Total 328 Quality Assurance / Control job vacancies in Camden, New Jersey

Job Summary

The Quality Assurance & Regulatory Affairs, Executive will report to the Regulatory Affairs & Quality Assurance, Manager and he/she will assume primary responsibility in providing quality assurance and control expertise to the Menarini team and Partners; and support the Regulatory Affairs & Quality Assurance, Manager in the regulatory affairs and quality assurance functions. He/she will also be responsible to undertake regulatory project management and ensure regulatory compliance in Singapore as required.

Job Responsibilities

• Prepare and conduct QMS audits with management review in accordance with SS 620 GDPMDS and/or HSA GDP requirements
• Prepare, review and maintain QMS required SOPs and ensure proper documentation in accordance with SS 620 GDPMDS and/or HSA GDP requirements
• Process and report product quality complaints/product defect to the authority, Regional and/or Partners. Review complaint investigations, CAPA plan and effectiveness review and monitoring of complaint trends and reporting the trends
• Manage deviations and CAPA and ensure timely investigation, closure and implementation
• Review and submit change controls to assess the impact of change and ensure timely implementation
• Liaise with distributor on the secondary repackaging requirements and prepare repackaging instructions and request forms
• Ensure product specifications, labels and related documentation are in alignment with current registered information
• Coordinate post marketing surveillance activities such as FSCA and product recalls
• Ensure compliance is in place for all product post market registration conditions
• Provide training for internal stakeholders on quality SOPs and ensure compliance with company policy
• Maintain database of registrations, change controls, deviations and product quality complaints
• Planning, preparing and submitting new marketing authorization applications for Singapore
• Planning, preparing and submitting post approval changes including variations, change notifications, renewals etc. for Singapore and work with relevant stakeholders to ensure business continuity
• Liaise with the local authorities to ensure timely regulatory approvals in meeting business plans
• Develop regulatory strategies during the preparation of new application, renewal and variation submissions to address gaps and communicate its impact
• Review and approve labels and promotional materials for regulatory compliance
• Supports any other relevant activities or as required

Requirements

• Candidate must possess at least a Bachelor's Degree in Science, Engineering or Pharmacy
• Understanding of regulatory standard related to cGMP, GDP, SS620, PIC/S, ISO 13485 and cold chain management
• Certified internal auditor for GDPMDS or ISO13485 is required
• Experience in audit, QA batch management, complaint management, deviation management, change control management, CAPA and recall management
• Minimum 2 years’ experience in commercial quality assurance in pharmaceutical or medical device industry
• Regulatory experience in therapeutic products, medical devices, cosmetics, traditional medicine and/ or health supplement is a bonus
• Ability to work both as an individual and as a team player
• Ability to influence and collaborate with people at all levels effectively
• Proficient in both oral and written English
• Computer literate
• Attention to details and results oriented
• Flexible and adaptive to changes

Interested applicants are invited to apply directly at the NUS Career Portal.

Your application will be processed only if you apply via NUS Career Portal.

We regret that only shortlisted candidates will be notified.

Job Description

AI Singapore (AISG) is a national AI programme launched by the National Research Foundation (NRF) to anchor deep national capabilities in Artificial Intelligence (AI).

The programme office is hosted by the National University of Singapore (NUS) and brings together all Singapore-based research institutions and the vibrant ecosystem of AI start-ups and companies developing AI products to perform use-inspired research, grow the knowledge, create the tools, and develop the talent to power Singapore's AI efforts.

We are seeking a part time staff who can assist in data creation, evaluating the collected data’s reliability, validity, and accuracy and improving the data quality.

Duties & Responsibilities

• Assisting with translation and data creation in Burmese language so proficiency in Burmese is a must.
• Evaluating the collected data’s reliability, validity and accuracy
• Verifying data by cross-checking with other sources
• Making recommendations for improving data quality

Qualifications

• Proficiency in Burmese as well as knowledge in Burmese culture due to usage of Burmese language for data collection and creation.
• Able to commit to the project for 6 months
• A Bachelor’s degree in any discipline

Job Scopes

• In charge of assist accounts payable and receivable

• Help with the preparation of monthly landed cost reports (Detention, Demurrage, Freight Charges, and Unstuffing Charges).

• Review and establish minimum selling prices for sales products, reporting to the director and business director

• Establish the item's asking price and manage its acquisition and subsequent sale.

• Assist with logistics to ensure stock balance in actual

• Calculate the cost of processing raw materials into the finished goods.

