Senior QC Chemist

Thermo Fisher Scientific; Singapore; On-site; SGD 80,000 - 110,000; Full time

Job summary

A leading pharmaceutical company in Singapore is seeking a Quality Control Specialist with over 7 years of experience in the pharmaceutical or medical devices industry. The candidate will lead testing processes and ensure compliance with GMP standards. A university degree in chemistry or life sciences is required along with extensive knowledge of regulatory expectations and analytical techniques. This role entails managing daily laboratory operations and mentoring team members.

Qualifications

• At least 7 years of experience in pharmaceutical or medical devices industry.
• Proven knowledge of regulatory expectations (PICS, ICH, HSA, EMA, FDA).
• Experience with Health Agency/internal audits is required.

Responsibilities

• Lead the testing process from sampling to release of materials.
• Ensure compliance and timely testing of chemistry analyses.
• Manage daily operations of the laboratory.
• Communicate with cross-functional teams and participate in problem-solving.

Skills

Quality Control

HPLC

cGMP compliance

Interpersonal skills

Analytical techniques

Education

University degree in chemistry or life sciences

Tools

UPLC

CE

Job description

• Support new equipment qualification, lab computerized systems, and chemistry lab setup.
• Perform transfer, verification, and validation of laboratory procedures.
• Prepare technical documentation, including protocols, analytical write-ups, standard operating procedures, specifications, investigations, and reports.
• Analyze incoming goods, intermediates, and finished products under cGMP conditions for QC release and stability studies.
• Lead the testing process from sampling to the release of raw materials, drug substances, process aids, and packaging materials.
• Ensure timely and compliant testing of all chemistry-related analyses, including HPLC, GC, and stability analysis.
• Manage daily laboratory operations, ensuring compliance with GMP standards.
• Identify and address compliance gaps with updated pharmacopoeia and regulations.
• Lead laboratory investigations, deviations, and ensure timely closure in line with quality management systems.
• Review analytical and laboratory data for accuracy and compliance.
• Perform maintenance and calibrations on laboratory equipment.
• Troubleshoot technical issues related to analytical equipment and methods.
• Manage QC chemical, reference standard, and consumable stock levels.
• Train fellow chemists, serving as a mentor and expert.
• Maintain a detailed understanding of international regulatory requirements.
• Communicate effectively with cross-functional teams and participate in problem-solving activities.
• Act as a Subject Matter Expert during audits and inspections.
• Undertake internal audits and support continuous improvement initiatives.
• Promote a culture of quality and adherence to cGMP, EHS, and 5S standards.
• Be prepared to support shift work if needed.

Minimum Requirements/Qualifications

Education:

• University degree or equivalent experience in chemistry, biochemistry, or life sciences.

Experience:

• At least 7 years of proven experience in the pharmaceutical or medical devices industry, with a focus on Quality Control.
• Extensive knowledge of regulatory expectations including PICS, ICH, Singapore HSA, EMA, and US FDA.

Proficiencies:

• Knowledge and exposure to cGMP environment.
• Sound technical knowledge of QC chemistry techniques (HPLC, UPLC, CE, etc.).
• Strong interpersonal and communication skills in English.
• Ability to work cross-functionally and meet timelines and objectives.
• Experience with Health Agency/internal audits.