QC Systems Validation Specialist – Pharma/ Contract

6 Months Contract Location: Tuas Up to $8,000 depending on experience Industry: Pharmaceutical

Our client aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to better address vaccine business challenges.

Job Summary: Expertise in equipment validation, with a focus on qualifying critical QC instruments such as environmental monitoring air samplers and particle counters

Responsibilities: Support the implementation and maintenance of QC GxP Systems in compliance with company’s Standards and Regulatory guidance, which includes: Write and/ or execute IQ and OQ test protocols for QC Laboratory Computerized systems/ electronic equipment, including writing of exception reports. Author Qualification Summary Report for QC Equipment. Author QC Systems associated procedures such as administrative SOPs and configuration specifications, as required. Partner with QC to conduct data integrity risk assessment.

Requirements: Bachelor’s or Master’s Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 5-7 years of experience in QC raw material testing. Experience in method validation/ verification in the pharmaceutical or biotechnology industry Good understanding of good laboratory practices, good documentation practice and data integrity requirements. Experienced in start-ups will be ideal

Lim Pey Chyi -  Apple.lim@manpower.com.sg Recruitment Consultant (R2090579) Manpower Staffing Services (S) Pte Ltd EA Licence: 02C3423