IPQA Officer – Quality Assurance | Rusoma Healthcare Private Limited | Indore, Madhya Pradesh, India
Rusoma Healthcare Private Limited is hiring qualified professionals for the role of IPQA Officer at its Indore, Madhya Pradesh pharmaceutical manufacturing operations. This full-time opportunity is suitable for candidates with 2 to 5 years of experience in in-process quality assurance, pharmaceutical compliance systems, production monitoring, quality inspections, and documentation management. The selected candidate will support IPQA activities, monitor manufacturing processes, conduct quality checks, maintain compliance records, and ensure adherence to pharmaceutical regulatory standards across production operations. Candidates with expertise in GMP compliance, batch documentation review, in-process inspections, and pharmaceutical quality systems will be preferred. This role offers valuable exposure to regulated pharmaceutical manufacturing environments, operational quality systems, process monitoring technologies, and compliance-driven production operations focused on product quality, regulatory standards, operational discipline, and continuous quality improvement initiatives.
Location
Indore, Madhya Pradesh, IndiaEmployment Type
Full-timeExperience Required
2 to 5Compensation & Benefits
Competitive compensation package with pharmaceutical quality operations exposure and long-term professional development opportunities.About Rusoma Healthcare Private Limited
Rusoma Healthcare Private Limited operates in the pharmaceutical manufacturing sector with expertise in regulated production systems, healthcare manufacturing operations, and quality-focused pharmaceutical processes.Position Overview
The IPQA Officer will monitor in-process quality systems, production compliance activities, and pharmaceutical documentation procedures.Key Responsibilities
- Conduct in-process quality inspections during manufacturing.
- Monitor compliance with GMP and pharmaceutical standards.
- Review batch records and production documentation.
- Coordinate with production and quality departments.
- Support investigations related to quality deviations.
- Maintain IPQA reports and operational records.
- Monitor manufacturing processes for compliance adherence.
- Ensure implementation of approved quality procedures.
- Support audit preparation and compliance activities.
- Participate in continuous quality improvement initiatives.
Required Skills & Competencies
- Knowledge of pharmaceutical IPQA systems and GMP.
- Understanding of production monitoring and compliance.
- Strong documentation and reporting abilities.
- Communication and coordination skills.
- Problem-solving and analytical thinking expertise.
- Attention to detail and operational discipline.
- Ability to review batch and quality records efficiently.
- Awareness of pharmaceutical regulatory standards.
- Team collaboration and inspection capabilities.
- Capability to work in regulated pharmaceutical facilities.