GSK Hiring Senior Regulatory Specialist

GSK Recruitment 2026 – Senior Regulatory Specialist

GSK is inviting applications for the Senior Regulatory Specialist position in Bengaluru, India. This opportunity is suited to professionals with experience in pharmaceutical regulatory affairs, Chemistry, Pharmacy, or related scientific disciplines. The role focuses on Chemistry, Manufacturing and Controls (CMC) regulatory submissions, global dossier strategy, and regulatory compliance across multiple vaccine projects. Candidates with 3–8 years of experience and knowledge of global regulatory requirements may be suitable for this opportunity.

Company Overview

GSK is a global biopharmaceutical company focused on developing medicines and vaccines to prevent and treat diseases. Its research and development activities span respiratory diseases, immunology and inflammation, oncology, HIV, and infectious diseases.

The company brings together science, technology, and talent to advance drug development and improve patient health worldwide.

Job Details

Job Role & Responsibilities

The Senior Regulatory Specialist will represent the CMC Delivery team on regulatory networks and matrix teams, supporting Pharma Supply Chain, Commercial, Quality Assurance, third-party Contract Manufacturing Organizations, and the Office of the Chief Medical Officer in preparing components for global regulatory dossiers.

Key responsibilities include:

• Independently manage multiple vaccine CMC regulatory submission assignments across different dosage forms.

• Execute agreed dossier strategies and ensure regulatory submissions meet their intended requirements.

• Assess data and documentation to confirm that regulatory dossiers are fit for purpose.

• Identify risks associated with submission data and information packages.

• Escalate issues with potential business impact to the line manager.

• Review and approve dossiers prepared by peers, where required.

• Identify opportunities to improve regulatory processes, policies, and systems.

• Interpret regulations, guidelines, procedures, and policies related to pharmaceutical product registration and manufacturing.

• Support the submission, review, and approval of global regulatory applications.

• Provide subject matter expertise and regulatory guidance within the department and to external stakeholders.

• Mentor and train new team members.

• Build effective working relationships with relevant stakeholders, including Pharma Supply Chain, Local Operating Companies, and other project teams.

• Communicate project and policy matters across GSK to support appropriate regulatory and business decisions.

Eligibility & Qualifications

Candidates should have a bachelor’s degree in Chemistry, Pharmacy, or another related scientific or technical discipline.

Relevant qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Chemistry, M.Sc. Chemistry, B.Sc. Pharmaceutical Sciences, M.Sc. Pharmaceutical Sciences, or other related scientific or technical qualifications. The official posting specifies the relevant degree disciplines rather than an exhaustive list of accepted courses.

Experience Requirements

• 3–8 years of experience in a relevant regulatory or scientific environment, as stated in the posting.

• Experience working in a complex scientific organization.

• Knowledge of global or EMAP regulatory submissions.

• Understanding of regulatory agency guidelines and submission requirements.

• Broad understanding of the pharmaceutical industry, drug development, and research and development processes.

• Ability to interpret and advise on global regulatory guidelines and requirements.

Required Skills

Applicants should demonstrate the following capabilities:

• Strong organizational skills and attention to detail.

• Commitment to delivering high-quality work under regulatory submission deadlines.

• Excellent written and verbal communication skills.

• Ability to present regulatory information clearly and concisely.

• Understanding of the regulatory environment and pharmaceutical manufacturing requirements.

• Ability to manage multiple assignments and changing priorities.

• Strong stakeholder management and collaboration skills.

• Ability to work effectively in a matrix organization.

• Flexibility in responding to shifting project timelines and business requirements.

• Ability to provide regulatory guidance and share knowledge with colleagues.

Work Location & Arrangement

The position is based in Bengaluru, India. The job details identify the arrangement as hybrid, while the work arrangement description states that the role is on-site in India and involves collaboration with local and global colleagues, including virtual meetings. Candidates should check the official listing for the applicable work arrangement.

Salary & Benefits

The job posting includes a salary range of PLN 144,750 to PLN 241,250 as a location-specific pay-transparency disclosure. This is a Polish złoty salary range and should not be interpreted as the salary offered for the Bengaluru position.

How to Apply

Interested candidates can review the full job description and submit their applications through GSK’s official careers website.

Apply here: GSK Senior Regulatory Specialist – Official Careers Page

GSK does not charge any recruitment fee. Applicants should avoid paying individuals or agencies for job applications, interviews, or recruitment opportunities.

Job Summary