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Search Results: 68 vacancies
£51.9k - £60.5k per annum
...commensurate with the level of risk. * Perform timely review and approval of site procedures and documentation to ensure compliance with GMP and regulatory requirements. * Review and approval of validation protocols/ reports and related documentation to ensure compliance...SuggestedContract workCounty Sligo5 days ago£38.9k - £47.5k per annum
...regulatory standards. * Implement corrective actions to resolve any issues and prevent recurrence. * Ensure compliance with all relevant EU GMP regulations. * Oversee the validation and verification of new testing procedures and technologies. * Troubleshoot technical issues...SuggestedPermanent employmentCounty Sligo12 days ago£43.2k - £51.9k per annum
...other relevant technical subject area * 2+ years direct experience in the use of single use materials for biologics manufacturing in GMP environment e.g., in operations, technical operations, and process validation. * 1+ years experience in the design, onboarding, and qualification...SuggestedPermanent employmentCounty Sligo17 days ago£86.4k - £103.7k per annum
...accordance with the requirements of the Product Specification File (PSF)/Marketing Authorisation (MA) and with Good Manufacturing Practice (GMP) for products manufactured * Ensure that products are manufactured in accordance with the relevant GMPs. * The Quality Assurance...SuggestedContract workSligo, Co. Sligo11 days ago- ...Ballina, Co. Mayo. You shall be reporting to the Microbiology Functional Manager. The main duties & responsibilities shall be; • GMP Compliance. • Perform Endotoxin testing, Sterility testing, Efficacy of Antimicrobial Effectiveness test, Environmental Monitoring...SuggestedContract workWorldwideFlexible hours
- ...required timelines i.e. scheduling of tests, review of basic data, liaising with QA, generation of CoA etc.) Generation and updating of GMP compliant SOPs, Protocols and reports. Sourcing, purchasing and stocking consumables, standards and reagents required for testing....SuggestedContract workFor subcontractorWorldwideFlexible hours
- ...qualification in an Engineering discipline ~ Trade qualified will also be considered ~3-5 years experience in a regulated environment (GMP preferable) ~ Strong IT knowledge is required. ~ Strong trouble shooting and documentation skills ~ Working knowledge of ATEX...SuggestedFull timeContract workFor contractorsShift workAfternoon shift
- ...in Quality Assurance activities supporting the qualification and validation of manufacturing operations, while ensuring compliance with GMP and regulatory standards. Responsibilities: Serve as the site QA point of contact, providing technical expertise, feedback, and...SuggestedPermanent employmentFull time
- ...delivery of medical devices that change lives. Responsibilities: Ensure compliance to all applicable regulatory standards and current GMP procedures and practices. Perform product defect analysis. Routine final functional testing, product release criteria testing/...SuggestedPermanent employment
- ...Remain updated on correct procedures by reviewing current and updated SOP's relating to the job and the department. Adhering to GMP cleanroom behavioural procedures at all times. Completing all GMP paperwork RFT, in a timely manner and as per GDP, allowing for review...SuggestedContract workFixed term contract
- ...Qualifications In this role you will need; ~3rd level qualification, preferably in Engineering or Science related fields OR 2+ years in a GMP regulated environment ~ Experience of operating in a highly automated environment ~ Experience in safe handling of dangerous...SuggestedFull timeFixed term contractShift work
- ...compliance to all quality requirements, including Good Manufacturing Practice, Good Laboratory Practice and Good Documentation Practice (GMP, GLP and GDP). ~ Perform and assist with additional duties as may be directed by the Supervisor. ~ Identify and implement...SuggestedWorldwide
€32k - €35k per annum
...production environments. A background in biotechnology, pharmaceutical sciences, engineering, or a related field, along with knowledge of GMP, would be essential. Certifications related to aseptic processing, environmental monitoring, or EHS standards would be advantageous....SuggestedContract work- ...Your Key Activities will include, but are not limited to: Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system Perform activities associated with the compounding, filling and capping of an aseptic process. Prepare components...SuggestedFull timeContract workFixed term contractShift workNight shiftWeekend workWeekday work
- ...the generation of all departmental quality documents including audit responses, facility replies and deviation reports. Generation of GMP compliant SOPs, Protocols and reports Generate risk assessments for laboratory and test items as required. Maintain Laboratory...SuggestedContract workWorldwideFlexible hours
- ...AQLs, and the incoming inspection and disposition of raw materials, consumables, packaging. Assist in preparation and presentation of GMP training programmes. Participate in initiatives and action plans for the development of QA and improvement of GMP compliance....Worldwide
Jazz Pharmaceuticals
Roscommon Town, Co. Roscommon4 days ago - ...Perform high-precision wiring tasks, ensuring components meet exact specifications. Conduct quality checks to ensure compliance with GMP and ISO standards. Prepare parts for anodising and assist in mechanical assembly during machine builds. Perform daily maintenance...Permanent employmentContract work
- ...& Development: Be part of a company where your skills will grow with you Commitment to Quality & Safety: Join a company focused on GMP, cleanroom standards, and QESH excellence Key Responsibilities Perform preventive and reactive maintenance on production equipment...Permanent employmentFull timeFor contractorsLong term contractAfternoon shiftWorking Monday to Friday
- ...problems, effect changes in procedures and ramp up line speeds or throughput. Ensure strict compliance with all procedures, regulatory and GMP requirements, quality procedures including record keeping, inspection standards, product disposition and validation protocols....Full timeFlexible hoursShift workNight shiftMonday to Thursday
- ...continuous improvement objectives. The role requires an individual with expert level technical skills with HMI and PLC systems, gained in a GMP (Medical Devices, Pharma, Life Sciences or Biotech) environment. Essential Duties and Responsibilities include, but are not limited...Permanent employmentFull timeFor contractorsRemote workRelocation
