Senior Executive -Global Regulatory Deficiency Centre
Aarti Pharmalabs · Mumbai · onsite · Posted 48d ago
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About this role
Role & responsibilities
Key Responsibilities:
API Process Development & Optimization:
- Perform feasibility studies, process optimization, and scale-up of API processes. Conduct process verification and identify Critical Process Parameters (CPPs) and Critical Quality Attributes (CQAs).
- Plan lab work, prepare Reference Standards (RS)/Working Standards (WS), and ensure their characterization.
- Initiate the technology transfer process to the pilot plant or production facility.
Regulatory Affairs & Compliance Support:
- Provide timely technical support for regulatory queries, especially those related to DMF preparation.
- Ensure accurate preparation of specification sheets and MSDS for raw materials and intermediates.
- Prepare the Development History Report for regulatory submission and archival. Conduct initial stability studies for developed products.
Cross-Functional Coordination:
- Coordinate with the Regulatory Affairs (RA), Analytical Development Lab (ADL), IPR, and Development Quality Assurance (DQA) teams.
- Manage coordination between officers working in R&D.
Required Qualifications & Experience:
- Education: M.Sc. (Organic Chemistry) or Ph.D. (Organic Chemistry) Experience: 2 to 8 years of relevant experience
Sourced from naukri
Skills
About Aarti Pharmalabs

Aarti Pharmalabs
Pharma
2.0k+
employees
Mumbai
India
₹6.6L PA avg
Avg at Aarti Pharmalabs
About
Aarti Pharmalabs Limited (APL) is a leading Indian manufacturer of Pharmaceuticals and Nutraceuticals with a global footprint. We deliver process chemistry expertise, with a scale-up engineering competence, regulatory support and long-term supply by maintaining quality and timely delivery to create a sustainable future.
Over the last two decades, APL serving global clients with top notch scientific knowledge, industry experts, state-of-the-art R&D and USFDA, EUGMP, EDQM, KFDA inspected manufacturing facilities. We manufacture Generic APIs, Intermediates and Xanthine derivatives. We offer CDMO services for small molecules drug substances (API/NCE/RSM/Intermediate) process development and manufacturing focusing on Ph-I/II/III, launch and commercial phase projects for Innovator Pharmaceutical and Biotech companies. We have been helping our clients to bring their molecules to market quickly and efficiently from clinical development through commercial stage manufacturing.
We have dedicated facilities to manufacture HPAPIs, Corticosteroids, Cytotoxic and Oncology products.
We are one of the preferred partner for Beverages and Nutraceuticals Industries for our flagship product ‘Caffeine’.
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