Total 32 job vacancies by Msd International Gmbh (singapore Branch)

Maintenance Engineer (WDA) 2 year contract

• Based in Singapore, the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on the Straits Times and Statista’s list of Best Employers in Singapore for two consecutive years (2020, 2021).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

WHAT YOU WILL DO

Responsibilities include, but are not limited to:

· Provide technical expertise for all the DPI equipment related activities in the manufacturing process and support Maintenance Technicians.

· Execute maintenance, improvement, DPI maintenance activities, ensure preventative maintenance is completed according to schedule requirements, and support equipment change control implementations.

· Utilize technical skills to lead equipment and Utilities system deviation/atypical investigations, safety incidents and ensure effective root cause analysis is conducted.

· Provide solutions to recurring failures by performing RCA and identifying corrective action.

· Implement technical solutions to improve equipment uptime and asset utilization through use of Continuous Improvement mindset (Lean methodologies).

· Responsible for improving the reliability of DPI equipment and maintenance processes by applying the principles of Reliability Centered Maintenance.

Corrective Maintenance

· Ensure resolution and timely follow-up of identified production equipment and facility related equipment issues, unplanned events, and new opportunities identified by Maintenance team.

· Provide technical expertise and support the Maintenance Technicians for equipment breakdown, troubleshooting and recovery to ensure the timely and effective resolution of issues.

· Ensure equipment breakdowns are resolved in a timely manner and update the Preventive Maintenance Plan.

· Apply effective root cause analysis and troubleshooting Techniques to support the resolution of equipment-related incident and deviation/atypical investigation.

Preventive Maintenance

· Ensure all planned internal and external Preventive Maintenance (PM) activities are executed and completed.

· Update equipment critical spare part list and set minimum re-order levels.

· Review existing maintenance RAs promptly and to develop new one when necessary.

Compliance – Safety

· Participate in and support the implementation of actions for Incident Investigations and Audits

· Ensure required risk assessments, including HAZOPS, are carried out in a timely manner, recommendations provided, and implemented as agreed.

· Ensure permit requirements met IPT maintenance activities.

• Proactively review and challenge current activities to reduce safety risk for employees and quality risks for company’s products.

Compliance – Quality & Change control

· Prepare SOPs and Job Aids to ensure compliance with regulatory standards and ensure PM related documents are generated and maintained according to required standards and frequency.

· Ensure all deviations/atypical and customer complaints are fully investigated with any equipment related actions effectively implemented within the agreed time frame to continually improve processes, prevent waste, and eliminate rework.

· Ensure all out-of-tolerance equipment findings are appropriately documented and investigated in a timely manner.

· Support implementation of Equipment change by participating in impact assessments and executing field equipment modifications, including management of project schedules, resource plans, vendor coordination, and material purchases.

· Prepare and complete IQ, OQ documentation and ensure that documentation meets required regulatory standards.

Equipment reliability

· Utilize Lean Six Sigma Tools, such as Six Sigma, Kaizen, SMED, and 5S, to support execution of continuous improvement and OE projects intended to increase agility, flow and throughput, and also to reduce cycle time and inventory.

· Support development of a continuous improvement framework within the maintenance group and works with the Maintenance Lead to identify opportunities.

· Lead plant improvement processes to enhance availability, reliability, cost-effectiveness and efficiency of the plant.

· Collect and analyze data and follow up with recommendation to improve equipment’s reliability and reduce equipment failures. Work with COE’s to execute a Reliability-Centered Maintenance (RCM) plan and to share best practices and lessons learned, with objective of improving asset utilization.

· Participate in equipment/system-based Root Cause Failure Analysis (RCFA) investigations and update equipment reliability plans.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Degree in Mechanical / Mechatronics / Electrical or Instrumentation & Control Engineering
• 3-5 years of maintenance work experience in Pharmaceutical (Preferred), Chemical, Semiconductor, aviation, oil & gas or Petrochemical industry.
• Knowledge and experience working within a Computerized Maintenance Management System (CMMS). Familiarity with SAP is a plus.
• Knowledge of parts inventory management, mechanical and electrical equipment design reliability principles
• Project management skill, including problem-solving, developing and implementing technical solutions.
• Experience in HVAC and water system operation and maintenance principle.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace

The User Experience Product Line Lead is a core and leadership position in Digital Services, our Digital Manufacuring Division responsible for leading the definition and implementation of User Experience strategy in our Digital Manufacuring Division. The Product Line Lead drives priorities setting and holistic value delivery of the UX capabilities across squads and products in Digital Services. The Product Lead collaborates and partners closely across product teams, our company value and enabling teams, our Manufacturing Operations, and IT CTO with product line UX professionals, UX researchers, UX/UI Designers, product managers, and business stakeholders at all levels to define, implement, maintain, and make innovative improvements to deliver user-centric and outcome-driven products and solutions.

The UX Product Line Lead sets the vision for best-in-class products, anticipating future business capabilities, emerging technologies, designs and best practices, ensuring that vision is realized through implementation and value delivery. This role will lead a product line team to create, scale and maintain our Digital Manufacuring Division UX solutions and capabilities to support digital transformations.

Primary Responsibilities:

