GSK
Pharmaceuticals
QualityOversightSpecialist
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Oversight Specialist at GSK. Skills: GMP, Quality assurance, Process oversight. Ensure GMP processes and personnel adhere to procedures. Minimize risk of non-compliance”
Industry & Context.
Quality issue resolution
Shift-based presence, Out of hours support
What They're Looking For.
Must Have
Degree, HND/HNC or equivalent in life science, chemistry, microbiology or related subject, or substantial practical laboratory experience, Experience of the pharmaceutical industry, Excellent working knowledge of QMS / GMP, Related manufacturing aspects / experience in resolving cGMP issues, Influencing, communication and coaching skills, Ability to effectively contribute to Department project activities
Nice to Have
Familiarity with investigation tools, Managing CAPA processes, Proven experience preparing for audits and inspections, Prior experience in on-site pharmaceutical manufacturing
What You'll Do.
Ensure GMP processes and personnel adhere to procedures
Minimize risk of non-compliance
Maintain inspection readiness
Support initial management of quality issues
Provide guidance during GMP activities
Detect potential quality issues through active observation
Prevent deviations and defects
Provide Quality support for site Management monitoring audits
Ensure adherence to frequency of oversight
Check facilities are maintained in good state
Escalate deviations from standards
Role model GPS standards
Foster a Quality Starts With Me culture
Provide coaching to employees on following procedures
Out of hours support for SLE process confirmation
How You'll Work.
Team & Collaboration
Tiered accountability meetings
Communication Scope
Communication skills
Full Job Description
Quality Oversight Specialist Closing Date: 15th June 2026 (COB) 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 To ensure adherence to GMP standards and procedures through independent oversight of GMP processes. To improve the effectiveness of quality in preventing, identifying and addressing quality issues by encouraging proactive quality culture and continuous improvement. To maintain shift based presence and be accountable for key quality decision-making or quality escalations. To provide first line support to operational areas (for example: rapid response to quality issues, provide guidance and coaching) and maintain inspection-readiness through independent checks. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: * Ensure that all GMP processes and operational personnel adhere to current local or area specific procedures, minimising risk of non-compliance and always maintaining inspection readiness. * Maintain presence across area of responsibility and be the first line of contact to support initial
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