Emplois actuels liés à Scientific Affairs Specialist for Medical Devices - Courbevoie, Île-de-France - ProductLife Group
-
Scientific Affairs Specialist for Medical Devices
il y a 4 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinJoin Our Team as a Scientific Affairs Associate for Medical DevicesWe are seeking a highly skilled Scientific Affairs Associate to strengthen our self-care medical device division. As a key member of our team, you will play a crucial role in evaluating the efficacy and safety of health products in the European market.In this role, you will work closely with...
-
Scientific Affairs Associate for Medical Devices
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinProductLife Group is seeking a Scientific Affairs Associate for Medical Devices to strengthen our self-care medical device division. This role involves evaluating the efficacy and safety of health products in the European market.As a Scientific Affairs Associate, you will work closely with Senior Consultants in a small dynamic team, overseeing the entire...
-
Scientific Affairs Associate for Medical Devices
il y a 4 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinJob Title: Scientific Affairs Associate for Medical DevicesWe are seeking a highly skilled Scientific Affairs Associate for Medical Devices to join our team at ProductLife Group. As a key member of our self-care medical device division, you will play a crucial role in evaluating the efficacy and safety of health products in the European...
-
Scientific Affairs Associate for Medical Devices
Il y a 2 mois
Courbevoie, Île-de-France ProductLife Group Temps pleinJoin Our Team as a Scientific Affairs Associate for Medical DevicesWe are seeking a highly skilled Scientific Affairs Associate to strengthen our self-care medical device division at ProductLife Group. As a key member of our team, you will play a crucial role in evaluating the efficacy and safety of health products in the European market.Key...
-
Scientific Affairs Expert for Medical Devices
il y a 4 jours
Courbevoie, Île-de-France ProductLife Group Temps pleinTo strengthen our medical device division, we are seeking a Scientific Affairs Expert for Medical Devices to evaluate the efficacy and safety of health products in the European market.This role involves working closely with Senior Consultants to oversee the life cycle of self-care medical device development, from conception to European registration.Self-care...
-
Scientific Affairs Associate for Medical Devices
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinAt ProductLife Group, we are seeking a highly skilled Scientific Affairs Associate for Medical Devices to strengthen our self-care medical device division. This role involves evaluating the efficacy and safety of health products in the European market, working closely with Senior Consultants in a dynamic team.The ideal candidate will have experience in...
-
Scientific Affairs Associate for Medical Devices
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinStrengthen our self-care medical device division by joining our team as a Scientific Affairs Associate for Medical Devices with experience in evaluating the efficacy and safety of health products in the European market.In this role, you'll work closely with Senior Consultants in a small dynamic team, overseeing the entire life cycle of self-care medical...
-
Scientific Affairs Associate for Medical Devices
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinTo strengthen our self-care medical device division, ProductLife Group is seeking a Scientific Affairs Associate for Medical Devices with experience in evaluating the efficacy and safety of health products in the European market.In this role, you'll work closely with Senior Consultants in a small dynamic team, overseeing the entire life cycle of self-care...
-
Regulatory Affairs Specialist
Il y a 2 mois
Courbevoie, Île-de-France ProductLife Group Temps pleinAbout the JobWe are seeking an experienced Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our Regulatory Affairs team, you will play a crucial role in the implementation of our regulatory strategy for the development and registration of oncology projects.ResponsibilitiesProvide regulatory support for all requests...
-
Courbevoie, Île-de-France ProductLife Group Temps pleinAbout the JobWe are seeking an experienced Regulatory Affairs Specialist to contribute to the implementation of our regulatory strategy for the development and registration of oncology projects.ResponsibilitiesDevelop and implement regulatory strategies for oncology products, evaluating local and global options.Contribute to the development and registration...
-
Regulatory Affairs Specialist
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinAbout the JobWe are seeking an experienced Regulatory Affairs Specialist to contribute to the implementation of our regulatory strategy for the development and registration of oncology projects. In this role, you will be responsible for regulatory referrals, developing regulatory strategies, and participating in the construction of global development...
