350 Quality Control Analysts jobs in Singapore

About the Role:

We are looking for a QC Analyst (Microbiology) to support our QC lab operations, ensuring testing and documentation are completed accurately and in compliance with cGMP standards.

Responsibilities:

• Perform routine microbiological testing of raw materials, drug substances, finished products, and packaging/stability samples.
• Manage sample handling, storage, and documentation.
• Ensure compliance with cGxP, GMP, HSE, and data integrity requirements.
• Support audits, inspections, and laboratory equipment documentation.

Requirements:

• Diploma/Degree in Microbiology, Biotechnology, Life Sciences, or related field.
• Preferably with lab or pharmaceutical industry experience.
• Knowledge of aseptic techniques, microbiological methods, and GxP standards an advantage.
• Strong attention to detail, teamwork, and communication skills.

Why Join Us?

• Be part of a global biotech/pharma company committed to quality and patient safety.
• Gain hands-on laboratory experience in a regulated environment.
• Continuous learning and professional growth opportunities.
• Collaborative and supportive work culture.

About the Role

We are seeking a QC Analyst 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, ensuring the quality and timely delivery of products.

Key Responsibilities

• Perform analytical testing and documentation of raw materials, drug substances, drug products, packaging, complaints, and stability samples
• Manage sample storage and stability programs
• Maintain, calibrate, and qualify laboratory equipment
• Ensure compliance with cGxP, data integrity, and HSE guidelines
• Participate in training and contribute to continuous improvement initiatives

Performance Measures

• Accurate and timely completion of analysis and documentation
• Compliance with GMP, SOPs, and regulatory standards
• Readiness for inspections with no critical findings
• Contribution to cost and process optimization

Qualifications & Experience

• Diploma, apprenticeship, or equivalent training in a relevant scientific field (e.g., Chemistry, Biochemistry, Biotechnology, Life Sciences)
• Preferably with 2-5 years of experience in a pharmaceutical laboratory environment (QC, QA, or production)
• Knowledge of GMP/cGxP standards, laboratory techniques, and QC processes
• Strong teamwork, resilience, and problem-solving skills
• Basic proficiency in English

Why Join Us

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

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking an experienced Quality Control Analyst with experience in pharmaceutical company/Life Science industries for a role in Singapore.

Key Responsibilities:

• Sample storage and management
• Prepare and support analytical testing
• Analytical testing and documentation
• Perform lab housekeeping activities
• Perform administrative documentation
• Comply with all HSE guidelines
• Detect and report potential accident, risks and propose solutions
• Responsible for participating in initial training and retraining

Qualifications:

• Proficient in English.
• Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production).
• Nitec or Diploma holders

Why PharmEng Technology?

Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone's unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.

EEOC Statement

At PharmEng Technology, we don't just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.

About the Role:

We are looking for a QC Analyst (Microbiology) to support our QC lab operations, ensuring testing and documentation are completed accurately and in compliance with cGMP standards.

Responsibilities:

• Perform routine microbiological testing of raw materials, drug substances, finished products, and packaging/stability samples.
• Manage sample handling, storage, and documentation.
• Ensure compliance with cGxP, GMP, HSE, and data integrity requirements.
• Support audits, inspections, and laboratory equipment documentation.

Requirements:

• Diploma/Degree in Microbiology, Biotechnology, Life Sciences, or related field.
• Preferably with lab or pharmaceutical industry experience.
• Knowledge of aseptic techniques, microbiological methods, and GxP standards an advantage.
• Strong attention to detail, teamwork, and communication skills.

Why Join Us?

• Be part of a global biotech/pharma company committed to quality and patient safety.
• Gain hands-on laboratory experience in a regulated environment.
• Continuous learning and professional growth opportunities.
• Collaborative and supportive work culture.

SCG Cell Therapy Pte Ltd is a Singapore based clinical-stage biotechnology company focusing on the development of novel immunotherapies for patients with pathogenic infections and associated cancers.

WHAT WE'LL OFFER YOU:

• The opportunity is based at the global headquarters of a fast-growing pre-IPO company dedicated to making positive differences in people's health. SCG is a company that provides employees with clear motivational goals and has a strong and positive employer brand in our field.
• A chance to develop your skills and advance in your career in a rapidly evolving business environment. This position is new in our organization, and thus you will have an excellent opportunity to impact the role and its responsibilities, build up a strong team and grow together with the company. This position offers significant career growth opportunity as the business is entering into a fast growth phase and high visibility to senior level management.
• A culture that is transparent, ambitious, international and where a team of experienced professionals with diverse backgrounds share a passion for helping patients and families in need.

The candidate will perform routine assays and assist the QC team leader in validating new assays used for in-process and final product release testing. The candidate will also be expected to support the routine maintenance and upkeep of the QC laboratory, and contribute to the continuous improvement of QC processes.

