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Kindeva Drug Delivery is seeking a detail-oriented candidate for a pharmaceutical manufacturing role in Missouri. Responsibilities include strict adherence to batch records, SOPs, and cGMPs, qualifying inspection systems, inspecting units for defects, and maintaining accurate records.
The position emphasizes compliance, safety, and continuous improvement in a sterile manufacturing environment. Qualifications require a high school diploma or GED and at least 1 year of relevant experience,
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
California residents should review our Notice for California Employees and Applicants before applying.
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.