Quality Assurance Specialist

SwissCo Services AG / Aenova Group; Carugate; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading contract manufacturer and developer in the pharmaceutical industry is seeking a Quality Assurance Specialist for its Carugate site. The role involves ensuring product quality, compliance with GMP standards, and facilitating effective change controls. Candidates should have a scientific degree and be adept in quality assurance protocols. Join a culture that prioritizes excellence and patient health!

Competenze

• Degree in scientific disciplines required.
• Knowledge of European and international GMP standards essential.
• Experience with semi-solid and/or liquid formulations is a plus.

Mansioni

• Ensure compliance with company quality standards and GMP regulations.
• Support timely investigations into quality deviations.
• Maintain status reports on all changes to ensure timely interventions.

Conoscenze

Knowledge of European and international GMP standards

Proficiency in English

Formazione

Degree in scientific disciplines

Descrizione del lavoro

Quality Assurance Specialist

for the site Carugate MI, Italy

Would you like to make a valuable contribution to the health of patients? And do something really meaningful on your own responsibility? Then we look forward to hearing from you! Excellence beyond manufacturing - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 sites. Our site in Carugate is a competence center for semisolids, including creams and gels.

Your key responsibilities

• Ensure that the products have the required quality characteristics.
• Ensure compliance with company quality standards required by current regulations (European and international GMP standards).
• Ensure compliance with company quality standards required by customers.
• Support the relevant business functions in ensuring an effective change control system by coordinating cross-functional risk evaluations of proposed changes to define appropriate action plans and implementation dates; maintain an up-to-date status report on the progress of all changes to ensure timely interventions for their implementation.
• Support the management of deviations by coordinating timely multi-disciplinary investigations to promptly identify issues and prevent impact extension; assess root causes and implement effective CAPAs.

Your profile

• Degree in scientific disciplines.
• Knowledge of European and international GMP standards.
• Knowledge of regulations related to the production of pharmaceutical products (experience with semi-solid and/or liquid formulations is a plus).
• Proficiency in English, both spoken and written.

Your motivation

Are you seeking new challenges in a highly competitive environment? Do you want to approach them creatively and with personal responsibility? Do you prefer a "get-it-done" culture and think in terms of solutions rather than problems? If so, what are you waiting for? We would be happy to explain our corporate benefits in a personal conversation!

If you have any questions, I - Chiara Fanasca / Human Resources - will be happy to assist you:

Temmler Italia S.r.l. • Member of the Aenova Group • Via delle Industrie 2 • 20061 Carugate MI, Italy