Essential Duties and Responsibilities

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

• Act as the primary point of contact with internal administrative functions to include Procurement, Finance, and Legal to enable the execution of the clinical activities.
• Serve as the main document control coordinator ensuring proper version control during critical document reviews and subsequent publication. 
• Assist with oversight of outside vendors, consultants, and clinical research organizations (CROs) and coordinate the needed interactions with internal vendors.
• Maintain, and continuously improve clinical veterinary operation functions. 
• Aid in developing additional tools and refining processes to ensure all clinical veterinary projects run efficiently and effectively.
• Ensure that assigned projects are properly monitored, and that data are accurate and collected uniformly among the various investigative study sites.
• Participate in regular meetings, follow-up on assigned tasks and issues, and transfer of important information to management.
• Assist in the coordination of all study activities, including start up, Investigator training, study conduct, site monitoring and close out.
• Assists Clinical Development with tasks required to conduct clinical veterinary studies during all phases of an assigned project or program.
• Assists in the authoring of clinical study protocols, amendments, deviations, and final reports as required.
• Utilize industry best practices, techniques, and standards throughout entire project execution for the timely completion of all clinical studies.
• Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.

• Bachelors’ degree in STEM is required.   
• Minimum 2 years as a clinical study coordinator/monitor in the pharmaceutical industry; preferably in the veterinary pharmaceutical industry. 
• Experience conducting/monitoring studies to Good Clinical Practice and/or Good Laboratory Practice standards.
• Experience with electronic data capture platform/ eClinical software.
• Experience working with Clinical Trial Management software platforms.
• Ability to multi-task and successfully handle multiple priorities simultaneously.
• A growth mindset with a proactive approach to challenges is a plus.
• Proven proficiency in Microsoft Office and use of cloud-based applications.  Proficiency in MS Word and scientific writing is a must. 
• Strong written, verbal communication and interpersonal skills with employees at all levels of an organization.
• Strong strategic and critical thinking skills; including problem solving.

Physical Environment and Requirements

• Ability to travel overnight up to 25%.
• Ability to be able to work remotely and have reasonable infrastructure to access the internet.
• Employee must be able to occasionally lift and/or move up to 15 pounds.

Expected Salary Range :

$91,300-$108,000

The salary range displayed is the minimum and maximum annual salary of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role.  Actual compensation for the role will be based on a number of different factors including but not limited to the candidate’s qualifications, education, knowledge, skills and experience.

American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

American Regent Inc. endeavors to make https://americanregent.com/Careers accessible to any and all users.  If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email hrtalentacquisition@americanregent.com.

Looking for an opportunity to make an impact?

At Leidos, we deliver innovative solutions through the efforts of our diverse and talented people who are dedicated to our customers’ success. We empower our teams, contribute to our communities, and operate sustainably. Everything we do is built on a commitment to do the right thing for our customers, our people, and our community. Our Mission, Vision, and Values guide the way we do business.

If this sounds like the kind of environment where you can thrive, keep reading!

Leidos National Security Sector combines technology-enabled services and mission software capabilities in the areas of cyber, logistics, security operations, and decision analytics to support our defense and intel customers’ mission to defend against evolving threats around the world. Our team’s focus is to ensure our customers have the right tools, technologies, and tactics to keep pace with an ever-evolving security landscape and succeed in their pursuit to protect people and critical assets.

Your greatest work is ahead!

The CSS Operation at Leidos is seeking a motivated individual to work in a dynamic environment with a team of Cyber Engineers in reverse engineering, vulnerability research, prototyping, design, development, integration, and test tasks to develop capabilities against various networking devices.  This work will leverage your ability to deconstruct and tear-down of a variety of hardware and software, focusing on network devices and technologies, and developing capabilities to utilize the vulnerabilities discovered. The candidate must be experienced in working with a dynamic team of cyber researchers and engineers through all stages of the product lifecycle – from vulnerability research to development and test. This position is contingent upon contract award.

What you’ll be doing:

• Active Top Secret/SCI (TS/SCI) security clearance required. Must be U.S. Citizen.
• Lead requirements, design, introduce innovation, collaborate with the customer.
• Software development for complex solutions.
• Manage Sprints and assist with monitoring schedules/deliverables.

What does Leidos need from me?

• Bachelor’s Degree in computer science, information systems or applicable engineering field and minimum ten years of experience in computer science, information systems, or network engineering.
• Minimum eight years of experience programming in Assembly, C, C++, Java, Perl, and/or Python.
• Minimum five years of experience programming cyber tools and/or techniques for the US Government or commercial sector.
• Experience performing open source research & vulnerability analysis.
• Experience utilizing reverse engineering tools such as IDA Pro to analyze firmware of embedded devices.
• Experience with disassembly of hardware.
• Experience using commercial off the shelf (COTS), and free open source (FOS) debugging and analyzer tools.
• Ability to analyze network traffic for vulnerabilities.
• Demonstrated experience with scripting and programming languages.
• Experience developing documentation and reports (analysis reports, test reports, etc.).
• Demonstrated ability to develop and deliver briefings, technical presentations, and program documentation to senior program management.

Favorable if you have:

• Experience applying an Agile methodology to the development of CNO capabilities.
• Experience in protocol and signal analysis utilizing tcpdump or Wireshark.
• Familiar with Advance Networking Concepts to include one or more of the following: MPLS, OSPF, BGP, IS-IS, NAT, VPN, VLAN, or VRF.
• Demonstrated experience programming techniques to evade host and/or network-based intrusion detection systems.
• Demonstrated experience developing programs to capture, analyze, and interpret raw network traffic.
• Demonstrated experience with network sockets programming including developing packet-level programs, expert packet-level understanding of IP, TCP, and application-level protocols.
• Demonstrated understanding of IP, TCP, and application-level protocols.

