




Job Summary: We are seeking a professional to organize manufacturing and supervise the production of bacterial autovaccines, ensuring regulatory compliance and process quality. Key Responsibilities: 1. Organization and supervision of bacterial autovaccine manufacturing 2. Verification of equipment and process compliance 3. Working with validated methods and qualified and calibrated equipment For a production position in Alcobendas, a degree in Health Sciences is preferred, along with expertise in pharmaceutical manufacturing according to Good Manufacturing Practice (GMP) standards, and skills in planning, coordination, and organization. Duties include organizing bacterial autovaccine manufacturing, supervising material receipt and registration, verifying equipment and process compliance, performing labeling and storage, drafting standard operating procedures (SOPs), participating in room and equipment cleaning and validation, generating documentation, and working with validated methods and processes using qualified and calibrated equipment. A full-time schedule from 7:30 AM to 3:30 PM is offered, with 30-minute flexibility, on-site work at a facility accessible by public transportation, an annual gross salary of €30,000 (negotiable), and an indefinite-term contract. **Required Prior Experience:** * Preferably, candidates should have relevant experience — at least 1 year in pharmaceutical preparation production cycles (in this case, microbiology for bacterial autovaccines) and in pharmaceutical technology issues.


