824 Quality Control Specialists jobs in Singapore

Job Id

Singapore, Singapore, Singapore

Job Type

Full-time

Work Your Magic with us

Ready to explore, break barriers, and discover more? We know you've got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Your Role:

Quality Control (QC) Specialist is to promote and integrate quality into every aspect of our BioReIiance biologics safety testing business in Singapore. Duties of the role include the support of QC operations (environmental monitoring and release of critical raw materials), data integrity and systems administration to ensure that laboratory testing operations are in full compliance with sound scientific practice, GxP and Standard Operating Procedures (SOPs). As a QC Specialist, you will ensure quarantine materials are received and released for use as per appropriate quality procedures. The ability to develop and maintain effective working relationships with operational, support services and quality assurance personnel will be critical for success in this role.

Who You Are:

• Graduate degree in life sciences or microbiology or higher related degree
• Minimum of 2-3 years of experience
• Demonstrable scientific expertise in microbiology related works
• Previous experience working in a Quality Control materials release environment
• Previous Pharmaceutical experience would be ideal; however, other industry backgrounds would be considered
• You will have previous work experience within a GLP / GMP regulated environment would be highly desirable
• You are strongly focused on quality and safety, with strong planning and organisational skills
• You have good communication and interpersonal skills and are highly self-motivated, with strong initiative and drive

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress

and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity

US Equal Employment Opportunities

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

Notice on Fraudulent Job Offers

Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information here.

Applicant Profile

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WHAT WE OFFER

Money makes the world go round. But at our company there's more than just financial rewards. We offer a range of attractive benefits to help you work your magic.

Saving & Finacial

Our 401(k) Plan includes a generous company-matching contribution and an additional discretionary contribution each year.

We also provide tax-advantaged accounts for you to save for healthcare, commuting expenses, company-provided and buy-up life insurance to help you protect your financial future.

Health & Wellness

We offer comprehensive medical, dental, & vision coverage-including virtual care through Telehealth & free behavioral health counseling sessions through our Employee Assistance Program.

We also offer a wellness incentive program and personalized support to help you navigate and use your benefits.

Voluntary Benefits

Our voluntary benefits provide additional protection from the high costs of healthcare not covered by health insurance.

We also have discount programs that offer exclusive savings on everything from auto, home, and pet insurance to low-interest personal loans.

Work/Life Support

We have several programs to support your work/life balance, including generous paid time off, back-up day care services, education assistance, and more.

OUR RECRUITING PROCESS

Depending on the position (level, functional area, country) the process can vary slightly.

You apply

Complete your online application for your preferred role(s) that match your interests and qualification. If you cannot find a suitable role please join our Talent Zone and stay connected for your next career opportunity.

We screen

We review your application and if we determine that you are a good fit we will move you to the selection process.

We assess

You are interviewed by phone, via video and/or face to face.

Mutual agreement

Ideally you are the perfect match for us We hope you consider us as your new employer.

Work your magic

To guarantee you a smooth start our onboarding preparation begins.

Haven't found the right job yet?

Join our Talent Community to stay connected and explore future opportunities.

• Perform routine microbiological testing on raw materials, finished products, water, and environmental samples.
• Conduct microbial limit tests, sterility testing, endotoxin testing, and microbial identification.
• Prepare culture media and maintain laboratory equipment in compliance with quality standards.
• Apply Good Laboratory Practices (GLP) and follow Standard Operating Procedures (SOPs).
• Support the investigation of non-conformities and participate in root cause analysis.
• Document and review test results in laboratory notebooks and LIMS systems.
• Assist with validation and verification of microbiological methods.
• Ensure all activities are aligned with regulatory and client-specific requirements

• Academic background: degree in Microbiology, Life Sciences, or related fields.
• Around 1 year of relevant experience in a QC microbiology role.
• Experience with microbiological techniques in pharmaceutical or biotech environment
• Experience with endotoxin testing, bioburden testing, and microbial identification
• Knowledge of GMP/GLP requirements and aseptic techniques
• Familiarity with environmental monitoring programs and cleanroom classifications
• You have an ability to synthetize and prioritize while maintaining strong attention to detail
• Comfortable with working in shift

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Pall Corporation, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. From airplane engines to hydraulic systems, scotch to smartphones, OLED screens to paper—everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place where you can thrive and amplify your impact on the world. Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation.

