Morepen Hiring Scientist, Chemist, QA Executive

Morepen PDR pharma R&D company focused on AI-driven drug discovery, NCEs, and regulatory excellence. Our mission is to deliver innovative and accessible therapies with speed, ethics, and global impact.

HIRING

Senior Formulation Scientist
M.Pharm with 8-12 Yrs experience Ph.D in Pharmaceutics with 5-10 Yrs Experience
• Expertise in Formulation R&D (OSD & Topicals; Injectables Preferred)
• Expertise in ANDA Development & Filings (USFDA, EU & RoW)
• Strong Knowledge of QbD, DoE, Digital Formulation & AI/ML
• Hands-on Experience in Tech Transfer, Scale-up & Process Development
• Sound Understanding of USP, ICH & cGMP Guidelines
• Strong Leadership, Project Management & Communication Skills

SR. Research Chemist
M.Sc Organic chemistry with 8-12 Yrs Ph.D in Chemistry with 5-10 Yrs experience
• Expertise in API R&D, Process Development, Scale-up, Tech transfer, PDR & DMF Documentation.
• Hands-on Experience in QbD, DoE, ICH guidelines & Troubleshooting.
• Experience in Team mentoring, Cross-functional Coordination & Timely Project Execution.
• Exposure to Digital Chemistry, AI/ML & Strong Analytical and Communication Skills.

Principal Scientist - API R&D
M.Sc Organic Chemistry with 12-18 Yrs Ph.D in Chemistry with 10-15 Yrs experience
• Extensive experience in API R&D with 10+ DMF filings, including CIP, Oncology & Non-Oncology API development for USFDA, EU, and RoW regulated markets.
• In depth understanding & implementation of QbD, DoE for atleast 3 DMF filings.
• Experience in Handling Multiple Teams. Design & implementation of project timelines as per ICH & market needs.
• Good exposure to digital chemistry, & AI/ML applications for API R&D.
• Business Proficiency in verbal & written communications.

QA Executive
M.Sc with 3-6 Yrs exp in QA/DQA
• 4+ Years of Experience in Analytical DQA / API DQA within a regulated pharmaceutical environment.
• Practical Experience with Phase Gate Systems, Project Trackers, ELN, QbD, DoE, SOPs & Stability Programs.
• Hands-on Exposure to Instrument Qualification, Method/Process Validation, Calibration, Change Control, Deviations, CAPA & Risk Assessment.
• Strong Understanding of GMP, GDP, Plant Operations, Regulatory Compliance (USFDA, EU, ICH) with Excellent Documentation & Communication Skills.