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- ...JOB DESCRIPTION Decontamination Technician - Sterile Services Reference No: 02.011 (2026) PURPOSE OF THE ROLE The Decontamination Technician will be responsible for ensuring that reusable medical devices such as endoscopes and other surgical devices e.g. instruments...SuggestedPermanent employmentFull timeContract workWork at office
- ...and problem solving with data and AI increasing our impact and delivering better and faster for patients. As the Vice President Sterility Assurance you will provide outstanding leadership in shaping and delivering a global sterility strategy across Engineering QA...SuggestedLong term contractFull timeLocal area
- ...Job Title: Sterility Engineer P2 Location: Cork Req Number: 618900 Contract Type: Permanent Reporting to: Senior Sterility Engineer - Elaine ORegan Closing Date: February 19th Apply through My Career Navigator attaching an updated CV. Queries to Lorna...SuggestedPermanent employmentFull timeContract workFor contractors
- JOB DESCRIPTION: Main Purpose of the Role Specialist professional individual contributor with comprehensive knowledge in the area of Pharmaceutical/Biological Process. Ability to execute highly complex or specialized projects. Adapts precedent and may make significant...SuggestedFull timeShift work
- ...industry ~ Experience with regulatory compliance in cGMP manufacturing and in-depth knowledge ofEudralexVolume 4 Annex 1 Manufacture of Sterile Medicinal Products. ~ Proven ability to work in a high paced matrix organization and effectively influence changeand escalate...SuggestedFull time
- ...Biotechnician in Cork Ireland. Reporting to the Drug Product Team Lead the successful candidate shall work as part of a team of Sterile Filling Technicians to complete both the manufacturing and visual inspection of sterile drug product as per the schedule for onward processing...SuggestedFull timeContract workWorldwideShift workRotating shift
- ...this role you will be accountable for ensuring that all products produced at the site adhere to the specified microbiological and sterilization standards. Responsibilities: • Responsible for maintaining up-to-date knowledge of all current relevant worldwide...SuggestedFull timeWorldwide
- ...job related computer applications required Report, standards, policy writing skills required Equipment and process validation Sterile filling processes and equipment Lean Six Sigma Methodology experience desired Our role in supporting diversity and...SuggestedFull timeContract workInterim role
Orion Engineering Services Limited
Carlow Town, Co. Carlow24 days ago - ...you will need: A third level qualification in a science or quality discipline Minimum 3 years Experience in Pharmaceutical or Sterile Manufacturing environment Experience with internal and external auditing Strong written and verbal communication skills Additional...SuggestedPart timeFixed term contract
- ...areas example cleaning CSV Aseptics process CPV ~ Understanding of Process Validation Computer system Validation SCADA systems CPV Sterilization Packaging systems and related technologies. ~ A strong understanding of current data integrity expectations would be a distinct...SuggestedPermanent employmentFull time
- ...of Design for Manufacturability (DFM) principles. Experience validating test methods, equipment or software . Background in sterile devices or electro-mechanical / software-containing medical devices . BENEFITS ~ Hybrid working model with flexibility. ~...SuggestedFull timeHybrid work
€48k - €72k per annum
...company that thinks differently to solve problems make progress and deliver meaningful innovations. Our Purpose At our Sterilization Validation Department in Medtronic plc we focus on product quality excellence and providing...SuggestedFull timeTemporary workFlexible hours- ...in a world-class supply organisation. Practical knowledge of execution of routine maintenance and calibration activities in a GMP Sterile Fill Facility. Experience of working in a cross functional environment. We keep the patient at the very heart of all that we...SuggestedFull timeHybrid workVisa sponsorshipLocal areaRelocationFlexible hoursShift work
- ...Work Flexibility: Hybrid or Onsite Position Summary The Staff Packaging Engineer plays a critical role in the design of sterile packaging for orthopedic implants. You will collaborate closely with implant product development operations vendor and program management...SuggestedFull timeHybrid work
- ...improvement. Strong knowledge in execution validation and development of microbiology related test methods i.e. Bioburden Endotoxin and Sterility testing. At least 5 years experience in the Microbiology Pharmaceutical industry or a similar operating environment....SuggestedFull timeContract workHybrid workImmediate startWorldwide
