At a Glance
- Tasks: Support global regulatory CMC for small molecule products and collaborate with cross-functional teams.
- Company: Dynamic company focused on innovative pharmaceutical solutions.
- Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
- Other info: Join a supportive team with diverse projects and career advancement opportunities.
- Why this job: Make a real impact in the pharmaceutical industry while developing your regulatory expertise.
- Qualifications: Experience in regulatory affairs and strong communication skills.
The predicted salary is between 50000 - 65000 £ per year.
The Chemistry Manufacturing Control Consultant will support the execution of multi-product global regulatory CMC for marketed products for small molecule products. This role contributes to the preparation and submission of regulatory CMC documentation and provides regulatory support to various cross-functional teams.
Key Duties and Responsibilities
- Execute commercial Lifecycle Management (LCM) strategy and submissions with a focus on Middle East and North Africa.
- Review CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies for small molecule products.
- Work with regulatory colleagues in development of global regulatory CMC strategies and submissions.
- Participate effectively on cross-functional teams and may serve as the primary regulatory CMC contact for assigned products and projects.
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Regulatory Consultant - CMC (CMC with small molecule products) in London employer: Syneos Health
As a leading employer in the pharmaceutical sector, our company offers a dynamic work environment that fosters collaboration and innovation. With a strong commitment to employee development, we provide ample opportunities for growth and advancement, particularly in the exciting field of regulatory consultancy for small molecule products. Located in a vibrant region, we also promote a culture of inclusivity and support, ensuring that every team member feels valued and empowered to contribute to our mission.
