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Kindeva Drug Delivery is seeking personnel to support quality inspection and batch record integrity in a GMP environment. The role requires strict adherence to SOPs and cGMP standards to ensure product quality and safety.
Responsibilities include qualifying manual and automated inspection systems, visually inspecting units for defects, and maintaining accurate batch documentation while supporting housekeeping and process-improvement efforts.
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
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.