Pharma Job at GSK for Submission Lead Role | Apply
GSK Careers are now open for a Submission Lead, focusing on Submission Delivery Excellence and Lifecycle Management, across Bangalore, Cairo, and Poznan. This role offers a unique opportunity to lead regulatory submission processes that impact millions of lives worldwide. This pharma job provides a unique opportunity to lead regulatory submission processes that impact millions of lives worldwide. If you’re a proactive, detail-oriented professional with a passion for compliance and collaboration, join GSK’s mission to unite science, technology, and talent to get ahead of disease together in this exciting pharma job opportunity.
Job Details
- Job Position: Submission Lead, Submission Delivery Excellence, Lifecycle Management
- Location: Bangalore, India
- Job ID: 428987
About the Company
Explore exciting opportunities at GSK Careers, where you can join a global biopharma company committed to uniting science, technology, and talent to get ahead of disease together. With a bold mission to positively impact the health of 2.5 billion people by 2030, GSK focuses on four key therapeutic areas: respiratory, immunology and inflammation, oncology, and infectious diseases. The company fosters an inclusive, innovative, and purpose-driven environment where employees can thrive while delivering transformative healthcare solutions. Consider applying for this pharma job if you are eager to contribute to GSK’s mission.
Job Description
The Submission Lead will play a key role in ensuring the timely, compliant, and high-quality delivery of regulatory submissions within the Lifecycle Management function. This pharma job requires working closely with cross-functional teams to manage submission deliverables that support global regulatory strategies.
Key Responsibilities
- Coordinate and deliver regulatory submissions that comply with local and global regulatory requirements.
- Collaborate with cross-functional teams to compile and review submission packages, including CMC (Chemistry, Manufacturing, and Controls) documentation.
- Monitor and interpret regulatory changes, providing guidance to internal teams.
- Support audits and inspections to ensure adherence to regulatory and company standards.
- Identify and implement process improvements in submission and documentation workflows.
- Foster effective relationships with internal and external stakeholders to ensure smooth submission processes.
Educational Qualification
Bachelor’s degree in Pharmacy, or Master’s degree in Regulatory Affairs, Pharmacy, or related discipline for this pharma job.
Experience and Skills
- Strong understanding of regulatory submission processes and lifecycle management.
- Excellent communication skills in English.
- Ability to manage multiple priorities in a fast-paced environment.
- Strong attention to detail and commitment to quality.
- Experience in a matrixed, international environment.
- Knowledge of global regulatory requirements (EU, US markets).
- Experience with regulatory systems such as Veeva Vault or similar.
- Proven ability to engage and influence senior stakeholders.