• Conduct scheduled in-process and product release testing
• Evaluate test data and generate test reports
• Conduct environmental monitoring of cleanrooms
• Draft standard operating procedures and QC related work instructions
• Support routine QC laboratory operations
• Contribute to the continuous improvement of QC procedures and processes
• Assist in the development, optimization and qualification of new test methods
• Apply good documentation practices on all records

• Diploma or Degree in the chemical or life sciences
• Candidates with cleanroom experience preferred
• Experience with cleanroom environmental monitoring would be advantageous
• Experience with cell and tissue cultures, flow cytometry, qPCR and plate-based fluorescence assays would be advantageous
• Assay development experience is a plus
• Experience with regulatory audits is a plus
• Candidates familiar with GDocP, cGMP, and GLP principles preferred

About the Role:
We are looking for a QC Analyst (Microbiology) to support our QC lab operations, ensuring testing and documentation are completed accurately and in compliance with cGMP standards.
Responsibilities:
Perform routine microbiological testing of raw materials, drug substances, finished products, and packaging/stability samples.
Manage sample handling, storage, and documentation.
Ensure compliance with cGxP, GMP, HSE, and data integrity requirements.
Support audits, inspections, and laboratory equipment documentation.
Requirements:
Diploma/Degree in Microbiology, Biotechnology, Life Sciences, or related field.
Preferably with lab or pharmaceutical industry experience.
Knowledge of aseptic techniques, microbiological methods, and GxP standards an advantage.
Strong attention to detail, teamwork, and communication skills.
Why Join Us?
Be part of a global biotech/pharma company committed to quality and patient safety.
Gain hands-on laboratory experience in a regulated environment.
Continuous learning and professional growth opportunities.
Collaborative and supportive work culture.
#J-18808-Ljbffr

SCG Cell Therapy Pte Ltd is a Singapore based clinical-stage biotechnology company focusing on the development of novel immunotherapies for patients with pathogenic infections and associated cancers.

WHAT WE'LL OFFER YOU:

• The opportunity is based at the global headquarters of a fast-growing pre-IPO company dedicated to making positive differences in people's health. SCG is a company that provides employees with clear motivational goals and has a strong and positive employer brand in our field.
• A chance to develop your skills and advance in your career in a rapidly evolving business environment. This position is new in our organization, and thus you will have an excellent opportunity to impact the role and its responsibilities, build up a strong team and grow together with the company. This position offers significant career growth opportunity as the business is entering into a fast growth phase and high visibility to senior level management.
• A culture that is transparent, ambitious, international and where a team of experienced professionals with diverse backgrounds share a passion for helping patients and families in need.

The candidate will perform routine assays and assist the QC team leader in validating new assays used for in-process and final product release testing. The candidate will also be expected to support the routine maintenance and upkeep of the QC laboratory, and contribute to the continuous improvement of QC processes.

• Conduct scheduled in-process and product release testing
• Evaluate test data and generate test reports
• Conduct environmental monitoring of cleanrooms
• Draft standard operating procedures and QC related work instructions
• Support routine QC laboratory operations
• Contribute to the continuous improvement of QC procedures and processes
• Assist in the development, optimization and qualification of new test methods
• Apply good documentation practices on all records

• Diploma or Degree in the chemical or life sciences
• Candidates with cleanroom experience preferred
• Experience with cleanroom environmental monitoring would be advantageous
• Experience with cell and tissue cultures, flow cytometry, qPCR and plate-based fluorescence assays would be advantageous
• Assay development experience is a plus
• Experience with regulatory audits is a plus
• Candidates familiar with GDocP, cGMP, and GLP principles preferred

Why working at Eurofragance?

In Eurofragance you will be part of the exciting world of smells and fragrances.

You will grow and learn in a company in constant growth and expansion.

You will have the opportunity to develop your career working with top professionals.

You will be part of a Global Company with Headquarters in Spain and subsidiaries in Dubai, Singapore, Mexico, Turkey, and India among others.

You will practice your language skills in a global and multicultural environment.

You will feel you play a role in society thanks to our Corporate Social Responsibility policy and our commitment to the Environment, which we demonstrate on a day-to-day basis with actions such as the Volunteer Day.

We are Passion, Performance & Entrepreneurship, we are Eurofragance

Enjoy a great work environment in Eurofragance

At our company, we're committed to creating an inclusive work environment where everyone feels welcome, regardless of their gender, age, sexual orientation, or any other factor. We encourage candidates from all walks of life to apply for this job vacancy, and we extend a particularly warm welcome to those with disabilities.

JOB MISSION:

The principal objective of this position is to carry out routine tasks related to quality control (QC) of raw materials and finished products to uphold quality standard of the company.

This person will need to prioritize urgencies accordingly and coordinate with relevant departments and/or parties.

