Regulatory Medical Document Coordinator

Our pharmaceutical organisation is seeking a Regulatory Documentation Specialist to provide support in preparing regulatory documentation for our global product portfolio.Key responsibilities include:Creating templates for study and regulatory documentation for CMC dossier, R&D reportsGenerating technical reports for regulatory submissions and preparing...

Regulatory Documentation Specialist RoleWe are seeking a meticulous and collaborative individual to provide product documentation, regulation, and compliance information internally and externally.This role requires timely creation, maintenance, and delivery of product documentation, registration, and certifications as well as responding to customer requests...

Key Position: Regulatory SpecialistThe successful candidate will be responsible for providing documentation, regulations, and compliance information to support the business strategy.Respond to queries related to product documentation, regulation, and compliance.Manage external product registration and certification processes.Regularly update databases with...

We are currently seeking a full-time, office based Study Start up Submissions Coordinator Entry to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. If you are interested in an exciting career where you can use your...

Regulatory Affairs SpecialistNavigate the complex landscape of medical devices and make a real difference in healthcare.Develop and implement regulatory strategies for product development and commercialization.Manage conformity planning, technical documentation, and post-market activities.Provide proactive regulatory guidance to cross-functional...

OverviewWe are currently seeking a full-time, office based Study Start up Submissions Coordinator Entry to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. If you are interested in an exciting career where you can use...

OverviewWe are currently seeking a full-time, office based Study Start up Submissions Coordinator Entry to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. If you are interested in an exciting career where you can use...

Document Management SpecialistThis exciting new role will work within the airfield team, supporting and coordinating activities in a highly regulated safety-sensitive working environment.The successful candidate will be instrumental in helping us implement a refreshed document control management system for the airfield, ensuring we meet regulatory...

Job OverviewWe are seeking a highly skilled professional to coordinate reviews and conduct assessments of submissions related to post-market medical device reviews.Key Responsibilities:Coordinate reviews and conduct assessments of submissions in relation to post-market reviews of medical devices.Provide expert advice and recommendations on complex medical...

">Job Overview">As a key member of our Regulatory Affairs team, you will play a critical role in supporting the registration, compliance, and life-cycle management of various products across Prescription Medicines, OTC, Complementary Medicines, Medical Devices, and Cosmetics in Australia and New Zealand.About the Role">Review and prepare quality regulatory...