Regulatory Affairs Specialist

**Job Overview**We are seeking a highly motivated Clinical-Regulatory Program Manager to join our team at Compremium AG. As a key member of our regulatory affairs team, you will be responsible for ensuring the compilation of pre-submission and submission packages, preparing pivotal clinical trials, and supporting continuous interaction with regulatory...

**Job Title:**We are seeking a talented Clinical-Regulatory Program Manager to join our team at Compremium AG. The successful candidate will have a strong background in clinical and regulatory affairs within the medical device sector and experience in regulatory approval pathways with FDA and EU notified bodies.About Our Culture:Compremium AG is a dynamic...

We are seeking an experienced professional to lead our team in developing regional strategies for the Cardio-Renal Therapeutic Area within the Intercontinental (ICO) Region.Main Responsibilities:Develop and implement regional regulatory strategies, ensuring compliance with CSL's Global Policies and Business Process Framework.Serve as a Subject Matter Expert...

Career Development Opportunities: CSL is seeking a highly motivated professional to fill the role of Regional TA Lead in the Intercontinental (ICO) Region. This key position requires the development and implementation of regional strategies for the Cardio-Renal Therapeutic Area, while ensuring compliance with relevant regulations and...

Job Description:The ideal candidate will be responsible for evaluating and ensuring that products adhere to industry standards, regulatory requirements, and compliance best practices. This includes collaborating cross-functionally with teams across production, development, supply chain, and more to drive compliance initiatives forward.Responsibilities also...

**Job Description:**We are looking for a highly skilled Clinical-Regulatory Program Manager to join our team at Compremium AG. The ideal candidate will have a strong background in clinical and regulatory affairs within the medical device sector and experience in regulatory approval pathways with FDA and EU notified bodies.About Our Mission:Compremium AG is a...

Job OverviewCompremium is seeking a skilled and highly motivated Clinical-Regulatory Program Manager to join our team. The ideal candidate will have a strong background in clinical and regulatory affairs within the medical device sector and experience in regulatory approval pathways with FDA and EU notified bodies. The successful candidate will ensure the...

Join us at CSL in this exciting opportunity to leverage your expertise in regulatory affairs and contribute to the success of our team. As a Regional TA Lead in the Intercontinental (ICO) Region, you will develop and execute regional strategies for the Cardio-Renal Therapeutic Area.Key Responsibilities:Lead the development of regional regulatory strategies...

Career OpportunitiesWe are looking for a Trade Compliance Director to join our EMEA Supply Chain team. As a seasoned professional, you will be responsible for leading our global trade compliance program and ensuring that all CSL entities operating worldwide are compliant with applicable customs and trade regulations.Your key objectives will include:Ensuring...

Career Opportunities at CSL: We're looking for a highly skilled professional to join our team as a Regional TA Lead in the Intercontinental (ICO) Region. The successful candidate will be responsible for developing and implementing regional strategies for the Cardio-Renal Therapeutic Area.About This Role:Regulatory Affairs LeadTeam LeadershipStrategic...

Forschungs- und Lehrassistent:in gesuchtDie Professur für Regulatory Affairs sucht eine/n Hilfsassistent:in zur Unterstützung in den Bereichen Forschung und Lehre sowie in administrativen Angelegenheiten. Besonders geeignet sind Studierende mit einem Interesse an interdisziplinärer Zusammenarbeit und dem schweizerischen Gesundheitswesen.

Key Responsibilities:Represent risk management in audits conducted by Notified Bodies, Competent Authorities, and pharma-customersCollaborate with development, usability engineering, and production teams to ensure effective communication and information flowAssist project and product management teams to implement risk control measuresContribute to the...

About the RoleAs a Medical Device Risk Management Specialist at CSL, you will play a crucial role in ensuring the safety and efficacy of our medical devices. Your primary responsibility will be to develop and implement risk management strategies that comply with relevant regulatory standards.You will represent risk management during audits conducted by...

**Job Summary:**We are seeking a skilled Clinical-Regulatory Program Manager to join our team at Compremium AG. The successful candidate will have a strong background in clinical and regulatory affairs within the medical device sector and experience in regulatory approval pathways with FDA and EU notified bodies.About Our Company:Compremium AG is a...

Oxford Global Resources is seeking a skilled Laboratory Equipment Acquisition Specialist to support the end-to-end acquisition process of laboratory equipment in a GxP-regulated environment. This role offers a great entry point into quality excellence, validation, and lab management.Responsibilities:Support the procurement of laboratory instruments, ensuring...

Cross Border Talents is looking for a highly skilled and motivated individual to fill the role of a Lisbon-Based Content Review Specialist. As a Content Review Specialist, you will play a vital part in maintaining a safe and secure online environment by reviewing user-generated content.This role requires a strong understanding of content policies and the...

At ITech Consult AG, we are seeking a highly skilled IT Business Analyst to join our team as an IT Product Compliance Specialist - Financial Services. This role involves working with global customers and market material compliance requirements for Comet PCT products.The ideal candidate will have a degree in material science, electrical/chemical engineering,...

We are seeking a skilled Mechanical Equipment Specialist to join our team at Proclinical. As a key member of our team, you will be responsible for maintaining, qualifying, and calibrating modern machinery within the pharmaceutical sector.The ideal candidate will have experience working with complex mechanical equipment, possess strong technical knowledge,...

Job ResponsibilitiesEvaluate and ensure that products adhere to industry standards, regulatory requirements, and compliance best practices.Collaborate cross-functionally with teams across production, development, supply chain, and more to drive compliance initiatives forward.Oversee laboratory tests to validate product conformity, ensuring standards are met...

Job Description:We are seeking a highly skilled and motivated Medical Scientific Liaison to join our team at Healthcare Businesswomen's Association. In this role, you will be responsible for developing and maintaining strong relationships with medical experts in the field of healthcare.Key Responsibilities:Relationship Building: Establish and maintain...