Learn about the Danaher Business System which makes everything possible.

The Quality Control Specialist is responsible for executing quality control activities within a filter manufacturing environment. This role involves performing analytical testing, inspections, and documentation to ensure products meet internal specifications, customer requirements, and regulatory standards. The QC Specialist also plays a key role in maintaining lab safety and supporting continuous improvement initiatives.

This position is part of the Quality Control Department reporting to the Senior Quality Manager and will be located in Benoi Sector, Singapore.

In this role, you will have the opportunity to:

• Conduct quality inspections, prepare samples for testing, assess product conformity (go/no-go decisions), and escalate issues related to failed or high-risk products.

• Verify and investigate laboratory-related non-conformances and develop effective corrective and preventive actions (CAPA). Oversee calibration activities for on-site equipment and tools to ensure accuracy and compliance.

• Establish and maintain QC protocols, revise Standard Operating Procedures (SOPs) and work instructions, ensure compliance with safety and risk assessment guidelines, and provide training on updated procedures and best practices.

The essential requirements of the job include

• Bachelor's degree in chemistry, Chemical Engineering, or a related scientific field, with a minimum of 3 years' experience in a QC or analytical lab—preferably in chemical manufacturing or similar industries.
• Proficient in analytical techniques including ICP-MS, GC-MS, NVR, LPC, and TOC, with understanding of ISO standards, GMP, and relevant regulatory frameworks.
• Working in 12 hours shift in a cleanroom environment with the gowning procedure.

It would be a plus if you also possess previous experience in:

• Experience in filter or membrane manufacturing environments.
• Proficiency in laboratory information management systems (LIMS) and understanding statistical process control (SPC) and data analysis tools.

Pall Corporation, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit

Job Duties

• Perform visual inspection on electronic components.
• Using various microscopic equipment and the naked eye, to ensure the component matches manufacturer specifications and no damage.
• Using alcohol swipe and scrape test to verify product has not been black topped.
• Determine if there are "red flags" that indicate a possible suspect part.
• Operate and maintain analytical instruments, perform tests in a laboratory such as, but not limited to, XRF, X-RAY, Microscopy, Decapsulation, Solderability, Curve Tracing, and C-SAM.
• Utilize our proprietary system to complete, in detail, the component inspection process and upload any documentation, including but not limited to test results.
• Prepare test reports in a timely manner and ensure tests are performed in accordance with industrial standards/customer specified testing plans
• Support testing method related work instructions in the laboratory
• Communicate/coordinate with 3rd party calibration/test houses to address equipment calibration/maintenance/additional customer testing requirements
• Support laboratory on tasks/processes related to ISO 17025 lab system/customer audits

Requirements

• 3+ years component or product inspection, testing, counterfeit detection
• Solid written and oral communication skills a must
• Multi-tasking and organization skills requirements
• Ability to work in a fast-paced lab environment
• Strong analytical skills and attention to details
• Knowledge of the electronics distribution field is a plus
• Knowledge of ESD controls/ISO 17025 lab system is a plus

What We Offer

We are committed to driving innovation and embracing diversity. At Smith, you will have the opportunity to expose to new opportunities and express your opinion to drive strategy and better results. We engage our people by our great culture, competitive remuneration, comprehensive fringe benefits, and progressive career opportunities.

• 5-day work week
• Annual Leave and Discretionary Day
• Group Medical, Dental and Life Insurance
• Recreational Sponsorship & Education Subsidy
• Comprehensive Wellness Programs and Year-round Company Activities

About Smith

Founded in 1984, Smith is celebrating 40 years of Intelligent Distribution. As a leading independent distributor of electronic components, we source, manage, test, and ship billions of components to partners worldwide in every industry and vertical. Offering a comprehensive suite of flexible and scalable supply chain solutions, Smith identifies and delivers customized service programs to support our customers' success. Our expertise is backed by decades of market data, cutting-edge technology, and a systems-based approach to quality excellence. Smith has generated more than USD $12.9 billion in global revenue since 2019 and ranks eleventh among all global distributors.

