QC Lab Analyst - Raw Materials (Validation/Verification/Pharma)

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

Job summary

A leading staffing service in Singapore is seeking a QC Lab Analyst for a 12-month contract in the pharmaceutical industry. The candidate will be responsible for method validation and verification for raw materials and must have 5-7 years of experience in QC testing. This role offers a competitive salary of up to $8,000, reflecting the candidate's experience.

Qualifications

• 5-7 years of experience in QC raw material testing.
• Experience in method validation/verification in the pharmaceutical or biotechnology industry.
• Understanding of good laboratory practices, good documentation practice and data integrity requirements.

Responsibilities

• Author method validation protocols and execute method validation/verification for raw material testing.
• Support laboratory start-up activities and equipment qualification activities.
• Perform QC tests for raw material samples including compendial tests.

Skills

QC raw material testing

Method validation/verification

Good laboratory practices

Data integrity

Routine laboratory operations

Education

Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology

Job description

Overview

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

Contact

Lim Pey Chyi - [e-mail]
Recruitment Consultant (R2090579)
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423

Desired Skills and Experience

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

Apple, Pey Chyi Lim EA License No.: 02C3423 Personnel Registration No.: R2090579

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