in working with spreadsheets. Trending of data/statistical knowledge. Method development experience. Experience in a food/chemical/Pharma laboratory. Competence in GLP/GMP. A willingness to be flexible in covering all roles in the laboratory area, including across site movement. Knowledge of HACCP and Food Safety more »
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 »
to their dynamic team Responsibilities Participate in pre-clinical and clinical bioanalytical projects through method development, validations and routine sample analysis in accordance with GLP and GCP regulations. Experience of running LC-MS/MS and or LBS s including equipment maintenance and troubleshooting. Experience in running Ligand Binding Assays. … Deliver projects as part of a team Demonstrate knowledge of GLP/GCP and conduct all work in a manner that is compliant to regulatory requirements Qualifications and experience A degree in life science or chemistry-related field Hands-on experience with LC-MS/MS and Ligand Binding assays … biological sample analysis. A good communicator with strong interpersonal skills. Has a delivery focus with a good work ethic. Experience in working in a GLP/GCP accredited facility Knowledge of software-specific platforms is preferred Benefits Competitive Salary Pension Scheme Private Healthcare Generous Holiday Package Career Progression Opportunities more »
or other plans Team player Review and sign of study data Responsible for regulatory compliance as assigned Ensure all processes are following GCP/GLP Liaising with clients regarding within agreed timescales Qualifications At least 3 years experience working in a regulatory bioanalytical laboratory. A degree in life sciences or … chemistry-related subject A good communicator with strong interpersonal skills. Experience working within a GLP/GCP accredited facility. Flexible and adaptable with an eye for detail Hand-on experience of LC-MS/MS, Sciex and Waters LC-MS/MS systems is an advantage Experience in Bioanalytical method more »
