Life Sciences Job at GSK | Regulatory Specialist | Apply Now
GSK is currently seeking a Regulatory Specialist for its CMC Renewals team, with vacancies across global hubs including Bengaluru (India), Poznan/Warsaw (Poland), and Cairo (Egypt). This Regulatory Job is a high-impact technical role focused on the Chemistry, Manufacturing, and Controls (CMC) lifecycle for GSK’s pharmaceutical and vaccine portfolios. If you are looking for a Life Sciences Job, you will be the technical architect behind regulatory submissions, ensuring that life-saving products remain compliant, safe, and available on international markets. If you are looking to advance a GSK Career within a digitally-forward environment, this position offers a front-row seat to the global biopharma landscape.
- Job Position: Regulatory Specialist
About the Company
GSK is a global biopharma company with a singular purpose: to unite science, technology, and talent to get ahead of disease together. The organization aims to positively impact the health of 2.5 billion people by the end of the decade. GSK focuses on four core therapeutic areas—respiratory, immunology and inflammation, oncology, and infectious diseases—while maintaining a world-leading presence in vaccines and HIV treatments. A GSK Career is built on a culture of being ambitious for patients, accountable for impact, and doing the right thing. The company is currently undergoing a significant digital transformation, integrating advanced data standards and technology (like Veeva Vault) into its core regulatory processes. In addition, GSK is renowned for fostering growth in life sciences job opportunities with a global outlook.
Key Responsibilities
In this Life Sciences Job, you will manage the technical documentation that proves a drug’s quality and consistency as it moves through its post-approval lifecycle.
- Dossier Authoring: Author, compile, and check regulatory submissions related to drug manufacturing and quality control for Pharma and Vaccines. As you author these dossiers, you are solidifying your role in a life sciences job at GSK.
- Renewal Management: Manage multiple CMC renewal assignments, including drafting responses to technical questions from global Health Authorities.
- Strategy & Compliance: Define regulatory strategies and complete data assessments to ensure dossiers comply with both internal processes and external international requirements. Compliance work further reflects the expertise required for a life sciences job in the regulatory domain.
- Risk Mitigation: Identify and escalate technical risks associated with submission data packages that could have a business impact.
- Stakeholder Synergy: Collaborate with Global Manufacturing & Supply (GMS) and Local Operating Companies (LOCs) across worldwide markets to deliver high-quality dossiers on time. These collaborations are essential in any life sciences job, especially within multinational biopharma organizations.
- Regulatory Intelligence: Monitor the global regulatory environment and proactively act on changes in manufacturing or registration requirements.
Qualifications and Requirements
GSK is looking for agile, detail-oriented professionals who possess a blend of scientific knowledge and digital fluency. To qualify for a life sciences job here, candidates must demonstrate the ability to adapt and apply their expertise in a fast-paced regulatory landscape.
- Education: Minimum of a Bachelor’s degree in Life Sciences or a related field. This educational background is the foundation for success in any Life Sciences Job.
- Experience: 1–2 years of relevant experience in regulatory affairs or the pharmaceutical industry.
- Technical Knowledge: Mandatory familiarity with post-approval CMC regulatory procedures and ICH CTD documentation.
- Digital Skills: A mindset that embraces innovation; knowledge of Veeva Vault is considered a strong asset.
- Communication: Excellent written and verbal English skills, with the ability to present complex technical information to diverse global teams. Candidates in a life sciences job must have outstanding communication to share scientific and regulatory concepts.
- Analytical Thinking: Ability to independently provide solutions to regulatory issues and propose process improvements.
In summary, the Regulatory Specialist (CMC Renewals) position is a definitive Regulatory Job for those who want to bridge the gap between science and global market access. Launching a GSK Career in this capacity allows you to master the complexities of ICH CTD documentation while playing a critical role in maintaining the supply of vaccines and medicines worldwide. Because this role is heavily involved in digital transformation, your ability to adapt to platforms like Veeva Vault and participate in virtual global meetings will be essential to your success. With the post date being March 24, 2026, this is a fresh opportunity to join one of the world’s leading biopharma organizations. Ultimately, pursuing a Life Sciences Job at GSK will open new doors for professionals seeking impact and innovation in healthcare.
