Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... processes are qualified, maintained, and compliant with applicable regulatory and industry ...

60 Kindeva Process Validation Engineer Jobs Hiring Near You
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... processes are qualified, maintained, and compliant with applicable regulatory and industry ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... processes are qualified, maintained, and compliant with applicable regulatory and industry ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... processes are qualified, maintained, and compliant with applicable regulatory and industry ...
Sr. MS&T Process Engineer II
Maryland Heights, MO · On-site
$100K - $130K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... The Sr. MS&T Engineer II authors and executes validation strategies, analyzes complex manufacturing ...
Sr. MS&T Process Engineer II
Maryland Heights, MO · On-site
$100K - $130K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... The Sr. MS&T Engineer II authors and executes validation strategies, analyzes complex manufacturing ...
Sr. MS&T Process Engineer II
Maryland Heights, MO · On-site
$100K - $130K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... The Sr. MS&T Engineer II authors and executes validation strategies, analyzes complex manufacturing ...
Sr. MS&T Process Engineer II
Maryland Heights, MO · On-site
$100K - $130K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... The Sr. MS&T Engineer II authors and executes validation strategies, analyzes complex manufacturing ...
Process Engineer
Brentwood, MO · On-site
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality Assurance , Validation , Microbiology , Regulatory , Supply Chain ...
Process Engineer
Brentwood, MO · On-site
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality Assurance , Validation , Microbiology , Regulatory , Supply Chain ...
Process Engineer
Brentwood, MO · On-site
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality Assurance , Validation , Microbiology , Regulatory , Supply Chain ...
Process Engineer
Brentwood, MO · On-site
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality Assurance , Validation , Microbiology , Regulatory , Supply Chain ...
Process Engineer
Brentwood, MO · On-site
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality Assurance , Validation , Microbiology , Regulatory , Supply Chain ...
Process Engineer
Brentwood, MO · On-site
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality Assurance , Validation , Microbiology , Regulatory , Supply Chain ...
Process Engineer
Brentwood, MO · On-site
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality Assurance , Validation , Microbiology , Regulatory , Supply Chain ...
Process Engineer
Brentwood, MO · On-site
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality Assurance , Validation , Microbiology , Regulatory , Supply Chain ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ...
Manufacturing Engineer
Maryland Heights, MO · On-site
$70K - $90K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA ...
Manufacturing Engineer
Maryland Heights, MO · On-site
$70K - $90K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ...
Manufacturing Engineer
$70K - $90K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA ...
Manufacturing Engineer
$70K - $90K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA ...
Manufacturing Engineer
Maryland Heights, MO · On-site
$70K - $90K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA ...
Manufacturing Engineer
Maryland Heights, MO · On-site
$70K - $90K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ...
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ...
Manufacturing Engineer
Maryland Heights, MO · On-site
$70K - $90K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA ...
Manufacturing Engineer
Maryland Heights, MO · On-site
$70K - $90K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA ...
Senior Manufacturing Engineer
Bridgeton, MO · On-site
$86K - $118K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... up, process validation, troubleshooting, and ongoing performance monitoring. * Ensure robust ...
Senior Manufacturing Engineer
Bridgeton, MO · On-site
$86K - $118K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... up, process validation, troubleshooting, and ongoing performance monitoring. * Ensure robust ...
Senior Project Engineer
Bridgeton, MO · On-site
$94K - $122K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... The Senior Project Engineer partners closely with Operations, Quality, Validation, Engineering ...
Senior Project Engineer
Bridgeton, MO · On-site
$94K - $122K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... The Senior Project Engineer partners closely with Operations, Quality, Validation, Engineering ...
Senior Manufacturing Engineer
Bridgeton, MO · On-site
$86K - $118K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... up, process validation, troubleshooting, and ongoing performance monitoring. * Ensure robust ...
Senior Manufacturing Engineer
Bridgeton, MO · On-site
$86K - $118K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... up, process validation, troubleshooting, and ongoing performance monitoring. * Ensure robust ...
Senior Manufacturing Engineer
Maryland Heights, MO · On-site
$87K - $120K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Author, execute, and review validation protocols (IQ/OQ/PQ, process validation, and computer system ...
Senior Manufacturing Engineer
Maryland Heights, MO · On-site
$87K - $120K/yr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Author, execute, and review validation protocols (IQ/OQ/PQ, process validation, and computer system ...
Kindeva Jobs Information
Do workers at Kindeva get paid breaks?
88% of people say they get paid breaks.
Based on data from 8 people who took the Breakroom Quiz between December 2024 and March 2026.
Does Kindeva pay people when they’re sick?
88% of people say they would get paid if they were sick but scheduled to work.
Based on data from 8 people who took the Breakroom Quiz between December 2024 and March 2026.
Do workers at Kindeva worry about hours?
100% of people report they don’t worry about getting enough hours.
Based on data from 6 people who took the Breakroom Quiz between December 2024 and August 2025.
Do Kindeva workers get to choose the shifts they work?
