Operational Quality Assurance Manager

Are you energized by a quality assurance role that allows you to accelerate compliance in a state of the art manufacturing environment?  If so, this Operational QA Manager role could be an ideal opportunity to explore.

As an Operational Quality Assurance Manager, you will be leading the whole process of the Quality Assurance department within the AB value stream.

This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:

• Review batch records, batch release, and GMP & regulatory compliance.
• Evaluate and approve quality event forms and deviation reports, corrective and preventive measures (CAPA), and effective CAPAs; Act as site Deviation process owner.
• Release finished products and raw materials/packaging materials with the operational quality team to release RM/PM and FP on time.
• Manage the OQ Shift team and ensure that GMP/GDP activities are supervised, including data integrity.
• Acts as RCA and HF process owner, providing necessary support during RCAs to ensure timely resolution of quality issues and to support batch release.
• Encourage Good Performance with integrity and enhance awareness and
• adherence to GSK policies and procedures.
• Create an atmosphere of respect and trust, where concerns can be fully raised.
• Ensure an effective process.
• Organize and conduct internal audits (L2 and L1) according to current standards (GMP, QMS, etc.) and in accordance with the predefined schedule. Write internal audit reports and ensure (preparation, follow-up) internal audits, L3 audits, and Regulatory inspections.
• Ensure the implementation and follow-up of corrective action plans defined following internal audits, deviations, customer complaints, and monitor the performance indicators of the department by identifying actions to achieve the department and site objectives.
• Contribute daily to the management of quality improvement activities in production areas, warehouse, and laboratory.
• Fully participate in the quality initiatives of our site and ensure compliance with quality standards.
• Participate in daily, weekly, and monthly quality meetings.
• Support new products and new projects.

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

• Bachelor of Science degree (Biological Sciences, Chemistry, Pharmacy or related scientific discipline)
• Min.5 years of experience of proven supervisory/management experience in Pharmaceutical Quality Assurance.

Post Closure Date: 04.Feb.2025

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.

Contact information:

You may apply for this position online by selecting the Apply now button.

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