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Sr Validation Engineer Jobs in Oak Ridge, TN (NOW HIRING)

Tjoapack

Senior Validation Engineer

Clinton, TN · On-site

Sr. Validation Engineer ???? Clinton, TN | Full-time At least one year of experience in a Pharmaceutical GMP setting is required for consideration. About Alcami Alcami is a contract development and ...

New

Ametek

Senior Electrical Engineer

Oak Ridge, TN · On-site

$102K - $133K/yr

Conceptualize, design, simulate, implement and validate low noise electronics using mixed signal ... The Senior Electrical Engineer will have: * BS in Electrical Engineering or equivalent required. MS ...

Amentum

Senior Mechanical Engineer

Oak Ridge, TN · On-site

$99K - $131K/yr

Senior Mechanical Engineer Amentum is a global leader in advanced engineering and innovative ... Valid driver's license is required * Ability to obtain and maintain a security clearance * Ability ...

MBI - Malibu Boats, Inc

Senior Data Engineer

Loudon, TN

$93K - $127K/yr

The Senior Data Engineer designs, builds, and supports the data pipelines, integrations, and ... Apply medallion architecture principles, preserving source fidelity in Bronze, creating validated ...

Malibu Boats, LLC

Senior Data Engineer

Loudon, TN · On-site

$93K - $127K/yr

The Senior Data Engineer designs, builds, and supports the data pipelines, integrations, and ... Apply medallion architecture principles, preserving source fidelity in Bronze, creating validated ...

Vital Services

Senior Data Engineer

Oak Ridge, TN · On-site +1

$110K - $130K/yr

As a Senior Data Engineer, you will work closely with our customer's department leads and project ... Own the monitoring and validation of data flows to ensure complete accuracy, quality, and ...

Malibu Boats Inc.

Senior Data Engineer

Loudon, TN · On-site

$93K - $127K/yr

The Senior Data Engineer designs, builds, and supports the data pipelines, integrations, and ... Apply medallion architecture principles, preserving source fidelity in Bronze, creating validated ...

Pae

Senior Mechanical Engineer

Oak Ridge, TN · On-site +1

$99K - $131K/yr

Senior Mechanical Engineer Amentum is a global leader in advanced engineering and innovative ... Valid driver's license is required * Ability to obtain and maintain a security clearance * Ability ...

Tjoapack

Senior Project Engineer

Clinton, TN · On-site

$81K - $105K/yr

Senior Project Engineer ???? Clinton, TN | Full-time At least one year of Pharmaceutical GMP is ... Additionally, the Project Engineer supports equipment and facility validation efforts by ...

Ametek

Senior Electrical Engineer

Oak Ridge, TN · On-site

$102K - $133K/yr

Conceptualize, design, simulate, implement and validate low noise electronics using mixed signal ... The Senior Electrical Engineer will have: * BS in Electrical Engineering or equivalent required. MS ...

AMETEK, Inc.

Senior Electrical Engineer

Oak Ridge, TN · On-site

$125 - $140/hr

Conceptualize, design, simulate, implement and validate low noise electronics using mixed signal ... The Senior Electrical Engineer will have: * BS in Electrical Engineering or equivalent required. MS ...

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All JobsSr Validation Engineer JobsSr Validation Engineer Jobs in Oak Ridge, TN

Sr Validation Engineer information

See Oak Ridge, TN salary details

$33

$61

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How much do sr validation engineer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for sr validation engineer in Oak Ridge, TN is $61.93, according to ZipRecruiter salary data. Most workers in this role earn between $49.42 and $70.34 per hour, depending on experience, location, and employer.

What is a Sr validation engineer?

Sr Validation Engineers are experienced professionals responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They lead validation projects, develop protocols, oversee testing, and document results to confirm compliance with industry regulations, such as those from the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and manufacturing, where product quality and safety are critical. Senior validation engineers also mentor junior staff and help improve validation processes within their organizations.

What are the key skills and qualifications needed to thrive as a Sr validation engineer?

To thrive as a Sr Validation Engineer, you need a solid background in engineering or life sciences, extensive experience with validation protocols, and a strong understanding of regulatory standards such as FDA, GMP, or ISO. Expertise in using validation software, risk assessment tools, and familiarity with documentation management systems is typically required, along with certifications like Six Sigma or ASQ CQE being advantageous. Exceptional problem-solving abilities, attention to detail, and effective communication skills help you lead teams and interact with cross-functional departments. These competencies are crucial for ensuring products and processes meet compliance standards, maintain quality, and support organizational success.

What are some common challenges a Sr validation engineer faces when managing multiple validation projects simultaneously?

A Sr Validation Engineer often manages several validation projects at once, which can present challenges such as coordinating timelines, ensuring compliance with regulatory standards, and balancing cross-functional communication. Keeping detailed documentation and staying organized are essential, as unexpected equipment issues or shifting project priorities may arise. Successful engineers proactively communicate with quality, manufacturing, and R&D teams to mitigate risks, maintain project momentum, and deliver results within required deadlines.

What is the difference between Sr Validation Engineer vs Validation Engineer?

