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Full Time Validation Engineer Jobs in Massachusetts

Validate functionality, reliability, performance, and stability across integrated robotic systems ... Equity and benefits are included for all full-time employees. If you believe you can contribute to ...

Jr QA Tester

Cambridge, MA · On-site

$55K - $58K/yr

... IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA ... ITE provides all its full-time employees with medical insurance. Health Insurance coverage (PPO ...

Jr QA Tester

Cambridge, MA · On-site

$55K - $58K/yr

... IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA ... ITE provides all its full-time employees with medical insurance. Health Insurance coverage (PPO ...

About This Role Textron Systems is seeking a full-time Principal level Mechanical Engineer to join ... Validate engineering requirements and designs by employing analytical models, simulations, test ...

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Full Time Validation Engineer information

What is a full time validation engineer?

Full Time Validation Engineers are professionals who work to ensure that products, systems, or processes meet specified requirements and function as intended. They design and execute tests, analyze data, and document results to demonstrate compliance with regulatory standards and internal quality guidelines. Validation Engineers are commonly employed in industries such as pharmaceuticals, biotechnology, manufacturing, and electronics, where product safety and consistency are critical. Their role is crucial in preventing defects and ensuring that products are safe and effective for their intended use.

What are some common challenges faced by full time validation engineers, and how can they be addressed?

Full Time Validation Engineers often encounter challenges such as tight project deadlines, evolving regulatory requirements, and the need to coordinate with cross-functional teams. Managing documentation and ensuring thorough testing while maintaining compliance can also be demanding. To address these challenges, it's important to stay organized, communicate proactively with colleagues in quality assurance, manufacturing, and R&D, and keep up-to-date with industry standards and regulations. Leveraging project management tools and regular team meetings can help streamline validation activities and minimize potential bottlenecks.

What are the key skills and qualifications needed to thrive as a full time validation engineer, and why are they important?

To thrive as a Full Time Validation Engineer, you need a solid background in engineering principles, quality assurance, and validation processes, typically supported by a degree in engineering or a related field. Familiarity with industry standards (such as GMP or FDA regulations), data analysis tools, and validation software like ValGenesis or TrackWise is commonly required. Strong attention to detail, analytical thinking, and effective communication skills set top performers apart in this role. These capabilities ensure that products and processes consistently meet regulatory standards and quality expectations, which is critical for compliance and operational success.

What is the difference between Full Time Validation Engineer vs Validation Technician?

AspectFull Time Validation EngineerValidation Technician
CredentialsBachelor's in Engineering or related field, certifications like GxP or IQ/OQ/PQAssociate's or Bachelor's, often with on-the-job training
Work EnvironmentDesigning validation protocols, analyzing data, overseeing validation processesExecuting validation tests, collecting data, supporting validation activities
Industry UsagePharmaceutical, biotech, medical device manufacturingSimilar industries, often as support staff
Search & ComparisonOften compared for roles involving validation planning and oversightCompared for hands-on testing and data collection roles

The Full Time Validation Engineer typically leads validation projects, requiring more technical expertise and planning skills, while the Validation Technician focuses on executing validation tests and supporting validation activities. Both roles are essential in regulated industries like pharmaceuticals and biotech, but they differ in responsibilities and required credentials.

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 Full Time Validation Engineer jobs in Massachusetts?

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

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

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

What cities in Massachusetts are hiring for Full Time Validation Engineer jobs?

Cities in Massachusetts with the most Full Time Validation Engineer job openings:

Infographic showing various Full Time Validation Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.

Sr. Validation Engineer

Alcami Corporation

Pepperell, MA • On-site

$43.27 - $53.49/hr

Full-time

Re-posted 14 days ago


Alcami rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

 

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary

The Senior Validation Engineer will plan, schedule, coordinate, and track all facets of assigned validation projects. Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer will execute protocols for Installation, Operational and Performance Qualification testing on chambers and rooms including: autoclaves, cryo-freezers, cold rooms, refrigerators, incubators, sterilizers, depyrogenation ovens, stability chambers, and warehouses. Also, Steam in Place (SIP) validation using biological indicators and projects requiring specialized knowledge or expertise (GMP manufacturing facilities and equipment, computerized systems). Process, assemble and review data, generate documentation and reports. The Sr. Validation Engineer will be a source of technical knowledge for validation staff and customers and will deliver excellent customer service, resulting in long-term relationships.

On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 4:30pm.
  • This position is for day shift but may require some occasional off shift and/or weekend coverage to accommodate schedules and/or project timelines.
Responsibilities
  • Perform pre- and post-validation verification on test equipment.
  • Perform calibrations incidental to validation including controllers, gauges, recorders, etc.
  • Create and execute validation protocols, procedures, and final reports; perform validation projects.
  • Perform peer review of validation reports.
  • Learn and execute troubleshooting strategies in the field.
  • Independently manage technical writing and documentation aspects of validation reports.
  • Write and work with clients to resolve deviations.
  • Maintain records of pertinent information for the project including project costs reconciliation.
  • Relay opinions or interpretations of results to customer.
  • Train validation team members.
  • Other duties as assigned.
Qualifications
  • BA/BS in technical or science related field of study preferred. Candidates with an HSD/GED, technical training, or an Associate's degree combined with mechanical aptitude or relevant industry experience considered.
  • 5+ years of direct validation experience required.
Knowledge, Skills, and Abilities
  • Experience with autoclave qualification and processes.
  • Experience with validation of temperature-controlled units and temperature mapping.
  • Experience with validation of sterilization processes (steam sterilizers, SIP).
  • Experience with validation of GMP laboratory and manufacturing equipment and computerized systems.
  • Calibration expertise (temperature, humidity, CO2, pressure, timer) is a plus.
  • Ability to perform tasks with high standard of quality and accuracy.
  • Spreadsheet and word processing applications experience, computer literacy.
  • Strong written and verbal communication skills.
  • Proficient with test instruments.
  • ISO 9001, ISO 17025, GMP and GLP knowledge.
Travel Expectations
  • Up to 80% travel expected. This position includes travel during the day to client sites.
Physical Demands and Work Environment

The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee will regularly stand, walk, and use hands, frequently reach, stoop, kneel, crouch or crawl and talk or hear, and occasionally sit and climb or balance. In this role, the employee will frequently work in an office, lab or at customer sites and be exposed to extreme cold (non-weather). The employee will occasionally be exposed to wet or humid conditions, work near moving mechanical parts, work in high places, near toxic or caustic chemicals, in outdoor weather conditions and exposure to vibration. The noise level that is typical for this position is loud.

Pay Range The base hourly pay range for this position is $43.27 - $53.49 per hour. Disclosure Statement The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. Actual base salary will be based on a number of factors including, but not limited to, relevant skills, competencies, and experience, and upon joining Alcami will be reviewed periodically. Alcami may change the published salary range based on company and market factors. Employment Type: FULL_TIME

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