back to search results


  • Head Office - Parkmore
Apply now
  • Job reference number:15256643
  • Client ID:RI/FRS24701
  • Posted on:17-JUL-2017
  • Location:CORK, CORK
  • Job type:CONTRACT

Are you looking for an opportunity to work for a global leader in medical device innovation?

Do you want to a job where your work that makes a real difference to people's health and lives?

If so this is could be the role for you.

My client, one of Ireland's largest medical device manufacturers, has a fantastic opening for a Senior Supplier Quality Engineer to join their world-class team. The company has an amazing facility with cutting edge technology and a dynamic, supportive working environment. This is an exciting chance to join a multinational industry leader with excellent opportunities for progression and development. If you are an experienced Quality Engineer from a Life Science or Pharma background looking for the next step up into a new role, this is an excellent fit for you.

Key Responsibilities:
Provide overall quality assurance leadership in the management of select contract manufacturing sites engaged in the production of company products.

Provide complex product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes.

Utilize multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), and international organization for standardization (ISO).

Report on contract manufacturer performance metrics.

Provide Quality Engineering support to suppliers including audits/assessments, inspection technique support, verification/validation activities, CAPA and change management.

Ensure External Manufacturers continue to meet Quality requirements with regard to Supplier Change Request process of the company

Promote continuous improvement and Process Excellence activities within the Global Supply Chain

Resolve problems & eliminate constraints to ensure project and supply targets are met.

This position will require some travel

Key Requirements:
- Batchelor's degree in Engineering, Life Science or related discipline
- 4 years experience in Medical Device / Pharmaceutical industry
- Knowledge of FDA and ISO regulation alongside FDA CFR Part 820 and ISO 13485
- Experience in root cause analysis

Nice to have:
- Auditing background
- Six Sigma, Lean or ASQ Certification and training

Apply now if interested in this position.
Please click on the link
If you just have some questions about the job or want to have a chat call James on (086) 464 8426 or connect with me on <> or <>

This job originally appeared on