Original Posting Date:

While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above.

Pay Range:

The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

Job Title

Job Description Summary

Job Description

Responsibilities:

• Gather, analyze, interpret, and present  real estate trends and information for business development opportunities, client support, and internal analysis for the office and industrial markets
• Compile and distribute research in the form of narratives, graphics, data summaries, etc. for internal (Brokers, Property Managers, Marketing)
• Analyze market statistics, generate market reports and/or collateral material based on statistical analysis conducted
• Interface with national research resources to produce standardized market reports and customized client research
• Educate internal clients on available research tools and resources
• Develop and maintain a proprietary commercial real estate database ensuring consistently accurate and current data
• Create and analyze spreadsheets utilizing data needed to generate graphs, tables, and written analysis and make recommendations to the Director of Research
• Generate statistics, tables, and graphs used in quarterly market and statistical reports
• Create quarterly market reports to include written analysis  explaining statistics and market activity, which may include drafting quarterly write-up
• Compile statistical data specific to client or service line by translating and converting data to graphs/tables/charts

Qualifications:

• Bachelor's Degree; Industry related field of study preferred
• 1+ years of real estate research or related business experience
• Or any similar combination of education and experience
• Experience in data entry/data management
• Proficient in Microsoft Office Suite
• Strong data software applications skills
• Demonstrated ability to work independently to meet goals and objectives
• Proven record of providing excellent internal and external customer service
• Excellent verbal and written communication skills
• Effective listening and critical thinking skills

In compliance with the Americans with Disabilities Act Amendments Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a position at Cushman & Wakefield, please call the ADA line at 1-888-365-5406 or email HRServices@cushwake.com. Please refer to the job title and job location when you contact us.

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.

We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As the Sr Clinical Project Lead, you will be responsible for overseeing, designing, planning, conducting, and reporting on clinical studies, supporting life cycle management activities, post-market studies and training Medical Affairs teams located remotely in the United States!

Key Responsibilities:

• Crafting and providing oversight of clinical research programs to deliver study outcomes within schedule, budget, quality/compliance and performance standards, and ensuring the studies meet scientific objectives, and are aligned with commercial needs.

• Serves as single point of contact in core teams in R&D, leads Clinical Sub-Teams, and acts as the medical/scientific consultant to marketing or research project teams and government regulatory agencies.

• Contributes to operational excellence through process improvement and knowledge sharing.

• Provides clinical functional review and expertise on the assigned projects/tasks, updates on clinical study progress and performance metrics.

• Forms relationships with key opinion leaders and applies their input to improve study design, protocols, and identified initiatives as appropriate.

• Leads the planning, conduct, and reporting of clinical studies throughout the product development and life cycle management including development of scientific publications and peer reviewed manuscripts.

• May be responsible for site or vendor selection as appropriate, post-marketing studies, and training for customer facing Medical Affairs associates worldwide.

Key Requirements/Minimum Requirements

• Bachelor’s Degree or Equivalent years of directly related experience (or high school+15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs)

• The ability to fluently read, write, understand, and communicate in English.

• 7 Years of Proven Experience

Travel Requirements: 20%

Relocation Assistance: No

Sponsorship Available: No

Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

Job Description Summary

Job Description

Primary Work Location

Additional Locations

Work Shift

Graco manufactures and markets premium equipment to move, measure, control, dispense and spray a wide variety of fluid and powder materials. What does that mean? Well, we pump peanut butter into your jar, and the oil in your car. We glue the soles of your shoes, the glass in your windows and the screen on your phone. We spray the finish on your vehicle, coatings on your pills, the paint on your house and texture on your walls. Graco is part of your daily life.

Graco’s Industrial Division is a fast-paced, high-performing, and growing business, with global operations and hundreds of millions of dollars in annual sales. Our equipment helps solve some of the world’s most complex manufacturing challenges. Graco technology is used by automotive companies to achieve the highest quality paint finishes; electronics manufacturers rely on our solutions to manage heat inside 5G equipment and gaming consoles; battery producers use our technology to get the extra mile out of electric vehicles; and Graco enables solar panel manufacturers to increase efficiency while reducing footprint, just to name a few applications. Many of our end user customers are household names that are synonymous with technology thought leadership.  Graco’s Industrial Team is built for performance, innovation and service within these markets, with Leading Technology and Proven Quality.

Job Purpose

To assist experienced mechanics efficiently performing maintenance and repair on Company assembly equipment, machine tools, machining equipment, and manufacturing equipment by using cost-saving strategies and ensuring Graco quality standards are met.

Essential Duties

• Perform preventative maintenance and simple repairs of all company-owned machine tools, assembly equipment, and Graco-owned manufacturing assets.

• Perform simple testing and repair in the area of hydraulics, mechanical elements, electrical, and electronics.

• Promptly respond to customer maintenance requests concerning equipment breakdowns.

• Troubleshoot issues to determine the course of action and consult with CNC Mechanic A for advice if necessary.

• Provide support to departmental personnel as workload dictates.

• Keep accurate maintenance records.

• Order parts/supplies and maintain inventory accuracy.

• Meet operational requirements and expectations for accuracy of work, while minimizing waste by caring for product, equipment, and facilities.

• Maintain a productive and efficient work environment.

• Follow all required safety guidelines and utilize the proper personal protective equipment (PPE).

• Perform other duties as assigned.

Position Requirements

Education & Experience:

• Associates degree in maintenance/maintenance-related field (electrical, electronics, hydraulics, fluid power, or robotics, etc.) and meet experience requirements.

• 0 – 1+ years of machine maintenance experience.

Requirements with No Degree –

• Must meet experience requirements.  If no degree must start associate's degree in maintenance or related field to be eligible for promotion to next pay grade.

