At a Glance
- Tasks: Lead regulatory submissions and ensure compliance for innovative pharmaceutical products.
- Company: Join a dynamic pharmaceutical company focused on impactful healthcare solutions.
- Benefits: Competitive salary, professional development, and a supportive work environment.
- Other info: Opportunity to manage complex projects and grow your career in a fast-paced industry.
- Why this job: Make a difference in healthcare by navigating complex regulatory landscapes.
- Qualifications: Degree in life sciences and substantial regulatory experience required.
The predicted salary is between 51750 - 63250 £ per year.
Select Pharma Recruitment provided pay range
This range is provided by Select Pharma Recruitment. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
- Base pay range
- Direct message the job poster from Select Pharma Recruitment
Responsibilities
- Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applications.
Manages increasingly complex submissions making decisions independently and with minimal referral to line manager.
- Ensure regulatory submissions are made on time and any delays are communicated to all relevant stakeholders in a timely manner so as to minimize impact to the business
- Provide regulatory input on pharmaceutical development and CMC and review quality documentation to ensure regulatory compliance with UK and EU legislation
- Provide regulatory input on artworks and ensure approval in time for product launch and compliance with legislation and guidelines.
Qualifications and Required Experience
- Degree in a suitable scientific discipline (biological/chemistry/life sciences).
- Substantial regulatory experience across the full product lifecycle.
- Strong due diligence and report writing; ability to write up a report with the information found (deficiencies, errors etc in the dossier or territory specific updates needed prior to submission)
- Strong CMC regulatory experience, including preparation and review of Module 3 CTD.
- Solid understanding of pharmaceutical manufacturing processes, analytical methods and regulatory expectations for CMC compliance.
- Broad experience of managing relevant regulatory submissions, with demonstrated ability to work independently and manage complex projects.
- In depth knowledge of UK and European regulatory affairs legislation and guidance.
- Planning and organisation skills - Ability to handle multiple tasks/projects and manage priorities accordingly.
- Able to work under pressure and to strict deadlines.
- A confident credible communicator with good negotiation skills.
- Able to build relationships at all levels of the business.
- Excellent written communication skills with attention to detail.
- Able to independently identify and initiate tasks/projects.
- Seniority level
- Mid-Senior level
- Employment type
- Full-time
- Job function
- Science
- Industries
- Pharmaceutical Manufacturing
- #J-18808-Ljbffr
Principal Regulatory Affairs Officer employer: Select Pharma Recruitment
Join a dynamic and innovative pharmaceutical company that values compliance and integrity, offering a supportive work culture where your expertise in Regulatory Affairs will be recognised and rewarded. With a strong focus on employee development, you will have access to continuous training and growth opportunities, all while working in a collaborative environment that prioritises teamwork and open communication. Located in a thriving area, this role not only provides a chance to make a significant impact but also offers a fulfilling career path in a sector dedicated to improving health outcomes.
