Company Description UNILITE INDIA is a leading pharmaceutical manufacturer specializing in precision-driven liquid formulations from its GMP and GLP compliant facility in Lodhi Majra, Baddi, Himachal Pradesh. The company focuses on liquid injections, eye drops, ear drops, and nasal drops, serving both leading domestic pharmaceutical brands and international partners through reliable third-party manufacturing solutions. With state-of-the-art infrastructure and advanced technologies, UNILITE INDIA maintains stringent quality controls to ensure products meet high standards of purity, safety, and efficacy. The organization is committed to continuous improvement, innovation, and strong regulatory compliance, enabling partners to grow confidently in a dynamic healthcare landscape. Above all, UNILITE INDIA emphasizes trust, consistency, and long-term value in its role as a quality-driven healthcare partner. Role Description The QA Manager role at UNILITE INDIA is a full-time, on-site position based at the manufacturing facility in Baddi, Himachal Pradesh. The QA Manager will oversee the quality management system, ensuring compliance with GMP, GLP, and relevant regulatory standards across all liquid formulations, including injections and ophthalmic, otic, and nasal products. Day-to-day responsibilities include developing and updating SOPs, supervising in-process and finished product quality checks, coordinating validations and qualifications, and managing documentation, change control, and deviation handling. The role also involves conducting internal audits, supporting regulatory inspections,



mentoring QA team members, and collaborating closely with production, R&D;, and QC to drive continuous improvement. The QA Manager will be expected to identify quality risks, implement corrective and preventive actions, and maintain a strong culture of quality and safety throughout the organization. Qualifications
• Solid expertise in pharmaceutical quality assurance, including GMP/GLP compliance, documentation control, and quality management systems.
• Experience with sterile and liquid formulation manufacturing processes, preferably in injections, eye drops, ear drops, and nasal drops.
• Proficiency in internal auditing, deviation and CAPA management, change control, risk assessment, and validation/qualification activities.
• Knowledge of national and international regulatory requirements, guidelines, and quality standards relevant to pharmaceutical manufacturing.
• Effective leadership and people management skills, with the ability to train, mentor, and develop QA teams.
• Robust analytical, problem-solving, and decision-making abilities, with attention to detail and a focus on data-driven improvements.
• Excellent written and verbal communication skills for cross-functional collaboration and regulatory interactions.
• Relevant academic background such as a degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related discipline.
• Prior experience in a similar QA leadership or managerial role in the pharmaceutical industry is highly desirable.
• Commit

📌 QA Manager (Baddi)
🏢 UNILITE INDIA
📍 Baddi