• Accountable for Product roadmap (e.g., key capabilities delivered to the business) for designing, building, delivering, and maintaining UX products and technological capability enhancements
• Optimize team setup and delivery models across all functional areas, working with functional leads, while removing roadblocks and impediments, enabling efficient and effective product team delivery
• Translate business goals and end user needs into UX strategy, communicate product priorities to the development team, other matrixed teams, and vendor partners
• Oversee delivery of applications in the products and the on-going operations of cohesive & integrated applications
• Design, develop, and deliver a consistent product line vision, strategy, and roadmap for several products related to Experience Design, UX/UI, User Research, and Technical Product Management relevant to our company user environment.
• Partner with Product teams across our Digital Manufacuring Division and IT to develop, test, and deliver high quality, scalable, and reusable data and digital products
• Oversee Agile Scrum processes for product teams to define and prioritize backlog, create user stories, drive sprint planning and execution, standups, product demos, track velocity, burndown, and deliver retrospectives
• Demonstrated experience in leading strategic design and user-centric research and usability studies, and applying change management approaches to understand user needs and deliver results
• Manage, monitor and calibrate relevant metrics on UX effectiveness
• Demonstrated experience in leading UX designs using a variety of techniques, tools, and best practices to improve product usability, accessibility and desirability
• Lead, develop, upskill, and grow a high-performing and diverse User Experience team
• Set strategy for resource management within systems development, accountable for the allocation of resources for systems development programs, and maintain an overview of the contribution of such program to organizational success. Manage the quality and appropriateness of the work performed and delivers measurable business benefits
• Engage and partner with cross-functional stakeholders (value teams, domain leads, business partners, product owners, etc.) to build project plans and business cases that drive our Manufacuring Division business outcome and value realization while maintaining scalability of UX capabilities
• Ensure senior leaders and business stakeholders are consistently well informed about product strategy, capabilities, priorities, timelines, releases, issues, and risks
• Drive and reinforce highest standards and best practices in technical and operational excellence relevant for user experience
• Accountable for the management and optimization of the product line’s total cost of ownership (TCO)

Education:

• Bachelor’s degree in Computer Science, Engineering, Graphics Design, or related field.

Required Experience and Skills:

• Minimum of 8 years of relevant experience in a delivery lead, team lead, product owner, or product line lead capacity.
• Minimum of 5 years of relevant experience in leading the development and delivery of User Experience, Experience Design, UX Strategy.
• Demonstrated experience in software development lifecycle, agile methodologies e.g. Scrum, and relevant tools such as Jira and Confluence
• Experience in pharmaceutical manufacturing or similar area, building, managing, and leading high-performing, diverse, collaborative and geographically distributed digital product teams
• Solid knowledge and experience in UX capabilities, methodology, and tools to enable User Research, UX/UI Design, and Digital Product capabilities in Manufacturing, Quality, and Supply Chain domains.
• Strong leadership and team building skills and must be able to collaborate effectively with a group of high performing individuals in a fast-paced, agile, dynamic operational environment
• Experience in product and people management with Experience Design, Graphics Design, User Experience, and Data & Digital products knowledge, roadmap, and implementation (e.g., in an organizational unit with 10+ team members)​
• Demonstrated experience owning and delivering digital products​ throughout their entire lifecycle
• Proven ability to facilitate and break down complex product requirements into actionable strategy, implementation plan, and user stories
• Strong leadership skills and the proven ability to drive organizational change​ and alignment, and communicate technical information to senior executives
• Outstanding written and verbal communication skills – able to effectively communicate complex concepts in simple ways​
• Active coach and mentor whose goals are to grow, upskill, and maximize the squads’ potential​
• Strong understanding of modern architecture patterns​
• Demonstrated ability to partner with business stakeholders and navigate across conflicting priorities to balance critical tactical and strategic needs ​to achieve business goals and OKRs
• Strategic leader, with demonstrated ability to work in a global, broad, and diverse environment with a fair amount of ambiguity
• Growth and global mindset and ownership mentality with a passion to challenge status quo to find new solutions and drive out of the box ideas

Preferred Experience and Skills:

• MBA or Master’s degree in a relevant field
• Previous experience working in a global environment and transformational change
• Experience with manufacturing shopfloor or lab environments and digital culture is a plus
• Experience with P&L responsibility is a plus

Who we are

We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

What we look for

Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.

THE OPPORTUNITY

• To work in a culturally diverse and high-performance team who has built a lot of capabilities in Pharmaceutical Manufacturing.
• Based in Singapore, the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on The Straits Times and Statista’s list of Best Employers in Singapore for three consecutive years (2021, 2022, 2023).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

​

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products.

Reporting to the Engineering Manager, the Technician plans, organizes, performs engineering and maintenance activities related to the installation, modifications, troubleshooting, repairs, calibrations and maintenance of equipment / system to ensure that they are safe, efficiently, reliable and meet GMP/ regulatory / production requirements at production plant.

WHAT YOU WILL DO

• Provide support for calibration of instruments and preventative maintenance (PM's) plans, as requested.

• Responsible for written documentation of activities. • Responsible for SAP transactions and change control activities including spare part lists and Preventative Maintenance (PMs) plans.

• Actively supports, participates and embraces an inclusive team culture including significant interaction with Operations, Quality, Automation, Technology, and other groups as required.

• Provides support to complete work activities timely, efficiently and satisfactorily.

• Provides troubleshooting and diagnostic of equipment failure to determine the root cause and perform immediate corrective actions

• Standby for any emergency repair after office hours / weekends and public holidays.

• Operates and maintains production support equipment efficiently and reliably to support production activities.

• Performs and coordinates equipment shutdown, startup, swing over, and equipment servicing and inspection

• Identifies, executes and reports improvement on routine work activities

• Participates in the improvement to enhance equipment or system efficiency, reduce energy usage and other cost saving/avoidance projects.

• Performs jobs assigned by Maintenance Lead pertaining to installation, modification, fabrication, testing, servicing and repairs of equipment, with adherence to site change control procedures or minor projects

• Performs testing, commissioning, qualification (IQ, OQ) activities.

• Carries out Safety, Health, and Environment (SHE) improvement initiatives (i.e., audits, training, etc.) and submit recommendation.

• Performs job assignments by Maintenance Lead pertaining to equipment or system or documentation or housekeeping.

• Executes CMMS Work Instruction from process plants (e.g. leakages, replace faulty part, troubleshooting, repair).

• Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable.

• Supervise and oversee Third Party Contractors, where applicable.

• Any other duties as and when assigned by the Supervisor / Manager cGMP Standards Understands and follows proper cGMP principles and our company quality guidelines and policies related to the execution of assigned work.

