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- ...Senior Quality Assurance Systems Specialist Senior Quality Assurance Systems Specialist... ...for the communication of revised guidelines associated to Quality Systems. Responsible for sustained... ...necessary to perform the duties of the QA Specialist are typically acquired through...SuggestedContract work
- ...Cpl in partnership with SK pharmteco are hiring a permanent QA Senior Specialistto join QA Systems team for their site in Swords, Co. Dublin. ABOUT US? SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities...SuggestedPermanent employmentContract work
- ...Biotech Quality Systems QA Specialist, Dun Laoghaire, Dublin Office/Project Location: Dun Laoghaire, Dublin Employment Type: Contract... .../requirements and for the communication of revised guidelines associated to Amgen Quality Systems. Responsible for sustained...SuggestedHourly payContract workWork at officeShift work
- ...join our team and make a meaningful impact on patients’ lives. QA Associate - Shanbally, Ringaskiddy, Cork (day role) Closing Date - 31st... ...and continuous improvement of new and existing processes / systems to meet customer needs. Exercise judgment to determine appropriate...SuggestedImmediate startWorldwide
- ...Acorn Regulatory’s ongoing growth has created an opportunity for a QA Specialist & Responsible Person to join our award winning... ...complaints etc. as required • Maintenance of the supplier management system, including completion of supplier evaluations, assessment and repeat...SuggestedFull timeContract workPart timeFixed term contractLocal areaRemote workHybrid work
- ...animation_direction="left" animation_speed="0.3" animation_offset=""] QA Resources is currently recruiting for a Senior QA Specialist on... ...implementation and improvement of the local Quality Management System. They will provide hands on Quality on the Shop floor compliance...SuggestedLocal area
- ...responsible to: Guarantees cGMP compliance in all activities and systems related to Projects and Products execution. Assures that working... .../ reporting of KPIs for the team Develop and accumulate strong QA expertise, sharing knowledge of new developments and methodologies...SuggestedContract workWorldwide
- ...responsibility. What you'll be doing Finished product positive release Customer Complaint Investigations Conduct internal quality system audits Support audit readiness and participate in internal and external inspections Accountable for managing the resolution and...SuggestedPermanent employmentFull timeLocal area
- ...Select how often (in days) to receive an alert: QA Specialist II (Senior) - External Manufacturing, Combination Products & Quality... ...area with responsibility for day-to-day implementation of Quality Systems and Compliance functions appropriate for Emergent (EBSI) combination...SuggestedLocal areaHybrid workFlexible hours
- ...in the administration and implementation of the Quality Management System in the context of manufacturing, commercialisation, and post... ...further develop their career path by being exposed to many varied QA experiences in a fast-moving dynamic environment. There is also potential...SuggestedWork at office
- ...QA Specialist - Dublin, Ireland - 12 Months Contract One of the top 10 best companies... .../Investigations CAPAs Other associated documentation ~ Support OpEx programs and... ...understanding of cGMP requirements for QA systems and compliance and/or manufacturing. Detailed...SuggestedContract work
- ...QA CSV Specialist - Ireland, Limerick - 6 Months Initial Contract We are recruiting... ...Responsibilities include: Ensure Computer System Quality across all site systems... ...approval Provide training on CSQ Support associated Computer System maintenance activities...SuggestedContract workLocal area
- ...Play a key role in supporting the Quality Management System (QMS) and ensuring that our site consistently meets both regulatory and customer... ...safety, compliance, and innovation. We are currently seeking a QA Officer to support our Quality Assurance team in maintaining high...Suggested
- ...site in setting up the quality function. Support validation and qualification of equipment, utilities, facilities, and computerised systems. Develop and execute validation protocols (IQ/OQ/PQ), cleaning validation, and process validation. Oversee the Quality...SuggestedPermanent employment
- ...possible, together. Job Description QA Specialist II position in QA Packaging Support... ...and approval of packaging and labelling associated documents, procedures, changes,... ...requires a sound knowledge of quality assurance systems, methods and procedures. The candidate will...SuggestedPermanent employmentFull timePart timeFor contractorsLocal area
- ...Position Overview: We are seeking a QA Specialist for a contract role within the Quality Assurance (QA) Department, specifically... ...This role requires a solid understanding of quality assurance systems, current Good Manufacturing Practices (cGMPs), and standard QA procedures...Contract work
- ...QA Facilitator – Systems and Compliance Summary of role Setting the standard and ensuring compliance in the areas of Sterling Pharma Ringaskiddy... ...ability to quickly learn new software, tracking tools and associated processes. Experienced in influencing people,...Contract work
- ...releaseresponsibility and ensures that effective and robust Quality systems are inplace to comply with required regulations, policies and... ...with manufacturing operations and/oranalytical expertise associated with biologics and/or vaccines. Asepticmanufacturing experience...Contract workFor contractorsRemote workWorldwide
- ...our R&D facility in Dunboyne. You will be reporting to the Associate Director of QA Operations within Global Development Quality (GDQ), the QA Specialist... ...GMP documentation. ~ Experience in quality management systems such as Veeva, SAP, PAS-X etc. ~ Demonstrated knowledge...Visa sponsorshipRelocationFlexible hoursShift work
- ...responsible to: # Guarantee cGMP compliance in all activities and systems related to Projects and Products execution. # Assure that... ...# Typically requires 5-8 years of relevant experience within a QA GMP environment within the Pharmaceutical Industry (mandatory)....Contract work