Walk-in Interviews For Staff / Technician - Injectable Manufacturing

Role & responsibilities: -

• Documentation & Compliance: Review and release Batch Manufacturing Records (BMR). Ensure absolute compliance with global regulatory guidelines (FDA, EMA, MHRA).
• Process Oversight: Monitor automated systems, process parameters (compounding time, filtration pressure, mixing speed), and cleanroom environmental metrics (temperature, differential pressure, relative humidity).
• Deviation & QMS Management: Identify, document, and initiate root-cause analysis investigations for any process exceptions or quality deviations on the line.
• Line Clearance: Perform and authorize line clearance before transitioning equipment or areas to a new batch or product.
• Cross-Functional Coordination: Collaborate with Quality Control (QC), Quality Assurance (QA), and Engineering teams to manage validations and audits.

Preferred candidate profile: -

• Required Experience: - 3 to 12 Years
• Required Educational Qualification: - B.Pharm. / Diploma / ITI

Regards,

Human Resources Team,

Intas Pharmaceuticals SEZ Plant