Descripción de la oferta
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.Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma‑derived medicines with presence in more than 100 countries, and a growing global team of over 20 000 people. That’s why we need a Manager, In‑Process‑Control like you.What your responsibilities will be- Define and establish sampling and control procedures in production processes, facilities, critical systems, and equipment.- Propose and apply sampling and/or control procedures and enhance their continuous improvement according to current regulations.- Ensure the suitability of the collected samples so that they are representative of the quality of the product, equipment, or facility.- Lead, organize, and plan tasks and human resources to ensure the proper execution of work procedures in accordance with production activity planning.- Propose the acquisition of materials or equipment for the development and improvement of control procedures, as well as supervise their proper maintenance.- Approve the results of the controls carried out while respecting the established deadlines.- Report the results and deviations obtained in the sampling and control procedures according to the established planning.- Conduct investigations related to detected deviations and propose or advise on corrective/preventive actions to be taken.- Attend evaluation committees related to their functions and propose or recommend improvement actions for the identified issues.- Supervise the traceability of the documentation generated in production procedures, ensuring compliance with established deadlines.- Advise on the design, implementation, or modifications of facilities or equipment to ensure compliance with current GMP regulations.- Advise other departments on the required quality levels based on the purpose of the facility or equipment.- Propose control frequencies and procedures compatible with production processes in collaboration with other departments.- Prepare and supervise work procedures affected by modifications or changes in facilities, systems, or equipment.- Present the sampling and control procedures applied to facilities and equipment to regulatory agencies or audits as required.- Provide the necessary information regarding their activities to official agencies or audits upon request.- Prepare the necessary documentation to demonstrate the proper condition of equipment and facilities through obtained results.- Prepare the necessary technical reports to support compliance with current regulations.Who you areTo 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).- A Bachelor’s Degree in health sciences, preferably in Pharmacy.- Minimum of 5 years of experience in a pharmaceutical multinational environment.- Integrated, adaptable to organizational needs, with technical knowledge and practical sense.- Skilled in internal communication and work presentation, effective in tasks, achieving high commitment from collaborators.- Ability to develop talent, motivate, and lead team members to foster teamwork.- Availability to travel: periodic travel to the plant in Egypt will be required.- Advanced English.What we offerIt’s a brilliant opportunity for someone with the right talents.Grifols understands you want a challenging and rewarding career in a critical function. As Manager, In‑Process‑Control, you can grow professionally.We look forward to receiving your application.Grifols is an equal opportunity employer.Flexible schedule: Monday‑Thursday 7‑10 to 16‑19h and Friday 8‑15h.Benefits packageContract of Employment: Permanent positionFlexibility for U Program: 2 days remote working#J-18808-Ljbffr
