Adecco Italia Spa_Life Science is looking, on behalf of a pharmaceutical company operating in the development and manufacturing of semi-solid and liquid dosage forms, for a highly qualified and experienced Qualified Person (QP).
Required Qualifications
* A degree in scientific disciplines such as Chemistry and Pharmaceutical Technologies, Pharmacy, Chemistry, Industrial Chemistry, Biological Sciences, Medicine and Surgery, or Veterinary Medicine.
* 10 years of significant professional experience, ideally within the chemical-pharmaceutical industry, with a strong background in quality management systems and GMP standards.
* Proven eligibility to practice as a Qualified Person, certified by AIFA (art. 52 Legislative Decree 24 April 2006 n. 219), and registration in the relevant professional register.
* A solid track record in coordinating and managing QA and QC departments, including resource planning and activity oversight.
* Advanced proficiency in the MS Office suite.
* Fluency in English, both spoken and written.
Job Responsibilities
* Oversee and manage Quality Assurance and Quality Control operations, ensuring optimal resource allocation and adherence to industry regulations.
* Ensure the analysis and market release of each batch in compliance with GMP standards and legal requirements, both in Italy and in destination countries.
* Maintain the site's production authorization by ensuring all production activities meet regulatory requirements.
* Collaborate on development plans, focusing on the integration of new products and technologies while maintaining regulatory compliance and obtaining necessary authorizations.
* Oversee the review and update of production-related documentation and the execution of stability studies in alignment with ICH guidelines.
* Foster collaboration between departments, including Quality, Production, Supply Chain, and Warehouse, to ensure seamless operations.
* Serve as the primary liaison with the Ministry of Health/Italian Medicines Agency (AIFA), supporting inspections and managing regulatory interactions.
* Promote the professional development of team members, evaluating performance and providing recommendations for recognition in line with company policies.
Work Location: Northern Province of Milan, Italy
Additional Notes: This is a full-time, permanent position offering a competitive salary and an attractive benefits package, including a company car.
Contract Type: Permanent, full-time employment.
Working Hours: Standard business hours.
I curricula ricevuti potranno essere comunicati all'azienda nostra cliente o ad altre che ne facciano richiesta per valutare un'eventuale assunzione, salvo diversa volontà del candidato. "I candidati ambosessi (L.903/77) sono invitati a leggere su www.adecco.it l'informativa sulla privacy (art.13, D.Lgs. 196/03). Per esercitare i diritti di cui all'art. 7 del citato Decreto è possibile scrivere al seguente indirizzo e-mail: customer.service@adecco.it. Un facsimile di domanda di candidatura, comprensivo di informativa sulla privacy (art. 9, comma 3, D.Lgs. 276/03), è presente al seguente indirizzo internet: http://www.adecco.it/it-IT/privacy/privacy-candidato/Pages/default.aspx
Adecco Italia S.p.A. (Aut. Min. Prot. N.1100-SG del 26.11.2004).