Skip to main content
Post your CV and find your next job on Indeed!

Medical Device Europe jobs

Sort by: -
    • Minimum 5 years’ experience in GMP production environment, preferably in medical device or pharma industry.
    • Develop and lead the site safety management with a…
    • Through our support of international pharmaceutical and medical device companies, we very much see Q1 Scientific as being part of a customer’s own operational…
    • Assembles medical products on an assembly operation, performing a variety of tasks on a rotating basis Maximise output by operating efficiently and minimising…
    • Good working knowledge of ISO 13485, FDA requirements and medical device Quality Systems.
    • Take ownership of quality activities across manufacturing, ensuring…
    • Perform inspections, checks, tests, and sampling procedures of incoming materials, parts and components used in the manufacture of medical devices, partially…
    • This role is based in the company’s European facility in Athenry on our Day Shift. .
    • Day shift hours are Monday - Thursday 7am - 3:30pm and 7am - 1pm on…
    • Assembles medical products on an assembly operation, performing a variety of tasks on a rotating basis Maximise output by operating efficiently and minimising…
  • View similar jobs with this employer
    • You operate within a multidisciplinary team that integrates technology and business expertise to devel-op and deliver professional solutions.
    • Experience in pharmaceutical, medical device, food or other regulated manufacturing environments.
    • Machinelab is seeking an experienced, practical Automation…
    • Install, maintain, and repair wiring, containment, distribution boards, protective devices, lighting, and controls in domestic and commercial settings.
  • View similar jobs with this employer
    • Our Fermoy, Ireland, facility is FDA registered and certified to ISO ISO13485:2016 for the manufacture of high-quality PCBAs, subassemblies and complete devices…
    • Programming of PLC’s, HMI’s, Robots, Servos, Instrumentation devices.
    • The Automation Controls Engineer is a highly technical role that is crucial to the success…
  • View similar jobs with this employer
    • Please note any offer of employment for this position is conditional upon the successful completion of a pre-employment medical examination, including drug and…
    • Previous manufacturing engineering experience, ideally within a medical device or regulated environment.
    • 5+ years’ experience within medical manufacturing or a…
    • Certified Time served Electrician skilled in Industrial - Medical device installations and live working environments.
    • Full Irish Driving Licence (required).

People also searched:

europe remote
europe visa sponsorship
medical administration
medical device
medical receptionist
medical secretary
medical secretary, administration
senior house officer
sho
sweden

Job Post Details

Safety Manager, Medical Device Manufacturing Facility, Waterford - job post

APS Materials Inc.
2.0 out of 5 stars
Waterford, County Waterford
€60,000–€70,000 a year - Full-time

Job details

Pay

  • €60,000–€70,000 a year

Job type

  • Full-time

Location

Waterford, County Waterford

Benefits

Pulled from the full job description

  • Sick pay
  • Employee assistance program
  • Company pension
  • Private medical insurance
  • Bike to work scheme
  • Company events

Full job description

Responsibilities:

  • Develop and lead the site safety management with a view to attaining ISO45001.
  • Conduct Risk Assessments, JSAs (Job Safety Analysis) and safety reviews.
  • Develop and maintain Housekeeping and 6S program requirements.
  • Lead incident investigations and implement corrective actions.
  • Develop and deliver OHS training programs to employees.
  • Drive safety culture through employee engagement and communication (site induction, toolbox talks, etc.) to ensure personnel are understanding of their duties and responsibilities.
  • Manage and maintain emergency response and security programs including fire safety, site security and business continuity planning.
  • Liaise with contractors for safe working practices, RAMs, method statements, insurance certs.
  • Liaise with consultants for specialist requirements: ATEX, chemicals, occupational noise, industrial hygiene etc.
  • Ensure that inspection records are maintained and preserved for all activities and plant equipment.
  • Ensure compliance with EHS laws, standards, corporate policies and insurance requirements.
  • Provide OHS guidance for change management processes, including review and approval of equipment and machinery modifications and process changes.
  • Participate in pre-start up safety reviews, internal and external auditing, site safety inspections and walkdowns.
  • Achieve a series of effective EHS KPI’s for the site.
  • Support Company quality programs and initiatives.

Education / Qualifications (Desirable but not Essential)

  • Minimum Level 8 in OHS discipline from an accredited institution.

Training / Experience (Desirable but not Essential)

  • Minimum 5 years’ experience in GMP production environment, preferably in medical device or pharma industry.

Skills / Attributes

  • Excellent interpersonal skills and the ability to effectively communicate and collaborate with all levels of the organization.
  • Self-starter with demonstrated efficient work methods, problem-solving skills and ability to handle multiple tasks in a fast-paced environment.

Benefits Include

  • Private medical cover
  • Defined contribution pension scheme up to 6% of salary matched by employer
  • Life assurance cover on death in service
  • Study support scheme
  • Annual sick pay bonus up to 5 days
  • Employee Assistance Programme

Job Type: Full-time

Pay: €60,000.00-€70,000.00 per year

Benefits:

  • Bike to work scheme
  • Company events
  • Company pension
  • Employee assistance program
  • Private medical insurance

Work Location: In person

Let Employers Find YouUpload Your Resume