Executive Quality Assurance

Azis Labs

Pithampur, Madhya Pradesh

Department: Quality Assurance

Experience: 3-5 Years

Industry: Pharmaceutical

Education: BSc Msc BPharm MPharm

Job Description

Executive Quality Assurance – Quality Assurance | Azis Labs | Pithampur, Madhya Pradesh, India

Azis Labs is inviting applications for the position of Executive – Quality Assurance at its pharmaceutical manufacturing facility in Pithampur, Madhya Pradesh. This opportunity is ideal for candidates with 3 to 5 years of experience in quality assurance functions within the pharmaceutical industry. The role involves ensuring compliance with GMP standards, reviewing batch manufacturing records, handling deviations, and supporting regulatory audits. The selected candidate will play a key role in maintaining product quality, documentation accuracy, and regulatory compliance. This position provides excellent exposure to pharmaceutical quality systems and regulatory practices. Candidates with strong knowledge of QA processes, documentation control, and audit handling will be preferred. This is a strong career opportunity for professionals looking to grow in pharmaceutical quality assurance functions within a structured and compliance-driven environment.

Location

Pithampur, Madhya Pradesh, India

Employment Type

Full-time

Experience Required

3 to 5 Years

Compensation & Benefits

Competitive salary as per pharmaceutical industry standards along with opportunities for career advancement and exposure to regulatory environments.

About Azis Labs

Azis Labs is a pharmaceutical manufacturing company committed to delivering high-quality products while adhering to stringent regulatory standards and GMP compliance. The company focuses on quality-driven processes and continuous improvement in manufacturing and quality systems.

Position Overview

The Executive – Quality Assurance will be responsible for ensuring compliance with quality systems, reviewing documentation, and supporting regulatory and internal audits.

Key Responsibilities

Review batch manufacturing and packing records.
Ensure compliance with GMP and regulatory requirements.
Handle deviations, CAPA, and change control processes.
Maintain QA documentation and records.
Conduct internal audits and support external audits.
Ensure SOP implementation and compliance.
Coordinate with production and QC departments.
Monitor documentation accuracy and data integrity.
Support validation and qualification activities.
Ensure adherence to quality management systems.

Required Skills & Competencies

Strong knowledge of GMP and QA systems.
Experience in pharmaceutical documentation.
Understanding of audit processes.
Deviation and CAPA handling skills.
Attention to detail.
Analytical and problem-solving skills.
Communication and coordination abilities.
Knowledge of regulatory guidelines.
Documentation control expertise.
Ability to work in compliance-driven environments.

Educational Qualification

BSc / MSc / BPharm / MPharm

About the Project & Industry

This role is part of pharmaceutical manufacturing operations where quality assurance ensures product safety, efficacy, and compliance with regulatory standards. The pharmaceutical industry requires strict adherence to GMP guidelines and quality systems.

Why Join Azis Labs?

Opportunity to work in a regulated pharmaceutical environment, gain exposure to audits and quality systems, and build a strong career in QA functions.