912 Quality Analyst jobs in Singapore

• Carry out incident investigation, VDR analysis, on board audits / inspections and training as assigned.
• Assist the company with business development, where possible.
• Perform duties of Training Faculty when required.
• Visit and assess vessels for compliance with owners / managers requirements, industry regulations and best practices.
• Under the direction of the General Manager / Team Lead, ensure all assigned jobs are delivered in line with its expectations and ensure quality standards are uniformly maintained.
• Keep up to date with national, regional, and international legislative requirements and practices to support company compliance with all relevant regulations.
• Perform tasks as per the deliverables agreed with the client.
• Interface with vessel operators to ensure vessel performance standards.

• Carry out incident investigation, VDR analysis, on board audits / inspections and training as assigned.
• Assist the company with business development, where possible.
• Perform duties of Training Faculty when required.
• Visit and assess vessels for compliance with owners / managers requirements, industry regulations and best practices.
• Under the direction of the General Manager / Team Lead, ensure all assigned jobs are delivered in line with its expectations and ensure quality standards are uniformly maintained.
• Keep up to date with national, regional, and international legislative requirements and practices to support company compliance with all relevant regulations.
• Perform tasks as per the deliverables agreed with the client.
• Interface with vessel operators to ensure vessel performance standards.

Job Role:

As a Water Testing Specialist, you will play a pivotal role in ensuring the accuracy and reliability of water analysis results.

The key responsibilities of this position include sample preparation for analysis, conducting thorough water testing using various methods and instruments, and maintaining our ISO 17025 system to guarantee high-quality results.

You will work closely with the laboratory team to ensure seamless operations and contribute to the maintenance of our quality management system.

Additionally, you will be responsible for adhering to strict protocols and procedures to ensure accurate results and compliance with regulatory requirements.

Key Responsibilities:

• Prepare samples for analysis to ensure accurate and reliable results.
• Conduct water testing using various methods and instruments to analyze water quality.
• Maintain our ISO 17025 system to guarantee high-quality results.

Requirements:

• A degree in Chemistry or a related field is required.
• Previous experience in water testing is highly desirable.

Key Responsibilities

• Manage the storage and inventory of laboratory samples
• Conduct analytical testing and documentation for APIs, drug substances/products, complaints, packaging materials, and stability samples
• Ensure strict compliance with cGxP standards, including data integrity requirements
• Execute and document stability testing (if not centralized), including storage, testing, and reporting to cGxP standards
• Follow all Health, Safety, and Environment (HSE) guidelines
• Identify and report safety risks or potential incidents, and propose preventive solutions
• Participate in mandatory training and retraining programs
• Support operations during rotating day/night shifts

Role Requirements

Essential Qualifications and Experience

• Prior experience in a laboratory setting within the pharmaceutical industry (QA, production), with exposure to aseptic techniques preferred
• Proficiency in administrative and documentation tasks compliant with GMP and HSE standards
• Demonstrated strengths in:
• Breakthrough analysis and problem-solving
• Resilience and adaptability
• Operational efficiency and continuous learning
• Digital fluency and technical skills

Technical Competencies

• Hands-on knowledge of laboratory instruments and QC testing procedures
• Strong command of GxP, TQM principles, and lab excellence standards
• Ability to maintain QC IPC/DS laboratory equipment and systems in accordance with cGMP compliance
• Competent in executing product testing within timelines and contributing to validation and method transfer protocols
• Skilled in performing routine in-process, release, and stability testing, including documentation review
• Capable of supporting lab investigations and leading root cause analysis
• Detail-oriented in preparing and verifying QC documentation to ensure accuracy, consistency, and regulatory compliance
• Proactively identifies opportunities to optimize testing procedures
• Supports audit readiness and participates in internal audits and inspections by health authorities

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

• Conduct quality checks on final product according to established procedures.
• Keep proper record of all analysis results.
• Identify and raise a nonconformance form when the product quality does not meet the specification.
• Provide support to the Production, R&D or Sales departments on an ad-hoc basis.
• Perform calibration and maintenance of lab equipment as planned.
• Properly store and label all retained samples and documentation in the designated storage area.
• Ensure compliance to statutory and corporate requirements related to Health, Safety, Environment and Quality.

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Manfield Employment Services Pte Ltd (Lic. No: 95C2823)

Posting Personnel: Quennie Chen

EA Personnel Reg No.: R1222837

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

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

This position is for 12-hr day shift, 2-3-2 basis.

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.