(E082) Medical Devices & Row Materials Quality Control Manager

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.

We are looking for an Instruments & Raw Materials Quality Control Manager to join Diagnostic Grifols SA, dedicated to the design and manufacture of in vitro diagnostic systems for blood typing.

What your responsibilities will be

1. Manage the quality control team for raw materials, intermediates, and final products.
2. Establish quality control processes for the product in accordance with applicable quality and regulatory requirements to determine compliance with specifications.
3. Establish processes and procedures for conducting quality control of raw materials, intermediates, and final products.
4. Set up workflows in the laboratory to optimize resources to meet planning and ensure the integrity of analytical data.
5. Ensure proper investigation and definition of corrective and preventive actions for non-conformities originating in the laboratory.
6. Ensure that there are methods in place to guarantee control over laboratory equipment and facilities.
7. Ensure that there are methods to guarantee the use of appropriate samples, tools, standards, etc., for the controls to be performed.
8. Supervise the transfer of methods from Instrument Development and ensure the validation status.
9. Ensure that changes made within the laboratory are carried out in a controlled manner.
10. Collaborate on internal quality system audits and external audits of material suppliers.
11. Ensure the application and compliance in your area with Quality, Safety and Health, and Environmental Standards, as well as with the procedures and instructions that affect the tasks performed in the area.

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.

• Bachelor's degree in Engineering (industrial, mechanical, electronics or similar).
• Minimum 2 years of experience in a similar position, preferably within pharma or medical devices sector.
• Knowledge in GMP is valuable.
• English: Advanced level.
• High knowledge in MS Office.
• SAP user or similar ERP.
• Strong leadership skills.
• Excellent communication skills.
• Ability to analyze in an agile and decisive way.
• Ability to expose the issues in a clear and organized way focused on the objective.
• Ability to work as part of 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.

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: Occasionally remote. Flexible schedule: Monday-Thursday 8h to 17h and Friday 8-15h. Benefits package. Contract of Employment: Permanent position. Location: Parets del Vallès, SPAIN.

Learn more about Grifols.