237 Quality Control Specialist 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.

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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

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• 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

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.

1. Perform and implement method development / qualification / validation / verification for new product and method introduction, compendial updates.

2. Keeps up-to-date on regulations / development of QC activities to ensure QC operations are in compliance to applicable regulatory and external agency regulations.

3. Lead and perform laboratory investigation and deviation.

4. Responsible to conduct effective training to ensure methods/knowledge are effectively transferred to routine testing team.

5. Write / reviews change controls, events' deviations, CAPA and GMP documents (e.g. SOP, protocols, reports, specification).

6. Provides technical expertise and consultation to routine testing team on technical matters.

7. Performs review of compendium updates timely and accurately.

8. Perform periodic review of test methods to ensure compliance to latest compendium requirements.

9. Ensure real time documentation, maintain data integrity and appropriate traceability.

10. Responsible for the accurate, timely and compliant execution of assigned projects, analytical testing and related documentation.

11. Responsible for checking all results in LIMS/RDS and reporting of any observed results that do not meet the requirement (OOS/OOT/Deviation) for further investigation.

12. Subject-Matter-Expect (SME) audit frontier for assigned.

13. Any other activities as and when assigned by the Superior.

EDUCATION:

Degree / Diploma in science related discipline (e.g. Chemistry, Chemical Engineering, Biomedical Engineering, Biotechnology).

KNOWLEDGE & SKILLS:

1. Possess working knowledge of GMP in the pharmaceutical industry.

2. A good team player with positive learning attitude.

3. Able to work independently, shows initiative and able to work with all levels of staff.

4. Excellent interpersonal and analytical skills, good verbal and written communication skills.

KEY DUTIES AND RESPONSIBILITES:

• Responsible for the analysis of RM, finished product/in-process/stability/validation/utility samples for MLT by referring current version of specification/STP/SOP with relevant product code.

• Responsible for the analysis of water samples by referring current version of specification/STP/SOP with relevant code, based on of monthly schedule.

• Responsible for the analysis samples of EMP by referring current version of SOP.

• Perform identification of microorganism isolate by microscopy.

• Perform the assay test as per STP/SOP by Microbiological method.

• Check the sample integrity with respect to labelling, container, packing, time point, sampling point, etc., along with availability of reagent/chemical/media as per STP/SOP and within the validity.

• Preparation of all microbiological media/diluent/sample as per SOP/STP.

• Ensure maintenance, review and availability of media/cultures and miscellaneous materials.

• Ensure implementation of SOP for all corresponding activities.

• Write controlled documentation related to Microbiology Laboratory operations or testing such as SOP's, analytical protocols, analysis reports and forms.

• Ensure real time documentation, maintain data integrity and appropriate traceability.

• Responsible for checking all results in LIMS/RDS and reporting of any observed results that do not meet the requirement (OOS/OOT/Deviation) for further investigation.

• Responsible for preventive maintenance and calibration of microbiological lab instrument.

• Responsible for microbiology lab and equipment/instrument cleanliness.

• Responsible for procuring and receipt of microbiology lab glassware and consumables.

• Preserve all sample media petri plates till the completion and confirmation of results.

• Responsible for disposition of samples upon confirmation.

• Any other activities as and when assigned by the Superior.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche.

As a Quality Control Analyst based in Singapore, you will join our Microbiology/Environmental Monitoring (EM) team. You'll be responsible for testing environmental and product stream samples, ensuring we meet release timelines and maintain compliance with cGMP regulations. Your work will directly support our manufacturing operations and contribute to a culture of continuous improvement, helping us deliver safe and effective diagnostic solutions.

The Opportunity

• You will perform routine and non-routine testing of environmental, raw material, and product samples in accordance with Standard Operating Procedures (SOPs) and Test Methods.
• You will conduct Environmental Monitoring (EM), including sampling HVAC systems, biological safety cabinets, and compressed gases, as well as monitoring fingertips.
• You will document and review results in our Laboratory Information Management System (LIMS) and other documents to ensure compliance.
• You will perform problem-solving and troubleshooting for testing-related issues and equipment.
• You will support investigations into microbial contamination and help implement corrective actions.
• You will contribute to projects, validation, and process improvement works, and assist in preparing EM reports for lot release and trend analysis.
• You will cooperate with the team to foster a strong team spirit and embody our lean principles and continuous improvement mindset.

Who You Are

• You hold a Bachelor's degree in Microbiology, Biology, Biochemistry, or a related Life Sciences discipline.
• You have 1-3 years of relevant work experience, preferably in a biotech or pharmaceutical environment.
• You have knowledge of cGMP standards and laboratory safety procedures.
• You possess strong communication skills, both written and verbal, in English.
• You are a collaborative and proactive team player with the ability to work effectively with others.
• You are organized and can plan your work effectively to meet deadlines.
• You demonstrate initiative and a proactive attitude, turning ideas into action to support team goals.
• You are committed to promoting a positive safety culture and complying with all Safety, Health & Environment (SHE) requirements.

Who we are

A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let's build a healthier future, together.

Roche is an Equal Opportunity Employer.

Key Responsibilities:

• Quality Performance Dashboard: Collaborate with all Business Units to collect and analyze monthly performance data, identify trends, and prioritize quarterly governance action plans.
• Continuous Improvement: Partner with Business Units on audits, RFCs, and quality risk assessments to identify improvement areas and promote a strong food safety culture.
• GTQM Resource Database Leadership: Maintain and update TQM resource documents, manage user access, and oversee approval matrices.
• Document Management: Support creation and maintenance of R&D policies, guidelines, and procedures in line with international standards.
• Vendor Qualification: Evaluate new/alternative vendors for ingredients and packaging through document reviews, supplier liaison, technical assessments, and audits to meet quality standards.
• Process Qualification: Plan and execute sterility tests, cleaning, sanitation, and hygiene verification for new or modified production lines before commercial approval.
• Quality Plan Development: Develop and maintain quality plans for all Business Units, ensuring alignment and implementation across stakeholders.
• Additional Projects: Undertake other assignments/projects as assigned to meet business needs.

Requirements:

• Min. Degree in Food Technology, Food Science, or related Science/Engineering fields.
• Min. 5 years of QA/QC experience in the dairy or beverage industry.
• Willingness to travel for business.
• Knowledge in food packaging qualification; certified lead auditor qualification is an advantage.

If interested, please email me at or telegram @alexgohhl

Alex Goh Hock Leong

(CEI.No: R l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)