Mission

A Bioanalytics Scientist is sought to join the Bioanalytics, CMC Product Development area within the Scientific Innovation Office at Grifols, a company specialized in the research, development, and manufacturing of purified plasma-derived therapeutic proteins obtained through the fractionation of human plasma.

Main Mission

The successful candidate will be responsible for initiating, planning, coordinating, and executing the technical aspects of assigned projects within the established timelines. They will ensure that all analytical developments, method validations, and related activities are performed in compliance with internal procedures and applicable Good Manufacturing Practice (GMP) regulations.

What your responsibilities will be

- Design, plan, and oversee laboratory studies and experimental activities to ensure high-quality scientific outcomes.
- Analyze and interpret experimental data, including statistical analysis, trend evaluation, and graphical data presentation.
- Prepare and present scientific results through clear technical reports, presentations, and cross-functional communications.
- Develop, optimize, and validate new laboratory methods in accordance with applicable scientific and regulatory standards.
- Conduct scientific literature reviews and bibliographic research to support project development and innovation.
- Ensure the stability, characterization, and analytical evaluation of biological products throughout the product lifecycle.
- Author study protocols, technical reports, and scientific documentation, ensuring accuracy, traceability, and compliance with quality requirements.

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.

- Bachelor's degree in Life Sciences, such as Pharmacy, Biology, Chemistry, Biochemistry, or a related field.
- A Master's and/or PhD in a relevant discipline is considered an advantage.
- At least 2 years of research experience, preferably within the pharmaceutical industry.
- Experience with in vitro and/or in vivo studies is highly desirable.
- Solid knowledge of GMP, GLP, ICH guidelines, and other relevant regulatory standards.
- Strong understanding of statistical analysis and data interpretation.
- Advanced English proficiency (C1 level), both written and spoken.
- Proficiency in Microsoft Office, particularly Excel, experience with GraphPad Prism is a plus.
- Excellent time management and prioritization skills.
- Strong communication and presentation abilities.
- High level of analytical thinking, attention to detail, and accuracy.
- Ability to work effectively in cross-functional teams.
- A proactive, committed, and enthusiastic attitude, with a genuine passion for scientific research and continuous improvement.

Benefits package

Flexibility for U Program: On site.

Contract of Employment: Temporary position.

Equal Employment Opportunity

Grifols is an equal opportunity employer. We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

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📌 BIOANALYTICS SCIENTIST (Parets)
🏢 Grifols
📍 Parets