Bioanalytics Scientist, Stability
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 opportunities that foster an inclusive environment.
Misión del Rol
Her main responsibility will be to initiate, plan, coordinate, and execute the technical aspects of assigned projects within the established timelines. She will ensure that all developments, validations, and related activities are carried out in accordance with internal procedures and GMP regulations.
What Your Responsibilities Will Be
* Generate study protocols, reports, and standard departmental documentation.
* Review analytical results and related processes for assigned projects.
* Provide guidance and coordination to the team on specific work activities.
* Ensure knowledge and application of applicable working standards (GMP, SOPs, internal guidelines, GLP, etc.) in line with established procedures.
* Ensure accurate completion of records when required.
* Adhere to quality, safety, hygiene, and environmental regulations and standards.
* Report any incidents impacting normal operations to the direct supervisor.
* Perform tasks corresponding to lower professional levels when necessary.
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.
* Degree in Health Sciences (Pharmacy, Biology, Chemistry, Biochemistry, Biotechnology); Master’s and/or PhD desirable.
* Minimum of 2 years’ experience in the pharmaceutical industry, within the stability area.
* Knowledge of GMP, GLP, ICH, and related guidelines.
* English level: B2.
* Proficiency in Microsoft Office (especially Excel) and SAP QM.
* Strong time management and prioritization skills.
* Excellent communication, analytical skills, and attention to detail.
* Strong ability to work effectively within a team.
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.
Flexible schedule
Monday-Thursday 8:00h – 17:00h and Friday 8:00 - 15:00h (with the same flexible start time).
Benefits Package
* Contract of Employment: Permanent position.
* Flexibility for U Program: Hybrid Model.
* Location: Parets del Vallès.
Grifols is an equal opportunity employer.
Information about Grifols is. 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! Learn more about Grifols.
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