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- ...QA Facilitator – Systems and Compliance Summary of role Setting the standard and ensuring compliance in the areas of Sterling Pharma Ringaskiddy’s Auditing Programs including: Internal Audit/ Self Inspection Supplier Audits Customer Audits Health Authority...SuggestedContract work
- ...QA CSV Specialist - Ireland, Limerick - 6 Months Initial Contract We are recruiting on behalf of a leading global pharmaceutical client based in the surroundings of Limerick. Due to a large capital investment and multiple projects on site, the client is looking for aQA CSV...SuggestedContract workLocal area
- ...Engineering, Pharmaceutical Sciences or similar scientific field (mandatory). # Typically requires 5-8 years of relevant experience within a QA GMP environment within the Pharmaceutical Industry (mandatory). # Experience of working in a GMP operational environment (mandatory)....SuggestedContract work
- ...Gilead and help create possible, together. Job Description QA Specialist II position in QA Packaging Support, Gilead Sciences Ireland... ..., returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-...SuggestedPermanent employmentFull timePart timeFor contractorsLocal area
- ...animation_direction="left" animation_speed="0.3" animation_offset=""] QA Resources is currently recruiting for a Senior QA Specialist on... ...****@*****.*** ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa...SuggestedLocal area
- ...outcomes. We’re now looking for a Quality Assurance Labelling Assistant to join our team in Tipperary. Job Description What... ...qualification (or equivalent) in Science, Engineering, Pharma or QA (desirable) Ideally 2+ years’ experience in a regulated medical...SuggestedFull timeLocal area
- About the role Here at Kerry, we are currently recruiting for a Quality Assurance Officer to join our team in Charleville. Your role as a Quality Assurance Officer will involve a number of tasks such as batch review, approval of incoming raw material requests and subsequent...SuggestedLocal area
- ...responsible for performing activities in support of dispositioning product and/or raw materials while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents. This is a 12-month temporary contract. A...SuggestedTemporary workLocal area
- In this position you will be responsible for the disposition of raw materials and ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents. Please note this is a 12/7 shift position which is extended...SuggestedLocal areaShift workDay shift
€50k - €70k per annum
...collaborating with a Biotech company who are in search of a Specialist in QA Validation. The chosen individual will offer supervision for the... ...reports. Provide supervision to project-related deviations. Assist generation of Process and Q/C Equipment Installation, and...SuggestedPermanent employmentFor contractors- ...Department (“Department”). This position will functionally report to the QA and Training Audit Director. This role requires a strong,... ...expertise in the firm’s audit methodology. Key tasks include: Assist with update, delivery, management and post-course review for technical...SuggestedFlexible hours
- ...systems, programs and quality events are robust and meet regulatory agency expectations. The position will liaise with the IT and broader QA organizations to ensure all aspects of IT related programs are in compliance with regulatory agency expectations and internal company...SuggestedLocal area