Explore Top Pharma Jobs | Join GSK as a CMC Regulatory Project Manager
Looking to take your next step in pharma jobs or advance your career in Regulatory Affairs Jobs? Join GSK Careers as a CMC Regulatory Project Manager, where science, innovation, and purpose come together. In this exciting opportunity, you’ll play a key role in global Regulatory Affairs, ensuring that safe, high-quality medicines reach patients across the world. At GSK, your work shapes the future of healthcare making this one of the most rewarding pharma jobs in the industry.
- Job Position: CMC Regulatory Project Manager
- Job ID: 429428
- Location: Bengaluru, India
- Department: Regulatory Affairs
- Posted Date: October 27, 2025
- Closing Date: November 10, 2025
About This Pharma Job Opportunity at GSK
As a CMC Regulatory Project Manager in GSK’s Global Regulatory Affairs team, you will ensure uninterrupted access to essential medicines worldwide. You’ll develop global regulatory strategies, support lifecycle management for marketed small molecules, and collaborate with cross-functional teams in Quality, Technical, and Supply Chain to maintain compliance with global standards as part of your pharma job role.
Key Responsibilities in Regulatory Affairs Jobs
- Develop and deliver global and regional regulatory strategies for product submissions.
- Provide expert guidance on regulatory policies, requirements, and scientific standards.
- Support lifecycle management and ensure compliance with regional guidelines in your pharma job role.
- Collaborate across Regulatory, Development, Quality, and Manufacturing teams to enhance your career in pharma jobs, fostering growth and innovation.
- Manage regulatory activities ensuring continuous market supply.
- Drive innovation to adapt to evolving regulatory landscapes.
- Share best practices and promote efficiency across CMC teams.
Qualifications for GSK Careers in Pharma
Basic Qualifications:
- Bachelor’s degree in Pharmacy, Chemistry, or a related scientific discipline.
- Proven experience in CMC regulatory affairs or product development within pharma sector, particularly in pharma jobs like this one.
- Strong knowledge of global CMC regulatory requirements and submission processes.
- Excellent communication, project management, and problem-solving skills.
Preferred Qualifications:
- Master’s or Ph.D. in Pharmacy, Chemistry, or related discipline.
- Regulatory Affairs Certification (RAPS) or equivalent.
- Demonstrated ability to lead global regulatory strategies and influence stakeholders.
- Recognized expertise in a CMC subject area, crucial for numerous pharma jobs.
Why Join GSK?
GSK provides an inclusive and growth-oriented environment where employees thrive. The company offers competitive compensation, annual bonuses, comprehensive healthcare, pension plans, and share programs. With hybrid working options under the Performance with Choice model, employees enjoy flexibility and work-life balance. Join GSK to explore various jobs in pharma and benefit from a supportive environment.
At GSK, your work directly contributes to advancing healthcare innovation and improving patient lives globally through various pharma occupation opportunities.
Equal Opportunity Statement:
GSK is an Equal Opportunity Employer. All qualified applicants will receive equal consideration regardless of gender, race, religion, disability, age, or sexual orientation.
