
Regulatory Affairs Manager
4 weeks ago
Job Title: Senior Regulatory Manager – RoW Market
Department: Regulatory Affairs
Job Summary:
The Senior Regulatory Manager will be responsible for the preparation, review, and submission of high-quality regulatory dossiers and documents for pharmaceutical products intended for Rest of the World (RoW) markets, ensuring compliance with country-specific regulatory requirements. The role involves coordination with internal teams, external partners, and regulatory authorities to ensure timely product approvals and lifecycle management.
Key Responsibilities:
- Thorough knowledge of - Dossier Preparation & Review: Prepare and review CTD/eCTD/non-CTD dossiers for new product registrations, renewals, and variations for RoW markets (e.g., Africa, Southeast Asia, CIS, LATAM).
- Ensure dossiers are in line with current regulatory guidelines and client expectations.
- Regulatory Submissions & Approvals: Coordinate with agents for regulatory submission and queries.
- Track and manage timelines for submissions and approvals to ensure compliance with project milestones.
- Regulatory Intelligence & Compliance: Monitor changes in regulatory guidelines and keep relevant stakeholders informed.
- Ensure all submissions and regulatory strategies align with applicable national and international regulations.
- Lifecycle Management: Manage regulatory documentation for product variations, renewals, packaging/labelling updates, and post-approval changes.
- Audit & Documentation: Maintain and update regulatory databases and trackers.
Required Qualifications & Experience:
- Must have experience handling RoW markets.
- Strong knowledge of CTD/non-CTD formats and regulatory requirements of RoW markets.
- Experience in dealing with distributors/agents for regulatory submissions.
Key Skills:
- In-depth understanding of pharmaceutical regulatory processes.
- Strong documentation and technical writing skills.
- Ability to interpret and apply regulatory guidelines effectively.
- Excellent communication, coordination, and project management skills.
- Proficiency in MS Office and regulatory databases.
-
Regulatory Affairs
2 weeks ago
Ahmedabad, Gujarat, India VITAL INTELLIGENCE TECHNOLOGY PRIVATE LIMITED Full time ₹ 6,00,000 - ₹ 12,00,000 per year**Vivanza Biosciences Limited** is seeking a highly motivated and detail-oriented professional to join our team as a **Regulatory Affairs Executive** in Ahmedabad, Gujarat. This role is ideal for an individual with foundational experience in the pharmaceutical industry who is keen to grow their career in regulatory compliance and submissions for global...
-
Regulatory Affairs Officer
2 days ago
Ahmedabad, Gujarat, India CLAPS Industries Private Limited Full time ₹ 9,00,000 - ₹ 12,00,000 per yearCompany DescriptionCLAPS Industries Pvt Ltd. is a global pharmaceutical company founded by a team of visionary and successful individuals in the pharmaceuticals field. With a focus on delivering top-quality healthcare products and services worldwide, CLAPS is rapidly growing through product diversification, strategic manufacturing expansions, and strong...
-
regulatory affairs
1 week ago
Ahmedabad, Gujarat, India Sunrise Remedies Full time ₹ 15,00,000 - ₹ 28,00,000 per yearSunrise Remedies Job Opening for Regulatory Affairs (RA) officer.Experience: 1 YearIndustries: Pharmaceutical CompanyEducation: B.Sc. | M.Sc | B.Pharm | M.PharmJob Location: Santej Ahmedabad.Facilities Provided:– Transportation Facility Available (As Per Circumference Of Sunrise Remedies)*– Mediclaim and Food Facility provide By Company.*Key...
-
Regulatory Affairs Executive
2 weeks ago
Ahmedabad, Gujarat, India Vital Group Full time ₹ 12,000 - ₹ 14,90,645 per yearJob Opening: Regulatory Affairs Executive | Vital GroupLocation: SG Highway, AhmedabadExperience: 1–3 years (Pharma Industry)Key Responsibilities:Preparation and submission of dossiers, CTD/ACTD, and regulatory documents.Handling regulatory queries and compliance requirements.Coordination with internal teams to ensure timely submissions.Support in product...
-
Regulatory Affairs Executive
1 week ago
Ahmedabad, Gujarat, India Prompt Career Consultants Full time ₹ 15,00,000 - ₹ 28,00,000 per yearPrepare, submit regulatory dossiers for new product registrationsCoordinate and manage the submission of regulatory documents Facilitate communication with health authorities, responding to queries Required Candidate profileM. Pharm (Female Candidate Preferred)1 year of experience in Regulatory Affairs in Pharmaceutical Formulations unit desired.Excellent...
-
Regulatory Affairs Executive
1 week ago
Ahmedabad, Gujarat, India Uniza Group Full time ₹ 6,00,000 - ₹ 12,00,000 per yearCompany DescriptionUniza is part of the $150 M+ Pashupati group of companies, specializing in India Business, International Business, and the manufacturing of tablets, capsules, creams, and ointments. With a strong distribution network across 28 states in India, Uniza has established a significant presence in Dermatology, Cardio-Diabetic, Gynecology, and...
-
Ahmedabad, Gujarat, India Claps Industries Full time ₹ 8,00,000 - ₹ 12,00,000 per yearWe are hiring an International Regulatory Affairs Executive/Manager with expertise in regulatory documentation, CTD dossiers & query handling. Immediate joiners preferred. Candidates with 1+ year experience may also apply. Join our growing team
-
Regulatory Affairs Associate
1 week ago
Ahmedabad, Gujarat, India Smart Lion Full time ₹ 4,00,000 - ₹ 12,00,000 per yearRegulatory Affairs Associate Responsible for preparation, review & submission of regulatory documents (US FDA, EMA, ICH), ensuring compliance with guidelines, supporting product approvals, maintaining records & coordinating with authorities. Required Candidate profileBSC/MSC/B.Pharm or Life Sciences graduate with knowledge of regulatory guidelines, dossier...
-
Regulatory Affairs Specialist
5 days ago
Ahmedabad, Gujarat, India, Gujarat Frisch Medical Devices PVT LTD Full timeJob Title: Regulatory Affairs Junior ManagerLocation: At Ahmedabad Office , Near Thaltej Crossroads Department: RA Reports To: RA Head and Regulatory Department at HO /Director Employment Type: Full TimeOffice hours : 9,30 AM to 6 PMWeek of: Sunday and Saturday Half Day Preferred Gender : M/FExperience: Minimum 2 years Job Summary:We are seeking a...
-
Regulatory Affairs Manager
5 days ago
Ahmedabad, Gujarat, India, Gujarat Red Envelope Consultants Full timeJob Title: Senior Regulatory Manager – RoW MarketDepartment: Regulatory AffairsJob Summary:The Senior Regulatory Manager will be responsible for the preparation, review, and submission of high-quality regulatory dossiers and documents for pharmaceutical products intended for Rest of the World (RoW) markets, ensuring compliance with country-specific...