Kusum Healthcare Pvt Ltd Walk-in 16th Feb 2025 for R&D (FRD and ADL)

Kusum Healthcare Pvt Ltd Walk-in Interview.Kusum Healthcare Pvt Lt Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue.

Vacancy details:

  • Department: R&D (FRD and ADL)
  • Experience: RA/SRA: 2-5 years RS: 9-12 years
  • Qualification: M.Pharma (Pharmaceuticals)/MS/M.Sc(Science) in Chemistry,
  • Salary:₹Not Disclosed
  • Contact – Yogendra Mishra ( 09785080066 )

Important Details :

  • Work Location: New Delhi
  • Selection Process: The selection will be on the basis of Interview.
  • Mode of Interview: Face to face
  • Interview Rounds of Interview: HR

For ARD Candidate:

  • To perform routine & stability analysis of R&D batches of solid & liquid dosages form as assigned.
  • Independently execute day to day allotted work and timely release of COA.
  • To adhere with departmental SOPs and company SOPs.
  • Maintenance and calibration of analytical instruments.
  • Being aware of, and keeping up to date with, health and safety issues in all aspects of the work undertaken.
  • Able to understand pharmacopoeia and guidelines.
  • Accountable to maintain code of conduct inside the lab and in company premises.

Below is the Candidate application Link :

https://forms.office.com/Pages/ResponsePage.aspx?id=oc5Y6SySv0iZPi3tGKfjcszqR28cyNFGpZJgpTQnp1xUN0Y5S0dUOFhKMkpIR0lHR1BWWDZCNEZBQS4u

Perks and benefits

5 Days working

Transportation Facility

Detailed Profile:

Pre formulation studies of Pharmaceutical & Medicinal Devices and to check the compatibility of the API with different excipients

Formulation development of Pharmaceutical & Medicinal Devices

Execution of successful technology transfer at commercial site

Literature survey and to design strategy for the formulation of the projects

Day to day execution of the planned batches in the laboratory

Manufacturing of lab-scale stability batches, involves monitoring of stability batches with review of Routine and stability data

Setting of QTPP for Pharmaceutical product development

Optimization of the prototype formulation by evaluating the Critical Process Parameters and Critical Quality attributes

Improvement in existing formulations and possibility of new dosage forms

Checking in-process parameters during product development

Preparation of documents like PDR and Stability Guideline as per requirement

Scale up activity at the production plant

Coordinating with the Cross Functional Team for timely execution of project work

LNB Writing, preparation of Master formula card and Product development reports

Walk In Drive Details Below

Date: Sunday, 16th Feb ’25

Location: R&D Centre New Delhi

Address: D, 158A, Pocket D, Okhla Phase I, Okhla Industrial Estate, New Delhi, Delhi 110020

SWARNALATHA B

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