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Site Quality Head

Your RoleAn exciting opportunity to lead the Quality Unit at the biotechnology site of Tres Cantos - Madrid (Quality Assurance, Quality Control and local Regulatory Compliance) to ensure that materials and products manufactured, controlled, stored and shipped by production meet the appropriate Quality Standards and are in compliance with current Good Manufacturing Practices (cGMPs), Healthcare Quality Systems and Regulatory files.

You will ensure the implementation and the monitoring of the site Quality System and to maintain up to date the registration and operational documents including Procedures, Specifications and Site Master File. You will guarantee the release of the drug substances, following GMP normative, the quality standards and corporate policies and procedures. You will provide a Quality Unit service to meet requirements and the company's business plans and strategies. You will be the site contact with Health Authorities for quality related activities.

 

 

Who you are: 

  • You have a Master Degree in Science or equivalent
  • You have a minimum of 10 years of experience in the Pharmaceutical industry in quality or manufacturing roles
  • You have demonstrated experience in Leadership roles
  • You are fluent in English (mandatory) and highly recommended Spanish

 

 

Job Requisition ID:  202704
Location:  Tres Cantos
Career Level:  E - Professional (10+ years)
Working time model:  full-time

US Disclosure
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our HR Services team at 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday.


Job Segment: Biotech, Pharmaceutical, QA, Quality Assurance, Quality, Science, Technology

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