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Search Results: 15 vacancies
- ...Job Description We are seeking a Data Reviewer to join our exciting Gene Therapy team in Dungarvan Co Waterford. 3+ years' GMP Pharma experience is required to apply for this role. The purpose of this job is the data review of scientific test procedures used...SuggestedFull timeContract workWorldwideFlexible hours
- Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients...SuggestedFull timeContract workWorldwide
- ...The QP will be involved in the review and certification of batches intended for use in clinical trials, to ensure compliance with EU GMP, the Product Specification File and the Clinical Trial Application. This role will encompass product manufactured across the company...SuggestedContract workTemporary work
€43.97k - €73.62k per annum
...communication skills. • Analytical problem-solving skills. • Active listening skills and ability to integrate diverse perspectives. • Timely decision making. • Ability to respond to changing priorities. • Experience of working in strongly regulated GMP environment...SuggestedContract workFixed term contract- ...Working experience in requirement analysis, design document creation and other validation documents; ITIL service delivery processes and GMP validation processes; Knowledge on GMP change control processes; Develop system validation documentation and ensure the system...SuggestedPermanent employmentLocal area
- ...Skills and Requirements: Familiarity with pharmaceutical laboratory operations. Strong understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Attention to detail and a proactive, team-oriented mindset. Ability to follow safety...SuggestedPermanent employment
- ...required. Qualifications A degree in microbiology or a related discipline At least 6 months microbiology testing experience in a GMP laboratory Experience with any of the following; bioburden, MLT and ID testing Good team player, organised, accurate, have strong...SuggestedFull timeContract workFixed term contractWorldwideRotating shiftWeekend work
- ...Mechanical or Manufacturing. ~5+ years of experience in a medical device or pharmaceutical manufacturing setting. ~ Strong understanding of GMP/HPRA/FDA regulatory requirements and current Health and Safety Regulations legislation. ~ Familiarity with industry regulations and...SuggestedPermanent employment
- ...Experience in manufacturing environments, preferably in regulated industries like medical devices or pharmaceuticals. Knowledge of GMP, regulatory requirements, and health and safety regulations. Strong problem-solving, communication, and decision-making skills. Ability...SuggestedPermanent employment
- ...with this role include, but are not limited to the following: Carry out all work safely, cost effectively and to the highest GMP standards, while maintaining good relations with our suppliers, contractors, customers and fellow employees Carrying out all routine...SuggestedPermanent employmentFor contractorsImmediate startShift work
- ...manufacturing facility, including commercial product release Ensure implementation of Consumer Healthcare Quality standards and current GMP requirements within the site Manufacturing plant Deploy Quality and Compliance systems (HQS) and ensure they are in place and in use...SuggestedLocal areaWorldwide
- ...Key Skills: ~Strong leadership and team development skills ~Excellent troubleshooting and problem-solving abilities ~Knowledge of GMP, food safety, and regulatory compliance ~Effective communication and interpersonal skills ~IT proficiency and fluency in English (written...SuggestedPermanent employmentFull time
- ...investigations and assist in resolving any identified issues. Key Skills and Requirements: Experience working as a production operator in a GMP environment is a must. Strong commitment to workplace safety and quality standards. Ability to follow detailed instructions and...SuggestedPermanent employmentShift work
€45k - €60k per annum
...ATEX system management. Strictly adherence to all site safety Policies. Compete all work according to site Quality standards and GMP-Documentation and housekeeping. Skills Required: ~4+ years’ experience carrying out Mechanical & Electrical Maintenance Repairs....SuggestedContract workFor contractors- ...communication skills. Analytical problem-solving skills. Active listening skills and ability to integrate diverse perspectives. Timely decision making. Ability to respond to changing priorities. Experience of working in strongly regulated GMP environment....SuggestedFull timeContract workWorldwide