Pharmaceutical Labeling Expert
il y a 6 jours
Key Responsibilities
- Coordinate and manage the Labelling team in charge of the Linguistic Review for the products of one of our key clients
- Contribute to labelling related regulatory activities related to the Linguistic Review process for Centralized Procedure (CP) medicinal products
- Manage the relationship with the Translation partner and manage the translation tool to facilitate the review and coordination of Linguistic Review processes with internal and external stakeholders
- Provide ongoing support to the project teams to ensure project concerns are planned and accounted for
Requirements
- At least a Bachelor's Degree in Life Sciences. Ideally a Pharmacy Degree (PharmD)
- At least 1-2 years' experience in Regulatory Labelling Operations in a Pharmaceutical Company or Service Provider
- Good knowledge of regulatory labelling procedures
- Experience in Project Coordination/Management
- Good IT skills/knowledge and the ability to learn appropriate softwares
- Fluent English is mandatory, including excellent grammar skills (written and verbal fluency)
-
Global Labelling Strategist
il y a 6 jours
Paris, Île-de-France Cpl Healthcare Temps pleinJob Description:We are looking for a Global Labelling Strategist to join our team at Cpl Healthcare. As a key member of our regulatory affairs team, you will be responsible for developing and implementing global labelling processes for our pharmaceutical products.Key Responsibilities:Develop, implement and operate global labelling processes for a...
-
Head of Global Labeling Strategy
il y a 3 semaines
Paris, Île-de-France Cpl Healthcare Temps pleinJob Title: Head of Global LabelingJob Type: Full-time permanent positionLocations: UK, France, Germany, Ireland, Netherlands, Norway, and the United States of America (Remote)Remuneration: Competitive salary and benefits packageAbout the RoleWe are seeking a highly experienced and skilled Head of Global Labeling to join our team at Cpl Healthcare. As a key...
-
Regulatory Compliance Expert
il y a 6 jours
Paris, Île-de-France Cpl Healthcare Temps pleinJob Summary:We are seeking a highly experienced Regulatory Compliance Expert to join our team at Cpl Healthcare. As a key member of our regulatory affairs team, you will be responsible for providing expert regulatory knowledge and strategy to the business regarding healthcare industry regulatory requirements.Key Responsibilities:Implement and manage...
-
Pharmaceutical Manufacturing Automation Expert
il y a 6 jours
Paris, Île-de-France Auto Strunk Temps pleinPharmaceutical Manufacturing Automation ExpertWe are looking for a highly skilled Pharmaceutical Manufacturing Automation Expert to join our team at Auto Strunk. The ideal candidate will have a strong background in automation engineering and experience with iFix systems.Key Responsibilities:Design and develop automation systems for pharmaceutical...
-
Regulatory Affairs Director
il y a 1 semaine
Paris, Île-de-France Cpl Healthcare Temps pleinCpl Healthcare is seeking a highly experienced Regulatory Affairs professional to join our team as a Head of Compliance. This is a fantastic opportunity to provide expert regulatory knowledge and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations, and post-market compliance....
-
Pharmaceutical Safety Expert
il y a 6 jours
Paris, Île-de-France Healthcare Businesswomen's Association Temps pleinJob OverviewWe are seeking a highly skilled Country Patient Safety Head to join our team at the Healthcare Businesswomen's Association. As a key member of our organization, you will be responsible for establishing and driving Patient Safety (PS) strategy and operational excellence at the country level.Key Responsibilities:Collaborate with the global patient...
-
Pharmaceutical Development and Manufacturing Expert
il y a 6 jours
Paris, Île-de-France Adragos Pharma GmbH Temps pleinAbout UsAdragos Pharma is a dynamic and ambitious Contract Development and Manufacturing Organization (CDMO) in the pharmaceutical industry, private equity backed and focused on drug products. Our mission is to provide innovative solutions for the development and manufacturing of small molecule drugs, enhancing the health and well-being of patients...
-
Head of Regulatory Affairs
il y a 6 jours
Paris, Île-de-France Cpl Healthcare Temps pleinJob Title: Head of Regulatory AffairsJob Summary:We are seeking a highly experienced Head of Regulatory Affairs to join our team at Cpl Healthcare. As a key member of our regulatory affairs team, you will be responsible for providing expert regulatory knowledge and strategy to the business regarding healthcare industry regulatory requirements.Key...
-
Pharmaceutical Process Specialist H/F
Il y a 2 mois
Paris, Île-de-France PAGE PERSONNEL Temps pleinPosition: Pharmaceutical Process SpecialistPAGE PERSONNEL, a prominent player in the pharmaceutical industry, is seeking a Pharmaceutical Process Specialist to enhance their operational capabilities.Key Responsibilities:Formulate the validation framework, evaluate potential risks, and ensure compliance with quality and regulatory standards.Leverage...
