GSK Career: Chemistry Job in Bangalore | Regulatory Associate Manager Position
Are you looking for a rewarding Chemistry Job that lets you shape the future of global healthcare? GSK is offering an incredible opportunity as a Regulatory Associate Manager – CMC Variations, Small Molecules in Bengaluru, India or Poznan, Poland. This position is ideal for professionals passionate about pharmaceutical science and eager to grow their GSK career. Explore one of the most sought-after Chemistry Jobs in Bangalore and make a difference in patients’ lives worldwide.
Position Summary
In this role, you will lead regulatory activities for product variations, ensuring compliance and quality across multiple projects. You will collaborate closely with supply chain, quality assurance, and commercial teams to support global regulatory submissions. This is a perfect opportunity for professionals looking to expand their Chemistry Job expertise and grow their GSK career in a collaborative, innovative, and inclusive environment.
Job Details
- Job Post: Regulatory Associate Manager
- Location: Bangalore
- Req ID: 430069
Responsibilities
- Manage regulatory activities for product variations across multiple projects, ensuring timely delivery and compliance.
- Collaborate with internal and external stakeholders to produce high-quality components for global regulatory dossiers.
- Assess data to ensure submissions are fit for purpose and identify risks associated with submission packages.
- Act as a reviewer or approver for regulatory dossiers prepared by peers, driving process improvements.
- Provide guidance on regulatory requirements, policies, and procedures to expedite submission and approval processes.
- Build effective networks within the organization to share knowledge and promote best practices.
Basic Qualification
- Experience managing multiple project assignments, including CMC variations, source transfers, and handling Health Authority Questions (HAQs) for finished products and active ingredients.
- Ability to execute dossier strategies, complete data assessments, and ensure compliance with GSK regulatory processes and global requirements.
- Expertise in preparing, reviewing, and coordinating submission-ready documents.
- Strong collaboration skills with Product Owners, Project Managers, and global regulatory teams.
- Proven ability to monitor regulatory intelligence and identify improvement opportunities for CMC processes.
Preferred Qualification
- Bachelor’s or Master’s degree in chemistry, biotechnology, pharmacy, or a related technical field.
- Relevant experience in regulatory affairs within the pharmaceutical industry.
- Strong understanding of ICH CTD documentation (Modules 2 and 3) and change management processes.
- Excellent communication, interpersonal, and analytical skills.
- Ability to handle multiple priorities and deliver results under pressure.
Why GSK?
At GSK, our purpose is to unite science, technology, and talent to get ahead of disease together. We are a global biopharma leader committed to impacting the health of 2.5 billion people by the end of the decade. Our focus spans specialty medicines and vaccines across four therapeutic areas: respiratory, immunology and inflammation, oncology, HIV, and infectious diseases. We foster an environment where people can thrive — being ambitious for patients, accountable for impact, and doing the right thing. If you are passionate about regulatory science and seeking a fulfilling Chemistry Job that advances your GSK career, we encourage you to apply today. If you’re searching for Chemistry Jobs in Bangalore with global exposure and professional growth, this position offers the ideal platform to excel in your GSK career.
