Regulatory Affairs CMC Manager / Snr Manager EU & US – Small Molecules, Berkshire, UK

Employer
Advanced Regulatory (UK & Europe)
Location
Berkshire, 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 / Snr Manager EU & US – Small Molecules, Berkshire, UK

About the company

Our client is growing, and to strengthen their Global Regulatory Affairs CMC team, they are looking to hire a Global Regulatory Affairs Manager / Snr Manager in Berkshire, UK.

This is an established Pharmaceutical company that has been transforming patients’ lives for decades, developing novel medicines and new generation therapies. This is an R&D driven business that has been successfully pushing the boundaries of what is possible, innovating and making a real difference to patients’ lives.

This is an opportunity to:

  • Lead assigned regional projects and take responsibility for the regulatory CMC support of chemical entities throughout the Life-Cycle (early to late development, CTA writing of IMPDs and INDs, authoring CMC sections of initial MAA/BLAs/NDAs and module 3 for post approval variations)
  • Contribute to the preparation of global regulatory CMC submission documentation to deliver timely approvals
  • Define, plan and implement regional regulatory CMC strategy and have input into the global regulatory CMC strategy
  • Lead and/or provide regulatory CMC input to Health Authority responses - authoring and managing the interactions with agencies on CMC matters in assigned regions. 

You will be responsible for:

  • Taking accountability by managing regulatory CMC projects yourself and authoring global CMC documentation (based on technical source reports) for submissions in line with agreed global regulatory strategy
  • Developing and implementing the regional CMC regulatory strategy and submission plans for assigned small molecule projects to deliver timely approvals
  • Ensuring effective communication of CMC regulatory strategy, risks, and overall plan for assigned projects to the Regulatory Affairs Teams and cross functional teams as delegated and agreed by the Global Regulatory CMC Lead.

 You should have:

  • At least 4-5 years of relevant pharmaceutical industry experience in a regulatory affairs CMC function. Previous experience in pharmaceutical manufacturing, analytical development and QA/QC technical field would be an advantage
  • Proven track record of successful writing / authoring and contribution to delivering regulatory CMC sections of CTAs, MAA/NDAs or Variations for chemical or biological entities
  • “Hands on”, “Can do” attitude and problem-solving abilities working within the regulatory affairs and enjoying a multicultural, international matrix environment where English is the business language.

Package, flexibility & Bens

  • My client is offering Manager or Senior Manager grading, for this position, including a bonus, and incentives plan. The role comes with great overall package and great career and promotion prospects
  • The company is willing to consider individuals that want to work from home for 2 days a week post-Covid
  • You will receive continual training and mentoring, from individuals with 15-20 years each in regulatory CMC
  • During the next few months, my client will hire and on board you virtually, so you will be interviewed, inducted and on-boarded from home. After Covid-19, this role will be based in Berkshire, UK.
     

To Apply!

To apply, please send a full CV to CV@AdvTalent.com or call Oli Dimitrov or Theo Moore on +44 (0)207 801 3388 or +44 (0)207 801 3384. 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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