[ref. g70615000] Laboratory Test Technician (GMP Medical Devices)

placeDublin calendar_month 

Who we are

PM Group is an employee owned, international project delivery firm with a team of 3,700 + people. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations.

We are focused on growing a sustainable business centred around our people, our clients and trade partners.

We are looking for a Laboratory Test Technician to join our Medical Device Client's (GMP accredited manufacturer) to join the Research and Development (R&D) team. The successful candidate will have a strong technical knowledge base and experience in laboratory equipment, as well as experience with R&D testing and quality documentation.

  • Daily Responsibilities
  • Product testing to support program milestones.
  • Participate in the generation of laboratory equipment operation, maintenance, calibration, and cleaning SOPs to ensure adherence to approved laboratory procedures.
  • Using the laboratory with adherence to good laboratory practices (GLP) for product testing and good documentation practices (GDP) through planning, performing, monitoring, recording and reporting on product testing.
  • Providing support in testing of root cause investigations on malfunctioning product.
  • Ensuring that all work is carried out in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs).
  • Maintaining the laboratory and equipment to good safe working order and ensure readiness of the laboratory for internal/customer/regulatory inspections within the laboratory.
  • Working as part of a dynamic team to collaboratively reach project targets and milestones.
  • Maintaining appropriate recording and reporting systems on all engineering related matters (calibrations etc).
  • Manage stock, including allocation and removal of products and waste.
  • Requirements
  • The successful candidate will have a third level Engineer/Technical/Science qualification.
  • You must have a clear understanding of R&D testing and have experience in a laboratory environment.
  • The ideal candidate will have experience of working with mechanical testing equipment and tools.
  • Ability to work autonomously and meet project deadlines with diligence.
  • Good communications and time management skills.

As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2025 business strategy.

Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.

PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.

#LI-BW1

business_centerHigh salary

Medical Devices Manufacturing Operator

apartmentOsborneplaceDublin
Medical Devices Manufacturing Operator A leading medical device company in Dublin are looking for a Manufacturing Operator to join their growing team. This role will require someone with a commitment to quality, ability to work well in a team...
apartmentCPLplaceDublin
On behalf of our client, a growing global medical devices company, we are recruiting for a Sales Account Manager for B2B. This role will look after the European market. The role will be based hybrid role, with approx 2/3 days a week in South Dublin...
local_fire_departmentUrgent

QA Specialist - Dublin - ref. n41786415

apartmentMorgan McKinleyplaceDublin
We are seeking a Quality Assurance Specialist to join our clients team and help ensure the quality, safety, and regulatory compliance of their medical devices. In this role, you'll play a critical part in maintaining and improving their Quality...