Browse by job sector

Quality Assurance Specialist

  1. Midlands (Ireland)
Carlow
  1. Contract
Competitive
  1. Compliance / Quality Assurance
33211

This vacancy has now expired

Quality Assurance Specialist -  Pharma - Carlow, Ireland - 11-Month Contract 

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

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:
  • Review and approval of all manufacturing batch documentation including electronic batch records, real time reports, master data using the site systems.
  • Review and approval of SOP's, cleaning verification/validation data and other documents as necessary for the IPT department.
  • Drive effective writing/revising/ rolling out of accurate operational procedures, training materials and maintenance procedures for various Quality related systems; ensure all work is subsequently carried out in line with same.
  • Support the development and implementation of improved quality reporting measures.
  • Liaise with the Quality Specialists/QP/QA Lead to resolve queries relating to batch manufacturing process.
  • Provide effective real time on the floor support for day-to-day manufacturing operations for example area clearances, batch record reviews, aseptic operations.
  • Provide quality input into decision making process on the shopfloor ensuring that product quality is maintained.
  • Provide training in all aspects of Quality Management Systems and GMP.
  • Ensure all work is carried out in line with SOP’s, training, or other quality systems such as change controls where applicable.
  • Facilitate compliance direction for the site by assisting in the adherence to divisional policies and guidelines as well as regulatory requirements.


Experience, Knowledge & Skills:
  • Relevant experience in a quality role, ideally in a pharmaceutical manufacturing environment.
  • Knowledge of US and European cGMP guidelines, and other international regulatory requirements, as applicable to the site.
  • GMP Audit experience in the pharmaceutical industry
  • Third Level Degree qualified in a Science/Technical or related discipline.


If this role is of interest to you, please apply now! 

 #LI-CH3
Save as a job alert
List #1

Similar Jobs

Senior Construction Manager

Salary

Competitive

Location

Frankfurt ( Oder)

Salary

Competitive

Sector

Compliance / Quality Assurance

Job type

Contract

Location

Germany

Frankfurt

Description

Senior Construction Manager - Germany, Frankfurt - 18 Month Contract We are recruiting on behalf of a leading global pharmaceutical client based in the surroundings of Frankfurt. Due to a large

Reference

37306

Expiry Date

01/01/0001

Amy Baxter

Author

Amy Baxter
Amy Baxter

Author

Amy Baxter
Read more
Read more
Quality Auditor

Salary

Competitive

Location

City Of London

Salary

Competitive

Sector

Compliance / Quality Assurance

Job type

Contract

Location

England

London

Description

Quality Auditor - UK, London - 6 Month Contract Do you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our

Reference

37310

Expiry Date

01/01/0001

Christopher Hutchinson

Author

Christopher Hutchinson
Christopher Hutchinson

Author

Christopher Hutchinson
Read more
Read more
Safety Advisor

Salary

Competitive

Location

Dublin

Salary

Competitive

Sector

Compliance / Quality Assurance

Job type

Contract

Location

Ireland

Dublin

Description

Safety Advisor - Ireland, Dublin - 12 Month Contract One of the top 10 best companies to work in Ireland is looking for EOHSS Safety Advisor for their large-scale new facility in Dublin. Is this

Reference

37311

Expiry Date

01/01/0001

James Smithson

Author

James Smithson
James Smithson

Author

James Smithson
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