Ocular Health R&D Engineer

Aequor; Fort Worth (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Aequor in Fort Worth, TX is seeking a hands-on QA engineer for equipment validation and testing support in ophthalmic pharma packaging projects. You will perform IQ/OQ, write protocols, and analyze data under supervision.

We value 2+ years directly related experience with a Bachelor’s degree (or a Master’s with 0 years), strong documentation, problem solving, and collaboration with engineers to improve test methods and ensure regulatory compliance.

Qualifications

• Hands-on testing per SOP and methods.
• Analyze test results; identify trends or failures; summarize findings.
• Draft and maintain protocol and test reports; ensure documentation.
• Conduct engineering studies, testing, and data analysis under supervision.
• Drive compliance with QS requirements and assist in investigations.

Responsibilities

• Perform standardized tests per SOP and methods.
• Analyze results, identify trends and summarize findings.
• Draft protocols and reports; maintain documentation.
• Execute engineering studies and data analysis under supervision.
• Ensure quality system compliance with QS requirements.
• Collaborate with engineers and supervisors.

Skills

Technical testing

IQ/OQ validation

Data analysis

Root cause analysis

Documentation

Education

Bachelor's degree or equivalent

Mechanical Engineering major

Job description

Description: Top 3 must haves:
oHands-on Technical Testing Competency
oEquipment Validation Experience (IQ/OQ)
oTechnical Documentation, Problem Solving and Root Cause Analysis

Schedule: 40 hours per week, Monday - Friday.
Years of experience: 2+ years of directly related experience with a Bachelor's degree, or +0 years of experience with a Master's degree

Job Description:

• Hands-on and Technical Testing Competency o Ability to perform standardized tests per SOP and test methods. o Understands protocols, data collection, and proper use of lab equipment. o Focused on accuracy, repeatability, and compliance o Perform equipment validation (IQ/OQ, etc.) o Prior experience working with *** is strongly preferred.
• Data Analysis & Documentation o Capable of analyzing test results, identifying trends or failures, and summarizing findings clearly. o Writes structured test protocol, reports and maintains documentation aligned with quality and regulatory requirements
• Problem Solving & Root Cause Analysis o Can identify potential issues in performance and support investigations (e.g., basic CAPA input, troubleshooting test failures). o 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 supervisors.
• General use, set-up and upkeep of laboratory, including equipment/instrumentation

Key Requirements/ Minimum Qualifications:
• Bachelor's Degree or Equivalent + 2 years of directly related experience (or high school +8 yrs; Assoc.+6yrs; M.S.+0 yrs), Mechanical Engineering major is desired
• The ability fluently read, write and communicate in English.
• Work efficiently and productively with other team members and external partners.
• Adheres to ***'s guidelines for appropriate workplace behaviors and attitudes
• Prior experience working with *** is strongly

Custom Fields:
Name: Worker Time Type
Value: Full Time

Name: Workspace
Value: None

Name: Invoice Type
Value: USA-ARL-Staffing-USD

Name: System Access Required
Value: Yes

Name: Badge ID Required
Value: Yes

Name: Remote Worker
Value: No

Name: Supervisory Org
Value: OH Device Packaging(James Yin)-60003120

Name: Work Desk Phone Number Required
Value: Yes