Regulatory Associate Manager - Global Labelling

Posted:
1/28/2026, 3:14:04 PM

Location(s):
Karnataka, India ⋅ Bengaluru, Karnataka, India

Experience Level(s):
Senior

Field(s):
Business & Strategy ⋅ Legal & Compliance

Workplace Type:
Hybrid

Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
Find out more:
Our approach to R&D Position Summary You will lead global labelling activities that help prescribers and patients use our products safely and effectively. You will work closely with clinical, safety, regulatory and commercial colleagues across multiple regions. We value clear scientific thinking, practical collaboration, strong writing, and a drive to improve how we work. This role offers high visibility, growth opportunities, and the chance to contribute directly to GSK’s mission of uniting science, technology and talent to get ahead of disease together. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Lead and coach a small team of labelling professionals to deliver global and local labelling content on time and to quality. - Manage updates to Global Product Information, including drafting text, coordinating expert input, and preparing materials for governance review. - Manage country and regional labelling activities worldwide, including coordination of localised documents, artwork updates, and responses to regulatory questions. - Act as subject matter expert for labelling processes and regulatory requirements, advising cross-functional teams on content and compliance. - Drive process improvements, standardisation and training to improve labelling quality, cycle time and consistency. - Build strong stakeholder relationships and represent labelling in cross-functional forums and governance committees. Why You? This role is based in India and follows a hybrid working model with regular office presence required. We welcome applicants who are motivated to grow, who bring clarity and care to their work, and who enjoy collaborating across teams. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: - Bachelor’s degree in life sciences, pharmacy, regulatory affairs, or related field. - At least 8 years’ relevant regulatory or labelling experience in a regulated environment. - Experience leading people or small teams and delivering regulatory outputs to time and quality. - Strong written and verbal communication skills in English, with clear scientific writing ability. - Solid understanding of global labelling content and lifecycle maintenance processes. - Proven ability to manage multiple priorities and work with cross-functional stakeholders. Preferred Qualification If you have the following characteristics, it would be a plus: - Advanced degree (Master’s or PhD) in life sciences, pharmacy or related field. - Experience with major regulatory markets and product information requirements (for example EU, US, and other key markets). - Experience with label management or regulatory content systems and document management tools. - Familiarity with global governance processes and committee preparation. - Demonstrated track record in driving process improvements and standardisation. - Strong stakeholder management and influencing skills at senior levels. What we offer You will join a team where your work makes a meaningful difference for patients. You will gain exposure to global regulatory partners and complex labelling challenges. You will be supported to develop your skills and take on increasing responsibility. How to apply If this role matches your experience and ambition, we would like to hear from you. Please apply now and tell us how your skills and values align with this opportunity. If you need any adjustments during the recruitment process, please contact the recruitment team to discuss your needs.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Inclusion at GSK:

As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.

Please contact our Recruitment Team at [email protected] to discuss your needs.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.

GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.

If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing [email protected], so that we can confirm to you if the job is genuine.

 

Glaxosmithkline Plc

Website: https://gsk.com/

Headquarter Location: London, England, United Kingdom

Employee Count: 10001+

Year Founded: 1929

IPO Status: Public

Last Funding Type: Grant

Industries: Biotechnology ⋅ Health Care ⋅ Pharmaceutical