Quality Assurance Specialist - Provincia di Latina, Lazio, Italia - Recordati Group

Recordati Group

Azienda verificata

Provincia di Latina, Lazio, Italia

2 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

Recordati, established in 1926, is an international pharmaceutical group, listed on the Italian Stock Exchange (Reuters RECI.MI, Bloomberg REC IM, ISIN IT , with a total staff of more than 4,300, dedicated to the research, development, manufacturing and marketing of pharmaceuticals. Headquartered in Milan, Italy, Recordati has operations in Europe, Russia and the other C.I.S. countries, Ukraine, Turkey, North Africa, the United States of America, Canada, Mexico, some South American countries, Japan and Australia. An efficient field force of medical representatives promotes a wide range of innovative pharmaceuticals, both proprietary and under license, in several therapeutic areas including a specialized business dedicated to treatments for rare diseases. Recordati is a partner of choice for new product licenses for its territories.

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About the Quality Assurance Specialist position

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We are looking a Quality Assurance Specialist to work together to ensure the high quality of our operations and services, with the goal of ensuring the long-term success of our business.

Your duties include inspecting procedures and products, identifying errors or nonconformity issues in products and related manufacturing processes and analysis.

Establish quality and safety standards and criteria to be met.

Establish procedures for monitoring achievement of standards.

Analyze and supervise business processes from production to marketing of products and draft related documentation.

Quality Assurance Specialist responsibilities are

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Product Quality Review
Supplier qualifications
Process Validation
SOPs revision
Other quality system related tasks

Quality Assurance Specialist requirements are

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Experience of 2+ years working as a Quality Assurance Specialist or other similar position in a GMP regulated pharmaceutical environment or equivalent.
Significant experience using quality assurance methodologies and standards and managing GMP documents and version control.
Significant experience in data analysis and statistical methods.
Good handson experience with MS Office and databases.
Statistical skills, great attention to detail, and a resultsoriented approach.
Strong communication, organizational and leadership skills.
Strong ability to work on own initiative or in a crossfunctional team.
Bachelor's degree in a scientific discipline.
Quality control certification, such as ISO 9000, will be a bonus.

At Recordati, we believe in equal opportunities and we guarantee that everyone can achieve their potential.

We see diversity as a value and will not tolerate any discrimination based on ethnicity, nationality, gender, sexual orientation, disability, age, political or religious belief, or any other personal characteristics.

At Recordati, we work hard to create a safe and inclusive work environment, where we all have our rights to physical and psychological integrity respected on a daily basis, as well as our right to freedom of opinion and association.

We recognise that we each have a role to play in the success of our business and we implement staff development policies through which everyone's contribution and achievements can be appropriately rewarded.