PROBLEM SOLVING:

• Use tools like Real time problem solving (RTPS), Fishbone or 5 Whys to solve problem

• Assesses simple issues and suggest paths towards resolution

• Able to properly assess the situation and understand when to escalate to a higher-level Leading Self or Others, and Department

• Works with minimum direct supervision

• Trains and guides technicians in the day/shift teams

• Seeks advice in personal and professional development • Apply inclusive behavior in the work environment and day to day activity

WHAT YOU MUST HAVE

Qualification:

• NTC / ITC / Diploma in Electrical Engineering, Instrument & Control or Mechanical Engineering or its equivalent • PUB electrician's license will be an advantage

Experience:

• Preferably 3 to 5 years of working experience in electrical/instrumentation in the manufacturing, petrochemical or related industries

• Good working experience in Electrical & Instrumental discipline will be an advantage

• Knowledge of cGMP and good documentation practice is an advantage Other Personal Attributes:

• Demonstrate our company’s Inclusive Behaviors

• Initiative, drive and ability to work independently

• Good interpersonal and communication skills

This is a Career Conversion Programme (CCP for Advanced Biopharmaceuticals Manufacturing Professionals (Place-and-Train) under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• PMETs/Mid-Careerist with no prior work experience in Biopharma industry are welcome to apply
• Singaporeans/PRs only

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Pharmaceutical Manufacturing.
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

WHAT YOU WILL DO:

As a member of Document Control Team in Singapore, you will be able to learn good documentation practices and how to ensure all data and records we generate are in compliance with the data integrity or ALCOA principles, meeting stringent requirement imposed by regulatory agencies and authorities around the world.

The Document Administrator key responsibilities are as follows:

• Member in decommissioning project.

• Identify documents related to equipment undergoing decommissioning.

• Isolate identified documents.

• Pack into carton box and prepare for shipment.

• Perform necessary transactions in Document management system.

• Perform disposal of documents as per Document Retention policy.

• Perform other archival and retrieval of documents.

• Support initiatives to improve straight through documentation.

• Participates in continuous improvement proposals of the department, especially supporting Right First Time (RFT) documents.

WHAT YOU MUST HAVE

• Current study in Diploma or bachelor’s degree in a technical field, preferably in a science or engineering.

• Demonstrated capability in application of sound engineering and scientific principles, project management skills and structured/analytical problem-solving techniques

• An excellent team player who is able to readily take on responsibilities and work independently

• Strong interest in working in a engineering and operational environment

• Excellent communication and facilitation skills

• Have a positive, proactive, can-do attitude

• Keen to learn

• Good team player

• Strong problem-solving skills

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide

The Maintenance Technician organizes, performs engineering and maintenance activities related to the installation, modifications, troubleshooting, repairs, calibrations and maintenance of equipment I system to ensure that they are safe, efficiently, reliable and meet regulatory and production requirements. Other engineering activities include maintaining spares and parts storage, operation of utilities supplies and up-keeping of facilities.

WHAT YOU WILL DO

Main Responsibilities:

• Assists team to complete work activities timely, efficiently and satisfactorily.
• Follow up and continue with the previous shift or day incomplete work.
• Collates and reports the team shift or day activities to the team lead.
• Provides simple troubleshooting and diagnostic of equipment failure to determine the root cause and perform immediate corrective actions.
• Standby for any emergency repair after office hours, weekends, and public holidays
• Operates and maintains Utilities or Production support equipment efficiently and reliably to support production activities.
• Performs and coordinates utilities shutdown, start-up, swing over, and equipment servicing and inspection.
• Identifies, executes, and reports improvement to routine work activities.
• Assists in the improvement to enhance equipment or system efficiency, reduce energy cost/usage and other cost saving/avoidance projects
• Performs jobs assigned by Supervisor pertaining to installation, modification, fabrication, testing, servicing and repairs of equipment with adherence to site change control procedures or minor projects.
• Perform chemical cleaning, Gasket and Diaphragm replacement activities and complete all the activities timely.
• Assists in performing testing, commissioning, qualification (IQ, OQ, PQ) activities
• Participates in Safety, Health, and Environment (SHE) improvement initiatives (i.e., audits, training, etc.)
• Performs corrective and preventive maintenance for the MEI systems and facilities to ensure efficient running of equipment (e.g. checking line components, servicing of sensors, lubrication of bearings, servicing of dryer)
• Performs calibrations and preventive maintenance on all types of industrial instruments for temperature, pressure, level, flow, RH and analysers (e.g. Sensors, indicators, recorders, transmitters, transducers, control valves, annunciators, pH and conductivity meters).
• Work as team to perform weighing scale calibration.
• Executes CMMS Work Instruction from process plants (e.g. Isolation and Reconnection of electrical supply, leakages, replace faulty part, troubleshoot, repair any E/I or mechanical faults)
• Performs basic troubleshooting of the PLC, BMS, EMS and FAS systems. Troubleshoot AHU repair and replace motor belt and do laser alignment.
• Have knowledge on machining and fabrication activities. Perform tire repair and replacement of Tank agitator and mechanical seal.
• Participate in SHE, Business Compliance, and all other compliance-related matters, where applicable
• Supervise and oversee Third Party Contractors, where applicable
• Any other tasks as and when assigned by Supervisors

Problem Solving

• Assesses simple issues and suggest paths towards resolution
• Able to properly assess the situation and understand when to escalate to a higher level

Leading Self or Others and Department

• Works under direct supervision
• Seeks advice in personal and professional development

WHAT YOU MUST HAVE

To be successful in this role, you will have:

Qualification

• Diploma / ITC/ NTC in Mechanical, Mechantronics, Electrical or Instrumentation & Control Engineering

Experience

• Work experience required; 2 to 5 years’ experience in maintenance or related fields;
• Have work experience in the chemical, semiconductor or oil and gas industry
• PUB electrician license will be an advantage
• Fitting and welding skills will be an added advantage

Leadership

• Demonstrates Ethics & Integrity
• Drive Results
• Focus on Customers & Patients
• Make Rapid Disciplined Decisions
• Act with Courage & Candor
• Build Talent
• Foster Collaboration

Other Competencies and Personal Attributes

• Ability to prepare simple report
• Communicates in a clear and unambiguous manner

This is a career conversion programme under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• Singaporeans/Singapore PRs only
• PMETs/Mid-Careerist with minimum 2 years working experience
• Open to two years contract
• shift work (12 hours rotating shift including Sat/Sun. Shift allowance will be provided)

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

WHAT YOU WILL DO

Job Purpose:

• Operate and monitor the chemical production activities in the plant, ensure that processes are run according to process description, complete batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner.
• Assist Production Lead to supervise a section of Chemical Technicians to meet production targets/schedules while maintaining satisfactory standards of Good Manufacturing Practice, safety, and housekeeping.

