Quality Assurance Officer

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

Job summary

A leading recruitment company in Manchester is seeking a QA Officer to manage document lifecycles and ensure compliance with GMP regulations. Candidates should have at least 1 year of Quality Assurance experience in a pharmaceutical facility. Responsibilities include documentation review, compliance checks, and managing supplier issues. This position offers competitive salary and benefits.

Qualifications

• Minimum of 1 year experience in Quality Assurance within a Pharmaceutical (GMP) facility.
• Understanding of GMP and regulatory requirements within the pharmaceutical industry.
• Experience working with analytical laboratories and GMP production areas.

Responsibilities

• Ensure effective management of the document lifecycle, ensuring compliance.
• Creating, reviewing, and approving documentation such as SOPs and protocols.
• QA review and dossier collation of GMP production documentation.

Skills

Quality Assurance

Document management

Regulatory compliance

Internal auditing

Education

Degree in a relevant scientific discipline

Job description

Job Overview

Job Title: QA Officer

Salary: Highly competitive basic salary, bonuses & benefits!

Location: Manchester

SRG is exclusively working with an award-winning pharmaceutical organisation who are increasing their manufacturing and quality teams due to success.

Responsibilities

• Ensure effective management of the document lifecycle, ensuring compliance with regulations and industry best practices.


• Creating, reviewing, and approving key documentation such as specifications, SOPs, protocols, and methods associated with a product.


• QA review and dossier collation of GMP production and analytical documentation prior to QP release.


• Ensure compliance with SOPs and regulatory standards.


• Investigating and addressing deviations to prevent future occurrences.


• Managing supplier suitability and any issues and supplier mitigation steps for supplier complaints raised.


• Assessing changes and their impact on the site through Change Controls.


• Evaluating site compliance and implementing improvements through internal audits.


• Proactively identify and manage site improvements for Quality Improvement through CAPAs.


• Trained and competent in internal auditing is desirable but not essential.

Qualifications & Experience

• Minimum of 1 years\' experience in Quality Assurance within a Pharmaceutical (GMP) facility, preferably Investigational Medicinal Products (IMPs)


• Degree in a relevant scientific discipline desired


• Experience in working with analytical laboratories and GMP production areas.


• An understanding of GMP and regulatory requirements within the pharmaceutical industry.

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.

If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit www.srg.co.uk to view our other vacancies.