Analytical Development Chemist (12 months contract)
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From GSK’s original posting
To assist the Analytical Tech Transfer Manager, ensure that testing activities or methods and specifications introduced or changed as part of product lifecycle are validated or verified in compliance with current Good Manufacturing Practice (cGMP) and regulatory requirements that meet the defined quality standards. To support all analytical testing activities required for the resolution of process and method problems / issues, method validation, and the introduction of new measurement technologies and analytical tests as part of new product introduction. Key Responsibilities • Draft, compile, review and update appropriate laboratory documents such as analytical methods and specifications, method validation/equivalency protocols/reports, local procedures and guidelines relating to GMP and operational framework of the laboratory • Ensure that all data supporting the resolution of process and method issues have sufficient accuracy to allow for the correct actions to be taken to address the issue. • Contribute to the formulation and development of the plans for the implementation of new or improved testing technologies and/or methods for products and or cleaning processes. • Ensure a…
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