Main Responsibilities

• Operate and monitor the chemical processes assigned:

Each of these processes may comprise the following activities:

• Participate in an appropriate hand-over of the process(es) on which he / she is working.
• Obtain, follow and complete process related documentation. Check prior shifts' documentation for accuracy and thoroughness.
• Clean vessels and lines prior to and following batches as required.
• Conduct all required pre-batch checks.
• Charge vessels with solids or liquids as directed in procedures.
• Conduct post-charge verification checks and take any necessary corrective action.
• Adjust and monitor (using all information available, including automation input/outputs and personal inspection) process conditions as required.
• Carry out routine sampling, testing some samples as necessary.
• Transfer process streams to other units in coordination with other staff.
• Monitor process; both with DCS and manually observing temperature, pressure, flow, PH, volume, colour, salt content, moisture content and adjusting the parameters accordingly.
• Perform Batch / Offloading operations.
• Operate general facility service equipment such as vacuum pumps, water systems, VOC scrubbers.
• Record all operational and analytical data on the appropriate documents and inform the Shift Production Lead of any process abnormalities.
• Put on appropriate clothing and personal protective equipment for the process and the processing area.
• Maintain material segregation and label appropriately and accurately all containers, bags and vessels.
• Carry out routine checks and scheduled cleaning procedures, for both process and facilities as required.
• Obtain and verify materials necessary for processing, monitor materials stock and notify Shift Production Lead as necessary in the event of a material or supply abnormality.
• Notify Shift Production Lead of requirement for maintenance. Prepare equipment before maintenance work for example depressurizing, cleaning of lines and equipment, de-energizing, etc.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Higher NITEC or Diploma in Engineering (Chemical, Mechanical, Electrical) or Science or equivalent operations experience.
• 1 to 2 years of relevant technical experience in the Pharmaceutical, or manufacturing-based industry, including manufacturing operations support.
• Good stewardship awareness (including cGMP, regulatory inspection preparation, SHE)
• Good knowledge in applicable regulations and divisional policies/guidelines (especially cleaning/housekeeping/maintenance, environmental control, process/cleaning/equipment validation, change control and manufacturing practices).
• Demonstrate Ethics & Integrity & Result Driven
• Focus on Customers & Patients & Make Rapid Disciplined Decisions
• Act with Courage & Candor, Build Talent & Foster Collaboration
• Demonstrate Our Company's Inclusive Behaviors & Effective communication skills
• Open to 12 hours rotating (day/night) including Sat/Sun. Shift allowance will be provided

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Pharmaceutical Manufacturing.
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

The Process Engineer provides technical support for the manufacturing and cleaning processes in the various manufacturing facilities at the site, along with equipment support for the main process technology platforms.

WHAT YOU WILL DO

• Supports routine supply manufacture by providing on going technical support to the IPT and proactively monitoring performance of equipment/module(s) or unit operations during manufacturing and cleaning.
• Participates in developing continuous process verification (CPV) plans and contributes to the CPV reports and annual product review.
• Provides technical expertise related to equipment and manufacturing/cleaning processes in response to deviations to understand and eliminate the root cause.
• Supports filing activities by assisting with process qualification activities, equipment qualification and cleaning validation.
• Any other duties as assigned by Supervisor

After one year, you will be competent in current Good Manufacturing Practices which is applied across the pharmaceutical industry. You will be able to provide technical support fairly independently to the integrated process team for process/product/equipment issues and changes.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Bachelor or Masters Degree in a technical field, including Chemical/ Mechanical Engineering, or Pharmaceutical Sciences
• Knowledge of problem-solving tools (such as fishbone analysis, 5 WHY, logic fault tree etc.) and troubleshooting skills
• Knowledge of data analysis (familiarity with use of statistical software such as Minitab or JMP is preferred)
• Good verbal communication skill and technical writing skill
• Attention to detail

This is a Career Conversion Program (CCP for Advanced Biopharmaceuticals Manufacturing Professionals (Place-and-Train) under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• PMETs/Mid-Careerist with minimum 2 years of working experience
• Singaporeans/PRs only

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

THE OPPORTUNITY

• Based in Singapore, the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on The Straits Times and Statista’s list of Best Employers in Singapore for two consecutive years (2020, 2021).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.
• Our Company is committed to provide patients and customers with a reliable supply of high-quality, safe and effective medicines and vaccines. Our global supply strategy relies on manufacturing capabilities and expertise to achieve this mission. Singapore is one of the key strategic manufacturing sites for our Company and patients. The local site operates multi-product facilities that manufactures active pharmaceutical ingredients, oral solid dosage, inhalation and sterile drug products.
• Looking for a change? The following presents an opportunity to work in the Packaging team.

Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.

In this role, you will:

• Act as subject matter expert (SME) in IPT Maintenance team with in-depth knowledge in Purified water system, HVAC and Electrical & Instrumentation.
• You will take ownership for the HVAC and purified water system day to day support and continues improvement.
• Experience in manufacturing in a GMP HVAC environment utilizing ISO 14644-1 classifications.
• Respond to BMS/EMS alerts, investigate and feedback on any outstanding issues or events and respond to emergency situations and be on standby duty as required.
• Develop and implement maintenance program, preventive maintenance procedures and spare parts strategy for safe, reliable, and efficient operation of the systems/Equipment’s.
• Shape data-driven decisions that solve business challenges and deliver on desired outcomes and people experience.
• Drive innovation, every plant area is a model area using our Production System.

