QA Supplier Relations Officer

SRG; Leeds; On-site; GBP 80,000 - 100,000; Full time

Job summary

A leading recruitment company is seeking a QA Officer for a global pharmaceutical company in West Yorkshire. This role involves managing supplier relations and ensuring compliance with quality assurance standards. Candidates should have a relevant degree and at least 2 years of experience in a pharmaceutical GMP environment, with a focus on quality assurance. Competitive salary and benefits are offered.

Benefits

Bonuses

Benefits

Qualifications

• A minimum of 2 years recent experience in a pharmaceutical GMP environment.
• At least 1 year's experience in pharmaceutical QA.

Responsibilities

• Write quality documents and reports with supervision.
• Identify issues during QA activities and raise deviations.
• Support quality events investigations and root cause analysis.
• Revise standard operating procedures per company policies.
• Raise and progress Change Controls as required.

Skills

Quality Assurance activities

Regulatory compliance

Statistical analysis

Root cause analysis

Education

Relevant University degree

Tools

SAP

Job description

Overview

Job Title: QA Officer - Supplier Relations

Location: West Yorkshire

Salary: Highly competitive basic salary, bonuses & benefits!

SRG is exclusively working with a global pharmaceutical company who require a QA Officer to join their well-established Quality and Operations team, responsible for managing supplier relations.

This role involves ensuring all Quality Assurance activities are planned and executed in line with company SOPs and GMP Requirements and Regulations.

Responsibilities

• Write Quality documents and reports with supervision in accordance with procedural requirements and current regulatory standards.
• Identify issues and problems during QA activities, raising deviations if required and ensuring timely closure.
• Support quality events investigations/ root cause analysis.
• Revise standard operating procedures and WRKs in line with company policies and procedures.
• Raise and progress Change Controls as required.
• Complete CAPA and assigned actions as required.
• Complete statistical analysis as per the in-house procedures (PQR).
• Support Internal Auditor
• Ensure compliance to MHRA, FDA, Regulatory and Company requirements / standards
• Provide relevant solutions and proposals to facilitate any decision-making processes
• Technical Agreement, Supply Chain Map/ Pedigree and template Risk Assessment Author
• Excipient Risk Assessment Author
• Material management process: Creating and Release of RM codes within SAP, liaising with Manufacturers/ Suppliers regarding Change Notifications, Specifications, queries etc.
• Maintenance of Raw Material Dossiers

Requirements

• Relevant University degree along with a minimum of 2 years recent experience of working in a pharmaceutical GMP environment of which, at least 1 years' experience is in pharmaceutical QA.

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy