Finoso Pharma Hiring for Project Management & Regulatory Affairs Roles in Hyderabad | 0–4 Years Experience

Apply now for high-paying jobs at Finoso Pharma in Hyderabad! Openings for Assistant Manager – Project Management and Regulatory Affairs Executive. Ideal for B.Pharm/M.Pharm graduates with 0–4 years’ experience. Work in a USFDA-compliant CDMO. Send resume to hr@finoso.com

🔬 Finoso Pharma Job Openings 2025 – Project Management & Regulatory Affairs in Hyderabad | Apply Now!

Are you looking for high-paying pharma jobs in Hyderabad? Finoso Pharma Pvt. Ltd., one of India’s fastest-growing CDMO (Contract Development and Manufacturing Organizations), is inviting applications for exciting roles in Project Management and Regulatory Affairs at its USFDA-compliant facility in Hyderabad.

This is a golden opportunity for B.Pharm/M.Pharm graduates with 0 to 4 years of experience to build a strong career in pharmaceutical operations, regulatory strategy, and project execution.

🏢 About Finoso Pharma

Founded in 2009 and headquartered in Hyderabad, Finoso Pharma Pvt. Ltd. offers end-to-end support in formulation development, analytical R&D, and regulatory filing services. With projects across the US, EU, Canada, and emerging markets, Finoso is known for precision, quality, and customer-centric innovation.

✅ USFDA-compliant infrastructure
✅ Specialization in NDAs, ANDAs, CTD/eCTD submissions
✅ Partnered with top global pharma firms
✅ Strong presence in formulation research and regulatory consulting

Rated 4.0/5 on AmbitionBox, Finoso offers a promising workplace with:

• 🌱 Skill Development: 4.2/5

• 🔒 Job Security: 4.1/5

• 🤝 Positive Culture: 4.0/5

• 🕒 Work-Life Balance: 3.9/5 (single weekly off and travel demands)

💼 Current Openings – Hyderabad Facility

1️⃣ Assistant Manager – Project Management

• Qualification: B.Pharm / M.Pharm

• Experience: 4+ years in pharmaceutical project management

• Location: Hyderabad, Telangana

• Department: Project Management

• Openings: 1–2

🧾 Responsibilities:

• Coordinate cross-functional teams (FR&D, AR&D, RA, QA, QC)

• Monitor project milestones and timelines

• Facilitate tech transfer and scale-up from R&D to production

• Oversee risk management and GMP compliance

• Conduct stakeholder meetings and ensure timely project delivery

🧠 Required Skills:

• Project timeline tracking and status reporting

• Good understanding of formulation & GMP procedures

• Leadership in cross-department collaboration

• Excellent verbal and written communication

• Willingness to travel for meetings or audits

2️⃣ Executive / Senior Executive – Regulatory Affairs

• Qualification: B.Pharm / M.Pharm

• Experience: 0–3 years in regulatory affairs

• Location: Hyderabad, Telangana

• Department: Regulatory Affairs

• Openings: Multiple

🧾 Responsibilities:

• Compile and submit CTD/eCTD dossiers for regulatory filings

• Assist in USFDA, EMA, Health Canada submissions

• Coordinate internal documentation and quality audits

• Respond to regulatory queries and ensure compliance

• Maintain SOPs, logs, and audit readiness

🧠 Required Skills:

• Familiarity with eCTD software and dossier submission formats

• Strong understanding of ICH, USFDA, and EU guidelines

• Team coordination, accuracy in documentation

• Basic knowledge of GMP and compliance protocols

• Entry-level applicants with internships or academic projects are welcome.

📩 Application Process

Apply By: Priority deadline – June 15, 2025
How to Apply:
Email your CV to hr@finoso.com with the subject line:

"Application for [Position Name] – June 2025"

🗂️ Documents Required:

• Updated CV with photograph

• Copies of B.Pharm / M.Pharm certificates and marksheets

• Experience certificates / relieving letter (if applicable)

• Latest 3 months’ payslips and increment letter (for experienced)

• Government ID: Aadhaar & PAN Card

🌟 Why Work at Finoso Pharma?

If you’re aiming to grow in formulation development, regulatory strategy, or project leadership, Finoso provides a robust platform:

• Work with global clients and regulatory bodies

• Get hands-on exposure to dossier compilation, ANDA/NDA filings, and tech transfer activities

• Strong internal mentorship and professional development programs

• Excellent job stability in a USFDA-audited facility

Pros:

• 📈 Rapid career growth in formulation and regulatory jobs

• 🌐 Exposure to global regulatory frameworks

• 🔄 Dynamic work environment with learning curve

• 🧑‍🎓 Fresh graduates with regulatory internships encouraged to apply

Cons:

• 🔁 Weekly off limited to Sundays

• 🚕 Field visits and client meetings may require inter-city travel

• ⏱️ Fast-paced with tight regulatory deadlines

📍 Why Hyderabad?

Hyderabad is India’s pharma capital, home to leading R&D, CDMO, and biotech companies. The city provides:

• 🌐 Access to global clients and regulatory infrastructure

• 🎓 Proximity to top pharma colleges and research centers

• 🚇 Good living standards (though facility commuting may require planning)

• 💼 Career ladder opportunities in project management, regulatory affairs, and QA/QC.

⚠️ Important Notes

• 🎓 Eligibility: B.Pharm / M.Pharm graduates

  • Project Management: Minimum 4+ years of relevant experience

  • Regulatory Affairs: 0–3 years (entry-level welcome)

• 🧑‍💼 Male candidates preferred for roles involving travel or shift-based work

• ❌ No application fees – Finoso Pharma does not charge for recruitment

• ⚠️ Beware of job scams; use only official contact – hr@finoso.com

• 🔁 Candidates interviewed in the past 6 months are not eligible to reapply.

📣 Don’t Miss Out – Build Your Career at Finoso Pharma

Whether you’re a fresh graduate in pharmaceutical sciences or a seasoned project manager, Finoso Pharma offers career-defining roles in Hyderabad’s thriving pharmaceutical ecosystem. Take the next step in your professional journey and work on projects that impact global healthcare.

📧 Email your CV to hr@finoso.com by June 15, 2025

🔍 Mention your desired role in the subject line