At a Glance
- Tasks: Lead CMC projects in drug development, collaborating with top scientists and industry experts.
- Company: Dynamic biotech organisation in Oxfordshire focused on oncology therapeutics.
- Benefits: Enjoy a competitive salary, bonus, private healthcare, and 25 days holiday.
- Other info: Hybrid work model with opportunities for professional growth and learning.
- Why this job: Make a real impact in the future of medicine while growing your career.
- Qualifications: Background in Life Sciences and experience in Project Management within Biotech/Pharma.
The predicted salary is between 63000 - 77000 £ per year.
- Overview
- CMC Project Manager
- Oxford, UK | Hybrid (1–2 days on site per week)
Are you ready to take full ownership of projects that will shape the future of oncology therapeutics? We’re looking for a
CMC Project Manager who can hit the ground running, thrive in a collaborative environment, and bring real impact to a growing Biotech organisation in Oxfordshire.
This is your chance to work at the cutting edge of drug development, partnering with talented scientists and industry experts while driving critical CMC programmes forward.
Responsibilities
- Leading CMC projects from start to finish – planning, execution, delivery and everything in between.
- Acting as the driving force between internal teams (Preclinical, Clinical, Regulatory, CMC and Quality) and external CDMO partners.
- Managing vendor relationships, budgets, timelines and risks to keep high-priority programmes moving smoothly.
- Supporting regulatory submissions and ensuring quality standards are met.
- Being a key member of the Project Management Office, sharing learnings, improving processes and ensuring best practice.
- Be part of a team that’s expanding its CMC capability at a crucial stage of growth.
- Work in a hybrid model – typically 1–2 days in office.
- Enjoy a comprehensive benefits package including discretionary bonus, pension, life insurance, private healthcare and 25 days holiday (plus bank holidays).
Qualifications
- A background in Life Sciences (degree or equivalent).
- Solid experience as a Project Manager within Biotech/Pharma.
- Hands-on knowledge of CMC projects, ideally with exposure to small molecules.
- Direct experience working with CDMOs – you understand the challenges and how to navigate them.
- A proactive, confident communicator who can work cross-functionally and independently.
- PM qualifications (e. g. PMP) and regulatory/c GMP knowledge would be a bonus.
- Seniorities
- Mid-Senior level
- Employment type
- Full-time
- Job function
- Project Management
- Industries
- Biotechnology Research, Pharmaceutical Manufacturing, and Research Services
- Oxford, England, United Kingdom 4 days ago
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CMC Project Manager employer: Next Phase Recruitment
As a Process Validation Lead at Next Phase Recruitment, you will join a dynamic team that values collaboration and innovation in the heart of a thriving manufacturing hub. Our commitment to employee growth is reflected in our comprehensive training programmes and opportunities for cross-functional engagement, ensuring you can advance your career while contributing to meaningful projects that impact product quality and safety. With a supportive work culture that prioritises work-life balance and professional development, we offer an exceptional environment for those looking to make a significant impact in the industry.
