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From Home Validation Engineer Ii Jobs (NOW HIRING)

The Impact You Will Make The Floater Validation Engineer II provides validation engineering support across two pharmaceutical aseptic manufacturing facilities and one inspection and packaging site.

Validation Engineer II

Carlsbad, CA · On-site

$30 - $33/hr

Validation Engineer II Location: 2251 Faraday Ave, Carlsbad, CA 92008 Duration: 10 Months Work Arrangement: 100% Onsite Position Summary We are seeking a Validation Engineer II to support validation ...

KPI Solutions is seeking a Validation Engineer II to join our growing team as a primary execution ... Lead software integration and validation of automation systems from planning through go-live

$70K - $105K/yr

Software Validation Engineer 2 Life Unlimited. At Smith+Nephew we design and manufacture technology ... Adhere to applicable regulatory requirements from multiple countries * Support and drive non ...

Position Summary Validation Engineer II will be responsible for leading the commissioning, qualification, and validation (CQV) for a newly announced facility expansion for biologics that includes a ...

We look forward to hearing from you. Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex ...

We look forward to hearing from you. Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex ...

We look forward to hearing from you. Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex ...

PR · On-site

We look forward to hearing from you. Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex ...

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From Home Validation Engineer Ii information

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How much do from home validation engineer ii jobs pay per hour?

As of Jun 17, 2026, the average hourly pay for from home validation engineer ii in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Validation Engineer Ii jobs? The most popular types of Validation Engineer Ii jobs are:

Validation Engineer II

kindeva

Saint Louis, MO • On-site

Other

This job post has expired today. Applications are no longer accepted.


Kindeva rating

6.8

Company rating: 6.8 out of 10

Based on 6 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 Floater Validation Engineer II provides validation engineering support across two pharmaceutical aseptic manufacturing facilities and one inspection and packaging site. This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers flexible, cross-site validation coverage while executing protocols, performing testing, and authoring validation documentation under the direction of the Validation Manager.

Responsibilities

• Provide validation support across multiple sites based on business priorities.

• Assist in equipment qualification (IQ/OQ/PQ), cleaning validation, process validation, and CSV.

• Execute and author validation protocols and reports.

• Support aseptic manufacturing and inspection/packaging validation activities.

• Issue validation data, protocols, reports, and technical memos.

• Support site change management programs and maintain validated states.

• Assist with Validation Master Plans and Continuous Process Verification activities.

• Review vendor turnover packages and User Requirement Specifications.

Qualifications

  • Bachelor’s degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related discipline
  • 5+ years of relevant validation or pharmaceutical manufacturing experience, or equivalent combination of education and experience.
  • Knowledge of cGMP and regulatory guidance.
  • Experience in aseptic manufacturing and inspection/packaging operations.
  • Ability to interpret technical documentation and identify deviations.

• Proficiency with Microsoft Office applications.

  • Regular travel between sites required; ability to adapt to multiple GMP environments.

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