855 Quality Control Specialist jobs in Singapore

Dingdong Maicai, a leading fresh grocery e-commerce platform, is expanding its successful B2B fresh grocery delivery model to Singapore's vibrant F&B sector. Building on our proven track record in markets like Dubai, we are dedicated to provide efficient, high-quality fresh product solutions to restaurants, cafes, and food establishments across Singapore. Join our dynamic team and play a key role in shaping the future of fresh food supply chain in Singapore.

Responsibilities

• Inspect incoming fruits & vegetables, check freshness and quality.
• Monitor warehouse stock, prevent defective products.
• Supervise sorting and ensure product standards.
• Handle quality issues and coordinate with supply chain teams.

Requirements

• Diploma in Food Science or related fields.
• 2+ years in fresh produce/food quality inspection preferred.
• Knowledge of food safety standards; HACCP/ISO22000 is a plus.
• Good communication and responsibility.

Working Schedule

• 6 days work / 1 day off
• Night shift required

Registration No D

EA No. 25S2678

EA Personnel: R

• 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 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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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.

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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.

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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.

• 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

We seek a qualified professional to support quality control operations within our biotech drug substance site. The role is responsible for executing laboratory testing, sample management, and equipment maintenance in compliance with cGxP standards.

The successful candidate will be responsible for performing analytical testing and documentation of raw materials, drug substances, drug products, packaging, complaints, and stability samples. Additionally, they will manage sample storage and stability programs, maintain, calibrate, and qualify laboratory equipment, and ensure compliance with cGxP, data integrity, and HSE guidelines.

• Sample Management: Manage sample storage and stability programs
• Laboratory Equipment Maintenance: Maintain, calibrate, and qualify laboratory equipment
• Compliance: Ensure compliance with cGxP, data integrity, and HSE guidelines
• Documentation: Perform analytical testing and documentation of raw materials, drug substances, drug products, packaging, complaints, and stability samples

To be successful in this role, you should have a diploma or equivalent training in a relevant scientific field (e.g., Chemistry, Biochemistry, Biotechnology, Life Sciences). Additionally, you should have preferably 2-5 years of experience in a pharmaceutical laboratory environment (QC, QA, or production) and knowledge of GMP/cGxP standards, laboratory techniques, and QC processes.

• Degree: Diploma, apprenticeship, or equivalent training in a relevant scientific field
• Experience: Preferably 2-5 years in a pharmaceutical laboratory environment
• Knowledge: GMP/cGxP standards, laboratory techniques, and QC processes

This role offers the opportunity to directly impact product quality, compliance, and patient safety while working in a collaborative and innovative environment.