Create, review, and approve documents including standard operating procedures
Work with Manufacturing and Project Engineers to develop inspection and test methods and related acceptance criteria
Assist with Quality Assurance reviews of processes
Provide metrics reporting and status updates to Quality management relating to the facility (PD lab, GMP Facility and QC)
Management of all documents, manual and electronic documents using Master Control
Provide daily QA support for general operation activities, calibration status and preventive maintenance status of equipment and system in PD and QC laboratory and GMP Facility
Support continuous improvement and oversight of Quality management System
Work within a culture of continuous improvement and system efficiencies
Minimum of Bachelor's degree in Biology of Chemistry (or related)
Experience in a Quality Assurance position within a highly regulated industry
Relevant GMP experience in a Pharma/Biotech company, working within quality system and regulated GMP environment
Strong understanding of quality control standards and testing techniques
Knowledge of cGMP/ICH/FDA/EU regulations and guidance
Proficient in using Microsoft applications (Microsoft Word, Microsoft Excel, Microsoft PowerPoint)
Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact us at +44 (0)20 3854 7700.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Legal, Other, and Quality Assurance
Industries
Biotechnology Research and Pharmaceutical Manufacturing
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