Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunity fostering an inclusive environment where diversity makes us be outstanding.
We are looking for a Quality Systems Specialist to join Quality department at Biomat SA, company dedicated to analyzing and controlling the plasma used by Instituto Grifols SA as raw material for the production of plasma derivatives.
What your responsibilities will be
* Coordinate the change control process for processes, facilities and equipment, both within Biomat S.A. and for change notifications received from suppliers. Evaluate the potential regulatory and operational impact in connection with the approved Plasma Master Files.
* Coordinate the management of deviations, complaints, and CAPA, acting as the process manager who oversees workflows and coordinates the editing and execution of tasks in the system.
* Review process documentation, validations and qualifications.
* Participate in the company’s global quality projects.
Who you are
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
* Bachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry), being valuable to have a Master or Postgraduate degree in the pharmaceutical sector.
* You have 3 years of experience in similar position within pharma quality.
* Knowledge in GMP.
* You have advanced level of English.
What we offer
It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.
Information about Grifols is available atwww.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!
We look forward to receiving your application!
We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.
Grifols is an equal opportunity employer.
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).
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