Research Scientist

Piramal Pharma Solutions; Ahmedabad District; On-site; INR 700,000 - 1,150,000; Full time

Job summary

Piramal Pharma Solutions is hiring a Research Scientist to lead formulation and process development, ensuring timely delivery within cost and specifications.

The role involves executing GMP batches, preparing technical documents, and training junior scientists while adhering to GDP and GxP standards in a GMP environment.

Qualifications

• Experience in pharmaceutical formulation development and process development.
• Familiarity with GMP batches and GDP guidelines.
• Knowledge of QbD principles and documentation practices.

Responsibilities

• Development and execution of NCE, generic, and line extension projects using QbD principles.
• Prepare literature summaries and development reports for assigned products.
• Execute formulation development, process development, and GMP batch manufacturing for the product.

Skills

Formulation development

Process development

GMP knowledge

QbD principle

Job description

Job Description

Job Description:

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Research Scientist

Job Description

Delivery of project within timelines, cost and specifications. Formulation development and manufacturing of solid oral and other dosage form.

Job responsibilities are listed below

• Development and execution of NCE projects, generic projects and line extension projects using QbD principle.
• Preparation of literature summary and development report to the assigned product.
• Involve in execution of formulation development, process development and manufacturing of GMP batches to the assigned product.
• Preparation of technical documents like MFC, BMR, BPR and Stability protocol etc. following the GDP.
• Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same.
• Execution of scale up and pilot/clinical batches in pilot under GMP condition.
• Performing calibration and maintenance of R&D instruments and equipment
• Procuring/ indenting materials and machines change parts related to concern projects
• Maintain safe and hygienic condition in respective department
• Ensuring the use of personal protective equipment whenever required during batch execution
• Attending training related to FD, EHS and QA (as applicable)
• All generated waste to be sent to concerned person and must be comply with EHS requirements
• Preparation of technical presentations and presenting to client
• Training and monitoring of junior scientists for activities related to FD.