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

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading staffing agency in Singapore is seeking a QC Lab Analyst for a 12-month contract. The candidate will be responsible for authoring method validation protocols, executing QC tests, and supporting laboratory activities. The ideal applicant holds a Bachelor’s or Master’s in relevant fields and has 5-7 years of experience in QC raw material testing. The role is based in Tuas with a salary of up to $6,000, depending on experience.

Qualifications

• At least 5-7 years of experience in QC raw material testing.
• Experience in method validation/verification in the pharmaceutical or biotechnology industry.
• Experienced in routine laboratory operations.

Responsibilities

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

Skills

QC raw material testing

Method validation

Good laboratory practices

Good documentation practice

Data integrity requirements

Education

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

Job description

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

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.

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