Job Title: QA Manager Department: Quality Assurance Location: Surendernagar, Gujarat. Qualification: M.Pharm / B.Pharm / M.Sc Experience: 8 - 10 years in pharmaceutical QA Reporting To: Head Quality / Plant Head Key Responsibilities: Lead QMS activities: deviations, change control, CAPA, risk assessments, and quality audits. Manage validation activities: process, cleaning, equipment qualification. Review and approve SOPs, BMRs, BPRs, and validation protocols. Handle regulatory inspections and customer audits; ensure effective CAPA implementation. Drive compliance with data integrity and continuous improvement initiatives. Supervise and mentor QA team; collaborate with cross-functional departments. Mandatory Requirements: Must have hands-on exposure to regulatory audits like EU-GMP, MHRA, TGA, and USFDA. Deep understanding of cGMP, quality systems, and global compliance expectations. Skills & Competencies: Strong leadership in quality assurance and regulatory compliance. Excellent communication, documentation, and team management skills. Should Be able to handle the Team .

Job Title: QC Executive Location: Surendranagar, Gujarat Experience: 15 years Department: Quality Control Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry) Key Responsibilities: Perform analysis of raw materials, packaging materials, in-process & finished products. Operate instruments: HPLC, GC, UV, Dissolution Apparatus, etc. Ensure documentation as per cGMP & ALCOA+ principles. Conduct stability studies & routine instrument calibration. Handle OOS/OOT/deviation investigations. Comply with GLP, GMP & regulatory requirements. Preferred Skills: Experience in regulated pharma (WHO-GMP/USFDA/EU-approved plants). Knowledge of LIMS/Chromeleon/Empower preferred. Good communication & documentation skills.

Job Title: Production Executive Nasal Formulation Location: Surendranagar, Gujarat, India Department: Production – Nasal Formulations Experience: 2–4 years (including international/non-domestic experience) Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc or equivalent Key Responsibilities: Oversee end-to-end manufacturing operations for Nasal formulations (sprays, drops, etc.). Ensure adherence to production schedules, batch planning, and resource allocation. Monitor and enforce cGMP, safety, and hygiene practices across the Nasal production area. Review and maintain production documentation including BMRs, BPRs, and SOPs. Coordinate with Quality Assurance, Quality Control, Engineering, and Warehouse for seamless operations. Identify and troubleshoot production issues to minimize downtime and rejections. Participate in internal and external audits; ensure timely CAPA implementation. Drive process improvement initiatives to increase productivity and reduce waste. Ensure proper maintenance and calibration of production equipment used in Nasal manufacturing.