Walk-in || Formulation R&D
The Pharma Patashala · Hyderabad · onsite · Posted 57d ago
About a minute. You'll make an account on the way through.
About this role
ob Title: Trainee Research Associate Formulation R&D (Oral Dosage)
Roles & Responsibilities:
Assist in the development and optimization of oral solid dosage forms including tablets, capsules, and pellets .
Support pre-formulation activities such as excipient compatibility studies and stability assessments .
Perform formulation trials and operate lab-scale equipment (granulators, blenders, tablet press, dissolution tester) under supervision .
Maintain accurate documentation of experimental data, observations, and results in lab notebooks and trial records as per GLP and GMP guidelines .
Coordinate with Analytical R&D and QC teams for timely sample analysis and interpretation .
Ensure strict adherence to safety protocols and quality standards in the R&D lab .
Assist in the preparation of development reports, batch records, and technology transfer documents .
Option 2: For Experienced Scientists (2-10 Years)
Paste this if you have 2 to 10 years of experience. (For those at the higher end of this range, you can adapt this for a "Senior Scientist" title.)
Job Title: Formulation Scientist / Senior Scientist – Oral Dosage R&D
Roles & Responsibilities:
Independently design, execute, and lead formulation and process development experiments for oral solid dosage forms (tablets, capsules, etc.) for regulated markets .
Conduct pre-formulation studies, excipient selection, and formulation optimization to ensure product robustness, scalability, and cost-effectiveness .
Perform and support formulation work using various technologies including wet granulation, dry granulation, direct compression, and functional coating .
Execute scale-up batches and lead technology transfer activities to pilot plant and commercial manufacturing sites .
Author, review, and approve technical documents including product development reports, batch records, stability protocols, and CMC sections for regulatory submissions (USFDA, EMA, etc.) .
Troubleshoot formulation and process issues arising during R&D development, scale-up, and production .
Collaborate with cross-functional teams including Analytical Development, QA, Production, and Regulatory Affairs to ensure seamless product development .
Mentor and provide technical guidance to junior scientists and associates .
Option 3: For Group Leaders (2-10 Years for Senior / 5-10 Years for Group Lead)
Paste this if you are applying for a Group Leader / Team Lead role.
Job Title: Group Leader – Formulation R&D (Oral Dosage)
Roles & Responsibilities:
Lead and manage the formulation development strategy for oral dosage forms, ensuring on-time, cost-effective, and quality delivery of projects .
Approve formulation strategies and project plans, streamlining processes to reduce development timelines and facilitate on-time commercial delivery .
Drive innovation by developing platform technology products and advanced drug delivery solutions .
Ensure compliance with regulatory requirements (ICH, FDA, EMA) through all stages of formulation development and adapt to regulatory changes .
Oversee and mentor cross-functional teams, fostering technical excellence and engagement .
Drive and resolve issues related to manufacturing, analytical, regulatory, and APIs across all manufacturing locations .
Lead technology transfer, scale-up activities, and troubleshooting for commercial manufacturing .
Support lifecycle management of commercialized products including regulatory queries, variations, and troubleshooting .
Ensure compliance with QbD, GMP, GLP, and EHS standards across all R&D operations .
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