Skip to main content

QA Compliance Specialist

  1. Ireland, East
Sligo
  1. Contract
Competitive
  1. CAPEX Projects
36378
QA Compliance Specialist - Dublin, Ireland - 12 Months Contract 

Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a QA Compliance Specialist 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:
  • Leading / Assisting in investigations arising out of product or manufacturing processes non-compliance.
  • Review/Audit of completed Batch Records.
  • Review of Manufacturing Logs as required.
  • Completion of quality review of operations documentation (SOPs, JSTMs, Risk Assessments)
  • Completion of Incoming Raw Material checks, including product status maintenance (as required).
  • Provide Stability Program Support, e.g. sample pulls, weekly checks, protocol generation (as required).
  • Administration of Quality Logs, e.g. QA Hold, Sample Request.
  • Lead operations floor daily walk around of manufacturing areas.
  • Drive continuous improvements and simplify site processes and procedure, specifically relating to the Operations function to ensure compliance is maintained at all times.
  • Other support as deemed necessary
Desirable Experience:
  • Third level degree in a science, quality or engineering discipline.
  • Previous experience in a quality role
  • A minimum of three years’ experience in a quality/operations role in a highly regulated GMP environment. Experience in biologics manufacturing is highly desirable
  • Experience in aseptic processing gained within either a quality or operations role is highly desirable.
  • A strong knowledge of regulatory requirements is required.
  • Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times.
  • Requires proven problem-solving skills and the ability to adapt to new requirements.
  • Requires innovative thinking, where new and untested solutions are proposed, demonstrated and implemented on a regular basis.
If this role is of interest, please apply now!
 #LI-JS4
Save as a job alert
List #1

Similar Jobs

QC Systems Specialist

Salary

Competitive

Location

Ireland

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Ireland

Dublin

Description

QC Systems Specialist - Ireland - 6-12 Months Contract  Do you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines,

Reference

36932

Expiry Date

01/01/0001

Christopher Hutchinson Read more
CQV Project Coordinator

Salary

Competitive

Location

North Carolina

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

North America

East Coast

Description

CQV Project Coordinator - United States, North Carolina - 6-12 Months Contract Our client, a global pharmaceutical manufacturing organization are looking for a talented CQV Project Coordinator to

Reference

36934

Expiry Date

01/01/0001

Mark Chaumeton Read more
Senior Planning Manager

Salary

Competitive

Location

Ohio

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

North America

United States

Description

Senior Planning Manager - Ohio, United States - 12 Months Contract This is a fantastic opportunity for a Senior Planning Manager to join our major, global pharmaceutical client on their latest

Reference

36828

Expiry Date

01/01/0001

Annabel Nangle Read more

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.