22/04/2024 | Fulltime | | United Kingdom | CV-LibraryProduction Scientist to join the rapidly growing London based CMC division. Job Description - Responsible for day-to-day operation and manufacture of the RPE ATMPs in a GMP facility - Maintain batch records, equipment logs and other production records to comply with cGMP in collaboration with fellow team
Save for later15/04/2024 | Fulltime | | United Kingdom | CV-Library | €45,000 - €50,000 / Year We have an opportunity for a Projects Team Manager to work for an expanding Pensions and Benefits consultancy in Bristol. You would be responsible for managing a team of around 15 people that are focused on GMP related projects over the next few years. The team consists of Data Analysts
Save for later26/04/2024 | Fulltime | | United Kingdom | Totaljobs 12 pcGMP) audits of process, people and work in process product. - Carry out Internal audits against a defined sched
Save for later22/03/2024 | Fulltime | | United Kingdom | CV-Library | €15 / Hour GMP Production Manufacturing Technician Opportunity – Kent Opportunity An exciting opportunity has been created due to company growth. My client a global pharmaceutical manufacturing company are looking to recruit a Production Manufacturing Technician based in Kent where you will be working
Save for later22/03/2024 | Fulltime | | United Kingdom | CV-Library | €15 / Hour GMP Production Manufacturing Technician Opportunity – Kent Opportunity An exciting opportunity has been created due to company growth. My client a global pharmaceutical manufacturing company are looking to recruit a Production Manufacturing Technician based in Kent where you will be working
Save for later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | In Ballina, Co. Mayo Reporting to the Immunoassay Supervisor this role shall be responsible for the following Conduct immunoassays in both an R and D and GMP environment. Assist in the development and validation of different immunoassays (ELISA, Western Blot, ELISPot, etc.) and activity based assays
Save for later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | With ICH guidelines, where appropriate. Draw up study plans and implement studies in strict accordance with study plan ensuring full GMP regulatory compliance as appropriate. Liaise with the Quality Department for the generation of audit responses, deviation reports and for the compilation of study
Save for later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | Procedures like generic ELISA, MAT assay, microplate assays or clients specific immunoassays. Receipt and processing of test samples in LIMS. Safe and compliant disposal of all laboratory generated waste. Generation of GMP compliant SOPs, Protocols and reports. Carry out data calculations and basic
Save for later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | Evaluation of mammalian cells (e.g. cell morphology, count and viability) Receipt and processing of test samples in LIMS. Support update current standard operating procedures. Assist in laboratory investigations where necessary. Support generation of GMP compliant SOPs, Protocols and reports Generate
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