Principal Regulatory Affairs Consultant (CMC Biologics) in Plymouth

Principal Regulatory Affairs Consultant (CMC Biologics) in Plymouth

Plymouth Full-Time 80000 - 100000 € / year (est.) Home office (partial)
Scendea

At a Glance

  • Tasks: Provide strategic regulatory advice and lead innovative drug development plans for clients.
  • Company: Join Scendea, a global leader in regulatory consulting with a passion for healthcare innovation.
  • Benefits: Enjoy a competitive salary, generous vacation, and professional development opportunities.
  • Other info: Remote work with flexible hours and a supportive, inclusive company culture.
  • Why this job: Make a real impact in the biotech field while mentoring and leading a dynamic team.
  • Qualifications: PhD or equivalent in biomedical sciences and extensive CMC regulatory experience required.

The predicted salary is between 80000 - 100000 € per year.

Scendea is seeking a highly motivated individual to join our global team as a full-time Principal Consultant (CMC Biologics). This is a remote position, affiliated to either our Bishop's Stortford (UK), Brisbane (AUS) or Washington, D.C. Office (USA), with a requirement to work in the office a minimum of one day per month. This is an excellent opportunity to progress your career at a rapidly growing product development, regulatory, and compliance consultant group. You will have the opportunity to play a key role in the development and mentoring of colleagues whilst providing high-quality regulatory technical advice and product development strategies for clients.

Role Requirements

  • Provide strategic, technical and regulatory advice/services to clients with a special interest in CMC development of human medicinal products.
  • Provide innovative drug development plans, data gap analyses and international regulatory strategies from a CMC perspective for complex products within the changing regulatory environment.
  • Contribute to technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Paediatric plans/applications, Investigator Brochures, IMPDs, Marketing Authorisation Applications, New Drug Applications, Biologic License Applications, DMFs according to area of expertise.
  • Lead multi-jurisdiction programs of work and deliver consulting services within your respective area of expertise.
  • Represent clients in regulatory agency interactions and provide regulatory solutions to agency objections.
  • Ensure delivery of project goals within agreed timelines, maintaining oversight of project budgets.
  • Lead meetings with internal and external stakeholders on matters related to any current and/or future projects, contracts, or new business opportunities.
  • Support Scendea's Business Development in sales/marketing introductions and generate additional business from current clients.
  • Line manage, train, and mentor members of the Scendea Operational team, including providing technical leadership.

Skills and Experience

  • A high scientific calibre with a relevant science focused BSc (or equivalent), and a higher degree in a biomedical field or equivalent (e.g., a life/physical science focused MSc or preferably a PhD).
  • Extensive experience in CMC strategy and a minimum of ten years of experience in CMC development and regulatory compliance.
  • Expertise in CMC-related regulatory requirements, including FDA, EMA, ICH guidelines.
  • A minimum of ten years of regulatory experience, working with either FDA, and/or MHRA/EMA/TGA submissions, including meetings/negotiation. Regulatory experience may include time within a National Competent Authority.
  • Experience with a broad range of products would be beneficial, including recombinant proteins and peptides (including antibodies), prophylactic and therapeutic vaccines, biosimilar products, advanced therapy medicinal products (tissue, cell and gene therapy), RNA or DNA based products, and live biotherapeutics.
  • Direct experience preferred in providing strategic regulatory planning from early-stage development up to marketing authorisation, and a proven ability to define and deliver creative scientifically driven solutions to technical development and regulatory issues.
  • Experience in consultancy and/or an outgoing personality that supports the ability to showcase their expertise and the business to new potential clients.
  • Proven ability and willingness to lead a team and deliver education and training in chosen field, both internally, and at scientific conference presentations.
  • Exemplary organisational and time management skills with a high level of attention to detail, and the proven ability to work both proactively and autonomously.
  • High level of verbal communication and presentation skills in English, computer literacy, and competency in MS Office programs.
  • Willingness to work flexible hours and travel for short periods, sometimes at short notice, within the country of employment, or internationally.

The Company

Scendea is an international product development, regulatory, and compliance consulting group delivering market-leading scientific expertise & regulatory solutions, to advance healthcare innovation worldwide. We are passionate about delivering strategic and operational support to clients, with a strong commitment to problem-solving and redefining customer service. Our goal is to streamline the product development process, reduce time-to-market, and minimise overall development costs.

