We are seeking to hire a Manager, Quality Assurance Operations & QP to join our Italian QUALITY TEAM at Pessano con Bornago.

If any of the below describes you, we would love to meet you!

Job Summary

The Manager, Quality Assurance Ops acts as lead for the QA Operation group and carries out and covers the following responsibilities:

• Manages the QA Specialist/Sr Specialist group of the site for the deviation/ investigation, Batch Record reviews and release functions and ensures their correct training and professional growth
• Manages the QA Specialist/Sr Specialist quality on the floor of the site for the oversight of production activities
• Is the first point of contact with customer relating deviation, CAPA and complaints
• Acts as a Qualified Person at Pessano site
• Supervise and verify that each batch of medicine is produced and controlled by preparing all the necessary operations and measures to allow the aforementioned controls to be carried out
• Is responsible for managing the documentation relating to the production and controls of the products and its availability
• Ensure the management of narcotic and psychotropic substances and drug precursors
• Identifies areas and activities for improvement from a procedural point of view, promotes the drafting of the Standard Operating Procedures and their approval and application
• Manages the personnel who deal with the deviations and non-conformities found, ensuring the quality of the outgoing product and verifying the effectiveness of the corrective actions taken
• Manages the personnel who deal with customer complaints with related investigation, corrective activities, response and closure of complaints
• Works cooperatively with managers, supervisors, collaborators, customers and the public
• Complies with the policies, procedures and regulations in force in the company.

Required Skills and Qualifications

• Master's Degree in Scientific Disciplines: Chemistry and Pharmaceutical Technology (CTF ), Biological Sciences, Pharmacy or similar
• Ten years of experience in the pharmaceutical GMP field
• English full working proficiency (proven fluency)
• Recognition by AIFA as a Qualified Person
• Proven experience in resource management
• Excellent interpersonal written and oral communication skills
• Ability to coordinate, contribute to and work within a cross-functional team.

Also as per D.Lgs n. 205/03 and n. 206/03, Adare Pharma is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status.

Adare is an organization that works daily to break down any gender gap, in the awareness that the full valorization of female talent represents a fundamental element for a greater creation of economic and human value. In Adare both genders are equally represented even in the case of managerial roles. In Adare we have structured a management system useful for the certification of gender equality; therefore, we work daily to combat any form of non-inclusion in our management processes and in our internal and external communication. The selection process is no exception: our staff in charge of selection and recruitment are prohibited from asking questions that directly or indirectly relate to the topics of pregnancy, marriage or - in general - the responsibility of care. If you are a woman and you are reading this announcement, know that your gender will not represent an obstacle to the selection process.

PRINCIPALS ONLY
NO AGENCIES OR THIRD PARTIES