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

Risk Management Medical Device jobs

Sort by: -
  • View similar jobs with this employer
    • Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed.
    • Bachelor's Degree in Engineering.
  • View similar jobs with this employer
    • Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed.
    • Bachelor's Degree in Engineering.
    • Experience in medical device or similar regulated industries preferable.
    • Minimum +3 years project management experience or related discipline.
    • Participate in risk management and change control activities.
    • Previous experience within a regulated industry, ideally medical devices, pharmaceuticals, or…
    • Analyze user behavior and contextual risk signals sourced from various systems to identify potential insider threats, in line with approaches where insider risk…
    • Prior experience in a GMP or medical device manufacturing environment.
    • Good project management and communication skills.
    • Provide technical support for projects.
    • Experience within a regulated manufacturing environment, ideally medical devices, is advantageous.
    • Champion Lean methodologies by facilitating Kaizen events,…
    • Experience with risk management and quality system practices.
    • Impact: Your work directly contributes to ensuring quality, compliance, and customer trust in…
  • View similar jobs with this employer
    • Effectiveness of planning escalation management and recovery actions.
    • Working experience in a manufacturing environment (Medical devices desired).
    • Lead new business development efforts within medical device OEM markets.
    • Experience in medical device, healthcare OEM, or related technical industries.
    • Ensures rapid communication of quality issues and risks to appropriate management and leaders.
    • Support with the raising of change controls and risk assessments.
    • How many years of project management experience do you have within the pharmaceutical, biopharmaceutical, or medical device manufacturing industry?
    • Collaborate with peers and management to meet production targets and escalate issues promptly when output schedules are at risk.
    • Strong understanding of engineering principles and medical device development processes.
    • Documentation: Maintain detailed documentation of design control, risk…
    • Minimum of 2 years' experience in a quality or compliance role within a pharmaceutical, medical device, or regulated life sciences environment.

People also searched:

medical receptionist
medical secretary
medical secretary, administration
risk analyst
risk management
risk manager
senior house officer
sho
management trainee
mba

Job Post Details

Process Engineer - medical device: South Dublin (DT18673) - job post

ICDS Recruitment Consultants
South Dublin, County Dublin
Permanent, Full-time

Job details

Job type

  • Permanent
  • Full-time

Location

South Dublin, County Dublin

Full job description

Process Engineer - medical device: South Dublin.

In this role you will support a high-volume, fully automated manufacturing environment, with responsibility for process development, troubleshooting, maintenance, and continuous improvement of production processes and equipment within the assigned area.

Responsibilities:

  • Develop, design, and evaluate equipment and/or processes. Requirement for novel and innovative approaches in relation to fixtures / jig design and scalability.
  • Develop knowledge to become the subject matter expert for assigned processes.
  • Drive process improvements through identification of problem areas/opportunities and collaborate with internal groups and external vendors using Lean / Six Sigma and project management techniques. Assist with Quality Non-conformances, Customer Complaints and CAPA investigations
  • Liaise with external equipment manufacturers / suppliers in terms of equipment / fixture design and manufacture.
  • Manage projects related to product & equipment development
  • Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed.
  • Liaise with R&D teams as required, providing design for manufacture input on component / assembly development projects.
  • Provide support to operations, optimising existing processes as needed to ensure that engineering work orders / production related goals are met.

Requirements for this role:

  • Bachelor's Degree in Engineering
  • At least 3 years' process engineering experience within a regulated manufacturing environment
  • Process optimisation with strong background in design of experiments essential.
  • Experience with Cognex or other Vision Systems, pick and place operations, and form fill seal would be desirable.
  • High speed automation experience, test equipment fixture design and documentation is advantageous.

Job Types: Full-time, Permanent

Work Location: In person

Let Employers Find YouUpload Your Resume