Job Description

Conduct

pre-formulation and formulation development

of new pharmaceutical dosage forms (solid, liquid, semisolid, etc.). Perform

compatibility studies

for Drug-Excipient interactions. Design and execute

laboratory-scale

and

pilot-scale trials

. Develop and optimize

manufacturing processes

, ensuring scalability and reproducibility. Maintain

batch manufacturing records (BMRs)

and

development reports

. Support

analytical development

teams with stability and validation studies. Assist in

technology transfer

to production and contract manufacturing sites. Ensure adherence to

GMP, GLP, and regulatory guidelines

(e.g., USFDA, MHRA, WHO). Collaborate with cross-functional teams: QA, QC, Regulatory Affairs, and Production. Troubleshoot formulation and process-related issues. Participate in product

lifecycle management

and

cost optimization

initiatives.

Key Skills:

Strong knowledge of

formulation principles and pharmaceutical excipients

. Experience in

process optimization

and

scale-up

. Familiarity with

equipment

like granulators, tablet presses, blenders, etc. Attention to detail and

documentation accuracy

. Good communication, problem-solving, and team collaboration skills.
Job Type: Full-time

Pay: ?40,000.00 - ?70,000.00 per month

Benefits:

Food provided Leave encashment Paid sick time Provident Fund
Schedule:

Day shift
Work Location: In person