We are always looking for talented individuals to join our dynamic, friendly, and professional team environment. Located in more than 20 offices around the world, you'll find a home here as part of the Smith family.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working a

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

As a global leader in clinical diagnostics,
Beckman Coulter Diagnost
ics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.

Learn about the Danaher Business System which makes everything possible.

The
Director of Operations
is responsible for provide strategic direction and collaborates closely with the Beckman Coulter-Dx leadership team to develop manufacturing strategies specifically for India, ensuring alignment with broader corporate goals. This position reports to the Vice President of Operations and is part of operations located in India and will be fully remote.

In this role, you will have the opportunity to:

• Direct and develop operations for Beckman Coulter Dx India, ensuring cost-effectiveness, financial prudence, high quality and safety results.
• Develop long-term operational strategies in collaboration with senior management to optimize workflows and enhance productivity and performance.
• Devise strategies to maximize output and minimize costs across Manufacturing, Operations, Engineering, Facilities, EHS, and DBS

The essential requirements of the job include:
Educational Background:

• Bachelor's degree in a relevant field with at least 18 years of experience
• Master's degree with at least 14 years of experience or Doctoral degree with a minimum of 12 years of experience

Operational Expertise:

• Extensive experience in an operations environment, including manufacturing, supply chain, engineering, logistics, or distribution.

Leading Critical Initiatives:

• Proven leadership experience in managing large, complex projects and teams.

Contract Acumen:

• Experience working with contract manufacturers and a deep understanding of contractual requirements.

Navigation of Matrix Organization:

• Demonstrated ability to manage and influence within a matrix organizational structure.

Process Improvement Skills:

• Lean/Six Sigma proficiency, with certification.
• Strong problem-solving capabilities and a track record of driving continuous improvement initiatives.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel 50% of the time

It would be a plus if you also possess previous experience in:

• Building Relationships: Cultivate strong relationships both internally and externally, effectively liaising with contract manufacturing teams.
• Innovation and Problem-Solving: Foster a collaborative, innovative problem-solving environment, demonstrating excellence in execution.

At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit

Counterfeit Detection – Quality Control Specialist

Key Responsibilities:

• Perform visual inspections of electronic components using microscopes and the naked eye to ensure they meet manufacturer specifications and are free of damage.
• Conduct alcohol swipe and scrape tests to verify products have not been black topped.
• Identify "red flags" indicating possible suspect or counterfeit parts.
• Operate and maintain analytical laboratory instruments, including XRF, X-RAY, microscopy, decapsulation, solderability, curve tracing, and C-SAM.
• Accurately document inspection processes and upload test results using proprietary systems.
• Prepare detailed test reports promptly, ensuring compliance with industry standards and customer testing plans.
• Support laboratory testing methods and update work instructions as needed.
• Coordinate with third-party calibration and testing services for equipment maintenance and additional customer testing requirements.
• Assist with tasks related to ISO 17025 lab accreditation and customer audits.

Requirements:

• Minimum 3 years of experience in component or product inspection, testing, and counterfeit detection
• Familiarity with ESD controls and ISO 17025 laboratory systems is an advantage
• Knowledge of the electronics distribution industry is a plus
• Excellent multitasking and organizational abilities
• Ability to thrive in a fast-paced laboratory environment
• Strong analytical skills with keen attention to detail
• Strong written and verbal communication skills

What We Offer:

We are committed to driving innovation and embracing diversity. At Smith, you will have the opportunity to expose to new opportunities and express your opinion to drive strategy and better results. We engage our people by our great culture, competitive remuneration, comprehensive fringe benefits, and progressive career opportunities.

