GMP QA Technician - Aseptic & Line Compliance

Kindeva; Missouri; On-site; USD 28,000 - 48,000; Full time

Job summary

Kindeva Drug Delivery is seeking a QA Technician to oversee quality across aseptic manufacturing environments, ensuring adherence to specifications and cGMPs. The role includes readiness walkthroughs, line clearance, in-process checks and documentation reviews to support manufacturing and regulatory readiness.

The position emphasizes detail orientation, strong communication, and the ability to work with cross-functional teams to drive continuous improvement and accurate investigations.

Qualifications

• HS/GED; Bachelor's degree in a scientific field preferred.
• Strong attention to detail and organizational skills.
• Ability to follow instructions and procedures.
• Basic knowledge of cGMPs (USFDA, Health Canada, PIC/S and/or Eudralex).
• Demonstrated decision making ability with emphasis on quality and timelines.
• Effective written and oral communication skills.

Responsibilities

• Reviews manufacturing related documentation to ensure processes adhereance and compliance with SOPs and cGMPs.
• Performs inspection readiness walk-throughs, line clearance and in-process checks in support of manufacturing activities.
• Provides QA support for manufacturing and testing including: shop floor oversight, deviation investigations, change management and batch documentation review.
• Proactively identify and address non-conformances in manufacturing operations.
• Collaborate with cross-functional teams to support continuous improvement activities and regulatory audits.

Skills

Attention to detail

Organizational skills

Written and verbal communication

Team player

Problem solving

Education

HS/GED; Bachelor's degree in a scientific field preferred

Job description

Kindeva Drug Delivery is seeking a QA Technician to oversee quality across aseptic manufacturing environments, ensuring adherence to specifications and cGMPs. The role includes readiness walkthroughs, line clearance, in-process checks and documentation reviews to support manufacturing and regulatory readiness.

The position emphasizes detail orientation, strong communication, and the ability to work with cross-functional teams to drive continuous improvement and accurate investigations.