Global Regulatory Lead Jobs in Camberley

Blackfield Associates - Slough, United Kingdom (+1 location)

Develop and drive the implantation of both regional and global regulatory strategies for a broad portfolio, including premarket and marketed/ established products Minimum 10 years of experience in regulatory...

from: uk.lifeworq.com (+2 sources) - 4 days ago

farnborough, england, United Kingdom

Conduct and lead user research, usability testing (formative and summative), task analysis, and risk assessments (usability FMEA), and generate documentation for regulatory submissions (FDA, EU-MDR, CMDE)...

from: jobleads.co.uk - 3 days ago

slough, england, United Kingdom

Serve as the Regulatory point of contact on the assigned projects with senior management and/or at other internal meetings providing the agreed global regulatory strategic recommendations, aligned timelines...

from: jobleads.co.uk - 15 days ago

Complete Regulatory | An IPG Health Company - Woking, United Kingdom (+7 locations)

We are seeking experienced Senior Regulatory Writers to join our growing team. You’ll play a key role in writing and reviewing a broad range of regulatory documents, with a particular focus on strategic...

from: uk.lifeworq.com (+1 source) - Yesterday

Bracknell, England, United Kingdom

The Senior Director, Global Regulatory Affairs (GRA)-EMEA or Regional Regulatory Scientist is accountable to establish the local regulatory strategy and plan for assigned product(s) in region/country,...

from: jobleads.co.uk - 6 days ago

Life Sciences Recruitment - Woking, United Kingdom (+7 locations)

As one of the most competitive and fast-paced industries globally, succeeding and growing in the life sciences business requires a combination of creativity, technical expertise, and business savvy. At...

from: uk.lifeworq.com (+1 source) - 25 days ago

Warman O'Brien - Slough, United Kingdom

This is a unique opportunity to shape and support regulatory strategy across unlicensed medicines, clinical trials, and commercial access programs. You’ll act as a central source of intelligence, keeping...

from: uk.lifeworq.com (+1 source) - Yesterday

STADA Arzneimittel AG - Reading, United Kingdom

The post-holder is accountable for global execution and delivery of assigned studies across therapy areas to time, budget and quality as defined in the study protocol; in accordance with local regulations... Competitive

from: newscientist.com (+2 sources) - 6 days ago

Arevna - Windsor, United Kingdom

Ensure the company’s Quality Management System and product documentation meet MDSAP audit requirements across applicable markets (e.g., US, Canada, Australia, Brazil, Japan). Knowledge of international...

from: uk.lifeworq.com (+1 source) - 5 days ago

Warman O'Brien - Slough, United Kingdom

This is not your average regulatory position. You’ll be working across a broad spectrum of regulatory pathways - from Expanded Access Programs (EAPs) and Named Patient Programs to Compassionate Use and...

from: uk.lifeworq.com (+1 source) - Yesterday