• Determine and advise strategies to lower the landed cost from shipping lines.

• Modify the system's data to ensure managers can forecast selling prices.

• Verify that the supplier's billing matches the sales confirmation.

• Dealing with bank applications for trade financing

• Monitoring the order desk to ensure for the correct selling price

• Assist in inventory stock take

• Planning for bid preparation for company

• Dealing with the supplier to confirm payment & Portnet release for the container

• Any other ad hoc tasked assigned by superior

Requirements:

• Minimum relevant diploma qualifications

• At least 2 years’ experience in handling full set of accounts preferred

• Ability to multi-task and work independently under pressure.

• Fluency in Chinese and English languages.

• Proficiency in Microsoft Office (Excel, Word).

Working Day:

5.5 working days

8:00am to 5.00pm (Mondays to Fridays)

8.00am to 12.00pm (Saturdays)

What’s the role?

Your primary accountabilities as a Process Control Senior Engineer includes:

• Improve robustness of Base Layer control performance, delivery of high uptime and low operator intervention rates.
• Conduct daily base layer performance monitoring, provide technical support and lead troubleshooting for control and safeguarding related issues.
• Maximize benefits from optimization applications through the implementation of unit wide Advanced Process Control (APC) and Real Time Optimization (including Advanced Analytics) systems.
• Sustain the performance of existing APC and optimization systems.
• Identify opportunities for improvements in the area of control strategy and control configuration.
• Design, modify and tune base layer controls and Advanced Process Control applications to maximize benefits and save energy.
• Support Production team activities for e.g. alarm management and ensure plan delivery
• Participate in design or safety review and provide process control and safeguarding related inputs to projects.
• Participate in major activities like factory acceptance and site acceptance tests for Distributed Control System (DCS), Oil Movement System (OMS) and Instrumented Protective System (IPS) systems and unit startup support.
• Contribute to multifunctional teams in site wide initiatives, such as unit shutdown/startup preparation and coordination.
• Lead and engage with other engineers from Shell to maximize value delivered from process automation, control and optimization technology.
• Guide and coach, the less experienced process control staffs and help develop their technical competences.
• Demonstrate strong learner mindset and commits to be digitally literate to drive value creation through digitalisation.

What we need from you

We are keen to speak to individuals with the following:

• Chemical engineer or similar background by either education or by experience
• Knowledge of oil/chemical manufacturing processes
• At least 6-8 years of relevant Process Control experience in oil/gas industry.
• Knowledge competency level for APC technology such as PACE
• Knowledge competency level with Yokogawa DCS system and ability to execute engineering changes.
• Be able to tune, design and implement process control loops independently.
• Excellent written and verbal communication skills, and interpersonal relation skills.
• Good collaboration and team working skills, with a keen ability to develop a good rapport with Process Operating teams.
• Be able to prioritize and manage expectations in the case of competing requests from stakeholders.
• Familiarity with Yokogawa DCS & Prosafe
• Knowledge in Process Automation Systems Engineering
• Knowledge in Safety Instrumented Systems and Safeguarding
• Knowledge in Advanced Process Control and Modelling & Real Time Optimization
• Knowledge in Compressor Control
• Skilled in Base Layer Control

If you don’t see yourself reflected in the job requirements on the posting above, we still encourage you to reach out and apply. Shell is committed to creating a more diverse, equitable and inclusive workplace and we encourage individuals of all backgrounds to send in your applications.

Company Description

Shell is an international energy company that uses advanced technologies and takes an innovative approach to help build a sustainable energy future. Here in Singapore, Shell has a long history and is one of the country’s largest foreign investors. It has businesses spanning trading and marketing of liquefied natural gas; refining, trading, marketing and shipping of oil products, lubricants and chemicals; low carbon solutions; and operating a network of service stations through retailers, as well as electric vehicles charging.

An innovative place to work

There’s never been a more exciting time to work at Shell.

Join us and you’ll be adding your talent and imagination to a business with the ambition to shape the future – whether by investing in oil, gas, and renewable energy to meet demand, exploring new ways to store energy, or developing technology that helps the world to use energy more efficiently, everyone at Shell does their part.

An inclusive place to work

To power progress, we need to attract and develop the brightest minds and make sure every voice is heard. Here are just some of the ways we are nurturing an inclusive environment – one where you can express your ideas, extend your skills, and reach your potential.

