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    • Minimum 5 years’ experience in GMP production environment, preferably in medical device or pharma industry.
    • Develop and lead the site safety management with a…
    • Train and support operators on production equipment.
    • Please note that any offer of employment is conditional upon the successful completion of a *pre-employment…
    • Train and support operators on production equipment.
    • Please note that any offer of employment is conditional upon the successful completion of a *pre-employment…
    • Working to deadlines and production targets.
    • Operating machinery in line with production plans and quality standards.
    • Attractive salary based on experience.
    • Maintain production logs and required documentation following Standard Operating Procedures.
    • Strong analytical skills and a problem-solving mindset to address…
    • Good working knowledge of ISO 13485, FDA requirements and medical device Quality Systems.
    • Play an active role in new product introduction (NPI), partnering with…
    • 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…
    • Achieving all production and quality targets.
    • The Product Builder will work in a manufacturing team producing smoke and gas detection systems.
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    • Or relevant technical work experience in assembly, manufacturing, maintenance, or production.
    • You will receive training and support from experienced colleagues.
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    • Or relevant technical work experience in assembly, manufacturing, maintenance, or production.
    • You will receive training and support from experienced colleagues.
    • Demonstrate flexibility in supporting changing business and production needs.
    • 5+ years’ experience within medical manufacturing or a similarly regulated…
    • Train and support operators on production equipment.
    • Please note that any offer of employment is conditional upon the successful completion of a *pre-employment…
  • View similar jobs with this employer
    • Or relevant technical work experience in assembly, manufacturing, maintenance, or production.
    • You will receive training and support from experienced colleagues.
  • View similar jobs with this employer
    • Or relevant technical work experience in assembly, manufacturing, maintenance, or production.
    • You will receive training and support from experienced colleagues.
    • Train and support operators on production equipment.
    • Please note that any offer of employment is conditional upon the successful completion of a *pre-employment…

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

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