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Validation Manager Jobs in Chicopee, MA (NOW HIRING)

SCA Pharma

Validation Engineer

Windsor, CT · On-site

Manage a schedule for outsourcing HEPA Filter recertification. Oversee and approve the outsourced activities. * Effectively coordinate and communicate all due validation/qualification activities with ...

SCA Pharma

Validation Engineer

Windsor, CT

Manage a schedule for outsourcing HEPA Filter recertification. Oversee and approve the outsourced activities. * Effectively coordinate and communicate all due validation/qualification activities with ...

Cadence Inc

Validation Engineer II

Suffield, CT · On-site

Conduct risk assessments and manage change controls. * Ensure regulatory compliance. (GMP, GLP, CSV, data integrity) * Collaborate cross-functionally to support validation strategy and training.

Aspen Square Management

Community Manager

South Hadley, MA · On-site

$50K - $68K/yr

Join Aspen Square Management , where we cultivate successful teams by empowering our team members ... Must possess a valid driver's license, have reliable transportation to and from work, and ability ...

Aspen Square Management

Community Manager

South Hadley, MA · On-site

$50K - $68K/yr

Join Aspen Square Management , where we cultivate successful teams by empowering our team members ... Must possess a valid driver's license, have reliable transportation to and from work, and ability ...

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Validation Manager information

See Chicopee, MA salary details

$47.7K

$106K

$161.3K

How much do validation manager jobs pay per year?

As of Sep 1, 2026, the average yearly pay for validation manager in Chicopee, MA is $105,965.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,900.00 and $132,700.00 per year, depending on experience, location, and employer.

What is a validation manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

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

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

How does a validation manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What is the difference between Validation Manager vs Quality Assurance Specialist?

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

More about Validation Manager jobs

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What cities near Chicopee, MA are hiring for Validation Manager jobs?

Cities near Chicopee, MA with the most Validation Manager job openings:

Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Chicopee, MA as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $105,965 per year, or $50.9 per hour.

Validation Engineer

Springfield, MA • On-site

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

Contractor

Re-posted 8 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/