hireejobs
Hyderabad Jobs
Banglore Jobs
Chennai Jobs
Delhi Jobs
Ahmedabad Jobs
Mumbai Jobs
Pune Jobs
Vijayawada Jobs
Gurgaon Jobs
Noida Jobs
Oil & Gas Jobs
Banking Jobs
Construction Jobs
Top Management Jobs
IT - Software Jobs
Medical Healthcare Jobs
Purchase / Logistics Jobs
Sales
Ajax Jobs
Designing Jobs
ASP .NET Jobs
Java Jobs
MySQL Jobs
Sap hr Jobs
Software Testing Jobs
Html Jobs
IT Jobs
Logistics Jobs
Customer Service Jobs
Airport Jobs
Banking Jobs
Driver Jobs
Part Time Jobs
Civil Engineering Jobs
Accountant Jobs
Safety Officer Jobs
Nursing Jobs
Civil Engineering Jobs
Hospitality Jobs
Part Time Jobs
Security Jobs
Finance Jobs
Marketing Jobs
Shipping Jobs
Real Estate Jobs
Telecom Jobs

Senior Executive, Regulatory Affairs, Pre Approval Injectable USA Market

Fresher   Ahmedabad, Gujarat   26 Oct, 2025
Job LocationAhmedabad, Gujarat
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaNot Mentioned
EmploymentTypeFull-time

Job Description

    Role Overview:As a Regulatory Affairs Specialist at Amneal, your primary responsibility will be to prepare regulatory strategies for complex products such as injectables, ophthalmic, otic, topical gel, and 505(b)(2) products for both the US and EU markets. You will be drafting Pre-ANDA/Pre-IND/ScA meeting packages, controlled correspondences, and deficiency responses for complex products. Additionally, you will review API and finished product in-vitro characterization reports, collaborate with cross-functional teams, and ensure compliance with regulatory standards.Key Responsibilities:- Prepare Regulatory strategies for Complex Products including injectables, peptides, microspheres, liposomes, nano-suspensions, etc., as well as 505(b)(2) Products for the US and EU market.- Draft Pre-ANDA/Pre-IND/ScA meeting packages for the US and EU market.- Draft controlled correspondences on complex issues.- Draft Deficiency responses for Complex Products and 505(b)(2) Products.- Review API and FP in-vitro characterization/sameness reports.- Collaborate and work closely with cross-functional teams.Qualifications:- Suitably qualified individuals with a strong Scientific and Regulatory background.- Academic degree in Pharmacy (M. Pharm), preferably with a specialization in Regulatory Affairs or Pharmaceutics.- Minimum 3 years of experience in Regulatory Affairs with hands-on experience in Injectable dosage forms, including submission of ANDA, responding to deficiencies, and FDA communications.- Possess good judgment on regulatory, quality, and technical compliance issues.- Demonstrate high personal integrity, trustworthiness, and a strong compliance and quality mindset.- Solution-oriented with a strong sense of ownership and accountability.- Collaborative and team-oriented approach, capable of working cross-functionally and in a matrixed and integrated way.(Note: Additional details about the company and the Human Resources team have been omitted as per the instructions),

Keyskills :
InjectablesPeptidesMicrospheresLiposomesAPIRegulatory strategiesComplex ProductsNanosuspensionsOphthalmicOticTopical gelDDCP505b2 ProductsPreANDAPreINDScA meeting packagesDrafting controlled correspondencesDeficiency responsesFP invitro

Senior Executive, Regulatory Affairs, Pre Approval Injectable USA Market Related Jobs

© 2019 Hireejobs All Rights Reserved