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Job Details

Validation Specialist - Dublin

Company: Just Pharma
Reference: JBIRQVS
Closing Date: 17 Dec 17
Type: Permanent
Salary (£): Competitive

Job Summary:

A leading global pharmaceutical company is seeking a validation professional to join their office in Dublin.


The Validation Specialist is responsible for the coordination of all validation activities on site ensuring compliance with current regulatory requirements. The Validation Specialist will have specific and varying duties as assigned by the Quality Director. Some key tasks and responsibilities are outlined below



•             Provide expertise in the area of validation at the company, ensuring compliance with current industry regulations, guidelines and trends.

•             Coordinate execution of all validation activities at the company including the following:

  1. Qualification of premises, equipment and utilities.
  2. Computer system qualification.
  3. Laboratory equipment validation.
  4. Process validation.
  5. Cleaning validation.

•             Prepare and maintain policies and SOPs associated with validation.

•             Prepare and maintain company validation master plans, protocols and reports

•             Review validation documents prepared by other personnel as required.

•             Execute validation protocols when required, including preparation of, and review of, deviations associated with validation activities.

•             Participate in cross-functional project teams as the validation representative.

•             Coordinate the periodic review and revalidation programme.

•             Ensure that all change controls are assessed for impact on validation.

•             Participate in Continuous Improvement programmes.



•             Participate fully in any cross functional training initiatives.

•             Actively foster, in cooperation with other staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.

•             Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.

•             Ensure timely completion of all SOP, reading, training and assessment.

•             Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.



•             Primary degree in scientific discipline.



•             A minimum of 5 years’ experience in a validation role in the pharmaceutical industry.

•             Computer systems validation experience is required

Apply for this job: Validation Specialist - Dublin

Contact Information:

Address:  Head Office
2nd Floor Albany Chambers, Bridge Road East, Welwyn Garden City, Hertfordshire
Tel:  0044 1707 830300
Website:  Visit Our Web Site

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