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Validation Engineer

Actalent

Andover, MAContract$43–53/hrSeen todaySeen in employer's feed today

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At a glance

Compensation
$43–53/hr
Location
Andover, MA
Schedule
Contract
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

The Validation Engineer develops and executes validation and commissioning protocols for general equipment in a biopharmaceutical facility. The role supports equipment qualification projects, prepares commissioning and IOQ documents, and maintains lifecycle documentation. It also involves reviewing and redlining requirements and design documents, supporting change management, and coordinating with customers. The position is contract-to-hire and fully onsite in Andover, Massachusetts.

Skills & qualifications

RequiredNice to have

Skills

cGMP, nice to haveChange Control, nice to haveCommissioning, nice to haveEquipment Qualification, nice to haveIQ, nice to haveOQ, nice to havePQ, nice to haveValidation Protocols, nice to haveAseptic Processing, nice to haveCleaning Validation, nice to haveFill Finish, nice to havePackaging Lines, nice to haveFDA Validation Guidelines, requiredGDP, required21 CFR 210 and 211, required21 CFR Part 11, requiredOrganizational Skills, requiredCommunication, requiredPeople Skills, requiredClient-Facing Consulting, requiredProject Environment Experience, required

Qualifications

Bachelor's in Engineering, Science, or Related Field or Master's in Engineering, Science, or Related Field, required3+ Years Equipment Qualification Experience or 2+ Years With Master's, required

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off

Full job description

Description

The Validation Engineer is responsible for development and execution of validation and commissioning protocols for general equipment in Biopharma facility. The position requires general knowledge of Biopharmaceutical equipment, cGMP, and GDP. Duties: Perform and support execution of validation protocols/projects Develop, review, and redline URS/FRS/DDS Support change management process Support project level customer communications and coordination efforts Prepare and execute commissioning documents Prepare and execute IOQ documents and summary reports Maintain project lifecycle documentation in accordance with Mangan Biopharm internal procedures and client procedures

Skills

cgmp, change control, commissioning, equipment qualification, iq, oq, pq, validation protocol, aseptic processing, cleaning validation, fill finish, packaging line

Top Skills Details

cgmp,change control,commissioning,equipment qualification,iq,oq,pq,validation protocol

Additional Skills & Qualifications

Bachelors degree in engineering, science, or related field with at least (3) years of experience or Masters degree in engineering, science, or related field with two (2) years of experience in equipment qualification in Biotechnology or Pharmaceutical cGMP environment Must possess a solid understanding of FDA validation guidelines, GDP, and industry best practices and be able to implement validation standards daily Working knowledge of 21CFR 210, 211 and Part 11 Excellent organizational, communication, and people skills Experience working in a client-facing consulting or project environment

Experience Level

Intermediate Level

Job Type & Location

This is a Contract to Hire position based out of Andover, MA.

Pay and Benefits

The pay range for this position is $43.00 - $53.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)

Job Type & Location

This is a Contract to Hire position based out of Andover, MA.

Application Deadline

This position is anticipated to close on Nov 25, 2026.

Workplace Type

This is a fully onsite position in Andover,MA.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

How this job compares

Set against the 441 open Validation Engineer jobs on Olive Jobs, counted November 12, 2026.

Pay
  • This posting$43–53/hr
  • US median$50–60/hr31 hourly ranges

This range's midpoint, $48/hr, is 13% below the US median midpoint ($55/hr) — in the middle half of Validation Engineer hourly ranges across the US.

Openings
Olive Jobs lists 22 open Validation Engineer jobs in Massachusetts and 441 across the US. Under 1% of them nationwide are listed as remote or flexible.
Hiring the most in Massachusetts
Experience
This posting asks for at least 2 years of experience — less than three in four Validation Engineer postings that state a minimum ask for (median 5 years, across 337 postings).
Education
241 of the 441 open Validation Engineer jobs (55%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 12, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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