QA Executive – Quality | Aculife Healthcare | Ahmedabad, Gujarat, India
Aculife Healthcare is hiring skilled professionals for the role of QA Executive at its pharmaceutical manufacturing facility in Sanand, Ahmedabad, Gujarat, India. This full-time walk-in opportunity is suitable for candidates with 0 to 5 years of experience in quality assurance operations, pharmaceutical documentation systems, compliance monitoring, validation support, and GMP-related activities. The selected candidate will support QA documentation processes, monitor quality systems, coordinate with production teams, and ensure compliance with pharmaceutical quality standards and regulatory requirements. Candidates with strong understanding of quality assurance systems, SOP management, batch documentation review, and pharmaceutical compliance processes will be preferred. This role offers excellent opportunities to work in a professional pharmaceutical manufacturing environment with exposure to quality management systems, regulatory operations, and process-driven industrial standards focused on maintaining product quality and operational excellence.
Location
Sanand, Ahmedabad, Gujarat, IndiaEmployment Type
Full-timeExperience Required
0 to 5Compensation & Benefits
Competitive salary package with opportunities to work on pharmaceutical quality systems, regulatory operations, and long-term professional growth in quality assurance management.About Aculife Healthcare
Aculife Healthcare is a pharmaceutical manufacturing company focused on quality-driven healthcare solutions, industrial manufacturing systems, and regulatory-compliant pharmaceutical operations.Position Overview
The QA Executive will support quality assurance operations, documentation systems, compliance monitoring, and pharmaceutical quality management activities.Key Responsibilities
- Maintain QA documentation and compliance records.
- Review batch manufacturing and quality documents.
- Support validation and quality assurance activities.
- Coordinate with production and quality control teams.
- Ensure adherence to GMP and SOP guidelines.
- Monitor compliance with pharmaceutical regulations.
- Assist in audits and inspection preparation activities.
- Support deviation handling and corrective action processes.
- Prepare quality reports and operational documentation.
- Ensure maintenance of quality management systems.
Required Skills & Competencies
- Knowledge of pharmaceutical quality assurance systems.
- Understanding of GMP and compliance procedures.
- Strong documentation and reporting skills.
- Analytical and problem-solving capabilities.
- Communication and coordination abilities.
- Knowledge of validation and audit processes.
- Attention to detail and quality standards.
- Ability to handle quality records and documentation.
- Awareness of pharmaceutical manufacturing operations.
- Capability to work in regulated environments.