Overview
Life Science recruiter helping scientists find exciting jobs in a regulated space, from discovery through to commercial release.
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 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 here.
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