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Quality Control Director - Vaccines - Madrid

This job is no longer available

Employer
SEC Recruitment
Posted
Thursday, June 21, 2012
Closes
Saturday, July 21, 2012
Ref
2106a
Contact
Beatriz De Luis
Location
Madrid
Jobseeker Type
Professional
Organization Type
Corporate
Contract Type
Employee
Hours
Salary
Negotiable

Further information


TITLE - TITLE: Quality Control Director/Vaccines - Madrid


For a confidential consultation call Beatriz de Luis on 0044 (0) 207 255 6665 or email your CV to beatriz.deluis@secpharma.com


Job Summary:

My client, global biopharmaceutical company dedicated to development and production of vaccines, is lloking for a Quality Control Director to join their manufacturing site in Madrid. In this position you will report to the Quality Affairs Director.


Accountabilities/Responsibilities

*Main purpose: The position is responsible for GMP compliance in Quality control micro and physico-chemical as well as In process controls. The position is responsible also of KPI proposal and development and Annual Quality report data compilation and management.
*Develop and implement the quality department's strategy, to ensure it meet the business requirements and customers deliverables.
*Maintain and improve department´s operational performance in order to meet regulatory authorities requirements with regard to company standars and external/intenal customers.
*Continuous improvement of department's procedures/documentation to assure they meet drugs updates and current regulations.
*Ensure proper investigation of errors, events and deviations that required documented review and action.
*Ensure good relations and communication with all team members and between departments.
*Monitoring and compliance of GMP´s.
*Collaborate with external and internal audits.


Essential Skills & Capabilities:

*Pharmaceutical degree or equivalent level
*Languages: English and Spanish good communications skills (oral and written)
*Expert scientific/technical knowledge in the area of relevance for the specific position (GxP)
*Experience: At least 5 years of relevant working experience in Production, Galenic and Analitycal Developmentor Quality Control and Quality Assurance.
*Previous solid experience managing teams and developing people are crucial.
*Expert user of Microsoft Office

In return, my client offers the opportunity to join a leader and growing company and a competitive salary package.

For further details or a confidential conversation please contact me directly:

Beatriz de Luis
Pharmaceutical, Healthcare & CRO Division
Spain and International Biotech
Tel: +44 (0) 207 255 6665
Beatriz.deluis@secpharma.com
http://uk.linkedin.com/in/beatrizdelulis

SEC Recruitment

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