As the Quality Control Manager for injectable products, your primary responsibility is to ensure the adherence to quality control procedures in compliance with cGMP and regulatory standards such as FDA and EMA. You will oversee the testing and release of raw materials, in-process materials, and finished products, ensuring the proper documentation and traceability of quality control processes. Leading and managing the quality control team is a key aspect of your role, where you will provide mentorship, training, and motivation to ensure the team's effectiveness. Daily coordination of activities, task assignments, and setting priorities to meet production schedules are essential tasks. Regular performance evaluations and fostering continuous improvement within the team are also part of your responsibilities. You will be in charge of supervising the inspection and testing of injectable products for stability, sterility, endotoxins, potency, and other specifications. Sampling of materials and products for testing, as well as reviewing and approving laboratory test results, fall under your purview. Ensuring regulatory compliance with local and international standards, managing quality audits, and inspections by regulatory agencies, and implementing corrective and preventive actions are crucial aspects of your role. Root cause analysis of quality-related issues, initiating corrective actions, and collaborating with other departments for issue resolution are also part of your responsibilities. Overseeing the qualification and calibration of QC equipment, ensuring validation of analytical methods, and maintaining accurate documentation of test results and quality-related activities are essential tasks. Leading initiatives for continuous improvement, developing training programs for employees, and maintaining industry standards and SOPs are also key responsibilities. To qualify for this role, you should have a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related field, along with 5-8 years of experience in quality control in a pharmaceutical or injectable manufacturing environment. Strong knowledge of cGMP, FDA, EMA guidelines, laboratory testing methods, and quality management systems is required. Strong leadership, organizational, and communication skills, problem-solving abilities, and attention to detail are essential skills for this role. Proficiency in Microsoft Office and quality control software systems is also necessary. Excellent decision-making skills, interpersonal skills, and a proactive approach to quality management and compliance are personal attributes that will contribute to your success in this role.,
PPIC Executive/Manager (Injectables Plant) Company: Kesar Drugs Pvt. Ltd. Location: Panchkula, Haryana (Corporate Office / Injectables Manufacturing Unit) Department: Production Planning & amp; Inventory Control (PPIC) Position: Executive / Manager – PPIC (Injectables) About the Company Farlex Pharmaceuticals Pvt. Ltd., with 1000+ products across diverse therapeutic areas, is one of India’s fastest-growing pharmaceutical companies. With our own injectables manufacturing facility (Kesar Drugs Pvt. Ltd.) , we are committed to innovation, quality, and timely delivery of healthcare solutions across India. Role Overview We are looking for a highly organized and proactive PPIC Executive/Manager to oversee production planning, scheduling, and inventory control at our injectables manufacturing unit (Kesar Drugs Pvt. Ltd. . The role requires close coordination between production, QA, QC, purchase, warehouse, and regulatory teams to ensure smooth operations and on-time delivery. Key Responsibilities Develop and implement production plans as per market demand, sales forecast, and regulatory requirements. Monitor raw material, packing material, and finished goods inventory to ensure uninterrupted production. Coordinate with procurement and warehouse teams for timely availability of inputs. Prepare daily/weekly/monthly production schedules for injectables . Track WIP (Work in Progress) and finished goods to meet dispatch timelines. Maintain accurate records of BMR/BPR status, production reports, and stock reconciliation. Liaise with QA/QC, regulatory, and production teams for smooth compliance- driven operations. Implement cost-effective inventory control systems to minimize wastage. Prepare and analyze MIS reports for management review. Ensure adherence to GMP, cGMP, and regulatory guidelines in planning and execution. Key Requirements Education : B.Pharma / M.Pharma / MBA (Operations / Supply Chain) Experience: 5–10 years in PPIC, production planning, or supply chain in a reputed pharmaceutical injectable plant. Strong knowledge of GMP guidelines, production workflows, and inventory management systems. Excellent analytical, coordination, and communication skills . Proficiency in ERP/MS Excel/MS Office tools. Ability to handle pressure and ensure timely delivery with zero stock-outs. Why Join Us? Opportunity to work with a fast-growing pharmaceutical company with a strong presence across India. Exposure to state-of-the-art injectable manufacturing operations . Growth-oriented environment with focus on learning, innovation, and career development. How To Apply :- Interested candidates can share their CV's on hradmin@farlex.in or call us at 9875998082. Job Type: Full-time Pay: From ₹50,000.00 per month Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: ppic: 5 years (Preferred) Injectable Plant : 5 years (Preferred) Work Location: In person