Research Associate : Pharma Analytical

Qvents.In; Pune District, Pimpri-Chinchwad; On-site; INR 450,000 - 650,000; Full time

Job summary

Lupin Limited in Pune, Maharashtra, invites applications for a Research Associate in R&D/ARD to conduct analytical method development, validation, and method transfer, including analysis of developmental samples.

The role requires 2–5 years of Pharma QC/ARD experience with GCMS, LCMS, ICPMS, IC, and a Masters in Analytical Chemistry or Pharmacy. It is a full-time position with SOP preparation, IQ/OQ/PQ involvement, and collaboration with manufacturing.

Qualifications

• 2–5 years Pharma QC/ARD experience
• Experience with GCMS, LCMS, ICPMS, IC instrumentation
• Experience in Analytical Development and Method Validation

Responsibilities

• Analysis and Review of projects by various techniques in the laboratory.
• Support on all analytical activities in laboratory.
• Preparation / review of SOPs.
• Responsible for analytical method development, validation, and study reports.
• Involvement in IQ/OQ/PQ activities for instruments.
• Calibration and maintenance of instruments per SOP and GLP.
• Review of Analytical data and test results.
• Support to Manufacturing site for various activities.

Skills

GC-MS

LC-MS

ICP-MS

IC

Analytical development

Method validation

Pharma QC

Education

Masters in Analytical Chemistry

Masters in Pharmacy

Tools

GCMS

LCMS

ICPMS

IC

Job description

Designation : Research Associate

Function : R&D

Functional Area : AR&D

Job Role Summary : Analytical method development, validation, method transfer, Analysis of developmental samples

Job Profile

• Analysis and Review of projects by various techniques (e.g. Extractable and Leachable study by using instruments like GCMS, LCMS, ICPMS, IC, and other instruments) within the laboratory.
• Supporting on all analytical activities in laboratory.
• Preparation / review of Standard Operating Procedures (SOP’s).
• Responsible for analytical method development, validation, preparation of protocol and study reports.
• Involving in the IQ/OQ/PQ activities performed for different instruments in Laboratory.
• Calibration and maintenance of instruments as per SOP according to the GLP practices.
• Effective utilization of all available resources like instruments, apparatus etc.
• Review of Analytical data and test results.
• Support to Manufacturing site for various activities.

Job Requirements

• Pharma Formulations QC experience
• Experience in Analytical Instrumentation like GCMS, LCMS, ICPMS, IC
• Experience in Analytcal Development, Method Validation

Work / Job Experience : 2-5 Years

Type of Experience : Pharma QC, ARD Experience

Academic Qualifications

• Masters in Analytical Chemistry or Pharmacy

Job Post Link : https://tinyurl.com/3nx3jrem

• Full Time
• India | Maharashtra | Pune
• Posted 1 week ago

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