QA Technician

Posted Tuesday, February 3, 2026 at 5:00 AM

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The QA Technician supports manufacturing operations by performing quality checks and verifications on equipment, materials, and processes in aseptic and environments. Responsibilities include conducting readiness walk-throughs, line clearances, and in-process inspections to ensure compliance with established specifications, procedures, cGMPs, and regulatory requirements. The QA Technician works closely with production teams to identify and address issues, document findings, and assist with continuous improvement activities, investigations, and change implementations as needed.

• Reviews manufacturing related documentation to ensure processes adherance and compliance with approved SOP’s and cGMPs.
• Responsible for performing inspection readiness walk-throughs, line clearance and in-process checks in support of manufacturing activities
• Provides QA support for manufacturing and testing activities including: shop floor oversight, deviation and laboratory investigations, change management, SOP revisions and batch documentation review
• Proactively identify and address non-conformances in manufacturing operations
• Able to work in a team environment within own team and interdepartmental teams independently, with minimal guidance and under short timelines while maintaining quality work.
• Collects, reports and is responsible for departmental data.
• Alerts management promptly to any issues identified during batch production / record reviews that may adversely impact manufactured products, demonstrating accountability and a commitment to maintaining high-quality standards.
• Reviews SOPs, Forms, Logbooks, and Master Batch Records to ensure accuracy and compliance with established procedures.
• Participates in internal GMP audits and supports customer and regulatory audits.
• Assists in training Quality Assurance colleagues.
• Has the ability to understand and demonstrate aseptic techniques and behaviors required in aseptic processing areas.
• Performs ERP transactions, as applicable.
• Must be willing to work overtime and weekends as needed to support business initiatives.
• Other tasks assigned by management.

• HS/GED. Bachelors degree in a scientific field and industry experience is preferred.
• The individual must have strong attention to detail and organizational skills.
• The individual must be able to follow instructions and procedures
• Basic knowledge of cGMPs (USFDA, Health Canada, PIC/S and/or Eudralex).
• Demonstrated decision making ability with emphasis on overall quality, site priorities, results and achievements.
• Works well in a team environment within own team and interdepartmental teams.
• Must work under short timelines while maintaining quality work.
• Must have effective written and oral communication skills.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

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