QC Systems Validation Specialist – Pharma/ Contract

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 - [email protected]

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423