Manufacturing Engineer II Jobs 2026 at Aequor Houston Texas
Aequor is hiring a Manufacturing Engineer II contractor for their Houston, Texas location with estimated hourly compensation between $35 and $45. This position focuses on validating and implementing manufacturing processes for ophthalmic medical devices used in cataract and vitroretinal surgeries, combining engineering expertise with quality control and statistical analysis.
The role suits engineers with at least one year of medical device manufacturing experience who understand validation protocols, statistical process control, and CAD design. If you hold a Bachelor’s degree in Engineering or Biomedical Engineering and want hands-on involvement developing manufacturing processes for life-changing medical devices, this contract opportunity offers meaningful technical work in the medical device sector.
Job Overview
Medical device manufacturing requires rigorous validation ensuring equipment and processes consistently produce safe, effective products meeting regulatory standards. The Manufacturing Engineer II leads validation activities including Installation Qualification, Operational Qualification, and Performance Qualification protocols supporting automated and semi-automated production equipment.
Your responsibilities span the complete manufacturing engineering lifecycle from designing and developing processes through validation, implementation, and ongoing optimization. Working with ophthalmic devices helping restore vision to cataract and vitroretinal surgery patients adds meaningful purpose beyond abstract engineering work.
The position balances strategic process development with hands-on equipment support, statistical analysis ensuring process capability, and creating documentation maintaining compliance with medical device regulations. You’ll apply Lean and Six Sigma methodologies optimizing production efficiency while maintaining the quality standards critical for medical device safety.
Available Positions
Manufacturing Engineer II Contractor
The engineer leads, executes, documents, and manages validation activities necessary for introducing or revising production equipment and processes. Designing, developing, validating, and implementing manufacturing processes for ophthalmic medical devices requires understanding both engineering principles and regulatory requirements governing medical device production.
Supporting production process optimization through Lean and Six Sigma methodologies reduces waste and variation. Applying Statistical Process Control concepts ensures processes transferred to production remain monitored and controlled maintaining equipment in validated states compliant with quality standards.
Continuous statistical analysis of Critical Quality Attributes and process capability indicators confirms existing processes meet product specifications. Hands-on equipment support before, during, and after production release means troubleshooting technical issues and ensuring reliable operation.
Designing fixtures and creating CAD drawings in SolidWorks supports production operations with tools enabling efficient manufacturing. Creating standard work procedures documents best practices ensuring consistent high-quality output. Maintaining project schedules and timelines keeps process improvements and equipment introductions on track.
Eligibility Criteria
Aequor seeks candidates combining engineering education with medical device manufacturing experience and specific technical competencies.
Educational Background
Bachelor of Science in Engineering or Biomedical Engineering represents the minimum educational requirement. Master of Science in Engineering or Biomedical Engineering is preferred, providing deeper technical foundation though isn’t mandatory for strong candidates with relevant experience.
Professional Experience
One or more years of professional experience specifically in medical device manufacturing environments demonstrates your familiarity with regulatory requirements, validation protocols, and quality systems governing this highly regulated industry. Generic manufacturing experience without medical device exposure won’t satisfy this requirement.
Technical Skills
Medical device validation experience with IQ/OQ/PQ protocols is essential. Statistical Process Control capabilities and statistical analysis skills including Design of Experiments, ANOVA, Gage R&R, T-Tests, and Process Capability analysis enable data-driven process development.
MiniTab statistical software proficiency supports analysis work while SolidWorks CAD design experience enables fixture development. Technical writing skills document processes and validation protocols while public speaking abilities support presentations and training.
Age Requirements
No age restrictions apply. Aequor evaluates candidates based on engineering qualifications and relevant experience.
How to Apply
Applications are managed through a life sciences recruitment platform.
Visit the official posting at HireLifeScience careers portal where the Manufacturing Engineer II position details and application interface appear.
Review the complete job description carefully, confirming your medical device manufacturing experience and validation knowledge align with stated requirements.
Prepare your resume emphasizing your engineering education, medical device manufacturing background, specific validation projects you’ve led, statistical analysis experience, and CAD design capabilities with concrete examples.
Complete the online application accurately and submit your materials demonstrating your qualifications for this specialized medical device engineering role.
Monitor email for responses from Aequor’s recruitment team regarding interview scheduling or technical assessments.
Important Instructions
This is a contractor position rather than direct permanent employment, meaning different employment terms regarding benefits, duration, and job security compared to full-time staff roles. Understanding this distinction helps set appropriate expectations.
Medical device manufacturing experience is specifically required, not just general manufacturing backgrounds. Ophthalmic device experience provides particular advantage though isn’t mandatory if you have strong medical device validation foundations from other device types.
The hands-on nature means you’ll physically work with manufacturing equipment troubleshooting issues and supporting production, not purely desk-based engineering analysis.
Deadline
The posting does not specify an application deadline, suggesting Aequor reviews qualified candidates continuously for this contract engineering position. Applying promptly improves your chances for consideration.
Additional Career Resources
While exploring manufacturing engineering opportunities, consider browsing senior executive assistant jobs 2026 for diverse career opportunities across different professional fields.
Common Questions
Can engineers from other manufacturing industries apply without medical device experience?
The posting specifically requires “1+ year of professional experience in a Medical Device Manufacturing Environment,” making this mandatory rather than preferred. Medical device manufacturing involves unique regulatory requirements, validation protocols, and quality standards differing significantly from other industries. Engineers from automotive, aerospace, or consumer products manufacturing lack the FDA compliance, design control, and validation experience essential for this role despite strong general engineering backgrounds.
What does IQ/OQ/PQ validation actually involve?
Installation Qualification verifies equipment is installed correctly per specifications. Operational Qualification confirms equipment operates as intended across its operating ranges. Performance Qualification demonstrates the equipment consistently produces results meeting predetermined specifications under actual production conditions. These staged validation protocols prove equipment and processes reliably produce safe, effective medical devices meeting regulatory requirements, forming the foundation of quality assurance in medical device manufacturing.
Is this contractor position eligible for benefits like health insurance?
Contractor positions typically don’t include employer-provided benefits like health insurance, paid time off, or retirement contributions offered to direct employees. Contractors usually receive higher hourly rates compensating for self-funding benefits. The $35-45/hour range reflects contractor compensation. Clarifying exact employment terms including contract duration, extension possibilities, and any benefits provided through staffing agencies during interviews provides complete understanding of the employment arrangement.
Final Thoughts
Aequor’s Manufacturing Engineer II contract position in Houston offers meaningful engineering work developing and validating manufacturing processes for ophthalmic medical devices. The estimated $35-45/hour compensation reflects the specialized medical device validation expertise required.
If you hold a B.S. in Engineering or Biomedical Engineering, bring at least one year of medical device manufacturing experience, possess validation protocol knowledge, demonstrate statistical analysis capabilities, have SolidWorks proficiency, and want to contribute to manufacturing processes producing vision-restoring surgical devices, submit your application through HireLifeScience emphasizing your medical device validation accomplishments and hands-on engineering capabilities.
