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Job Details

Validation Engineer

Company: Optimus Search Limited
Location: Dublin
Reference: BBBH9815
Closing Date: 07 Mar 18
Type: Contract
Salary (£): Negotiable

Job Summary:

Are you a Validation Engineer interested in working for one of the Irelands leading names in High-Tech Pharmaceutical Engineering?Are you looking for something new?!Then stop what you are doing and read on!


Are you a Validation Engineer interested in working for one of the Irelands leading names in High-Tech Pharmaceutical Engineering?
Are you looking for something new?!
Then stop what you are doing and read on!

Title: Validation Engineer

Rate: Negotiable

Location: Dublin, Ireland

Positions Available: 1 Engineer

Type: Contract (12 Months Rolling)

A Fantastic new role has just opened up at one of our leading Dublin based clients offering the successful candidate the opportunity to join a hard-working team working on exciting projects in the pharmaceutical sector.

The proposed start date is ASAP- We need YOU

Responsibilities include:

* Prepare, execute and report validation protocols and SOPs with responsibility across equipment / production / facilities & utilities / Analytical Methods /computer systems / cleaning studies in GMP environment.

* Follow Biotech/Pharmaceutical/Medical Device industry standards in generating and updating supporting documentation such as P&IDs, material and equipment specifications, and requirement specifications.

* Implement validation strategy based on current regulatory and pharmaceutical industry standard and quality expectations.

* Ensure validation is delivered on time to support product introductions/launches and any regulatory requirements are met either as a result of licence activity or site audit.

* Maintenance of validation system ensuring all processes, equipment and validation services remain current to GMP standards.

* Ensure validation gaps and risks are identified and addressed, to support ongoing release, licence submission/renewal, and ensure an audit ready situation.

* Planning and managing validation of CAPEX projects and strategic systems using risk based approaches (identification of CCPs, FMEA, ICH Q9).

* Working in a multicultural and multidisciplinary environment (production, QA, laboratories, suppliers, engineering and technical teams).

* Co-ordination of validation activities with key support functions.

* Maintenance of validation master plan to agreed timelines.

* Ensure validation is conducted on fully developed processes.

* Ensure that validation requirements allow launch/routine product delivery times.

* Validation reporting delivered to meet launch commitments.

* Capturing all operational requirements to ensure processes meet GMP and operational effectiveness requirements.


* Life Science / Engineering degree.

* 2 to 3 years pharmaceutical experience or associated manufacturing industry experience.

* In-depth knowledge and experience of manufacturing technology applied on manufacturing site.

* Knowledge in sterile, solid and liquid dosage forms.

* Experience in Validating processes, equipment, cleaning methodologies, utilities/facilities, computer and analytical methods.

* Broad knowledge of pharmaceutical manufacturing processes.

* Good inter-personal skills and presentation skills. Can influence at all levels.

If you are interested please do not hesitate to email or call me!

+44 20 30969 392

Apply for this job: Validation Engineer

Contact Information:

Address:  Head Office
171-177 Great Portland Street, London
Tel:  +44 (0) 20 3418 8033
Fax:  +44 (0) 20 7287 4908
Website:  Visit Our Web Site

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