QC Chemist I

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, No contact lens allowed; prescriptive glasses will be provided, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

Job Description

Join the Thermo Fisher Scientific team to experience meaningful work, innovative ideas, and a customer-centric culture. Our work is significant, from supporting cancer research to safeguarding the environment, ensuring food safety, and providing COVID-19 solutions. As the industry leader in scientific services, we foster an environment that encourages our colleagues to excel and make unique contributions. We are dedicated to offering our colleagues around the world the resources and opportunities they need to create a meaningful difference while building a fulfilling career with us.

Location/Division Specific Information

Singapore/PSG

Position summary:

The role reports to the QC Manager Chemistry. Responsibilities include writing lab procedures, verifying/validating methods, and supporting the manufacture and release of pharmaceutical materials and products. The role also involves building and maintaining the QC lab's cGMP system, delivering analytical solutions to clients, and conducting various testing activities.

Responsibilities:

• To support new equipment qualification, lab computerized system and new chemistry lab set up where required
• To perform transfer/verification/validation of laboratory procedures within the team where required
• To prepare technical documentation including but not limited to protocols, analytical write-ups, standard operating procedures, specifications, investigations and reports.
• To perform analysis of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies.
• To review analytical and laboratory data within the department for accuracy, completeness and compliance with detailed procedures.
• To perform planned preventative maintenance and performance calibrations on equipment.
• Management of QC chemical, reference standard and consumable stock levels
• To maintain own training records
• Participate/chip in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab
• Support and encourage a “Quality Culture” and company 4i values throughout QC
• Ensure cGMP is applied in their area of work and align with cGMP in all areas of the business.
• To work with HSE, cGMP and 5S in mind at all times.
• Undertake ad-hoc activities that may be required by the business
• To support shift work (if necessary) in future

Keys to Success:

This is a fixed term (1 year) role.

Education

Degree in Chemistry or equivalent experience in a strongly related scientific field

Experience

• At least 3 years relevant industrial experience
• Ability to work independently and adhere to critical timelines
• Excellent attention to detail
• Excellent organisational skills