Bioanalytics Supervisor

Grifols, S.A; Parets del Vallès; Híbrido; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

A global healthcare leader in Spain is seeking a Bioanalytics Supervisor to oversee bioanalytical activities and ensure compliance with quality standards. The ideal candidate will have experience in laboratory supervision and knowledge of GMP and GLP regulations. This position offers a permanent contract and a supportive working environment for professional development.

Servicios

Brilliant opportunity for career development

Flexible schedule

Benefits package

Formación

• At least 6 months experience as a Laboratory supervisor or similar position.
• 2 years of experience in applying work standards (GMP, SOP, etc.).
• Knowledge and application of quality, safety, hygiene standards.

Responsabilidades

• Supervise bioanalytical activities under quality standards.
• Review completed work logs and data.
• Ensure compliance with GLP and GMP regulations.

Conocimientos

Laboratory supervision

GMP knowledge

Analytical skills

Proficient in Office suite

Teamwork

Educación

CFGS in Laboratory, Chemistry or similar

Herramientas

Graphpad

SAP

Descripción del empleo

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 are looking for Bioanalytics Supervisor to join Development Department within Scientific Innovation Office Division at Instituto Grifols SA, a company specialized in the research, development, and production of purified plasma proteins with therapeutic properties obtained from the fractionation of human plasma.

Role Mission

Supervise and ensure the execution of bioanalytical activities under quality standards, ensuring the generation of reliable data and compliance with GLP and GMP regulations; as well as supervise the technical team in the development, validation and application of bioanalytical methods, promoting continuous improvement, operational efficiency and regulatory compliance in the laboratory.

What your responsibilities will be

• Review completed work logs.
• Verify that the data obtained is generated according to the procedural instructions.
• Evaluate and report the results generated according to the procedural instructions.
• Review the results reported in the available systems.
• Observe the trends in the data obtained.
• Apply the pre-established study protocol according to the scope, procedure, and evaluation criteria.
• Prepare the predefined resources to conduct the study within the established timeframe.
• Collect data and prepare documentation related to the pre-established study protocols.
• Monitor critical equipment and/or materials used in the unit.
• Prepare documentation related to the maintenance of critical equipment and materials in the unit.
• Prepare documentation related to unit procedures. 13. Ensure ongoing training for staff and the availability of necessary resources.
• Organize unit resources to complete planned tasks on time and to the established quality standards.
• Ensure adequate working conditions within your area of responsibility by complying with preventive measures adopted in each case, including health surveillance.

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.

• CFGS in Laboratory, Chemistry or similar,
• Experience of at least 6 months, as a Laboratory supervisor or similar position (Essential).
• 2 years of experience in the application of work standards (GMP, SOP, INS, GLP, etc...) in accordance with the defined procedures.
• Knowledge and application of established quality, safety, hygiene and environmental standards.
• You are proficient in the Office suite (especially Excel and Word), and knowledge of Graphpad and other laboratory software will be valued.
• Knowledge of SAP will be valued.
• You manage your time well and know how to prioritize.
• You have analytical skills and attention to detail.
• You can work in a team. You are committed and enthusiastic about your work.

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.

Flexibility for U Program: Hybrid Model

Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

Benefits package

Contract of Employment: Permanent position