Principal Consultant (CMC)

Scendea; England; Hybrid; GBP 70,000 - 100,000; Full time

Job summary

Join Scendea as a Principal Consultant (CMC) to advance your career in a rapidly growing Regulatory Consultancy. This hybrid position requires strategic regulatory advice and technical leadership, with opportunities for mentoring staff and contributing to innovative drug development plans. You will work within a collaborative international team, influencing healthcare innovation and ensuring regulatory compliance.

Benefits

Generous bonus program

26 days’ vacation plus additional days

Employer pension contribution

Private Healthcare insurance

Employee Assistance Programme

Coaching and mentoring support

Qualifications

• High scientific calibre with relevant BSc; higher degree in biomedical field preferred.
• Ten years of CMC development and regulatory compliance experience required.
• Experience with FDA, EMA, and ICH guidelines essential.

Responsibilities

• Provide strategic regulatory advice for CMC development of human medicinal products.
• Lead multi-jurisdiction programs and deliver consulting services.
• Manage and mentor team members, ensuring project goals and budgets are met.

Skills

Regulatory compliance

CMC strategy

Technical leadership

Education

BSc in Science

MSc or PhD in Biomedical field

Job description

Scendea Bishop's Stortford, England, United Kingdom

Principal Consultant (CMC)

Scendea Bishop's Stortford, England, United Kingdom

1 day ago Be among the first 25 applicants

Direct message the job poster from Scendea

Scendea is seeking a highly motivated individual to join our global team as a full-time Principal Consultant (CMC). This is a hybrid position, affiliated to either of our UK, Netherlands, Australia, or US offices, 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 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, MHRA, and/or EMA 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.
• Generous bonus program, which rewards success.
• 26 days’ vacation plus discretionary additional days for birthday and work anniversary and public holidays.
• Employer pension contribution
• Provision/Contribution 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 office locations and 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/Netherlands./US/Australia without the requirement for sponsorship now or in the future. Closing date for applications is Monday 16th June 2025 and candidates will be notified of the outcome of their application no later than Friday 20th June 2025.

Seniority level

Seniority level

Mid-Senior level

• Seniority level

  Mid-Senior level

Employment type

Employment type

Full-time

• Employment type

  Full-time

Job function

Job function

Consulting

• Job function

  Consulting

• Industries

  Pharmaceutical Manufacturing

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