Executive QA – Quality Assurance | Azis Labs | Pithampur, Madhya Pradesh, India
Azis Labs is inviting applications for the role of Executive QA at its pharmaceutical manufacturing operations in Pithampur, Madhya Pradesh. This full-time opportunity is suitable for professionals with 1 to 5 years of experience in pharmaceutical quality assurance systems, GMP documentation, compliance monitoring, batch record review, deviation management, and quality-focused manufacturing operations. The selected candidate will support QA activities related to production compliance, documentation verification, audit readiness, SOP implementation, and quality control coordination within regulated pharmaceutical environments. Candidates with expertise in pharmaceutical quality systems, validation support, documentation management, and regulatory compliance procedures will be preferred. This position provides excellent exposure to pharmaceutical quality assurance operations, manufacturing compliance systems, audit preparation activities, and regulated production environments focused on product quality, operational accuracy, GMP adherence, and continuous process improvement within pharmaceutical manufacturing facilities.
Location
Pithampur, Madhya Pradesh, IndiaEmployment Type
Full-timeExperience Required
1 to 5Compensation & Benefits
Competitive salary package with pharmaceutical quality assurance exposure, compliance management opportunities, and long-term professional growth.About Azis Labs
Azis Labs operates in the pharmaceutical industry specializing in regulated manufacturing systems, pharmaceutical quality operations, and compliance-driven production environments.Position Overview
The Executive QA will manage quality assurance documentation systems, monitor GMP compliance activities, and support pharmaceutical manufacturing quality operations.Key Responsibilities
- Review batch manufacturing and packaging records.
- Monitor GMP compliance across manufacturing operations.
- Support deviation handling and CAPA implementation.
- Maintain QA documentation and quality records.
- Coordinate internal audits and inspection readiness.
- Verify SOP implementation and compliance systems.
- Support validation and qualification activities.
- Coordinate with QC and production departments.
- Ensure adherence to pharmaceutical quality standards.
- Prepare quality reports and operational documentation.
Required Skills & Competencies
- Strong understanding of pharmaceutical QA systems.
- Knowledge of GMP and regulatory compliance standards.
- Documentation review and audit coordination skills.
- Attention to detail and operational accuracy.
- Communication and departmental coordination abilities.
- Problem-solving and compliance management capabilities.
- Understanding of pharmaceutical manufacturing workflows.
- Ability to manage quality timelines effectively.
- Awareness of validation and SOP systems.
- Team collaboration and reporting skills.