Job Location Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072 Job Shift Day
Assist in the execution of formulation and process technology transfers from R&D to manufacturing sites (in-house and CMO).
Conduct scale-up and exhibit batches under supervision, ensuring proper documentation and parameter tracking.
Support in the preparation and review of Batch Manufacturing Records (BMRs) and validation protocols/reports
Coordinate with R&D, QA, QC, Regulatory Affairs, and Manufacturing teams for effective knowledge transfer and execution.
Participate in process investigations, troubleshooting, and deviation handling during trial and validation batches.
Assist in equipment selection and capacity assessment based on product-specific requirements.
Ensure document readiness for regulatory submissions, respond to technical queries, and support audit preparation.
Support internal and external/vendor audits by providing required documentation and technical inputs.
Contribute to continuous improvement initiatives and support knowledge-sharing activities within the MSTG team.
Prepare data summaries, technical reports, and presentations as per project or management requirements.
Maintain accurate records, follow applicable SOPs, and ensure strict GMP compliance in all operations.
B.Pharm / M.Pharm in Pharmaceutics or Pharmaceutical Technology.
2–5 years of experience in formulation development, MS&T, or technology transfer.
Exposure to solid orals, liquids, or softgel capsule dosage forms.
Understanding of scale-up principles, equipment functionality, and validation practices
Familiar with regulatory expectations (USFDA, EU, etc.) and cGMP standards.
Good communication, documentation, and teamwork skills.
Willingness to travel to manufacturing sites as per project requirements.
We are a US based Global Pharmaceutical company with a primary focus on developing complex high barrier to entry Generics and Specialty Pharmaceutical products that would help increase accessibility to high quality medication thereby leading to the creation of next generation healthy communities. We are driven by an earnest pursuit of redefining the accepted standards in pharmaceutical product development and commercialization. We consistently aspire to challenge standard thought processes to arrive at dependable solutions that create a paradigm shift in product development, quality, clinical affairs, regulatory sciences, and commercial strategy. Our talented team with some of the brightest minds have developed a holistic understanding of the nuances associated with the development of unique, commercially viable and difficult product lines across varying therapeutic areas and a broad array of dosage forms such as Injectables, Ophthalmics, Topicals, Biologicals, Drug Devices, Soft Gels, Solid Orals & Suspensions.
