Are you an experienced pharmaceutical professional looking for your next career opportunity? Morepen Proprietary Drug Research (Morepen PDR) has announced multiple openings for highly skilled candidates in Formulation R&D, API Research & Development, Quality Assurance, and Research Chemistry. If you have experience in pharmaceutical research, product development, quality systems, or API development, this is an excellent opportunity to join an innovation-driven organization committed to developing high-quality medicines for global markets.
Candidates meeting the required qualifications and experience can apply by sending their updated resume through the official email provided by the company.
Job Overview
Company Name: Morepen Proprietary Drug Research (Morepen PDR)
Job Location: India
Employment Type: Full-Time
Application Mode: Email
Available Positions:
- Senior Formulation Scientist
- Principal Scientist โ API R&D
- Senior Research Chemist
- QA Executive
Vacancy Details
Senior Formulation Scientist
Qualification
- M.Pharm with 8โ12 years of experience
- OR Ph.D. in Pharmaceutics with 5โ10 years of experience
Key Skills
- Formulation R&D (OSD, Topicals, Injectables preferred)
- ANDA development & regulatory filings (USFDA, EU & ROW)
- QbD, DoE, Digital Formulation and AI/ML
- Technology Transfer
- Scale-up & Process Development
- USP, ICH & cGMP guidelines
- Leadership, project management and communication skills
Principal Scientist โ API R&D
Qualification
- M.Sc. Organic Chemistry with 12โ18 years of experience
- OR Ph.D. in Chemistry with 10โ15 years of experience
Key Skills
- API R&D experience
- DMF filings including CIP
- API development for USFDA, EU and ROW markets
- QbD & DoE implementation
- Team leadership and project management
- Digital chemistry and AI/ML exposure
- Strong verbal and written communication
Senior Research Chemist
Qualification
- M.Sc. Organic Chemistry with 8โ12 years of experience
- OR Ph.D. in Chemistry with 5โ10 years of experience
Key Skills
- API R&D
- Process Development
- Scale-up
- Technology Transfer
- PDR & DMF documentation
- QbD, DoE, ICH Guidelines
- Troubleshooting
- Team mentoring
- Digital Chemistry & AI/ML
- Strong analytical and communication skills
QA Executive
Qualification
- M.Sc.
- 3โ6 years of experience in QA/DQA
Key Skills
- Analytical DQA / API DQA
- Phase Gate Systems
- ELN
- Project Trackers
- QbD & DoE
- SOPs
- Stability Programs
- Instrument Qualification
- Method & Process Validation
- Calibration
- Change Control
- Deviations
- CAPA
- Risk Assessment
- GMP, GDP and Regulatory Compliance (USFDA, EU, ICH)
Roles & Responsibilities
- Conduct research and development activities as per project requirements.
- Develop and optimize pharmaceutical formulations or API processes.
- Prepare technical and regulatory documentation.
- Ensure compliance with GMP, ICH and global regulatory standards.
- Support technology transfer, process validation and commercialization activities.
- Collaborate with cross-functional teams for timely project execution.
- Maintain quality systems, documentation and continuous improvement initiatives.
Required Qualifications
Candidates with the following qualifications are eligible depending on the position:
- M.Pharm
- M.Sc. Organic Chemistry
- Ph.D. in Pharmaceutics
- Ph.D. in Chemistry
Relevant pharmaceutical industry experience as mentioned for each position is mandatory.
Salary & Benefits
Expected Salary: โน12 LPA โ โน40 LPA (Approximate, based on role, qualifications and experience)
Employee Benefits
- Competitive salary package
- Career growth opportunities
- Exposure to global pharmaceutical projects
- Learning and development programs
- Collaborative and innovation-focused work culture
How to Apply
Interested and eligible candidates can send their updated CV to the official recruitment email.
Email: jobs@morepenpdr.com
Contact Number: 6302451459
Apply as early as possible since the company has not mentioned a specific application closing date.