AspectSr Validation EngineerValidation Engineer
Required CredentialsBachelor's/Master's in Engineering, certifications like CQE or ASQ, experience in validation processesBachelor's in Engineering or related field, some certifications preferred, less experience required
Work EnvironmentPharmaceutical, biotech, or manufacturing industries; leading validation projectsSupporting validation tasks under supervision, often in similar industries
Employer & Industry UsageUsed by companies requiring compliance with FDA, ISO, or GMP standardsCommonly used in manufacturing and quality assurance roles

The main difference between a Sr Validation Engineer and a Validation Engineer lies in experience, responsibility, and expertise. The Sr Validation Engineer typically leads validation projects, has more advanced certifications, and plays a strategic role in compliance. Validation Engineers support validation activities and often work under supervision. Both roles are essential in regulated industries like pharmaceuticals and manufacturing, but the senior role involves greater leadership and technical oversight.

What are popular job titles related to Sr Validation Engineer jobs in Oak Ridge, TN?

For Sr Validation Engineer jobs in Oak Ridge, TN, the most frequently searched job titles are:

What job categories do people searching Sr Validation Engineer jobs in Oak Ridge, TN look for?

The top searched job categories for Sr Validation Engineer jobs in Oak Ridge, TN are:

What cities near Oak Ridge, TN are hiring for Sr Validation Engineer jobs?

Cities near Oak Ridge, TN with the most Sr Validation Engineer job openings:

Sr Validation Engineer jobs near you
Infographic showing various Sr Validation Engineer job openings in Oak Ridge, TN as of July 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $128,805 per year, or $61.9 per hour.

Senior Validation Engineer

Tjoapack

Clinton, TN • On-site

Full-time

Posted 2 days ago

New

Job description

Sr. Validation Engineer

???? Clinton, TN | Full-time

At least one year of experience in a Pharmaceutical GMP setting is required for consideration. 


About Alcami

Alcami is a contract development and manufacturing organization headquartered in North Carolina with over 40 years of experience advancing products through every stage of the development lifecycle. At Alcami, we are a team of dynamic, agile individuals committed to developing life-saving drugs around the world. A mindset of collaboration, innovation, responsiveness, accountability, and customer focus inspires us to be the most efficient, safe, and reliable choice for our customers and the patients they serve. In return, we offer challenging careers, professional growth, and the opportunity to be part of our skilled team with over 40 years of experience as champions that are dedicated, trustworthy, and relentless to advancing products through every stage of the development cycle.

 ????Summary of the Role:

This role is responsible for leading validation and qualification activities that support compliant pharmaceutical packaging operations, including packaging equipment, utilities, facilities, and computerized systems. The Sr. Validation Specialist develops and executes validation protocols, maintains validation documentation, manages change controls, and ensures systems remain inspection-ready and compliant with cGMP, data integrity, and 21 CFR Part 11 requirements. The position partners closely with engineering, quality, operations, IT, contractors, and equipment vendors to support the installation, qualification, and ongoing performance of packaging-related equipment and systems. Additionally, the role serves as a validation subject matter expert during audits, provides technical guidance, authors SOPs and validation plans, and helps drive continuous compliance across packaging and operational processes.


 ✅Your Expectations:

Validation & Qualification

  • Partner with Engineering, Operations, Quality, IT, vendors, and contractors on qualification and validation initiatives.
  • Support the planning, installation, startup, and validation of new or updated equipment and systems.
  • Serve as the primary validation resource for contractors and external service providers.
  • Analyze complex technical and compliance issues and recommend effective solutions.

Validation Program Management

  • Develop validation procedures, protocols, and project plans to support business and compliance objectives.
  • Maintain qualification and validation documentation, ensuring accuracy, completeness, and audit readiness.
  • Author and revise SOPs and Master Validation Plans (MVPs).
  • Manage ongoing validation lifecycle activities, including change controls and periodic system reviews.

Cross Functional Project Support

  • Partner with Engineering, Operations, Quality, IT, vendors, and contractors on qualification and validation initiatives.
  • Support the planning, installation, startup, and validation of new or updated equipment and systems.
  • Serve as the primary validation resource for contractors and external service providers.
  • Analyze complex technical and compliance issues and recommend effective solutions.

Compliance, Training, & Technical Leadership

  • Ensure validation activities are conducted in accordance with cGMP requirements and internal quality standards.
  • Exercise technical judgment to resolve validation and compliance-related challenges.
  • Act as a certified trainer and support validation-related training programs.
  • Provide subject matter expertise on validation practices, compliance requirements, and system qualification strategies.


????Requirements:

  • Bachelor's degree in Engineering, Chemistry, Biology, or related field is required. 
  • At least one year of experience in a Pharmaceutical cGMP Manufacturing setting is required. 
  • Minimum 10 years of experience in a regulated manufacturing environment, preferably pharmaceutical, biotech, medical device, or consumer healthcare packaging.
  • Experience qualifying and validating equipment, utilities, and computerized systems within a cGMP-regulated pharmaceutical, biotech, medical device, or packaging environment.
  • Proven ability to lead validation projects, support new equipment implementation, manage change controls, and maintain systems in a validated state throughout their lifecycle.
  • Strong analytical skills with the ability to work effectively across Engineering, Quality, Operations, IT, and external vendors to resolve complex technical and compliance challenges.
  • Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint) required; experience with project management and scheduling tools preferred.
  • Strong technical, analytical, and problem-solving skills with the ability to manage multiple priorities in a fast-paced environment.
  • Excellent communication, presentation, and stakeholder management skills with the ability to collaborate effectively across all levels of the organization.


????Selection Process:

Submit your Application à Complete a Phone Screening with Tjoapack’s Recruiter à Complete your Hiring Manager Interview à Complete an Onsite Interview à 15 Minute Site Leader Interview via Teams


All Offers are conditional pending successful completion of Tjoapack’s Pre-Employment Drug Screening, Physical Examination, and Background Check.