+Rekrutacja · Dyrektor ds. Spraw Regulacyjnych · GSK istnieje od 2008 roku i ma siedzibę w Gdańsku. · +Zakres obowiązków · - Rozwijanie strategii regulacyjnych dla produktów farmaceutycznych; · - Pracowanie nad projektem Farmakopea Polska XIII; · +KwalifikacjeKandydat powinien mi ...

We are looking for a Regulatory Affairs professional to join our team. The role involves registration activities, maintaining the QMS and liaising with suppliers. · ...

The role holder will lead a team responsible for setting the strategic framework to manage monitoring identifying interpreting and communicating of new and updated product regulation in global markets excluding US. · This role will manage partnerships with key internal and extern ...

Regulatory Affairs Specialist is responsible for leading global regulatory and safety strategy for Air Care products. The role involves representing the Regulatory function in cross-functional teams, overseeing global registration and notification processes, partnering with count ...

Job summaryIn this role your key responsibility is to maintain regulatory compliance obligations to international regulations and organisation of related technical documentation. · ...

An exciting opportunity has arisen for an experienced Regulatory Affairs Executive to join a busy and collaborative pharmaceutical regulatory team. · This role will see you managing a varied portfolio of UK licences, · taking ownership of submissions and ensuring ongoing complian ...

An exciting opportunity has arisen for an experienced Regulatory Affairs Executive to join a busy and collaborative pharmaceutical regulatory team. · ...

++Cure Talent are delighted to be partnered with a medical device manufacturer as they look to strengthen their Regulatory Affairs capability. We have an exciting opportunity for a Regulatory Affairs Specialist to join an established regulatory team and support international mark ...

An exciting opportunity to join an established and growing IVD manufacturer. · Preparing and compiling regulatory documentation · Coordinating and executing regulatory submissions in compliance with ISO13485, · IIVD2017/746 Regulation,FDA21 Code of Federal Regulations (CFRs),Biol ...

Job summary As part of our next phase of growth, we are seeking an experienced Regulatory Affairs Specialist to join the business as a partner... · ...

SRG are recruiting a Regulatory Affairs Training Manager to support the rollout and ongoing adoption of Veeva RIM within a global pharmaceutical organisation. · ...

The role is accountable for undertaking a variety of regulatory activities across a range of products and licensing routes for the UK market including developing regulatory strategy and contributing to regulatory filing activities and documentation. Ensures regulatory strategies ...

At Johnson & Johnson, we are committed to addressing and solving some of the most meaningful unmet medical needs through creating an environment where our employees feel valued and can reach their potential. · ...

We have partnered with a specialist CRO who are looking to hire a Regulatory Affairs Associate to join them on a permanent basis.We are looking for an experienced and talented · Risk Management Consultant to help us develop our risk management function. · ...

We are currently seeking a talented Regulatory Affairs Consultant to join our dynamic team. · ...

This is a part-time position as Regulatory Affairs Consultant. The consultant will oversee regulatory compliance processes and manage regulatory submissions. · ...

An exciting opportunity has arisen for an experienced Regulatory Affairs Executive to join a busy and collaborative pharmaceutical regulatory team. · Managing and maintaining your own licence portfolio · Preparing high-quality regulatory submissions with a strong first-time appro ...

A leading medical device manufacturer based in South Wales is seeking a Regulatory Specialist to join its Regulatory Affairs team. · This is an excellent opportunity to be part of a growing, multinational organisation with a diverse portfolio of medical devices marketed globally. ...

The client is a leading organisation in the healthcare and diagnostics sector committed to delivering innovative solutions and maintaining the highest standards of regulatory compliance. · This is an exciting opportunity to work in a fast-paced environment where your expertise wi ...

Maintain regulatory compliance obligations to international regulations and organisation of related technical documentation. · ...

Job summary · Joining Thermo Fisher Scientific means engaging in meaningful work that positively affects the world.The purpose of this role is to increase market access for Microbiology Division's (MBD) clinical IVD products through successful pre-market licenses, renewals, and s ...