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Validation Engineer I Jobs in Massachusetts (NOW HIRING)

Emvia, Inc.

Automation Validation Lead

Andover, MA · On-site +1

Finalize the Automation Validation Plan Work with a team of Engineers and System Integration (SI ... Allen Bradley PLCs and I/O o The ideal candidate would have experience with the following software:

Ralliant

Manufacturing Engineer I

Boxborough, MA · On-site

$74 - $137/hr

The Manufacturing Engineer I will support the development, documentation, and implementation of ... Perform engineering pilot runs for part and process validation. * Provide manufacturing engineering ...

Dynavac

Controls Engineer I

Hingham, MA · On-site

$76K - $95K/yr

Controls Engineer I Join Dynavac --a leader in high‑vacuum process equipment--and help us support ... Perform system integration tasks including I/O checkout, system validation, and performance testing ...

Ralliant

Manufacturing Engineer I

Boxborough, MA · On-site

$70K - $91K/yr

The Manufacturing Engineer I will support the development, documentation, and implementation of ... Perform engineering pilot runs for part and process validation. * * Provide manufacturing ...

Axcelis

Mechanical Engineer III

Beverly, MA

$106K - $159K/yr

Mechanical Engineer III Axcelis is seeking a Mechanical Engineer I to support the design and ... Support the design, development, and validation of mechanical components and subsystems * Apply ...

Abbott

System Engineer I

Burlington, MA · On-site

Job Title Systems Engineer I Working at Abbott At Abbott, you can do work that matters, grow, and ... and validation. What You'll Work On * Analyzes input requirements for medical devices and ...

Abbott

System Engineer I

Burlington, MA · On-site

Job Title Systems Engineer I Working at Abbott At Abbott, you can do work that matters, grow, and ... and validation. What You'll Work On * Analyzes input requirements for medical devices and ...

Genezen

Automation Engineer I/II/III

Lexington, MA · On-site

... validation, and performance monitoring.Essential Compensation: The compensation range for this ... Automation Engineer I - $70,000-$90,000 Automation Engineer II - $90,000-$110,000 Automation ...

DPS Group

CQV Engineer

Framingham, MA · On-site

Equipment validation protocol development, including drafting documents, managing review cycles and ... Supporting engineer will be resident at the Client facility or a previously agreed upon location (i ...

BCforward

Mechanical Engineer I

Westborough, MA · On-site

$28.37/hr

Mechanical Engineer I Westborough, MA, USA, 01581 02/27/2017 to 02/25/2018 $28.37/hr on w2 Role ... Write design verification/validation plan, perform testing and write verification/validation report ...

restor3d

Manufacturing Engineer I

Wilmington, MA · On-site

$80K - $85K/yr

Description Job Summary: The Manufacturing Engineer I will be responsible for the selection ... process validation plans and reports, using sound, data/stats supported results. - Play a major ...

restor3d

Manufacturing Engineer I

Wilmington, MA · On-site

$80K - $85K/yr

Job Summary: The Manufacturing Engineer I will be responsible for the selection, development ... process validation plans and reports, using sound, data/stats supported results. - Play a major ...

Axcelis

Manufacturing Test Engineer I

Beverly, MA

Second Shift Manufacturing Test Development Engineer I Location: Beverly, MA (Onsite) Schedule ... About the Role In this role, you will design, implement, validate, and maintain electrical and ...

CitraLabs, LLC

Manufacturing Engineer I

Braintree, MA · On-site

$74K - $95K/yr

What You Can Expect The manufacturing engineer I is an entry-level position, responsible for ... process validation, tool design, and trouble shooting. How You'll Create Impact * Assist in ...

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All JobsValidation Engineer I JobsValidation Engineer I Jobs in Massachusetts

Validation Engineer I information

See Massachusetts salary details

$24

$56

$85

How much do validation engineer i jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for validation engineer i 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 Validation Engineer I?

A Validation Engineer I is an entry-level professional responsible for ensuring that systems, equipment, or processes meet regulatory standards and function as intended. They typically work in industries like pharmaceuticals, biotechnology, medical devices, or manufacturing, performing tasks such as creating validation protocols, executing tests, and documenting results. Their work helps maintain product quality and compliance with industry regulations. Validation Engineer I roles often involve collaboration with quality assurance and production teams. This position is ideal for those with a background in engineering or science seeking to start a career in quality and compliance.

What are some common challenges faced by a Validation Engineer I during project execution?

As a Validation Engineer I, one common challenge is managing tight project timelines while ensuring all validation protocols and documentation meet regulatory standards. New engineers often need to quickly familiarize themselves with complex equipment, processes, and compliance requirements specific to the industry, such as FDA or ISO guidelines. Collaboration with cross-functional teams, such as manufacturing, quality assurance, and R&D, is essential to troubleshoot issues and ensure smooth validation processes. Developing effective communication skills and attention to detail will help you overcome these challenges and contribute positively to project success.

