Are you ready to apply your bioprocess expertise to deliver life-changing therapies for people living with rare diseases? Join a manufacturing team where precision, ownership, and cross-functional collaboration turn complex science into reliable supply for patients
This is what you will do: The QA Validation Specialist performs review and approval activities to support validation activities in Alexion ARDU cGMP commercial and clinical requirements for the Alexion Manufacturing Facility. The responsibilities will include performing review
This is what you will do: The QA Validation Specialist performs review and approval activities to support validation activities in Alexion ARDU cGMP commercial and clinical requirements for the Alexion Manufacturing Facility. The responsibilities will include performing review
Are you ready to apply your bioprocess expertise to deliver life-changing therapies for people living with rare diseases? Join a manufacturing team where precision, ownership, and cross-functional collaboration turn complex science into reliable supply for patients
The Senior Director MSAT will serve as a senior leader within the Tech Ops organisation, playing a central role in shaping future technical capability and driving sustained excellence across a complex and expanding neuroscience portfolio. Reporting
If you are a current Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We
This is what you will do: The management and oversight of the following QC activities: analytical, microbiological; sample management; direct laboratory testing support; equipment management & maintenance support to ensure fully compliant, effective and safe Quality
This is what you will do: The management and oversight of the following QC activities: analytical, microbiological; sample management; direct laboratory testing support; equipment management & maintenance support to ensure fully compliant, effective and safe Quality
Introduction to role: Are you ready to safeguard the quality of life-changing medicines and keep patient supply flowing without compromise? Do you thrive at the intersection of compliance, investigation, and continuous improvement, turning complexity into clear,
Quality Assurance Specialist Location: Athlone, Ireland Business Area: Operations – Quality Job Type: Full‑time | Grade C | On‑site Worker Type: Employee Scheduled Hours: 37.5 per week Make a meaningful impact by ensuring the highest standards
Quality Assurance Specialist Location: Athlone, IrelandBusiness Area: Operations – QualityJob Type: Full‑time | Grade C | On‑siteWorker Type: EmployeeScheduled Hours: 37.5 per week Make a meaningful impact by ensuring the highest standards of product quality At
Position Title: Process Project Engineer (PE). Reporting to: WPO Project Lead for Process Equipment. Department / BU: Engineering / Capital Expansion Emerging Technologies. JOB SUMMARY: The Process Equipment Project Engineer (PE) is responsible for safely coordinating and leading Equipment
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting Job Description Scientist III (Inhalation), Pharma At PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Laboratory
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Scientist III - LCMS - Pharma At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab
Work ScheduleStandard (Mon-Fri) Environmental ConditionsLaboratory Setting, Office Job Description At PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission
eir business talent are seeking applications for a Senior Commissioning & Qualification Project Lead, this is a long-term day rate contract based in Athlone. This role is part of the expansions team and will support the
Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Athlone. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best
Overview Our organisation is undertaking a major expansion program to support the retrofit of a brownfield site to produce oral medicines. This role is part of the Athlone Expansions team and will support the delivery of