QC Lab Analyst Raw Materials

Manpower Singapore; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A recruitment consultancy is seeking a QC Lab Analyst for a 12-month contract in Singapore. The ideal candidate will have 5-7 years of experience in QC raw material testing and be familiar with method validation and verification in pharmaceutical settings. Responsibilities include authoring validation protocols, supporting laboratory start-up activities, and performing QC tests for raw materials. Candidates with a Bachelor's or Master's Degree in relevant fields are encouraged to apply. Competitive pay up to SGD 5,000.

Qualifications

• 5-7 years of experience in QC raw material testing.
• Experience in method validation/verification in pharmaceuticals or biotechnology.
• Experienced/participated in method transfer and verification for raw material testing.

Responsibilities

• Author method validation protocols for raw material testing.
• Support laboratory start-up activities and equipment qualification.
• Perform QC tests and QC sampling of incoming raw materials.

Skills

Good understanding of good laboratory practices

Good documentation practice

Data integrity requirements

Experience in routine laboratory operations

Experience in method validation/verification

Education

Bachelor's or Master's Degree in related life sciences or technology

Job description

QC Lab Analyst – Raw Materials (Method Validation/ Verification/ Pharma)

12 Months Contract
Location: Tuas
Up to $5,000 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 tests 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.
• Experience in start‑ups will be ideal.

Our client is building agile, modular, tech‑driven facilities to meet evolving vaccine challenges with adaptable, multi‑product manufacturing.

Lim Pey Chyi – [e-mail]
Recruitment Consultant (R2090579)
Manpower Staffing Services (S) Pte Ltd