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Validation Manager Jobs in Hackettstown, NJ (NOW HIRING)

CYNET SYSTEMS

Validation Lead

Raritan, NJ · On-site

$48 - $53/hr

Provide Validation guidance, timely reviews, and escalations to management. * Work with global project teams during the initial project planning phases. * Provide guidance on validation strategy and ...

R3tek

Validation Engineer

Hillsborough, NJ · On-site

R3 Technology Inc. seeks Validation Engineer or it Hillsborough NJ office to gather requirements to ... Must have Master's degree in Industrial Engineering, Supply Chain Management or related degree and ...

R3TEK

Validation Engineer

Hillsborough, NJ · On-site

R3 Technology Inc. seeks Validation Engineer or it Hillsborough NJ office to gather requirements to ... Must have Master's degree in Industrial Engineering, Supply Chain Management or related degree and ...

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

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

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 · 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 ...

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 ...

Cloud think technologies LLC

MES Engineer

Raritan, NJ · On-site

Manage the validation and qualification processes for developed MBR's, ensuring they meet user requirement and specification. · Documentation: Maintain comprehensive documentation of automation ...

CAI

Senior Validation Engineer

Bridgewater, NJ · On-site

$87K - $94K/yr

... Management - Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities - Coordinate with project contractors and equipment vendors to execute required ...

CAI

Senior Validation Engineer

Bridgewater, NJ

$87K - $94K/yr

... Management - Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities - Coordinate with project contractors and equipment vendors to execute required ...

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Validation Manager information

See Hackettstown, NJ salary details

$49.1K

$108.9K

$165.8K

How much do validation manager jobs pay per year?

As of Aug 19, 2026, the average yearly pay for validation manager in Hackettstown, NJ is $108,925.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $136,400.00 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 cities near Hackettstown, NJ are hiring for Validation Manager jobs?

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

Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Hackettstown, NJ as of August 2026, with employment types broken down into 82% Full Time, 17% Part Time, and 1% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $108,925 per year, or $52.4 per hour.

Validation Engineer III

Kashiv Biosciences LLC

Piscataway, NJ • On-site

$70K - $90K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 11 days ago

Job description

Job Type
Full-time
Description
Company Overview
Creating a Healthier World through Accessible Biologics:
Kashiv BioSciences, LLC is a fully integrated biopharmaceutical company. Kashiv BioSciences, LLC in the United States, and its subsidiary, Kashiv BioSciences Private Limited in India (together "Kashiv BioSciences"), operate together with robust infrastructure and highly skilled teams that provide global R&D, clinical, manufacturing, regulatory, and IP capabilities. We believe our people, partners, and shared purpose fuel our work to advance patient care and access to important medicines.
Position Summary
The Validation Engineer III is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC, in Piscataway, NJ. This employee will be responsible for developing, testing, modifying, and creating solutions to technical problems.
Essential Duties & Responsibilities:
  • Draft and implement Quality System documentation including SOPs and Traceability Matrix designed to establish good validation practices within the organization.
  • Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and internal quality standards.
  • Coordinate all validation activities with vendors, cross functional team and assemble results, and draft validation reports.
  • Serve as the validation representative during FDA, customer, and internal audits.
  • Provide input on user and/or functional requirements of current and future processing equipment, and draft appropriate documentation. Additionally, interface with Contract Manufacturers to ensure all relevant user and functional requirements are met.
  • Lead or participate in deviation/CAPA investigations related to qualification failures, equipment malfunctions, or out-of-specification results, applying root cause analysis methodologies (5-Whys, Ishikawa, Fault Tree).
  • Prepare, Review and approve vendor qualification documentation, Factory Acceptance Test (FAT) and Site Acceptance Test (SAT) protocols and execution reports.
  • Develop and maintain the site Validation Master Plan (VMP), including validation impact assessments, criticality ranking, and lifecycle change management for validated systems.
  • Provide support to non-engineering Staff, including those from R&D and Manufacturing, to ensure successful technology transfer and continuous improvement.
  • Maintain validation status tracking dashboards and periodic system health reviews to ensure all validated systems remain in a continuous state of inspection readiness.
  • Execute assigned duties on time and pro-actively telegraph delays and other issues to validation manager and other relevant stakeholders.
  • Comply with all regulatory, corporate, and Quality System policies.

Requirements
Position Requirements and Qualifications
Minimum Qualifications:
Education:
  • Degree in engineering / Pharmaceuticals or another relevant discipline.

Experience:
  • 8+ years of experience working within a medical device environment or other FDA-regulated environments.
  • Experience with Biological products is highly desirable.

Preferred Qualifications:
SPECIALIZED KNOWLEDGE AND SKILLS:
  • Experience in the areas of Design Documentation (URS, FRS, DS, and other engineering specifications), Validation (IQ, OQ, PQ, PV, CSV, MVP, etc.), Quality Systems (Change Control, Non-Conformances, Requalification, etc.), Understanding of cGxP principles and familiarization with ISO guidelines.
  • Working knowledge of Computer Systems Validation lifecycle and documentation.
  • Proficient in Microsoft Word, Excel, and PowerPoint.
  • Must be able to work independently with adequate supervision, multitask, and support several projects simultaneously.
  • Must demonstrate strong communication, interpersonal and teamwork skills.
  • A strong understanding of technical writing and presentation skills is required.

Compensation:
  • Validation Engineer III - Base Salary Range and Yearly Bonus - $70,000 to $90,000 (dependent on years of experience and fit for the position) with up to a yearly 10% (discretionary) cash bonus

Benefits/Perks:
  • Medical Insurance - Aetna
    • Prescription Converge Rx
    • Virtual Visits - Aetna/Teladoc
    • Health Savings Accounts (HSA)
    • Flexible Spending Accounts (FSA)
  • Dental Insurance - Aetna
  • Vision Insurance - VSP
  • Life and AD&D Insurance
  • Disability Benefits
  • Supplemental Benefits
    • Legal Services
    • ID Theft Protection
    • Travel Assistance
  • Value Added Benefits & Services
    • Health Advocate
    • Life Assistance Program (LAP)
    • Student Loan Assistance Program
  • 401K
  • Monthly Cell Phone Allowance

Hours:
This position is onsite 5 days a week from 9 AM EST to 5:30 PM EST
WORKING ENVIRONMENT/PHYSICAL REQUIREMENTS:
  • Noise: No extraordinary noise levels.
  • Standing/Lifting: Must be able to lift at least 25 lbs.
  • Visual: No extraordinary requirements.
  • Stress: High-paced, demanding environment to meet ambitious project goals.
  • Travel required as needed 20%- 30%

Supervisory Responsibility, if any: No
This position description is not a complete list of all responsibilities, duties, or skills required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.
Kashiv BioSciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Kashiv BioSciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

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