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.

• Ensures manufacturing, cleaning, and sterilization validations.

• Develops validation protocols (IQ, OQ, PQ) and final reports.

• Evaluates deviations and proposes 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 the English and Arab language – C1.

• Availability to travel frequently.

• Minimum 1 year of experience in validation areas, production procedures within the pharmaceutical sector.

• You have user-level skills in MS Office

• Knowledge of GMP environment is essential.

• You are 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.

Information about Grifols is available at www.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!

Grifols is an equal opportunity employer.

Third Party Agency and Recruiter Notice:

Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law. We will consider for employment all qualified Applicants in a manner consistent with the requirements of applicable state and local laws.

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

Benefits package.

Professional Group: 6

Contract of Employment: Permanent position

Parets del Vallès

Learn more about Grifols (https://www.grifols.com/en/what-we-do)

Req ID: 526047

Type: Indefinido tiempo completo

Job Category: