Quality Control – QMS

StrainX Biotech; Hyderabad; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Biopatrika in Hyderabad is seeking a Quality Control - QMS professional to uphold product quality and regulatory standards in a regulated pharmaceutical environment.

The role involves reviewing analytical data, validating methods, supporting CAPA and investigations, and driving audit readiness across cross-functional teams to ensure compliant operations and data integrity.

Qualifications

• Review and approve analytical data, method validation, stability studies, and QC documentation
• Drive QMS compliance, investigations, CAPA management, and audit readiness
• Support root cause analysis for OOS/OOT, incidents, and customer complaints
• Collaborate with cross-functional teams to ensure timely investigation closures and compliance effectiveness
• Ensure adherence to global quality standards through lab oversight and data review

Responsibilities

• Review and approve analytical data, method validation, stability studies and QC documentation
• Drive QMS compliance, investigations, CAPA management, and audit readiness
• Support root cause analysis for OOS/OOT, incidents, and customer complaints
• Collaborate with cross-functional teams to ensure timely investigation closures and compliance effectiveness
• Ensure adherence to global quality standards through lab oversight and data review

Skills

Quality Assurance

Quality Control

Regulatory Compliance

Education

B.Pharm

Post-Graduation in Life Sciences

Job description

Quality Control - QMS

Are you passionate about ensuring quality, compliance, and data integrity in a regulated pharmaceutical environment? Join us and play a critical role in maintaining the highest standards of product quality and regulatory compliance.

• Review and approve analytical data, method validation, stability studies, and QC documentation
• Drive QMS compliance, investigations, CAPA management, and audit readiness
• Support root cause analysis for OOS/OOT, incidents, and customer complaints
• Collaborate with cross-functional teams to ensure timely investigation closures and compliance effectiveness
• Ensure adherence to global quality standards through lab oversight and data review

Qualification: B.Pharm / Post-Graduation in Life Sciences

Experience: 4+ years in Manufacturing, Quality Control, Quality Assurance, or within the pharmaceutical industry