We have opening for Sr. IPQA for OSD for Pharma Industry for Amreli Location.
Job Description (JD) for IPQA in Pharma
Role Objective
Ensure quality assurance during manufacturing of oral solid dosage forms (tablets, capsules, etc.).
Prevent deviations and defects by real-time monitoring of production processes.
Key Responsibilities
Line Clearance: Verify cleanliness, area labeling, and readiness before starting production
Guidelines - SOPs
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Process Monitoring: Check blending, granulation, compression, coating, and packaging steps for compliance with SOPs.
Sampling & Testing: Collect in-process samples (e.g., weight variation, hardness, friability, disintegration) and verify against specifications.
Documentation: Record observations in batch manufacturing records and logbooks.
Deviation Handling: Identify, report, and assist in investigating deviations or non-conformities.
GMP Compliance: Ensure adherence to Good Manufacturing Practices and regulatory guidelines
Royed Training
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Training & Guidance: Support production staff in following SOPs and quality standards.
Audit Readiness: Maintain documentation for internal and external audits.
Skills & Competencies
Strong knowledge of OSD manufacturing processes (granulation, compression, coating).
Familiarity with regulatory requirements (FDA, EMA, WHO GMP).
Attention to detail and ability to detect process deviations early.
Good communication and documentation skills.
Qualifications
3- 8years of experience in quality assurance or production in OSD manufacturing.
Interested candidate please revert over mail or WhatsApp.
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