With a current team of over 50 staff based in the UK, Netherlands, Australia, and the US, Scendea is undergoing a period of significant growth, with the addition of new service lines to facilitate the delivery of expert and strategic global regulatory consulting services to our rapidly growing client base. We are equally committed to making a positive impact on society by managing our environmental impacts and contributing to a low-carbon economy. Our inclusive work culture values transparency, ethical collaboration with clients, and employee involvement in key decision-making processes, ensuring that our team is respected, supported, and engaged.

Benefits

  • A competitive salary.
  • Generous bonus program, which rewards success.
  • 26 days’ vacation plus discretionary additional days for birthday and work anniversary and public holidays.
  • Employer pension contribution/compensation in line with country specific legislation.
  • Compensation of Private Healthcare insurance.
  • Access to Employee Assistance Programme.
  • Employee Ownership Trust Scheme.
  • A challenging and stimulating position for a dynamic and competent scientist, looking to contribute to a growing business and a rapidly expanding team.
  • Coaching, mentoring and support of your continuous learning, and professional development within a highly recognised international team.

As a Scendea Employee

Part of what makes Scendea successful is the highly motivated people who work for us and their enthusiasm for what we do and stand for. We recruit individuals whose passion, drive, integrity and customer orientation shines through. You are a motivated individual who can instil trust and confidence in our customer relationships whilst having a natural aptitude for getting the best out of people internally. You will inspire others through your commitment, motivation, expertise, professional manner and always placing the customer at the centre of everything you do.

Eligibility & Conditions

Applicants must reside and be eligible to work in either the UK, Australia or United States without the requirement for sponsorship now or in the future.

Principal Regulatory Affairs Consultant (CMC Biologics) in Plymouth employer: Scendea

Scendea is an exceptional employer that fosters a collaborative and inclusive work culture, offering employees the chance to thrive in a dynamic environment focused on healthcare innovation. With generous benefits including a competitive salary, extensive vacation time, and opportunities for professional development, employees are empowered to grow their careers while making a meaningful impact in the regulatory affairs sector. The company's commitment to employee involvement in decision-making and its focus on ethical collaboration ensures that every team member feels valued and engaged.

Scendea

Contact Detail:

Scendea Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Principal Regulatory Affairs Consultant (CMC Biologics) in Plymouth

Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings or can put in a good word for you.

Tip Number 2

Prepare for interviews by researching the company and its projects. Familiarise yourself with their recent work in CMC development and regulatory affairs. This will help you tailor your responses and show that you're genuinely interested in what they do.

Tip Number 3

Practice your pitch! Be ready to explain how your experience aligns with the role of Principal Regulatory Affairs Consultant. Highlight your expertise in CMC strategy and any successful projects you've led to demonstrate your value.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our team at Scendea and contributing to our mission in healthcare innovation.

We think you need these skills to ace Principal Regulatory Affairs Consultant (CMC Biologics) in Plymouth

CMC Development
Regulatory Compliance
FDA Guidelines
EMA Guidelines
ICH Guidelines
Technical Authoring
Project Management

Some tips for your application 🫡

Tailor Your Application:Make sure to customise your CV and cover letter for the Principal Regulatory Affairs Consultant role. Highlight your experience in CMC development and regulatory compliance, and don’t forget to mention any specific projects that align with what we do at Scendea.

Showcase Your Expertise:We want to see your knowledge shine through! Include details about your experience with FDA, EMA, and ICH guidelines, as well as any innovative drug development plans you've worked on. This is your chance to show us how you can contribute to our team.

Be Clear and Concise:When writing your application, keep it straightforward and to the point. Use clear language and avoid jargon unless necessary. We appreciate a well-structured application that makes it easy for us to see your qualifications and fit for the role.

Apply Through Our Website:Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team at Scendea.

How to prepare for a job interview at Scendea

Know Your CMC Inside Out

Make sure you brush up on your knowledge of CMC development and regulatory compliance. Familiarise yourself with the latest FDA, EMA, and ICH guidelines, as well as any recent changes in the regulatory landscape. This will not only help you answer technical questions but also show your passion for the field.

Prepare Real-World Examples

Think of specific projects or experiences where you've successfully navigated complex regulatory challenges. Be ready to discuss how you provided strategic advice or led multi-jurisdictional programmes. This will demonstrate your hands-on experience and problem-solving skills, which are crucial for this role.

Showcase Your Leadership Skills

Since the role involves mentoring and leading teams, be prepared to talk about your leadership style and experiences. Share examples of how you've trained or guided colleagues, and how you foster collaboration within a team. This will highlight your ability to inspire and manage others effectively.

Ask Insightful Questions

At the end of the interview, don’t forget to ask thoughtful questions about the company’s future projects or their approach to regulatory challenges. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.