QA Validation Specialist

BSP Pharmaceuticals S.p. A focuses on the development and manufacturing of anticancer drugs with high potency and cytotoxic characteristics for the pharmaceutical industry.
BSP has been at the forefront in the fight against cancer since 2006.
Innovation is the hallmark of BSP with investments in new technologies and production methods in a high containment plant.
We are one of the most important Contract Development and Manufacturing Organization (CDMOs) for anticancer drugs.
The fight against cancer is ours too.
We are currently looking for a  QA Validation Specialist  for our Quality Assurance Validation Team.
Main Activities    Analysis of technical documentation
Ensure the analysis and evaluation of technical documentation related to manufacturing processes or cleaning and sanitization procedures that have to be submitted for validation.
Defining Protocols
Drafting the Validation Protocols, by researching and acquiring data and information from other business functions.
Validation
Ensure the correct validation of the processes, cleaning in compliance with company protocols and procedures through the execution of the operational activities.
Preparation of Validation Reports.
Data Analysis
Ensure correct analysis of validation activities through data collection and analysis, in compliance with company protocols and procedures.
Main Requirements     MA degree (CTF/Chemistry..)
1/2 years of experience in similar roles in complex organizations
Knowledge of GMP
English working knowledge
At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect the diversity, the different backgrounds and experiences and provide equal opportunity for all.
We are BSP
Seniority level   Mid‑Senior level

Employment type

Full‑time
Job function   Quality Assurance
Industries   Pharmaceutical Manufacturing

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