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Job Details

QA Validation Consultant – Tech Transfer - Global Pharma – Ireland, Dublin – 6 Month Contract – Excellent Rates

Company: Meet
Reference: MD-LEP-QAV-IRE-4
Closing Date: 04 Jul 18
Type: Contract
Salary (£): Competitive

Job Summary:

This leading pharmaceutical company are looking for a specialist contractor in Validation and Tech Transfer to perform QA Oversight of validation protocols for equipment, utilities and process validation. Get in touch with Matt Dixon on +442030196006 or email for more details.


This multinational Pharmaceutical company is looking for a QA Validation contractor that is experienced in GMP QA review of Validation life-cycle documentation to come in and hit the ground running on a 6 month contract. This full-time role, is part of an NPI Tech Transfer project based at their manufacturing site in Dublin, Ireland.

This is a fantastic opportunity to get on board with a company that has a global presence in the industry and has a reputation as being a great company to work for.


My client is transferring the manufacturing operations of one of their patented products from one of their 3rd party CMO sites in Europe to their facility in Dublin.

Role Responsibilities

Working as a QA Validation Consultant your main responsibilities will be:

  • QA Oversight of Validation activities for NPI/ transfer project from 3rd party site to Dublin
  • GMP QA Review of full validation life-cycle documentation including Risk Assessments, IOQ, PQ, equipment and cleaning validation.
  • Gap analysis of current procedures and updating SOPs as necessary to be GMP compliant and compliant to LEO Pharma internal Quality System.
  • Communication with stakeholders of Project activities and Quality Impacts

Suitable For

This role is ideal for a contractor that has experience working in a high potency manufacturing environment and is also experienced with solid-dosage tablet production. If you have experience of writing and reviewing validation protocols for manufacturing equipment and conducting QA review of said protocols and manufacturing documentation you will be ideal for this opportunity!

Get in touch with Matt Dixon at or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.

Skills Required

  • Bachelor's degree in science, pharmacy, biological science or related field is preferred.
  • Hands-on international Quality Assurance experience in a solid-dose tablet manufacturing environment is essential
  • Experience working with high potency products from QA/Validation perspective is essential.
  • Strong understanding of cGMP requirements and the ability to implement and actions needed to implement this within the QMS.
  • Experience of writing and executing validation protocols for solid-dose manufacturing equipment (DQ, IQ, OQ, PQ).
  • Excellent verbal and written communication skills, ability to work well in teams or independently and the ability to prioritise work and manage multiple projects while maintaining quality and compliance.


Commutable Locations: Republic of Ireland, Dublin.

Rate: Competitive

Full job description and company details are available upon application, apply below. The position is being dealt with by Matt Dixon at Meet, call us on 0203 019 6006 or email directly at to discuss in confidence.

Meet are good people wo are great at recruitment. We’re proud to partner with the industry’s leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available. We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way.

Find out more about us at

Apply for this job: QA Validation Consultant – Tech Transfer -  Global Pharma – Ireland, Dublin – 6  Month Contract – Excellent Rates

Contact Information:

Address:  meet
Irongate House, 30 Dukes Place, London
Tel:  +44 203 178 7488
Website:  Visit Our Web Site

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