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 »
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 »
Middlesbrough, North Yorkshire, North East, United Kingdom
E3 Recruitment
Skills and Qualifications: Education: Degree in Chemistry. Experience: Minimum 2 years as a QC Analyst in the Fine Chemical or Pharmaceutical industry (GMP/GLP environment). Technical Skills: Proficiency in forensic investigation techniques such as HPLC, GC, GC-HS, LC-MS, GC-MS, FT-IR, XRF, RAMAN, NMR, and more »
Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC Experience Responsibilities more »
Middlesbrough, North Yorkshire, North East, United Kingdom
E3 Recruitment
Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC Experience Responsibilities 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 »
Macclesfield, Cheshire, North West, United Kingdom
Russell Taylor Group Ltd
new quotes via literature searches. Providing an indication of any potential difficulties with bioanalytical methods and assisting with client calls and visits. Working to GLP/GCP and showing good documentation practice. The Person A successful candidate will have previous experience working in a regulatory bioanalysis lab with experience performing … either a PhD or relevant degree in any chemistry or life science related subject. The ideal candidate will have previous experience of working to GLP/GMP Must be IT literate with competent use of the Microsoft systems. The ideal candidate will have previous experience of using LC-MS/ 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 »
within the Bioanalytical Services –Small Molecules group. You will be responsible for delivering high quality results to our Sponsors and Clients in compliance with GLP and GCP. WHAT WE OFFER: Auto Enrolment Pension Comprehensive Benefits Package Working within a Global organisation Career Advancement Opportunities including Apprenticeships KEY RESPONSIBILITIES: Quality: Follow … knowledge of large molecule analysis in support of PK and PD studies. Experience working in a regulatory environment, managing studies that are compliant with GLP/GCP Experience in a client facing role with the ability to provide high level advice and guidance to clients Non-Smoker: due to the more »