07/05/2024 | Fulltime | | United Kingdom | CV-LibraryAnalytical Development Team Leader Due to continuous growth, I am working with a pharmaceutical manufacturing site based 10 miles outside of Manchester, this is a good opportunity to get involved with inhalation analytical development a very sought after industry, enhancing your skills within
Save for later07/05/2024 | Fulltime | | United Kingdom | CV-Library | €30,000 - €35,000 / Year Experienced in HPLC Analysis and Methodology, LC-MS, UPC2 or ICP Experience Beneficial - Minimum of 2-3 Years Quality Control or Research and Development Laboratory Experience in the Pharmaceutical, Nutraceutical or Food Industry - Experience in Method Development/Transfer and Validation Beneficial
Save for later07/05/2024 | Parttime | | United Kingdom | CV-Library | €400 - €450 ERP Project Manager Redhill, Surrey Outside IR35 Summary A Project Manager or Business Analyst is required to lead an ERP implementation project within a small to medium enterprise within the pharmaceutical engineering industry. The client An SME acting as a UK-based, technical agent for three
Save for later07/05/2024 | Fulltime | | United Kingdom | CV-Library | €400 - €450 ERP Project Manager Redhill, Surrey Outside IR35 Summary A Project Manager or Business Analyst is required to lead an ERP implementation project within a small to medium enterprise within the pharmaceutical engineering industry. The client An SME acting as a UK-based, technical agent for three
Save for later03/05/2024 | Fulltime | | United Kingdom | CV-LibraryWe are currently looking for a QC Analyst to join a leading Pharmaceutical company based in the Lancashire area. As the QC Analyst you will be responsible for routine testing of radiopharmaceuticals. KEY DUTIES AND RESPONSIBILITIES Your duties as the QC Analyst will be varied however the key
Save for later03/05/2024 | Fulltime | | United Kingdom | CV-LibraryQuality Control QC Microbiology Microbiologist Pharmaceutical Biopharmaceutical Quality Testing GMP GLP Good Manufacturing Practice Good Laboratory Practice Quality Documentation Compliance Regulated Environment Environmental Monitoring Aseptic Monitoring CAPAs SOP Bioassay
Save for later03/05/2024 | Fulltime | | United Kingdom | CV-Library | €30,000 / Year A fantastic opportunity has come up for an experienced process development analyst with our client based in the North West of England. This role will involve developing methods for the analysis of pharmaceutical products and raw materials. We are looking for candidates who have previous experience
Save for later02/05/2024 | Fulltime | | United Kingdom | CV-Library | €70,000 - €90,000 / Year Research, pricing, reimbursement and market access strategy projects to a client base including several pharmaceutical, biotech and medical device - diagnostics manufacturers. The Principal Consultant will be a key member of the market access leadership team, responsible for managing projects
Save for later01/05/2024 | Fulltime | CV-Library | €38,500 - €42,700 / Year Environment. - Must have experience in aseptic techniques, formulation, aseptic filling of sterile product and/or visual inspection of Parenteral products. - Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role. - Comprehensive understanding
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