• 4+ years machine/mechanical maintenance experience (no degree) OR currently enrolled in an associate's degree program for at least 1 year OR more than 2 years experience at Graco in a maintenance capacity.

Knowledge, Skills & Abilities:

• Mechanical aptitude.

• Understand safety rules and regulations to prevent unsafe set-ups, operations, or acts, which might cause injury to self, others, or the environment.

• Read and understand mechanical prints and electrical schematics.

• Ability to work independently.

• Ability to take work direction and complete tasks in an organized and timely manner.

• Good written, verbal, and interpersonal communication skills.

#LI-EG1

Power to Be

At Graco, the Power to Be means providing the support, resources and freedom to pave your own way. Bring your unique attributes to the table, along with a commitment to being your best self, and you can be a part of a culture that rewards effort, celebrates uniqueness, and gives you the tools you need to succeed and become your best, fullest self along the way. Our culture empowers employees to chart their own career path. Our managers provide support and opportunities while offering freedom for employees to find their own Power to Be. Whether you decide to move up within the same department or expand to another cross-functional group, you will gain the well-rounded experience to succeed on your own terms.

Graco has excellent opportunities available to individuals who want to be part of a fast-moving, growing company that is committed to quality, innovation and solving fluid handling problems for our customers. Graco is proud to be named a Best Place to Work by Fortune Magazine in 2016, 2018, 2019, 2021 & 2022. Graco offers attractive compensation, benefits and career development opportunities. Graco’s comprehensive benefits include medical, dental, stock purchase plan, 401(k), tuition reimbursement and more.

Our company uses E-Verify to confirm the employment and eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.

Proven Quality. Leading Technology. Launch your career with Graco!

Job Title

Job Description

Federal Accounts Manager (AM&D) - Northeast

The Federal Accounts Manager will primarily be responsible for orchestrating the sales process from lead identification, prospect new business, maintain and grow existing government accounts and ensure sales strategies meet revenue objectives while promoting Philips ECG Solutions products and services.

 Federal Accounts Manager (AM&D)

• Build and forge strong relationships throughout the respective geographic responsibility and represent Philips ECG Solutions professionally in all client and prospect interactions to extend the One Philips Solution.

• Drive sales revenue and overall market share within the government as well as nurturing existing accounts. Serve as the primary contact with all government accounts across the territory and provide updates and sales reports to the Emerging Markets Leader regarding territory status, including forecasts, sales proposals, and business reviews. 

• Implement a government territory business plan with clearly defined strategies and objectives. Communicate the company’s competitive differentiation and value proposition to enhance sales and convert competitive accounts.

• Responsible for government Requests for Proposals (RFPs) and Requests for Information (RFIs), VISN leadership business development, VA ECG Solutions Sales with collaboration on sales with other Philips Sales Divisions.

• Travel can be up to 50% within the territory.  

You’re the right fit if:

• You have a Bachelor’s degree or equivalent experience.

• You have Three (3) or more years’ sales experience reflecting a track record of proven success within the Medical Device and / or Biotechnology arena

• You have Four(4) or more years experience working in the government arena space.  Prior Military experience preferred

• You have a demonstrated track record of consistently meeting or exceeding an annual quota of more than $1M. Good understanding of government contracts, RFPs and standard bid requests.  Advanced selling capability that showcases commitment to sales and company strategy, customer satisfaction, negotiation, and ability to close. Significant experience in negotiating and closing new business and / or budgeting. Excellent strategic selling skills (strategy development and execution). Outstanding problem-solving skills and technical aptitude with Microsoft programs (PowerPoint, Excel). Well versed on concepts, practices and procedures related to field sales

• Strong interpersonal skills with the ability to develop and maintain productive, cooperative, and interdependent working and business relationships. Exemplary presentation skills with the ability to present in front of large and small groups of people.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
• Read more about our employee benefits.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

Philips Transparency Details

Total Target Earnings is composed of base salary + target incentive. At 85% to 120% performance achievement, the Target Earning potential is $156,500 to $198,00 annually, plus company fleet/car.  Total compensation may be higher or lower dependent upon individual performance. 

Target Earnings pay is only one component of the Philips Total Rewards compensation package, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.  Details about our benefits can be found here.

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position.  For this position, you must reside in or within commuting distance to the Northeast US and near a metropolitan airport.

#LI-PH1

#LI-Remote

Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.

Job Title

Job Description

Federal Accounts Manager (AM&D) - West

The Federal Accounts Manager will primarily be responsible for orchestrating the sales process from lead identification, prospect new business, maintain and grow existing government accounts and ensure sales strategies meet revenue objectives while promoting Philips ECG Solutions products and services.

 Federal Accounts Manager (AM&D)

• Build and forge strong relationships throughout the respective geographic responsibility and represent Philips ECG Solutions professionally in all client and prospect interactions to extend the One Philips Solution.

• Drive sales revenue and overall market share within the government as well as nurturing existing accounts. Serve as the primary contact with all government accounts across the territory and provide updates and sales reports to the Emerging Markets Leader regarding territory status, including forecasts, sales proposals, and business reviews. 

• Implement a government territory business plan with clearly defined strategies and objectives. Communicate the company’s competitive differentiation and value proposition to enhance sales and convert competitive accounts.

• Responsible for government Requests for Proposals (RFPs) and Requests for Information (RFIs), VISN leadership business development, VA ECG Solutions Sales with collaboration on sales with other Philips Sales Divisions.

• Travel can be up to 50% within the territory.  

You’re the right fit if:

• You have a Bachelor’s degree or equivalent experience.

