Responsibilities:
- Timely completion and data verification of all testing of raw material, intermediates, in-process control samples and final product.
- Maintain comprehensive, up-to-date, and accurate records for all conducted tests.
- Serve as a SME for a range of instruments and techniques, offering support as needed for both simple and complex issues.
- Lead and perform any method transfer or method validation protocols or equipment qualifications and support the transfer of new products
- Demonstrate understanding and adherence to cGMP 6S concepts.
- Able to present clearly and lead confidently during audits and site leadership inquiries
- Write/revises procedures as necessary and make recommendations for process improvement
- Perform variety of laboratory techniques with minimal error
- Train new analysts and technicians on instruments and techniques.
- Assist the lab supervisor in following up with corrective actions
- Lead laboratory investigations, collaborating with QA to ensure successful closure.
- Participate in tier meeting for manufacturing updates on incoming raw materials/in-process samples and final API
- Ensure a safe work environment by enforcing EHS standards, procedures, and policies
Requirements:
- Bachelors in biology, biochemistry and chemistry or related science degree
- Minimum 1-3 years of experience in pharma manufacturing
- Able to commit to 12 hour rotating day/night shift
Interested candidates please send a copy of your resume in MS Word to
EA Personnel: Alvin Lee Peck Keong
CEI No.: R1104781
Recruit Express Pte Ltd, EA License No.: 99C4599
