1,663 Quality Control Specialists jobs in Singapore

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

• 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

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

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

Along with our brand-new career site, we've also revamped our application process. If you've applied for a position before April 16th 2025, you can log into your old profile to see the status of past applications. For the application you've will completed, and any in the future, you can create a new profile to check in on your status.

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.

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We are seeking a highly skilled professional to fill the role of Technical Specialist .

• Perform quality control activities, including incoming and outgoing checks.
• Liaise with clients to address product specifications and quality issues.
• Update quality standards regularly to meet client requirements.
• File and update QC testing records or reports.
• Review and verify daily routine QC results.
• Liaise with Logistics Coordinator for outgoing shipment activities.
• Report abnormalities to QA Supervisor.
• Prepare quality-related reports.
• Participate in ISO 9001:2015 Internal Quality Audits (IQA) activities.

Able to lift heavy parts. Physically fit.

Any other duties assigned by management from time to time.

The ideal candidate will possess strong analytical skills and be able to work effectively in a team environment.

Excellent communication and problem-solving skills are essential for this role.

Candidates should have a high level of attention to detail and be able to maintain accurate records.

A strong understanding of quality control principles and practices is required.

This is an excellent opportunity for a career-minded individual to join our organization and contribute to our success.

The successful candidate will receive comprehensive training and support to ensure their success in the role.

Ongoing professional development opportunities will be available to enhance your skills and knowledge.

Please note that all applicants must be willing to undergo a background check as part of the hiring process.

We are seeking a quality control specialist with hands-on experience in temperature mapping of controlled environments. The role focuses on validation, documentation, and compliance to ensure the reliability of temperature-controlled spaces in regulated settings.

• Develop and execute temperature mapping plans for various chambers including cold rooms, freezers, incubators, and stability chambers.
• Create and review protocols, reports, and validation deliverables using systems such as Kneat.
• Perform data integrity assessments and ensure compliance with GDP and Alcoa+ principles.
• Design, review, and maintain SOPs related to temperature mapping and qualification activities.
• Support audit/inspection readiness through accurate documentation and reporting.
• Collaborate with QC, QA, and engineering teams to ensure compliance and operational readiness.
• Contribute to process improvements for chamber qualification and environmental monitoring.

• Bachelor's degree or diploma in life sciences, engineering, or related discipline.
• 2-5 years' experience in temperature mapping of chambers within pharmaceutical/biotech or regulated industries.
• Knowledge of GDP, Alcoa+ principles, and validation requirements.
• Experience with protocol drafting and use of electronic validation systems, e.g., Kneat.
• Strong analytical and documentation skills.
• Ability to work cross-functionally and support compliance initiatives.

Job Summary:

As a QC Laboratory Expert, you will play a pivotal role in ensuring the quality of raw materials used in pharmaceutical production. Your primary responsibilities include:

• Developing and executing method validation protocols for raw material testing.
• Supporting laboratory start-up activities, including equipment qualification, generation of user requirement specifications, SOPs, and configuration specifications.
• Performing quality control tests for raw material samples, including compendial tests and identification tests.
• Conducting quality control sampling of incoming raw materials.
• Authoring and revising raw material specifications and other quality-related documents.
• Assisting with laboratory activities such as housekeeping and equipment maintenance.

Requirements:

The ideal candidate will have a Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, or related life sciences or technology, with at least 5-7 years of experience in QC raw material testing. Additionally, they should possess expertise in method validation/verification, good laboratory practices, and data integrity requirements. Experience with routine laboratory operations and participation in method transfer, method validation, and method verification for raw material testing is highly desirable.

What We Offer:

We provide a dynamic and challenging work environment that allows professionals to grow and develop their skills. Our team is passionate about delivering high-quality results and making a meaningful impact in the industry.

We are seeking a highly skilled M&E professional to oversee the delivery of high-quality work and ensure compliance with statutory requirements.

• Ensure Contractors deliver high-quality work and maintain good safety practices in accordance with regulatory standards
• Attend all project meetings, including site, progress, variation, coordination, QAQC etc.
• Provide ongoing supervision for construction of civil and structural works as needed, ensuring compliance with project specifications, construction drawings, and the Building Control Act and Regulations.
• Carry out supervision and inspection M&E works including concreting, pavement, drainage, compaction, curing of concrete, formwork, re-props and removal of props, quality & erection of precast components and steel works.
• Manage and supervise Resident Technical Officers under his charge.
• Coordinate with safety team and provide overview of WASH and aerodrome safety management systems and implementation of safe working practices on site.
• Ensure all construction works will not impact or affect operations of the client.
• Verify all reports and claims relating to M&E works submitted by contractors.
• Inspect quality of work and materials delivered to site, take corrective actions for any non-compliance, and report any materials that do not conform to specifications to Operations In-Charge.

• At least 8 years of experience in M&E discipline, 3 years in major construction works deep excavation, drainage, pipe jacking, ground improvement, flexible/rigid aircraft pavement, supervising & installation of monitoring instruments and collating of monitoring data.
• Degree in M&E discipline recognized by Project Evaluation Board.
• Accredited as Resident Engineer with Institution of Engineers Singapore (Preferred).
• Able to perform shift work.