Consultant CMC & Regulatory Affairs
Location: Warsaw & Madrid/Barcelona- hybrid work
Type: Full-time
Join our CMC Regulatory Affairs team and work on complex projects supporting the development, registration, and lifecycle management of medicinal products.
You will combine your CMC expertise with client-facing consulting, supporting regulatory submissions, pharmaceutical development, GMP documentation, and Health Authority interactions.
What you’ll be doing
Provide solutions and expert support related to the development and registration of medicinal products.
Prepare, review, and deliver CMC documentation for regulatory submissions covering both development-stage and commercial products.
Support clients in resolving CMC-related matters and responding to Health Authority questions and requests.
Ensure the timely delivery of high-quality projects in compliance with regulatory requirements, agreed scope, and budget.
Collaborate closely with clients and internal teams to facilitate the successful execution of projects.
Provide technical expertise in drug substance and drug product development and lifecycle management, supporting regulatory submissions throughout the product lifecycle, including clinical development, marketing authorization, and post-approval variations.
Review and work with GMP documentation related to manufacturing sites for medicinal products.
Verify manufacturing documentation, including batch records.
Participate in projects involving pharmaceutical development, regulatory submissions, and lifecycle management activities.
What you bring
Master's degree in Pharmacy, Chemistry, Biotechnology, Pharmaceutical Sciences, Life Sciences, or a related field.
Minimum 4 years of experience in CMC Regulatory Affairs, pharmaceutical development, manufacturing, quality assurance, or a related area.
Strong knowledge of CMC requirements for the development, registration, and lifecycle management of medicinal products.
Fluency in English, both written and spoken.
Excellent communication and organizational skills, with the ability to prioritize and manage multiple activities effectively.
Strong problem-solving skills, accountability, and the ability to work independently.
What’s in it for you?
Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices.
Grow within a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.
Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations - because your contribution deserves to be valued.
Who you are
Our culture is driven by values If this sounds like you, you’ll fit right in:
You’re resilient and tackle challenges with a positive mindset
You’re curious and always up for learning something new
You have a no non-sense approach honest, clear, respectful
You’re innovative and bring ideas, not just opinions
And above all, you’re serious about your work, but not too serious about yourself
About us
We support life sciences companies from idea to patient - offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 700 experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma. Since January 2025, SciencePharma has been part of QbD Group, joining forces to deliver comprehensive end-to-end solutions.
We believe in JPEG:
Joy. Partnership. Going the Extra Mile. Getting Things Done.
You won’t just be taking a job - you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.
Interested? Let’s talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family.