50% report that they don’t have enough control over which shifts they work.
Based on data from 6 people who took the Breakroom Quiz between December 2024 and May 2025.
How easy is it to get time off at Kindeva?
89% of people report it’s easy to get time off.
Based on data from 9 people who took the Breakroom Quiz between December 2024 and March 2026.
Do Kindeva managers change schedules at the last minute?
86% of people say their manager doesn’t change their shift schedule at the last minute.
Based on data from 7 people who took the Breakroom Quiz between December 2024 and August 2025.
Do jobs at Kindeva spill into time workers aren’t paid for?
14% of people report that their job takes up time that they don’t get paid for.
Based on data from 7 people who took the Breakroom Quiz between December 2024 and August 2025.
How easy is it to take sick days at Kindeva?
100% of people report that it’s easy to take time off if they are sick.
Based on data from 7 people who took the Breakroom Quiz between December 2024 and December 2025.
Do people at Kindeva feel treated with respect by their managers?
71% of people say they’re treated with respect by their managers.
Based on data from 7 people who took the Breakroom Quiz between December 2024 and December 2025.
Do people at Kindeva get to take their breaks without interruption?
78% of people report that they get to take their breaks without interruption.
Based on data from 9 people who took the Breakroom Quiz between December 2024 and March 2026.
Is it stressful to work at Kindeva?
56% of people say they often feel stressed out at work.
Based on data from 9 people who took the Breakroom Quiz between December 2024 and March 2026.
Do people at Kindeva recommend working with their team?
78% of people report that they wouldn’t recommend working with their immediate team to a friend.
Based on data from 9 people who took the Breakroom Quiz between December 2024 and March 2026.
Do people get enough training when they start at Kindeva?
44% of people report they didn’t get enough training when they started working here.
Based on data from 9 people who took the Breakroom Quiz between December 2024 and March 2026.
Do people get support to advance at Kindeva?
In the last year, 63% of people report not being given support to advance their career here.
Based on data from 8 people who took the Breakroom Quiz between December 2024 and March 2026.
Do people think Kindeva’s headquarters understands what’s happening where they work?
89% of people think that this employer’s headquarters or owners don’t have a good understanding of what’s really happening where they work.
Based on data from 9 people who took the Breakroom Quiz between December 2024 and March 2026.
Do workers feel well informed about how Kindeva is doing?
63% of people feel that they aren’t kept well informed about how the company is doing as a whole.
Based on data from 8 people who took the Breakroom Quiz between December 2024 and March 2026.

Kindeva rating
6.7
Based on 9 frontline employees who took The Breakroom Quiz
Job description
Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
The successful candidate will support laboratory instrument qualifications, and continuous compliance initiatives within a cGMP-regulated laboratory environment. This role is responsible for ensuring laboratory instruments; computerized systems, and supporting processes are qualified, maintained, and compliant with applicable regulatory and industry standards. The position works closely with Quality, Metrology, and IT as well as write and execute qualification protocols of various types under the direction of Laboratory Validation Manger.
Role Responsibilities
- Execute and support qualification activities for laboratory instruments, and computerized systems, including IQ, OQ, requalification, and periodic review activities; ensuring laboratory equipment and systems remain compliant with GMP requirements, FDA regulations, Data Integrity expectations, and internal quality systems.
- Develop and manage qualification lifecycle documentation and activities including qualification plans, protocols, reports, change controls, and deviations.
- Author and review User Requirement Specifications (URS) for laboratory instruments and systems to ensure operational, regulatory, data integrity, and business requirements are clearly defined and traceable throughout the qualification lifecycle.
- Collaborate with cross-functional teams such as Quality Assurance, Laboratories, Metrology, Engineering, IT, and external vendors to ensure successful qualification execution.
- Evaluate and apply risk-based qualification approaches aligned with current industry guidance and standards.
- Write periodic reviews and support continuous monitoring of qualified systems and laboratory equipment.
- Ensure compliance with ALCOA/ALCOA+ data integrity principles and electronic records requirements.
- Assist in development and improvement of qualification strategies, procedures, and best practices.
Qualifications
- Bachelor's degree in biology, Chemistry, Engineering, Pharmaceutical Sciences, or
- 5+ years of laboratory testing experience in a GMP-regulated environment with a sound working knowledge of the operation of various laboratory instruments and equipment.
- 3+ years of experience qualifying laboratory equipment and systems.
- Knowledge of analytical instrument qualification (AIQ) practices.
- Strong technical writing, communication, and organizational skills.
- Sound knowledge of GMP regulations, internal SOPs, FDA regulations applicable to laboratory operations, 21 CFR Part 11 requirements, Data Integrity principles, change control, and deviation management.
- Familiarity with audit trail review processes and electronic data management systems preferred.
- Experience authoring User Requirement Specifications (URS) and qualification documentation for laboratory instruments and computerized systems preferred.
- Strong knowledge of laboratory instrumentation and qualification lifecycle methodologies preferred.