Key Responsibilities:

Safety & compliance

• Lead or support investigation, participate in trouble shooting and root cause analysis for various operational events, and also ensure that all relevant engineering CAPA are completed within agreed timeline.
• Lead and manage change control on project activities or act as technical advisor for plant modifications, capital projects and other identified plant improvement projects in line with defined specifications, budget and qualification of facilities in accordance with site to approved procedures.
• Proactively review and challenge current activities to reduce safety risk for employees and quality risks for company’s products.
• Assist in overseeing testing, commissioning, qualification (IQ, OQ) activities are executed accordingly and in compliance.
• Maintain HVAC and Purified water systems are in optimum condition in compliance with Good Manufacturing Practice (GMP) & EHS requirements.
• Familiar with current applicable our standard & external standard for clean room/building environment and HVAC. When required, will also be familiar with other standards to provide full end to end support.
• Lead/participate in equipment failure troubleshooting and deviation investigations whenever required.
• Provide input during Basis of Design (BOD) and Detailed Design during large capital projects, applying good maintenance and reliability engineering principles whenever required.

Enhance and uphold maintenance quality.

• Implements technical solutions to improve equipment uptime and asset utilization through use of Continuous Improvement mindset (Lean methodologies)
• Supports Maintenance Lead to meet Profit Plan targets, optimize maintenance and product standard cost effectiveness in accordance with cGMP and Safety guidelines
• Responsible for improving the reliability of equipment and maintenance processes by applying the principles of Reliability Centered Maintenance.
• Lead and develop Business and GMP processes, formalized them into site procedures required for startup and commercial launch.
• Lead and perform Root Cause Analysis (RCA) for surfaced issues and implement a robust solution.

Operations excellence

• Plans, monitors, schedules, and implements measures on the Planned Preventive Maintenance Program and also ensures that the work is done in accordance with schedule and specification.
• Regularly review and revise maintenance program and procedures to increase equipment reliability, reduce waste and improve overall asset care process & cost efficiency.
• Work with Engineering & Safety, Health & Environment (SHE) to execute a 'reliability-centric’ maintenance plan
• Share best practices and lessons learned with the objective of improving asset utilization.
• Undertake activities to support realization of production, maintenance and product cost effectiveness with emphasis on equipment reliability and maintenance expenses.
• Conducts Maintenance effectiveness / optimization reviews along with IPT maintenance leads/Engineers/Technicians

Continuous Improvements (CI)

• Utilize Lean methodologies such as 5S, Standard Work, real-time problem solving (RTPS), to support execution of continuous improvement activities.
• Support the development of continuous improvement framework and work with the Maintenance team to identify opportunities.
• Compile and review data and develops action plans for critical HVAC systems and Purified water systems to improve reliability and reduce M&R cost.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Degree in Mechanical / Mechatronics / Electrical or Instrumentation & Control Engineering.
• 5 to 8 years of maintenance work experience in Chemical, Semiconductor, aviation, oil & gas or Petrochemical industry.
• Analytical and Problems solving skill with regard to Purified water system and HVAC Systems
• Knowledge in HVAC and Purified water system operation and Maintenance principle.
• Experience in manufacturing in a GMP HVAC environment utilizing ISO 14644-1 classifications.
• Knowledge of various clean room standards across the Pharmaceutical Manufacturing Industry will be an added advantage.
• Familiar with Life cycle of the HVAC system (from design, operations, controls monitoring, maintenance and obsolescence management).
• Knowledge and experience working within a Computerized Maintenance Management System (CMMS). Familiarity with SAP is a plus.
• Demonstrated use of Reliability analysis tools such as FME, RCFA, etc.

Professional Competencies

• Resilient and resourceful
• Good oral/written communication and interpersonal skills
• Continuous learning mindset
• Foster team collaboration
• Strong work ethics

Who we are

We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

What we look for

Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today

The E&I Engineer provides technical expertise (Electrical & Instrumental) for all equipment troubleshooting and maintenance support to maintenance technicians. They also need to organize, plan, direct, and support production, project (Equipment Change Control), Validation and PM (Preventive Maintenance plan) CM (Corrective Maintenance plan) activities. This role also actively supports, participates and embraces an inclusive team culture including significant interaction with Operations, Quality, Automation, Engineering, and other groups as required.

WHAT YOU WILL DO

• Provides support to maintenance manager (E&I) and maintenance technician (E&I) to complete planned work activities timely, efficiently and satisfactorily.
• Participate and lead in Quality/Safety related investigation. Ensure the deviations are fully investigated with any actions effectively implemented within agreed time frame.
• Develops standard operating procedures (SOP's), Job aids and preventative maintenance (PM's) plans. Ensure the developed instructions are compliance with regulatory requirements and company guidelines and standards.
• Provides technical oversight and support maintenance technicians with troubleshooting and diagnostic of equipment failure and determining the root cause and perform immediate corrective actions.
• Coordinates and support equipment shutdown, start-up, swing over, and equipment servicing and inspection with stakeholders. Support installation, modification, testing, servicing, commissioning, qualification activities (IQ, OQ), as well as site change control procedures or minor projects.
• Supervise and oversee Third Party Contractors, vendors and service providers.
• Participates in the improvement initiatives to enhance equipment or system efficiency, reduce energy usage and other cost saving/avoidance projects.
• Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable

After one year, you will be able to handle small project and lead investigation independently.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Bachelor’s degree or Diploma of Electrical Engineering and Instrument & Control Engineering (Preferred).
• Bachelor’s Degree in Engineering. Mechanical Engineering, Chemical Engineering or its equivalent can be also considered if the candidate demonstrates strong willing to work and learn in E&I areas.
• PUB electrician's license will be an advantage.
• Minimum 2 years relevant technical experience in the manufacturing industry, including but not limited to Process/ facilities design, equipment operation, reliability and maintenance planning, project management, problem-solving, developing and implementing technical solutions, planning and scheduling implementations, and working with multi-functional teams.
• Good working experience in Electrical & Instrumental will be an advantage.
• Ability to work independently
• Good interpersonal and communication skills

This is a career conversion programme under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• Singaporeans/Singapore PRs only
• PMETs/Mid-Careerist with more than 2 years working experience
• Open to two years contract

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

Reporting to the Manager of Engineering, the Technician will provide maintenance and engineering support in the manufacturing plant.

