Quality Assurance Lead, Devices

About the role

Lupin is seeking a strategic and results-driven Quality Assurance Lead, Devices to lead quality systems and compliance activities for our growing portfolio of drug-device combination products. In this critical role, you will establish and maintain robust quality management systems, ensure adherence to FDA and global regulatory standards, and collaborate with cross-functional teams throughout the product lifecycle. The successful candidate will combine deep quality expertise with strong leadership, project management, and communication skills to drive a culture of quality, compliance, and continuous improvement while supporting the successful development and commercialization of innovative healthcare solutions. This role will be responsible for ensuring compliance with FDA, ISO 13485, ICH, and other applicable regulatory requirements.

Responsibilities

• Design, implement, and maintain quality systems tailored to the unique needs of drug-device combination products. Ensure full alignment with FDA 21 CFR Part 820, ISO 13485, and relevant ICH guidelines. Develop and maintain procedures for design control, risk management, change control, and supplier quality oversight.
• Collaborate with R&D, Regulatory Affairs, Manufacturing, and Clinical teams to embed quality into each stage of the product lifecycle. Provide quality planning and execution support to combination product teams, ensuring quality is proactively managed across disciplines.
• Prepare for and support both internal and external audits, ensuring all quality systems and documentation are audit-ready. Monitor regulatory changes and proactively update systems to maintain ongoing compliance with evolving standards and requirements.
• Author, review, and maintain Standard Operating Procedures (SOPs), quality manuals, and technical documentation. Develop and deliver training programs for cross-functional teams on the specific quality requirements for combination products.
• Identify and implement opportunities for process optimization and enhancements to the quality system. Lead Corrective and Preventive Action (CAPA) investigations and root cause analyses related to combination product issues.

Requirements

• Standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing.
• In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply.
• This position may require lifting up to 15 pounds occasionally.
• Generally work is performed in an office environment.

Qualifications

• Bachelor’s or master’s degree in engineering, Life Sciences, or a related field.
• Minimum of 8 years’ experience in Quality Assurance or Quality Systems within the pharmaceutical or medical device industry.
• Strong understanding of combination product regulations, including FDA and ISO standards.
• Experience with women’s health products or nasal delivery systems is a significant plus.
• Demonstrated excellence in communication, leadership, and project management.
• Prior experience establishing quality systems for combination products.