- ...LIMS system for logging of samples. Environmental Monitoring of Cleanrooms. Microbial Limit Testing of Products and Active Ingredients (Sterile and Non – Sterile – TAMC, TYMC, Absence of Specific Organisms) Bioburden Testing on Medical Devices. ~ Phase 2: Accelerate – Turn...Long term contractPermanent employmentFull timeContract work
- ...~ A minimum of 2 Years cGMP industrial experience ideally covering Operations Engineering Projects within Proteins manufacturing or Sterile manufacturing ~ Experience with dealing with vendors on scoping and pricing jobs. ~ Key Competencies: ~ Planning and organizing...Full timeHybrid workRelocation packageFlexible hours
- ...manufacturing, packaging, or assembly Experience working in a GMP or ISOregulated environment is an advantage. Prior cleanroom or sterile assembly experience beneficial. Knowledge, Skills & Abilities Knowledge of: GMP, GDP (Good Documentation Practices), and...Permanent employmentImmediate startWorking Monday to FridayNight shift
- ...new product development and sustaining project teams with responsibilities for development of packaging solutions for packaging for sterile medical devices (instruments), , package design verification, shelf life testing and compliance related activities. This resource will...Fixed term contractWorldwide
€ 70 - 80 per hour
...an initial 12-month contract. Responsibilities: Development and execution of CQV testing documentation for Equipment for the Sterile Drug product facility. Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related documentation...Hourly payContract workFor contractors- ...system performance and critical equipment cycles (e.g. CIP SIP VHP aseptic filling autoclaves lyophilization depyrogenation heat sterilization). Investigate and address automation alarms and proactively trend system performance developing action plans as needed. Partner...Full time
- ...required checklists and documentation. ~ Assist radiologists and radiographers during diagnostic and interventional procedures maintain sterile technique position patients safely and operate monitoring equipment effectively. ~ Administer IV contrast sedation analgesia and...Permanent employmentFull timeOverseasWorking Monday to Friday
- ...following areas: Sterilisation – Autoclaves, SIP of vessels Cleaning – Parts Washer and CIP of vessels Isolator (Filling, Sterility & Material Transfer isolators) - HVAC, VHP, E-Beam and Depyrogenation systems Controlled Temperature Units (CTU) – Temperature/Humidity...Full timeContract workHybrid workWork at officeWorldwide
Orion Engineering Services Limited
Carlow Town, Co. Carlow11 days ago - ...and sterilise RIMDs in line with department procedures 7. Clean and Decontaminate Endoscopes and Probes. 8. Stocking shelves of sterile supplies non-sterile disposable items and assisting with stock control and requisitioning. 9. Maintenance of records where appropriate...Permanent employmentFull timeFlexible hoursShift workNight shiftWeekend work
- ...Eligible to act as a QP under directive 2001/83/EC (preferably under the permanent provisions) Experienced in aseptically produced sterile products and ideally lyophilized dosage form Ideally, experience of QP certification for release of clinical trial materials...Permanent employmentContract workPart timeLocal areaOverseas2 days week
- ...systems Ability to design/build validation plans from project concept to system end of life Knowledge of process validation CPV sterilization and packaging systems Demonstrated interpersonal and communication skills for cross-functional teamwork Preferred...Full time
€ 65 - 85 per hour
...Extensive knowledge and demonstrated experience managing Validation activities for Pharmaceutical / Biotechnology projects Experience of sterile / biotech equipment within the pharmaceutical industry is preferred. Demonstrated strong Communication and Leadership skills....Hourly payContract workHybrid workWork at office- ...validations and re-qualifications as required. Review of validation files for compliance. Strong interactions, maintenance and support of sterility suppliers. Interpreting sampling and monitoring data, applies statistical and analysis techniques, to determine control and...Full timeTemporary workFixed term contractLocal area
- ...third level qualification in a science or quality discipline Minimum 2 years Experience in a similar role in a Pharmaceutical or Sterile Manufacturing environment Excellent written and verbal communication skills with a strong attention to detail. Additional Information...Full time
- ...Validation Engineer II based in Carlow, you will be at the forefront of ensuring the integrity and compliance of critical equipment and sterilization processes. This is a fantastic opportunity to apply your technical expertise in a dynamic, collaborative environment, supporting...Hybrid work
