Deviation Management Specialist, PHARMA 6 Months Contract #HJN

Your tasks

Job Responsibilities

• Lead and manage manufacturing deviation investigations within a GMP-regulated pharmaceutical/biopharmaceutical environment.
• Conduct root cause analysis (RCA) using tools such as 5 Whys and Fishbone Analysis.
• Identify root causes and drive corrective and preventive actions (CAPA) through to closure.
• Work closely with cross-functional teams, including Manufacturing, QA, QC, MSAT and Engineering, to resolve manufacturing issues.
• Assess product quality impact and support batch disposition decisions.
• Prepare investigation reports and ensure timely closure of deviations and CAPAs.
• Support deviation trending and continuous improvement initiatives while ensuring GMP compliance.

Requirements

Job Requirements

• Min Diploma or Degree in Biotechnology, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, Life Sciences or a related discipline.
• Relevant experience in pharmaceutical or biopharmaceutical manufacturing, preferably within biologics, vaccines, API or drug substance manufacturing.
• Proven experience in managing manufacturing deviation investigations, root cause analysis and CAPA implementation.
• Good understanding of GMP requirements, manufacturing processes and quality management systems.

How to apply

OR Email me at janeve.ng@recruitexpress.com.sg

EA Personnel : Janeve Ng Choy Tong

Other

C.E.I: R25159176

Company Registration No: 99C4599

Recruit Express Pte Ltd