• We’re creating a space where people with disabilities can excel through transparent recruitment process, workplace adjustments and ongoing support in their roles. Feel free to let us know about your circumstances when you apply, and we’ll take it from there.
• We’re closing the gender gap – whether that’s through action on equal pay or by enabling more women to reach senior roles in engineering and technology.
• We’re striving to be a pioneer of an inclusive and diverse workplace, promoting equality for employees regardless of sexual orientation or gender identity.
• We consider ourselves a flexible employer and want to support you finding the right balance. We encourage you to discuss this with us in your application.

A rewarding place to work

Combine our creative, collaborative environment and global operations with an impressive range of benefits and joining Shell becomes an inspired career choice.

We’re huge advocates for career development. We’ll encourage you to try new roles and experience new settings. By pushing people to reach their potential, we frequently help them find skills they never knew they had, or make career moves they never thought possible.

This is a 4 months contract subject to renew.

This role responsibles for ensuring that all piping and welding work meets industry standards, regulations, and specifications. This role involves inspecting, testing, and verifying the quality and integrity of piping systems and welded joints to ensure they are constructed and maintained according to project requirements and safety standards.

Key Responsibilities:

· Inspection:

o Conduct thorough inspections of piping systems and welded joints to ensure compliance with industry codes, standards, and specifications.

o Review and interpret engineering drawings, schematics, and specifications to ensure correct implementation.

o Perform visual inspections, non-destructive testing (NDT), and other relevant testing methods.

· Testing:

o Execute various tests such as pressure tests, leak tests, and weld quality assessments.

o Document test results and maintain accurate records of inspections and findings.

· Compliance:

o Ensure all work adheres to relevant codes and regulations (e.g., ASME, API, ASTM).

o Verify that all materials and components used in piping and welding meet required specifications and standards.

· Reporting:

o Prepare detailed inspection reports, including findings, deviations, and recommendations.

o Communicate with project managers, engineers, and other stakeholders regarding inspection results and quality issues.

· Troubleshooting:

o Identify and report any defects or non-compliance issues and work with relevant teams to develop and implement corrective actions.

o Provide technical support and advice on welding and piping-related issues.

· Documentation:

o Maintain and organize inspection records, test results, and compliance documentation.

o Ensure proper documentation and certification for all inspected and tested components.

Requirements:

· Candidate must possess at least Professional Certificate/NiTEC, Diploma/Advanced/Higher/Graduate Diploma, Bachelor's Degree/Post Graduate Diploma/Professional Degree in Engineering or equivalent

· At least 5 Year(s) of working experience in the related field is required for this position

Responsibilities:-

• Person in charge of the workplace on environmental regulations pertaining to the Environmental Public Health (Registration of Environmental Control Officers) Regulations 1999 Person in charge of the workplace implementation and revision of Environmental Management in the worksite
• Act as an Earth Control Measures Officer (ECMO)
• Establish, update, maintain, and implement the Environmental Management System and Environmental Impact Aspect assessment
• Conduct / Plan site environmental inspection and ensure effective implementation and continual improvement on all environmental matters. Advise occupier of the workplace or other person in charge of the workplace on environmental health problems and recommend remedies to establish a healthy working environment
• Oversee the installation of noise meters at site vicinity and monitoring of construction works noise to ensure it does not exceed the permissible noise levels throughout various stages of construction phases
• Coordinate with external pest control operator visits to carry out fumigation, mosquito oiling and rodent control measures. This is to ensure effective control on site
• Liaising with National Environment Agency & Public Utilities Board (PUB) on environmental issues and other statutory requirements of compliance by sites
• Updates on codes of practice & environmental literature and circulates information to each level of employees

Requirements:-

• Must possess Environmental Control Officer Certificate and registered with National Environmental Agency (NEA)
• Min 2 years’ relevant experience

Responsibilities:

Corporate Secretary

• Manage all local corporate secretarial work for a portfolio of about +25 entities incorporated in various Asia countries (ie. Singapore, Indonesia, Thailand, Malaysia, Vietnam, Philippines, etc.) in compliance with all relevant local laws and regulations.
• Liaise with & give instructions to corporate secretarial agents & other relevant government authorities
• Monitor deadline for statutory filings (eg. annual returns, etc.) and generally compliance with relevant Companies Act
• Co-ordinate/Liaise with other in-house departments (ie tax, finance, treasury, etc.) to ensure smooth running of the day-to-day administrative and corporate secretarial related matters
• Maintain and timely update the secretarial database (eg. registration certificate, business license certificate, etc.)
• Prepare & Circulate resolutions, board meeting of directors and shareholders and ensure timely signing
• Update from time to time any movements and/or changes in the organization (eg. change of name, registered address, change of directors, etc.)
• Prepare & implement automatic resignations in respect of all directors in all entities in South East Asia and Taiwan
• Check the invoices for the services rendered by the corporate secretarial agents
• Develop efficient and effective system for the management of corporate secretarial procedures
• Consolidate corporate secretary information for all Asia entities (about 60 entities in total)
• Provide regular updated corporate secretary reports & legal structure chart to the French headquarters
• Handle notarization of legal documents upon request
• Support the Legal counsel in charge of the legal restructuring works

