Walk-in || Engineering / Technical Services

Pharma Engineering / Technical Services HVAC, Electrical, Instrumentation & Utilities | Hyderabad

A reputed Pharmaceutical Formulations manufacturing company in Hyderabad is hiring experienced technical professionals across

Engineering & Technical Services.IPQA 2 - 5 Years: Monitor in-process quality activities, GMP compliance, batch records, deviations, and production processes.

1. Validation & Qualification .. 5 - 6 Years: Execute and document equipment, process, cleaning, and facility validation/qualification activities as per GMP requirements.
2. Document Issuance 2–4 Years: Manage issuance, control, tracking, and distribution of GMP-controlled documents in compliance with QMS procedures.
3. QMS Team – 2–4 Years: Manage QMS activities including deviations, CAPA, change controls, OOS/OOT, and compliance documentation.
4. Finished Product Release – 2–4 Years: Review batch documentation, test results, and quality records to ensure timely and compliant finished product release.
5. Document Preparation – 2–4 Years: Prepare GMP documents, SOPs, protocols, reports, and quality records in line with regulatory requirements.
6. Document Review – 4–6 Years: Review GMP documentation, batch records, SOPs, and quality records for accuracy, completeness, and compliance.
7. AQA – 4–6 Years: Manage analytical quality assurance activities including laboratory compliance, data review, investigations, and GMP adherence.
8. Candidate Profile: ITI / Diploma / B.Tech / relevant technical qualification with relevant industrial or pharmaceutical plant experience.