Quality Engineer (NPI)

I8936

DPS are currenty recruiting on behalf of a Pharmaceutical / Medical Device Client for a Quality Engineer for a New Product Introduction in South Dublin.

Category:
Control Cost
Location:
Ireland
Years of Experience Req.:
3-5 Years+
Date Posted:
16/11/2021
Days Remaining:
27
Employment Type:
Contract
Education Level Req.:
See Description

Quality Engineer (NPI)

DPS is a leading Project Management and Engineering Company delivering Full Service Engineering with a ‘client first’ mentality and personal touch across a range of market sectors: Project and Programme Management, Procurement, Design, Construction Management, Health & Safety Management, Commissioning, Qualification and Start-up. We have one goal: to deliver more than our clients expect first time, every time. We’ve been serving industry around the world for 40 years plus, relied on for our agility, original thinking, sound judgement and high-calibre people. What sets us apart is the rapport we build with our clients and the care we take to gain a fundamental understanding of our client’s businesses. We employ over 1700+ people out of our thirteen office locations and we serve a broad range of clients ranging from multinational companies to small generic producers.

Quality Engineer (NPI)

DPS are currenty recruiting on behalf of a Pharmaceutical / Medical Device Client for a Quality Engineer for a New Product Introduction in South Dublin.

Responsibilities:

  • Be a key driver of cGMP practices within Operations and Quality divisions
  • Provide support for the relevant Quality Systems
  • Responsible for ensuring consistency to all internal and external regulatory requirements
  • Become an active member of the site internal audit team, collaborating closely with Regulatory auditors
  • Prepare and maintain documentation in compliance with the appropriate regulatory requirements
  • Support production personnel in continuous improvement activities (Six Sigma etc.)

Requirements:

  • A minimum of 5 years work experience in a relevant quality system environments, coupled with a background in Medical Devices/Pharmaceutical Industry.
  • Experience in the preparation of Technical Documentation.
  • Knowledge of Statistical Process Control and Six Sigma methodologies (Greenbelt Certification would be advantageous).
  • Experience in CAPA system management
  • A proven understanding of FDA& ISO requirements
  • Experience in process validation and working in a clean room environment.
  • Proven track record of working in a multi-functional team environment.

DPS is an Equal Opportunities Employer

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