Pharmaceuticals production head and quality head

Euploid Pharmaceuticals Private Limited · Mysore, India

Company Description Euploid Pharmaceuticals Private Limited is a pharmaceuticals OSD company WHO GMP Certified with 100% EU GMP Compliance located at Mysore near Mysore airport, headquartered in Bangalore, Karnataka, India. The organization focuses on developing and manufacturing pharmaceutical products with a strong emphasis on quality and regulatory compliance. As a growing company, Euploid Pharmaceuticals offers opportunities to contribute to modern biotech and pharma manufacturing practices. Team members work in a collaborative environment that values scientific rigor, safety, and innovation. The company is committed to building reliable, high-quality production capabilities to support healthcare needs.

Role Description This is a full-time, on-site role based in Mysore for a Pharmaceuticals Production Head and Quality Head. The role involves overseeing day-to-day production operations, including planning batches, managing manufacturing schedules, coordinating staff, and ensuring adherence to standard operating procedures. The position also includes leading quality assurance and quality control activities, monitoring compliance with GMP and regulatory guidelines, supervising documentation, and reviewing quality records such as deviations, change controls, and CAPA. The individual will collaborate with cross-functional teams to optimize processes, implement continuous improvement initiatives, and ensure timely, compliant product delivery. The role requires hands-on leadership on the shop floor, active mentoring of team members, and regular reporting to senior management on production performance and quality metrics.

Qualifications

• Strong expertise in pharmaceutical production management, including batch planning, resource allocation, and process optimization.
• Demonstrated experience in quality assurance and quality control, with deep knowledge of GMP, GLP, and relevant regulatory requirements.
• Ability to lead and develop manufacturing and quality teams, with skills in people management, training, and performance monitoring.
• Proficiency in documentation and compliance activities, including SOP development, deviation handling, change control, and audit readiness.
• Experience with sterile or non-sterile dosage form manufacturing, validation, and equipment qualification is highly beneficial.
• Bachelor’s or Master’s degree in Pharmacy, Biotechnology, Chemistry, or a related field; prior leadership experience in pharma manufacturing preferred.
• Strong analytical, problem-solving, and decision-making skills, with the ability to work effectively in a fast-paced, on-site environment.
• Excellent communication and collaboration skills to coordinate with regulatory, R&D, supply chain, and senior management stakeholders.