VALIDATION SPECIALIST AT GEPD

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.

Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20,000 people. That’s why we need a Validation Specialist - GEPD like you.

Role Mission

Ensure that validations are executed in GEPD with Grifols standards and within the established timeframes.

What your responsibilities will be

• Support the new GEDP validation team in managing work teams.
• Prepare documentation (VMP, SOP, validation reports).
• Provide support for the execution of validations to ensure they are carried out properly and on schedule.
• Ensure manufacturing, cleaning, and sterilization validations.
• Develop validation protocols (IQ, OQ, PQ) and final reports.
• Evaluate deviations and propose corrective and preventive actions (CAPAs).
• Ensure the qualification of production equipment, laboratories, and critical services.
• Review and approve suppliers' technical documentation.
• Ensure compliance with international regulations (FDA, EMA, ISO, ICH, PIC/S).
• Keep documentation and procedures up-to-date with GEPD regulatory changes.

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 Biochemistry, Biotechnology, Biomedical Engineering, Health Sciences or related fields.
• Master's degree in the field of science (Biotechnology, Biology, Biochemistry, Chemistry...) (Desirable).
• Excellent verbal and written communication skills in English and Arabic – C1.
• Availability to travel frequently.
• Minimum 1 year of experience in validation areas, production procedures within the pharmaceutical sector.
• User-level skills in MS Office.
• Knowledge of GMP environment is essential.
• Proactive, methodical and eager to learn.

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.

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!

Grifols is an equal opportunity employer.

Schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h

Benefits package.

Professional Group: 6

Contract of Employment: Permanent position

Location: Parets del Vallès