Global Regulatory Lead

Job OverviewTeva Pharmaceuticals is seeking a talented Global Medicines Regulatory Lead to join our Regulatory Affairs team.As a key member of our team, you will be responsible for developing and implementing regulatory strategies for innovative medicinal products in the EU and globally.Key ResponsibilitiesYou will develop regulatory strategies during...

About the CompanyTeva Pharmaceuticals is a leading manufacturer of generic medicines and specialty pharmaceuticals.We are committed to making good health more affordable and accessible to millions of people around the world.Our company has a long history of innovation, quality, and customer satisfaction, and we are always looking for talented individuals to...

Global Regulatory Compliance SpecialistWe are seeking a highly skilled individual to join our team as a Global Regulatory Compliance Specialist.In this role, you will be responsible for ensuring compliance with all relevant regulations and laws across different regions.Key Responsibilities:To develop and implement regulatory compliance strategies.To...

Role OverviewIn this exciting role, you will have the opportunity to work closely with a dynamic team to contribute to our mission. As a Medicines Regulatory Specialist, you will be responsible for developing regulatory strategies, collaborating with cross-functional teams, and developing your skills in a fast-paced environment. The successful candidate will...

At Lifelancer, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. This mission bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds.The company is working with the worlds leading manufacturer of innovative generic medicines, and the...

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. Our mission is to make good health more affordable and accessible.At Lifelancer, you'll be part of a diverse team working with leading manufacturers of innovative generic medicines. You'll help millions around the world enjoy healthier lives.We're looking for a highly skilled Regulatory...

We are seeking a skilled Regulatory Affairs Manager to join our client, a global leader in generics and biopharmaceuticals, in Harlow. This role offers the opportunity to work on regulatory submissions, post-approval obligations, and product development.Key ResponsibilitiesOwnership of UK/IE Marketing Authorisation Applications for new productsDeliver new...

Job OverviewWe are seeking an experienced Regulatory Affairs Manager Lead to join our Global Regulatory Affairs – Innovative Medicines (Europe) team.About the RoleThis is a key opportunity for a professional with a strong scientific background and European regulatory affairs experience to develop regulatory strategies during development, approval, and...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Leader to join our team in Harlow, UK. As a key member of our Global Regulatory Affairs – Innovative Medicines (Europe) team, you will be responsible for developing regulatory strategies during development, approval, and post-approval phases for submissions to EU Competent Authorities.As a...

A Day in the LifeAs a Manager/Senior Manager in our Global Regulatory Affairs team, you'll play a crucial role in developing key regulatory strategies for Innovative products. You'll work closely with teams covering European and global licensing for medicines and OTC products. Our Centre of Excellence (CoE) for Regulatory Affairs is based in Harlow, where...

Join Our Mission:We're on a journey to improve healthcare outcomes and increase accessibility to high-quality medicines. This Regulatory Affairs Specialist role will play a vital part in achieving our vision.Key Responsibilities:You will be responsible for developing and implementing regulatory strategies, managing complex projects, and building strong...

About UsWe're on a mission to make good health more affordable and accessible. We aim to help millions around the world enjoy healthier lives, united by our shared goal.Our Company Overview:Teva is the world's leading manufacturer of innovative & generic medicines, part of a diverse team from nearly 60 countries.Job Description:This role will focus on...

OverviewTeva Pharmaceuticals is committed to making good health more affordable and accessible to millions of people around the world.We are recruiting for a Manager or Senior Manager - Regulatory Affairs to work within the Global Regulatory Affairs - Innovative Medicines (Europe) team.This role offers a competitive salary of £65,000 - £85,000 per annum,...

About the JobWe are seeking a highly skilled and motivated individual to join our global team as a Medicines Regulatory Specialist. In this role, you will have the opportunity to contribute to our mission by working closely with a dynamic team. The successful candidate will be responsible for developing regulatory strategies, collaborating with...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Director to join our Global Regulatory Affairs – Innovative Medicines (Europe) team at Teva Pharmaceuticals.This is an exciting opportunity to work with key innovative products part of our Pivot to Growth strategy. You will be responsible for developing regulatory strategies during...

Job DescriptionWe are seeking an experienced Regulatory Affairs Manager to join our Global Regulatory Affairs - Innovative Medicines (Europe) team.You will be responsible for developing regulatory strategies during development, approval and post-approval phases for submissions to EU Competent Authorities.The ideal candidate will have a strong scientific...

Data-Driven Decision MakingWe are seeking a skilled Qlik Developer to join our team at PE Global, where you will be responsible for unlocking the value in large and complex datasets. With a strong background in data management and analytics, you will be able to provide high-quality, insightful, and accurate internal and external business performance...

Job DescriptionPE Global is currently recruiting for a Qlik Developer for an initial contract role with a leading multinational Pharma client based in Harlow - hybrid. This position offers the opportunity to unlock the value in the most appropriate datasets, improving business decisions and performance by maintaining in-depth knowledge of relevant databases....

Copello Global invites applications from exceptional individuals to fill the role of Embedded Systems Architect Lead.About UsWe work with cutting-edge technology to deliver complex and high-profile programmes to customers in the UK.Key ResponsibilitiesDefine and perform unit level and subsystem level testing for embedded software.Work alongside our embedded...

Job Title: Regulatory Affairs Expert - Innovative MedicinesEstimated Salary: £70,000 - £90,000 per annum (dependent on experience)Company OverviewLifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. We connect talented professionals with opportunities in these domains.About the RoleWe are seeking an experienced Regulatory Affairs Expert...