- Standard Operating Procedures (SOPs): Drafts, updates, and maintains clear instructions for every operational task to reduce variability. [1, 2]

- Batch Release Authority: Reviews all production, testing, and processing data to give final approval before a drug goes to market. [1]

- Validation and Qualification: Confirms that equipment, facilities, and analytical methods perform reliably through strict testing (IQ, OQ, PQ). [1, 2]

- Deviation and CAPA Management: Investigates production errors and builds Corrective and Preventive Actions (CAPAs) to stop issues from happening again. [1, 2]

- Audit and Inspection Readiness: Conducts internal checks and prepares the facility for external regulatory reviews by agencies like the FDA. [1, 2]

Pay: ₹15,000.00 - ₹30,000.00 per month

Advantages

- Commuter assistance

- Flexible schedule

- Health insurance

- Leave encashment

- Life insurance

- Paid sick time

- Paid time off

Education

- Bachelor's (Required)

Experience

- Qa: 1 year (Required)

Work Location: In person

📌 Qa pharma background (Roorkee)
🏢 Manvik Placement
📍 Roorkee