Regulatory Affairs Jobs in Lincolnshire Eng

As an Associate Director / Director Global Medical Affairs at Theramex you will be a critical member of the Global Medical Affairs team setting strategic direction and leading the development and implementation of bestinclass Medical Affairs plans across our Womens Health Osteoporosis portfolio.You...

Were looking for a Regulatory Affairs Consultant to help us shape and deliver our regulatory strategy across the this role youll collaborate with colleagues at all levels and play a key part in maintaining transparent constructive relationships with our regulators. If youre proactive detailfocused...

Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies in-depth regulatory know-how manufacturing and process development help our customers to safeguard nutrition health and infrastructure efficiently through chemistry and biotechnology that enhanc...

DescriptionJoin our Control Management team as a Vice President within Securities this dynamic role you will be at the forefront of managing the risk and control framework for Trading Services including Agency Securities Finance Margin Services and Tri-Party. As a key member of the Control Manageme...

There has never been a more exciting time to join Wirral Council. Weve got ambitious targets to meet and to achieve everything we have promised to our residents we need people who are ready to deliver the very best for our communities and show how they can #BeTheDifference. Our vision is to secure t...

Were building a relationship-oriented bank for the modern world. We need talented passionate professionals who are dedicated to doing whats right for our clients.At CIBC we embrace your strengths and your ambitions so you are empowered at work. Our team members have what they need to make a meaningf...

DescriptionDiscover yourself in Lewisham where what you do makes a difference to our vibrant and culturally diverse communities!We have a rich history of welcoming people from all over the world and are proud to be recognised as the UKs first Borough of Sanctuary for our work in championing the righ...

Company OverviewAt GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to tran...

Head of Regulatory ServicesWhat we offer youPermanent Full-Time OpportunitySalary: Commencing at $196312.00 Super vehicle package availableFlexible Working Arrangements: Hybrid work options and flexible hoursAdditional Benefits:Leadership development programs wellbeing initiatives and generous lea...

About the roleThis role is responsible for acting as a Qualified Person (QP) under UK and EU regulatory frameworks ensuring that medicinal products released to the UK and EU markets fully comply with GMP Marketing Authorisations and applicable legislation. Reporting to the Quality Leadership Group i...

Arxada is a pioneering leader with a powerful legacy of more than 120 years in creating specialty chemicals and solutions that enhance the performance of our customers and their products. Our solutions expertise and support enable our customers to be more efficient more effective and more sustainabl...

You will manage CMC (Chemistry Manufacturing and Controls) regulatory projects for a portfolio of devices (standalone and all types of drug-device combinations). You will work closely with colleagues across supply technical quality and local operating companies. We value clear thinkers who build str...

Qualified Person (QP) Pharmaceutical Manufacturing & QualityIndustry: Global Pharmaceuticals / Life SciencesLocation: London United Kingdom (On-site / Manufacturing & Corporate Quality Office)Type: Full-Time PermanentSalary Band:BenefitsExperience Level: Senior (815 Years)The Role (Why This Exists)...

In collaboration with line manager and/or Area Product Lead is responsible for implementation of registration strategy to ensure the regulatory approval of commercially successful pharma products in the Europe region. Is responsible for ensuring effective product maintenance and lifecycle management...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee youll be part of a continually growing organization working alongside e...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

CK Group are recruiting for a Labelling Manager to join a company in the pharmaceutical industry on a contract basis for 12 months. This is a hybrid role 50% office working at the clients site in Tadworth. Salary: 30.27 ph PAYE or 39.18 ph via Umbrella Labelling Manager Role:Produces labelling-rela...

The Head of Clinical Data Management is a strategic leadership role responsible for ensuring the integrity quality and timely delivery of all clinical trial data across our oncology portfolio. This individual will provide expert leadership and direction for data management activities from study star...

DescriptionThe Micro:bit Educational Foundation is seeking an outstanding Product Compliance and Manufacturing Manager to lead product compliance quality and manufacturing oversight. This role works cross-functionally with internal teams and external partners to deliver safe high-quality and legally...