Browse by job sector

QAV Engineer

  1. Ireland, West
Sligo
  1. Contract
Competitive
  1. Life Sciences
38215
Apply to this job Save job
QAV Engineer - Ireland, Sligo - 12 Month Contract 

Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a QAV Engineer to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow.

Essential duties and responsibilities for this role include, but are not limited to, the following:
  • Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with policies, FDA, European cGMP and GAMP standards.
  • Generation/maintenance/execution of the Site Validation Master Plan.
  • Generation/maintenance/execution of Project Validation Plans and schedules.
  • Generation of validation protocols and final reports to cGMP standards.
  • Generation of validation investigations and implementation of corrective actions.
  • Creation/Review/Approval of various quality documents and test data.
  • Management of validation, exception event, and change control processes.
  • Maintenance and tracking of validation equipment, if applicable.
  • Completing all required training before executing a task.
  • Documenting all activities in line with cGMP requirements.
  • Updating of validation procedures, job instructions and batch documentation to reflect current best practices.
  • Performing cross training within the team and training of new team members.
  • Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.
  • Coordinating activities to maximise the effectiveness of all of the team members.
  • Maintaining the overall cGMP compliance of the production areas.
  • Communicating with peers and management regarding activities in the area, including elevation of events or concerns. 
Desirable Experience:
  • Qualification and/or degree in engineering or scientific discipline.
  • Requires extensive validation/Quality experience in medical device plastics processing, moulding or assembly operations.
  • Extensive knowledge of cGMP and regulatory requirements relating to the medical device industry.
  • Strong communication (written and oral), presentation and troubleshooting skills required
  • Effective interpersonal and organisational skills.
  • Ability to work well both independently and in a team environment.
  • Capable of prioritising work and multitasking.
If this role is of interest, please apply now!
#LI-JS4

Apply to this job Save job
Save as a job alert
List #1

Similar Jobs

Project Administrator

Salary

Competitive

Location

Central London

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

England

London

Description

Project Administrator - UK, London - 6 Months Initial Contract This is your opportunity to work for a global data centre operator that has been recognised for as one of fastest growing and

Reference

38175

Expiry Date

01/01/0001

Becky Daly

Author

Becky Daly
Becky Daly

Author

Becky Daly
Read more
Read more
Aviva PI Specialist

Salary

Competitive

Location

Remote work

Salary

Competitive

Sector

Life Sciences

Job type

Permanent

Location

Remote

Description

Aviva PI Specialist - Remote Working - Permanent Contract Do you want to be involved with exciting pharmaceutical projects?   Our client specialises in data-intelligence, data-driven technology

Reference

38212

Expiry Date

01/01/0001

Farhan Younas

Author

Farhan Younas
Farhan Younas

Author

Farhan Younas
Read more
Read more
Project Manager

Salary

Competitive

Location

Dublin

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Ireland

Dublin

Description

Project Manager - Ireland, Dublin - 12 Month Initial Contract  Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of a Project Manager. A leader in the

Reference

38195

Expiry Date

01/01/0001

Read more
Read more

Insights

QCS Staffing Validation Engineer Jobs: In-Demand Skills and Career Paths

Validation Engineer Jobs: In-Demand Skills and Career Paths
Read more

05/27/2025

QCS Staffing A Guide to Pharmacovigilance Careers

A Complete Guide to Pharmacovigilance Careers
Read more

05/15/2025

Living and working in Ireland
Read more

03/12/2025

VIEW ALL

Send us your CV

Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.

Send your CV
Upload your CV