Acme Generics Regulatory Affairs Executive Recruitment 2026 | B.Pharm M.Pharm Jobs in Ahmedabad for EU Regulatory Affairs Professionals
Acme Generics Regulatory Affairs Executive / Senior Executive Jobs 2026
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(Acme Generics Regulatory Affairs Executive Recruitment 2026) |
Introduction
Acme Generics has announced new recruitment opportunities for Regulatory Affairs Executive and Senior Executive positions at its Ahmedabad facility. This latest pharmaceutical job opening is ideal for professionals with experience in EU Regulatory Affairs, eCTD dossier preparation, lifecycle management, pharmaceutical compliance, and regulatory submissions.
Candidates looking for Regulatory Affairs jobs in Ahmedabad, EU market pharmaceutical jobs, eCTD submission careers, or international regulatory affairs opportunities can explore this opening. The company is seeking qualified professionals who can support European regulatory operations and ensure compliance with global pharmaceutical standards.
About Acme Generics
Acme Generics is a well-established pharmaceutical company engaged in the development, manufacturing, and marketing of high-quality pharmaceutical products for domestic and international markets. The company focuses on regulatory compliance, quality assurance, research-driven development, and global market expansion.
With growing operations in regulated markets, Acme Generics continues to strengthen its regulatory affairs team to support product registrations, lifecycle management, and compliance activities across multiple international regions.
Company Details
Company Name: Acme Generics Pvt. Ltd.
Headquarters: Ahmedabad, Gujarat, India
Industry: Pharmaceuticals
Business Area: Generic Pharmaceuticals, Regulatory Affairs, International Markets
Founded: Pharmaceutical industry presence for several years, with growing global operations
Employee Strength: 500+ Employees (Approx.)
Focus Markets: European Union, International Regulated Markets
Job Overview Summary
Acme Generics is hiring experienced Regulatory Affairs professionals for its EU Market Regulatory Affairs division. The selected candidates will be responsible for preparing and managing pharmaceutical dossiers, regulatory submissions, lifecycle management activities, and compliance documentation for European markets.
This role provides excellent exposure to international pharmaceutical regulations, EU submissions, regulatory approvals, and global compliance processes.
Vacancy Details
Company Name: Acme Generics
Position: Regulatory Affairs Executive / Senior Executive
Department: Regulatory Affairs
Location: Ahmedabad, Gujarat
Employment Type: Full-Time
Qualification: B.Pharm / M.Pharm
Experience Required: 3–10 Years
Market Focus: European Union (EU)
Industry: Pharmaceutical Industry
Job Role Explanation
The Regulatory Affairs Executive role focuses on ensuring pharmaceutical products meet European regulatory requirements before and after market approval.
Professionals in this role work closely with regulatory authorities, internal departments, and international partners to support product registrations, dossier submissions, lifecycle management, and regulatory compliance activities.
The position is highly suitable for candidates interested in long-term careers in Regulatory Affairs, International Pharmaceutical Compliance, and Global Product Registration.
Key Responsibilities
Selected candidates will be responsible for handling various regulatory affairs functions for EU markets.
Major responsibilities include:
Preparing and reviewing eCTD and NeeS dossiers.
Compiling CTD Modules 1 to 5.
Managing pharmaceutical product submissions.
Supporting EU regulatory approval activities.
Handling variations, renewals, and post-approval changes.
Preparing responses to deficiency letters and regulatory queries.
Supporting PSUR and PBRER submissions.
Maintaining regulatory databases and submission trackers.
Reviewing labeling, artwork, SmPC, and PIL documentation.
Coordinating with R&D, QA, QC, Production, and Packaging teams.
Supporting DCP and MRP regulatory procedures.
Monitoring updates in EU regulatory guidelines.
Ensuring continuous compliance with EMA requirements.
Supporting inspections and regulatory audits.
