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Medical Device jobs in Athlone, County Westmeath

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    • Pharmaceutical or medical device industry: 2 years (required).
    • Experience within pharmaceutical, biotechnology, medical device or regulated manufacturing…
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    • Previous experience within a regulated industry, preferably medical device manufacturing, is highly desirable.
    • Knowledge or experience of EU MDR requirements.
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    • You will operate high-precision CNC manufacturing equipment producing orthopaedic medical devices that improve patients' quality of life.
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    • Experience within medical device, orthopaedic, aerospace or other high-precision manufacturing environments.
    • This is a highly technical position that will play…
    • We are excited to announce an opening for 3 x Maintenance Technician (Shift) with our client, a Global - Medical Device organisation in Athlone.
    • Medical / Healthcare Background (A Major Advantage): Prior experience in pharmaceutical sales, medical device representation, healthcare administration,…
    • Practical experience working with commercial or industrial HVAC systems, preferably in a GMP, pharmaceutical, biotechnology, medical device, food, or other…
    • View all Thermo Fisher Scientific jobs - Athlone jobs - Facilities Technician jobs in Athlone, County Westmeath
    • Salary Search: Facilities Specialist/HVAC / Facilities Technician salaries in Athlone, County Westmeath
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    • Knowledge of materials associated with medical devices such as polymers (nylons, PVC, polyethylene, polypropylene, Pebax, PTFE, polycarbonate, films, Tyvek, etc…
    • Your new company are a multinational player in the medical device manufacturing field, they have a strong presence in Westmeath and the finance leadership team…
    • As a Calibration Technician you will support Facility/calibration team in ensuring all equipment is calibrated in line with schedule and specifications to meet…
    • Supporting production equipment in a medical device healthcare environment.
    • 8 + years experience in a similar technical role within the medical device or…
    • Supporting production equipment in a medical device healthcare environment.
    • 5years experience in a similar technical role within the medical device or similar…
    • 2-5 years of warehouse experience within a pharmaceutical, biopharmaceutical, medical device, or life sciences manufacturing environment.
    • Engineering experience within the pharmaceutical, biotechnology, medical device, or related regulated manufacturing industries.
    • We install modular systems in the pharmaceutical and medical device sector.
    • Safe Pass and Manual Handling required.
    • Pay: €17.00-€20.00 per hour.

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Engineering Calibration Planner & Scheduler
Full-time

Job details

Pay information not provided
Full-time
Ireland

Full job description

Innopharma Technical Services, part of Innopharma Group, specialise in the training and provision of highly skilled, project ready, Contract Engineers & Scientists to the (Bio) Pharmaceutical and MedTech Manufacturing Sector.

We are now seeking a Calibration Planner & Scheduler Specialist to support within our client’s Site Engineering Department in Leinster Region.

About the Position:

We are seeking a highly organized and technically capable Specialist, Engineering (Calibration Planner & Scheduler) to support and coordinate the site-wide Calibration and Gas Detection Programs. The role is responsible for the planning, scheduling, coordination, and performance management of calibration activities across all manufacturing, utility, laboratory, warehouse, and support areas.

The successful candidate will act as the primary focal point for calibration planning activities, ensuring compliance with GMP requirements, maximizing equipment availability, optimizing contractor performance, and maintaining regulatory inspection readiness.

Responsibilities

  • Own the end-to-end planning and scheduling process for site calibration and gas detection activities.
  • Develop and maintain weekly, monthly, quarterly, and annual calibration schedules.
  • Coordinate calibration activities across manufacturing, laboratories, utilities, warehouse, and support functions.
  • Create, plan, release, and manage calibration work orders within SAP and associated maintenance systems.
  • Manage calibration backlog and drive timely closure of work orders.
  • Coordinate site-wide calibration programs for instrumentation and gas detection systems.
  • Lead the calibration daily meetings and maintain calibration KPI dashboards.
  • Manage scheduling and coordination of external calibration vendors.
  • Support audit readiness through maintenance of accurate records and planning documentation.
  • Lifecycle management of Instruments.
  • Drive improvements in planning, scheduling, and work management processes.
  • Drive a culture of compliance, reliability, and operational excellence.
  • Maintain inspection readiness and support regulatory inspections.
  • Adhere to Data Integrity and ALCOA+ principles.
  • Demonstrate ownership and accountability for calibration planning performance.

Preferred Experience:

  • Minimun Level 7/ 8 Degree qualification in Engineering, Instrumentation, Maintenance Management or related discipline.
  • Minimum 3 years experience in planning, scheduling, maintenance, calibration, or engineering support within a GMP environment.
  • Experience within pharmaceutical, biotechnology, medical device or regulated manufacturing industries.
  • Knowledge of Instrumentation and Calibration Practices.
  • Experience using SAP or equivalent CMMS/EAM system.
  • Experience with ProCal or equivalent calibration management system.
  • Knowledge of GMP, Data Integrity and regulatory inspection requirements.

Application question(s):

  • Are you authorised to work in Ireland without Visa sponsorship

Education:

  • Bachelor's (required)

Experience:

  • Calibration : 3 years (required)
  • Scheduler / planner: 3 years (required)
  • instrumentation: 3 years (preferred)
  • ProCal or equivalent calibration management system.: 2 years (preferred)
  • using SAP or equivalent CMMS/EAM system: 2 years (preferred)
  • Pharmaceutical or medical device industry: 2 years (required)
  • Gas Detection Programs: 1 year (preferred)

Work Location: In person

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