Senior Consultant in England

Senior Consultant in England

England Full-Time 36000 - 60000 £ / year (est.) No working from home possible
Scendea

At a Glance

  • Tasks: Provide strategic regulatory advice and mentor staff in a dynamic consultancy environment.
  • Company: Join Scendea, a rapidly growing global regulatory consultancy with a passion for healthcare innovation.
  • Benefits: Enjoy competitive salary, generous vacation, bonuses, and professional development opportunities.
  • Other info: Flexible hybrid work model with opportunities for travel and continuous learning.
  • Why this job: Make a real impact in drug development while working with a talented international team.
  • Qualifications: PhD or MSc in biomedical field, with 5+ years of regulatory experience required.

The predicted salary is between 36000 - 60000 £ per year.

Scendea is seeking a highly motivated individual to join our global team as a full-time Senior Consultant (CMC). This is a hybrid position, affiliated to either our Bishop's Stortford, Brisbane or Washington, D.C. Office, 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 Regulatory Consultancy. You will have the opportunity to play a key role in the development and mentoring of staff 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 Chemistry, Manufacturing, and Controls (CMC) development of human medicinal products.
  • Establish and maintain a high level of technical knowledge in product development and international regulatory affairs.
  • 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).
  • Authoring of CMC sections of regulatory documentation is required. MAA/BLA experience is highly desirable.
  • A minimum of five years of drug development experience.
  • A minimum of five years of regulatory experience, working with either FDA, EMA, and/or MHRA submissions, including meetings/negotiation. Regulatory experience may include time within a National Competent Authority.
  • Demonstrated experience with a broad range of products, 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, live biotherapeutics and small molecule NCE and/or generic chemical entities.
  • 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.
  • 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.

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.

The Company

Scendea is an international product development and regulatory 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.

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. Closing date for applications is Friday 20th March 2026 and candidates will be notified by of the outcome of their application no later than Friday 27th March 2026.

Senior Consultant in England employer: Scendea

Scendea is an exceptional employer that fosters a dynamic and inclusive work culture, offering employees the chance to thrive in a rapidly growing Regulatory Consultancy. With competitive salaries, generous vacation policies, and a strong emphasis on professional development, employees are encouraged to grow their careers while contributing to meaningful healthcare innovations. The hybrid work model allows for flexibility, and the supportive environment ensures that every team member feels valued and engaged in their work.

Scendea

Contact Details:

Scendea Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Consultant in England

Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can land you that dream job.

Tip Number 2

Prepare for interviews by researching the company and its culture. We recommend practising common interview questions and even role-playing with a friend. The more comfortable you are, the better you’ll perform when it counts!

Tip Number 3

Showcase your expertise! Bring along examples of your previous work or case studies that highlight your skills. We want to see how you’ve tackled challenges in the past and how you can bring that experience to Scendea.

Tip Number 4

Don’t forget to follow up after your interview! A simple thank-you email can go a long way in showing your enthusiasm for the role. We love candidates who take the initiative and keep the conversation going.

We think you need these skills to ace Senior Consultant in England

Regulatory Affairs
Chemistry, Manufacturing, and Controls (CMC)
Drug Development
Regulatory Documentation Authoring
FDA, EMA, MHRA Submissions
Project Management
Strategic Regulatory Planning

Some tips for your application 🫡

Tailor Your Application:Make sure to customise your CV and cover letter for the Senior Consultant role. Highlight your relevant experience in Chemistry, Manufacturing, and Controls (CMC) and how it aligns with what we’re looking for at Scendea.

Showcase Your Expertise:Don’t hold back on showcasing your scientific background and regulatory experience. We want to see your knowledge in drug development and your ability to provide strategic regulatory planning. Make it shine!

Be Clear and Concise:When writing your application, keep it clear and to the point. Use bullet points where necessary to make it easy for us to read through your qualifications and experiences. We appreciate a well-structured application!

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows you’re keen on joining our team at Scendea!

How to prepare for a job interview at Scendea

Know Your Stuff

Make sure you brush up on your knowledge of Chemistry, Manufacturing, and Controls (CMC). Familiarise yourself with the latest regulatory guidelines and be ready to discuss how your experience aligns with the role's requirements. This will show that you're not just a candidate, but a knowledgeable expert.

Showcase Your Leadership Skills

As a Senior Consultant, you'll be expected to lead and mentor others. Prepare examples of how you've successfully managed teams or projects in the past. Highlight your ability to inspire and educate others, as this is key to fitting into Scendea's culture.

Prepare for Technical Questions

Expect to dive deep into technical discussions during your interview. Be ready to explain your experience with regulatory submissions and product development strategies. Practising answers to common technical questions can help you feel more confident and articulate.

Engage with the Interviewers

Interviews are a two-way street! Prepare thoughtful questions about Scendea’s projects, team dynamics, and future goals. This not only shows your interest in the company but also helps you assess if it's the right fit for you.