Quality Validation Engineer at Collins McNicholas Recruitment
Kilkenny, County Kilkenny, Ireland -
Full Time


Start Date

Immediate

Expiry Date

30 Jun, 25

Salary

60.0

Posted On

30 Mar, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Information Technology/IT

Description

This is an exciting opportunity for an experienced Quality Validation Engineer to join our client, a leading Life Science company based in their new manufacturing facility in Kilkenny.

Role Responsibilities:

  • The development and maintenance of Quality System procedures.
  • Investigate/troubleshoot validation problems for components, equipment, and/or performance processes.
  • Monitoring and maintaining the quality and compliance status of associated quality records.
  • Writes, reviews, approves, and/or executes documentation for new and current validation procedures and technical reports related to components, equipment, products, and/or processes.
  • May assist with establishing corporate validation policies.
  • Maintaining the quality and compliance status of associated Procedures, work instructions, and training materials.
  • Presenting and communicating status, reporting metrics, identifying trends potential issues, and improvement initiatives, as applicable.
  • Basic understanding of design controls and design transfer.
  • May be responsible for creating or participating in risk analyses and FMEAs.

Education And Experience

  • Minimum 2 years experience in a similar industry
  • Minimum Level 7 NFQ qualification or equivalent in a relevant discipline
Responsibilities

FOR A CONFIDENTIAL DISCUSSION AND MORE INFORMATION ON THE ROLE, PLEASE CONTACT KEVIN GRIFFIN

Kevin Griffin
kevin.griffin@collinsmcnicholas.ie
(021) 2427108

Role Responsibilities:

  • The development and maintenance of Quality System procedures.
  • Investigate/troubleshoot validation problems for components, equipment, and/or performance processes.
  • Monitoring and maintaining the quality and compliance status of associated quality records.
  • Writes, reviews, approves, and/or executes documentation for new and current validation procedures and technical reports related to components, equipment, products, and/or processes.
  • May assist with establishing corporate validation policies.
  • Maintaining the quality and compliance status of associated Procedures, work instructions, and training materials.
  • Presenting and communicating status, reporting metrics, identifying trends potential issues, and improvement initiatives, as applicable.
  • Basic understanding of design controls and design transfer.
  • May be responsible for creating or participating in risk analyses and FMEAs
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