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 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 a Manager, Stability, like you.

Role Mission

Plan, coordinate, and oversee assigned development and stability study projects, ensuring their proper execution in line with company-defined objectives, timelines, and quality standards, while guaranteeing compliance with applicable regulations and alignment with the current scientific and technical state of the art.

What your responsibilities will be

• Lead the planning and execution of development projects and stability studies.
• Define the technical strategy and ensure adherence to deadlines and objectives.
• Design and optimize products, materials, and manufacturing processes.
• Coordinate multidisciplinary teams and monitor project progress.
• Analyze and interpret experimental results to inform decision-making.
• Ensure compliance with applicable regulations (GMP, GLP, among others).
• Oversee the preparation and review of technical and regulatory documentation.
• Prepare for and attend regulatory audits.
• Manage the department's budget and ensure the efficient use of resources.

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 in Pharmacy, Chemistry, Biotechnology, Chemical Engineering, or a related field, and Master's degree in the Pharmaceutical and Parapharmaceutical Industry is a plus.
• You have an advanced level of English (C1).
• You have experience in stability studies and product development in regulated environments (GMP, GLP). (Indispensable).
• You have 3 - 5 years of experience in similar roles within R&D in the pharmaceutical or biotechnology industry.
• You have experience in scientific project management.
• Previous experience in team management will be highly valued.
• You are proficient in the Office and have basic SAP user skills.

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 7:00 -10:00 to 16:00 -19:00h and Friday 8:00-15:00h (with the same flexible start time).

Contract of Employment: Permanent position

Flexibility for U Program: 2 day remote working

Location: Parets del Vallès

www.grifols.com

Learn more about Grifols