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products.

WHAT YOU WILL DO

Your responsibilities will include but are not limited to:

• Performs scheduled calibrations and preventive maintenance on all types of industrial instruments and electrical devices and mechanical equipment.
• Executes work request from process plants for equipment, instruments and electrical breakdown.
• Operates and maintenance of utilities and facilities.
• Performs modifications, fabrication, fittings, and installation for minor projects.
• Performs equipment/system testing, commissioning and/or qualification (IQ, OQ, PQ).
• Performs basic trouble shooting of the PLC, BMS, EMS and FAs system.

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Min NITEC Diploma in Mechanical, Mechatronics, Electrical or instrumentation and control engineering
• Min 2 years' experience in maintenance field preferably from oil and gas or semiconductor industries
• PUB electrician license will be an advantage

This is a career conversion program under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• Singaporeans/Singapore PRs only
• PMETs/Mid-Careerist with more than 2 years working experience
• Open to two years contract
• 12 hours rotating shift (day/night) including Sat/Sun. Shift allowance will be provided
• Work location Tuas (shuttle bus provided)

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Pharmaceutical Manufacturing.
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

WHAT YOU WILL DO

JOB PURPOSE:

• Provide support for calibration of instruments and preventative maintenance (PM's) plans, as requested.
• Responsible for written documentation of activities.
• Responsible for SAP transactions and change control activities including spare part lists and Preventative Maintenance (PMs) plans.
• Actively supports, participates and embraces an inclusive team culture inluding significant interaction with Operations, Quality, Automation, Technology and other groups as required.
• Provides support to complete work activities timely, efficiently and atisfactorily.
• Provides troubleshooting and diagnostic of equipment failure to determine the root cause and perform immediate corrective actions
• Standby for any emergency repair after office hours / weekends and public holidays.
• Operates and maintains production support equipment efficiently and reliably to support production activities.
• Performs and coordinates equipment shutdown, startup, swing over, and equipment servicing and inspection
• Identifies, executes and reports improvement on routine work activities
• Participates in the improvement to enhance equipment or system efficiency, reduce energy usage and other cost saving/avoidance projects.
• Performs jobs assigned by Maintenance Lead pertaining to installation, modification, fabrication, testing, servicing and repairs of equipment, with adherence to site change control procedures or minor projects
• Performs testing, commissioning, qualification (IQ, OQ) activities.
• Carries out Safety, Health, and Environment (SHE) improvement initiatives (i.e., audits, training, etc.) and submit recommendation.
• Performs job assignments by Maintenance Lead pertaining to equipment or system or documentation or housekeeping.
• Executes CMMS Work Instruction from process plants (e.g. leakages, replace faulty part, troubleshooting, repair).
• Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable.
• Supervise and oversee Third Party Contractors, where applicable.
• Any other duties as and when assigned by the Supervisor / Manager

cGMP Standards

• Understands and follows proper cGMP principles and our company quality guidelines and policies related to the execution of assigned work.

PROBLEM SOLVING:

• Use tools like Real time problem solving (RTPS), Fishbone or 5 Whys to solve problem
• Assesses simple issues and suggest paths towards resolution
• Able to properly assess the situation and understand when to escalate to a higher-level Leading Self or Others, and Department
• Works with minimum direct supervision
• Trains and guides technicians in the day/shift teams
• Seeks advice in personal and professional development • Apply inclusive behavior in the work environment and day to day activity

WHAT YOU SHOULD HAVE

Qualification:

• NTC / ITC / Diploma in Electrical Engineering, Instrument & Control or Mechanical Engineering or its equivalent • PUB electrician's license will be an advantage

Experience:

• Min 2 years of working experience in electrical/instrumentation in Petrochemical or related industries
• Good working experience in Electrical & Instrumental discipline will be an advantage
• Knowledge of cGMP and good documentation practice is an advantage

Other Personal Attributes:

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• Initiative, drive and ability to work independently
• Good interpersonal and communication skills

This is a career conversion programme under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• Singaporeans/Singapore PRs only
• PMETs/Mid-Careerist with more than 2 years working experience
• Open to two years contract

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

The Pharmaceutical Technical Operations (PTO) Process Engineer or Chemist provides technical supply support on the commercialization and manufacture of all drug products

WHAT YOU WILL DO

• Supports all technical or process activities, for example, investigations, validation and qualification processes, risk and impact assessments and process safety management activities
• Supports continuous process improvement activities to enhance site performance metrics and contributes to the global company technical network to share site experiences and knowledge and continuously expands on personal expertise.
• Supports the introduction of new products to the site and the transfer of drug products to other facilities

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• Bachelor’s Degree in Chemistry, Biological, Pharmaceutical, and/or Chemical/Mechanical Engineering
• Minimum 2 years of relevant experience from oil and gas, semiconductor or manufacturing industries preferred
• Good verbal communication skill and technical writing skill
• Attention to detail

This is a Career Conversion Program (CCP for Advanced Biopharmaceuticals Manufacturing Professionals (Place-and-Train) under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• PMETs/Mid-Careerist with minimum 2 years of working experience
• Singaporeans/PRs only

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

Reporting to the Engineering Manager, you are responsible for supporting and executing the setup of the Packaging operations. This involves working closely together with the Capital Project team to ensure Safety, Quality, Compliance and Operational aspects of the packaging lines are adequately included during the design and construction phase. Post construction and qualification, as the team prepares for commercial supply, you will support the engineering and maintenance activities to ensure they meet GMP, regulatory and supply requirements.

WHAT YOU WILL DO

• Participate actively as part of the Site start-up team in equipment FATs and site qualification activities (IQ, OQ and PPQ) for Syringe and Vial Packaging lines
• Shape data-driven decisions that solve business challenges and deliver on desired outcomes and people experience.
• Drive innovation, every plant area is a model area using company production system
• Build future-ready manufacturing facility and position company as strategic site for new products and innovation solutions in the Global Network.

