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- ...and follow-through in executing responsibilities. Understanding of risk management methodologies (ISO 14971). Experience with sterilization (EtO/Gamma), biocompatibility, and transportation testing is a plus. Prior involvement in audits or inspections is an advantage...SuggestedPermanent employmentFull timeImmediate start
- ...exposure to FDA, HPRA or other authorities of similar standing. · Biologics manufacturing experience highly desirable · Experience in Sterile Manufacturing and/or Clinical Trials Regulations highly desirable · High level technical skills including analytical, auditing,...SuggestedWorldwideHybrid work
- ...Regulation 536/2014. • Strong organisational and communication skills; ability to work on global teams. • Hands-on experience with sterile, non-sterile, biologics, vaccines, gene therapy, or ATMPs is preferable with at least 2 years’ experience in Quality Assurance or...SuggestedContract work
- ...manufacturing operations. Fill Finish is the department where product which treat rare conditions is filled and finished in a highly automated, sterile, controlled and regulated environment. For more than 20 years, our Waterford team has continued to grow and diversify to serve...SuggestedContract workFixed term contractLocal areaFlexible hoursShift work
- ...experts through comprehensive training. Become a trusted guide for customers - conducting piercings, educating on aftercare, maintaining a sterile environment, addressing questions and concerns throughout the process. Store Operations: Keep the heartbeat of our store strong by...SuggestedPermanent employmentFull timeShift work
- ...Cork Hybrid - 3-4 days onsite Your key responsibilities: Define local quality strategy to deliver safe, high-quality clean and sterile products while maintaining regulatory compliance Oversight of Micro & Sterility key processes cleaning, cleanroom, sterilization...SuggestedLocal areaHybrid work
- ...compliance in area of responsibility to cGMP ’ s of all medical device regulatory agencies ( e . g . FDA and TUV ). Management of Sterile Returns and IDD processes. Provide functional expertise to other support functions on quality related issues ( e . g . regulatory...SuggestedWorldwide
- ...environment. Key Responsibilities: Lead, mentor, and develop a team of R&D Technicians to support product builds, testing, and sterilization activities. Manage the R&D lab facility, including equipment calibration, maintenance, and material inventory. Establish...SuggestedWorldwide
- ...change conditions and testing different variables. With a focus on fermentation, microfiltration, separation, liquids blending, sterilization and spray-drying, this is an advanced and technical site. About Kerry Kerry is the world's leading taste and nutrition...SuggestedPermanent employment
- ...tourniquet with confirmation of limb pressure with individual surgeon. Assist with draping of patient within surgeons guidelines maintaining sterility. Maintain integrity of the sterile field. - Assist in the safe transfer of patients between wards, and from the theatre to the...SuggestedPermanent employmentFull timeImmediate start
- ...~ Pharma manufacturing experience. ~ Capital Project Management Experience in Pharma manufacturing facilities, such as: Bulk API, sterile products, secondary packaging, Devices and to a lesser extent lab projects. ~ Experience in the following areas: GMP manufacturing,...SuggestedTemporary workFor contractorsFor subcontractorLong term contractLong distanceFlexible hours
- ...to be named as a Qualified Person (QP) and to have maintained CPD. ~ Practical experience with disposition of product types such as Sterile, Nonsterile, Biologics, Vaccine, Gene Therapy or ATMP, is preferable ~2 year’s experience in quality assurance or qualitative...SuggestedContract workHybrid work
- ...The QC chemist's responsibilities will support testing of finished products across a variety of techniques for the solid oral dosage, sterile, and biologic product portfolio. THE ROLE: Review of analytical data and documentation to ensure compliance with appropriate...SuggestedFull timeContract workFixed term contractWork at office
- ...supplier quality management. Familiarity with ISO 14971 and risk management practices. Experience with validation of test methods, sterilization (EtO or Gamma), packaging, biocompatibility, and labelling is a plus. Demonstrated ability to lead audits, CAPA processes, and...SuggestedPermanent employmentFull timeContract workImmediate start
- ...Laboratories, ensuring regulatory compliance and product quality requirements are met at all times. This will involve routine entry to the sterile facility. They will support qualification and ongoing monitoring of suppliers and service providers including execution of external...SuggestedLocal area
- ...examination rooms. Assist the Sonographer/Radiologist with their workload, including managing the daily patient list and assisting with sterile procedures. Monitor Ultrasound vetted in-patient list on RIS system and liaise with wards re patient transport and preparation for...Permanent employmentFull timeWork at officeLocal areaFlexible hoursShift workDay shiftSaturday2 days week3 days week
- ...compliance with applicable Corporate and Divisional Policies and procedures. Key Responsibilities: 1. Leads team that conduct sterilization qualification for new products and/or changes to existing products. 2. Leads team that performs sterilization validation for...Full time
- ...experts through comprehensive training. Become a trusted guide for customers - conducting piercings, educating on aftercare, maintaining a sterile environment, addressing questions and concerns throughout the process. Keep It Fresh: Maintain an Insta-worthy store with perfect...Permanent employmentPart timeShift work
- ...comprehensive site services, bioreactors and fermenters, filtration and chromatography systems, prep and hold systems, and cleaning/sterilization systems. Roles we have available: Mechanical Assemblers/Polishers Day shift (7am - 3:30pm) Evening shift (3:15pm - 11...Permanent employmentDay shiftAfternoon shift
- .... What You’ll Do: Lead packaging projects for new product development and changes to existing products Develop and validate sterile and non-sterile packaging systems Drive cost savings and continuous improvement initiatives Ensure global regulatory compliance...Worldwide
- ...and follow-through in executing responsibilities. Understanding of risk management methodologies (ISO 14971). Experience with sterilization (EtO/Gamma), biocompatibility, and transportation testing is a plus. Prior involvement in audits or inspections is an advantage...Contract workVisa sponsorshipLocal areaImmediate startWork visa
- ...Eligible to be named as a Qualified Person (QP) and to have maintained CPD. Practical experience with disposition of products such as Sterile, Non-sterile, Biologics, Vaccines, Gene Therapy, or ATMP, with at least two years of experience in quality assurance or qualitative...Contract workTemporary workWorldwide