• You have Three (3) or more years’ sales experience reflecting a track record of proven success within the Medical Device and / or Biotechnology arena

• You have Four(4) or more years experience working in the government arena space.  Prior Military experience preferred

• You have a demonstrated track record of consistently meeting or exceeding an annual quota of more than $1M. Good understanding of government contracts, RFPs and standard bid requests.  Advanced selling capability that showcases commitment to sales and company strategy, customer satisfaction, negotiation, and ability to close. Significant experience in negotiating and closing new business and / or budgeting. Excellent strategic selling skills (strategy development and execution). Outstanding problem-solving skills and technical aptitude with Microsoft programs (PowerPoint, Excel). Well versed on concepts, practices and procedures related to field sales

• Strong interpersonal skills with the ability to develop and maintain productive, cooperative, and interdependent working and business relationships. Exemplary presentation skills with the ability to present in front of large and small groups of people.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
• Read more about our employee benefits.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

Philips Transparency Details

Total Target Earnings is composed of base salary + target incentive. At 85% to 120% performance achievement, the Target Earning potential is $156,500 to $198,000 annually, plus company fleet/car.  Total compensation may be higher or lower dependent upon individual performance. 

Target Earnings pay is only one component of the Philips Total Rewards compensation package, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.  Details about our benefits can be found here.

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position.  For this position, you must reside in or within commuting distance to Western US.

#LI-PH1

#LI-Remote

Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.

At Pitney Bowes, we do the right thing, the right way.

Bei Pitney Bowes können Sie das auch.

Wir schaffen dies mit besonderem Fokus auf die vier Stützpfeiler von Pitney Bowes: client. team. win. innovate.

Unsere tollen Kolleginnen und Kollegen sind das Fundament, die Inspiration und die treibende Kraft unseres Unternehmens.

Wir freuen uns auf Kolleginnen und Kollegen, die:
•    sich leidenschaftlich für den Kundenerfolg einsetzen.
•    Freude an der Zusammenarbeit haben.
•    danach streben, Erwartungen zu übertreffen.
•    mutig vorangehen auf der Suche nach hervorragenden und marktorientierten Lösungen.

Job Description:

Zur Verstärkung unseres Team von Service Technikern suchen wir einen

Mechatroniker/Servicetechniker im Außendienst (m/w/d)

für digitale Postbearbeitungs-Systeme und andere spannende technische Geräte

Wohnort: Raum Brandenburg / Berlin.

Einsatzgebiet: PLZ-Gebiete 01-19

Vollzeit (40 Std. pro Woche) und unbefristet

Diese abwechslungsreichen Aufgaben warten auf Sie:

• Ihr Start erfolgt mit einer gründlichen Einarbeitung durch unser erfahrenes Team und Produkt-Schulungen in unserem Trainingscenter in Darmstadt.
• Vernetzen Sie sich durch Ihr Firmen-iPad oder iPhone und Sie sehen, genau welche Aufgaben bei unseren Kunden auf Sie warten. Sie können sich zusätzlich jederzeit mit Ihrem Team abstimmen.
• Und wenn es mal „brennt“ und Sie nicht mehr weiterkommen, helfen Ihnen unsere Supportteams durch zielgerechte Eskalationsstufen.

Es fällt Ihnen leichter, wenn Sie

• eine technische Grundausbildung, z.B. als Mechatroniker und wertvolle Erfahrungen als Servicetechniker im Außendienst mitbringen.
• sich in der Mechanik und vor allem in Elektro- und Netzwerktechnik gut auskennen.
• Ihnen analytisches Denken Spaß macht.
• mit Freude, Respekt und offenen Augen Ihren Kunden gegenübertreten und sie beraten können.
• sich so zu organisieren wissen, dass Ihr Kunde nicht warten muss und Sie alles Notwendige dabeihaben.

Was Sie neben diesen abwechslungsreichen Aufgaben bekommen:

• Ein attraktives und marktgerechtes Gehalt
• Ford/Skoda Kombi, den Sie selbstverständlich auch privat nutzen dürfen
• Hochwertige Werkzeuge und optimale technische Ausrüstung incl. iPhone, iPad
• Schritt für Schritt Einarbeitung durch qualifizierte Kollegen
• Freiheit bei der Umsetzung Ihrer Ideen
• Ein breites Weiterentwicklungs- und Schulungsprogramm
• Kostenloses E-Learning Angebot zur persönlichen Weiterbildung
• Eine attraktive betriebliche Altersversorgung
• Persönliche Unterstützung in unserem Mitarbeiter Assistance Programm
• Ein interessanter Job in einem über 100-jährigen, innovativen und erfolgreichen Konzern
• Unbefristeter Arbeitsvertrag, 30 Tage Urlaub plus Sonderurlaub

Werden Sie Teil eines internationalen Konzerns und gestalten Sie Ihre Zukunft gemeinsam mit uns! 

Wir bei Pitney Bowes verstehen Diversität und Inklusion schon lange in all ihren Facetten als Bereicherung für unsere Teams. Chancengleichheit ist uns seit Jahrzehnten ein besonderes Anliegen, die Gleichbehandlung von Menschen ein grundlegendes Prinzip unserer Unternehmenspolitik.

Wir freuen uns über Bewerbungen von Menschen mit Behinderung.

Wenn wir Ihr Interesse wecken konnten, freuen wir uns auf Ihre Bewerbung an Birgit Correll: birgit.correll@pb.com oder direkt über unsere Karriereseite auf www.pitneybowes.com/de.

Pitney Bowes Deutschland GmbH

Poststraße 4-6

64293 Darmstadt

Germany

Unser Versprechen:

• Die Möglichkeit sich weiterzuentwickeln und Ihre Karriere voranzutreiben.
• Ein integratives Umfeld, das unterschiedliche Perspektiven und Ideen fördert.
• Herausfordernde und einzigartige Möglichkeiten, um zum Erfolg einer sich wandelnden Organisation beizutragen.
• Weltweit umfassende Benefits (PB Live Well)

Key Role:

Work closely with a variety of clients to capture and document information requirements, formulate data collection plans, and implement normalization processes. Interpret results independently using a variety of techniques, ranging from simple data aggregation to more complex data analysis. Work with the client and project leadership to identify analytical requirements and synchronize, integrate, and operate working R model. Adapt quickly to comprehend requirement and model constraints and needs and resolve those challenges, applying data analysis expertise to create solutions through the application of appropriate analytical techniques and methods.  

