Equipment & Process Validation Enginneer
Parets del Valles, ES
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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. |
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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 an Equipment & Process Validation Engineer like you.
Role Mission
Ensure that equipment and processes comply with quality standards, regulatory standards, and operational requirements through validation and qualification activities. Their work includes the design and execution of validation protocols, risk analysis, technical documentation, and the implementation of improvements to optimize process efficiency and safety. They contribute to compliance with good manufacturing practices (GMP) and other applicable industry regulations.
What your responsibilities will be
- Analyze and monitor the reagent plant's manufacturing processes.
- Perform monthly CPV monitoring of the data obtained.
- You will draft and approve CPV monitoring documents (protocols, reports).
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.
- You have a B2 level of English. (Essential).
- Master's degree or Postgraduate degree in the Biotechnology, Biology, Biochemistry, Chemistry... Pharmaceutical Industry. (Desirable)
- You have at least 6 months of experience in a similar position.
- You have user-level skills in MS Office
- Knowledge of GMP environment is essential.
- You are proactive, methodical and eager to learn.
- Knowledge in SAP system and Minitab software (desirable).
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 8:00h – 17:00h and Friday 8:00h 15:00h.
Benefits package
Contract of Employment: Temporary
Flexibility for U Program: 1 day remote working
Location: Parets del Vallès