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 **** 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.
Role Mission
In the Validations Department at Laboratorios Grifols, we need to recruit an Equipment and Process Validations Technician.
Their primary role will be to manage and execute assigned validation projects in accordance with current regulations, ensuring the validity of production processes.
What Your Responsibilities Will Be
You will draft and execute assigned qualification/validation protocols.
You will draft and track qualification/validation reports.
You will edit deviations and change control assessments associated with validations.
You will validate the plant, at the equipment and process level, throughout its various stages of design qualification (DQ), installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ), as well as cleaning validation (CV) and process performance qualification (PPQ).
You will generate and review primary data associated with assigned validations.
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).
You have a University Degree in Engineering, Biochemistry, Biotechnology, Experimental Health Sciences or similar.
Minimum of 2 years experience in the area of validations or quality systems of the pharmaceutical industry (GMP) or ISO quality systems.
(Necessary).
You have an level of English (minimum B2).
You are proficient in the Office suite and have basic SAP user skills.
Available to reside in Murcia
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.
Grifols is an equal opportunity employer.
Versátil schedule:
Monday-Thursday 8:00h – 17:00h and Friday 8:00h 15:00h.
Benefits Package
Contract of Employment:
Permanent position
Flexibility for U Program:
1 day remote working
Location: Murcia
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