Qp Head

Act as a liaison between the plant and the National Public Health Authorities, National Public Safety Authority, and other relevant bodies in relation to drugs and controlled drugsEnsure that each batch of drug is produced and controlled in strict compliance with current laws and the conditions defined in the product marketing authorizationRelease finished products for the market (Batch Release) and authorize the release of unpacked products for delivery to clientsEnsure all required documentation, as per law and Good Manufacturing Practices (GMP), is properly compiled and filed for the appropriate period of timeCollaborate actively during inspections by Health Authorities and ensure timely compliance with any requested actionsCertify that pharmacologically active substances used within the plant have been produced in compliance with GMPRequirementsProven experience in the pharmaceutical fieldProven track record in the QP role, according to 219/06 legislative decreeProficiency in Italian and English languagesAbility to navigate sophisticated contexts and optimally manage relationships with authoritiesAt Thermo Fisher Scientific, we value diversity and believe that an inclusive workforce drives innovation and success.
We are an equal opportunity employer and welcome applications from all qualified individuals, regardless of race, gender, age, disability, sexual orientation, or religion.Application InstructionsTo apply for the position of QP Head at Thermo Fisher Scientific Inc., please submit your resume and cover letter highlighting your meaningful experience and qualifications.
We appreciate all applications; however, only candidates selected for an interview will be contacted.Join us !