Grifols

Quality Manager – In-Process Control

Grifols

full-time

Posted on:

Location Type: Hybrid

Location: Sant Cugat del Valles • Spain

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About the role

  • 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.

Requirements

  • A Bachelor’s Degree in health sciences, preferably in Pharmacy
  • Minimum of 5 years of experience in 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.
Benefits
  • Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h
  • Benefits package
  • Contract of Employment: Permanent position
  • Flexibility for U Program: 2 days remote working
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
sampling procedurescontrol procedurescontinuous improvementquality assuranceGMP regulationstechnical reportinginvestigative analysiscorrective actionspreventive actionsdocumentation traceability
Soft Skills
leadershipteam motivationinternal communicationorganizational skillsadaptabilitycollaborationpresentation skillscommitmenttalent developmentproblem-solving
Certifications
Bachelor’s Degree in health sciencesPharmacy degree