Winter Co-op​/Quality Control Systems

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines.

We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included.

Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

The Quality Control (QC) organization includes several teams:
Systems, Chemistry, Chromatography, Immunology, and Microbiology. The Systems group is responsible for supporting the QC laboratory in various functions, including but not limited to, fridge/freezer oversight and management, stability sample management, sample receipt, shipment receipt from external sites, setting up outgoing shipments, and setting up analytical systems utilized by the laboratory.

The Chemistry team is responsible for utilities testing (TOC, Conductivity, Nitrates), compendial testing/assays, incoming materials and component release testing.

Receive and prepare quality control samples for further processing by in-house and external testing labs following cGMPs. Performs any or all sample coordinator functions including oversight and performance of a variety of complex standard tasks and sample tasks (receipt, accessioning, routing, storage, aliquotting, shipping, discard, destruction, etc.) in support of the sample management department. Performs routine departmental GMP activities (lab instrument calibrations, preventive maintenance, audits, work orders, etc) to support our group, as well as supporting other laboratory groups.

This can also include performing chemistry testing for utilities and incoming materials/component release. This role involves interacting and coordinating with various other departments and with the other teams within the QC organization.

• Pursuing a Bachelor’s (Junior/Senior level) or Master’s degree in Chemistry, Biochemistry, or science related fields.
• Organizational skills, ability to follow procedures (SOPs), understanding of GMPs, and experience with biopharmaceutical products/testing.
• Ability to quickly learn new processes/techniques.
• Must be able to work full-time (40 hours/week) throughout the duration of 6-month co-op (January ~ June 2027, flexible based on academic schedules).
• Must have an active student status and/or within 12 months post-graduation from a BS or MS degree program. Post-doctoral candidates are not eligible.

• Assays/experiences include (but not limited to) – pH, Appearance, Osmolality, HPLC/UPLC, PCR, FTIR, TOC, Conductivity, Wet Chemistry, aliquotting, shipping/sample logistics, project management.
• System experience preferred – SAP/ERP, Labware LIMS/LES, Agentry, Info Logs, Microsoft Office, GLAMS (artwork database for component release).
• Working knowledge of cGXP, ICH guidelines, FDA, USP/EP/JP and…