Primary Manufacturing and Process Engineer

Virtual Incision; Lincoln (NE); Sur place; USD 75 000 - 105 000; Plein temps

Avantages offerts par ce poste

Medical/Dental/Vision

Disability/Life Insurance

401(k)

Flexible working hours

PTO

Résumé du poste

Virtual Incision is seeking a Manufacturing & Process Engineer to join the Operations team onsite in Lincoln, NE. You will design, prototype, test, and implement manufacturing processes for miniature robotic systems, driving quality, yield, and efficiency improvements.

You will partner with Engineering, Quality, Supply Chain and Operations to support production, new product introductions, and design transfers in a fast-paced, highly regulated setting.

Qualifications

• Bachelor degree in engineering or related technical discipline.
• 1–4 years of manufacturing/process engineering experience.
• Proficient in reading engineering drawings and specs.
• Strong problem-solving and analytical skills.
• Experience with statistics and process improvement methodologies.
• Excellent communication and cross-functional collaboration.

Responsabilités

• Develop and implement manufacturing processes, tools, and equipment.
• Support design transfer and manufacturing readiness for new products.
• Create and validate production process controls and validations.
• Perform IQ/OQ/PQ qualification activities and documentation.
• Analyze processes using DMAIC, Cp/Cpk, and SPC.
• Drive process improvements to improve quality and efficiency.
• Collaborate with Engineering, Quality, Supply Chain and Ops.
• Work with suppliers for equipment and tooling development.
• Support risk assessments including FMEA.
• Ensure compliance with QMS and regulatory standards.

Connaissances

Problem solving

Statistical analysis

Reading drawings

Communication

Collaboration

Independent work

Formation

Bachelor of Science in Engineering

Outils

SolidWorks

CAD software

Statistical tools

Description du poste

Job Title: Primary Manufacturing & Process Engineer Date: October 14,2026

Department: Operations Location: Onsite, Lincoln,NE

Virtual Incision is advancing robotic-assisted surgery with a focus on expanding access to minimally invasive care. We are a growing medical technology company where experienced leaders have the opportunity to make a meaningful and visibleimpact.

Why VirtualIncision:

• Work on innovative robotic surgical technology with the potential to improve patientcare.
• Join an experienced, collaborative team focused on clinical excellence and disciplined execution.
• Take meaningful ownership of products and programs in a hands-on environment.
• Work in a culture that values technical rigor, practical problem-solving, andteamwork.
• Competitive benefits including medical, dental, vision, disability, and life insurance, 401(k), flexible working hours, andPTO.

Job Summary:

As a Manufacturing & Process Engineer at Virtual Incision, you will be part of a team that designs, prototypes, tests, and produces innovative miniature surgical robots and related equipment that advance the field of surgery. This role is responsible for developing, validating, implementing, and continuously improving manufacturing processes that support the production of Virtual Incision's robotic surgicalsystems.

The Manufacturing & Process Engineer partners closely with Engineering, Quality, Supply Chain, and Operations to support production, new product introductions, design transfers, process improvements, and manufacturing scale-up activities. The successful candidate will be a hands-on problem solver who thrives in a fast-paced, highly regulated environment and is passionate about improving product quality, manufacturing efficiency, and operational performance.

Responsibilities:

• Develop and implement manufacturing processes, tools, fixtures, equipment, and facility infrastructure to support productionoperations.
• Support design transfer activities and ensure manufacturing readiness for new products and productchanges.
• Develop and implement production process controls, including risk analysis activities, facility monitoring, process validations, and test method validations.
• Perform qualification activities and maintain associated documentation, including IQ/OQ/PQ protocols and reports whererequired.
• Analyze and improve manufacturing processes, components, and products using statistical and continuous improvement methodologies such as DMAIC, Gage R&R, Cp, Cpk, andSPC.
• Identify and implement process improvements that improve product quality, manufacturing yield, throughput, cycle time, and operational efficiency.
• Troubleshoot manufacturing issues and drive root cause investigations to implement effective correctiveactions.
• Develop, maintain, and improve manufacturing process documentation, including assembly procedures, inspection procedures, work instructions, and product specifications.
• Collaborate with Engineering, Quality, Supply Chain, and Operations teams to ensure successful implementation of manufacturing and process improvements.
• Work with suppliers and vendors to support equipment procurement, tooling development, process improvements, and ongoing manufacturing support.
• Support the development and implementation of manufacturing test systems for complex electromechanical products.
• Participate in manufacturing risk assessments, including process FMEAactivities.
• Ensure compliance with company policies, Quality Management System requirements, and applicable regulatorystandards.
• Support internal and external audits asneeded.
• Participate in continuous improvement initiatives that enhance manufacturing performance, product quality, and operational scalability.
• Perform other duties asassigned.

Qualifications:

Required

• Bachelor of Science degree in Engineering or a related technicaldiscipline.
• 1–4 years of manufacturing engineering, process engineering, production support, or related engineering experience.
• Strong problem-solving and analyticalskills.
• Experience with statistical analysis and process improvement methodologies.
• Ability to read and interpret engineering drawings, technical documentation, and manufacturing specifications.
• Strong communication and collaboration skills.
• Ability to work independently and effectively within cross-functional teams.

Preferred

• Mechanical design and CAD software experience, with SolidWorks experiencepreferred.
• Experience building and implementing manufacturing test systems for complex electromechanical assemblies.
• Experience within the medical device industry or another regulated manufacturing environment.
• Knowledge of FDA Quality System Regulations and ISO13485.
• Experience facilitating manufacturing risk assessments using pFMEA methodologies.
• Experience sourcing, qualifying, and implementing manufacturing equipment.
• Experience collaborating with suppliers and contract manufacturers.
• Experience supporting robotic, electromechanical, or advanced technologyproducts.
• Lean Manufacturing and/or Six Sigmaexperience.

Status: Exempt

Virtual Incision is an Equal Opportunity Employer and values diversity in itsworkforce.

Disclosure and Important Safety Information

The MIRA Surgical System is intended for prescription use only. Patients should talk to their doctor to decide if surgery with a MIRA Surgical System is right for them. Patients and doctors should review all available information on nonsurgical and surgical options and associated risks in order to make an informeddecision.

Serious complications may occur in any surgery, including minimally invasive surgery with the MIRA Surgical System, up to and including death. Serious risks include, but are not limited to, injury to tissues and organs, and/or conversion to other surgical techniques which could result in a longer operative time and/or complications.

For important safety information, including surgical risks and considerations, please also refer to www.virtualincision.com/safety-information . For the product’s indications for use, risks, full cautions, and warnings, please refer to the associated user manual(s).

Individual outcomes may depend on a number of factors, including but not limited to patient characteristics, disease characteristics, surgeon, and/or hospitalexperience.

MIRA Surgical System PrecautionStatement

The demonstration of safety and effectiveness for the representative specific procedures was based on evaluation of the MIRA Surgical System as a surgical device and did not include evaluation of outcomes related to the treatment of cancer (overall survival, disease-free survival, local recurrence) or treatment of the patient’s underlying disease/condition. Device usage in all surgical procedures should be guided by the clinical judgment of an adequately trainedsurgeon.

Contact

Virtual Incision
1501 Old CheneyRd
Lincoln, NE68512