At a Glance
- Tasks: Lead regulatory strategies and mentor a dynamic team in the biotech field.
- Company: Join Scendea, a global leader in regulatory consulting for healthcare innovation.
- Benefits: Enjoy competitive salary, generous vacation, and professional development opportunities.
- Other info: Flexible remote work with a vibrant, inclusive culture focused on growth.
- Why this job: Make a real impact in healthcare while advancing your career in a supportive environment.
- Qualifications: PhD or MSc in biomedical field with extensive CMC regulatory experience.
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 our 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 Portsmouth employer: Scendea
Scendea is an exceptional employer that fosters a collaborative and inclusive work culture, providing employees with the opportunity to grow professionally while making a meaningful impact in the healthcare sector. With competitive salaries, generous vacation policies, and a strong commitment to employee development through coaching and mentoring, Scendea empowers its team members to excel in their roles as they contribute to innovative regulatory solutions. The remote nature of the Principal Regulatory Affairs Consultant position allows for flexibility, while the chance to engage with a diverse global team enhances the overall work experience.
StudySmarter Expert Advice🤫
We think this is how you could land Principal Regulatory Affairs Consultant (CMC Biologics) in Portsmouth
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant webinars, and join professional groups. 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 recent projects. Tailor your responses to highlight how your experience aligns with their needs, especially in CMC development and regulatory compliance.
✨Tip Number 3
Showcase your expertise! Create a portfolio of your past projects and achievements that demonstrate your skills in regulatory affairs. This will help you stand out during interviews and discussions.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about joining our team at Scendea.
We think you need these skills to ace Principal Regulatory Affairs Consultant (CMC Biologics) in Portsmouth
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, as well as any specific projects that align with what we do at Scendea.
Showcase Your Expertise:Don’t hold back on showcasing your knowledge of FDA, EMA, and ICH guidelines. We want to see how your expertise can contribute to our team and help us deliver top-notch regulatory solutions.
Be Clear and Concise:When writing your application, keep it clear and to the point. Use bullet points where possible to make it easy for us to see your key achievements and skills. We appreciate a well-structured application!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity 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 instances where you've successfully navigated complex regulatory challenges or led multi-jurisdictional projects. Be ready to discuss these examples in detail, highlighting your strategic thinking and problem-solving skills. This will demonstrate your hands-on experience and ability to deliver results.
✨Showcase Your Leadership Skills
As a Principal Consultant, you'll be expected to mentor and lead teams. Prepare to discuss your leadership style and provide examples of how you've trained or guided colleagues in the past. This will illustrate your capability to inspire and develop others, which is crucial for this role.
✨Engage with the Interviewers
Don't just wait for questions; engage with your interviewers by asking insightful questions about Scendea's projects and future directions. This shows your genuine interest in the company and helps you assess if it's the right fit for you. Plus, it can make the conversation more dynamic and memorable!