Finoso Pharma Pvt. Ltd., a rapidly growing global Contract Development and Manufacturing Organization (CDMO) founded in 2009, is expanding its leadership team in Project Management and Regulatory Affairs at its Hyderabad facility.
With a mission rooted in precision, performance, and partnership, Finoso collaborates with global pharmaceutical companies to deliver innovative formulation development and regulatory solutions. Join our team to drive excellence in a dynamic, USFDA-compliant environment!
About Finoso Pharma
Headquartered in Hyderabad, Finoso Pharma specializes in formulation research, analytical development, and regulatory filings for generics and NDAs across the US, Europe, Canada, and emerging markets.
Rated 4.0/5 on AmbitionBox for its positive work culture, Finoso excels in skill development (4.2/5) and job security (4.1/5), though work-life balance (3.9/5) is impacted by a single weekly off and travel requirements. With a focus on innovation, Finoso handles numerous products annually, fostering career growth (4.0/5).
Job Opportunities at Hyderabad Facility
We are hiring for Assistant Manager – Project Management and Executive / Senior Executive – Regulatory Affairs roles. Candidates with relevant experience in formulation development or regulatory affairs are preferred. Below are the details.
Assistant Manager – Project Management
- Qualification: B.Pharm / M.Pharm
- Experience: 4+ years in pharmaceutical project management
- Department: Project Management
- Work Location: Hyderabad, Telangana
- Responsibilities:
- Coordinate cross-functional teams (FR&D, AR&D, RA, QA/QC) to ensure project alignment
- Track project timelines, milestones, and deliverables
- Facilitate technology transfer and scale-up activities
- Manage risk assessments and ensure GMP compliance
- Required Skills:
- Strong cross-functional coordination and communication skills
- Expertise in timeline and milestone tracking
- Understanding of tech transfer, scale-up, and GMP processes
- Familiarity with formulation development and project execution
- Openings: 1-2
- Note: Role may involve travel within the city for client meetings or site visits.
Executive / Senior Executive – Regulatory Affairs
- Qualification: B.Pharm / M.Pharm
- Experience: 0-3 years in regulatory affairs
- Department: Regulatory Affairs
- Work Location: Hyderabad, Telangana
- Responsibilities:
- Prepare and compile eCTD/CTD dossiers for regulatory submissions
- Coordinate with internal teams for documentation and compliance
- Support regulatory filings for USFDA, EMA, Health Canada, and other agencies
- Maintain accurate records and respond to regulatory queries
- Required Skills:
- Knowledge of regulatory guidelines and documentation
- Proficiency in eCTD/CTD dossier compilation
- Strong team coordination and attention to detail
- Basic understanding of GMP and regulatory compliance
- Openings: Multiple
- Note: Entry-level candidates (0 years) with relevant academic projects or internships are encouraged to apply.
Application Details
- How to Apply: Share your profile via email to hr@finoso.com with the subject “Application for [Position Name] – June 2025.”
- Application Deadline: Not specified; apply by June 15, 2025, for priority consideration.
- Contact: hr@finoso.com
- Website: www.finoso.com
Documents Required
- Updated CV with passport-sized photograph
- Copies of B.Pharm/M.Pharm certificates and mark sheets
- Experience certificates and relieving letters (if applicable)
- Last 3 months’ payslips and increment letter (for experienced candidates)
- Aadhaar Card and PAN Card
Verified by Trusted HRs
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Why Join Finoso Pharma?
Finoso Pharma offers a vibrant, innovation-driven workplace with exposure to global markets and advanced formulation technologies. Employees benefit from robust skill development (4.2/5) and strong job security (4.1/5), supported by a collaborative culture.
However, the single weekly off and city travel may challenge work-life balance (3.9/5). Join a company recognized for handling numerous products annually and driving pharmaceutical research excellence.
Why Hyderabad?
Hyderabad is a global pharmaceutical hub, hosting Finoso’s state-of-the-art R&D and manufacturing facilities. The city offers unparalleled career opportunities, though commuting to the facility may be required.
Important Notes
- Eligibility: B.Pharm/M.Pharm graduates only. Project Management requires 4+ years; Regulatory Affairs accepts 0-8 years. Male candidates preferred for roles involving travel or shifts.
- Disclaimer: Finoso Pharma does not charge fees for job applications. Use only official contact hr@finoso.com. Beware of fraudulent offers.
- Note: Candidates interviewed in the last 6 months need not reapply. Be prepared for a fast-paced environment with opportunities for learning but demanding timelines.
Don’t miss this chance to grow with Finoso Pharma! Apply now and contribute to precision-driven pharmaceutical solutions in Hyderabad!
