Ocular Health R&D Engineer

BioPharma Consulting JAD Group; Fort Worth (TX); In loco; USD 55.000 - 75.000; Tempo pieno

Descrizione del lavoro

BioPharma Consulting JAD Group seeks a testing professional to perform standardized lab tests, analyze data, and document results for ophthalmic pharma packaging and devices. You will work under supervision, draft protocols, and assist in design and method improvements.

Requirements include a Bachelor’s degree or equivalent with 2+ years related experience (Mechanical Eng preferred), strong English communication, and hands-on testing competency. Contract position with potential extension.

Competenze

• Bachelor’s degree or equivalent + 2 years directly related experience (Mechanical Eng preferred)
• 2+ years directly related experience with a bachelor’s degree, or 0+ with a Master’s
• Fluent read/write/communication in English
• Hands-on technical testing competency
• Equipment validation experience (IQ/OQ)
• Technical documentation and problem solving abilities

Mansioni

• Perform standardized tests per SOP and test methods with accuracy and repeatability
• Document experiments thoroughly in lab notebooks and prepare technical documents
• Draft and route standard operating procedures as required
• Collaborate with engineers to improve designs and test methods
• Support development of packaging/devices for ophthalmic pharma products
• Handle data collection, analysis, and reporting of test results
• Execute engineering studies and tests under supervision from senior staff

Conoscenze

Hands-on technical testing

Data analysis & documentation

Problem solving & root cause analysis

English communication

Formazione

Bachelor’s degree or equivalent (Mechanical preferred)

Strumenti

Lab equipment IQ/OQ validation

Descrizione del lavoro

• Hands-on and Technical Testing Competency o Ability to perform standardized tests per SOP and test methods.


• Understands protocols, data collection, and proper use of lab equipment. o Focused on accuracy, repeatability, and compliance o Perform equipment validation (IQ/OQ, etc.)


• Data Analysis & Documentation o 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 supervisors.


• General use, set-up and upkeep of laboratory, including equipment/instrumentation

• 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


• Years of experience: 2+ years of directly related experience with a Bachelor's degree, or +0 years of experience with a Master's degree


• The ability fluently read, write and communicate in English.


• Hands-on Technical Testing Competency


• Equipment Validation Experience (IQ/OQ)


• Technical Documentation, Problem Solving and Root Cause Analysis

• Schedule: 40 hours per week, Monday - Friday.


• Contract position with posible extension