Northwich, Cheshire, North West, United Kingdom Hybrid / WFH Options
Dechra
will have responsibility for duties including: Designs and oversees the implementation quality management systems for CMC development activities including the release of product for GLP and GCP studies. Provides quality expertise in accordance with the global quality requirements in the creation of product characterisation, product specifications, method validation, stability and … process, including in the collaboration with C(D)MOs. Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may more »
development and development of medical devices is a plus. Strong knowledge of Clinical Development and Research operations and regulatory landscape. Deep knowledge of GCP, GLP, GPVP, GCP for Labs and a general understanding of GMP. Expert in process development, industry standard problem-solving approaches, in alignment with Lean and Lean more »
projects on behalf of vaccine manufacturers. The Group has extensive experience in assay development and validation and operates to several Quality Systems including GCP, GLP and GMP. Main duties of the job Job description The purpose of this job is to perform routine duties related to and to provide general more »
City Of London, England, United Kingdom Hybrid / WFH Options
Proclinical Staffing
development and development of medical devices is a plus. Strong knowledge of Clinical Development and Research operations and regulatory landscape. Deep knowledge of GCP, GLP, GPVP, GCP for Labs and a general understanding of GMP. Expert in process development, industry standard problem-solving approaches, in alignment with Lean and Lean more »