Basic Qualifications:

• 2+ years of experience working directly with clients to gather requirements, facilitate analysis, and deliver high quality results

• Experience deconstructing analysis, showing analytic process and methodology, validating the tools used to create analysis, and making recommendations based on analysis

• Secret clearance

• Bachelor's degree

Additional Qualifications:

• Experience with analysis at strategic and operational levels

• Experience with data science

• Experience with R and R Shiny

• Experience using Microsoft Excel and PowerPoint

• Knowledge of basic statistics

• Knowledge of data visualization tools

• Possession of excellent data-gathering, analytical, and problem-solving skills

• Top Secret clearance

Clearance:

Applicants selected will be subject to a security investigation and may need to meet eligibility requirements for access to classified information; Secret clearance is required.

Create Your Career: 

Grow With Us 

Your growth matters to us—that’s why we offer a variety of ways for you to develop your career. With professional and leadership development opportunities like upskilling programs, tuition reimbursement, mentoring, and firm-sponsored networking, you can chart a unique and fulfilling career path on your own terms.  

A Place Where You Belong 

Diverse perspectives cultivate collective ingenuity. Booz Allen’s culture of respect, equity, and opportunity means that, here, you are free to bring your whole self to work. With an array of business resource groups and other opportunities for connection, you’ll build your community in no time. 

Support Your Well-Being 

Our comprehensive benefits package includes wellness programs with HSA contributions, paid holidays, paid parental leave, a generous 401(k) match, and more. With these benefits, plus the option for flexible schedules and remote and hybrid locations, we’ll support you as you pursue a balanced, fulfilling life—at work and at home.  

Your Candidate Journey 

At Booz Allen, we know our people are what propel us forward, and we value relationships most of all. Here, we’ve compiled a list of resources so you’ll know what to expect as we forge a connection with you during your journey as a candidate with us.  

Compensation

At Booz Allen, we celebrate your contributions, provide you with opportunities and choices, and support your total well-being. Our offerings include health, life, disability, financial, and retirement benefits, as well as paid leave, professional development, tuition assistance, work-life programs, and dependent care. Our recognition awards program acknowledges employees for exceptional performance and superior demonstration of our values. Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible to participate in Booz Allen’s benefit programs. Individuals that do not meet the threshold are only eligible for select offerings, not inclusive of health benefits. We encourage you to learn more about our total benefits by visiting the Resource page on our Careers site and reviewing Our Employee Benefits page.

Work Model
Our people-first culture prioritizes the benefits of flexibility and collaboration, whether that happens in person or remotely.

• If this position is listed as remote or hybrid, you’ll periodically work from a Booz Allen or client site facility.
• If this position is listed as onsite, you’ll work with colleagues and clients in person, as needed for the specific role.

EEO Commitment

We’re an equal employment opportunity/affirmative action employer that empowers our people to fearlessly drive change – no matter their race, color, ethnicity, religion, sex (including pregnancy, childbirth, lactation, or related medical conditions), national origin, ancestry, age, marital status, sexual orientation, gender identity and expression, disability, veteran status, military or uniformed service member status, genetic information, or any other status protected by applicable federal, state, local, or international law.

The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.

Moderna is seeking a Medical Science Liaison for North Germany, based in the Hamburg area, to develop key relationships with healthcare practitioners and support mRNA platform development. This role focuses on scientific engagement, clinical research support, and maintaining compliance with medical and regulatory standards. It offers the opportunity to work at the forefront of innovative medicine, collaborating with professionals in the vaccination community and other therapeutic areas.

Here's What You’ll Do:

Within 3 Months, You Will…

• Initiate and cultivate strategic peer-to-peer relationships with key healthcare practitioners (HCPs) in the vaccination community across the regions of Niedersachsen, Bremen, Schleswig-Holstein, Hamburg, and Mecklenburg-Vorpommern.

• Conduct detailed study and familiarization with Moderna’s mRNA technology platform, focusing on its application in various therapeutic areas, particularly in vaccination.

• Engage actively in presenting scientific data to healthcare professionals, tailoring the delivery to suit the audience, and ensuring clarity and compliance with scientific accuracy.

• Respond promptly and accurately to medical information requests from HCPs, ensuring all communications are in line with Moderna’s standards and regulatory guidelines.

• Start reporting any adverse events (AEs) and/or Product Quality Complaints (PQC) encountered in the field, ensuring timely and compliant documentation and communication of such incidents.

Within 6 Months, You Will…

• Develop and implement personalized HCP Engagement Plans, catering to the unique needs and interests of key healthcare practitioners in your region, in alignment with Moderna’s strategic goals.

• Expand your knowledge and understanding of clinical development processes, with a particular focus on rare diseases and vaccines, integrating this knowledge into your daily activities and discussions.

• Take an active role in coordinating and managing regional Medical Affairs initiatives, including educational programs, advisory boards, and medical conferences, fostering Moderna’s presence and reputation in the medical community.

• Work closely with physicians and other medical experts to facilitate medical education opportunities and develop advisory boards, ensuring the scientific integrity and relevance of these initiatives.

• Begin to develop training materials and content for internal stakeholders, highlighting key scientific and medical topics relevant to Moderna’s therapeutic areas.

Within 12 Months, You Will…

• Be fully integrated into the role, recognized as a key driver in medical science liaison activities and research initiatives within your region, contributing significantly to Moderna’s presence and influence in the healthcare community.

