Salary: Up to $7,000/month
Contract: 6 months, renewable/extendable
Completion bonus: 0.5 month
Start: By end November
Job Responsibilities
- Lead manufacturing deviation investigations from initiation to closure.
- Conduct root cause analysis and assess potential product quality impacts.
- Develop CAPAs and monitor their effectiveness.
- Coordinate investigations with Manufacturing, QA, QC, MSAT and Engineering teams.
- Prepare investigation reports and ensure timely closure in line with GMP requirements.
- Support deviation trending and continuous improvement.
Requirements
- Min. Diploma/Degree in Biotechnology, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, Life Sciences or a related field.
- Relevant pharmaceutical or biopharmaceutical manufacturing experience.
- Hands-on experience independently leading end-to-end manufacturing deviation investigations is essential.
- Strong knowledge of RCA, CAPA, product impact assessments and GMP operations.
- Good technical writing, problem-solving and stakeholder management skills.
- TrackWise, Veeva Vault or similar system experience is an advantage.
Email your resume to ************* or Telegram @alexgohhl
Alex Goh Hock Leong
CEI No.: R1763413
Recruit Express Pte Ltd (Healthcare & Life Sciences)
EA Licence No.: 99C4599