Site Name:UK - Hertfordshire - Stevenage

Posted Date:Jan 23 2025

QC Senior Analyst

Closing Date for Applications – 6th February (COB)

Quality Control: Conducts a wide range of quality control tests and analyses on products to uncover defects. Reports to management who make the decision to allow or deny the release. Testing for process monitoring. Testing of Raw Materials Job Family Group - Quality: Develops and implements programs to establish and maintain quality standards of existing products, and internal systems and processes. Develops policies, procedures and methods to check product, material, components and/or operational quality and improve same.

In this role you will:

As a Senior Quality Control Analyst, you will play an integral role in the continued success of our analytical laboratories. You will have responsibility to train new Analysts in the laboratory and thus set the tone for the way in which a new analyst generates data for the release of products and materials.

• Conduct routine analytical testing of finished products and environmental samples using approved methods and various instrumentation while adhering to cGMP and established policies. Interpret validity of own test data and other members within the team and generate accurate results.
• Support/ lead all aspects of laboratory investigations. Including troubleshooting test methods and laboratory instrumentation.
• Assist in basic technical writing such as specifications, laboratory work sheets, standard operating procedures and technical reports.
• Provide technical support by executing protocols and evaluating results for non-routine testing.
• Independently organize daily work activities and those of other staff, as needed. Participate in interdepartmental project teams or committees.
• Conduct training of laboratory personnel on methods, instrumentation and computer systems.

Qualifications & Skills:

We are looking for professionals with these required skills to achieve our goals:

• BSc or MSc in Biochemistry, chemistry or related life science
• Previous GMP experience
• Good knowledge and level of understanding of procedures, processes, analytical skills and technical knowledge.
• Strong verbal and written communication skills.
• Good ability to motivate and inspire colleagues, and work with others to drive, implement and support continuous improvement.

Preferred Qualifications & Skills:

If you have the following characteristics, it would be a plus:

• Ability to work in high pressure environment, often under tight deadlines.
• Good knowledge of Microsoft, Teams and online systems like Labware.
• Good communication skills.

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.

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