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Contract Validation Engineer Jobs in Massachusetts

Spryte Medical Inc

Quality Engineer (Contract)

Bedford, MA · On-site

$45 - $55/hr

The Quality Engineer participates in all phases of the product development process. This includes ... Support Process/Design Validation/Verification activities including process validation, IQ/OQ/PQ ...

National Grid

Lead Contract Manager

Waltham, MA · Hybrid

$142K - $166K/yr

... Engineering, Safety and Emergency Planning. * Ensure alignment of construction contracts with ... Valid driver's license with a safe driving history that meets National Grid's Safe Driver policy ...

National Grid

Lead Contract Manager

Waltham, MA · On-site

$142K - $166K/yr

... Engineering, Safety and Emergency Planning. * Ensure alignment of construction contracts with ... Valid driver's license with a safe driving history that meets National Grid's Safe Driver policy ...

FSTONE Technologies

Contract manager

Boston, MA · On-site

$96K - $129K/yr

Work closely with Product Owners, developers, QA, and technology teams to deliver business ... Analyze data and develop validation checks and reports to ensure accurate business processing.

New

campus4tech

Contract System Test Engineer

Newton, MA · On-site

We are currently looking for an ambitious Contract System Test Engineer to join our Endovascular ... validation phases • Determining sample size for tests based on statistical processes • ...

Zelis

Contract Analyst I

Boston, MA · On-site

$75K - $90K/yr

... programming and development teams in the creation and vetting of calculation methods, database ... Validate and test contract configurations for claims pricing accuracy. * Maintain feeschedulein ...

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All JobsContract Validation Engineer JobsContract Validation Engineer Jobs in Massachusetts

Contract Validation Engineer information

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How much do contract validation engineer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for contract validation engineer in Massachusetts is $56.79, according to ZipRecruiter salary data. Most workers in this role earn between $43.08 and $69.04 per hour, depending on experience, location, and employer.

What is a contract validation engineer?

A Contract Validation Engineer is responsible for ensuring that systems, processes, and products meet regulatory and contractual requirements. They typically work on a temporary or project basis, verifying compliance through testing, documentation, and analysis. Their role involves collaborating with engineering teams to validate designs, troubleshoot issues, and ensure quality standards are met. This position is common in industries like pharmaceuticals, aerospace, and manufacturing, where strict validation protocols are required.

What are the primary responsibilities of a contract validation engineer on a typical project?

A Contract Validation Engineer is primarily responsible for reviewing and verifying that project deliverables, processes, and products comply with contractual requirements and industry standards. This includes conducting thorough documentation reviews, performing technical validations, and collaborating with project managers, legal teams, and quality assurance professionals to resolve any discrepancies. You will also support audits, maintain compliance records, and participate in meetings to ensure all stakeholders remain informed and aligned. The role often involves both independent analysis and teamwork, providing an excellent environment for those who enjoy balancing technical expertise with cross-functional collaboration.

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

To thrive as a Contract Validation Engineer, you need strong analytical skills, a degree in engineering or a related field, and a deep understanding of contract requirements and industry regulations. Proficiency with validation software, quality management systems (QMS), and relevant certifications such as Six Sigma or ISO standards is often preferred. Outstanding attention to detail, effective communication, and the ability to work collaboratively across departments are crucial soft skills. These competencies ensure accurate contract assessments, regulatory compliance, and seamless integration of contractual obligations into engineering projects.

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

The most popular types of Validation Engineer jobs in Massachusetts are:

What are popular job titles related to Contract Validation Engineer jobs in Massachusetts?

For Contract Validation Engineer jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Contract Validation Engineer jobs in Massachusetts look for?

The top searched job categories for Contract Validation Engineer jobs in Massachusetts are:

What cities in Massachusetts are hiring for Contract Validation Engineer jobs?

Cities in Massachusetts with the most Contract Validation Engineer job openings:

Contract Validation Engineer jobs near you
Infographic showing various Contract Validation Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 87% Full Time, 8% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $118,116 per year, or $56.8 per hour.

EXPANSION Validation Specialist

Piramal Pharma Limited

Lexington, MA • On-site

Full-time

Re-posted 4 days ago

Job description

Be the First to Apply

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

EXPANSION Validation Specialist

Job Description

Business: Pharma Solutions
Department: Validation
Location: Lexington

Job Overview
Reporting to the Validation Supervisor, the Validation Specialist executes validation and qualification protocols of manufacturing, packaging, laboratory, utility systems and other equipment, in accordance with current Good Manufacturing Practices (cGMPs), Good Engineering Practices (GEP) and change control.


Reporting Structure
This position reports to theValidation Supervisor.


Key Responsibilities:

Write, schedule, plan, manage and execute validation and qualification protocols
Act as technical interface between the company and 3rd parties for discussions surrounding the on-site validation activities
Coordinate and interface with Operations, Technical Services, Facility Engineering, Microbiology, and Quality Assurance groups to ensure successful project execution
Lead qualification activities and timelines for equipment purchased for manufacturing purposes
Coordinate order timelines and equipment requirements with Technical Services group.
Represent validation at project team meetings and provide expert validation advice.
Independently design, plan and manage own studies.
Manage the development of the following documents for new equipment:
User requirement specification (URS)
Design qualification (DQ)
Commissioning (CX)
Risk assessment (RA)
Maintain and develop state of the art knowledge regarding existing and future validation processes and maintain up-to-date knowledge on regulatory expectations
Lead investigations related to validation discrepancies and ensure thoroughness of investigation, documentation and closure.
Implement preventive/corrective actions as necessary
Conduct periodic validation reviews of equipment, facilities, utilities, and sterilization cycles
Author assigned Standard Operating Procedures (SOPs) for Validation department


Qualifications:

Bachelor's Degree in the physical or biological sciences or engineering

2+ years of QA and/or Regulatory experience in a cGMP/FDA regulated environment
Sterile manufacturing of injectables strongly preferred

Thorough knowledge of cGMP (Current Good Manufacturing Practice) regulations, guidance, and general compliance expectations.
Technical writing skills
In-depth understanding of investigational techniques, including but not limited to root cause analysis, risk assessment, impact evaluation, and technical report writing
Working knowledge of cGMP data management systems (EDMS, Trackwise, and/or SAP)
Thorough understanding of Common Technical Document (primarily Chemistry and Manufacturing Controls (CMC) format, content, and filing requirements for US and EU.
High level of proficiency operating all Microsoft Office applications
Excellent communication skills, both verbally and in writing
Detail oriented and organized

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