Pharma Jobs in Ahmedabad – Regulatory Affairs & Business Development Careers
Cubit Lifesciences LLP is hiring experienced professionals for its Regulatory Affairs and Business Development departments in Ahmedabad, Gujarat.
The openings are suitable for experienced pharma professionals with expertise in regulatory affairs, international markets, business development and pharmaceutical licensing.
Cubit Lifesciences LLP Hiring for Below Positions
1) Department: Regulatory Affairs
Designation: Regulatory Affairs Manager
Experience: 10–15 Years
Qualification: B.Pharm / M.Pharm
Work Location: Ahmedabad, Gujarat
Key Skill / Job Description:
- Planning, preparation & review of registration/re-registration dossiers in CTD, eCTD, ACTD, Country specific formats.
- Compilation and submission of queries and variations.
- Review of documents, artworks.
- Review of change controls, deviations.
- Gap analysis and regulatory strategies preparation for new product filing.
- Maintaining product Life cycle.
- Liaising with various stakeholder internal & external for submission documents, payments.
- Key Responsibilities:
- Lead and guide the regulatory team and ensure timely submissions.
- Ensure compliance with global regulatory requirements and standards.
- Coordinate with cross-functional teams (Quality, R&D, Production, RA).
- Mentor and develop team members; drive process improvements.
- Handle audits, inspections and regulatory queries.
- Strategic planning for market expansion and new product filings.
2) Department: Business Development
Designation: Business Development (BD)
Experience: 10–12 Years
Qualification: B.Pharm / M.Pharm / MBA
Work Location: Ahmedabad, Gujarat
Key Skill / Job Description:
- Lead Business Development via Out-Licensing in multiple global markets.
- Take full ownership of assigned countries – from deal structuring to execution.
- Negotiate and finalize commercial agreements with international partners.
- Maintain long-term strategic relationships with existing clients.
- Design regional product portfolios and oversee development & registration activities.
- Manage supply chain, administrative, and operational needs for customers.
- Collaborate across teams to ensure execution and client satisfaction.
- Key Responsibilities:
- Identify and develop new business opportunities across global markets.
- Manage end-to-end BD process – from lead generation to deal closure.
- Build and maintain strong relationships with international partners.
- Work with R&D, Regulatory and Supply Chain for product licensing and launches.
- Monitor market trends, competition and growth opportunities.
- Achieve revenue and business targets with strategic planning.
- Represent the company at global conferences and business forums.
How To Apply Cubit Lifesciences Jobs
Step 1: Check the qualification and experience requirements for the position.
Step 2: Prepare your updated CV highlighting relevant pharmaceutical experience.
Step 3: For the Regulatory Affairs position, candidates with the required regulatory affairs experience can approach the company for the walk-in opportunity.
Step 4: Candidates can share their CV at hr@cubitgroup.in.
Frequently Asked Questions
1. What is the experience required for the Regulatory Affairs Manager position at Cubit Lifesciences?
The required experience is 10–15 years, with relevant regulatory affairs experience in OSD/injectables and international markets.
2. Is international pharmaceutical experience required for the Business Development position?
The job poster asks for experience involving international markets, out-licensing, business development, licensing or partnerships.
3. Does Cubit Lifesciences offer opportunities related to international pharmaceutical markets?
Yes. The company highlights international markets and its official profile describes its activities across domestic and international pharmaceutical markets.
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Cubit Lifesciences LLP Jobs – Regulatory Affairs Manager and Business Development openings in Ahmedabad.
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