• 5-day work week
• Annual Leave and Discretionary Day
• Group Medical, Dental and Life Insurance
• Recreational Sponsorship & Education Subsidy
• Comprehensive Wellness Programs and Year-round Company Activities

About Smith

Founded in 1984, Smith is celebrating 40 years of Intelligent Distribution. As a leading independent distributor of electronic components, we source, manage, test, and ship billions of components to partners worldwide in every industry and vertical. Offering a comprehensive suite of flexible and scalable supply chain solutions, Smith identifies and delivers customized service programs to support our customers' success. Our expertise is backed by decades of market data, cutting-edge technology, and a systems-based approach to quality excellence. Smith has generated more than USD $12.9 billion in global revenue since 2019 and ranks eleventh among all global distributors.

We are always looking for talented individuals to join our dynamic, friendly, and professional team environment. Located in more than 20 offices around the world, you'll find a home here as part of the Smith family.

The Opportunity

Esco Lifesciences Group is Singapore's most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.

Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.

Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.

We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.

Who we're looking for

Physical/Mental Requirements/Work Environment

· Ability to understand protocols, technical reports and technology transfer documents.

· Ability to understand standard operating procedures and other related documents.

· Able to commit to weekend work when needed, off in lieu will be given for work on weekends and public holidays.

· Repetitive motions due to certain laboratory techniques.

· Good Understanding of Aseptic Techniques.

· Work performed in a clean room environment wearing PPE.

· Ability to define problems, collect data, establish facts and draw conclusions.

· Ability to focus regardless of circumstances and stress induced pressure.

· Ability to take proactive approach.

· Meticulous and systematic.

· Commitment to continuous learning and staying updated with industry best practices.

· Have a strong focus on safety, quality and timeliness.

· Have strong critical thinking skills.

Report To:

Selected candidate will report to Quality Control Manager and others as assigned.

The Scope

You will be part of Esco Aster's Quality Control team and contribute to the overall site mission and objectives. Specifically, you will contribute to microbial-related analytical testing and operational activities.

Primary work location: Ayer Rajah Crescent, Singapore

Job Responsibilities

· Establishment of QC procedures (drafting and reviewing QC functional SOPs including QC testing SOPs).

· Responsible for Environmental monitoring (Viable and Non-Viable) of Cleanrooms, water and gases as per SOPs.

· Responsible for the Microbiological Testing of Water/Raw Material/in-process/ finished product / stability/validation/utility samples as per approved SOPs.

· Manage coordination and communication with external laboratories for Growth Promotion Testing, Sterility Testing, and Microbial Identification testing services.

· Support Sample Management functions.

· Ensure testing support media and consumable inventory timely manner to avoid delay in testing.

· Write, review and update standard operating procedures timely manner to operate EM and Microbiology operations and to ensure that specifications are in compliance with current GMP requirements/standards.

· Maintain data integrity and appropriate traceability.

· Responsible to identify OOS/OOT/Deviation and participate in Root Cause Analysis (RCA) and recommend corrective and preventive actions as applicable.

· General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc. Responsible for microbiology lab and equipment/ instrument cleanliness.

· Responsible for disposition of samples upon confirmation.

· Collaborate with other functional teams in new processes/equipment/method qualifications.

· Explore and implement new technologies for rapid release such as rapid sterility testing.

· The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor and QC Management from time to time to support GMP Facility.

Requirements

· Degree with at least 3 years or Diploma with at least 5 years of experience in QC (Microbiology and Environmental Monitoring) from a highly regulated cGMP manufacturing environment (Biologics, Pharmaceuticals & ATMPs etc.).

· Candidates with experience in ATMPs (Cell & Gene) manufacturing are highly preferred but not mandatory.

· Ability to prioritize work and multitask.

· Knowledge and experience in QC laboratory operations and procedures, analytical test methods, troubleshooting and evaluation of analytical results

· Thorough knowledge and understanding of current regulatory requirements of cGMP manufacturing.

· Good knowledge and understanding of Biologics manufacturing, aseptic operations and cleanroom behavior.

· Experience cell and gene therapy operations is an added advantage.

· Demonstrated ability to supervise, train, and manage technical staff.

· Demonstrated knowledge in Quality Control operations as it relates to QC testing, method validations and QC system implementation.

