Job Title: PPIC Executive Industry: Pharmaceuticals / Cosmetics Location: Tehsil Inodra, Kangra (HP), near by Pathankot Experience Required: 410 years Education: B.Sc / B.Pharma / B.Tech / MBA in Supply Chain / Operations preferred Key Responsibilities: Prepare monthly and weekly production plans based on sales forecasts and inventory levels. Coordinate with production, warehouse, and procurement teams to ensure timely availability of raw materials and packaging materials. Monitor daily production schedules and update any deviations or delays. Maintain optimal inventory levels to avoid stock-outs or overstock situations. Analyze consumption trends and prepare material requirement plans (MRP). Ensure proper documentation and compliance with GMP, ISO, and regulatory requirements. Maintain master data for BOM (Bill of Materials), routings, and item masters in ERP systems (SAP / Tally / Oracle, etc.). Prepare and share regular MIS reports on production status, inventory health, and material availability. Coordinate with QA/QC, warehouse, and logistics for smooth production and dispatch planning. Identify gaps in supply chain processes and suggest improvements to enhance efficiency. Key Skills Required: Production Planning & Scheduling Inventory Control & Management Material Requirement Planning (MRP) ERP Knowledge (SAP / Oracle / Tally, etc.) Coordination & Communication Skills Analytical and Problem-solving Abilities Knowledge of GMP / GLP / Regulatory Compliance MS Excel Advanced proficiency

Department: Quality Control Location: Tehsil Inodra, Kangra (HP). Near by Pathankot Reporting to: QC Manager / Head Quality Department Key Responsibilities: Conduct routine testing of raw materials, in-process materials, and finished products as per approved specifications and standard test procedures (STPs). Perform chemical and instrumental analysis using HPLC, UV, IR, GC, KF, etc. Maintain accurate and up-to-date laboratory records, worksheets, and logbooks. Ensure timely calibration and maintenance of laboratory instruments and equipment. Review and follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Assist in method development and method validation activities as required Conduct stability testing and prepare stability summary reports. Ensure compliance with company SOPs, quality standards, and regulatory requirements (such as USFDA, MHRA, WHO, etc.). Participate in internal and external audits and implement corrective and preventive actions (CAPA). Manage sampling, labeling, and storage of test samples as per SOPs. Handle out-of-specification (OOS), out-of-trend (OOT), and deviations according to quality procedures. Coordinate with production, QA, warehouse, and other departments for quality-related issues. Monitor environmental conditions of the lab as per the standard protocol. Desired Candidate Profile: Education: B.Pharm / M.Pharm / B.Sc / M.Sc Chemistry or related field Experience: 2–10 years in QC role within a pharmaceutical formulation plant Skills Required: Proficient in operating analytical instruments (HPLC, GC, etc.) Knowledge of GMP, GLP, ICH guidelines Strong documentation and communication skills Attention to detail and ability to work under pressure Good analytical and problem-solving skills