QC Analyst (Sampling)

Duration: 12 Months Contract

Location: Tuas

Our client is a fully integrated, global immunotherapy powerhouse who have been working on automated and digitized processes and build continuously capabilities for specialized manufacturing, either for individualized vaccines or for large-scale products like COVID-19 vaccine.

Job Summary:

• Responsible for performing laboratory specific activities, such as sampling, sample administration and simple analytical testing, laboratory supplies inventory control.

Responsibilities:

• Clean Room and Clean Utility sampling and testing

• Incoming raw material sampling and identification testing as per sampling plan and testing plan.

• Sample management for all QC laboratories including receiving, labelling and safely storing samples to be tested. Arrange sample shipment to external testing laboratories.

• GMP-compliant and on time completion documentation of sample administration and analyses and the associated activities as required by method SOPs, control regulations, QC planning documentation, and pharmacopoeia.

• Enters analysis results into the SAP/LIMS system, stores and archives source data and ensures data integrity for the assigned work, permanently monitors assigned analysis methods, including trend controls of data.

• Maintains and calibrates analysis equipment with associated documentation, assists qualifications of analytical equipment with associated documentation and schedule control.

• Promptly informs the laboratory manager about nonconforming analysis values or exceeded limit values, and initiates and processes non-conformance reports (non-conformances and OOx)

• Assists with preparing reports and with drafting and revising test procedures and SOP's.

• Assists and trains new employees/trainees

• Performs all assigned activities while observing all internal and regulatory requirements (safety and quality)

Requirements:

• Diploma or equivalent with experience in the pharmaceutical sector or comparable qualification with multiyear professional experience in a quality control function sciences

• At least 5 years of industry experience in an analytical, cGMP-regulated environment

• High degree of conscientiousness and diligence (documentation, order and cleanliness at the workstation)

• Sense of ownership and honesty (proactive handling of errors)

Lim Pey Chyi (Apple) - Apple.lim@manpower.com.sg

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423