e.g., pharmaceutical, biotechnology, manufacturing). Knowledge of regulatory requirements and compliance standards relevant to laboratory operations (e.g., FDA 21 CFR Part 11, ISO 17025, GLP, GMP). Experience with relational databases Oracle, SQL Server, Postgres. Experience with cloud services and infrastructure highly desirable Excellent problem-solving skills and ability to more »
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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and GoodLaboratory 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 »
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 »
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 »
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 »
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 »
complex scientific information to both technical and non-technical audiences. Knowledge of biopharmaceutical development processes and regulatory expectations for bioanalysis Previous experience in a GLP & GCP bioanalysis -compliant environment. What LabCorp Drug Development can offer you: A comprehensive training plan; with the ability to develop your technical and managerial skills. 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 »
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 »
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 »
projects on behalf of vaccine manufacturers. The Group has extensive experience in assay development and validation and operates to several Quality Systems including GCP, GLP and GMP. Main duties of the job Job description The purpose of this job is to perform routine duties related to and to provide general more »
Clydebank, Dunbartonshire, Scotland, United Kingdom
SGS United Kingdom Limited
Responsibilities: - Execute laboratory tasks and data analysis promptly and to an exceptional standard, adhering to all relevant procedures, Study Plans, and SOPs. - Comply with GLP/GMP standards, ensuring all activities meet health and safety guidelines and understanding all risk assessments related to the tasks (COSHH, GMO, etc.). - Maintain 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 »
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 »
