Kindeva
Kindeva

20 Kindeva Senior Validation Engineer Jobs Hiring Near You

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. As a Validation Engineer, you will play a critical role in ensuring ...

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. As a Validation Engineer, you will play a critical role in ensuring ...

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. As a Validation Engineer, you will play a critical role in ensuring ...

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. As a Validation Engineer, you will play a critical role in ensuring ...

Our Work Matters At Kindeva, we make products that save lives, ensuring better health and well ... The Impact You Will Make As a Senior Validation Manager, you will provide strategic and technical ...

Our Work Matters At Kindeva, we make products that save lives, ensuring better health and well ... The Impact You Will Make As a Senior Validation Manager, you will provide strategic and technical ...

Our Work Matters At Kindeva, we make products that save lives, ensuring better health and well ... The Impact You Will Make As a Senior Validation Manager, you will provide strategic and technical ...

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Bachelor's degree in biology, Chemistry, Engineering, Pharmaceutical Sciences, or * 5+ years of ...

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being ... Bachelor's degree in biology, Chemistry, Engineering, Pharmaceutical Sciences, or * 5+ years of ...

Senior Project Engineer

Bridgeton, MO

$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

$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 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 ...

Kindeva Jobs Information

Do workers at Kindeva get paid breaks?

Yes. Most people 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?

Yes. Most people get paid 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?

Most people don’t worry about getting enough 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?

Some people don’t get to choose which 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?

Most people find it easy to get time off.
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?

Most managers don’t change people’s 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?

Rarely. The job doesn't usually spill into unpaid time.
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?

Most people find it easy to take sick days.
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?

Most people 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?

Most people get 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?

Some people feel stressed out here.
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?

Not many people 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?

Some people didn’t get enough training when they started.
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?

Only some people are given support to advance their career here.
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?

Most people think headquarters doesn’t understand 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?

Only some people feel well informed about how the company 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.

Sr. Validation Engineer

kindeva

Lexington, KY • On-site

Other

Re-posted 21 days ago


Kindeva rating

6.7

Company rating: 6.7 out of 10

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.

As a Validation Engineer, you will play a critical role in ensuring our pharmaceutical manufacturing systems and processes meet rigorous regulatory and quality standards. You will lead and execute validation activities—including equipment, utilities, facilities, and process validations—to ensure our operations remain compliant and inspection-ready. Your expertise in cGMP, risk-based validation, and technical writing will directly impact the safety, efficacy, and consistency of the drug products we deliver. This is a highly visible, hands-on role ideal for a detail-oriented professional passionate about quality and continuous improvement in a dynamic, fast-paced environment

Responsibilities:

Validation Strategy & Execution

  • Develop, execute, and maintain validation protocols and reports (IQ, OQ, PQ) for equipment, utilities, and manufacturing processes.
  • Support commissioning and qualification (C&Q) activities for new equipment and facilities, ensuring compliance with FDA, EU, and global regulatory expectations.
  • Author and review validation lifecycle documentation, including plans, protocols, deviations, and final reports.
  • Partner with Engineering, Manufacturing, Quality, and Regulatory Affairs to ensure effective cross-functional validation planning and execution.
  • Perform periodic reviews and revalidation activities in accordance with lifecycle requirements.

Compliance & Risk Management

  • Lead risk assessments (FMEA, gap assessments) to determine validation strategy and appropriate testing requirements.
  • Provide validation input during change control, deviation investigations, and CAPA execution.
  • Ensure data integrity and good documentation practices in all validation records.
  • Act as subject matter expert (SME) during internal and external audits and inspections.

Continuous Improvement

  • Evaluate validation program effectiveness and recommend process improvements to enhance compliance, efficiency, and scalability.
  • Stay current with industry best practices and evolving regulatory guidance to ensure validation activities remain aligned with expectations.

Qualifications:

  • Bachelor’s degree in engineering, life sciences, or a related technical field.
  • 5 or more years of validation experience; or 3 years with a Master’s degree 
    in a regulated pharmaceutical, biotech, or medical device environment.
  • Demonstrated knowledge of FDA, EU, and ICH regulatory requirements including 21 CFR Part 11 and Annex 15.
  • Experience in developing and executing validation documentation (IQ/OQ/PQ, protocols, reports).
  • Strong organizational, communication, and technical writing skills.
  • Ability to collaborate cross-functionally and manage multiple priorities in a deadline-driven environment.

Preferred Qualifications:

  • Familiarity with validation of automated systems and computerized system validation (CSV).
  • Experience with nasal or respiratory drug delivery systems, aseptic manufacturing, or cleanroom validation.
  • Working knowledge of validation tools and systems (e.g., TrackWise, ValGenesis, Veeva).
  • Lean Six Sigma or other continuous improvement training/certifications.

#LI-Onsite


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