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Position Summary: The Deputy Technical Director ensures the quality and safety of medicinal products and compliance with Good Manufacturing Practices (GMP) in radiopharmaceutical preparation. Key Responsibilities: 1. Lead quality and safety in radiopharmaceutical manufacturing 2. Manage and plan the operation of radioactive facilities 3. Manage personnel and resources to ensure smooth plant operation **About Curium** Curium is the world’s largest nuclear medicine company, with over a century of experience in the industry. We develop, manufacture, and distribute high-quality radiopharmaceutical products to help patients worldwide. Our proven legacy, combined with a pioneering approach, defines our commitment to innovation, excellence, and unparalleled service. With manufacturing facilities across Europe and the United States, Curium provides SPECT, PET, and therapeutic radiopharmaceutical solutions for life-threatening diseases to more than 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactivity researchers Marie and Pierre Curie—after whom the radioactive element curium was named—and underscores our focus on nuclear medicine. The motto ‘Life Forward’ reflects our commitment to securing a brighter future for all those we serve: better quality of care for our patients; a trusted partner for our customers; and an employer that supports our valuable team. **Summary of Position** ----------------------- * ***Permanent contract*** * ***Shifts: 00:00\-7:00; 7:00\-14:00*** * ***Some public holidays and Saturdays required*** * ***Category 6*** * ***Remuneration: €35,000\-42,000 gross annual*** * ***Immediate start*** * ***Location: Málaga*** As Deputy Technical Director, your mission is to ensure the quality and safety of medicinal products and to comply with and enforce Good Manufacturing Practices (GMP) applicable to radiopharmaceutical preparation. * Ensure that each batch of medicinal products has been manufactured and controlled in accordance with applicable legislation and the requirements stipulated for marketing authorization. * In all cases—and particularly before releasing medicinal products to the market—the Technical Director must certify, in a register or equivalent document established for this purpose, that each manufacturing batch complies with the provisions of this article; such register or equivalent document must be kept up to date as operations are performed and made available to the competent health authority for a minimum period of five years. * The Technical Director must assist inspection authorities in carrying out their duties and serve as the laboratory’s liaison with the competent health authorities regarding matters covered by this Royal Decree. **Essential Functions** ----------------------- * Manage and plan the operation of the radioactive facility and the activities of operators in accordance with the facility’s authorization resolution, any other official documents, and applicable legislation. To this end, establish all necessary operational procedures. * Keep official documents up to date * Archive all documents and records required by applicable legislation. Documents and records from radioactive facilities shall comply with Instruction IS\-16\. * Submit quarterly and annual reports on activities carried out, as well as any potential anomalies. * The supervisor shall schedule and oversee all operations and remain reachable and available during facility operation. * Be responsible for proper facility operation, including monitoring radiation-emitting equipment, equipment inspections, and all protective equipment—both during operation and inspection—as well as dosimeters, area monitors, etc. * Monitor operator radiation doses, their dosimetric histories, and medical examinations and histories. * Release batches of medicinal products * Participate in all internal and external audits and in all inspections conducted by competent authorities. * Manage plant personnel and resources to ensure smooth operation of the manufacturing plant. * Manage and/or support the logistics plan. * Open, review, investigate, and close deviations, Out-of-Specification (OOS) results, and change controls within prescribed timeframes. * Open customer complaints received at the supervisor’s own site **Requirements** ---------------- * University degree in Pharmacy, Medicine, Chemistry, Pharmaceutical Technology, or related fields * Minimum two years’ professional experience in companies holding authorization as pharmaceutical manufacturing laboratories or laboratories performing qualitative analysis of medicinal products, quantitative analysis of active substances, and tests and verifications required to ensure medicinal product quality. * FIR/QIR/BIR specialization * Radioactive Facility Supervisor * English: intermediate\-advanced level * Knowledge of GMP **Competencies** ---------------- **Disclaimer** The above statements are intended to describe the general nature and level of work performed by employees assigned to this classification. They should not be interpreted as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position. **Equal Opportunity Employment** Curium is an equal opportunity employer and believes everyone deserves respect, dignity, and equality. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
