Overview
Life Science recruiter helping scientists find exciting jobs in a regulated space, from discovery through to commercial release.Job Title:
QA OfficerSalary:
Highly competitive basic salary, bonuses and benefitsLocation:
ManchesterSRG 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 and Experience
Minimum of 1 year''s experience in Quality Assurance within a Pharmaceutical (GMP) facility, preferably Investigational Medicinal Products (IMPs).Experience in working with analytical laboratories and GMP production areas.An understanding of GMP and regulatory requirements within the pharmaceutical industry.For more information, please apply ..... full job details .....