Quality Assurance Technician – Aseptic GMP Oversight

Kindeva; Brentwood (MO); On-site; USD 55,000 - 75,000; Full time

Job summary

Kindeva is seeking a QA Technician to provide quality oversight of Operations in aseptic and controlled environments, ensuring conformance to specifications, procedures, and cGMPs. You will conduct readiness walk-throughs, line clearance, and in-process verifications, collaborating with cross-functional teams to support manufacturing activities and continuous improvement.

You will review documentation, support audits, train QA colleagues, and address non-conformances while maintaining high

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 with emphasis on quality and priorities.
• Works well in a team and meets tight deadlines.
• Effective written and oral communication skills.

Responsibilities

• Review manufacturing documents to ensure adherence to SOPs and cGMPs.
• Perform inspection readiness walk-throughs, line clearance, and in-process checks.
• Provide QA support for manufacturing and testing activities including investigations and change management.
• Identify and address non-conformances in operations.
• Collaborate with cross-functional teams to support continuous improvement.
• Assist in training QA colleagues and participate in internal GMP audits.

Skills

Attention to detail

Organizational skills

Written and verbal communication

Team collaboration

Decision making

Education

HS/GED

Bachelor's degree in a scientific field

Job description

Kindeva is seeking a QA Technician to provide quality oversight of Operations in aseptic and controlled environments, ensuring conformance to specifications, procedures, and cGMPs. You will conduct readiness walk-throughs, line clearance, and in-process verifications, collaborating with cross-functional teams to support manufacturing activities and continuous improvement.

You will review documentation, support audits, train QA colleagues, and address non-conformances while maintaining high