QA Specialist

Overview

GlaxoSmithKline (GSK) is a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We are on an audacious journey to impact the health of 2.5 billion people over the next decade. Our R&D division is at the forefront of this mission, dedicated to the discovery and development of groundbreaking vaccines and medicines. We are transforming the landscape of medical research by integrating cutting-edge science and technology and harnessing the power of genetics and new data. By fostering a collaborative environment that unites the talents of our people, we are revolutionizing R&D to pre-empt and defeat diseases. Join us in our commitment to uniting science, technology, and talent to get ahead of disease together.

Position Summary

GSK are the lookout for a Biopharmaceuticals Testing Laboratory (BioCTL) QA Specialist to join the team in Stevenage. This person will ensure that the BioCTL complies with all QMS and relevant regulatory standards in relation to data generation and laboratory testing and approval.

Key Responsibilities

• Review, approve and issue QC data to support timely release of medicines to the market.
• Provide coaching and support to improve Right First Time performance.
• Perform document control activities, including controlled printing, reconciliation and archiving.
• Assist in the preparation for and participation in inspections and audits.
• Author GMP documents.
• Initiate and participate in quality events such as deviation investigations and change controls.
• Participate in GEMBA and process confirmations of quality systems and processes to improve compliance and efficiency.

Minimum Requirements/Skills

• Bachelor of Science or equivalent work experience.
• Background in Science, Engineering or other technical discipline.
• Ability to interpret complex data and draw conclusions about scientific and technical data.
• Experience working in a regulated environment, preferably in a GMP environment in a role directly related or supporting Quality or Manufacturing.
• Competency in Microsoft Office.

 Why GSK?

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.

Inclusion at GSK

GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

If you need any adjustments in the recruitment process, please get in touch with our Recruitment team () to further discuss this today.

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