Manager, QA Validation (Sterile Manufacturing) at Mannkind

Danbury, Connecticut, United States -

Full Time

Start Date

Immediate

Expiry Date

29 Jul, 26

Salary

174000.0

Posted On

30 Apr, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Validation, Sterile manufacturing, Fill-finish operations, Aseptic processing, Quality assurance, GMP, People management, Risk management, Equipment qualification, Process validation, Cleaning validation, Computer system validation, Regulatory compliance, Sterilization, Environmental monitoring, Data integrity

Industry

Pharmaceutical Manufacturing

Description

MannKind is committed to developing and commercializing innovative therapeutic products for patients living with endocrine and orphan lung diseases. We are on a mission to give people control of their health and the freedom to live life. At MannKind, 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 MannKind’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 MannKind, 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. Position Overview The QA Validation Manager manages the validation activities supporting sterile drug product manufacturing and fill–finish operations. This role ensures that validation/qualification program/activities meet regulatory expectations and maintain a state of control across aseptic processing areas. The ideal candidate brings strong technical expertise in validation, proven project and people management skills, and deep understanding of sterile manufacturing and fill–finish processes. Adheres to quality and safety policies and procedures. Key Responsibilities Validation and People Management * Develop risk-based qualification/validation strategy to support the activities * Support generation, review and approval of validation deliverables such as plans, protocols and reports (supporting equipment, facility, utility, computerized systems and processes) * Supervise validation engineers/specialists (direct or contract) ensuring high technical competency and adherence to cGMP. Aseptic & Fill–Finish Support * Provide QA oversight for validation activities including process validation, cleaning validation, equipment qualification (IQ/OQ/PQ), utility qualification, and computer system validation. * Oversee validation activities related to aseptic processing, sterilization (e.g., autoclaves, dry heat ovens), and environmental monitoring systems. * Evaluate and support qualification of cleanrooms, HVAC systems, compressed gases, WFI, and clean steam. * Participate in aseptic process simulations (media fills) and ensure validation readiness. * Support validation of formulation processes, sterile filtration, container closure systems, and visual inspection technologies. * Assess validation impact for changes to equipment, components, formulations, or process parameters. * Identify opportunities to optimize fill–finish validation strategies while maintaining compliance and product quality. * Contribute to development and revision of SOPs, templates, and quality standards related to aseptic processing and fill–finish validation. Quality Systems and Compliance * Apply Quality Risk Management (ICH Q9) principles to validation strategies and decisions. * Support investigations related to validation deviations, equipment failures, or sterility assurance risks * Ensure validation activities align with FDA, EMA, ICH, Annex 1, and industry best practices for sterile and fill–finish operations. * Support regulatory inspections and internal audits, serving as the subject matter expert for validation. Required Qualifications/Skills * Bachelor’s or master’s degree in engineering, Life Sciences, or related field. * 8+ years of experience (6+ years for master’s degree) in validation/QA within a GMP sterile manufacturing or fill–finish environment. * 3+ years of experience in people management (direct or contract) * Strong understanding of aseptic processing, sterilization, contamination control, fill–finish and packaging operations. * Working knowledge of validation lifecycle principles, risk management, and data integrity requirements. * Familiarity with regulatory expectations including FDA, EMA, ICH Q7–Q10, and EU Annex 1. * Excellent communication, documentation, and cross functional collaboration skills. Preferred Qualifications * Experience with isolator‑based sterility testing and aseptic filling technologies. * Experience supporting regulatory inspections (FDA, EMA, MHRA). * Lean/Six Sigma or continuous improvement training.

Responsibilities

The QA Validation Manager oversees validation activities for sterile drug product manufacturing and fill-finish operations to ensure regulatory compliance. This role involves supervising validation engineers and developing risk-based strategies for equipment, facility, and process qualifications.