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SRG is exclusively working with a global pharmaceutical company who require a QA Supplier Management Supervisor to join their well-established Quality and Operations team, supervising a team of 4 responsible for supplier management.
This role involves managing a state of compliance, providing hands-on leadership in pro-active improvement in the related Supplier Relations Quality systems. Ensuring activities are planned, tracked and executed in line with company SOPs and GMP and GDP Requirements and Regulations.
Responsibilities:
* Ensure Supplier Qualification Activities are scheduled to plan or risk assessed as required, supporting the site and wider business, as required.
* Maintenance and improvement of Quality Supplier Qualification systems (including but not limited to the procedures linked to: Technical Agreement, External Vendor, Material management, Supplier Management).
* Ensure the Approved Supplier list is accurate and up to date. Support Departments across the site on quality GMP matters related to Supplier Qualification activities.
* Work closely with QA CMO management, Supply Chain, Business Development, Commercial and Project management, etc to ensure queries are handled in a timely manner, Project timelines are met, and Supplier Qualification activities are communicated and completed as required.
* Perform QA Supplier Relations activities (including Technical Agreements, Auditing (to provide additional Audit Capacity only), including deputising for the QA Officers/ Auditors during periods of absence.
* Act as Quality GMP advisor on site projects such as new product introductions or CAPEX projects.
* Host training sessions on GMP QA related topics.
* Support QA Manager in relation to site document and QMS reviews/approvals.
Requirements:
* Extensive recent experience in a leadership role within a GMP Quality Assurance environment, preferably Supplier Relations/ Qualification Activities.
* Line Management Experience within a quality assurance team in a GMP environment.
* Proved track record of development, improvement and maintenance of process/ systems.
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Quality Assurance
Industries: Pharmaceutical Manufacturing
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