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Associate Scientist

Job in Indiana Borough, Indiana County, Pennsylvania, 15705, USA
Listing for: Lupin Ltd
Full Time position
Listed on 2026-09-13
Job specializations:
  • Pharmaceutical
  • Healthcare
    Medical Science, Clinical Research, Data Scientist
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below

Job Description

Literature search, Idea generation and preparation of technical reports.

  • Preparation of product development strategy – keeping in mind technical, IP, regulatory & clinical requirements – for a variety of sterile drug products.

Screening & selection of raw materials (APIs, excipients, packaging components)

  • Pre-formulation & solution chemistry studies
  • Process development & optimization – complex injectable development
  • Stability evaluation applicability of QbD principles in product development

Basic physico-chemical testing and understanding of regulatory framework pertaining to product development & filing (ICH, regulated markets)

Handling of technology transfer batches and submission in regulated market

  • Following GDP, cGMP, GLP & laboratory safety practices during work.

Multi-tasking capability along with ability to think out-of-the-box.

Good interpersonal skills, effective verbal & written communication skills

Work Experience

PhD with 2-3 years experince

Education

Doctorate in Pharmaceutical Technology or Polymers

Job Description

Literature search, Idea generation and preparation of technical reports.

  • Preparation of product development strategy – keeping in mind technical, IP, regulatory & clinical requirements – for a variety of sterile drug products.

Screening & selection of raw materials (APIs, excipients, packaging components)

  • Pre-formulation & solution chemistry studies
  • Process development & optimization – complex injectable development
  • Stability evaluation applicability of QbD principles in product development

Basic physico-chemical testing and understanding of regulatory framework pertaining to product development & filing (ICH, regulated markets)

Handling of technology transfer batches and submission in regulated market

  • Following GDP, cGMP, GLP & laboratory safety practices during work.

Multi-tasking capability along with ability to think out-of-the-box.

Good interpersonal skills, effective verbal & written communication skills

Work Experience

PhD with 2-3 years experince

Education

Doctorate in Pharmaceutical Technology or Polymers

Position Requirements
10+ Years work experience
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