Talent.com
Validation Engineer III

Validation Engineer III

AbbVieBranchburg Township, NJ, US
30+ days ago
Job type
  • Full-time
Job description

Job Description

Job Description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

An engineering professional that works with project owners, subject designers / engineers and other project team members to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes etc.in line with project, operations and quality objectives. Level of responsibility and performance is commensurate with grade level. The main objective is to establish evaluation, testing and documentation for risk management, commissioning and validation applying product and regulatory requirements and risk management to result in robust, high quality products. This includes optimizing systems that support the work in and around this area of responsibility.

This position is fully onsite Monday-Friday but may have periods of time that require nights or weekends (approx. quarterly)

Responsibilities :

Work with end-user and project engineer to develop User Requirements Specifications and Functional / Design Specifications for new or modified equipment, facilities, and utilities.

  • Support Factory Acceptance Testing in conjunction with Project Engineer to confirm unit is acceptable.
  • Identify risk controls, critical elements and traceability of equipment design based on FMEA or other risk assessment.
  • Develop and execute commissioning, qualification and validation test protocols to ensure that the unit functions according to specifications.
  • Perform minor troubleshooting of issues encountered during commissioning and documentation of unresolved issues.
  • Able to support broader aspects of projects at times including : project leadership, developing operational procedures, support training of maintenance / technical staff / operators on new equipment, reviewing new or modified product documentation to ensure compatibility with qualified equipment and implementing changes in equipment parameters or recipes.
  • Leads Execution of Risk Management. including, periodic review and update per the Validation Master Plan, interface with best practices, establishing team's work practices including overall program, ccRA. Understands risk management principles. Can find and review documentation. Understands controls, impact of change, trace controls, and can estimate ratings using appropriate scale. Timely. Demonstrated success in FMEA authorization / facilitation.
  • Qualification as QRM facilitator commensurate with responsibility.
  • May supervise contract validation resources in the timely completion of activities in his / her area of responsibility

Qualifications

  • Bachelor’s Degree in Engineering, science, or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 3+ years of significant engineering and / or operational experience.
  • Process and Cleaning Validation Experience
  • Equipment Qualification (IOQ / PQ)
  • Quality System Experience (Veeva, Trackwise, ComplianceWire)
  • Medical Device or Pharmaceutical Experience Required. Preferred Medical Device with 3-5 Years
  • Statistical Analysis (Minitab or JUMP)
  • Experience in the development of commissioning, qualification, validation and risk management deliverables including specifications and testing protocols that can stand up to regulatory scrutiny.
  • 6+ years of overall experience in Manufacturing, Quality or Engineering including 4 major validation subjects (e.g. Computer, Equipment, Cleaning, Process, etc.) preferred
  • A technical background in medical devices, pharmaceutical, or similar industries (preferred).
  • ISO5 Clean Room Manufacturing experience strongly preferred
  • Strong interpersonal, communication, and negotiation skills with demonstrated ability to work within a team environment.
  • Knowledge of quality / compliance management as well as regulations and standards affecting API, Bulk Drug or Finished goods manufacturing preferred
  • Ability to supervise junior or contract team members (prior supervisory experience preferred)
  • Ability to manage complex projects and multiple projects (5+) simultaneously
  • Additional Information

    Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law :  ​

    The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time ofthis posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

    We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),  medical / dental / vision  insurance and 401(k) to eligible employees.​

    This job is eligible to participate in our short-term incentive programs. ​

    This job is eligible to participate in our long-term incentive programs​

    Note : No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

    AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer / Veterans / Disabled.

    US & Puerto Rico only - to learn more, visit  https : / / www.abbvie.com / join -us / equal-employment-opportunity-employer.html

    US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more :

    https : / / www.abbvie.com / join -us / reasonable- accommodations.html

    Create a job alert for this search

    Validation Engineer • Branchburg Township, NJ, US

    Related jobs
    • Promoted
    Validation Engineer

    Validation Engineer

    IPS-Integrated Project Services, LLCSomerset, NJ, United States
    Full-time
    At IPS, we apply our knowledge, skills, and passion to make a difference in the lives of people, solving complex challenges related to life sciences. We are looking for a dedicated.In this role, you...Show moreLast updated: 4 days ago
    • Promoted
    Quality Engineer

    Quality Engineer

    1014 AD FederalAlpha, MA, United States
    Permanent
    NASDAQ : ADI ) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologie...Show moreLast updated: 30+ days ago
    • Promoted
    Validation Engineer

    Validation Engineer

    Kasmo GlobalPrinceton, NJ, United States
    Full-time
    Title : Validation Engineer 10 Openings.Medical domain, medical implants.IQ, OQ PQ , equipment qualification, process qualification in medical device manufacturing. IQ, OQ PQ protocols, Execute and r...Show moreLast updated: 30+ days ago
    • Promoted
    Validation Engineer

