26 to 42 of 42 GLP Jobs

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 »

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 »

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 »

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 »

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 »

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 »

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 »

to embark onto a Level 4 apprenticeship to further their skills development through internal training programmes. Apprenticeship Standard Business administrator (level 3) Training Provider GLP TRAINING LTD Working Week Monday - Friday (Times to be confirmed). Expected Duration 18 Months Positions Available 2 Closing Date Sunday, 30th June 2024 Start more »

on the toxicological effect of chemicals. The studies are carried out in vitro and in vivo in accordance with international test regulations and the GLP guidelines. You be responsible for scientific writing of toxicological studies (e.g. in vivo) conducted in our testing facility. Moreover, you will generate reports of various … as well as work in scientific projects whenever possible. PhD or master in life sciences or an equivalent qualification familiar with toxicological studies under GLP conditions knowledge of basic toxicology, laboratory animal science and animal welfare understanding of chemical analytics strong communication skills in English and German Gross annual salary more »

the company to a full-time position and structured salary increases. Apprenticeship Standard Building services engineering service and maintenance engineer (level 3) Training Provider GLP TRAINING LTD Working Week 8am to 4.30pm Monday to Friday (30 mins for lunch) Expected Duration 48 Months Positions Available 1 Closing Date Wednesday, 19th more »

Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills in a collaborative environment with cross-functional departments. A successful candidate more »

in 2021 to address the changing needs of commercial organizations developing modern therapeutics. AmplifyBio brings decades of experience to accommodate a wide variety of GLP and non-GLP studies in all in vivo models and dose routes. Among the investments that AmplifyBio has made to empower preclinical assessments of advanced … hours a week (including weekend and holidays) when needed to accomplish necessary tasks. Knowledge of Food and Drug Administration's (FDA) Good Laboratory Practice (GLP) Regulations, 21 CFR Part 58 for the conduct of nonclinical laboratory studies. At AmplifyBio , we're committed to growing and empowering an inclusive community within more »

Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills in a collaborative environment with cross-functional departments. A successful candidate 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 »

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 »

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 »

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 »