Key Responsibilities:

Safety & compliance

• Uphold and comply with safety standards and never compromise on patient, team and personal safety.
• Participate in Safety, Health, and Environment (SHE) improvement initiatives.
• Implement corrective and preventive actions as recommended from investigations, regulatory inspections and internal audits.
• Understand and ensure Safety and cGMP requirements are met. Ensure equipment related activity is completed according to established procedures and all associated documentation is completed to a high standard.
• Participate in Emergency Response Team (ERT) as a team member when assigned.

Enhance and uphold Maintenance quality

• Execute maintenance and improvement activities within the IPT, ensure preventative maintenance is completed according to schedule requirements, and support equipment change control implementations
• Reduce equipment downtime and enhance equipment performance through quality preventive maintenance works.
• Executes CMMS Work Instruction from Packaging line (e.g. Isolation and Reconnection of electrical supply, replace faulty part, troubleshoot, repair E/I and mechanical faults).

Operations excellence

• Support and meet performance metrics of the assigned operations
• Proactively assess and carry out preventive maintenance and corrective repair works on packaging, robotic and conveying system.
• Contribute to maintain a high level of good housekeeping and carrying out operations within accepted GMP and HSE practices.
• Resolve issues in a timely manner and minimize equipment down time.
• Participate in Continuous improvement initiatives. Identify and report improvement for routine work activities.
• Highly effective worker; resourceful with a “get-it-done, can-do” attitude.

Problem solving

• Analyze and recommend solutions for identified issues
• Support Production and Maintenance teams on problem solving and troubleshooting.
• Able to properly assess the situation and understand when to escalate to a higher level.
• Work together with the Engineering team to use 5S tool to maintain the working environment and perform Kaizen for improvement activities.

WHAT YOU SHOULD HAVE

Qualifications & Experience

• Nitec/ Diploma in Mechanical / Mechatronics / Electrical or Instrumentation & Control Engineering.
• 3-5 years of maintenance experience in the chemical or semiconductor industry.
• Experience or knowledge of PLC’s/HMI’s, electrical protective devices will be an added advantage.
• Good oral/written communication and interpersonal skills.
• Knowledge and experience working within a Computerized Maintenance Management System (CMMS). ). Familiarity with SAP is a plus.
• Basic knowledge in using Microsoft Office, including MS Word, MS Excel, MS PowerPoint

Professional Competencies

• Resilient and resourceful
• Continuous learning mindset
• Foster teamwork and cross collaboration
• Strong work ethics
• Result driven mindset

Job Requirements

• Physically fit as the job requires employee to stand, walk, crouch, lift, twist, climb and reach.
• In addition, employee may be required to stand for a period of time, climb flights of stairs, and wear hearing protection equipment as required by the job.
• Role requires employee to work on shift
• May be required to be on standby for any emergency repair after office hours, weekends and public holidays

This is a Career Conversion Programme (CCP for Advanced Biopharmaceuticals Manufacturing Professionals (Place-and-Train) under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• PMETs/Mid-Careerist with no prior work experience in Biopharma industry are welcome to apply
• Singaporeans/PRs only

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Pharmaceutical Manufacturing.
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

WHAT YOU WILL DO

In this role, you will support the site energy sustainability program and introduce good energy management practices to improve energy efficiency and reduce environmental impact. The program shall be in alignment with the global energy conservation program and Singapore Energy Act. Support site to analyse energy efficiency opportunities, leverage expertise and manage projects to implement improvements.

Besides, you will support Engineering Services to meet profit plan targets, optimize cost effectiveness, and lower utility operation in accordance with cGMP and Safety guidelines, with emphasis on reliable and stable operation.

Cost Transformation and Energy Management

• Support cost transformation for utilities program. Will be the project owner, ensuring projects are implemented on schedule, validated in accordance to commitment and accuracy of reports. Conduct analysis; identify risks and proposal for mitigation and to report out to the governance committee.
• Support the site energy efficiency program and introduce good energy management practices to improve energy efficiency and reduce environmental impact. The program shall be in alignment with the global energy conservation program and Singapore Energy Act. Support site to analyse energy efficiency opportunities, leverage expertise and drive projects to implement improvements.
• Support the site energy conservation program with all stakeholders to ensure site wide consistency in energy awareness, energy conservation and active participation in our site energy conservation program
• Support the computerized energy monitoring system for the site to drive efficiency and sustainability
• Support the development of annual and long-term strategic energy capital projects to ensure continuous energy efficiency improvement and energy conservation sustainability, in alignment with the site’s energy policies.
• Provide expertise in conducting energy audit, evaluating options and providing solutions
• Promote energy efficiency program for the company to ensure high level of awareness by all employees in energy usage and energy efficiency in equipment operation
• Network with the energy subject matter experts from other sites, the Global Energy Team, other Pharma Energy Improvement team and the government to recommend proven or new energy savings program and initiatives and continuously seek new energy conservation technologies with subject matter experts
• Monitor and analyse key performance indices and take mitigation actions to ensure objectives are met and where appropriate to escalate

Engineering Services Support

• Coordinate with GES on site process engineering design, construction and equipment validation activities when appropriate
• Supports Energy Lead – Engineering to develop Profit Plan forecast, execute activities to meet production, cost effectiveness, and cost reduction targets
• Any other tasks as and when assigned by Energy Lead

Management of Maintenance, Utilities & Facilities

• Support utility / process / system energy efficiency program – compilation of data, analysis of data and recommendation to stakeholders to reduce wastage or find alternative energy efficient methodology
• Collaborate with maintenance and utilities managers to ensure all equipment have an effective PM or predictive program to ensure all equipment are in high energy efficiency operations
• Support the development of system and program to track energy conservation projects, cost savings from new initiatives and prepare stretch goal for each year to reduce cost of energy for the site
• Prepare utility budgets, monitor actual billing spending and track energy conservation projects against this budget. Analyse and report out risk and mitigation plans.
• Coordinate the implementation of energy projects with utilities operation with least impact to manufacturing
• Recommend energy efficient process, system or proven equipment to Project Engineers in their capital planning process or in their capital procurement plan
• Coordinate and update global energy project planning system to maintain a good energy conservation pipeline for each year and over a 3-5 years period to ensure energy sustainability and reducing site energy consumption levels
• Ensure projects are timely, on budget and completed in compliance to safety and quality
• Due to diversity of the site and the complexity of projects, priority of projects and changes of priority affects the planning process. This position is frequently required to take appropriate decisions and actions to engage stake holders from peer level or next level managers for resolution. For the energy reduction role, he is to analyze, develop projects, prioritize and plan for the resources to complete the projects.

