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£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 Sligo4 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 Sligo11 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 Sligo16 days ago- ...automation discipline, with a minimum of 5 years’ experience in industry, preferably in a pharmaceutical, biotechnology, blue chip or relevant GMP manufacturing environment. The ideal candidate will have excellent communication skills and strong problem skills. Candidates...SuggestedContract workFor contractorsRemote workRelocationHybrid work
£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- ...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
- ...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
- ...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....SuggestedFull timeFlexible hoursShift workNight shiftMonday to Thursday
- ...relevant experience may negate degree requirements. A minimum of 5 years of experience in production scheduling and planning within a GMP-regulated environment, preferably in the pharmaceutical or biotechnology industry. Proficiency in MS Excel is essential. Strong...SuggestedPermanent employmentLocal area
- ...planned and reactive—ensuring efficient, compliant operations. It involves cross-functional collaboration and ensures adherence to EU GMP, EHS, and company standards. Overview of your responsibilities ( full job description available on request ): As Maintenance Manager...SuggestedPermanent employmentFor contractors
- ...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...SuggestedFull time
- ...accordance with the requirements of the Product Specification File (PSF)/Marketing Authorisation (MA) and with Good Manufacturing Practice (GMP) for products manufactured at AbbVie Biologics Ballytivnan Sligo. · To ensure that products manufactured at AbbVie Biologics...SuggestedContract workTemporary work
- ...experience in process chemistry or process engineering, with a strong background in batch processing, technical transfers, and validation in a GMP pharmaceutical environment essential. ~ Proven leadership experience with a team of direct reports. ~ Excellent interpersonal and...SuggestedFull time
- ...Procedures. Qualifications What you will need: ~3rd level qualification in a relevant Science discipline ~2 years experience in GMP manufacturing ~ Antibody drug, ADC and drug substance purification experience preferable Additional Information Whatever your...SuggestedFull timeShift work
- ...help with 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. Maintain...Permanent employmentContract workFlexible hoursAfternoon shift
- ...required. Qualifications Qualifications ~ A thorough knowledge of aseptic and sterile processes together with experience within a GMP environment and knowledge of current EU/FDA/ICH/HPRA and Annex 1 guidelines. ~3 -5 years’ (minimum) experience in microbiology is a...Full timeImmediate start
- ...with vendors, and act as Engineering representative for pre-approval of vendor documentation. Skills Brief Experience in a GMP regulated environment is essential and only candidates with this experience can be considered (The following experience will be...Permanent employmentFor contractorsRelocation
- ...high standard of quality in their work. Key Responsibilities: - Qualification of new laboratory equipment as required. - Perform GMP compliant and timely transfer of analytical methods. - Generation of necessary documentation to support ongoing operation of the QC...WorldwideFlexible hoursWorking Monday to Friday
PHIBRO ANIMAL HEALTH CORP
Sligo, Co. Sligo5 days ago - ...Maximo CMMS. To manage and co-ordinate the site efforts in planning and executing a site electrical power down/up ensuring work is GMP & safety compliant with minimal impact to site activities. To represent the electrical program during FM Global inspections. Desirable...Contract work
Quanta Consultancy Services Ltd
Sligo, Co. Sligo2 days ago - ...assigned CORE COMPETENCIES Proactive at keeping current with literature and latest technologies. An excellent understanding of GMP, ICH and compendia regulations and guidance's. Demonstrated ability in leading root cause analysis and effective investigation...WorldwideWorking Monday to Friday
PHIBRO ANIMAL HEALTH CORP
Sligo, Co. Sligo2 days ago - ...secondary maintenance engineers to each eMaint asset. # Develop and implement preventive and predictive maintenance programs for all GMP critical assets. # Ensure maintenance activities comply with EU GMP, EHS, and other standards. # Manage service contracts and vendor...WorldwideWorking Monday to Friday
PHIBRO ANIMAL HEALTH CORP
Sligo, Co. Sligo4 days ago - ...accordance with the requirements of the Product Specification File (PSF)/Marketing Authorisation (MA) and with Good Manufacturing Practice (GMP) for products The Quality Assurance Specialist / Qualified Person (QP) is responsible for the disposition of bulk product...Contract work
Quanta Consultancy Services Ltd
Sligo, Co. Sligo4 days ago - ...The QA Specialist will be responsible for delivery of Quality Assurance activities to ensure product is manufactured in accordance with GMP and Regulatory requirements. The role will also include the review and approval of validation documentation and activities related to...WorldwideWorking Monday to Friday
PHIBRO ANIMAL HEALTH CORP
Sligo, Co. Sligo3 days ago - ...finish facility. Proven ability to work cross-functionally. Skills and Experience: Strong technical and business knowledge in a GMP environment, particularly in pharma/biologics. Thorough understanding of regulatory requirements. High attention to detail and a...Fixed term contractWorldwide
Allergan
Sligo, Co. Sligo3 days ago - ...accordance with the requirements of the Product Specification File (PSF)/Marketing Authorisation (MA) and with Good Manufacturing Practice (GMP) for products manufactured at Sligo site. To ensure that products manufactured at the site are manufactured in accordance with the...Permanent employmentImmediate start
Hero Recruitment
Sligo, Co. Sligo4 days ago - ...Ideally previous experience in a quality role A minimum of three years’ experience in a quality/operations role in a highly regulated GMP environment. Experience in biologics manufacturing is highly desirable. Experience in aseptic processing gained within either a...Contract work
Quanta Consultancy Services Ltd
Sligo, Co. Sligo3 days ago
