Browse by job sector

Quality Auditor

  1. Midlands (Ireland)
Carlow
  1. Contract
Competitive
  1. Compliance / Quality Assurance
33537

This vacancy has now expired

Quality Auditor - Pharma - Carlow, Ireland - 6 Month Contract + Possible Extensions

With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a Quality Auditor to join their team to support multiple capital projects taking place onsite in Leinster.

This is a fantastic opportunity to work on a state-of-the art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US. 


Role Summary:
  • Responsible for helping to ensure that the validated equipment on site maintains validated status. 
  • Act as quality support for validation and qualification activities of equipment, facilities, and associated processes on site to ensure they are maintained in accordance with global and local procedures. 
  • Ensure that quality issues are identified, addressed, and resolved in a timely manner.
  • Responsible for supporting deviation close out and initiating/following up on corrective and preventative actions.
  • Partner with colleagues cross functionally to provide support and advice on day-to-day basis and on a project, basis including communications, training, project work, audit/inspection duties, investigations etc.

Requirement: 
  • Bachelor’s degree or higher preferred; ideally in a related Science discipline
  • Lean Six Sigma Methodology experience desired.
  • Demonstrated ability in pharmaceutical equipment validation/qualification or quality support for same
  • Knowledge of EU/US quality related pharmaceutical regulations
  • Experience of Sterile manufacture preferred.
  • Ideally a minimum of 3 years’ experience in the FDA and/or EU regulated pharmaceutical environment; preferably in a manufacturing site in quality and/or engineering roles.
  • Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices requirements.
  • Knowledgeable in Industry Best Practices for quality and compliance related topics
  • Proven ability to effectively initiate and drive change.
  • Strong verbal and written communication skills, project management skills
  • Report, standards, policy writing skills required.
  • Proficiency in Microsoft Office and job-related computer applications required (electronic validation systems)

If this role is of interest to you, please apply now! 
  #LI-CH3
Save as a job alert
List #1

Similar Jobs

CQV Lead

Salary

Competitive

Location

Toulouse

Salary

Competitive

Sector

Compliance / Quality Assurance

Job type

Contract

Location

France

Description

CQV Lead - France, Toulouse - 6 Month Contract Are you looking for your next contract, and fancy the opportunity to work in Toulouse? Our client, a global biotechnology organisation, are recruiting

Reference

37373

Expiry Date

01/01/0001

Caroline O’Sullivan

Author

Caroline O’Sullivan
Caroline O’Sullivan

Author

Caroline O’Sullivan
Read more
Read more
Lab Project Manager

Salary

Competitive

Location

Dublin

Salary

Competitive

Sector

Compliance / Quality Assurance

Job type

Contract

Location

Ireland

Dublin

Description

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

Reference

36631

Expiry Date

01/01/0001

Katarina Chalanska

Author

Katarina Chalanska
Katarina Chalanska

Author

Katarina Chalanska
Read more
Read more
Cold Room Package Owner

Salary

Competitive

Location

North Carolina

Salary

Competitive

Sector

Compliance / Quality Assurance

Job type

Contract

Location

North America

East Coast

Description

Cold Room Package Owner - US, North Carolina - 12 Month Contract  Our client, a globally recognized pioneer in Biotechnology, are recruiting for the position of a Cold Room Package Owner. A leader

Reference

37343

Expiry Date

01/01/0001

Read more
Read more

Insights

A Day in the Life of a Quality Assurance Specialist in the Pharmaceuticals World

A Day in the Life of a Quality Assurance Specialist in the Pharmaceuticals World

Read more

10/27/2023

Your next step as a Validation Engineer
Read more

07/20/2021

Sourcing legally and compliantly
Read more

04/15/2019

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