QA Validation Specialist

BSP Pharmaceuticals S.p.A.; Latina; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading company in the fight against cancer is seeking a QA Validation Specialist for their Quality Assurance Validation Team. The role involves analyzing technical documentation, drafting validation protocols, and ensuring compliance with company procedures. Candidates should have a relevant MA degree and experience in similar roles, along with knowledge of GMP and a proactive attitude.

Competenze

• 1-2 years of experience in similar roles in complex organizations.
• Knowledge of GMP and English working knowledge.

Mansioni

• Analyze technical documentation related to manufacturing processes.
• Draft Validation Protocols and ensure correct validation of processes.
• Collect and analyze data for validation activities.

Conoscenze

GMP

Data Analysis

English

Formazione

MA degree (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 agains 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 datas and informations 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;
• Great can-do attitude.

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