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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…
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    • Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed.
    • Bachelor's Degree in Engineering.
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    • Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed.
    • Bachelor's Degree in Engineering.
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    • Good understanding of Quality and Regulatory requirements related to the medical device industry.
    • Conduct internal audits and participate in regulatory agency…
    • Foster and promote a strong quality culture centered on proactive risk management, continuous improvement, product quality, and operational excellence.
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    • Significant experience within a GMP pharmaceutical, sterile manufacturing, biologics, or medical device microbiology laboratory.
    • Have working knowledge of MODA.
    • 8-10 years of / Sourcing / Procurement Supply chain experience, preferably in medical devices or other highly regulated environments.
    • Manufacturing, medical device or SME experience.
    • Work in a modern, high-precision medical device manufacturing environment.
    • Job Types: Permanent, Full-time.
    • Collaborate with peers and management to meet production targets and escalate issues promptly when output schedules are at risk.
    • 5+ years' experience in an EHS leadership role within construction, manufacturing, engineering, pharmaceutical, medical device or industrial environments.
    • Hands on involvement in local office management in conjunction with other members of the senior management team.
    • Electrical Technical Director - Dublin or Cork.
    • Previous medical device manufacturing experience is preferred.
    • Our Fermoy, Ireland, facility is FDA registered and certified to ISO ISO13485:2016 for the…
    • Proficiency with quality tools, risk management, and continuous improvement methodologies.
    • Medical device industry experience preferred.
    • Managing project risks, issues, assumptions and dependencies through RAID management.
    • Excellent stakeholder management and communication skills.
    • Excellent stakeholder management and communication skills.
    • Strong project management and organisational abilities.

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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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