Job Title: QC Senior Analyst
Closing Date for Applications - 24th October (COB)
This is a site-based role in Worthing, UK.
Business Introduction
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance.
Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.
We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
Position Summary
As a QC Senior Analyst, you will play a vital role in ensuring the quality and compliance of our products. You will conduct analytical testing, support method validation and transfer, and contribute to the introduction of new technologies in our laboratories. Collaborating with cross-functional teams, you will help deliver high-quality medicines to patients while advancing your career in a supportive and inclusive environment. This role offers opportunities for growth, meaningful impact, and alignment with GSK's mission to unite science, technology, and talent to get ahead of disease together.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Perform quality control testing, validate analytical results, and ensure compliance with GMP standards.
- Coordinate laboratory investigations, including RCA and CAPA, ensuring timely and compliant resolution.
- Execute compliance activities such as audit trail reviews, method reviews, validation activities, and SOP updates.
- Lead GPS activities including problem-solving, standard work, 5S, and continuous improvement initiatives.
- Mentor and train analysts in laboratory techniques, processes, and procedures, acting as a Subject Matter Expert.
- Champion EHS activities within the laboratory, conducting risk assessments and maintaining safety standards.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
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