Looking for pharma jobs in India? Explore this excellent opportunity for Regulatory Affairs Manager roles in Pune with global market exposure across LATAM, APAC, Africa, and CIS regions.
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About the Company
Humano Forte is a professional talent and business solutions organization supporting pharmaceutical and healthcare companies with regulatory, compliance, and global market expansion requirements.
The organization focuses on innovation, quality standards, and regulatory excellence to help healthcare products reach emerging international markets efficiently.
With a strong emphasis on global compliance and documentation management, the company offers professionals an opportunity to work in a dynamic regulatory environment handling international product registrations and market approvals.
Candidates joining the organization can expect exposure to international pharmaceutical regulations, cross-functional collaboration, and strategic regulatory operations.
Pharmaceutical professionals seeking long-term pharmaceutical careers in India, especially in regulatory affairs, international business support, QA jobs, QC jobs, and production jobs, may find this role highly rewarding.
Job Details
- Company Name: Humano Forte
- Job Role: Regulatory Affairs Manager
- Experience: 9–15 Years
- Qualification: B.Pharm, M.Pharm, Microbiology, or relevant degree
- Location: Pune
- Market Focus: LATAM, APAC, Africa & CIS Regions
- Work Type: On-site
- Industry: Pharmaceutical Regulatory Affairs
- Department: Regulatory Compliance
Job Description
Humano Forte is hiring experienced pharmaceutical regulatory professionals to manage product registrations, compliance activities, and emerging market submissions.
The selected candidate will play a critical role in ensuring timely regulatory approvals and maintaining international compliance standards.
Regulatory Affairs Manager
- Department: Regulatory Compliance
- Market: LATAM, APAC, Africa & CIS
- Role: Regulatory Affairs Manager
- Experience: 9–15 Years
- Education/Qualification: B.Pharm, M.Pharm, Microbiology, or related degree
- Location: Pune
Skills & Qualifications
- Strong knowledge of emerging market regulatory requirements
- Expertise in CTD and ACTD dossier preparation
- Experience handling product registrations and renewals
- Excellent technical documentation skills
- Strong analytical and problem-solving abilities
- Effective communication and authority coordination skills
- Ability to manage multiple regulatory submissions simultaneously
- Knowledge of legalization and attestation processes
- Team management and leadership capabilities
- Strategic planning and compliance management expertise
Key Responsibilities
- Develop regulatory strategies for emerging markets
- Prepare and submit CTD/ACTD dossiers
- Coordinate technical documentation for submissions
- Address regulatory deficiencies and queries
- Track registration timelines and approvals
- Communicate with regulatory authorities effectively
- Monitor changing international regulations
- Support cross-functional compliance activities
- Manage tender documentation processes
- Handle manufacturer documentation management
- Maintain master product list records
- Support new client onboarding activities
- Oversee legalization and attestation tasks
- Manage interns and management trainees
Benefits & Perks
- Exposure to global pharmaceutical markets
- Career growth in regulatory affairs
- International compliance experience
- Collaborative and professional work culture
- Leadership and team management opportunities
- Learning opportunities in emerging market regulations
- Competitive salary and professional development
- Opportunity to impact global healthcare access
How to Apply
Interested and eligible candidates can share their updated resumes via email.
Official Email ID: Jobs@humanoforte.com
Candidates with strong experience in pharmaceutical regulatory compliance and emerging market submissions are encouraged to apply immediately.
Build your future in global pharmaceutical compliance and become part of a mission-driven organization shaping healthcare access worldwide.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Humano Forte career page.
For more pharma jobs, regulatory affairs openings, QA jobs, QC jobs, and pharmaceutical careers in India, visit Pharma Recruiter.
Why You Should Join
This opportunity offers professionals the chance to work in a highly specialized regulatory environment focused on global pharmaceutical compliance and international product registrations.
Employees gain exposure to diverse emerging markets and evolving regulatory frameworks.
The organization promotes professional growth, strategic involvement, and collaborative learning while supporting global healthcare accessibility.
Regulatory professionals seeking long-term career advancement and international exposure can benefit significantly from this role.
FAQs
Who can apply for this Regulatory Affairs Manager job?
Candidates with 9–15 years of pharmaceutical regulatory affairs experience and qualifications like B.Pharm, M.Pharm, or Microbiology can apply.
What markets will the selected candidate handle?
The role focuses on emerging markets including LATAM, APAC, Africa, and CIS regions.
Is this a walk-in interview?
No walk-in interview details have been mentioned for this position. Applications are accepted through email submission.
What are the growth opportunities in this role?
Candidates can gain international regulatory exposure, leadership opportunities, and long-term career growth in global pharmaceutical compliance.
