General Manager- Quality Control

SAVA Group; Surendranagar; On-site; INR 1,200,000 - 2,000,000; Full time

Job summary

A leading pharmaceutical company based in Surendranagar is looking for a Head of Quality Control to manage all QC activities ensuring compliance with cGMP and regulatory guidelines. The ideal candidate should hold an M.Sc. or B.Pharm degree and possess 12–18 years of experience in Quality Control within the pharmaceutical industry. Responsibilities include managing the QC department, supervising analytical testing, and coordinating with other departments for regulatory audits. The role requires strong analytical and leadership skills.

Qualifications

• 12–18 years of experience in Quality Control in the pharmaceutical industry.
• Minimum of 3–5 years in a leadership role in QC.
• Strong knowledge of analytical instruments.

Responsibilities

• Manage all quality control activities ensuring compliance with regulatory guidelines.
• Lead and manage the QC department including various labs.
• Coordinate stability studies and method validation activities.

Skills

Leadership

Analytical skills

Communication skills

Education

M.Sc. / B.Pharm / M.Pharm in Chemistry or Pharmaceutical Sciences

Tools

HPLC

GC

UV

IR

Job description

Job Title: Head Quality Control (QC)

Location: Surendranagar, Gujarat

Department: Quality Control

Reports To: Vice President - Technical

Role Summary

The Head of QC will be responsible for managing and overseeing all quality control activities at the Surendranagar site, ensuring compliance with cGMP, regulatory guidelines, and internal quality standards. The role includes supervision of analytical testing, documentation, method validation, and coordination with cross‑functional teams for timely product release and regulatory audits.

Key Responsibilities

• Lead and manage the QC department including chemical, instrumental, and microbiology labs.
• Ensure compliance with cGMP, GLP, ICH, and other regulatory requirements.
• Review and approve specifications, test procedures, and analytical reports.
• Oversee sampling and testing of raw materials, packaging materials, in‑process and finished products.
• Ensure timely release of materials and products with strict adherence to quality standards.
• Coordinate stability studies and method validation activities.
• Handle deviations, out‑of‑specification (OOS) results, investigations, and implement CAPAs.
• Interface with regulatory authorities and support audits/inspections (e.g., WHO‑GMP, EU, USFDA, etc.).
• Ensure continuous training and development of QC personnel.
• Maintain and review QC documentation, including SOPs, protocols, reports, and logbooks.
• Collaborate with QA, Production, RA, and other departments for smooth quality operations.

Qualifications & Experience

• M.Sc. / B.Pharm / M.Pharm in Chemistry, Pharmaceutical Sciences, or related field.
• 12–18 years of experience in Quality Control in the pharmaceutical industry.
• Minimum 3–5 years in a leadership role in QC.
• Strong knowledge of analytical instruments (HPLC, GC, UV, IR, etc.).
• Hands‑on experience with regulatory audits and compliance requirements.
• Excellent analytical, leadership, and communication skills.

Preferred Candidate Profile

• Experience in formulations (oral solids/Nasal) is desirable.
• Exposure to international regulatory standards (e.g., USFDA, EU, TGA) is an added advantage.
• Ability to drive quality culture and implement continuous improvement initiatives.