MAIN JOB FUNCTIONS:

• Perform routine QC testing, which includes organoleptic, physical-chemical and chromatographic analyses.
• Interpret and evaluate analysis results against established standards and specifications for product releases and/or rejections.
• Assist in the investigations for quality non-conformances.
• Responsible for clear entry of quality data and information.
• Maintain good housekeeping in the laboratory and sample retention room.
• Ensure the smooth operations of the laboratory with periodic checks and in-house maintenance of laboratory instruments/equipment.

EDUCATION & EXPERIENCE REQUIRED:

• Minimally a diploma in science related field(s), preferably chemistry or perfumery.
• Minimum of 1 year of relevant work experience in a laboratory, preferably in a quality control department.
• Knowledge with SAP and/or hands-on experience with gas chromatography is preferred.
• Fresh graduates are welcome to apply.
• Related experiences in a fragrance or flavour industry will also be considered. A basic olfactory test will be carried out

About Symrise AG

Symrise is a global supplier of fragrances, flavourings, cosmetic active ingredients and functional ingredients. Its clients include manufacturers of perfumes, cosmetics, food and beverages, the pharmaceutical industry and producers of nutritional supplements and pet food. Its sales of approximately € 5.0 billion in the 2024 fiscal year make Symrise a leading global provider. Headquartered in Holzminden, Germany, the Group is represented in more than 100 locations in Europe, Africa, the Middle East, Asia, the United States and Latin America. Symrise works with its clients to develop new ideas and market-ready concepts for products that form an indispensable part of everyday life. Economic success and corporate responsibility are inextricably linked as part of this process.

Symrise – always inspiring more…

Senior Quality Control Analyst (Scent & Care), Singapore

As a Senior/Quality Control Analyst in Scent & Care Division, you will be responsible for conducting routine physical, chemical and sensory analyses to ensure that raw materials and finished products meet defined quality standards, specifications and customer requirements. You will work closely with cross-functional teams to support timely material approvals and ensure seamless product release within QC lead times. This role requires strong technical capabilities in operating lab equipment as well as maintaining accurate documentation and quality records. You will play a key role in identifying root causes of quality deviations and customer complaints, raising non-conformances and supporting corrective and preventive actions.

Additionally, you will contribute to continuous improvement efforts focused on lab efficiency, safety and compliance while supporting business continuity by stepping into critical tasks as needed including during supervisor absences.

The Position:

• Conduct routine physical, chemical, sensory and other required analyses
• Operate laboratory equipment such as GC-FID, GC/MS, titrators etc., perform basic preventive maintenance, equipment and verification/calibration and analytical method verification
• Manage accurate data entry and documentation to ensure full traceability and compliance with internal and regulatory standards
• Perform risk assessments and make informed decisions regarding the approval/rejection of raw materials and finished products based on the test results against the set specifications and customer requirements
• Ensure timely testing and release of raw materials and finished products within QC lead times while supporting business-critical priorities as needed
• Make informed decisions regarding material rework based on historical trends and in consultation with senior team members
• Raise non-conformances for quality deviations in raw materials and finished goods and follow up to ensure proper closure of corrective and preventive actions (CAPA)
• Initiate investigations into customer complaints in coordination with relevant teams to identify root causes and implement corrective measures.
• Collect comprehensive evidence and key data to support investigations. Apply sound reasoning to propose potential root causes for customer complaints and internal rejections
• Ensure adherence to the company's quality standards in alignment with customer contracts and agreements
• Develop and maintain quality specifications and standards for raw materials, intermediates and finished products
• Keep quality control programs, policies, process flows, procedures and work instructions up to date and align with operational needs
• Identify and implement workflow optimizations to enhance productivity, sustainability and laboratory safety
• Communicate effectively and in a timely manner with key stakeholders to prevent delays
• Provide cross-functional support to other QC teams as needed to maintain smooth operations
• Step in to manage critical tasks in the supervisor's absence to ensure business continuity

The Ideal Candidate:

• Degree in Chemistry, Flavors/Fragrance, Food Science or related field with minimum 5 years of relevant experience. Candidates with Diploma and at least 7 years of relevant experience are welcomed to apply.
• Strong understanding of fragrance, flavor and/or aroma ingredients,
• Good knowledge of chemistry, particularly relevant to the flavor and fragrance applications
• Essential exposure to sensory analysis and good sensory skills, especially in odor profile evaluation
• Basic knowledge of production processes in fragrance, flavor or chemical manufacturing
• Experience with SAP
• Hands-on experience with laboratory instruments such as GC, GC/MS, HPLC is an added advantage
• Proficient in writing clear and concise technical reports and communications
• Knowledge of Lab Safety Protocols and Good Laboratory Practice (GLP)
• Proficient in Microsoft Office applications.

Job Reference: AP00997