Role & responsibilities
Review and evaluation of QC analytical data, including thorough electronic data and audit trail review to ensure data integrity.
Review of analytical specifications, STPs/analytical procedures, protocols, and laboratory-related SOPs.
Review of QC laboratory qualification/calibration status of analytical instruments.
Batch Release Management.
Hands on analytical experience.
Review of batch manufacturing and packaging records, including audit trail verification.
Preparation and Review of APR.
Oversight and review of QC laboratory activities to ensure adherence to SOPs and quality standards.
Initiation, investigation, and review of QMS elements such as Deviations, Change Controls, OOS, OOT, and CAPA.
Review and execution of cleaning validation activities in accordance with regulatory guidelines.
Support during regulatory inspections and customer audits.

Preferred candidate profile
Quick learner with excellent communication skills
Punctual with proven track record of dedication & reliability
A team player who is equally capable of working alone
Fluent in both written and spoken English
Knowledge /Experience in peptides

📌 Senior Executive Navi Mumbai (India)
🏢 Piramal Pharma
📍 India