Quality Assurance Jobs at Kindeva USA
Looking to advance your career in quality assurance jobs within the pharmaceutical industry? This Quality Assurance Supervisor position at Kindeva in Brentwood, Missouri offers a strong jobs opportunity for life science graduates and experienced professionals seeking leadership roles in aseptic manufacturing. Among competitive jobs in USA, this role stands out for candidates exploring growth-driven Kindeva careers focused on patient safety and regulatory excellence.
About Kindeva
Kindeva Drug Delivery is a global pharmaceutical company dedicated to developing and manufacturing products that save lives. Known for innovation, compliance excellence, and employee development, Kindeva offers some of the most respected quality assurance jobs in the industry. Through strong operational standards and people-first culture, Kindeva careers empower professionals to make a real impact on global health.
Job Details:
- Job Title: Supervisor, Quality Assurance
- Req #: 2396
- Location: Brentwood, MO, USA
- Job Type: Salary
- Shift: 2nd Shift (2:00 PM – 10:30 PM), Monday–Friday
- Posted: Thursday, January 29, 2026, at 10:30 AM
- Job Family: D – Quality – Quality Assurance
- Job Function: D – Quality
- Work Arrangement: Onsite Only
The Impact Quality Assurance Role Will Make
The QA Supervisor – Aseptic is primarily based in the Sterile Product Manufacturing (SPM) building and provides oversight to Quality Inspector colleagues. This role requires a strong working knowledge of aseptic processing principles, including aseptic behaviors, Good Documentation Practices (GDP), Good Manufacturing Practices (GMP), facility controls, and regulatory compliance requirements.
The incumbent facilitates timely resolution and escalation of manufacturing deviations and ensures effective communication with Production and Quality Assurance Management.
Key Responsibilities
- Demonstrates proficiency in internal manufacturing and quality assurance procedures, including regulatory and compliance requirements
- Reviews batch records for conformance to established procedures and critical process parameters
- Provides leadership and guidance to Quality Inspectors, ensuring adequate shift coverage through dynamic scheduling for APA and Grade D/CNC areas
- Ensures required training is completed for direct reports
- Generates daily written shift reports for Quality and Production Management with clear and concise documentation of relevant issues
- Solves problems independently and proposes solutions when escalating issues
- Successfully dons sterile gowning, completes gowning qualification requirements, and maintains qualification to support critical aseptic processing areas (APA)
- Participates in media fills as a Quality Observer when required
- Initiates incidents in QTS as applicable
- Trains on and performs line clearance and verification of critical areas
- Conducts daily on-line auditing in APA areas to ensure audit-ready conditions
- Supports manufacturing investigations through Root Cause Analysis and identification of Preventive Actions
- Assists in continuous improvement of Standard Operating Procedures (SOPs) and Master Batch Records
- Performs additional Quality Assurance functions as needed
- Attends and actively participates in daily shift huddles and Gemba meetings
Education For Quality Assurance Jobs
- Bachelor’s degree in Biology, Microbiology, or another science-related discipline
- In lieu of a bachelor’s degree, an associate degree with 2+ years of relevant experience will be considered
Experience
- Minimum of 3 years of pharmaceutical experience or an equivalent combination of education and experience
- Experience at an aseptic manufacturing site preferred
- At least 1 year of supervisory experience preferred
Additional Requirements
- Produces high-quality work with minimal guidance
- Demonstrates the ability to work effectively in team environments and across interdepartmental teams
Work Schedule, Travel, and Environment
- Regular onsite attendance is required; this position cannot be performed remotely or via telecommute (temporary or permanent)
- Must be able to multitask across multiple functions and manage competing priorities, including site responsibilities, frequent email and phone communications, and participation in meetings and conference calls
- Must work effectively under strict production, time, and performance deadlines
- Willingness and ability to work beyond standard hours, including potential weekends and holidays, as required.
