ARD Executive Jobs in Pellets Pharma Limited - Sangareddy, Telangana

ARD Executive Jobs in Pellets Pharma Limited - Sangareddy, Telangana

work outline icon3 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Pellets Pharma Limited

time outline iconSangareddy, Telangana, India

Posted on 14-04-2026

5 Vacancies

Description

  • Job Title: ARD Executive
  • Qualification: MSc (Master of Science)
  • Location: Pellets Pharma Limited - Sangareddy, Telangana
  • Work Experience: 3 to 5 Years

Job Description

  • Develop, validate, and optimize analytical methods for raw materials, intermediates, and finished formulations.
  • Conduct routine analysis using HPLC, GC, UV, FTIR, Dissolution Tester, and other analytical instruments.
  • Prepare method validation protocols, reports, and analytical data summaries as per ICH guidelines.
  • Perform stability studies and compile analytical data for regulatory submissions.
  • Support formulation and process development teams through analytical testing and troubleshooting.
  • Maintain and calibrate analytical instruments and ensure compliance with GLP/GMP standards.
Take this opportunity to join Pellets Pharma Limited - Sangareddy, Telangana as a ARD Executive in Sangareddy, Telangana and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

R&D / F&D / ADL

Preferred Education

MSc (Master of Science)

Key Skills

Team WorkCommunication SkillsPositive AttitudeAttention to Detail

About Organization

Pellets Pharma Limited is a pharmaceutical organization engaged in the manufacturing of high-quality formulations with a strong focus on regulatory compliance, product quality, and efficient production processes. The role involves working in a manufacturing or operational environment to support production activities and ensure adherence to industry standards. Responsibilities include assisting in production operations, following Good Manufacturing Practices (GMP), maintaining accurate batch records and documentation, monitoring equipment performance, and ensuring compliance with safety and hygiene protocols. The role also requires coordination with quality assurance and quality control teams, adherence to regulatory guidelines, and maintaining consistency in product quality and operational efficiency.

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