Quality jobs

• Cork
• Up to €50 per hour
• Posted 8 days ago

Responsibilities Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Conducts feasibility studies to verify capability and functionality. Develops new concepts from initial design to market release. Write an...

• Cork
• Up to €50 per hour
• Posted 8 days ago

Responsibilities Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Conducts feasibility studies to verify capability and functionality. Develops new concepts from initial design to market release. Write an...

• California
• Negotiable
• Posted 12 days ago

Field Evaluation Engineer Location: Greater Los Angeles/Southern California (Mandatory) We are looking for a skilled Field Evaluation Engineer to join our team. This role offers an exciting opportunity to work in a dynamic and fast-paced environment, ensuring product safety and compliance through...

• United States of America
• Negotiable
• Posted 18 days ago

EPM is collaborating with a leading medical device company in the USA to find a skilled Engineer specializing in the evaluation and testing of medical electrical devices. This role is crucial in ensuring products meet regulatory standards and industry requirements. Role Overview The Engineer will...

• Ohio
• Negotiable
• Posted about 1 month ago

Location: Midwest, USA (with Travel Requirements) EPM is working with an exceptional medical device company in the Midwest that is seeking experienced Senior Quality Engineers to join their team. This company specializes in ophthalmology, cardiovascular, and dental medical devices and is dedicate...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Key Responsibilities: Perform technical assessments of active medical devices, ensuring compliance with MDR 2017/745 and international regulatory standards. Conduct conformity assessments, design dossier reviews, and clinical evaluations for medical devices. Lead and participate in regulatory aud...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Key Responsibilities: Conduct technical file reviews, risk assessments, and clinical evaluations of non-active medical devices. Perform conformity assessments and certification evaluations under MDR 2017/745 and related standards. Lead and participate in regulatory audits (ISO 13485, MDSAP, MDR) ...

• Norway
• Negotiable
• Posted about 2 months ago

Job Description: Medical Device Assessor & Lead Auditor - Non-Active Devices Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct technical file reviews, risk assessments, and clinical...

• Germany
• Negotiable
• Posted about 2 months ago

Job Description: Integrated Clinician - Medical Devices (Active & Non-Active) Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct clinical evaluations and assessments of active and no...