QA / Quality Assurance Specialist - Pharmaceutical
4 weeks ago
Quality Assurance Officer - Pharmaceuticals
Contract: Permanent
Salary: up to £28,000 + shift allowance + bonus
Shift Based (Mon-Fri)
Would you like to work for a reputable scientific organisation, making a direct difference to patients’ lives across the globe?
My client, a leader in delivering high quality, processed biological materials is seeking a personable and detail-oriented Quality Assurance Officer to join their growing team in London. Key responsibilities of the Quality Assurance Officer - Pharmaceuticals include:
Review pharmaceutical batch manufacturing records, ensuring compliance with GxP / GMP and addressing any errors to facilitate batch release.
Act as the primary point of contact within Quality Assurance for document review and batch release.
LIMS and Quality Management System (eQMS).
Support QA activities relating to batch release e.g. non-conformities, change controls, deviations, CAPA’s & audits.
Ensure adherence to GMP / GxP / GLP and best practice always in accordance to internal policies and Standard Operating Procedures (SOPs).
To be considered for the Quality Assurance Officer - Pharmaceuticals, you will need the following skills and experience:
Prior experience working with pharmaceutical documentation, ideally batch manufacturing records, in line with GxP / GMP etc.
Experience of working with quality systems, ideally an eQMS.
A personable nature, so able to build strong relationships within the organisation to aid batch release and QA activities.
BSc or MSc in a relevant scientific discipline such as; Microbiology, Bioscience, Biochemistry, Chemistry or equivalent working experience.
Previous experience in a clean room or manufacturing environment would be highly advantageous.
This is an excellent opportunity to take the next step in your Quality Assurance career within an enthusiastic and growing Pharmaceutical team.
Please apply online or contact Katie-May Kress at CY Partners for more information.
Keywords: “Quality Assurance, QA, QA Documentation, QA Officer, Batch Release, Batch Review, Batch Manufacturing Record, Batch Record, Good Manufacturing Practice, GMP, GMP Compliance, Deviations, Quality Management Systems, QMS, eQMS, Pharmaceutical, Biopharmaceutical, London, North London”
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