Compliance & Governance

The Jobholder will also be a key player in the implementation of the Ethics & Compliance standards of Thales Group and, as such, will contribute to the evolution of its organization as well as its way of working in order to take into consideration the evolutions of its environment, new laws & regulations, and the best ethical and governance practices.

Therefore, the Jobholder will be responsible to actively contribute to the implementation of Thales Group ethics & compliance standards in the Regions and as such, will be in charge, in particular, of the following:

• Perform, analyze, implement and update the screening and due diligence files of any Third Party with whom Thales wishes to enter into a contractual relationship, in close coordination with the competent Compliance Officer as well as all the other relevant stakeholders (i.e. business capture leaders, country directors, and all relevant local functions and concerned Thales business units) in accordance with the applicable Third Party Integrity Assessment Instruction;
• Actively contribute and participate to the deployment throughout the Regions of the anti-corruption, ethics & compliance program and training plan, i.e. code of conduct, gifts and hospitality instruction, community investment, sponsorship, corporate membership instruction, compliance tools and platforms deployment, etc.
• With the support of the Compliance Officer and of the Correspondents, assist in the deployment and implementation of the other Group compliance pillars’ programs (Trade Compliance, Anti-trust and Competition laws, Personal Data Protection) in the Regions;
• Follow-up the companies of her portfolio business evolution to ensure delegation of authorities are up to date and consistent with the current activities,
• Report to the Compliance Officer any identified situations of non-compliance which would require the definition of a corrective action plan and/or a reporting to Chief Compliance Officer and VP Legal & Contract of TNSEA
• Support the Compliance Officer in addressing the internal control requirements, the audit reviews, corporate law, governance and compliance aspects for all the entities falling with the Regions scope

Requirements:

• At least a Master’s degree in Law and, eventually, ICSA or equivalent qualifications
• More than 10 years professional experience in corporate secretarial function and compliance matters, in house legal department or law firm
• Good command of English language, verbal and written
• Experienced user of Microsoft Office Applications
• Strong oft skills: rigorous, precise, organized, pro-active, research-oriented strong team player, solutions oriented, and logic, ability to work independently
• Ability to navigate in a global complex structure
• Good and effective communication skills as well as good inter-personal and inter-cultural awareness and interest to work in diverse teams

Responsibilities:-

• Person in charge of the workplace on environmental regulations pertaining to the Environmental Public Health (Registration of Environmental Control Officers) Regulations 1999 Person in charge of the workplace implementation and revision of Environmental Management in the worksite
  Act as an Earth Control Measures Officer (ECMO)
• Establish, update, maintain, and implement the Environmental Management System and Environmental Impact Aspect assessment
• Conduct / Plan site environmental inspection and ensure effective implementation and continual improvement on all environmental matters. Advise occupier of the workplace or other person in charge of the workplace on environmental health problems and recommend remedies to establish a healthy working environment
• Oversee the installation of noise meters at site vicinity and monitoring of construction works noise to ensure it does not exceed the permissible noise levels throughout various stages of construction phases
• Coordinate with external pest control operator visits to carry out fumigation, mosquito oiling and rodent control measures. This is to ensure effective control on site
• Liaising with National Environment Agency & Public Utilities Board (PUB) on environmental issues and other statutory requirements of compliance by sites

Requirements:-

• Must possess Environmental Control Officer Certificate and registered with National Environmental Agency (NEA)
• Min 2 years’ relevant experience

We are looking for a dedicated Quality Control Officer to join our team. The ideal candidate will have 2-3 years of experience in a factory setting and will be responsible for overseeing the quality control processes, specifically in the packing team. The QC Officer will ensure that sampling procedures and quality checks are conducted effectively to meet quality standards.

