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 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 QM Equipments & Facilities Specialist like you.
Role Mission
Its main mission will be to ensure that all critical production, quality control, and systems equipment are qualified, complying with requirements, regulatory standards (GMP, FDA, EMA), and internal policies.
What your responsibilities will be
You will monitor and document incidents that arise related to systems, facilities, and equipment. You will oversee the follow-up of corrective or preventive actions arising from the incidents that arise. You will analyze results trends. You will prepare system, equipment, or facility review reports based on the collected and analyzed data. You will coordinate monitoring teams to communicate assessments and trends. You will review documentation describing the operations and sampling of equipment and facilities. You will review validation and qualification documentation associated with systems, equipment, and facilities. You will prepare and submit documentation requested for audits conducted by national and international organizations and other companies.
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 accommodation may be made to enable individuals with disabilities to perform the essential functions).
Bachelor’s degree in industrial engineering, Pharmacy, Biology, Chemistry, or a related field. Master's or postgraduate degree in the pharmaceutical sector (Valuable). Advanced level of English – C1. (Necessary). 3 years of experience in the pharmaceutical sector, sterile area (Highly Advantageous). Experience in GMP environments and basic statistics. You have knowledge of MS Office and SAP. You define yourself as a curious person with strong analytical and synthesis skills, oriented toward proposing data-driven solutions and, ultimately, continuous improvement. You possess strong communication skills and enjoy working in a collaborative and dynamic environment.
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.
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).
Benefits package
Contract of Employment: Indefinite Full Time
Flexibility for U Program: 2 days of remote work per week
Location: Parest del Vallès
www.grifols.com
Learn more about Grifols