Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Executive, Labeling Reviewer

Amneal
Amneal
4-8 years
Not Disclosed
Ahmedabad, Gujarat, India
10 March 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Executive – Labeling Reviewer

Company: Pharmaceutical Organization
Location: Ahmedabad City, Gujarat, India
Job Type: Full-Time

Experience Required
Minimum 4–8 years of experience in regulatory labeling or pharmaceutical regulatory affairs with hands-on exposure to US FDA labeling requirements for ANDA submissions and post-approval regulatory activities.

Education
Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, Regulatory Affairs, or a related discipline.

Job Overview
The Senior Executive – Labeling Reviewer will be responsible for compiling, reviewing, and managing US regulatory labeling documentation to support ANDA submissions and lifecycle management activities. The role requires strong knowledge of US FDA labeling regulations and effective coordination with cross-functional teams to ensure labeling compliance, accuracy, and timely regulatory submissions.

The position also supports product launch readiness by ensuring that all labeling components are reviewed, approved, and available in accordance with regulatory timelines and company procedures.

Key Responsibilities
Compile and perform the initial review of US labeling documents for original ANDA submissions and additional strength submissions.
Coordinate with cross-functional teams to ensure alignment on regulatory priorities, responsibilities, and filing timelines.
Follow up with internal stakeholders to obtain labeling documents within defined timelines and ensure completeness of all labeling modules prior to submission.
Maintain up-to-date knowledge of US FDA labeling regulations, guidance documents, and industry best practices.
Ensure availability and readiness of labeling modules required for regulatory responses including Complete Response (CR), Information Request (IR), and Deficiency Response Letter (DRL) submissions.
Coordinate with cross-functional teams to gather and compile required documentation for regulatory responses.
Ensure launch readiness for all new products by issuing the most current approved labeling (Ok-To-Print) and ensuring timely availability of printed labeling materials.
Support drug listing completion for newly approved products during the initial launch phase.
Assist in reviewing Reference Listed Drug (RLD) labeling updates for oral solid dosage and injectable products and ensure timely submission of revised labeling modules.
Coordinate with supervisors and regulatory teams to align priorities related to labeling updates.
Initiate and facilitate Change Controls and Labeling Review Committee activities related to labeling modifications.
Track and manage labeling changes required for annual regulatory reporting.
Manage Safety Labeling Change Notifications in compliance with regulatory requirements.
Apply knowledge of patent and exclusivity considerations, including labeling carve-outs where applicable.
Support the development, revision, and compliance of labeling Standard Operating Procedures.

Required Skills and Competencies
Strong understanding of US FDA labeling regulations for oral solid dosage and injectable pharmaceutical products.
Excellent written and verbal communication skills in English.
Strong coordination, follow-up, and documentation management capabilities.
High attention to detail with the ability to review complex regulatory documents accurately.
Ability to manage multiple projects and priorities while meeting strict regulatory timelines.

Professional Skills
Strong analytical and problem-solving abilities.
Ability to collaborate effectively with regulatory, quality, and development teams.
Excellent organizational and time-management skills.
Commitment to maintaining regulatory compliance and high-quality standards in pharmaceutical labeling processes.