Qualification Specialist

BSP Pharmaceuticals S.p.A.; Latina; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceuticals company in Italy is seeking a Qualification Specialist to ensure proper qualification of equipment and utilities. The ideal candidate will hold a Master's degree and have at least 2 years of experience. Responsibilities include analyzing technical documentation and drafting qualification documents. This role supports innovation in the fight against cancer and thrives in an inclusive workplace.

Competenze

• At least 2 years of experience in the same role in complex organizations.

Mansioni

• Ensure analysis and evaluation of technical documentation.
• Draft qualification documents.
• Perform qualification of equipment and utilities.
• Prepare Qualification Reports.

Conoscenze

Knowledge of regulations regarding Equipment and Utilities validation

Can-do attitude

Fluent English

Formazione

Master's Degree in Chemical Engineering/CTF/Chemistry

Descrizione del lavoro

BSP Pharmaceuticals S.p. A is focused on the development and manufacturing of anticancer drugs with high potency and cytotoxitc characteristics for the Pharmaceuticals 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.

Position

We are currently looking for a Qualification Specialist - that will mainly ensure:

Main Activities

• Analysis of technical documentation Ensure the analysis and evaluation of technical documentation related to equipments and utilities to be qualified, in order to acquire information necessary for the definition of protocols and the execution of qualification activities in compliance with company procedures;
• Definition of qualification documents Ensure the drafting of qualification documents (Risk Assessment, DQ-IQ-OQ-PQ Protocols, Validation Master Plan, Validation Plan, Project Qualification Plan), by researching and acquiring from other corporate functions the data and information necessary to define their contents and to settle the qualification strategy;
• Qualification Ensure within the required tiem frame the proper qualification of equipments and utilities, through the execution of the operational activities provided for in the Protocols (DQ-IQ-OQ-PQ Protocols). In collaboration with the Purchasing function, formulate bid requests to suppliers and support the Manager, preparing a technical and economic analysis of the bids received;
• Qualification Reports Ensure the proper preparation of Qualification Reports (DQ-IQ-OQ-PQ Reports), based on the analysis of data generated from validation activities, in compliance with company protocols and procedures;

Qualifications

• Master's Degree in Chemical Engineering/CTF/Chemistry
• Knowledge of regulations regarding Equipment and Utilities validation, with particular reference to sterile departments
• At least 2 years of experience in the same role in complex organizations
• English
• Can-do attitude

Additional Information

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.