FULLTIME
Assistant Manager / Deputy Manager - Quality Control

Acme Formulation
Not specified · onsite · Posted 12d ago
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Section · 01
About this role
Manage QMS activities: Change Control, Deviation, CAPA, OOS, OOT, Lab Events.
Conduct Risk Assessments, SOP reviews, and assist in grievance handling.
Document & review: Specifications, SOPs, Test Data Sheets, Analytical Test Reports, and Master documents.
Review Method Validation Protocols & Reports.
Monitor calibration and preventive maintenance schedules.
Initiate procurement of impurity/reference standards, chemicals, reagents, columns, and laboratory glassware.
Develop and implement site policies and procedures ensuring regulatory compliance.
Supervise deviation and CAPA review, approval, and implementation.
Create QC goals, objectives, and metrics to drive continuous improvement.
Ensure data integrity systems are in place with frequent checks and challenge tests.
Lead root cause investigations.
Prepare experimental plans during investigations.
Implement CAPA parameters post-investigation.
Verify CAPA effectiveness.
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Section · 02
Skills
Section · Company
About Acme Formulation

Acme Formulation
Pharma
750
employees
2004
22 years old
Nalagarh
India
₹3.6L PA avg
Avg at Acme Formulation
About
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Employee ratings
10 reviews
Culture
2.9
Career growth
3.1
Work-life
2.7
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