Kindeva Drug Delivery · 9 hours ago
QA Technician
St. Louis County, MO
Full-time
Onsite
New Grad, Entry LevelKindeva Drug Delivery is committed to making products that save lives and improve health for patients worldwide. The QA Technician will support manufacturing operations by performing quality checks and verifications in controlled environments, ensuring compliance with established specifications and regulatory requirements.
Manufacturing
Responsibilities
Reviews manufacturing related documentation to ensure processes adhereance 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
Qualification
Required
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
Preferred
Bachelors degree in a scientific field and industry experience
Company
Kindeva Drug Delivery
Kindeva Drug Delivery is a global contract development and manufacturing organization (CDMO) in the pharmaceutical industry.
Founded in 2020
1001-5000 employees
H1B Sponsorship
Kindeva Drug Delivery has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (2)
2024 (4)
2023 (1)
2022 (3)
Funding
Current Stage
Late StageTotal Funding
$46.96MKey Investors
Global Britain Investment Fund
2023-08-03Grant· $41.96M
2022-11-14Acquired
2022-06-13Series Unknown· $5M
Leadership Team
Brian Schubmehl
Chief Human Resources Officer
Recent News
2026-01-16
Bizjournals.com Feed (2025-11-12 15:43:17)
2026-01-16
MarketScreener
2026-01-01
Company data provided by crunchbase