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Validation Manager Jobs in Holyoke, 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 · 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 ...

Socket.dev

Validation Engineer

Windsor, CT · On-site

$95 - $140/hr

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

$83K - $105K/yr

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

ECI

Engineering Manager

Westfield, MA · On-site

$150K - $200K/yr

Quantic ECI, a leading manufacturer of advanced magnetic components is seeking an Engineering Manager to design, develop, and validate custom magnetic devices--including transformers, inductors ...

Dunkin' | Askar Management

Assistant Manager

Windsor, CT · On-site

$20 - $22/hr

Oversee Brand Training Programs, schedule, train, validate, certify team and shift lead staff ... Manages cash in restaurant and ensures team members are following franchisee's cash management ...

Dunkin' | Askar Management

Assistant Manager

Windsor, CT · On-site

$20 - $22/hr

Oversee Brand Training Programs, schedule, train, validate, certify team and shift lead staff ... Manages cash in restaurant and ensures team members are following franchisee's cash management ...

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Validation Manager information

See Holyoke, MA salary details

$46.9K

$104.2K

$158.6K

How much do validation manager jobs pay per year?

As of Aug 25, 2026, the average yearly pay for validation manager in Holyoke, MA is $104,189.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,600.00 and $130,500.00 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 Holyoke, MA are hiring for Validation Manager jobs?

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

Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Holyoke, MA as of August 2026, with employment types broken down into 33% Full Time, 33% Part Time, and 34% Contract. Highlights an 100% In-person job distribution, with an average salary of $104,189 per year, or $50.1 per hour.

Validation Engineer

Windsor, CT • On-site

SCA Pharmaceuticals, LLC
Pharmaceutical Product Wholesalers • 501 - 1,000 employees
Learn more about SCA Pharmaceuticals, LLCexternal

Full-time

Posted 12 days ago

Job description

Description:

SCA Pharmaceuticals is a dynamic rapidly growing company consisting of passionate individuals who believe in our mission of providing high quality medications that are critical in saving and sustaining human life. SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and healthcare facilities across the United States. We do this through unyielding quality, safety and integrity, our commitment to accountability and ownership, teamwork and creating better solutions by simplifying the complex.

Summary:

The Validation Engineer oversees the aseptic process simulations (media fills), equipment qualification and requalification, facility and utility qualification and requalification. This position supports Operations and Quality and will maintain a compliant schedule of validation activities and will serve as a technical resource in process improvement initiatives that require a validation expertise.

Essential functions:

  • Execute validation and qualification activities (equipment, media fills, facility, utility, environmental monitoring system) to include protocol preparation, scheduling execution, protocol execution, and final report preparation.
  • Ensure that C&Q and Validation project deliverables (i.e., Specification, SOPs; Protocols/Reports; Risk Assessment; Traceability Matrix, etc.) are compliant with the current regulations, current industry practices, and internal policies and procedures.
  • Maintain a revalidation / requalification lifecycle and executes accordingly per Standard Operating Procedures (SOPs).
  • Execute airflow patterns (smoke studies) of compounding operations.
  • Manage a schedule for outsourcing HEPA Filter recertification. Oversee and approve the outsourced activities.
  • Effectively coordinate and communicate all due validation/qualification activities with relevant functional groups to enable compliance to the validation / qualification schedule.
  • Develops/improves validation and qualification programs as needed to remain current with cGMP’s and industry standards.
  • Represent validation in teams assembled to procure, install, troubleshoot systems, equipment, and processes.
  • Conduct and/or participate in deviation investigations as appropriate to identify root causes and define corrective and/or preventative actions (CAPA).
  • Drive CAPA’s assigned to the validation department
  • Generate and approve SCA Certificate of Compliance
Requirements:

Required Qualifications & Experience:

  • Bachelor’s degree in life sciences, engineering, or related discipline.
  • 5+ years of direct validation experience in pharmaceutical and/or life sciences.

Desired Knowledge, Skills, and Abilities:

  • Proficient in MS Word, Excel, and PowerPoint
  • Have effective communication (both written and verbal).
  • Demonstrated strong technical writing skills, decision making abilities and critical thinking.
  • Demonstrated knowledge and understanding of cGMP’s, industry guidance associated with aseptic processing, CAPA, root-cause analysis, risk assessment and investigation tools and techniques.
  • Knowledge and experience in leading aseptic process simulations (media fills)

SCA Pharma is an equal opportunity employer (Minorities/Females/Disabled/Veterans). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state, or local law.