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- ...industry, ideally including digital transformation and process innovation. Strong knowledge of end-to-end supply chain processes and GMP/GxP compliance. Technical expertise in supply planning and solid oral dosage manufacturing; SAP experience preferred. Excellent...SuggestedFull timeContract workFlexible hoursShift work
- ...managing diverse opinions Experienced in supporting digital transformation and innovation within planning processes Familiarity with GMP/GxP and pharmaceutical regulatory requirements Strong organizational, prioritization, and time management skills Comfortable...SuggestedFull timeFixed term contractTerm timeLocal areaFlexible hoursShift work
- ...support and guidance of ISL technical and operational staff. As applies to all SGS personnel, the focus is to maintain high technical and GMP standards, to ensure the safety of the medicine for the millions of patients who take the products we test. We also will ensure the...SuggestedFull timeFor contractorsWork at officeImmediate startFlexible hours
- ...contractors, during project conception and implementation stages. Experience of implementing and delivering large projects in complex GMP (Pharma, Life Sciences, Medical Devices) manufacturing environments is essential. Candidates without 2 or more years experience in this...SuggestedFor contractorsRelocationHybrid work2 days week3 days week
- ...General position summary: This role is responsible for providing support with real time inspection readiness activities supporting GMP quality. The role requires the ability to adapt to pipeline program milestones, whilst effectively ensuring alignment with corporate...SuggestedContract workTemporary workHybrid work
- ...Operating Procedures. Quality & Compliance ~Work closely with the Quality team to ensure adherence to Good Manufacturing Practices (GMP) during product development. ~Conduct and interpret chemical, physical, sensory, and microbiological tests, and take appropriate...SuggestedPermanent employmentFull timeContract work
€ 45 - 50 per hour
...SAP experience essential Supply Chain Mgr experience. This is an individual contributor role – no need for managing / leading team GMP experience Profiles such as Compliance Trade, Transport Logistics, etc. are not relevant to this role. This role is all about...SuggestedHourly payFull timeContract workWork at officeHybrid workFlexible hours2 days week1 day week€80 per hour
...Master’s degree in Engineering, Life Sciences, or a related field. 5–10+ years of experience in Commissioning & Qualification within a GMP-regulated environment, preferably in the pharmaceutical or biopharmaceutical sector. Proven leadership experience managing C&Q teams...SuggestedHourly payFull timeContract workFor contractorsWork at officeRemote workHybrid work€ 55 - 62 per hour
...project. Ensure the C&Q activities associated with the capital project are completed safely, as per schedule and in compliance with GMP and Quality Requirements. Commissioning & Qualification of Clean Utility Systems / Facility and Process equipment. Generation of...SuggestedHourly payFull timeContract workWork at office3 days week€50 per hour
...right now. * You will have experience of servicing/maintaining/trouble shooting equipment Chromatography Capital Equipment in a GLP/ GMP environment gained from working in, or servicing equipment for, the Pharmaceutical, Biopharma, CRO or Biotechnology industries * Must...SuggestedDaily paidPermanent employmentImmediate startRemote work- ...activities of the Quality Assurance team, including handling product information requests ~Monitor compliance with food safety, legal and GMP (Good Manufacturing Practices) requirements ~Assist in the preparation of bi-annual REPAK packaging reports ~Perform daily product...SuggestedPermanent employmentFull time
- ...interfaces with other SME’s scope of works. Ensure requirements are appropriately documented and agreed with project stakeholders. All GMP URSs to be documented and agreed with project stakeholders in basic design. Work collaboratively with project stakeholders,...Suggested
MALDI-TOF for Precise and Fast Microorganism Identification in Compliance with Updated EudraLex[...]
...innovative solution for quality control processes. Swift and accurate analysis with MALDI-TOF, a sophisticated mass spectrometer. GMP laboratory. High throughput with the capacity to analyse 95 samples per plate in under one hour. Multiple daily analysis sessions...Suggested- ...work. This is a place to make a difference in the world. The Role & What You Will Be Doing The Site Self-Inspection Lead ensures GMP compliance and inspection readiness at the manufacturing site. Key duties include leading self-inspections, conducting facility walk-throughs...SuggestedFull timeLocal areaWorldwide
- ...late stage R&D or Technical Support environment Previous experience of working as an Engineer or Scientist role in a regulated and GMP environment on injectable devices Previous experience in compiling analytical and/or manufacturing control sections of regulatory submissions...SuggestedFlexible hours
- ...pharmaceutical production. It is a critical quality control measure aimed at ensuring that the raw materials meet the required specifications and GMP standards. Working closely with our microbiological lab department, we offer a range of services, including: Assay Testing...