Technical Competencies

• Advance in Energy Conservation Technologies, Proven Energy Savings Program, Standards and Benchmarking.
• Advance in the practical application of theoretical engineering knowledge
• Advance in the development and monitoring of engineering budgets
• Advance in planning of engineering and non-engineering activities in support of role
• Advance in the principles and application of risk based decision
• Consistently applies and promote LSS, MPS and change management tools

SHE

• Consistently show safety leadership by demonstrating advance understanding of all safety procedures and standards
• Seek opportunities to improve company SHE standards and move company towards goal on injury free workplace & better environment

cGMP Standards

• Consistently demonstrates advanced understanding of the importance of cGMP and WQS standards
• Consistently demonstrates an advanced understanding of the importance of cGMP regulations related to their work and consistently develops and executes appropriate solutions
• Seek opportunities to improve company cGMP standards and move company towards goal of Sustainable Compliance
• Subsystem owner for Quality Management System – Plant Maintenance Calibration.

Problem Solving

• Demonstrate creativity, maturity and foresight in providing solutions which are highly innovative, practical for implementation and may have strategic impact
• Lead cross-functional teams in the evaluation and resolution of complex problems with potential impact across business units and demonstrates ability to make rapid rational decisions under pressure

ACCOUNTABILITIES

• Undertakes activities to realize cost reduction, energy reduction or continuous improvement projects to be on time, on budget and to meet compliance requirements
• Effectively implements the Performance Management Process (PMP), ensures that objectives are developed, provides timely continuous feedback to direct reports, and appropriately rewards team members based on performance and demonstration of our leadership standards
• Implement effectively any tasks or projects as assigned by Supervisor as prioritized by business need.

WHAT YOU MUST HAVE

• Engineering Degree or equivalent
• Singapore Certified Energy Manager (preferable)
• Advance degree, such as Masters, would be a plus
• Work experience required with 5-10 years’ experience in engineering, manufacturing, consultancy or equivalent industry
• Demonstrate leadership behavior in alignment with our leadership standards

Functional Competencies

• Demonstrated project management expertise to execute large and/or complex projects, work in cross-functional teams to complete projects successfully within budget, schedule and quality requirements.
• Knowledge of applicable regulations and divisional policies/guidelines, especially equipment design, equipment qualification, preventive maintenance and calibration.
• Demonstrated capability in vendor service contracts management.
• Demonstrated knowledge of our System Life Cycle Methodology.
• Understands maintenance programs and requirements (reliability-cantered, preventative, predictive).
• Stewardship awareness, including cGMP, regulatory inspection preparation, and SHE.
• Demonstrated capability in the application of appropriate troubleshooting and problem-solving techniques.
• Effective communication skills, ability to lead cross-functional teams.
• Performance planning: objectives setting, metrics, action plan, reviews and performance management.
• Understands the site value stream and is customer focused.

This is a career conversion programme under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• Singaporeans/Singapore PRs only
• PMETs/Mid-Careerist with more than 2 years working experience
• Open to two years contract

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WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

WHAT YOU WILL DO

JOB PURPOSE

Coordinate and work alongside a team of 3rd Party Service Provider Personnel in performing warehouse and logistics activities in receiving, sampling, shipping, staging, storing, issuing, pack-out, inventory counting, transportation and documents processing related to materials movements.

MAIN RESPONSBILITIES:

• Provide guidance to Warehouses Personnel and 3rd Part Service Provider on proper and safe handling of materials, compliance to cGMP practices/procedures, accurate entry and maintenance of inventory transaction records. (as per assigned).
• Coordinate weekly microbiology test and quarterly swab-test of the pack-out rooms and isolators (as per assigned)
• Receive incoming materials. Verify incoming materials against the delivery note/document. Stage materials received neatly and transfer to storage locations. Route documents for the materials received to the appropriate departments for further processing. Record and report any variance versus the delivery note/document.
• Assemble and stage materials per production pick list and issue the materials to the appropriate plants. Accurately document all transactions. Input transaction data into the business computer systems and file the documents accordingly.
• Perform pack-out activities and observe the cleanliness requirements in the pack-out work area. Perform sanitation and cleaning of pack-out rooms and isolators. Record and document the operating temperature and relative humidity of the work area. Accurately document the pack-out transactions. Input transaction data into the business computer systems and file the documents accordingly.
• Perform sampling operation and observe the cleanliness requirements in the sampling booth. Perform sanitation and cleaning of sampling booth. Accurately document the sampling operation activities. and file the documents accordingly.
• Assemble and stage materials per the shipment packing list and hand-over the goods to designate freight forwarding agent. Accurately complete shipping document in accordance with shipping instructions. Input transaction data into the business computer systems and file the documents accordingly.
• Operate pallet truck, stacker, forklift and other material handling equipment. Handle all materials according to safety, health and environmental procedures with special attention to the handling of hazardous chemicals and store materials in accordance to its controlled storage requirements.
• Conduct inventory counts as required and record the variances in accordance to operating procedures.

Qualification:

• GCE ‘O’ level or equivalent.

Experience:

• At least 5 to 8 years of related work experience.
• Experience and knowledge in materials handling, operating of materials handling equipment, basic safety knowledge.
• Must have good understanding of procedure/ document system used for materials movements.

Other Personal Attributes:

• Able speaks, read and write simple English; and perform basic mathematics.
• Familiar with applicable regulations and guidelines, example: inventory control and handling of dangerous goods.
• Familiarized with cGMP working environment.