Aseptic Process Validation Engineer II (276483)

Company:  ASK Consulting
Location: Fort Worth
Closing Date: 08/06/2026
Hours: Full Time
Type: Permanent

Job Description

Job Description Job Description

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment".


Job title: Aseptic Process Validation Engineer II

Location: Fort Worth, TX (onsite)

Duration: 12 months

Interviews: 2

Pay Rate: $35/hr. - $50/hr. on w2


Job Description:

Hands-on and Technical Testing Competency

  • Ability to perform standardized tests per SOP and test methods.
  • Understands protocols, data collection, and proper use of lab equipment.
  • Focused on accuracy, repeatability, and compliance
  • Perform equipment validation (IQ/OQ, etc.)


Data Analysis & Documentation

  • Capable of analyzing test results, identifying trends or failures, and summarizing findings clearly.
  • Writes structured test protocol, reports and maintains documentation aligned with quality and regulatory requirements


Problem Solving & Root Cause Analysis

  • Can identify potential issues in performance and support investigations (e.g., basic CAPA input, troubleshooting test failures).
  • Collaborates with engineers to improve designs, performance or test methods based on results.
  • Supports in the designs and development of a wide variety of packaging and/or device used for the protection, display, handling, and delivery of ophthalmic pharma products.
  • Performs assigned tasks under general supervision in support of approved projects
  • Executes engineering studies, conduct testing and data analysis under direction of senior OH team members. Receives technical guidance from senior OH staff on the design of experiments.
  • Applies general technical skills to complete assigned work and solves routine problems of limited scope.
  • Thoroughly and clearly documents experiments in laboratory notebook and assists in preparation of technical documents.
  • Drafts protocol and reports to document related activities
  • Drafts and routes standard operating procedures as required
  • Drives effective actions for compliance within the agreed timelines
  • Ensures continual quality system compliance by adherence to established and evolving QS requirements.
  • Communicates and collaborates with colleagues and with supervisor.
  • General use, set-up and upkeep of laboratory, including equipment/instrumentation


Key Requirements/ Minimum Qualifications:

  • Bachelors Degree or Equivalent + 4 years of directly related experience (or high school +8 yrs; Assoc.+6yrs; M.S.+0 yrs)
  • The ability fluently read, write and communicate in English.
  • Work efficiently and productively with other team members and external partners.
  • Adheres to clients guidelines for appropriate workplace behaviors and attitudes
  • Experience in medical device is preferred.
  • Familiarity with statistical analysis and software is preferred


About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities

ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

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