-
Pharmaceutical Qualification Validation Assistant Intern
Il y a 2 mois
Paris, Île-de-France Spie Temps pleinMission:Validate technical solutions for training materials.Revise existing training materials.Create new training materials and quizzes.Collaborate with technical experts to improve materials.Stay updated on regulatory changes.Profile:Spie is seeking a student in engineering studies with an interest in the pharmaceutical industry for a 1-2 month internship....
-
Pharmaceutical Sales Representative H/F
Il y a 2 mois
Paris, Île-de-France Michael Page Temps pleinJob Title: Pharmaceutical Sales RepresentativeCompany: Michael PageAs a key player in the commercial strategy, you will report directly to the Regional Director and take charge of driving the growth of your designated area. Your primary focus will be on promoting a diverse range of pharmaceutical products to pharmacies.Main Responsibilities:Engage in...
-
Pharmaceutical Sales and Business Development Expert
il y a 6 jours
Paris, Île-de-France Adragos Pharma GmbH Temps pleinKey ResponsibilitiesAs a Senior Business Development Manager at Adragos Pharma GmbH, you will be responsible for:Creating and implementing sales strategies to acquire new clients.Managing key account relationships to drive sustainable growth.Identifying and capturing new business opportunities.Collaborating with operations and manufacturing teams to ensure...
-
Regulatory Affairs Specialist
il y a 6 jours
Paris, Île-de-France Groupe ProductLife Temps pleinJob SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Groupe ProductLife. The successful candidate will be responsible for coordinating and managing the Linguistic Review process for Centralized Procedure medicinal products.Key ResponsibilitiesCoordinate and manage the Labelling team in charge of the Linguistic Review...
-
Linguistic Review Coordinator
il y a 6 jours
Paris, Île-de-France Groupe ProductLife Temps pleinWe are looking for a skilled Linguistic Review Coordinator to join our team at Groupe ProductLife. The successful candidate will be responsible for ensuring and coordinating the Linguistic Review (LR) for the Centralized products of one of our key clients.Key ResponsibilitiesCoordinate and manage the Labelling team in charge of the Linguistic Review for the...
-
Data Engineer
il y a 18 heures
Paris, Île-de-France emagine Consulting Temps pleinJob Overview:We are seeking a skilled Data Engineer to join our team at emagine Consulting. The ideal candidate will have experience with creating and maintaining ELT/ETL pipelines on cloud infrastructure, data operations, and programming languages like Python and SQL.Key Responsibilities:Design and implement data pipelines on cloud infrastructureDevelop and...
-
Scientific Translator Regulatory Affairs Specialist
il y a 1 semaine
Paris, Île-de-France Groupe ProductLife Temps pleinJob Title:Regulatory Affairs Officer / Linguistic Review CoordinatorJob Summary:We are seeking a highly skilled Regulatory Affairs Officer / Linguistic Review Coordinator to join our team. The successful candidate will be responsible for ensuring and coordinating the Linguistic Review for Centralized products of one of our key clients.Key...
-
Senior Project Manager
il y a 6 jours
Paris, Île-de-France HR One Group Temps pleinJob SummaryWe are seeking a seasoned Senior Project Manager to lead our efforts in pharmaceutical innovations. The successful candidate will oversee a diverse portfolio of intellectual property rights, ensuring seamless project implementation and meeting defined deliverables.Key ResponsibilitiesInfluential recommendations to Senior Management on TPPs, new...
-
Quality Assurance Officer
il y a 1 mois
Paris, Île-de-France Audensiel Temps pleinAbout Audensiel HealthcareAudensiel Healthcare is a young innovative company that brings expertise and responsiveness to its customers in the Pharmaceutical, Biotechnology, and Medical Devices sectors.Our MissionWe contribute to the improvement of our customers' productivity through complementary business expertise: Engineering and new works, Commissioning,...
-
Quality Assurance Officer
il y a 3 semaines
Paris, Île-de-France Audensiel Temps pleinAbout Audensiel HealthcareAudensiel Healthcare is a young innovative company that brings expertise and responsiveness to its customers in the Pharmaceutical, Biotechnology, and Medical Devices sectors.Our MissionWe contribute to the improvement of the productivity of our customers through complementary business expertise: Engineering and new works,...
-
Scientific Translator
il y a 3 semaines
Paris, Île-de-France Groupe ProductLife Temps pleinRegulatory Affairs Officer / Linguistic Review CoordinatorWe are seeking a highly skilled Regulatory Affairs Officer / Linguistic Review Coordinator to join our team at Groupe ProductLife. The successful candidate will be responsible for ensuring and coordinating the Linguistic Review (LR) for Centralized products of one of our key clients.Key...