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Medical Devices Company jobs in Boyle, County Roscommon

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    • A Bachelor’s Degree in Polymer, Science, Biomedical, or Mechanical Engineering - or strong experience in a Process or Assembly Technician role within a medical…
    • Experience and knowledge of medical device environment including Clean room manufacture, validations, process controls, etc.
    • At least 10 years' experience in Quality within the medical device industry, including a minimum of 3 years leading and developing teams.
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Job Post Details

Process Assurance Operator - job post

VistaMed Ltd.
3.5 out of 5 stars
Carrick-On-Shannon, County Leitrim
You must create an Indeed account before continuing to the company website to apply

Location

Carrick-On-Shannon, County Leitrim

Full job description

Working at Freudenberg: "We will wow your world!" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 52,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments. Freudenberg Medical is a trusted Contract Manufacturing Organization (CDMO) partner, delivering high-quality solutions from ideation and market launch to volume production for medical device and pharmaceutical companies. With proven expertise in materials and technologies, Freudenberg Medical offers an extensive range of vertically integrated capabilities: precision molding and extrusions, complex catheters, hypotubes, and coatings.


Join our team as a:


Process Assurance Operator


Responsibilities

  • Learn how to manufacture high-quality medical devices that make a real difference to patients' lives.
  • Work in a modern Cleanroom environment, following clear procedures and high-quality standards.
  • Carry out basic product checks and in-process inspections - full training will be provided.
  • Learn how to make process adjustments when required to maintain quality and efficiency.
  • Support smooth product changeovers and help reduce waste.
  • Identify, report, and help prevent any product or process issues and take part in investigations and problem-solving activities when required.
  • Participate in corrective action and continuous improvement activities.
  • Complete all internal training to help you learn, develop, and grow in the role.
  • Follow all Health & Safety, GMP, and environmental procedures to keep yourself and others safe.


Qualifications

  • No previous experience required - this is a great opportunity to start your career in medical device manufacturing
  • A good standard of education and willingness to learn and work in a regulated manufacturing environment
  • Strong attention to detail and a quality-focused mindset
  • Reliable, punctual, and able to follow procedures
  • Comfortable working as part of a team with good communication and interpersonal skills


Some of your Benefits

Cafeteria/ Canteen


Health Management

We support you to stay and become healthy and fit.


Corporate Events

We celebrate success as a team, because only together can we achieve our goals.


Education Reimbursement

Receive financial aid to help propel your career to the next level.


Welcome to career changers

We look forward to your application, even if you do not have specific prior experience. All you need is the willingness to grow and develop


The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

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