B Pharm Job at GSK | Supplier Quality Specialist Role | Apply Now
For professionals looking for a Pharma QA Job, GSK Careers offers an excellent opportunity in supplier quality management and pharmaceutical quality assurance. GSK is hiring a Supplier Quality Specialist responsible for supplier audits, GMP compliance assessments, CAPA management, and quality improvement initiatives. This role is ideal for pharma candidates with experience in pharmaceutical quality systems, manufacturing quality, and regulatory compliance.
- Job Role: Supplier Quality Specialist
- Job ID: 444830
- Department: Pharmaceutical Quality & Supply Chain
About The Company
GSK is a global biopharmaceutical company focused on developing innovative medicines and vaccines to improve healthcare outcomes worldwide. With a strong presence in pharmaceutical manufacturing and research, GSK uses advanced technologies, digital solutions, and smart manufacturing practices to deliver high-quality healthcare products. Through GSK Careers, professionals get opportunities to work on global quality initiatives, collaborate with cross-functional teams, and contribute to improving pharmaceutical supply chains.
Job Description
As part of GSK Careers, the selected candidate will contribute to pharmaceutical quality management activities and support a Pharma QA Job role focused on supplier quality operations. The candidate will manage supplier quality activities to ensure compliance with regulatory requirements, GSK quality standards, and approved specifications. The role involves conducting supplier audits, evaluating quality risks, managing corrective and preventive actions (CAPA), and supporting continuous improvement initiatives across the pharmaceutical supply chain.
Key Responsibilities
- Plan and conduct supplier quality audits and compliance assessments.
- Evaluate supplier compliance with GMP requirements, quality systems, and regulatory standards.
- Prepare audit reports and provide supplier approval recommendations.
- Manage CAPA plans resulting from audits, complaints, and quality incidents.
- Monitor supplier quality performance and compliance status.
- Maintain supplier quality records, audit documentation, and quality agreements.
- Identify and mitigate supplier-related quality and regulatory risks.
- Support regulatory inspections and customer audits.
- Collaborate with Procurement, Quality, Manufacturing, R&D, and external suppliers.
- Drive continuous improvement initiatives within supplier quality processes.
Eligibility Criteria
- Education: Bachelor’s degree in Pharmacy, Chemistry, Microbiology, Life Sciences.
- Experience: Experience in pharmaceutical quality assurance, supplier quality, manufacturing quality, or GMP compliance.
- Experience in supplier audits, compliance assessments, CAPA management, and quality systems.
- Experience working with pharmaceutical suppliers or contract manufacturing organizations is preferred.
Required Skills
- Strong understanding of GMP requirements and pharmaceutical quality systems.
- Knowledge of supplier qualification and risk assessment processes.
- Experience with CAPA management and change control procedures.
- Ability to conduct audits and evaluate supplier compliance.
- Strong documentation and reporting skills.
- Good communication and stakeholder management abilities.
- Ability to work collaboratively with global and cross-functional teams.
- Knowledge of regulatory expectations and quality compliance practices.
