Regulatory Affairs CMC Manager, Biologics, Uxbridge, UK

Employer
Advanced Regulatory (UK & Europe)
Location
Uxbridge, UK
Salary
Competitive
Closing date
14 Oct 2020

View more

Discipline
Regulatory Affairs, CMC, Compliance, Project Management, Regulatory Project Management
Hours
Full Time
Contract Type
Permanent
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Regulatory Affairs CMC Manager, Biologics, Uxbridge, UK

We have a permanent role for a Regulatory Affairs CMC Manager based in Greater London, with a global biotechnology company.

  • Work on Variety of projects from Phase 1 to Phase 3.
  • Gain initial MAA/BLA experience and consolidate your EU and US experience.
  • Work of fewer projects, but be more involved and take on responsibility early on.
  • Do you enjoy writhing not just compiling? You will be authoring IMPD and Module 3 hear and although we will expect you to already have writing experience you will get a lot of support to improve, learn and grow in this R&D based company.
     

Our client:

Our client is a successful biotechnology company with a global reach. They develop innovative medicines for unmet medical needs and have an impressive pipeline of new molecules (NCEs and NBEs) coming up in development. They have some exciting new products coming in Phase II, Phase III and a number of products in early development. This company is committed to increasing access to high-quality healthcare products around the world.
 

The role:

This role will provide regulatory CMC expertise, leadership and oversite of projects in development in our client’s portfolio. You will have the opportunity here to work on a variety of indications, but also have the opportunity to follow through a molecule from Ph2/Ph3 to MAA/BLA in the EU and the US. You will have an input and support the implementation of regulatory CMC strategy as well as lead responses to the health authorities.

In this role you will:

  • Lead as assigned and manage the Regulatory CMC aspects of Clinical Trial Applications for New Biological Entities.
  • Provide regional strategic and operational Regulatory Affairs CMC expertise
  • Write and review global and regional Regulatory CMC submission documents, IMPDs, INDs, new MAAs and NDAs etc.
  • Lead and manage CMC aspects of Health Authority questions and negotiations.
     

What are the requirements?

  • As a minimum you will have at least 2-3 years in the Pharmaceutical industry in a Regulatory Affairs CMC role.
  • You will have experience writing CMC documentation (Module 3, IMPD, IND, PIP etc.) for development products or lifecycle management – biologic or biosimilar.
  • You will have experience authoring high quality Module 2.3 and Module 3 of MAAs or NDAs as part of a larger team and also some experience in lifecycle management, filing major variations, renewals, tech transfer etc.
  • Experience preparing responses to CMC questions from Health Authorities.
     

What is there for you?

In this company you will be given the opportunity to support or lead a project from early to late stage or submission right away. They like giving responsibility to Managers from the very beginning and promotions here don’t take long for the right person. Here you will work alongside experienced leaders who will help you learn, develop and get to the next level in your career.

The role comes with a competitive salary, company bonus, car allowance, a comprehensive health and benefits plan including a high company pension contribution. It is possible to work 1-2 days from home and the location is easily accessible by car and commutable by public transport.

How does this sound? Feel free to inquire more information even if you are not sure that this is the right moment for you to have a career change. We look forward to hearing from you.
 

To Apply!

To apply, please send a full CV to CV@AdvTalent.com, or alternatively contact Theo Moore or Oli Dimitrov on +44 (0)207 801 3384 or +44 (0)207 801 3388. We are assigned these roles by our client and will provide you with support throughout the hiring process.

About Advanced Search & Our Network

Advanced Search, has a network of affiliated companies including ADV Regulatory, and ADV Talent Partners. Together, we are specialists in Regulatory Affairs and Life Sciences recruitment especially around mAbs and biologicals for roles in R&D and Commercialization and have been established and hiring in this area since 2005.

Our Regulatory Affairs team know their subject matter areas and our mission is to help you grow your career each and every step of the way. We have helped many of today's leading companies develop strong regulatory sciences functions and are known for hiring complimentary teams that work well with each other, at owner-contributor, strategy leading and people management levels.

Contact us today to see how we can help you make that next career move on

+44 (0)207 801 3380

All applications are kept in confidence and we invite applications from all members of the Academic, Research & Development based bio-pharmaceutical community.

Advanced Regulatory is a new recruitment organisation. Our consultants are industry known and highly experienced in Regulatory Affairs recruitment. We have assembled a team with competencies in databased contingency recruitment, Search & Selection as well as Creative & Campaign management. Our specialism is Regulatory Affairs. We know that successful submissions are underpinned not by one but many people, all working in cohesion. Whether you require a new career position or a new recruit at junior, mid or senior level, we would like to assist you. Our remit is to provide Regulatory Affairs professionals at all levels to pharmaceutical, regulatory consulting, biopharmaceutical and clinical research organisations.

Contact Us
  • Suite 8 Penhurst House
  • 352-356 Battersea Park Road
  • SW11 3BY
  • GB
  • +44 (0)20 7801 3380
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