ContractHealthcare & care· Posted 22 Sept

QC Specialist - Project (2-Year Contract)

GSKFrom company site

Salary

Not stated by the company

When

To be confirmed

Where

Tuas

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Start: Not stated
Work mode: On-site
Experience: Some experience

About the role

This role provides technical QC support to the projects team for new projects at a vaccines manufacturing site in Tuas. You will represent the local QC unit and work with global QC and MSAT colleagues on validation and operational activities. It suits an experienced QC or analytical laboratory professional who is comfortable leading method work and working within GMP requirements.

What you'll do

Lead method validation, development, verification, transfer and introduction of new equipment or technology
Perform testing for project-related activities when required
Advise the projects team on technical QC matters to keep activities compliant with corporate, regulatory and external agency rules
Ensure projects are implemented on time and in full compliance with applicable regulations

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Keep current on biopharmaceutical QC methods and technology so projects make good use of digitalisation, automation and robotics

Work with global and local QC stakeholders to develop and endorse analytical transfer plans, validation master plans, cost management and training plans

Collaborate with global QC networks on test method innovation and evaluation to support facility design or modification for QC operations

Write and review change controls, events and deviations, CAPAs and GMP documents such as SOPs, protocols and reports

Keep project spending within the target budget

Respect safety, security and laboratory policies on site and ensure SEHSS practices are followed

Plan and execute the move from project mode to routine QC operations

Manage knowledge retention and training so methods and knowledge transfer effectively to the routine testing team

Good to know

Two-year contract
Based in Tuas, Singapore
Full-time role

Requirements

Bachelor's degree in chemistry, biochemistry, microbiology, life sciences or a related discipline
At least 4 to 6 years of experience in a QC or analytical laboratory, preferably in pharmaceutical or life sciences settings
Practical knowledge of GMP principles and laboratory quality systems
Hands-on experience with analytical methods and laboratory investigations
Experience coordinating method validation, verification or transfer activities
Good written and verbal communication skills in English

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QC Specialist - Project (2-Year Contract)

About the role

What you'll do

Good to know

Requirements

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