Assistant General Manager Peptide Quality Control

Raks Pharma Pvt Ltd; Dahej; On-site; INR 3,500,000 - 6,000,000; Full time

Job summary

Raks Pharma Pvt Ltd invites applications for an AGM Quality Control to lead the quality control function for peptide API manufacturing. The role will establish and maintain robust analytical and microbiological control systems, ensure GMP compliance, data integrity, regulatory readiness, and scientific excellence across peptide manufacturing operations.

The position requires strong hands-on leadership in peptide analytical characterization, QC operations, upstream synthesis, downstream

Qualifications

• 15+ years of experience in QC for peptide API manufacturing.
• M.Sc. / M.Pharm / Ph.D. in Chemistry, Pharmaceutical Sciences, or related field.
• Strong leadership and hands-on expertise in analytical characterization and GMP.

Responsibilities

• Lead QC function and establish robust analytical and microbiological control systems.
• Ensure GMP compliance, data integrity, and regulatory readiness across peptide operations.
• Oversee method validation, tech transfer, and readiness for regulatory inspections.

Skills

Leadership

QC operations

GMP knowledge

Education

M.Sc. / M.Pharm / Ph.D. in Chemistry, Pharmaceutical Sciences, or related discipline

Job description

AGM Peptide Quality Control

• Department: Quality Control
• Function: Quality Control Lead with Peptide API Manufacturing
• Location: Dahej
• Experience: 15 + Years
• Qualification: M.Sc. / M.Pharm / Ph.D. in Chemistry, Pharmaceutical Sciences, or related discipline

Job Summary

We are looking for an experienced AGM Quality Control to lead the Quality Control function for Peptide API manufacturing. The role will be responsible for establishing and maintaining robust analytical and microbiological control systems, ensuring GMP compliance, data integrity, regulatory readiness, and scientific excellence across peptide manufacturing operations.

The position requires strong hands-on and leadership experience in peptide analytical characterization, QC operations, upstream synthesis, downstream purification, microbiological control, method validation, technology transfer, and regulatory inspection readiness.