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Job Details
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QA Validation Manager



Business Type: Pharmaceutical Company, Biotechnology Company, Other Business
Job Type: Biology, Biotechnology, Bioengineering, Validation
Job Level: Management
Position: Full Time
Salary: EUR80000 - EUR90000 per annum + Bonus + Relocation + Benefits
Location: Ireland (Eire)
Reference: EM/202581/13
Closing Date: 09/04/19
Job Details:

The most exciting project in Europe is ongoing and the company is looking for a permanent employee to join them in the role of a QA Validation Manager.
With the fastest growing Biotech site in Europe (soon to be the largest as well) and a business model that has the company as one of the best employers in Europe and most financially successful as well, you will find yourself in an experience that will write history in the industry.

Essential Duties and Responsibilities include, but are not limited to, the following:
* You will manage, develop and build a team of subject matter experts in various validation areas.
* Management of resources, planning and assigning work to Validations Specialists and/or contingent workers.
* Managing multiple and complex validation programs, coordinating with other departments or outside contractors/vendors to complete validation tasks.
* Lead technical and quality investigations.
* Collaborates with functional departments to resolve issues.
* Manage cross-functional projects with many stakeholders.
* Review and/or approve master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria.
* Coaching and mentoring of less experienced Specialists.
* If required, internal and external (regulatory) audits.
* Some travel may be required.

Experience and Required Skills: Education and Experience:
* BS/BA in Engineering, Chemistry, or Life Sciences with 6+ years of related experience within the field preferred; may substitute relevant experience for education.
* Previous team/people management experience essential.
* Previous cleaning validation and steam in place experience an advantage.
* Understanding of Biopharmaceutical Drug Substance manufacturing process an advantage.



Posted: 02/04/2019 | NPJ Ref: 233101
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