Adjunto(a) a coordinación de producción de vacunas

Solo para miembros registrados
Amer
EUR 30.000 - 45.000
Descripción del empleo

Join to apply for the Adjunto(a) a coordinación de producción de vacunas role at HIPRA.

HIPRA is a pharmaceutical and biotechnological company focused on prevention and diagnosis for animal and human health, with a wide range of highly innovative vaccines and advanced diagnostic services.

It has a strong international presence in over 40 countries, with subsidiaries, 11 diagnostic centers, and 6 strategically located production plants in Europe (Spain) and America (Brazil).

Research and development are at the core of its expertise. HIPRA dedicates 15% of its annual turnover to R&D activities, focusing on the latest scientific advances to develop high-quality innovative vaccines. To enhance its vaccination experience, the company also develops medical devices and traceability services.

Currently, we have new vacancies for adjunto/a a coordinador/a in two of our vaccine production units located at the headquarters in Amer (Girona).

We are looking for candidates who:

  • Have a degree in chemical engineering, biology, or similar.
  • Are careful, meticulous, organized, enjoy teamwork and working in industrial laboratories.
  • Possess leadership qualities, proactivity, and have managed teams.
  • Are seeking stable employment with continuous training.
  • Are motivated and eager to learn.
  • Are available to work rotating shifts (morning and afternoon) from Monday to Friday.

At HIPRA, you will find:

  • Continuous learning opportunities.
  • A growing multinational company.
  • A multicultural environment open to new ideas.
  • Stable job positions.

Main responsibilities of the position:

  • Supervise and coordinate production activities during the shift.
  • Transfer information between shift supervisors to ensure process continuity.
  • Supervise, coordinate, and motivate staff, fostering excellence and teamwork.
  • Identify training needs and participate in training processes.
  • Conduct periodic staff evaluations.
  • Ensure the health and safety of personnel.
  • Ensure compliance with Good Manufacturing Practices and follow established Quality System procedures.
  • Draft documents for the Quality System of the organizational unit and ensure their validity.
  • Assist in production planning.
  • Organize resources to meet planning goals.
  • Ensure proper documentation by personnel and external staff.
  • Ensure sampling and control procedures are followed.
  • Oversee batch documentation within deadlines.
  • Investigate and document deviations and non-conformities during manufacturing.
  • Implement corrective measures to address deviations and non-conformities.
  • Gather information, analyze processes, and propose improvements aimed at zero defects.
  • Participate in the development and manufacture of pilot batches.
  • Implement corrective actions during audits or inspections.
  • Maintain proper functioning, cleanliness, and order in facilities and equipment.
  • Ensure validations, calibrations, and qualifications are performed as per the Annual Plan.
  • Propose preventive maintenance and ensure their execution.
  • Manage breakdowns with maintenance.
  • Participate in projects by providing ideas and testing equipment and facilities.
  • Execute delegated tasks from the direct supervisor.
  • Cover absences or vacancies as assigned by the supervisor.