• Offer comprehensive scientific support and training to internal stakeholders, including sales and marketing teams, enhancing their understanding and ability to communicate Moderna’s scientific advancements effectively.

• Play an instrumental role in shaping and contributing to the strategic medical direction in North Germany, leveraging insights and relationships to inform company strategies and initiatives.

• Actively involve yourself in clinical trial activities, suggesting HCPs for participation in company-sponsored studies, providing scientific training at Site Initiation Visits, and ensuring clear role definition and responsibilities in collaboration with Clinical Research Associates (CRAs) and Medical Monitors.

• Continuously communicate insights gained from field interactions to the Medical Affairs Department, aiding in the refinement of medical strategies for Moderna’s therapeutic areas.

Here’s What You’ll Bring to the Table:

• Advanced scientific degree required– MD, PhD, PharmD, or MSc

• Minimum of 4 years of experience in Medical Affairs or Medical Science role

• Robust and current clinical development experience supporting drugs to treat rare diseases; prior vaccines/infectious disease(s) experience preferred

• Candidates will ideally have well-established networks, understanding of decision-making structures and active relationships with HCPs in the therapy area.

• Candidate must have a strong understanding of compliance frameworks and demonstrable ability to work compliantly in a field-based role, within the medical organization, as well as interacting with the commercial organization

• Proven ability to take initiative, determine priorities and exercise good judgment

• Ability to recognize opportunities/gaps/obstacles, then take ownership to find creative, innovative solutions that question convention, and then see them through to completion

• Accepts new challenges with curiosity and drive while remaining positive in the face of obstacles

• Strong interpersonal and relationship building skills

• Fluency in German and English

• Ability and willingness to travel up to 75% within assigned region

• Valid Driver's license

• Working knowledge of virtual presentation platforms, social media and Microsoft Office Suite (Word, PowerPoint, and Excel)

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:

• Quality healthcare and insurance benefits
• Lifestyle Spending Accounts to create your own pathway to well-being
• Free premium access to fitness, nutrition, and mindfulness classes
• Family planning and adoption benefits
• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
• Educational resources
• Savings and investments
• Location-specific perks and extras!

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. 

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com.  (EEO/AAP Employer) 

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The Role:

We are seeking a talented and experienced Director to lead our in vivo pharmacology research team. The successful candidate will play an integral role across our oncology research groups, overseeing the development of relevant in vivo animal and cell models, and the design and execution of pharmacology studies to propel our pre-clinical research and early development oncology pipeline in addition to Translational initiatives, such as in vivo combination evaluations. The Director will manage all internal and/ or external in vivo workflows, collaborating with various teams within Moderna, including Cancer Vaccine Research, Immuno-Oncology Research, and Research Operations. The ideal candidate will be a proven and effective team leader and people manager, highly collaborative team player, possess excellent communication skills, have a proven track record of independent research achievements, and bring innovative approaches to further our mission.

Here’s What You’ll do:

• Direct the execution and analysis of in vivo pharmacology studies that support oncology programs and platform initiatives

• Develop and refine in vivo murine tumor models and study protocols, ensuring compliance with regulatory, ethical, and quality standards; including serving as Principal Investigator on internal in vivo pharmacology protocols

• Identify new tumor models and new techniques that will further advance mRNA therapies

• Work closely with internal teams to optimize in vivo study designs and oversee their execution, whether conducted in-house or through external partners

• Establish and maintain partnerships with Contract Research Organizations (CROs), industry partners and academic institutions for all in vivo studies

• Manage the analysis, review, and summary of in vivo pharmacology data to ensure robustness as well as integration into big picture considerations

• Contribute to and co-author scientific reports for inclusion in regulatory submissions, internal and external presentations

• Lead and allocate team resources and timelines to ensure the efficient progression of studies and achievement of objectives across multiple programs and oncology-focused teams

Here’s What You’ll Bring to the Table:

• Advanced degree in Pharmacology, Oncology, or a related scientific field, with a PhD or DVM and at least 9+ years relevant experience

• Demonstrated expertise in in vivo pharmacology within oncology drug discovery and early development, preferably with a focus on nucleic acid therapeutics and vaccines

• Deep knowledge of immuno-oncology including current and emerging standards of care to inform forward translational studies

• Experienced in the creation and use of diverse in vivo cancer models for efficacy and PK/PD studies, including advanced local, systemic, disseminated, and orthotopic syngeneic, xenograft and genetically engineered murine models

• Knowledge in overseeing relevant cell model development to be deployed in vivo

• Highly experienced in in vivo study management, including pharmacological agent administration via IV, IP, SC, iTu, IM, and PO dosing routes including vaccination protocols; regular health and tumor growth monitoring; bioluminescence/fluorescence imaging using IVIS systems; necropsy and tissue collections

• Experienced in authoring, implementing and ensuring compliance to study protocols under IACUC guidelines

• Ability to mentor and develop junior scientists and research associates, and guide teams to successfully conduct in vivo studies, trouble shoot, and grow technically and scientifically

• Skilled in outsourcing studies and fostering productive relationships with CROs and/or academic collaborators

Additional Preferred Qualifications:

• Experience with cell line engineering, humanized models, or surgical/ resection models  

• Familiarity with regulatory guidelines and Good Laboratory Practice (GLP) standards

• Experience with bioinformatics tools relevant to pharmacology and oncology research

•  Facility with data analysis software tools such as GraphPad Prism

• Exceptional organizational abilities, attention to detail, scientific adaptability, and a results-driven approach

• Superior written and verbal communication skills, with the capacity to effectively engage with multiple teams

• A respectful, inclusive, and collaborative mindset, complemented by boldness, creativity, curiosity, and relentlessness

Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:

