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- Tasks: Lead global regulatory strategies for innovative cell and gene therapies.
- Company: Dynamic biopharmaceutical company focused on advancing cancer therapies.
- Benefits: Collaborative work environment with opportunities for professional growth.
- Why this job: Make a real impact in the field of cancer treatment through innovative therapies.
- Qualifications: 8-10 years in Regulatory Affairs for biologics and strong communication skills.
- Other info: Join a team dedicated to transforming healthcare and improving patient outcomes.
The predicted salary is between 48000 - 72000 £ per year.
A biopharmaceutical company in the UK seeks an experienced Associate Director, Regulatory Affairs CMC, responsible for leading global CMC regulatory strategies for its innovative cell and gene therapy products.
The ideal candidate will have 8-10 years of experience in Regulatory Affairs for biologics, excellent communication skills, and a proven track record in regulatory submissions and interactions with health authorities.
This role offers a dynamic work environment focused on teamwork and advancing cancer therapies.
Regulatory Affairs CMC Lead - Cell & Gene Therapies in London employer: Autolus Limited
Contact Detail:
Autolus Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs CMC Lead - Cell & Gene Therapies in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs space, especially those with experience in CMC for cell and gene therapies. Attend industry events or webinars to make connections that could lead to job opportunities.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of current regulations and guidelines related to biologics. We recommend practising common interview questions and scenarios specific to regulatory affairs to showcase your expertise.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It’s a great way to keep you on their radar.
✨Tip Number 4
Apply through our website! We’ve got a streamlined application process that makes it easy for you to showcase your skills and experience. Plus, it shows you’re genuinely interested in joining our team.
We think you need these skills to ace Regulatory Affairs CMC Lead - Cell & Gene Therapies in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Regulatory Affairs, especially with biologics. We want to see how your background aligns with the role of CMC Lead for cell and gene therapies.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about advancing cancer therapies and how your skills can contribute to our team. Keep it engaging and relevant!
Showcase Your Communication Skills: Since excellent communication is key for this role, make sure your application reflects that. Use clear and concise language, and don’t hesitate to share examples of successful interactions with health authorities.
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!
How to prepare for a job interview at Autolus Limited
✨Know Your CMC Inside Out
Make sure you brush up on your knowledge of Chemistry, Manufacturing, and Controls (CMC) specific to cell and gene therapies. Be ready to discuss your previous experiences with regulatory submissions and how you've navigated interactions with health authorities.
✨Showcase Your Communication Skills
Since excellent communication is key for this role, prepare examples that highlight your ability to convey complex regulatory information clearly. Think about times when you successfully communicated with cross-functional teams or presented to stakeholders.
✨Demonstrate Your Teamwork Spirit
This position emphasises teamwork, so be prepared to share stories that illustrate your collaborative approach. Discuss how you've worked with diverse teams to achieve regulatory goals, especially in fast-paced environments.
✨Stay Updated on Industry Trends
Familiarise yourself with the latest trends and regulations in the biopharmaceutical industry, particularly regarding cell and gene therapies. Being knowledgeable about current challenges and innovations will show your passion and commitment to advancing cancer therapies.
