developing injectable dosage forms for preclinical & clinical use, this will include formulation development and product characterisation Appreciation of the regulatory environment, ideally GMP/GLP You will be able to coordinate multiple projects simultaneously You will be an effective team player and have strong interpersonal skills to enable you to more »
molecule bioanalytical studies. 3. A working knowledge and practical experience using LC-MS/MS. Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified more »
and troubleshooting skills in previous positions. Worked as an engineer or come from an analytical background carrying out on site support. Experience working in GLP/GMP environment. Be prepared to travel and stay away as required. Package: Salary up to £43,000 D.O.E Bonus Scheme (£6.5k) Company Car + 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 »
health and safety procedures and guidelines. Education and experience: - Degree education in Chemistry, Chemical Engineering or other related Engineering discipline. - Knowledge of GLP (GoodLaboratoryPractice) quality requirements skills gained in similar work (or dissimilar but relevantly skilled work). - Awareness of REACH, CLP, ISO 21469, NSF, AS9100. - Awareness of more »
scientific discipline is ideal. 2. Proven industry experience in HPLC/LCMS as well as a background of maintenance and troubleshooting skills in a GLP/GMP environment. 3. Experience with other Analytical Instrumentation such as MALDI, Prep LC and SFC is beneficial but not essential. Key Words: Field Service … Engineer | HPLC | LCMS | MALDI | Prep LC | SFC | Maintenance | GMP | GLP | Service Schedules | Installation | Validation | Instrumentation | IQOQ | SAP | Troubleshooting | Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role more »
Safety and Environmental requirements are met including (but not limited to) workplace organisation, work instructions, risk assessments, COSHH assessments, housekeeping standards in accordance with GLP and GMP n Demonstrable evidence of understanding the importance creating a safe environment n Working in a safe manner n Follow appropriate and relevant practices … achieve high standards Data and computer literate, fluent user of typical office software application packages, especially Word and Excel Working knowledge of GMP/GLP Delivers on commitments as per timelines and quality standards Shows a positive attitude in difficult situations 2 years working in an analytical laboratory environment Experience more »
Macclesfield, Cheshire, North West, United Kingdom
Russell Taylor Group Ltd
now to avoid missing out! The Role Being part of a busy QA team Participating in QA audits, both internal and external Maintaining a GLP environment Performing 3rd party audits Inspecting study procedures, facilities and laboratory processes within the organisation The Candidate Will ideally have come from a QA background. … Will have dealt with CAPAs, non-conformances, internal and external audits, etc. Will ideally have experience working within a GLP setting. Will have previous experience performing internal and external audits. Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role more »