Company Description Lezivia Lifesciences is a reputable pharmaceutical company recognized for delivering high-quality products to patients. Most of its portfolio is manufactured at WHO-approved facilities, ensuring strict adherence to international quality and safety standards. The organization focuses on consistent product excellence and regulatory compliance across its manufacturing operations.

Lezivia

Lifesciences offers a professional environment where quality-focused team members can contribute to meaningful healthcare outcomes. The company values integrity, reliability, and continuous improvement in all aspects of its work.

Role Description This is a full time, on-site QA Lead (Sr. Manager) role based in Baddi. The QA Lead will oversee quality assurance activities for pharmaceutical manufacturing, with a focus on dosage forms such as ointments, sprays, oral solid dosage (OSD), inhalers, and eye drops.

Daily responsibilities include establishing and monitoring quality systems, reviewing batch manufacturing records, managing investigations and CAPA, and ensuring compliance with GMP and regulatory requirements. The role involves leading and mentoring QA teams, coordinating with production, QC, and regulatory departments, and supporting internal and external audits. The QA Lead will also participate in validation activities, risk assessments,



and continuous improvement initiatives to maintain product quality and patient safety.

Qualifications

- Strong expertise in pharmaceutical quality assurance for ointments, sprays, OSD, inhalers, and eye drops, with hands-on experience in manufacturing environments.
- Proficiency in GMP guidelines, regulatory requirements (national and international), documentation practices, and quality systems (change control, deviations, CAPA).
- Experience in validation and qualification activities, including process validation, cleaning validation, equipment qualification, and risk-based approaches.
- Demonstrated ability to lead QA teams, manage cross-functional coordination, supervise audits and inspections, and drive continuous improvement initiatives.
- Excellent analytical, problem-solving, and decision-making skills, with strong attention to detail and a focus on data integrity and compliance.
- Effective communication and stakeholder management skills, including the ability to prepare clear reports, SOPs, and training materials.
- Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, or a related field; prior experience in a QA leadership or senior management role in pharmaceutical manufacturing is highly preferred.
- Comfort working on-site in Baddi and willingness to engage in floor-level oversight, coaching, and collaboration with production and QC teams.

📌 Hiring: QA Lead (Sr. Manager) – Pharmaceutical Manufacturing | Experience in Ointments / Sprays / OSD / Inhalers / Eye Drops | CTC: Up to ₹12 LPA (Baddi)
🏢 Lezivia Lifesciences
📍 Baddi