Validation Engineer jobs in Oklahoma

Validation Engineer prepares all protocols and reports for validation work. Coordinates all validation activities by constant communication with affected departments and personnel; oversees and reviews validation area processes and procedures. Being a Validation Engineer may require a bachelor's degree. Typically reports to a manager or head of a unit/department. The Validation Engineer works on projects/matters of limited complexity in a support role. Work is closely managed. To be a Validation Engineer typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)

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Test Validation Engineer
  • MillenniumSoft Inc
  • Mannford, OK FULL_TIME
  • Position : Test Validation Engineer

    Location : Mannford, OK

    Duration : 10 Months

    Total Hours/week : 40.00

    1st Shift

    Client: Medical Device Company

    Job Category: Engineering

    Level of Experience: Mid-Level

    Employment Type: Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)

    Hours M-F 8-5 with 1 hour lunch or long as total hours are 40 per week maximum. 8 hours a day 5 days a week.

    Note: Will consider someone who is willing to relocate at their own expense. Please note on resume location if so.

    Must Haves

    Previous create/execute test method validations, technical writing skills, flexible work week to support timing of validation time availability in a manufacturing environment.

    • BS in Engineering
    • Three to five years’ experience in engineering or Quality engineering experience within the medical device, pharmaceutical, or equivalent industry.

    Job Description

    • We believe that the human element, across our global teams, is what allows us to continually evolve.
    • Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.

    Essential / Key Job Responsibilities

    EU-MDR Senior Quality Engineer - Validation

    • EU-MDR support of submission documents; supports Quality activities surrounding EU-MDR submission of products through execution of identified remediation.
    • Works with multi-functional teams to remediate gaps related to EU-MDR requirements and meets all deliverables in line with division and business goals.

    Project Management

    • Assists with creating strategic plans for EU-MDR elements of remediation.
    • Coordinates with team members, internal and external peers, and outside professionals to ensure project output meet business needs as well as applicable regulatory requirements.

    Design To Manufacturing Transfer

    • Supports product and system updates in line with EU-MDR requirements while maintaining design intent and smooth transfer to manufacturing as it applies.

    Test Method Development & Test Method Validation

    • Leads and creates the development and validation of clinically relevant test methods that adequately challenge product design and related processes.

    Testing

    • Leads and creates verification and validation activities for products and processes in support of EU-MDR requirements.
    • Other Responsibilities may include, however are not limited to:
    • Support/lead design and process root cause analysis and support non-conforming product and complaint investigations.
    • Ability to make and present risked based decisions.
    • Technical leadership skills including an understanding of medical device operations (e.g., medical device manufacturing, process development, quality assurance)
    • Leads and creates development of risk assessments and test methods
    • Leads and creates component qualifications, design validation / verification and process validation as applicable.
    • Leads and creates product investigations.
    • Assess product changes against product design when applicable.
    • Supports translation of design inputs into manufacturing control plans
    • Prepare and present project updates and technical discussions
    • Provide support to the regulatory department in writing technical submissions
    • Complies with company procedures and policies, government regulations
    • Other duties and projects, as assigned.

    Required Qualifications

    • Knows how products are used and impact the user(s) so that risk can be managed effectively.
    • Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)
    • Ability to lead creation of risk management files (e.g. PFMEA).
    • Ability to develop solutions with business impact
    • Advanced statistical and risk assessment techniques
    • Working knowledge and creating abilities for test method (development and validation), equipment qualifications, and validations, process and design validation, risk assessment techniques, and component qualification methodologies
    • Ability to make and present risk-based decisions
    • Strong interpersonal skills
    • Ability to analyze and optimize manufacturing and quality systems
    • Product, design & prototyping
    • Ability to create and provide training, review and coordinate test protocols and reports
    • Problem solving ability
    • Ability to generate engineering proposals
    • Oral and written presentation skills
    • Ability to Lead cross functional teams
    • Understanding of regulatory requirements including ISO 13485, ISO 14971.