• Highly competitive and inclusive medical, dental and vision coverage options
• Flexible Spending Accounts for medical expenses and dependent care expenses
• Lifestyle Spending Account funds to help you engage in personal enrichment and self-care activities
• Family care benefits, including subsidized back-up care options and on-demand tutoring
• Free premium access to fitness, nutrition, and mindfulness classes 
• Exclusive preferred pricing on Peloton fitness equipment
• Adoption and family-planning benefits
• Dedicated care coordination support for our LGBTQ+ community
• Generous paid time off, including:
  •    Vacation, sick time and holidays
  •    Volunteer time to participate within your community
  •    Discretionary year-end shutdown
  •    Paid sabbatical after 5 years; every 3 years thereafter
• Generous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents
• 401k match and Financial Planning tools
• Moderna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
• Complimentary concierge service including home services research, travel booking, and entertainment requests
• Free parking or subsidized commuter passes
• Location-specific perks and extras!

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. 

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com.  (EEO/AAP Employer) 

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Reporting to CSO, External Research Ventures of Moderna, the Senior Director (SD) of Pulmonary Research is responsible for overseeing our therapeutic pulmonary research projects as well as leading and managing our external pulmonary research collaborations.  The SD of Pulmonary Research will be responsible for building our internal pulmonary capabilities and expertise, overseeing mRNA drug discovery projects into preclinical development, and driving the strategy for this emerging therapeutic area.  The SD will work closely with multiple internal stakeholders across functions including Platform, Nonclinical Sciences, Translational, Clinical Development, and R&D Strategy in addition to key external stakeholders involved in our external collaborations.  This is a superb opportunity for a highly motivated leader with pulmonary drug discovery expertise to join our dynamic team and impact our early pipeline.

Here’s What You’ll Do:

• Build and establish internal pulmonary capabilities and expertise to enable the inhaled pulmonary modality and therapeutics area
• Lead and direct a range of internal pulmonary therapeutic research projects.  Define objectives for research projects and ensure high-quality execution of these projects, including oversight of assays, study designs, and data
• Advance pulmonary therapeutic research projects into early development
• Oversee and manage relationships with external partners and collaborators.  Serve as Program Lead for external collaboration, effectively managing a large cross-functional internal team and working closely with external stakeholders to scientifically direct collaborations
• Mentor and have direct management responsibilities for the pulmonary research team
• Stay up-to-date with the latest scientific advances in pulmonary research and identify opportunities to incorporate new research methods and technologies
• Promote cross-functional collaboration across the organization
• Effectively communicate research progress, challenges and results to a variety of stakeholders, including teams across R&D organizations

Here’s What You’ll Bring to the Table:

• Ph.D. in pulmonary pharmacology, respiratory medicine, or related field with 12 years of relevant experience in pulmonary research in industry setting
• Strong pulmonary physiology and pharmacology experience
• Excellent leadership and team building skills.
• Strong track record driving discovery projects into early development and leading successful research teams and projects
• Proven ability to oversee and manage strategic partnerships and collaborations.
• Deep understanding of the scientific aspects of drug discovery and development
• Excellent leadership and team building skills.
• Strong written and oral communication skills scaling through all levels of the organization, including senior management.
• Strong leadership skills and an ability to collaborate productively across multiple cross-functional project teams are paramount.
• Ability to thrive in a fast-paced environment; ability to adapt to changes with demonstrated flexibility to pivot as warranted and needed.
• Acts with urgency with the understanding that actions today compound lives saved tomorrow.
• Acts like an owner, obsesses over learning, questions convention, and strives to push past possible.
• Scientific rigor & commitment to excellence and innovation.

Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:

• Highly competitive and inclusive medical, dental and vision coverage options
• Flexible Spending Accounts for medical expenses and dependent care expenses
• Lifestyle Spending Account funds to help you engage in personal enrichment and self-care activities
• Family care benefits, including subsidized back-up care options and on-demand tutoring
• Free premium access to fitness, nutrition, and mindfulness classes 
• Exclusive preferred pricing on Peloton fitness equipment
• Adoption and family-planning benefits
• Dedicated care coordination support for our LGBTQ+ community
• Generous paid time off, including:
  •    Vacation, sick time and holidays
  •    Volunteer time to participate within your community
  •    Discretionary year-end shutdown
  •    Paid sabbatical after 5 years; every 3 years thereafter
• Generous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents
• 401k match and Financial Planning tools
• Moderna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
• Complimentary concierge service including home services research, travel booking, and entertainment requests
• Free parking or subsidized commuter passes
• Location-specific perks and extras!

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. 

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com.  (EEO/AAP Employer) 

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Job Description Summary

Job Description

We are the makers of possible 

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. 

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. 

Job Group/Grade: JG1, H06

D Shift: 6pm-6am  

Position Summary:             

Produce quality molding components at the rate or goal set for each line while working as a team with other operators.  Keep area and machines clean.  Complete quality checks at the frequency required.  Ensures compliance with BD quality systems, policies, procedures and best practices, and all local, state, federal and BD safety regulations, policies and procedures.  Regular, punctual attendance is an essential job function.  Ability to read and write and converse in English.  Willing and able to uphold BD Values. 

Duties/Responsibilities:     

• Continually monitor operations for product quality and equipment performance 

• Transport material between molding area and Needle Assembly area as well as the storage area 

• Keep material cleared from auxiliary molding equipment to maintain steady flow of product 

• Stock line with raw materials necessary to assemble product 

• Supplement line with molded components as needed to prevent downtime 

• Keep machinery, work area, and floors neat and orderly to comply with GMP requirements 

• Perform daily and weekly cleanings of specific area 

• Perform quality inspections, process tests and record data accurately as required 

• Communicate with mold technicians and line operators on changeover times 

• Work as a team member to develop optimal task methods 

• Other duties as required to support the needs of the business 

Education: 

• High School diploma/GED preferred 

• In lieu of High School diploma/GED, two years manufacturing experience is required 

Experience:     

• None required 

Knowledge, Skills and Abilities

• Ability to keep and maintain detailed documentation/communication - Proficient 

• Teamwork – Proficient 

• Organization skills - Basic 

• PCP Level:   3 

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

At BD, we strive to make healthcare a priority for our associates and their families. We have a variety of plans including a new HSA Basic plan option with Cigna.