    Validation Engineer

    Info Way SolutionsParsippany, NJ, United States
    Full-time
    The Quality Engineer is responsible for supporting sustaining activities through the application of Quality Engineering skills for medical devices. This person will understand, improve, and control ...Show moreLast updated: 30+ days ago
    • Promoted
    Validation Engineer

    Validation Engineer

    PrideStaffFairfield, NJ, US
    Full-time
    Responsible for Validation / PPAP Packages on new customer programs, as well as ensuring compliance is applicable regulatory bodies and standards (ISO13485, 21 CFR 820, GMP).Requires a 4-yr engineeri...Show moreLast updated: 30+ days ago
    • Promoted
    0013V Senior CSV Analytical Instrument Engineer / Senior Validation Engineer Consultant

    0013V Senior CSV Analytical Instrument Engineer / Senior Validation Engineer Consultant

    Two River Consulting PartnersSummit, NJ, US
    Full-time
    Analytical Instruments accompanied by a thorough understanding of CSV principles.Knowledge and demonstrated experience of Computerized System and Analytical Equipment Validation.Running test script...Show moreLast updated: 2 days ago
    • Promoted
    Engineering - Validation Engineer

    Engineering - Validation Engineer

    TechDigital CorporationSummit, NJ, United States
    Full-time
    Onsite position PURPOSE AND SCOPE OF POSITION : The Equipment Validation Engineer supports the successful implementation of various process / lab equipment at multi-use sites through interaction with ...Show moreLast updated: 4 days ago
    • Promoted
    Consultant Engineer I

    Consultant Engineer I

    FMBOONTON, New Jersey, United States
    Full-time
    If you enjoy variety, we will put your time-management and organization skills to use handling field visits, office work, and projects for large commercial clients. We will provide you with extensiv...Show moreLast updated: 4 days ago
    • Promoted
    HIL Verification and Validation Engineer

    HIL Verification and Validation Engineer

    Kasmo GlobalPlainsboro, NJ, United States
    Full-time
    HIL Verification and Validation Engineer.Required Degree : BS or MS Electrical Engineering or Computer Engineering.Electrical Engineering or Computer Engineering degree. NO Mechanical Engineers or ot...Show moreLast updated: 30+ days ago
    • Promoted
    Senior CSV Analytical Instrument Engineer / Senior Validation Engineer Consultant

    Senior CSV Analytical Instrument Engineer / Senior Validation Engineer Consultant

    Two River Consulting PartnersSummit, NJ, United States
    Full-time
    Looking for a strongresource with a diverse skillset focused around Analytical Instruments accompanied by a thorough understanding of CSV principles. Knowledge and demonstrated experience of Compute...Show moreLast updated: 1 day ago
    • Promoted
    Validation Engineer

    Validation Engineer

    CAIPrinceton, NJ, US
    Full-time
    CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide.For mission-critical and regulated industries needing to deliver essential solutions in high...Show moreLast updated: 16 days ago
    • Promoted
    Automation Validation Engineer

    Automation Validation Engineer

    Technical SourceRahway, NJ, US
    Full-time
    Our client provides industrial automation, process control, and operational excellence solutions to the energy, life sciences, and pulp & paper industries. Our client is seeking a Validation Eng...Show moreLast updated: 30+ days ago
    • Promoted
    Process Sustaining Engineer, 2nd Shift

    Process Sustaining Engineer, 2nd Shift

    1014 AD FederalAlpha, MA, United States
    Full-time +1
    NASDAQ : ADI ) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologie...Show moreLast updated: 30+ days ago
    • Promoted
    CSV Validation Engineer

    CSV Validation Engineer

    Katalyst Healthcares and Life SciencesSouth Plainfield, NJ, United States
    Full-time
    Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution.You should have excellent...Show moreLast updated: 30+ days ago
    • Promoted
    Validation Lifecycle & Technical Lead

    Validation Lifecycle & Technical Lead

    Legend BiotechRaritan, NJ, US
    Full-time
    Validation Lifecycle & Technical Lead.Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we...Show moreLast updated: 7 days ago
    • Promoted
    Production Control Supervisor

    Production Control Supervisor

    Trident Maritime System - Custom AlloyHigh Bridge, NJ, US
    Full-time
    We’re Hiring : Production Control Supervisor.Trident Maritime Systems – Custom Alloy Division.This leadership role is perfect for someone with strong organizational skills, manufacturing...Show moreLast updated: 3 days ago
    • Promoted
    Quality Engineer Intern

    Quality Engineer Intern

    1014 AD FederalAlpha, MA, United States
    Full-time +1
    Are you a problem solver looking for a hands-on internship position with a market-leading company that will help develop your career and reward you intellectually and professionally?.NASDAQ : ADI ...Show moreLast updated: 30+ days ago
    • Promoted
    Manufacturing Engineer

    Manufacturing Engineer

    1014 AD FederalAlpha, MA, United States
    Full-time +1
    NASDAQ : ADI ) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologie...Show moreLast updated: 30+ days ago