- ...and enforce relevant SOPs, Job Aids, and Company policies and procedures To assist in ensuring; that the appropriate standards of GMP and GDP are maintained. Origination, review, approval, maintenance and archiving of quality documentation. This will include but not...
- ...spectrometry, Pharmaceutical, Installation, Operational, Performance, Qualification, IQ, OQ, PQ, installation, maintenance, IQ/OQ/PQ, GMP, dissolution, repair, engineering, pharmaceutical, Dublin, Athlone, Ireland, VRS9086PC Follow VRS Recruitment on LinkedIn to view all...Full timeLocal area
€ 60 - 70 per hour
...ensuring that the Validation activities associated with a Syringe Filling Line for a Sterile fill finish facility are in compliance with GMP and Quality Requirements. Generation, execution, review and approval of CQV test Documentation (Factor Acceptance Testing (FAT),...Hourly payFull timeContract workWork at officeRemote workHybrid work- ...electronic instrumentation and ability to effectively perform associated calibration procedures ~ Knowledge and experience working in a GMP regulated facility. ~ Experience executing and documenting instrumentation work orders in Maximo or similar computerized maintenance...Permanent employmentApprenticeship
- ...business. Key Responsibilities: ~Ensure compliance with food safety and quality standards during production. ~Conduct daily checks on GMP, weights, dates, temperatures, CCPs/OPRPs, and hygiene. ~Perform audits (hygiene, structural, internal, and glass) and monitor...Permanent employmentFull timeContract workLong term contractShift workNight shift
- ...Engaging with equipment vendors to review electrical and hardwired control system elements, including those for critical utilities and GMP spaces. Supporting project commissioning and qualification (CQV) activities, including protocol review, troubleshooting, and system...Hourly payContract workFor contractorsLong term contractLocal areaWorldwideFlexible hours
- ...review, assessment, and approval activities related to: Change controls Deviations and investigations CAPAs Other relevant GMP documentation Qualifications and Experience: BSc in a scientific or related discipline Minimum of 2 years' experience in Supplier...Permanent employmentContract workTemporary work
- ...engineering discipline, with particular emphasis mechanical or process engineering. Extensive experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment. Demonstrated ability to work on own initiative and proactively respond to business needs....Contract workWorldwide
- ...and regulatory requirements to ensure all drug manufacturing, storage and shipping activities are compliant Providing oversight of GMP systems completed by CMO's and External Supply Chain function related to Drug Substance, Drug Product and Finished Product. Providing...Contract workFor contractorsFixed term contract
- ...Microbial Identification, Media prep, Water Sampling. • Understanding and application of principles, concepts, theories and standards of GMP QC microbiology laboratories • Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change...
- ...communicated clearly to the Owner. Ensure the technical team keeps to the project scope Take accountability for the delivery of the GMP compliant, functionality and robust performance of the technical packages (e.g. process, packing, automation, critical utilities, HVAC)...Permanent employmentContract workFor contractorsLocal areaWorldwide
€70k - €75k per annum
...electrical, and automation systems . Proven track record in project management , team leadership, and regulatory compliance (HACCP, GMP). Excellent problem-solving skills and a continuous improvement mindset . In return, you'll join a forward-thinking company...Permanent employment- ...measurement and control in Pharmaceutical Industry ~ Proven fault finding/trouble shooting skills ~ Knowledge and experience working in a GMP regulated facility. ~ Experience executing and documenting Calibration certificates ~ Ability to interpret loop sheets, electrical...Permanent employment
- ...a global pharmaceutical leader that is currently hiring a Process Engineer based in Dublin. This is a fantastic opportunity to join a GMP-regulated manufacturing site, where you'll take ownership of cleanroom process equipment and utility systems. The role involves providing...Contract work