-
Regulatory Affairs Specialist
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinAbout the JobWe are seeking an experienced Regulatory Affairs Specialist to contribute to the implementation of our regulatory strategy for the development and registration of an oncology project. The successful candidate will be responsible for regulatory referrals, developing regulatory strategies, and contributing to the construction of global development...
-
Regulatory Affairs Specialist
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinAbout the JobWe are seeking an experienced Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our Regulatory Affairs team, you will play a crucial role in the implementation of our regulatory strategy for the development and registration of oncology projects.ResponsibilitiesProvide regulatory referrals for all requests...
-
Regulatory Affairs Specialist
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinAbout the JobWe are seeking an experienced Regulatory Affairs Specialist to contribute to the implementation of our regulatory strategy for the development and registration of oncology projects.ResponsibilitiesRegulatory referral for all requests concerning products under responsibility.Develops regulatory strategy for products by evaluating local and global...
-
Regulatory Affairs Specialist
il y a 1 semaine
Courbevoie, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistThe ProductLife Group is seeking a skilled Regulatory Affairs Specialist to coordinate and manage the Linguistic Review for Centralized products of one of our key clients.About usGroup 10 ResponsibilitiesCoordinate and manage the Labelling team in charge of the Linguistic Review for the products of one of our key...
-
Regulatory Affairs Specialist
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our team, you will be responsible for coordinating and managing the Linguistic Review process for Centralized Procedure medicinal products.About the RoleThe successful candidate will have a strong background in...
-
Regulatory Affairs Specialist
il y a 1 mois
Courbevoie, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally.Key...
-
Regulatory Affairs Specialist
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinWe are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally (internationally).Key Responsibilities:Submission...
-
Regulatory Affairs Specialist
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to coordinate and manage the Linguistic Review process for Centralized Procedure medicinal products. The ideal candidate will have a strong background in regulatory labelling procedures and excellent project coordination skills.Key Responsibilities:Coordinate and...
-
Regulatory Affairs Specialist
il y a 3 semaines
Courbevoie, Île-de-France ProductLife Group Temps pleinWe are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company, ProductLife Group. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally.Responsibilities:Prepare and...
Scientific Affairs Specialist for Medical Devices
Il y a 2 mois
To strengthen our self-care medical device division, ProductLife Group is seeking a Scientific Affairs Associate for Medical Devices with experience in evaluating the efficacy and safety of health products in the European market.
Key Responsibilities- Evaluate scientific, clinical, and toxicology data to extract pivotal efficacy and safety information while assessing study quality.
- Conduct systematic and well-documented literature searches utilizing reputable databases (e.g., PubMed, Cochrane, Science Direct, Medline, Cosmed).
- Perform risk assessments based on clinical, scientific, and toxicology data.
- Collaborate with Senior Consultants to integrate literature search and evaluation outcomes into self-care medical device development strategies.
- Provide recommendations to address data gaps, ensuring robust evidence to support medical device products (e.g., clinical trial planning, endpoint development, toxicological testing, additional literature searches).
- Contribute to the writing of scientific, clinical, and biocompatibility reports compliant with medical device guidelines (e.g., MEDDEV 2.7/1, MDCG, ISO standards).
- Contribute to writing sections of medical device technical files for the EU as per MDR 2017/745 (e.g., Clinical Evaluation Report, Biocompatibility, Post Marketing Clinical Follow Up, Usability, Risk Assessments, and more).
- Facilitate coordination between clients and European laboratories for scientific testing.
- Identify and interpret relevant regulatory guidelines, particularly MDR 2017/745 Regulations.
- Participate in client calls to present findings and address questions.
- Degree in Science, Toxicology, Pharmacy, Chemistry, Medical Sciences, Biomedical Sciences
- Experience with European & UK medical device regulations.
- 2+ years demonstrated experience
- Proficiency in the use of MS Office, specifically Word, PowerPoint, and Excel.
- Ability to work independently with minimal supervision, and as part of a team.
- Desired qualities: autonomy, flexibility, communication, technical writing, team mindset.
