- Full Time
- Mahad, Raigad, Navi Mumbai, Maharashtra

Website Titan Laboratories Pvt. Ltd.
About Titan Laboratories Pvt. Ltd.
Titan Laboratories Pvt. Ltd. is among the few select pharmaceutical companies in India with a dedicated WHO-GMP certified state-of-the-art facility specializing in Sustained and Modified Release Pellets, DC Granules, and Taste-Masked Granules. Strategically located in the green belt of Mahad Industrial Zone (180 km from Mumbai), our facility is well-connected via the Mumbai-Goa Highway.
We are inviting experienced and enthusiastic professionals to join our formulation team in Mahad, Raigad and corporate office in Navi Mumbai.
🧩 Project Management Department
1. Executive – R&D Project Management
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Location: Navi Mumbai
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Qualification: B.Pharm / M.Pharm
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Experience: 2 to 5 years
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Responsibilities:
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Manage pharmaceutical R&D projects
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Coordinate cross-functional teams and ensure timely execution
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Utilize project management tools/software
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Strong planning, communication, and organizational skills
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Experience with regulated markets like EU, UK, Australia preferred
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2. Executive – MDO (Management Development Office)
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Location: Navi Mumbai
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Qualification: B.Pharm / M.Pharm
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Experience: 1 to 2 years
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Responsibilities:
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Maintain and track project progress using Excel and PM tools
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Update task lists and prepare milestone reports
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Collaborate with cross-functional teams for execution of MDO-related activities
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🌍 Sales & Business Development – Formulations
Manager / Sr. Manager – Asia Markets
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Location: Navi Mumbai
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Qualification: MBA / M.Sc / M.Pharm
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Experience: 8 to 12 years
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Responsibilities:
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Develop new international markets and client base
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Drive sustainable growth and manage product registrations
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Achieve sales targets and manage order fulfilment
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Oversee budgets and client communication
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Maintain strong client relations and follow up on payments
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📄 Regulatory Affairs
Executive / Sr. Executive – CIS, Asia & Africa
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Location: Navi Mumbai
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Qualification: MBA / M.Sc / M.Pharm
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Experience: 5+ years in Regulatory Affairs
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Responsibilities:
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Prepare and submit ACTD/CTD dossiers
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Review R&D and plant documentation for accuracy and compliance
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Monitor and implement updates in CIS and Asian regulations
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Maintain detailed submission records
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Provide regulatory support for Asia, Africa, and CIS regions
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📬 How to Apply
📧 Email your updated resume to:
vaibhavi.b@titanpharma.com
🗓️ Last Date to Apply: 30th June 2025
Note: Candidates with relevant pharmaceutical industry experience will be given preference.
Take the next step in your pharma career with a company that prioritizes quality, innovation, and global reach.
Titan Laboratories Pvt. Ltd. – Shaping the Future of Pharmaceutical Excellence.
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To apply for this job email your details to vaibhavi.b@titanpharma.com