Eligibility Criteria
Educational Qualification
Candidates must possess:
B.Pharm
M.Pharm
Experience Required
Minimum Experience: 3 Years
Maximum Experience: 10 Years
Preferred Background
EU Regulatory Affairs
International Product Registration
Dossier Preparation
Regulatory Compliance
Pharmaceutical Documentation
Lifecycle Management
Skills Required
Candidates should possess the following skills:
Strong understanding of EU pharmaceutical regulations.
Knowledge of eCTD publishing and dossier management.
Experience with CTD documentation.
Understanding of EMA guidelines.
Regulatory lifecycle management expertise.
Strong documentation skills.
Project coordination abilities.
Communication and stakeholder management skills.
Regulatory database management knowledge.
Analytical and problem-solving abilities.
Ability to manage multiple submissions simultaneously.
Attention to detail and a compliance-focused mindset.
Salary Estimate
Based on current pharmaceutical industry standards in Ahmedabad for experienced Regulatory Affairs professionals, the expected salary range may be:
Estimated Salary Range
₹6 LPA to ₹18 LPA
Actual compensation may vary based on:
Experience level
EU regulatory expertise
Submission exposure
Current salary package
Technical interview performance
Professional certifications
Why Join Acme Generics?
Working with Acme Generics offers several professional advantages:
Exposure to international pharmaceutical markets.
Hands-on experience with EU regulatory submissions.
Opportunity to work on global registration projects.
Career growth in Regulatory Affairs.
Learning opportunities in lifecycle management.
Exposure to DCP and MRP procedures.
Collaboration with cross-functional pharmaceutical teams.
Professional and compliance-driven work environment.
Interview Details
The company has not officially announced a walk-in interview schedule.
Shortlisted candidates may be contacted directly by the HR team for the selection process.
Expected Selection Process
Application Screening
HR Discussion
Technical Regulatory Affairs Interview
Document Verification
Final HR Round
Offer Release
Required Documents
Candidates should keep the following documents ready before applying:
Updated Resume/CV
Educational Certificates
B.Pharm or M.Pharm Degree Certificates
Experience Certificates
Current CTC Documents
Latest Salary Slips
Government Identity Proof
Passport Size Photographs
Regulatory Affairs Project Details (if applicable)
How to Apply
Interested and eligible candidates can send their updated resume to the official recruitment email.
Email ID: pratik.joshi@acmegenerics.in
Email Subject Line:
Regulatory Affairs Executive – EU Market
Candidates are advised to apply as early as possible.
Frequently Asked Questions (FAQs)
Q1. What is the job location?
The position is based in Ahmedabad, Gujarat.
Q2. What qualifications are required?
Candidates must possess B.Pharm or M.Pharm qualifications.
Q3. What experience is required?
Applicants should have 3–10 years of Regulatory Affairs experience.
Q4. Which market will candidates work for?
The role focuses on the European Union (EU) pharmaceutical market.
Q5. Is eCTD experience required?
Yes, knowledge of eCTD publishing and dossier preparation is highly preferred.
Q6. What is the expected salary?
The estimated salary range is approximately ₹6 LPA to ₹18 LPA.
Q7. What departments will candidates coordinate with?
R&D, QA, QC, Production, Packaging, and Regulatory teams.
Q8. How can candidates apply?
Candidates can apply by emailing their updated resume to pratik.joshi@acmegenerics.in.
Final Conclusion
The Acme Generics Regulatory Affairs Executive Recruitment 2026 presents an excellent opportunity for experienced pharmaceutical professionals looking to advance their careers in EU Regulatory Affairs and international pharmaceutical compliance.
The role provides exposure to dossier preparation, regulatory submissions, lifecycle management, EU market registrations, and pharmaceutical compliance activities. Candidates with strong regulatory knowledge and experience in EU submissions can benefit significantly from this career opportunity.
Interested professionals should review the eligibility criteria carefully and submit their applications at the earliest for consideration.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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