• $0 payroll contributions if your salary is below $50,000

• Plan covers 100% preventative care (annual wellness exam, and immunizations)

• Visit any provider

If you meet the eligibility and enrollment requirements, your coverage begins on your date of hire or the date you become a benefits-eligible associate.

BENEFITS:

BD provides comprehensive total rewards benefits for all of its employees. Most benefits start on day 1 of your employment with BD.

• Competitive pay

• Up to 6 weeks of paid parental leave

• Medical, dental, and vision insurance plans

• Education assistance ($5250.00 per year)

• Adoption assistance

• 401K plan with $.75 of every dollar matched up to 6% of compensation

• Basic life and AD&D provided

• Discounted home, auto, and pet insurance plans

• Paid holidays and vacation (pro-rated the first year based on actual start date)

Excited to grow your career?

We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!

Our people make all the difference in our success.

Why Join Us?

A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place. 

To learn more about BD visit https://bd.com/careers

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

Primary Work Location

Additional Locations

Work Shift

Why Patients Need You  

 Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.  

What You Will Achieve  

 Pfizer is making significant investment in the creation of novel, first-in-class therapeutics for the Pfizer pipeline.  We are seeking an exceptional in vitro pharmacologist and laboratory automation head to join the Primary Pharmacology Group (PPG) at our Groton, CT campus and drive expansion and strategic execution of Pfizer’s internal HTS capabilities for small molecule lead identification across the diverse Discovery & Early Development portfolio. Your work will play a key role in addressing the critical task of rejuvenating the Pfizer research pipeline with innovative, differentiated First in Class programs in the years to come. 
 
As an Associate Research Fellow, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will drive the rebuilding of Pfizer’s internal HTS capability within the Discovery Sciences department and its implementation. You will oversee the deployment of capital to assemble a state of the art screening infrastructure and build a dedicated team of scientists with relevant skills to ramp up internal HTS capabilities while leveraging external CROs as required. Thus, this role requires technical excellence in the execution of disease relevant pharmacology approaches to support HTS, laboratory automation, and data strategies. Additional desired areas of expertise include high content imaging or analytical expertise in mass spectrometry.  

The successful candidate will combine strong technical/scientific rigor, strategic planning, leadership and problem-solving skills with a demonstrated ability to build, energize and lead high-performing teams to drive impact across multiple drug discovery programs. This individual should therefore possess exceptional collaborative and written/verbal communication skills, a good sense of humor and be adept at building partnerships. The role will have high visibility across the research organization so an executive presence and ability to gain the respect of stakeholders is key.Through your expertise and extensive knowledge, you will be able to foster a culture that promotes innovation and thrives on doing better for patients and healthcare. 

How You Will Achieve It  

• We are seeking an experienced pharmacologist and automation specialist to build and lead the HTS laboratory to support small molecule drug discovery. The laboratory head will also be responsible for automation and data management and lifecycle strategies within PPG.

• As the HTS portfolio lead, you will be responsible for management, communication, and execution of the HTS portfolio as well as and the strategic vision for HTS moving forward. This will include extracting value from HTS data beyond immediate project needs.   
• This laboratory leader will maintain a ‘cutting edge’ awareness of technical developments and scientific advancements in the field and apply these innovatively to advance internal capabilities. The role includes opportunities to publish when appropriate.
• This HTS lead will lead interdisciplinary team(s) of biologists, medicinal chemists, and protein biochemists to effectively prosecute the HTS portfolio and actively interact with other groups in Discovery Sciences.
• As a laboratory supervisor, a commitment to coaching and guiding professional development is required.

Qualifications  

Must-Have  

• PhD in Molecular Biology, Biochemistry, Cell Biology, and/or Pharmacology with 10+ years post-degree experience, including industry experience
• Proven ability to build, lead, energize and develop a high-performing team of scientists.
• Demonstrated examples of strong scientific leadership, independent thought and creativity, and ability to integrally contribute to program strategies and execute plans.
• Experience successfully interacting with and meeting the needs of stakeholder groups is essential as well as having a customer focus.
• Demonstrated experience with multiple plate-based pharmacology formats (e.g. FRET, FACS, FP, ELISA, high content imaging, FLIPR, radioligand binding, nanoBRET etc.), mass spectrometry (HTMS, LC-MS, AEMS) including assay development and troubleshooting
• Demonstrated proficiency in laboratory automation and data analysis with excellent computer, verbal and written communication skills
• A strong publication and presentation record showcasing scientific leadership in pharmacology and drug discovery.

Nice-to-Have  

• Previous experience in multiple target classes (e.g. GPCRs, transporters, kinases, ion channels, DUBs, RNA) in a drug discovery setting
• Experience with phenotypic screening and hit deconvolution
• Demonstrated ability to forge strong collaborative and inclusive relationships inside and outside organizational walls and across multiple cultures: academic, industrial, and CROs

 
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
 

PHYSICAL/MENTAL REQUIREMENTS

Sitting, standing, lifting, bending, and walking.  Ability to perform practical laboratory bench work and work on a computer (while standing or sitting).  Ability to perform mathematical calculations and interpret data.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• Travel to attend appropriate meetings and conferences.
• Compliance with laboratory safety practices.

Relocation support available

Work Location Assignment: On Premise

Relocation assistance may be available based on business needs and/or eligibility.