Mechatronics Engineer

Mechatronics Engineer Lendex Technology Jacksonville, FL Job Details Contract $45 - $50 an hour 1 day ago Benefits Health insurance Paid time off Qualifications Supplier management GMP Microscope proficiency Bachelor's degree in engineering Bachelor's degree Decision making Vendor relationship management Design controls Manufacturing Project leadership Delegation Project stakeholder communication Cross-functional communication Full Job Description We are looking for a hands-on, technically strong Mechatronics Engineer to lead vendor-led development of cell therapy processing equipment for GMP manufacturing. This is a high-impact role where you will serve as the primary technical owner and bridge between internal cross-functional teams and external equipment suppliers — delivering robust, compliant, and scalable solutions that meet the demands of regulated biotech and pharma environments. If you thrive at the intersection of engineering rigor, project ownership, and quality-first thinking, this is your opportunity.

KEY RESPONSIBILITIES

Own the full lifecycle of vendor-led equipment development — scope, interfaces, acceptance criteria, and handoff to operations Lead design reviews, technical governance sessions, issue resolution, and change control processes Author and maintain User Requirement Specifications (URS) and Functional Requirement Specifications (FRS) with full traceability to V&V Oversee Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), commissioning, and qualification in partnership with Quality and CQV teams Ensure GMP compliance, data integrity, and controlled documentation across all vendor deliverables Drive cross-functional alignment and proactively manage technical risk across all project phases Translate complex process needs into clear engineering requirements that guide design decisions

REQUIRED QUALIFICATIONS

Bachelor's degree in Mechanical, Electrical, Automation, Mechatronics, or a related engineering field 10+ years of experience delivering complex equipment in regulated manufacturing environments (medical device, pharma, or biotech) Proven track record managing external vendors or system integrators through full project lifecycles Strong working knowledge of GMP principles, design control, and equipment qualification (IQ/OQ/PQ) Demonstrated experience with bespoke, non-standard automation equipment in a regulated environment Excellent communication skills — structured, clear, and effective with technical and non-technical stakeholders Strong leadership and decision-making capabilities; comfortable delegating and driving execution Highly organized, with effective planning habits and the ability to manage multiple workstreams Adaptable and composed when navigating ambiguity and evolving project requirements

PREFERRED / NICE-TO-HAVE

Hands-on experience with cell therapy processing equipment or biologics manufacturing Background in automation/controls integration and robotics Experience supporting equipment startup and stabilization in a GMP setting Prior employment with a 3rd-party automation vendor, CDMO, or equipment/technology supplier in a design or automation capacity Design for Manufacture (DFM) and Design for Automation (DFA) expertise

WHY JOIN US

Work at the cutting edge of cell therapy manufacturing technology High-ownership role with direct impact on product quality and patient outcomes Collaborative, cross-functional team environment with strong engineering culture Competitive compensation and benefits package

Pay:

$45.00 - $50.00 per hour

Benefits:

Health insurance Paid time off

Work Location:

In person