Regulatory Affairs Specialist
6 giorni fa
The resource, within Corporate Quality Assurance team, will ensure that a company's products are compliance with national and international regulations:
**Main Activities**:
- Monitor the developments of regulatory projects applicable to the products and keep up to date with national and international legislation, guidelines and customer practices
- Budgeting Formulation necessary to cover the regulatory obligations required and to identify the necessary resources and workloads
- Provide answers to customers and dialogue with them about products' normative and regulatory needs
- Training activities on regulatory policies or procedures
- Consult materials such as marketing literature or user manuals to ensure that regulatory agency requirements are met
- Contribute to the development or implementation of business unit strategic and operational plans
- Represent organizations before national or international regulatory agencies on related to the company's products and management of audit activities
- Within the Compliance team, collaborates with colleagues in order to ensure the correct management of the activities necessary to acknowledge the compliance achieved.
**Skills**:
- Enabling for Auditor activity
- Knowledge of current certifications and regulatory standard
- Fluency in English
- Team Work
- Proactivity
- Problem Solving
- Accuracy, planning, organization, excellent interpersonal and communication skills
**Education**:
- Technical or Scientific degree
**About us**:
Bormioli Pharma operates in a very close partnership with the pharmaceutical industry and all the companies that are shaping the future of healthcare.
An acknowledged world leader in the packaging sector, Bormioli Pharma serves the pharmaceutical and biopharmaceutical market with an integrated offer of bottles, closures and accessories, using advanced materials and technologies.
Being part of Bormioli Pharma means working in a stimulating environment, where innovation is at home and where every talent can express itself to the best of its potential thanks to the mix of skills guaranteed by the different professionalism employed. An environment where passion and commitment shine, and where initiative, proactivity, autonomy and flexibility are promoted.
**Equal Employees Opportunity**
In Bormioli Pharma we strongly believe in inclusiveness and diversity as an enrichment factor.
**Personnel search and selection agencies**
It is permitted to download and/or copy parts of the content of the advertisements related to open positions for personal and non-commercial use only, in particular it is prohibited to i) modify or alter the content in any way and ii) distribute, modify, transmit, reuse, republish or use the text, image and video for public or commercial purposes without prior written authorization obtained from Bormioli Pharma S.p.a..
-
Eu Regulatory Affairs Manager, Rare Diseases
4 giorni fa
Parma, Italia Chiesi Farmaceutici A tempo pieno**Date**:8 Oct 2025 **Department**:GRD Regulatory Affairs **Business Area**:R&D, Pharmacovigilance & Regulatory Affairs **Job Type**:Direct Employee **Contract Type**:Permanent **Location**:Parma, IT **_About us_** - Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience,...
-
Eu Regulatory Affairs Manager, Rare Diseases
7 giorni fa
Parma, Italia Chiesi Farmaceutici A tempo pienoAbout us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years' experience, operating in 31 countries with more than 7,000 employees (Chiesi Group).To achieve its mission of improving people's quality of life by acting responsibly towards society and the environment, the Group researches,...
-
Parma-Based Technical Regulatory Manager, Italy
6 giorni fa
Parma, Italia Barilla Group A tempo pienoA leading food company in Parma is seeking a Technical Regulatory Manager to oversee food regulatory matters. The role requires a Master's degree and 5 years of experience in the food industry, with a focus on regulatory affairs. The successful candidate will collaborate with internal teams and external experts, ensuring compliance with regulations and...
-
Parma, Italia Lincotek Group A tempo pienoCompany DescriptionLincotek,headquartered in Rubbiano, Parma, Italy, is a global contract manufacturer for services in markets including Industrial Gas Turbines, Aerospace and Medical Device applications, as well as a leading manufacturer of industrial coating equipment and one of the most respected producers in the Additive Manufacturing field....
-
Parma, Italia Lincotek Group A tempo pienoCompany Description Lincotek,headquartered in Rubbiano, Parma, Italy, is a global contract manufacturer for services in markets including Industrial Gas Turbines, Aerospace and Medical Device applications, as well as a leading manufacturer of industrial coating equipment and one of the most respected producers in the Additive Manufacturing field. The...
-
Technical Regulatory Manager Italy
2 giorni fa
parma, Italia Barilla Group A tempo pienoAt Barilla, we believe that every great journey begins with passion and a bold vision. From our humble beginnings in 1877 in a small shop in Parma, Italy, we’ve blossomed into a global leader in the food industry, guided by our commitment to progress and excellence.Today, Barilla is an international group present in more than 100 countries and we are proud...
-
QA - QA Specialist
2 settimane fa
parma, Italia LAMP SAN PROSPERO S.P.A. A tempo pienoQA- QA Specialist – LAMP San Prospero (MO)Località: San Prospero (Modena)Contratto: Tempo pieno – inserimento strutturato con percorso di crescitaSettore: Industria farmaceutica – CDMOLingue richieste: Italiano, IngleseChi siamoSiamo un Contract Development Manufacturing Organization (CDMO) leader nel Settore Farmaceutico, specializzati nella...
-
Director / Senior Director, Project Management
6 giorni fa
Parma, Italia Chiesi Farmaceutici S.p.A. A tempo pienoSenior Director, Global Patient Safety Science Department: Global Regulatory Affairs & Patient Safety Business Area: R&D, Pharmacovigilance & Regulatory Affairs Contract Type: Permanent Everywhere in Europe, IT Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 90 years’ experience,...
-
Legal specialist
1 giorno fa
Parma, Italia Bonatti A tempo pienoWe are looking for a Legal Specialist to join our Legal Department in ParmaThe successful candidate will be responsible for providing comprehensive legal support to the company and its group across a range of activities, with a particular focus on corporate governance, group corporate structure management and regulatory compliance.He/She will play a key role...
-
Legal Specialist
1 giorno fa
Parma, Italia Bonatti A tempo pienoWe are looking for a Legal Specialist to join our Legal Department in Parma The successful candidate will be responsible for providing comprehensive legal support to the company and its group across a range of activities, with a particular focus on corporate governance, group corporate structure management and regulatory compliance. He/She will play a key...