Officer - QA IPQA – Quality Assurance | Curefox Healthcare Pvt Ltd | Ahmedabad, Gujarat, India
Curefox Healthcare Pvt Ltd is inviting applications for the position of Officer - QA IPQA at its pharmaceutical manufacturing operations located in Ahmedabad, Gujarat, India. This full-time opportunity is ideal for candidates with 2 to 4 years of experience in quality assurance, IPQA activities, in-process quality checks, batch documentation review, GMP compliance, and pharmaceutical manufacturing operations within regulated environments. The selected candidate will monitor IPQA activities during manufacturing processes, maintain quality documentation, coordinate with production and quality teams, ensure compliance with regulatory standards, and support audit readiness across production operations. Candidates having expertise in in-process quality assurance systems, pharmaceutical quality documentation, deviation handling, and GMP compliance procedures will be preferred. This role offers excellent exposure to advanced pharmaceutical quality systems, IPQA operational practices, regulatory manufacturing environments, and compliance-driven healthcare operations focused on product quality, process consistency, operational accuracy, and continuous improvement.
Location
Ahmedabad, Gujarat, IndiaEmployment Type
Full-timeExperience Required
2 to 4Compensation & Benefits
Competitive salary package with pharmaceutical QA exposure, compliance learning opportunities, and long-term quality assurance career growth.About Curefox Healthcare Pvt Ltd
Curefox Healthcare Pvt Ltd operates in the pharmaceutical industry specializing in healthcare manufacturing, quality assurance systems, pharmaceutical production, and regulated compliance operations.Position Overview
The Officer - QA IPQA will support in-process quality assurance activities, documentation systems, and compliance monitoring operations.Key Responsibilities
- Perform in-process quality assurance and IPQA activities.
- Monitor manufacturing operations and quality parameters.
- Maintain QA documentation and batch manufacturing records.
- Coordinate with production and quality control departments.
- Ensure compliance with GMP and pharmaceutical standards.
- Support deviation handling and corrective action activities.
- Participate in audits and regulatory inspection preparation.
- Monitor process consistency and operational quality.
- Assist in quality improvement and compliance initiatives.
- Maintain safety and documentation accuracy within operations.
Required Skills & Competencies
- Strong understanding of pharmaceutical QA and IPQA systems.
- Knowledge of GMP and regulated manufacturing practices.
- Documentation and compliance management expertise.
- Communication and coordination abilities.
- Problem-solving and analytical thinking capabilities.
- Awareness of pharmaceutical quality standards.
- Ability to manage quality workflows efficiently.
- Attention to documentation accuracy and product quality.
- Operational monitoring and reporting skills.
- Adaptability to regulated pharmaceutical environments.