What are the key skills and qualifications needed to thrive as a Validation Engineer I, and why are they important?

To succeed as a Validation Engineer I, you typically need a bachelor's degree in engineering or a related field and a solid understanding of validation protocols and industry regulations. Familiarity with technical tools such as validation management software, data analysis programs, and documentation systems is common, as well as knowledge of GMP standards. Attention to detail, problem-solving abilities, and strong teamwork and communication skills help set top performers apart. These competencies are vital to ensure that processes and equipment meet regulatory requirements and function reliably within quality-driven industries.

What is the difference between Validation Engineer I vs Validation Engineer II?

AspectValidation Engineer IValidation Engineer II
Required CredentialsBachelor's in Engineering, Life Sciences, or related field; often entry-level certificationsSame as Validation Engineer I, with additional experience or certifications
Work EnvironmentManufacturing, pharmaceutical, or biotech facilities; supervised tasksMore independent responsibilities; oversight of validation processes
Employer & Industry UsageCommonly employed in regulated industries like pharma and biotechProgression role within the same industries
Search & Comparison IntentEntry-level validation roles; understanding career progressionMid-level validation roles; seeking advancement opportunities

The main difference between Validation Engineer I and Validation Engineer II lies in experience and responsibility. Validation Engineer II typically has more hands-on experience, handles more complex validation tasks, and may oversee Validation Engineer I activities. Both roles require similar educational backgrounds and certifications, but Validation Engineer II often involves greater independence and technical expertise.

Are validation engineers in demand?

Validation engineers are in demand across industries such as pharmaceuticals, biotechnology, and manufacturing, where regulatory compliance and quality assurance are critical. They often require knowledge of validation protocols, industry standards, and tools like GxP and risk management, making their skills valuable in regulated environments.

Do validation engineers make good money?

Validation engineers typically earn competitive salaries that vary by industry, experience, and location. Entry-level validation engineers can expect to start around $60,000 to $80,000 annually, with experienced professionals earning over $100,000, especially in regulated sectors like pharmaceuticals or biotech. Skills in validation protocols, regulatory compliance, and tools like GxP are valuable for higher compensation.

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

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

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

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

Validation Engineer I jobs near you
Infographic showing various Validation Engineer I job openings in Massachusetts as of August 2026, with employment types broken down into 87% Full Time, 7% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $118,116 per year, or $56.8 per hour.

Validation Engineer

Springfield, MA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 5 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Validation Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Validation Engineer
Location: Massachusetts
Duration: Long Term

Position Overview

We are seeking an experienced Validation Engineer to support qualification and validation activities within a pharmaceutical manufacturing environment. This role will focus on equipment qualification, process validation, cleaning validation, computerized system validation, documentation review, and compliance with FDA and cGMP requirements. The ideal candidate will work closely with Manufacturing, Engineering, Quality Assurance, and Regulatory teams to ensure validated systems remain compliant and inspection-ready.

Key Responsibilities

• Develop, execute, and review validation protocols and reports, including IQ, OQ, PQ, and requalification activities.
• Support equipment, utility, facility, process, and cleaning validation programs.
• Prepare and maintain validation documentation in accordance with cGMP and regulatory requirements.
• Coordinate validation activities with Manufacturing, Engineering, Quality Assurance, and project teams.
• Perform risk assessments and gap analyses to identify validation and compliance requirements.
• Investigate validation deviations, implement corrective actions, and support CAPA activities.
• Ensure validation lifecycle activities comply with FDA regulations, 21 CFR Part 210/211, and industry standards.
• Support commissioning and qualification activities for new equipment, facilities, and manufacturing processes.
• Participate in audits, inspections, and validation-related regulatory submissions.
• Contribute to continuous improvement initiatives to enhance validation processes and compliance.

Required Qualifications

• Bachelor's Degree in Engineering, Pharmaceutical Sciences, Biotechnology, Chemistry, Life Sciences, or a related technical discipline.
• 3–7+ years of Validation Engineering experience within pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
• Strong experience with equipment qualification (IQ/OQ/PQ), process validation, and validation lifecycle management.
• Knowledge of cGMP regulations, FDA requirements, data integrity principles, and validation industry standards.
• Experience supporting cleaning validation, computerized system validation (CSV), or utility validation is preferred.
• Familiarity with risk assessments, deviation investigations, CAPA, and change control processes.
• Strong technical writing, documentation, analytical, and problem-solving skills.
• Ability to manage multiple validation projects and work effectively in a cross-functional environment.
• Experience supporting regulatory inspections and audit readiness activities is highly preferred.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/