12 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.
Responsibilities
- Author method validation protocols and execute method validation/ verification for raw material testing.
- Support the laboratory start-up activities, participate in equipment qualification activities including (but not limited to) generation of user requirement specifications, SOPs and configuration specifications.
- Perform QC test for raw material samples including compendial tests and identification tests.
- Perform QC sampling of incoming raw materials.
- Author/ revise raw material specification and other QC related documents.
- Support laboratory activities such as housekeeping and equipment maintenance.
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 routine laboratory operations.
- Experienced/ participated in method transfer, method validation and method verification for raw material testing.
- Experienced in start-ups will be ideal
Lim Pey Chyi - [Confidential Information]
Recruitment Consultant (R2090579)
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423
