Junior Analytical Chemist

About Us

Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs.

Job Roles & Responsibilities

Analytical Method Development & Validation:

• Develop and optimize analytical methods for pharmaceutical compounds using HPLC, GC, UV-Vis, and other analytical techniques.
• Perform method validation studies including accuracy, precision, linearity, specificity, and robustness testing.
• Transfer analytical methods between laboratories and ensure successful implementation.
• Troubleshoot analytical methods and resolve technical issues.

Sample Analysis & Testing:

• Conduct routine analysis of raw materials, intermediates, and finished pharmaceutical products.
• Perform quantitative and qualitative analysis following established protocols and regulatory guidelines.
• Execute stability studies and analyze samples at designated time points.

Instrumentation & Maintenance:

• Operate and maintain analytical instruments including HPLC, GC, GC-MS, FTIR, UV-Vis spectrophotometers.
• Perform routine calibration.
• Troubleshoot instrument issues and coordinate with service technicians when needed.
• Ensure proper documentation of instrument performance and maintenance activities.

Data Management & Reporting:

• Analyze and interpret analytical data using statistical methods and software.
• Prepare technical reports, certificates of analysis, and regulatory submissions.
• Maintain accurate laboratory records and electronic data systems.

Knowledge & Experience

• Master's degree in Analytical Chemistry,

  Chemistry, or related field.

• 2 - 4 years

  of relevant experience in pharmaceutical, chemical, or analytical laboratory settings.
• Strong foundation in analytical chemistry principles and techniques.

Preferred Qualifications

• Experience with advanced analytical techniques (DSC, TGA).
• Previous experience in pharmaceutical or biotech industry.
• Understanding of stability testing and forced degradation studies.
• Knowledge of cleaning validation by UV / HPLC.

Why Join MPDRPL?

• Be part of an organization driving

  cost-effective global healthcare solutions

  .
• Work on

  end-to-end projects

  from concept to market.
• Collaborate with experts across departments in a

  quality-driven, innovation-centric environment

  .
• Access to

  modern formulation laboratories

  and pilot-scale facilities.
• Competitive compensation with

  performance-linked incentives

  .
• Professional development and

  career advancement opportunities

  .
• Comprehensive employee benefits including

  healthcare and retirement plans

  .