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.