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Director Validation Jobs in Missouri (NOW HIRING)

Park Lawn Corporation

Funeral Director

Kansas City, MO · On-site

Valid and applicable state Funeral Director License; reciprocal across states and in good standing. * Valid state issued driver's license in good standing and acceptable driving record. Additional ...

Park Lawn Corporation

Funeral Director

Raytown, MO

Valid and applicable state Funeral Director License; reciprocal across states and in good standing. * Valid state issued driver's license in good standing and acceptable driving record. Additional ...

Park Lawn Corporation

Funeral Director

Kansas City, MO · On-site

Valid and applicable state Funeral Director License; reciprocal across states and in good standing. * Valid state issued driver's license in good standing and acceptable driving record. Additional ...

Park Lawn Corporation

Funeral Director

Raytown, MO · On-site

Valid and applicable state Funeral Director License; reciprocal across states and in good standing. * Valid state issued driver's license in good standing and acceptable driving record. Additional ...

Saint Agnes Home

Activity Director

Kirkwood, MO · On-site

$18 - $24.75/hr

As our Activities Director, you will develop, coordinate, and oversee engaging programs designed to ... Must have valid driver's license, personal automobile liability insurance, and acceptable driving ...

Saint Agnes Home

Activity Director

Kirkwood, MO · On-site

$17.75 - $24.25/hr

As our Activities Director, you will develop, coordinate, and oversee engaging programs designed to ... Must have valid driver's license, personal automobile liability insurance, and acceptable driving ...

Saint Agnes Home

Activity Director

Kirkwood, MO · On-site

$17.75 - $24.25/hr

As our Activities Director, you will develop, coordinate, and oversee engaging programs designed to ... Must have valid driver's license, personal automobile liability insurance, and acceptable driving ...

Saint Agnes Home

Activity Director

Kirkwood, MO · On-site

$18 - $24.75/hr

As our Activities Director, you will develop, coordinate, and oversee engaging programs designed to ... Must have valid driver's license, personal automobile liability insurance, and acceptable driving ...

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Director Validation information

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$24.8K

$117.7K

$173.3K

How much do director validation jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director validation in Missouri is $117,709.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,460.00 and $162,418.00 per year, depending on experience, location, and employer.

What does a director validation do?

A Director of Validation oversees the validation processes in industries like pharmaceuticals, biotechnology, or medical devices to ensure compliance with regulatory standards. They develop and implement validation strategies for equipment, processes, and systems, ensuring they meet quality and safety requirements. This role involves managing validation teams, coordinating with regulatory bodies, and maintaining documentation to support audits and inspections. The Director also ensures adherence to industry guidelines such as FDA, EMA, or ISO standards.

What are the typical daily responsibilities of a director validation in a regulated industry?

A Director Validation typically oversees the planning, execution, and review of validation projects to ensure compliance with regulatory requirements. Daily responsibilities include leading teams, reviewing validation protocols and reports, coordinating with quality, engineering, and regulatory departments, and addressing any deviations or issues that arise during validation activities. The role may also involve direct communication with regulatory agencies during audits and inspections. This ensures products or processes meet the highest standards of quality and regulatory compliance, ultimately supporting the company’s overall operational success.

What are the key skills and qualifications needed to thrive in the director validation position, and why are they important?

To thrive as a Director Validation, you need extensive experience in validation processes, regulatory compliance, quality assurance, and a relevant scientific or engineering degree. Familiarity with industry standards, validation lifecycle management software, and certifications such as Six Sigma or PMP are highly valued. Strong leadership, strategic thinking, and excellent communication skills help to drive complex projects and foster cross-functional collaboration. These skills are vital to ensuring validated processes meet regulatory standards and support organizational goals efficiently.

What are the most commonly searched types of Validation jobs in Missouri?

The most popular types of Validation jobs in Missouri are:

What are popular job titles related to Director Validation jobs in Missouri?

For Director Validation jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Director Validation jobs in Missouri look for?

The top searched job categories for Director Validation jobs in Missouri are:

What cities in Missouri are hiring for Director Validation jobs?

Cities in Missouri with the most Director Validation job openings:

Director Validation jobs near you

Product Process Validation Manager

kindeva

Bridgeton, MO

Full-time

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.

The Impact You Will Make

The is an exciting opportunity as Product Process Validation Manager is a key member of the Manufacturing Science & Technology (MS&T) organization, responsible for leading process validation strategy and execution across the product lifecycle. This role oversees the design, authorship, and facilitation of technology transfer activities, Process Performance Qualification (PPQ) protocols and reports, and supporting ongoing Continued Process Verification (CPV). The manager partners closely with Process Development, Quality, Manufacturing, and Regulatory Affairs to ensure robust, compliant, and efficient validation programs. This position reports directly to the Director of MS&T.

Role Responsibilities

Process Validation & PPQ

  • Lead the development, authorship, and execution of process validation strategies in alignment with regulatory expectations (e.g., FDA, EMA, ICH Q8–Q11).
  • Write, review, and approve PPQ protocols, sampling plans, risk assessments, and final reports.
  • Facilitate cross-functional PPQ readiness, including coordinating activities with Manufacturing, Quality Control, and Quality Assurance.
  • Ensure validation deliverables meet internal standards and external regulatory requirements.

Technology Transfer

  • Serve as the MS&T lead for technology transfer of new products, processes, or scale-up activities into manufacturing.
  • Develop and maintain tech transfer plans, process descriptions, and knowledge transfer documentation.
  • Drive process fit-gap assessments, risk analyses, and mitigation strategies.
  • Support equipment and facility readiness, including URS development and process capability assessments.

Continued Process Verification (CPV)

  • Partner with data analytics and quality teams to monitor process performance, identify trends, and drive data-based decision-making.
  • Lead investigations and corrective actions related to process performance deviations or CPV signals.

Cross-Functional Leadership

  • Collaborate with Process Development to translate laboratory-scale processes into robust, scalable manufacturing processes.
  • Support Regulatory Affairs with process validation content for submissions, responses to regulatory queries, and inspections.
  • Provide technical leadership during audits and regulatory inspections.
  • Mentor and guide junior MS&T staff in validation and tech transfer best practices.

Documentation & Compliance

  • Ensure all validation and tech transfer documentation is accurate, complete, and audit-ready.
  • Maintain strong alignment with internal quality systems, change control, and document management processes.
  • Champion continuous improvement initiatives to enhance validation efficiency and process robustness.

Basic Qualifications

  • Bachelor’s or Master’s degree in Engineering, Life Sciences, Biotechnology, or related field.
  • 7+ years of experience in biopharmaceutical or pharmaceutical manufacturing, MS&T, process validation, or related technical functions.
  • Demonstrated expertise in PPQ, CPV, and technology transfer.
  • Strong understanding of cGMP regulations and global validation guidelines.
  • Excellent technical writing, communication, and project management skills.

Preferred

  • Experience with biologics, cell therapy, gene therapy, or aseptic manufacturing.
  • Familiarity with statistical tools (e.g., JMP, Minitab) for process analysis.
  • Prior leadership or team management experience.
  • Experience supporting regulatory inspections.

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