Job Summary: This role involves managing stability and reference samples, initiating stability studies, and performing administrative tasks within a quality control department. Key Highlights: 1. Being part of a dynamic work environment. 2. Flexible working hours. 3. Permanent contract. Reporting to the Quality Control Coordinator, this person will be assigned the following responsibilities: * Managing stability samples located in climate chambers. * Managing reference samples located at Synthon Hispania. * Managing finished product samples prior to analysis commencement in the AO laboratory. * Initiating stability studies. * Placing purchase orders in SAP. * Performing departmental administrative tasks (e.g., sample dispatch). * Carrying out assigned tasks responsibly, following applicable instructions (SOPs, etc.) as appropriate. * Understanding and complying with cGMP regulations as well as PRL, hygiene, environmental, and social responsibility regulations. * Performing specific backup tasks (e.g., purified water sampling, equipment cleaning, procurement, reagent inventory control, etc). **WE OFFER:** * Being part of a dynamic work environment built on trust and transparency. * Flexible working hours (Monday to Friday: arrival between 07:00 and 10:00; Monday to Thursday: departure between 16:00 and 19:00 – 45-minute lunch break; Friday: departure between 15:00 and 19:00 – 45-minute lunch break). * Permanent contract. * Attractive salary package, allowances, flexible remuneration plan, and social benefits package. * Vocational Training Qualification (CFGM) in Chemistry, Analysis and Control or equivalent. * 1–2 years’ experience in the described functions within the pharmaceutical sector. Experience with SAP is valued. * We seek detail-oriented individuals with strong organizational skills, communication abilities, and a people-oriented mindset.
David Muñoz
Indeed · HR
David Muñoz
Indeed · HR
