At a Glance
- Tasks: Provide strategic regulatory advice and lead innovative drug development projects.
- Company: Join Scendea, a dynamic consulting group in the pharma industry.
- Benefits: Enjoy a generous bonus, 26 days holiday, and professional development opportunities.
- Other info: Flexible working with a supportive and inclusive team culture.
- Why this job: Make a real impact in healthcare innovation while advancing your career.
- Qualifications: 5+ years in drug development and regulatory experience required.
The predicted salary is between 51750 - 63250 £ per year.
- Senior Consultant (CMC Small Molecules) UK
- Bishop's Stortford, United Kingdom | Posted on 31/07/2026
- Industry Pharma/Biotech/Clinical Research
- Province Hertfordshire
- City Bishop's Stortford
- Postal Code CM23 2EJ
- Country United Kingdom
About Us
Scendea is an international product development, regulatory, and compliance consulting group delivering market-leading scientific expertise & regulatory solutions, to advance healthcare innovation worldwide.
Scendea’s expert team delivers strategic and operational support in the fields of Non-Clinical, CMC, Clinical, Regulatory and Compliance to successfully guide products from early development to marketing approval.
Job Description
The Role
Scendea is seeking a highly motivated individual to join ourglobal team as a full-time Senior Consultant (CMC small molecules).
Thisis a hybrid position, affiliated to our UK Bishop's Stortford office, with arequirement to work in the office a minimum of one day per month.
This is an excellent opportunity to progressyour career at a rapidly growing product development, regulatory, and compliance consulting group.
You will have theopportunity to play a key role in the development and mentoring of staff whilstproviding high-quality regulatory technical advice and product development.
Requirements
- Role Requirements
- Providestrategic, technical and regulatory advice/services to clients with aspecial interest in Chemistry, Manufacturing, and Controls (CMC) development of human medicinal products.
- Establishand maintain a high level of technical knowledge in product developmentand international regulatory affairs.
- Provideinnovative drug development plans, data gap analyses and internationalregulatory strategies from a CMC perspective for complex products withinthe changing regulatory environment.
- Contributeto technical authorship and review of development regulatory documentsincluding 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.
- Leadmulti-jurisdiction programs of work and deliver consulting services withinyour respective area of expertise.
- Representclients in regulatory agency interactions and provide regulatory solutionsto agency objections.
- Ensuredelivery of project goals within agreed timelines, maintaining oversightof project budgets.
- Leadmeetings with internal and external stakeholders on matters related to anycurrent and/or future projects, contracts, or new business opportunities.
- Support Scendea's Business Development in sales/marketing introductions and generateadditional business from current clients.
- Linemanage, train, and mentor members of the Scendea Operational team, includingproviding technical leadership.
Skills and Experience
- Ahigh scientific calibre with a relevant science focused BSc (orequivalent), and a higher degree in a biomedical field or equivalent(e. g., a life/physical science focused MSc or preferably a Ph D).
- Aminimum of 5 years drug development experience.
- Aminimum of 5 years regulatory experience, working with either the FDA, MHRA, and/or EMA submissions, including meetings/negotiation.
Regulatoryexperience may include time within a National Competent Authority.
- Authoring of CMC sections of regulatory documentation is required. MAA/BLA Experience is highly desirable.
- Demonstratedexperience with a broad range of products, including recombinant proteins andpeptides (including antibodies), prophylactic and therapeutic vaccines, biosimilar products, advanced therapy medicinal products (tissue, cell andgene therapy), RNA or DNA based products, live biotherapeutics and smallmolecule NCE and/or generic chemical entities.
- Directexperience preferred in providing strategic regulatory planning from early-stagedevelopment up to marketing authorisation, and a proven ability to defineand deliver creative scientifically driven solutions to technicaldevelopment and regulatory issues.
- Provenability and willingness to lead a team and deliver education and training inchosen field, both internally, and at scientific conference presentations.
- Exemplaryorganisational and time management skills with a high level of attentionto detail, and the proven ability to work both proactively and autonomously.
- Highlevel of verbal communication and presentation skills in English, computerliteracy, and competency in MS Office programs.
- Willingnessto work flexible hours and travel for short periods, sometimes at shortnotice, within the country of employment, or internationally.
Benefits
Package
- Generousbonus program, which rewards success.
- 26days’ holiday plus discretionary additional days for birthday and workanniversary and public holidays.
- 5%employer pension contribution.
- Accessto Employee Assistance Programme.
- Employee Ownership Trust Scheme.
- Achallenging and stimulating position for a dynamic and competentscientist, looking to contribute to a growing business and a rapidlyexpanding team.
- Coaching, mentoring and support of your continuous learning, and professionaldevelopment within a highly recognised international team.
- The Company
Scendea is an international product development andregulatory consulting group delivering market-leading scientific expertise& regulatory solutions, to advance healthcare innovation worldwide.
We arepassionate about delivering strategic and operational support to clients, witha strong commitment to problem-solving and redefining customer service.
Our goalis to streamline the product development process, reduce time-to-market, andminimise 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 ofsignificant growth, with the addition of new office locations and service linesto facilitate the delivery of expert and strategic global regulatory consultingservices to our rapidly growing client base.
We are equally committed to makinga positive impact on society by managing our environmental impacts andcontributing to a low-carbon economy.
Our inclusive work culture values transparency, ethical collaboration with clients, and employee involvement in keydecision-making processes, ensuring that our team is respected, supported, andengaged.
As a Scendea Employee
Part of what makes Scendea successful is the highlymotivated people who work for us and their enthusiasm for what we do and standfor.
You are a motivated individual who can instil trustand confidence in our customer relationships whilst having a natural aptitudefor getting the best out of people internally.
You will inspire others throughyour commitment, motivation, expertise, professional manner and always placingthe customer at the centre of everything you do.
Eligibility & Conditions
Applicants must reside and be eligible to work in the UK without the requirement for sponsorship now or in the future.
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Senior Consultant (CMC Small Molecules) UK employer: Scendea Ltd
Scendea is an exceptional employer, offering a dynamic and inclusive work culture that prioritises employee growth and development. With a generous benefits package including a bonus program, extensive holiday allowance, and a commitment to professional mentoring, employees are empowered to thrive in their careers while contributing to meaningful healthcare innovations. Located in Bishop's Stortford, this role provides the unique opportunity to be part of a rapidly expanding international team dedicated to advancing regulatory solutions in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Consultant (CMC Small Molecules) UK
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We think you need these skills to ace Senior Consultant (CMC Small Molecules) UK
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Scendea Ltd!
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How to prepare for a job interview at Scendea Ltd
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Scendea Ltd that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
