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Validation Manager Jobs in Edison, NJ (NOW HIRING)

Bloomberg LP

Model Validation Expert

New York, NY · On-site

Model Validation Expert Location New York Business Area Legal, Compliance, and Risk Ref # 10052595 ... Management (MRM) program as Bloomberg navigates its obligations under ERR. This is a senior ...

Deloitte

Model Validation Consultant

New York, NY · On-site

You will execute validation activities, contribute to documentation and testing, and help teams assess model risk management practices and responsible AI deployment across industries such as ...

AbbVie

Validation Engineer II

Branchburg, NJ · On-site

$75K/yr

Technical review of Validation Documents. * Execution of qualification and requalification ... Manages multiple, often concurrent, projects and meets deadlines and balances multiple demands

AbbVie

Validation Engineer II

Branchburg, NJ · On-site

Technical review of Validation Documents. * Execution of qualification and requalification ... Manages multiple, often concurrent, projects and meets deadlines and balances multiple demands

AbbVie

Validation Engineer II

Branchburg, NJ · On-site

Technical review of Validation Documents. * Execution of qualification and requalification ... Manages multiple, often concurrent, projects and meets deadlines and balances multiple demands

CAI

Validation Engineer

Bridgewater, NJ · On-site

$72K - $80K/yr

... Team Management - Plan and coordinate work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or ...

CAI

Validation Engineer

Bridgewater, NJ

$72K - $80K/yr

... Team Management - Plan and coordinate work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or ...

CAI

Validation Engineer

Princeton, NJ · On-site

$72K - $80K/yr

... Team Management - Plan and coordinate work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or ...

CAI

Validation Engineer

Bridgewater, NJ · On-site

$72K - $80K/yr

... Team Management - Plan and coordinate work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or ...

CAI

Validation Engineer

Princeton, NJ

$72K - $80K/yr

... Team Management - Plan and coordinate work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or ...

ClifyX

Computer system Validation Tester

Somerset, NJ · On-site

... the project manager during the system implementation and validation process, and ensure compliance with corporate policies and procedures. • Provide training related to computerized systems ...

Legend Biotech US

IT Validation Specialist

Somerset, NJ · On-site

Maintain and manage validation documentation and test execution activities using VLMS, EDMS, and QMS systems. Experience with ValGenesis and Veeva Quality Vault preferred. * Support Change Controls ...

Pwc

Data Validation Risk - Manager

Florham Park, NJ · On-site

$99K - $232K/yr

Industry/Sector Not Applicable Specialism Data, Analytics & AI Management Level Manager & Summary The Opportunity As a Data Validation Risk Manager, you will play a pivotal role within our Risk ...

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Validation Manager information

See Edison, NJ salary details

$49.2K

$109.1K

$166.2K

How much do validation manager jobs pay per year?

As of Sep 12, 2026, the average yearly pay for validation manager in Edison, NJ is $109,131.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,100.00 and $136,700.00 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

What are the most commonly searched types of Validation jobs in Edison, NJ?

The most popular types of Validation jobs in Edison, NJ are:

What are popular job titles related to Validation Manager jobs in Edison, NJ?

For Validation Manager jobs in Edison, NJ, the most frequently searched job titles are:

What cities near Edison, NJ are hiring for Validation Manager jobs?

Cities near Edison, NJ with the most Validation Manager job openings:

Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Edison, NJ as of September 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $109,131 per year, or $52.5 per hour.

Validation Engineer II

East Windsor, NJ • On-site

Medvacon Life Sciences LLC
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Medvacon Life Sciences LLCexternal

Full-time

Re-posted 27 days ago

Key responsibilities

  • Manage the full lifecycle of Computer System Validation, including developing validation documentation for sterile and non-sterile manufacturing processes.

  • Oversee multiple validation projects to ensure timely, budget-compliant completion while driving continuous improvement in manufacturing efficiency.

  • Prepare, review, and approve technical documents such as SOPs and cGMP records, and support compliance activities including change control, quality investigations, and audits.

Job description

POSITION OVERVIEW:
The Validation Engineer II ensures compliance and operational excellence by managing validation processes across sterile and non-sterile manufacturing. It oversees multiple projects, develops documentation, and collaborates with teams to enhance efficiency, support product development, and drive continuous improvement aligned with our mission to provide high-quality, accessible medications.
ESSENTIAL JOB FUNCTIONS:
  • Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site Acceptance Testing, Installation Qualification, Operational Qualification, Performance Qualification, and Process Qualification for sterile and non-sterile manufacturing.
  • Oversees multiple validation projects, ensuring timely budget-compliant completion while driving continuous improvement to boost manufacturing efficiency.
  • Prepares, reviews, and approves technical documents, including Standard Operating Procedures and current Good Manufacturing Practice (cGMP) records, while managing change control, Corrective and Preventive Action, and quality investigations.
  • Operates and manages critical equipment, executing cleaning, sterilization, and lyophilization cycles.
  • Provides training, supports Research and Development and product development, manages contractors for Commissioning, Qualification, and Validation (CQV) activities, and assists with audits to ensure compliance.

QUALIFICATIONS:
  • Bachelor of Science degree in a scientific or engineering discipline.
  • 7 years Validation experience in the pharmaceutical or biotechnology industries.
  • Advanced knowledge of cGMP, CQV, sterilization process validation, and regulatory compliance, including Good Automated Manufacturing Practice and 21 Code of Federal Regulations Part 11.
  • Strong problem-solving, project management, and attention to detail, with proficiency in Microsoft Office Suite, Quality Management Systems, and experience in Computer System Validation and Cleaning Validation preferred.

KEY COMPETENCIES:
  • Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions.
  • Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement.
  • Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives.
  • Resourcefulness: Secures and deploys resources effectively and efficiently.
  • Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems.
  • Ensures Accountability: Holds self and other accountable to meet commitment.
  • Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations.
  • Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences.

VALUES:
  • People: Our people define who we are as a company, and we believe that understanding and addressing the needs of our team, clients, and community is fundamental to fostering a culture of support and growth.
  • Quality: Quality stands at the core of our mission, reflecting our commitment to excellence in every medication we produce.
  • Service: We are here to serve others. Every interaction with our patients, providers, employees, and other stakeholders comes from a place of service.
  • Innovation: By continuously exploring new methodologies and embracing technology, we ensure that every solution we offer is at the forefront of pharmaceutical care.

SUPERVISORY RESPONSIBILITIES:
This position does not have supervisory responsibilities.
CERTIFICATES, LICENSES, REGISTRATIONS:
Certified Quality Engineer Preferred.
Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to jobs@medvacon.com.

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