ARD Executive Jobs in Sunglow Lifescience Private Limited - Kanchipuram, Tamil Nadu

institute logo

ARD Executive Jobs in Sunglow Lifescience Private Limited - Kanchipuram, Tamil Nadu

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Sunglow Lifescience Private Limited

time outline iconKanchipuram, Tamil Nadu, India

Posted on 27-04-2026

1 Vacancy

Description

  • Job Title: ARD Executive
  • Qualification: MSc (Master of Science)
  • Location: Sunglow Lifescience Private Limited - Kanchipuram, Tamil Nadu
  • Work Experience: 0 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 Sunglow Lifescience Private Limited - Kanchipuram, Tamil Nadu as a ARD Executive in Kanchipuram, Tamil Nadu 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

Positive AttitudeAttention to DetailCommunication SkillsTeamwork

About Organization

Sunglow Lifescience Private Limited is a pharmaceutical manufacturing organization focused on delivering high-quality healthcare products with a strong emphasis on quality assurance, regulatory compliance, and efficient production operations. The position requires strict adherence to Good Manufacturing Practices (GMP), safety protocols, and regulatory guidelines. It involves monitoring production processes, ensuring proper handling of raw materials and finished products, maintaining hygiene and cleanliness in the production area, and collaborating with cross-functional teams for efficient operations. The role focuses on maintaining product quality, ensuring compliance, and supporting seamless manufacturing operations while upholding high standards in pharmaceutical production.

Aggregated job.

Learn more