Qc Analyst - OSD Formulation

Roles and Responsibilities

• Conduct quality control analysis of OSD formulations using HPLC, UV spectrophotometry, and other relevant instruments.
• Ensure compliance with cGMP guidelines and company SOPs during instrument analysis.
• Maintain accurate records of test results, batch records, and inventory management.
• Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.
• Participate in audits and inspections by regulatory authorities.
  

Desired Candidate Profile

• 2-5 years of experience in Quality Control (QC - OSD Formulation).
• B.Sc./ B.Pharmacy/ M.Sc./ M.Pharmacy
• Strong understanding of Good Manufacturing Practices (cGMP), Current Good Laboratory Practice (cGLP), and Quality Control principles.
• Proficiency in operating various analytical instruments such as HPLC, UV spectrophotometer, etc.
• Should be willing to work in shift operations.
  

Interested candidates can share their updated CV to jahnavi.kodali@granulesindia.com