    Preferred Qualifications

    • Quality Engineering Certification (ASQ) or equivalent.
    • Education and/or Experience:
    • BS in Engineering
    • Three to five years’ experience in engineering or Quality engineering experience within the medical device, pharmaceutical, or equivalent industry.
    • Physical Demands:
    • The employee is regularly required to stand, walk, sit, use sight, and use hands to manipulate, handle or feel objects, tools, controls, and office equipment.
    • They frequently verbally communicate with other associates, and may reach with hands and arms and stoop, kneel or crouch.
    • Work Environment:
    • While performing the duties of this job, the employee may be in an open cubicle environment.
    • Candidate must be able to work in a team-oriented, fast-paced environment.
    • Client is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce.
  • 14 Days Ago

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Mid-Level Air Quality Environmental Scientist or Engineer
  • Level Air Quality Environmental Scientist or Engineer - Tetra Tech Careers
  • Oklahoma, OK FULL_TIME
  • Tetra Tech, Inc., an industry leader and nationally recognized engineering and consulting firm, is seeking a motivated intelligent, and experienced professional for a Mid-Level Air Quality Environment...
  • 4 Days Ago

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Engineer
  • Leader Communications Inc. (LCI)
  • Oklahoma, OK FULL_TIME
  • Position SummaryProvides support to the 76 Commodities Maintenance Group (CMXG) at Tinker Air Force Base (AFB) to include engineering services to verify and validate test station and Unit Under Test (...
  • 2 Days Ago

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Engineer
  • MONTE R. LEE AND COMPANY
  • Oklahoma, OK FULL_TIME
  • Engineer:Job Description: Responsible for assisting in the design and overseeing the installation of telecommunications equipment for both inside and outside plant projects across the rural US. Facili...
  • 2 Days Ago

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Engineer
  • Crescent Hotels & Resorts
  • Afton, OK FULL_TIME
  • Position Summary: Under general direction of the Facilities Manager, undertake the responsibility to preserve the good condition and functionality of the properties. Perform maintenance tasks of great...
  • 17 Days Ago

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Engineer
  • Hilton
  • Tulsa, OK FULL_TIME
  • An Engineer is responsible for maintaining the physical functionality and safety of the facility in the hotel's continuing effort to deliver outstanding guest service and financial profitability.What ...
  • 23 Days Ago

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Process Validation Engineer (Contract)
  • a Biopharmaceutical company based out PA
  • Philadelphia, PA
  • Process Validation Engineer (Contract) RESPONSIBILITIES Overseeing and reviewing design and construction work related to...
  • 6/11/2024 12:00:00 AM

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Validation Engineer
  • Hays
  • Auburn Hills, MI
  • Validation Engineer – Contract – Auburn hills, MI – $30.00-$35.00/hr The final salary or hourly wage, as applicable, pai...
  • 6/11/2024 12:00:00 AM

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Validation Engineer
  • Merck & Co., Inc.
  • Lansdale, PA
  • Qualifications: Associate’s degree or higher preferred with 1-2 years of experience or 4-5 years working experience in m...
  • 6/11/2024 12:00:00 AM

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Process Validation Engineer
  • Technical Source
  • Technical Source is currently in search of a Process Validation Engineer for our pharmaceutical manufacturing client in ...
  • 6/10/2024 12:00:00 AM

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Process Validation Engineer
  • EQVAL
  • Las Piedras, PR
  • EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, B...
  • 6/10/2024 12:00:00 AM

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Validation Engineer
  • ACL Digital
  • San Diego, CA
  • Job Title: Systems Test Engineer (Silicon Validation) Location: San Diego, CA (Onsite) Duration: Contract Project Job De...
  • 6/10/2024 12:00:00 AM

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Validation Engineer
  • Experis
  • Longmont, CO
  • Experis is partnering with a global manufacturing company based in Longmont, CO to hire a Test Engineer to join their te...
  • 6/9/2024 12:00:00 AM

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Process Validation engineer (SME)
  • AR Validation Services
  • Boston, MA
  • Project Description: We are looking for a process validation engineer with experience in an aseptic/sterile environment....
  • 6/8/2024 12:00:00 AM

Oklahoma is the 20th-largest state in the United States, covering an area of 69,899 square miles (181,040 km2), with 68,595 square miles (177,660 km2) of land and 1,304 square miles (3,380 km2) of water. It lies partly in the Great Plains near the geographical center of the 48 contiguous states. It is bounded on the east by Arkansas and Missouri, on the north by Kansas, on the northwest by Colorado, on the far west by New Mexico, and on the south and near-west by Texas. Much of its border with Texas lies along the Southern Oklahoma Aulacogen, a failed continental rift. The geologic figure defi...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Validation Engineer jobs
$51,894 to $69,319

Validation Engineer in Muskegon, MI
As the Process Validation Engineer you will perform process validation activities to ensure cGMP requirements are met with regards to the IQ, OQ and PQs.
February 08, 2020
Validation Engineer in Ogden, UT
Knowledge of system validation “life-cycle” concept.
February 17, 2020
Validation Engineer in Baton Rouge, LA
There are validation engineer job opportunities across the entire industry including pharmaceutical, biotechnology and medical devices companies.
December 18, 2019