IPQA/QMS – Pharmaceuticals

Role Description The IPQA/QMS – Pharmaceuticals role is a full-time, on-site position based in Jaipur. The role involves overseeing in-process quality assurance activities on the production floor to ensure that all pharmaceutical products meet established quality standards and regulatory requirements. Day-to-day responsibilities include monitoring manufacturing operations, performing in-process checks, reviewing batch records, and ensuring adherence to standard operating procedures and Good Manufacturing Practices (GMP). The role also includes maintaining and improving the Quality Management System (QMS), coordinating deviations, change controls, and CAPA, and supporting internal audits and regulatory inspections. The IPQA/QMS professional will collaborate closely with production, QA, QC, and R&D teams to drive continuous quality improvement and compliance.

Qualifications
Candidates should possess strong domain knowledge in Pharmacy and Pharmaceuticals, with an understanding of dosage forms, formulations, and regulatory requirements.Candidates should possess solid expertise in Good Manufacturing Practice (GMP) and Quality Management Systems, including SOPs, documentation, audits, and compliance.Candidates should possess relevant Laboratory Skills, including familiarity with basic analytical techniques, in-process testing, and data recording.Candidates should possess effective communication and collaboration skills to work cross-functionally with production, QA, QC, and regulatory teams.Candidates should possess strong attention to detail, problem-solving abilities, and a structured approach to managing deviations, change controls, and CAPA.Relevant academic qualifications such as a Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, or a related discipline are preferred.Prior experience in IPQA, QMS, or a similar pharmaceutical manufacturing quality role will be considered an added advantage.