Specialist III, QA Sterile Manufacturing

At Mann Kind, we are dedicated to transforming chronic disease through innovative, patient-centric solutions designed to fit seamlessly into daily life. Our focus is on delivering therapies for people living with cardiometabolic and orphan lung diseases such as diabetes, pulmonary hypertension and fluid overload in heart and chronic kidney disease.

At Mann Kind, our employees are our number one asset, and we foster a tight-knit community where each of us plays a critical role in our collective success. We strive to provide a work environment where diversity of background, thought and perspective is valued and respected. Our team is also energized by the company’s entrepreneurial spirit that provides an environment in which you can evolve ideas quickly and nimbly.

Our Values serve as the foundation of Mann Kind’s culture. They define who we are, how we act, and guide our interactions every day—both with each other and the customers we serve. At Mann Kind, you will work with people who are experts in their fields, see challenges as opportunities, are tenacious and push boundaries, bring creative and solutions-based thinking forward, and always believe in winning together.

Serve as the primary Quality Assurance representative on the sterile manufacturing floor, providing independent oversight of production operations, ensuring compliance with current GMP requirements, approved batch records, SOPs, and quality systems while supporting the manufacture and release of sterile pharmaceutical products.

• * Comprehend and interpret GMP, ISO 13485:2016 and EU/FDA regulatory and quality standards.
• * Serve as the Quality Assurance point of contact on the sterile manufacturing floor, providing GMP guidance and support for batch record execution, material status, and manufacturing operations for commercial and clinical batches.
• * Review Master Batch Records for compliance, identify issues, and suggest possible resolutions.
• * Review executed batch records and associated data for compliance to requirements.
• * Administer the Material Review Board transactions including accessing the Rework Program.
• * Participate in deviation events and investigations as required.
• * Support investigations, CAPAs, change controls, and risk assessments related to manufacturing operations.
• * Perform data entry and execute records in electronic systems.
• * Perform or support the risk management program.
• * Identify, communicate and escal[e]ate basic technical issues. Identify options for resolutions and lead implementation of corrective actions.
• * Prioritize own work and works independently on day-to-day activities, additional supervision/guidance for new assignments.
• * Provide guidance/leadership to junior associates.
• * Identify and benchmark compliance best practices.
• * Perform routine visual inspection and dimensional measurements.
• * Observe and verify execution of manufacturing activities in accordance with approved batch records and SOPs.
• * Review and approve QA-designated steps within batch records.
• * Basic understanding of calibration requirements.
• * Ensure appropriate identification, segregation, and status labeling of materials and product throughout manufacturing operations
• * Perform line clearance and area clearance verification activities.
• * Ensure manufacturing personnel adhere to approved batch records and procedures.
• * Responsible for working with MNKD partner relating to their product (e.g. batch record questions, deviations, SOPs, etc.)
• * Provide real time quality oversight of manufacturing and packaging operations.
• * Support validation/qualification activities for equipment/systems/processes and aseptic process simulations, as required.
• * Ensure adherence to approved SOPs, validated processes, and data integrity…