We are seeking to hire an **Assistant/Technical Pharmacist** for our company. The selected candidate will work in coordination with the Technical Management, supporting the assurance that conditioning activities are carried out in compliance with current legislation, applicable Good Manufacturing Practices (GMP)/Good Distribution Practices (GDP), and regulatory requirements corresponding to each product type. **Functions and responsibilities** * Support Technical Management in supervising handling and packaging activities for cosmetic, pharmaceutical, and parapharmaceutical products. * Collaborate to ensure that each packaged batch complies with current regulations, administrative authorizations, and customer requirements. * Participate in communication with competent health authorities and support inspections and audits conducted by such authorities. * Support regulatory affairs management with public administrations, including maintenance of the packaging room authorizations and associated documentation. * Collaborate in reviewing and maintaining the Technical File and other applicable regulatory documentation. * Support reviewing and managing technical agreements with third parties for outsourced activities. * Actively participate in Quality System management, including: * Documentation and training on GMP/GDP or other applicable Good Practices according to product type. * Change control management. * Handling of CAPAs (Corrective and Preventive Actions). * Sample management (receipt, identification, distribution, review, and archiving). * Review of packaging documentation (Batch Record / packaging records). * Deviation management. * Updating and maintaining the company’s Quality Manual. * Participate in quality system and product review activities: * Annual Quality Management System Review. * Product Quality Review, where applicable. * Collaborate in preparing, reviewing, and maintaining SOPs (Standard Operating Procedures) related to packaging activities, ensuring their consistency within the Quality Management System. * Support management of general services impacting quality: cleaning control, environmental conditions (climate), and pest control. * Collaborate in defining, validating, and maintaining documentation related to products and processes under their responsibility. * Participate in supervising and approving training for personnel involved in handling and packaging activities. * Collaborate in developing and presenting quality and operations KPIs requested by Management. **Requirements:** * Degree or Bachelor’s degree in Pharmacy. Experience in a Pharmaceutical Laboratory and knowledge of GMPs. Other degrees may be accepted provided they include the pharmacy-related subjects required for the position of Technical Director, certified by the corresponding university. * Meet minimum requirements established under Royal Decree 824/2010 to hold the position of Technical Director. * Availability for required working hours. Specialty: Pharmacy Working hours: Monday to Friday, 7:00 a.m. to 3:00 p.m. In the future, split shift. Position type: Full-time Salary: €20,000.00–€28,000.00 per month Work location: On-site employment