with provision and review of reports. Requirements A BA or BS in Chemistry/Biochemistry/Microbiology or other related science. Experience in a GLP/GMP environment. Computer literacy (including MS Word and Excel). Ability to work well with others. Effective communication skills. Good organizational skills. If you more »
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 »
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 »
Peterborough, Cambridgeshire, East Anglia, United Kingdom
McCormick UK Limited
indicators. Support sensory activities: taste panels, sample preparation, sample collection, sample submissions, processing of results. Adhere to good manufacturing practices (GMP), goodlaboratory practices (GLP) and master cleaning schedules (MCS). Comply with Company, third party and Customer standards demonstrated by successful completion of Inter-lab proficiency schemes, routine refresher 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 »
experience will be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT skills Important Information: We endeavour more »
Previous experience of Validation Proven leadership skills. Computer literate with the ability to use CRM systems Experience and knowledge of H&S, COSHH, ISO, GLP and GMP A problem solver Due to the nature of the role, you will need excellent colour vision If you believe you meet the above more »
Dispensing of Medicines" (or willingness to undertake in first year of role) Current registration with the General Pharmaceutical Council Knowledge and understanding of GMP, GLP and Pharmaceutical Quality Systems Knowledge Essential Demonstrable post qualification experience particularly in the specialised area of Aseptic Services and Pharmacy Quality Assurance Experience of staff more »
Proficient in using industry-standard software lifecycle management tools such as Jira, Confluence, and AHA! Previous exposure to applying industry compliance and quality standards (GLP, GMP, 21CFRPart11) in software products. Effective communication and stakeholder management skills to facilitate seamless collaboration and alignment across diverse stakeholders. If you possess a passion 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 »
indicators. Support sensory activities: taste panels, sample preparation, sample collection, sample submissions, processing of results. Adhere to good manufacturing practices (GMP), goodlaboratory practices (GLP) and master cleaning schedules (MCS). Comply with Company, third party and Customer standards demonstrated by successful completion of Inter-lab proficiency schemes, routine refresher 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 »
will be made in this round of recruitment. Key experience: Previous QC or analytical chemistry experience essential Must have worked within a GMP or GLP setting An understanding of raw materials and finished product testing Experience in some of the following will be important – HPLC, GC, UV, FTIR A solid … Quality, control, qc, analytical, chemistry, HPLC, chromatography, GC, gas, high, performance, liquid, testing, product, raw, materials, pharmacopoeia, FTIR, UV, bench, laboratory, analyst, technician, GMP, GLP, manufacturing, pharmaceutical more »
Experience in aseptic technique and controlled environments with prevention of cross-contamination. Experience working within a Good Manufacturing Practice ( cGMP ) or GoodLaboratoryPractice ( GLP ) environment is highly advantageous but not essential. Strong interpersonal and communication skills. Touchlight Benefits Touchlight is a successful scale-up business with a record of more »
Are you already working in a GLP/GCP environment and want to consider Quality Assurance as your next career move? Do you want to be part of a company that helps build a healthier and safer world? Are you looking for industry recognised training and development opportunities? Labcorp is … a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. As a GLP Quality Assurance Auditor at Labcorp based in Harrogate, North Yorkshire , you will play an essential part in making this happen. We are looking for someone who is able to apply … preferred (or equivalent Life Science experience) Experience may be substituted for education Skills/Experience: Proven work history in a regulatory environment working to GLP/GCP Ability to apply basic relevant regulatory knowledge Ability to follow instruction e.g. QA documents (SOPs) Ability to assimilate/interpret operational documents such 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 »
protection and biocidal products and technical compliance of their fertilisers within the UK and EU. This wide-ranging role includes ongoing liaison with consultants, GLP laboratories and efficacy testing organisations alongside participation in various industry taskforces to ensure compliance with relevant UK and EU regulations. Location: This role is located … in Leicestershire Key Responsibilities: Manage the registration/renewal processes for the plant protection and biocidal products, coordinating with consultants and external GLP laboratories as well as overseeing product labelling and compliance. Conduct liaison with GLP laboratories to address data gaps and stay updated with changes to regulatory guidance. Support more »