Senior Associate Quality Control I (chemistry)

Amgen

Singapore, Singapore
On-site
Analytical testing of raw materials, water, in-process control, drug substance and stability samples
Troubleshooting analytical testing, techniques and equipment
Laboratory investigations and closure of capas and deviations
Amgen is seeking a Senior Associate Quality Control I (Chemistry) in Singapore to perform analytical testing and support laboratory operations in a GMP environment. The ideal candidate should have a strong background in chemistry, biochemistry, and relevant industry experience, along with skills in troubleshooting and effective communication

Job Summary

  • Plan, schedule, perform analytical testing and approval of test results on raw materials, water, in-process control, drug substance and stability samples in GMP pharmaceutical environment.
  • Train new/ junior laboratory staff and ensure all staff are appropriately trained and qualified to execute the duties assigned to them with respect to the job.
  • Amgen is one of the world’s leading independent biotechnology companies, pioneering breakthroughs to bring state-of-the-art medicines from laboratory to the patient.

Matching Summary

Match Score: 85

Amgen is seeking a Senior Associate Quality Control I (Chemistry) in Singapore to perform analytical testing and support laboratory operations in a GMP environment. The ideal candidate should have a strong background in chemistry, biochemistry, and relevant industry experience, along with skills in troubleshooting and effective communication.

Skills & Requirements

Must-have

  • analytical testing of raw materials, water, in-process control, drug substance and stability samples
  • troubleshooting analytical testing, techniques and equipment
  • laboratory investigations and closure of CAPAs and deviations
  • GMP pharmaceutical environment
  • UPLC, HPLC, LC-MS, GC-HS
  • Capillary Electrophosis, LOD, Autotitration, KF, Optical Rotation, FT-IR, Conductivity, TOC, pH, wet chemistry

Nice-to-have

  • continuous improvement initiatives and projects
  • method verification and method validation/transfer
  • laboratory housekeeping and document archival duties
  • support regulatory inspections

Key Requirements

  • Master’s degree in Chemistry, Biochemistry or related technological field OR Bachelor’s degree and 2 years of directly related experience OR Associate’s degree and 4 years of directly related experience OR High school diploma and 6 years of directly related experience
  • 4 years of relevant professional work experience within the pharmaceutical or biopharmaceutical industry
  • Strong knowledge and understanding of GMP pharmaceutical production
  • Immunosorbent Assay/Cell based Bioassay: Potency, Host Cell Proteins, ELISA

Work Rights

Not specified

Tailored Resume

Cover Letter