quality assurance

Evarastaffing; Panchkula; On-site; INR 1,421,784 - 1,703,016; Full time

Job summary

Evarastaffing in Panchkula is seeking a Senior Manager / AGM – Quality Assurance with 15+ years in pharmaceutical manufacturing to lead our QA operations. You will ensure regulatory compliance, governance, and robust documentation.

The role requires strong leadership, expert knowledge of GMP, and proven success in audits and CAPA, with a focus on batch release and risk management at scale.

Qualifications

• 15+ years of QA leadership experience in pharmaceutical manufacturing.
• Proven track record in regulatory audits and inspections.
• Strong documentation, CAPA, and change-control management.
• Experience with QMS, validation/qualification and deviation handling.

Responsibilities

• Lead the Quality Assurance function in pharma manufacturing to ensure compliance with regulatory requirements.
• Plan, coordinate, and support regulatory audits (USFDA, WHO-GMP, MHRA, etc.).
• Oversee CAPA, change control, deviations, and documentation practices across the site.
• Drive batch release decisions, risk assessments, and continuous improvement initiatives.

Skills

Quality Assurance in Pharma

cGMP, GLP & GDP

Regulatory Compliance

Documentation & Audit Management

QMS, CAPA, Change Control

Validation & Qualification

SOP Preparation & Review

Risk Assessment

Team Leadership

USFDA & WHO-GMP Audits

Root Cause Analysis

Vendor Qualification

Batch Release & Investigation

Communication & Problem Solving

Education

B.Pharm

M.Pharm

M.Sc or equivalent

Job description

Job Title

Senior Manager / AGM – Quality Assurance (Pharma Manufacturing)

Location

Panchkula

Experience

15+ Years

CTC

Up to ₹1.40 Lakh per Month

Job Description

We are looking for an experienced Quality Assurance professional with a strong background in pharmaceutical manufacturing.

Key Skills

• Quality Assurance in Pharma Manufacturing
• cGMP, GLP and GDP
• Regulatory Compliance
• Documentation and Audit Management
• QMS, CAPA, Change Control and Deviations
• Validation and Qualification
• SOP Preparation and Review
• Risk Assessment
• Team Handling and Leadership
• USFDA, WHO-GMP, MHRA and other regulatory audits
• Root Cause Analysis
• Vendor Qualification
• Batch Release and Investigation
• Excellent communication and problem-solving skills

Qualification

B.Pharm, M.Pharm, M.Sc or equivalent.

Skills

assessment,manufacturing,audit management,quality assurance