More jobs:
Manufacturing Process Engineer
Job in
Gainesville, Alachua County, Florida, 32635, USA
Listed on 2026-02-28
Listing for:
Advita Ortho
Full Time
position Listed on 2026-02-28
Job specializations:
-
Engineering
Manufacturing Engineer, Process Engineer, Quality Engineering, Lean Manufacturing / Six Sigma -
Manufacturing / Production
Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma
Job Description & How to Apply Below
Manufacturing Process Engineer
Department: Manufacturing Engineering
Employment Type: Full Time
Location: Gainesville, FL
Reporting To: Sr. Director Operations and Engineering
DescriptionThis role is accountable for designing, stabilizing, and continuously improving end-to-end manufacturing process flow. The Manufacturing Process Engineer focuses on how work moves through the system — people, materials, information, and controls — to ensure predictable, compliant, and efficient production of orthopedic medical devices.
Key Responsibilities Process Design & Flow Optimization- Design and maintain end-to-end manufacturing process flows across operations, including handoffs between workstations, inspection points, and downstream processes.
- Analyze throughput, constraints, and work balance to improve Safety, Quality, Delivery, and Cost (SQDC) outcomes.
- Develop future-state process flows and lead implementation of changes in partnership with Operations and Quality.
- Develop, implement, and sustain Operator Standard Work (OSW) and process-level documentation that defines the expected method of work.
- Establish visual management and tiered performance metrics to enable daily management and rapid problem identification.
- Ensure process changes are effectively transferred to production through training alignment and documentation updates.
- Lead structured problem-solving activities for process-related issues using data-driven root cause analysis.
- Facilitate continuous improvement activities focused on flow, stability, and waste reduction rather than tooling optimization.
- Support corrective and preventive actions related to process deviations and nonconformances.
- Support execution of process and equipment qualification and validation activities (IQ/OQ/PQ) from a process-flow and risk perspective.
- Ensure manufacturing processes comply with the Quality System and applicable regulatory requirements.
- Maintain controlled process documentation through change management systems.
- Bachelor’s degree in Engineering (Manufacturing, Industrial, Biomedical, Mechanical, or related discipline) or equivalent experience.
- 1–3 years of experience in manufacturing, process engineering, industrial engineering, or operations.
- Experience in regulated industries (medical device, pharmaceutical, aerospace) preferred.
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