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QC Lab Analyst - Raw Materials (Method Validation/ Verification/ Pharma)
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QC Lab Analyst - Raw Materials (Method Validation/ Verification/ Pharma)
Job summary
A staffing agency in Singapore is seeking a QC Lab Analyst for a 12-month contract. This role involves method validation and verification for raw materials in the pharmaceutical industry. Candidates should have a relevant degree and 5-7 years of experience in QC raw material testing. The position offers a competitive salary of up to $6,000, depending on experience.
Qualifications
- 5-7 years of experience in QC raw material testing.
- Experience in method validation/verification in the pharmaceutical industry.
- Good understanding of documentation practices.
Responsibilities
- Author method validation protocols.
- Perform QC tests for raw material samples.
- Support laboratory start-up activities.
Skills
Education
12 Months Contract
Location: Tuas
Up to $6,000 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.
- 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.
- 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 - Apple.lim@manpower.com.sg
Recruitment Consultant (R2090579)
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.