6 Months Contract Technical Deviation Investigator I PHARMA #HJN

Your tasks

Job Responsibilities

• Support manufacturing readiness activities, including preparation and revision of Master Batch Records (MBRs), change requests and other GMP documentation.
• Review and update manufacturing procedures, work instructions and controlled documents to ensure compliance with cGMP requirements.
• Conduct operational risk assessments and coordinate pre-campaign training to ensure manufacturing readiness.
• Support deviation investigations, including root cause analysis (RCA), impact assessments and implementation of Corrective and Preventive Actions (CAPA).
• Coordinate and follow up on deviation records, quality-related tasks, rejected materials and audit findings to ensure timely closure.
• Assist in product impact assessments and investigations to support batch review and lot disposition.
• Collaborate with Manufacturing, Quality Assurance and other cross-functional teams to resolve operational and quality-related issues.
• Ensure all activities and documentation comply with site procedures, regulatory requirements and GMP standards.

Requirements

Job Requirements

• Min Diploma or Degree in Biotechnology, Biopharmaceuticals, Chemical Engineering, Life Sciences or a related discipline.
• Relevant experience in pharmaceutical, biotechnology or biopharmaceutical manufacturing environments.
• Familiarity with cGMP requirements and pharmaceutical quality systems.
• Experience in GMP documentation, Master Batch Records (MBRs), deviation management and CAPA will be an advantage.
• Knowledge of root cause analysis (RCA), risk assessments and change control processes is preferred.

How to apply

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

Other

C.E.I: R25159176