Finished Products Regulatory Affairs Specialist - Offanengo, Italia - Chromavis

Chromavis

Azienda verificata

Offanengo, Italia

2 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

Funzione:
_ REGULATORY

Sede:_ Offanengo, Italy
Contratto:_ Full Time

To guarantee the finished products are compliant versus customer and internal expectations, following the regulation applicable on the different countries concerned and watch to its maintenance.

To ensure the regulatory compliance about the finished products.

To perform regulatory checks following Customers Ban list and international regulations regarding customers and internal briefs and requests. To prepare pre-safety assessment and submit them to the safety assessor.

To select external laboratories following liability, prices and delays in order to quote and organize safety and efficacy tests respecting product categories and claims.

To plan, to organize, to gather and to spread safety and efficacy testing

results while helping interpretation of them.

To check finished products labelling regarding the regulation in force

To evaluate PAO and Shelf life of the products.

To gather all documents for safety assessment requests and ask for safety assessment.

To register CPNP notifications where relevant.

To gather all data and documents needed in the Product Information File, OTC reports and specifications for sending to the customers and archive them.

To update Safety assessments, PIF/OTC reports and Specifications for existing products following the regulations in force in the case of change controls.

To follow new developments, answering to customers' requests or local authorities

and gathering complementary data if necessary.

To be regulatory support for customer's registrations and

legalizations.

To ensure Regulatory, scientific and technologic watch for Europe and International countries.

To manage regulatory watch on going topics when necessary.

To participate in building and maintenance of regulatory database.

To ensure that the data entered is accurate and justified to improve data centralization.

Communication - Comunicazione
70% INTERNAL - R&D, Sales, PM, Marketing, Procurement

30% EXTERNAL - Customers, External Labs., Suppliers, Ministery of Health

Education required for the role - Titolo di studio
Bachelor Degree or qualified experience in the position

Foreign Language knowledge - Conoscenza lingue straniere
Good knowledge of English

IT Knowledge - Conoscenza Information Technology
Good level of knowledge of SOP & other IT tools (COPTIS, Pack Office)

Work Experience - Esperienza Lavorativa
3 years of experience in the same role

Knowledge, Skills and Abilities - Altre conoscenze, competenze e abilità
Regulatory Knowledge

Toxicological Knowledge

Project data management ( RM, formula, process)

Rigor/Attention to detail, Adaptability. Collaboration, Organization and Communication skills

Good knowledge of GMP roles

Teamworking

Company equipement management

Respect company policy, safety & quality rules

Tact and Diplomacy

Employee