Solutions Preparation Supervisor

• You have a minimum educational qualification of a Higher Degree in the Chemistry field with extensive experience in Production Areas within the Pharmaceutical Industry, and knowledge of GMP regulations. A university degree or Engineering qualification will be highly valued.
• You have at least 2 years of experience in a similar position.
• You are a regular user of computer tools (ERP, Office, etc.).

• You have a good level of English.
• You are a person with good adaptability skills and are agile enough to respond appropriately within a high-activity environment, as well as being goal-oriented, in accordance with safety and quality procedures and standards.
• You enjoy and feel comfortable in a role that involves team management and interacting with different types of stakeholders at an interdepartmental level.

Being part of Grifols means the opportunity to work in an international environment where equal opportunities are promoted.

It means the opportunity to develop professionally, have continuous training, and integrate into a team of professionals where each individual's contribution counts. Our commitment is to maintain an environment that fosters the professional development of our employees in a good work atmosphere.

Grifols' human capital is key to both the development of activities and the company's expansion process.

If you are interested in growing with us and your profile matches this professional opportunity, send us your CV.

Schedule: Head office, Monday to Friday.

Employment contract: Permanent

Location: Parets del Vallès

www.grifols.com

Location: SPAIN : Spain : Parets del Valles:[[cust_building]]

Learn more about Grifols

Would you like to join an international team working to improve the future of the healthcare sector? Do you want to contribute to improving the lives of millions of people? Grifols is a global healthcare company that since 1909 has been improving the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and we 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 opportunities and our mission is to offer an inclusive environment where differences strengthen our company.

We are looking to hire a Supervisor for the Solutions Preparation department at Laboratorios Grifols S.A., a company within the Grifols Group dedicated to producing a wide range of non-biological products used in hospital pharmacies, surgery, clinical nutrition, fluid therapy, and products for other therapeutic uses.

Your main mission will be to plan, control, and improve the production processes of the water treatment plant, weighing, and manufacturing of intermediate products, acting and ensuring that others act in accordance with established procedures and regulations in order to meet planned production commitments and requirements with the required degree of quality and safety.

• You will review the production plan daily and on a 2-week forward-looking basis.
• You will complete a schedule of activities and equipment usage for the department.
• You will review the condition of the facilities and report deteriorated or damaged items to maintenance.
• You will meet with the team to identify opportunities for improvement in terms of safety and health.
• You will conduct weekly follow-up with maintenance regarding the preventive maintenance operations to be carried out and to agree with the department head on the time slots to perform them.
• You will follow up on the calibrations to be performed and facilitate their execution to ensure they are completed within the deadline.
• You will investigate any deviations that may occur during processes to find their root causes.
• You will complete all documentation related to quality notifications as required.
• You will carry out follow-up and implementation of immediate actions and CAPAs to eliminate failures and make processes and equipment more robust.
• You will coordinate vacation periods with the department head to ensure adequate coverage in the area.
• You will manage and follow up on the tasks to be carried out to implement projects in the department, both minor changes to facilities as well as changes to processes and procedures.
• You will manage the documentation related to the management of these projects (e.g., Change Controls).

To perform this job successfully, a person must be able to carry out the responsibilities satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.