Senior Research Associate-FD

Biopatrika

Gujarat

On-site

INR 700,000 - 1,100,000

Full time

12 days ago

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Job summary

Piramal Pharma Solutions in India is seeking a Senior Research Associate-FD to deliver formulation development and manufacturing of solid oral and other dosage forms within defined timelines and cost targets.

Responsibilities include executing NCE and generic projects using QbD principles, preparing literature summaries and development reports, and ensuring GMP-compliant batch manufacturing, process development, and documentation such as MFC, BMR, BPR and Stability protocols while maintaining

Qualifications

  • Delivery of the project within timelines, cost and specifications.
  • Formulation development and manufacturing of solid oral and other dosage forms.
  • Follow GxP (GMP, GDP etc.) for all processes.
  • Attending training related to FD, EHS and QA.
  • All generated waste must be compliant with EHS requirements.

Responsibilities

  • 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

Job description

Company Overview

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

Senior Research Associate-FD

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
Seniority level

Mid-Senior level

Employment type

Full-time

Industries

Pharmaceutical Manufacturing

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