· cGMP regulations and audit experience in USFDA, EU and HSA etc.

· Will be able to commit 5 working days per week in a fixed pattern.

· Excellent communication, interpersonal and organizational skills.

· Ability to speak and write in English.

Apply now by submitting a Cover Letter and CV to

The Opportunity

Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.

Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.

Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.

We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.

Who we’re looking for

Physical/Mental Requirements/Work Environment

· Ability to understand protocols, technical reports and technology transfer documents.

· Ability to understand standard operating procedures and other related documents.

· Able to commit to weekend work when needed, off in lieu will be given for work on weekends and public holidays.

· Repetitive motions due to certain laboratory techniques.

· Good Understanding of Aseptic Techniques.

· Work performed in a clean room environment wearing PPE.

· Ability to define problems, collect data, establish facts and draw conclusions.

· Ability to focus regardless of circumstances and stress induced pressure.

· Ability to take proactive approach.

· Meticulous and systematic.

· Commitment to continuous learning and staying updated with industry best practices.

· Have a strong focus on safety, quality and timeliness.

· Have strong critical thinking skills.

Report To:

Selected candidate will report to Quality Control Manager and others as assigned.

The Scope

You will be part of Esco Aster's Quality Control team and contribute to the overall site mission and objectives. Specifically, you will contribute to microbial-related analytical testing and operational activities.

Primary work location: Ayer Rajah Crescent, Singapore

Job Responsibilities

· Establishment of QC procedures (drafting and reviewing QC functional SOPs including QC testing SOPs).

· Responsible for Environmental monitoring (Viable and Non-Viable) of Cleanrooms, water and gases as per SOPs.

· Responsible for the Microbiological Testing of Water/Raw Material/in-process/ finished product / stability/validation/utility samples as per approved SOPs.

· Manage coordination and communication with external laboratories for Growth Promotion Testing, Sterility Testing, and Microbial Identification testing services.

· Support Sample Management functions.

· Ensure testing support media and consumable inventory timely manner to avoid delay in testing.

· Write, review and update standard operating procedures timely manner to operate EM and Microbiology operations and to ensure that specifications are in compliance with current GMP requirements/standards.

· Maintain data integrity and appropriate traceability.

· Responsible to identify OOS/OOT/Deviation and participate in Root Cause Analysis (RCA) and recommend corrective and preventive actions as applicable.

· General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc. Responsible for microbiology lab and equipment/ instrument cleanliness.

· Responsible for disposition of samples upon confirmation.

· Collaborate with other functional teams in new processes/equipment/method qualifications.

· Explore and implement new technologies for rapid release such as rapid sterility testing.

· The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor and QC Management from time to time to support GMP Facility.

Requirements

· Degree with at least 3 years or Diploma with at least 5 years of experience in QC (Microbiology and Environmental Monitoring) from a highly regulated cGMP manufacturing environment (Biologics, Pharmaceuticals & ATMPs etc.).

· Candidates with experience in ATMPs (Cell & Gene) manufacturing are highly preferred but not mandatory.

· Ability to prioritize work and multitask.

· Knowledge and experience in QC laboratory operations and procedures, analytical test methods, troubleshooting and evaluation of analytical results

· Thorough knowledge and understanding of current regulatory requirements of cGMP manufacturing.

· Good knowledge and understanding of Biologics manufacturing, aseptic operations and cleanroom behavior.

· Experience cell and gene therapy operations is an added advantage.

· Demonstrated ability to supervise, train, and manage technical staff.

· Demonstrated knowledge in Quality Control operations as it relates to QC testing, method validations and QC system implementation.

· cGMP regulations and audit experience in USFDA, EU and HSA etc.

· Will be able to commit 5 working days per week in a fixed pattern.

· Excellent communication, interpersonal and organizational skills.

· Ability to speak and write in English.

Apply now by submitting a Cover Letter and CV to .

• Assemble furniture components from raw materials.
• Conduct quality checks on finished products to identify defects or imperfections.
• Collaborate with the fabrication team to optimize production processes.
• Maintain a clean and organized work environment to promote efficiency and productivity.