QA IPQA

Company Description Allrite Healthcare is a growing pharmaceutical and healthcare manufacturing organization committed to delivering safe, high-quality products that meet regulatory and patient care standards. The company focuses on robust quality systems, compliant manufacturing practices, and continuous improvement across its operations. Allrite Healthcare values collaboration, integrity, and a culture of accountability, encouraging team members to contribute to process enhancement and innovation. Professionals joining the organization can expect a structured environment, clear quality objectives, and opportunities to develop their expertise in healthcare manufacturing and quality management.
Role Description The QA IPQA role at Allrite Healthcare is a full-time, on-site position based in Baddi. The role involves performing in-process quality checks on manufacturing and packaging activities, monitoring adherence to standard operating procedures and GMP requirements, and ensuring that batch records and documentation are accurate and complete. The QA IPQA professional will review and approve line clearance, oversee sampling and testing as per quality plans, and support investigations of deviations, non-conformances, and complaints. Responsibilities also include participating in internal audits, supporting implementation of corrective and preventive actions, and coordinating with production, quality control, and regulatory teams to maintain consistent product quality. The role requires maintaining detailed records, preparing reports, and communicating quality-related observations to relevant stakeholders in a timely manner.
Qualifications
Candidates should possess skills in Quality Control and Quality Assurance to monitor in-process activities and ensure product compliance with specifications.
Candidates should possess skills in Quality Management and Quality Auditing to support internal audits, continuous improvement initiatives, and maintenance of robust quality systems.
Candidates should possess strong knowledge of Good Manufacturing Practice (GMP) to ensure adherence to regulatory guidelines and industry standards in all onsite operations.
Relevant academic qualification such as a diploma or degree in Pharmacy, Chemistry, Life Sciences, or a related field.
Experience in pharmaceutical or healthcare manufacturing, ideally in QA/IPQA or a similar quality-focused role.
Strong attention to detail, documentation skills, and the ability to follow and enforce standard operating procedures.
Effective communication, teamwork capabilities, and readiness to work in a structured, compliance-driven environment at the Baddi facility.

Work arrangement
No