QC Samplers (Pharmaceutical Production/Testing/ Laboratory)

Manpower Staffing Services (Singapore) Pte Ltd; Singapore; On-site; SGD 36,000 - 60,000; Full time

Job summary

Manpower Staffing Services (Singapore) Pte Ltd in Singapore is seeking a Laboratory QA associate to manage GMP sampling across raw materials, intermediates and finished products.

You will follow GMP procedures, report issues promptly, support lab investigations, maintain 5S and EHS, participate in audits, and coordinate with QC, processing and warehouse teams to ensure compliant analytical activities.

Qualifications

• Experience in laboratory work within pharma/biotech environments.
• Familiar with GMP regulations and quality management.
• Ability to perform 12-hour rotating shifts.

Responsibilities

• In charge of sampling for raw materials, intermediates and final products.
• Follow GMP sampling procedures and report issues promptly.
• Support lab investigations and maintain lab safety and 5S/EHS compliance.
• Communicate with QC, processing and warehouse teams to ensure smooth analytical activity.
• Participate in customer audits and government inspections and address issues.
• Track work progress and maintain good relationships with internal and external clients.
• Understand pharmaceutical production, testing and quality management.

Skills

GMP compliance

Lab safety

5S

EHS

Communication

Investigation

Audits

Job description

• In charge of sample specimen for raw material, intermediate and final product.

• Follow related procedure for GMP sampling.

• Timely report the various issue associated with sampling process. Ensure GMP compliance.

• Involved in the procedure update and ensure execution.

• Communicate with QC project team, processing team and warehouse. Ensure the smoothness of analytical activities.

• Assist necessary Lab investigation, keep good Lab environment, meet 5S and EHS requirements, ensure Lab safety and the safety of Lab staff.

• Follow the requirements of Lab events, OOX, Deviation and involve the investigation if necessary.

• Participate in customer audits and government inspections, promptly address identified issues, and ensure GMP compliance

• Timely track work progress, strengthen communication with internal and external clients, and establish stable and good relationships

• Understand pharmaceutical production, testing, and quality management; familiar with GMP regulations.

• Experience of Laboratory related work

• Able to perform 12 hours rotating shift work