Looking for pharma jobs in regulatory affairs? GlaxoSmithKline (GSK) is hiring for a GRA Apprentice role in Bengaluru—an excellent opportunity to start a career in global pharma.
About the Company
GlaxoSmithKline (GSK) is a globally recognized biopharmaceutical leader committed to improving human health through innovation.
The company focuses on vaccines, specialty medicines, and infectious diseases, with strong capabilities in R&D, regulatory science, and global healthcare delivery.
GSK operates in multiple therapeutic areas including oncology, immunology, respiratory diseases, and HIV, aiming to impact over 2.5 billion people worldwide. Its strong ethical foundation, patient-centric approach, and innovation-driven culture make it one of the most preferred employers in the pharmaceutical industry.
Job Details
- Company Name: GSK (GlaxoSmithKline)
- Experience: Freshers / Entry-level with relevant exposure
- Qualification: M.Pharm
- Location: Bengaluru, India
- Work Type: Full-time
Job Description
GSK is hiring a GRA (Global Regulatory Affairs) Apprentice to support global regulatory processes, submissions, and pharmacovigilance activities.
This role is ideal for candidates who want to build a long-term career in regulatory affairs, drug safety, and global compliance. You will work closely with experienced professionals and gain hands-on exposure to international regulatory frameworks.
GRA Apprentice
- Department: Global Regulatory Affairs
- Market: Global Pharma / Biopharma
- Role: Regulatory documentation, submission support, and compliance tracking
- Experience: Entry-level (exposure to pharma industry preferred)
- Education/Qualification: M.Pharm
Skills/Qualifications
- Strong understanding of global regulatory processes and guidelines
- Basic knowledge of pharmacovigilance systems and methodologies
- Excellent written and verbal communication in scientific terminology
- Ability to analyze data and generate insights
- Attention to detail and accuracy in documentation
- Good interpersonal and teamwork skills
- Proficiency in MS Office and web-based applications
- Ability to manage multiple tasks and meet deadlines
- Adaptability and willingness to learn in a fast-paced environment
Key Responsibilities
- Assist in preparation and submission of regulatory documents
- Support pharmacovigilance and safety reporting activities
- Maintain accurate regulatory records and databases
- Review and analyze scientific and regulatory data
- Coordinate with cross-functional teams globally
- Ensure compliance with international regulatory standards
- Participate in audits and internal quality checks
Benefits/Perks
- Work with a globally reputed pharmaceutical company
- Exposure to international regulatory frameworks and systems
- Structured learning and career development programs
- Opportunity to transition into full-time regulatory roles
- Inclusive, diverse, and collaborative work environment
- Strong mentorship and guidance from industry experts
How to Apply
Interested candidates should apply through the official GSK careers portal before the deadline.
- Application Deadline: 24 April 2026
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the GSK Career page.
🔗 Click below to apply directly for this job
For more pharma job updates, visit:
👉 https://pharmarecruiter.in
Don’t delay—opportunities at GSK are highly competitive and close quickly!
Why You Should Join
Joining GSK means becoming part of a purpose-driven organization that values innovation, integrity, and patient impact.
You will gain exposure to global healthcare challenges, advanced regulatory systems, and a collaborative culture that encourages continuous learning and professional growth.
GSK’s focus on employee well-being, career progression, and global exposure makes it an ideal choice for building a long-term pharmaceutical career.
FAQs
Who can apply for this GSK job?
Candidates with an M.Pharm degree and interest in regulatory affairs can apply.
Is prior experience required?
No, freshers can apply, but basic knowledge of regulatory or pharmacovigilance is preferred.
What career growth can I expect?
You can grow into roles like Regulatory Affairs Associate, Specialist, or Manager over time.
Is this role suitable for long-term career growth?
Yes, regulatory affairs is a high-demand and stable career path in the global pharma industry.