Key Responsibilities:

• Monitor and oversee the quality control processes within the packing team.
• Ensure that sampling procedures are conducted in accordance with established protocols.
• Conduct quality checks throughout the production process to ensure compliance with quality standards.
• Collaborate with cross-functional teams to address quality issues and implement corrective actions.
• Maintain accurate records of quality control activities and report any deviations or non-conformities.
• Assist in the development and implementation of quality control procedures and guidelines.
• Participate in audits and inspections to ensure compliance with regulatory requirements.

• 2-3 years of factory experience in a quality control role.
• Familiarity with workflow processes from sampling to quality completion.
• Educational background in Chemistry, Chinese Medicines, Microbiology, Biochemistry, Pharmaceutical Studies, or related fields.
• Strong attention to detail and accuracy in conducting quality checks.
• Excellent communication and teamwork skills.
• Ability to work effectively in a fast-paced environment and prioritize tasks accordingly.
• Knowledge of quality control standards and practices.

• A career opportunity with the market leader in health product sector.
• Comprehensive health insurance from your first day at work.
• Casual wear everyday to enjoy your work.
• Free and convenient shuttles from various locations.
• Generous leave policies, including paid annual leave, birthday leave, and other special leaves
• Many opportunities to learn and grow together.
• Rapid growth opportunities for strong performers. 
• Attractive staff purchase discount from your first day at work.
• And more!!!!

Job description:

1. To plan, organize and monitor all activities relating to quality assurance to maintain quality standards and systems to meet customer requirements.

2. To define and control the characteristics of each part, affiliated with appropriate Inspection Plans; and make available the required facilities to verify these characteristics.

3. To oversee and approve First Article inspection procedures prior to sample submission to customers.

4. To issue material certificate to meet customer requirements.

5. To liaise with customers on matters related to quality.

6. To conduct/co-ordinate Material Review procedures to implement any Corrective/Preventive Action; and follow-up for a closure with result of satisfactory action taken.

7. To approve disposal of non-conforming items.

8. To ensure all inspections are conducted correctly.

9. To control and manage the Equipment Calibration System; setting the frequency of each calibration.

10. To report quality performance and critical discrepancy issues to General Manager.

11. To propose to General Manager an indicative rate of annual salary-increment and annual bonus of his subordinates reflected through the past year performance.

12. To approve the application of various type of Leave of his subordinates.

13. To approve petty-cash paid to his subordinates.

14. To recruit and upgrade his subordinates with relevant training programs and sue practical experiences.

15. To train subordinates in Sampling and Inspection techniques.

Experience Required:

At least 5 years experience in a Quality Control Management.

Skills required

1. Well-versed in ISO 9001:2000 requirement.

2. Quality Control System.

Qualification required

1. Mechanical/Manufacturing/Engineering Degree.

IT Exposure

1. Computer literate in MS Office.

2. Application knowledge in Autocad.

Role Summary

The job holder is responsible for applying a local Quality Assurance program for the R&D Test Facility in alignment with Good Laboratory Practice (GLP), other applicable regulations and company best practices. This is to assure Test Facility Management (TFM) and management that the facilities and studies are in compliance with Good Laboratory Practice regulations.

Additionally, the incumbent supports the implementation of applicable standards pertinent to non-clinical research and/or toxicological assessments in order to verify that the studies are performed in accordance with the applicable regulatory frameworks, QMS requirements and best practices.

The incumbent also supports the quality oversight of suppliers and contract laboratories for pre-clinical research and/or toxicological assessments, as well as to identify opportunities for quality and process improvements in pre-clinical development.

Responsibilities

• Plan, perform and report QA inspections and suppliers audits to assure TFM and management that procedures/standards are in compliance with relevant national and international requirements for GLP for both internal and external entities. Monitor and follow up on corrective actions and preventive actions (CAPAs) reporting in response to internal audits and regulatory inspections.
• Support the monitoring of pre-clinical studies throughout their conduct and reporting for compliance with the GLP principles.
• Support R&D Test Facility for inspection readiness, participating in regulatory inspections/accreditations, and managing the corrective and preventive actions (CAPAs) reporting in response to internal audits and regulatory inspections
• Provide administrative support for the QMS document/record/training management system, including QA review of records such as QMS documents (SOPs/WKIs/Forms), Training, Nonconformance (NC), Corrective Action Preventive Action (CAPA) and Lab Change Request (LCR) for key QMS processes. Provide regular training on the systems and QMS (e.g. Good Documentation Practice, GLP) for new and existing staff.
• Manage the archival process in accordance with established SOP and GLP principles
• Monitor and report quality Key Performance Indicators (KPI) during Quality Management Review (QMR)
• Perform QA review of equipment/instrument qualification plans, reports and related documentation for GLP activities, to assure that the laboratory equipment/instrument are suitable for their intended purposes
• Continue to be developed as an expert in understanding GLP compliance on a global basis including local compliance enforcement experience with Health Authorities

