Outsourcing Technical Coordinator

Ref. no.: J020022

Tags: Role Dublin Quality Assurance Career Keywords: Quality QC QA Quality Control Vacancy Energy Opportunity Ireland Validation Science Engineering Job Compliance Green

Location(s): Dublin North Dublin South Dublin West

Salary range (€): Negotiable

Additional benefits: Bonus,Canteen,Bupa

Minimum experience required: 0 - 1 Years

Employment type: Permanent Full-time

Minimum qualification: See Description

Contact person: Aileen Cahill

Contact e-mail: aileen.cahill@cpl.ie

Job description: Our client a leading pharmaceutical company based in Dublin is looking to recruit for an Outsourcing Technical Project Specialist

Job Responsibilities

• Reporting to the Technical Affairs Manager, the successful candidate will be responsible for the management of all technical projects being carried out at third party sites which impact the company's product.
• Specifically this person will co-ordinate the resolution of any technical issues which arise in the CMO's which may hinder production outputs and schedule commits, or the execution of projects aimed at cost efficiency, improved regulatory compliance or product improvement.
• In addition they will set up formal reporting structures with all CMO'C's on relevant KPI's and ensure this information is available and up to date as required.

Qualifications:

• Candidates must have a primary degree in science ideally Microbiology or Biotechnology.
• The person must have a minimum of 5 to 7 years experience in a sterile manufacturing pharmaceutical environment. Some of this experience should have been gained in the Production environment but someone having production experience combined with Validation or Technical experience would have a distinct advantage. Experience in a medical device or product produced in clean room environment is not adequate to meet this criteria. Knowledge of validation systems as they pertain to both sterile processing and equipment a distinct advantage
• They must have experience of working in an FDA environment and have had front line experience with dealing with FDA either through audits or submissions. So the fact that someone works in a Plant which is FDA approved is not sufficient.
• Candidates would need to be able to work abroad for several months at a time if necessary and travel at short notice.

All applications will be treated with the strictest of confidence

CPL Contact:

To apply or for further information please contact Aileen Cahill or e-mail with your updated CV to aileen.cahill@cpl.ie

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