Requirement

• Bachelor degree in scientific discipline (Life Sciences, Biology, Chemistry etc) or equivalent
• Minimum 3 years of work experience in a laboratory environment (chemical/biologic analyses) and participation in quality assurance related to activities in tobacco, food, pharmaceutical or similar industry and/or at least 3 years experience as a specialist in a relevant area of activity. Experience in another quality standards eg. ISO 17025 would be an advantage
• Working knowledge of OECD principles of Good Laboratory Practice, knowledge of other quality systems such as FDA GLP Principles, cGMP, ISO, GCP and AAALAC is an advantage

We are seeking an experienced QC Supervisor (Microbial) with over 5 years of relevant experience and a strong background in team management. The ideal candidate will possess in-depth knowledge of Good Manufacturing Practices (GMP) and will lead a team in ensuring the quality and safety of various materials including starting materials, packaging materials, and finished products.

Key Responsibilities:

• Arrange and oversee sampling and testing for various materials, including starting materials, packaging materials, and finished products.
• Review and manage Batch Production Records, various record forms, and test reports to ensure compliance with quality standards.
• Conduct and supervise microbiological testing of food, traditional Chinese medicine (TCM), and pharmaceutical products.
• Collaborate with cross-functional teams to ensure quality assurance throughout the production process.

Qualifications:

• Minimum of 5 years of experience in quality control, with prior team management experience.
• Strong knowledge of Good Manufacturing Practices (GMP) is essential.
• Background in microbiology, biochemistry, pharmaceutical studies, or related fields is preferred.
• Experience with microbiological testing in food, TCM, and pharmaceuticals is a plus.
• Open to candidates with diverse educational backgrounds.

• A stimulating career opportunity with the market leader
• Be a part of a growing team.
• Work comfortably and confidently in our fun and welcoming environment with a casual attire
• Convenient free shuttles from multiple locations.
• Fast-track your career with our performance-based growth opportunities
• Performance-based bonuses offered at our discretion
• Comprehensive medical coverage available from day one under our company's medical insurance
• Competitive salary depending on experience

Please note that only short-listed candidate will be contacted.

#LI-AA1

Key Responsibilities:

• Conduct Inspections: Perform comprehensive inspections of mobile cranes and crawler cranes to assess structural integrity, operational functionality, and compliance with safety regulations and manufacturer specifications.
• Document Findings: Prepare detailed inspection reports outlining findings, deficiencies, maintenance requirements, and recommendations. Ensure all documentation is accurate, thorough, and compliant with regulatory standards.
• Quality Assurance Processes: Develop and implement quality assurance processes specific to mobile and crawler crane inspections to maintain consistency and reliability in inspections across different types and models.
• Compliance Monitoring: Monitor and enforce adherence to relevant safety regulations, standards, and codes applicable to mobile and crawler crane operations and maintenance.
• Collaboration: Work closely with crane operators, maintenance teams, and project managers to address inspection findings promptly. Provide guidance on corrective actions and ensure compliance with safety protocols.
• Continuous Improvement: Identify opportunities for improving crane inspection protocols, procedures, and equipment to enhance operational efficiency and safety standards.

Requirement:

• Minimum ITE / Higher Nitec / Diploma qualification or equivalent.
• Minimum 3 to 5 years of experience working in crane inspection.
• Computer literacy, including proficiency in Microsoft Office Applications (Word, Excel, Outlook)
• Work closely with maintenance teams to address inspection findings; proficiency in Mandarin is essential.
• Ability to work independently with minimal supervision and as part of a team.
• Commitment to upholding safety standards and ensuring quality excellence in crane operations.

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking an experienced Quality Control Analyst with experience in pharmaceutical company/Life Science industries for a role in Singapore.

Key Responsibilities:

• Sample storage and management
• Prepare and support analytical testing
• Analytical testing and documentation
• Perform lab housekeeping activities
• Perform administrative documentation
• Comply with all HSE guidelines
• Detect and report potential accident, risks and propose solutions
• Responsible for participating in initial training and retraining

Qualifications:

• Proficient in English.
• Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production).
• Diploma or Bachelor's Degree graduate

This position is for permanent 12-hr night shift, 2-3-2 basis.

Why PharmEng Technology?

Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.

EEOC Statement

At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.