Maintenance Reliability Engineer

TEXAS

Chemicals

Perm/Full-Time

Equipment Maintenance; Reliability Engineering

SUMMARY

Collaborate with Plant Departments and Corporate Engineering to develop, document and implement specific and effective measures to improve plant asset management strategies, procedures, work process, and effectiveness of the plant reliability programs as measured by Unit / Plant Reliability KPI’s. Promote a culture of continuous improvement in Equipment Reliability.

REQUIREMENTS

BS in Mechanical Engineering preferred. 10+ years of Equipment Maintenance/Reliability experience in a Chemical Plant. Problem-solving techniques like PDCA or 5 Why

Maintenance Planner

TEXAS

Chemicals

Perm/Full-Time

Plant Maintenance; Supervision

SUMMARY

Work directly with the Maintenance Supervisors to prepare Daily, Weekly, Monthly and Annual Maintenance Work Schedules to provide direct support to the production, Co-Gen, quality and shipping departments performing all routine running maintenance, preventive and predictive maintenance and production unit turnarounds.

REQUIREMENTS

4+ years in plant maintenance. Experience with Preventive Maintenance, Predictive Maintenance, RCM / TPM processes and other rotating equipment reliability programs.

Manufacturing Engineer

WISCONSIN

Medical Devices

Perm/Full-Time

Process Engineering; Manufacturing Engineering

SUMMARY

Lead/support customer complaint investigations and internal non-conformance. Lead manufacturing quality investigations and assist with improvements. Monitor process inspection and audits. Develop documentation on process capabilities. 

REQUIREMENTS

3+ years' experience in a related process/manufacturing role in a medical device environment.

Materials Process Engineer

WISCONSIN

Medical Devices

Perm/Full-Time

Ceramic Engineering; Process Engineering

SUMMARY

Select and develop ceramic materials and process technology. Works with cross-functional teams to execute assignments. Assess industry trends and new opportunities. Assists with technical issues regarding materials.

REQUIREMENTS

3+ years' experience in a materials process engineering role in a medical device manufacturing environment. Knowledge of materials analysis techniques and industrial statistics desired.

Sr. Staff Quality Engineer

CALIFORNIA

Medical Devices

Perm/Full-Time

Quality Systems; Quality Assurance

SUMMARY

Develop, apply, revise, and maintain quality standards. Design and implement methods and procedures. Write protocols and coordinate work for employees. Perform design reviews and assessments. 

REQUIREMENTS

3+ years & PhD OR 10+ years & bachelor degree. Medical device manufacturing experience. Skilled using Minitab.

Polymer Process Engineer

CALIFORNIA

Medical Devices

Perm/Full-Time

Process Engineering; Polymer Engineering

SUMMARY

Collaborate to continually improve manufacturing processes. Set up, operate, and troubleshoot molding equipment. Design and perform DOE and other studies. 

REQUIREMENTS

4+ years' experience in a process improvement/engineering role in a medical device manufacturing environment.

Process Development Engineer

CALIFORNIA

Medical Devices

Perm/Full-Time

Catheter Development; R&D

SUMMARY

Develop and optimize process parameters for manufacturing. Evaluate specifications and decide on needed equipment to support product line. Train technicians, operators, and engineers in assembly techniques, inspections methods, and documentation. 

REQUIREMENTS

5+ years of hands-on experience with a variety of catheter production equipment, such as: hot boxes, die-bonders, braiders, coil winders, laminators, ovens, UV adhesive light welders, laser welders, and others. Strong understanding of materials typical to catheter production: Pebax, Nylon, Polyurethanes, PEEK, PTFE, FEP, CA and UV adhesives, Stainless steel, NiTi, etc. Strong Solidworks skills.

Textile Technician

RHODE ISLAND

Medical Devices

Perm/Full-Time

Textile Engineering

SUMMARY

Support textile engineering efforts with operation of Comez machines and other looms or knitters.

REQUIREMENTS

3+ years' experience operating looms or knitters. Medical device manufacturing experience.

Process Development Engineer

TEXAS

Medical Devices

Perm/Full-Time

Catheter Development; R&D

SUMMARY

Develop and optimize process parameters for manufacturing. Evaluate specifications and decide on needed equipment to support product line. Train technicians, operators, and engineers in assembly techniques, inspections methods, and documentation. 

REQUIREMENTS

5+ years of hands-on experience with a variety of catheter production equipment, such as: hot boxes, die-bonders, braiders, coil winders, laminators, ovens, UV adhesive light welders, laser welders, and others. Strong understanding of materials typical to catheter production: Pebax, Nylon, Polyurethanes, PEEK, PTFE, FEP, CA and UV adhesives, Stainless steel, NiTi, etc. Strong Solidworks skills.

Textile Engineer

RHODE ISLAND

Medical Devices

Perm/Full-Time

Textile Engineering; Product Development; Process Development

SUMMARY

Design and develop prototype medical textile based structures and processes to demonstrate feasibility for meeting customer needs. Develops products based on customer needs and specifications.

REQUIREMENTS

12+ years' developing textile solution for new products with focus on process development and validation related activities.

Metrology Development Technician

RHODE ISLAND

Medical Devices

Perm/Full-Time

Optical Metrology

SUMMARY

Develop processes and specify needed tools. Responsible for method development, calibration, needed equipment, measurement development, laboratory auditing, root cause and Gage R&R analysis for optical metrology.

REQUIREMENTS

Experience using MicroVu and other optical demnsional metrology systems. Experience in preparing laboratory documentation.

Quality Engineer

WISCONSON

Medical Devices

Perm/Full-Time

Quality Systems

SUMMARY

Use metals/machining and quality systems experience to lead quality department.

REQUIREMENTS

Hands-on experience with metal machining. ISO certified.

Technical Superintendent

TEXAS

Chemicals

Perm/Full-Time

Project Engineering; Plant Maintenance

SUMMARY

Manage all Plant Projects from conception and design through Construction and Commissioning.

REQUIREMENTS

5+ years' of Maintenance or Technical Management

Business Development Coordinator

Virtual/Remote

Recruiting

Perm/Full-Time

Inside Sales; Business Development; Medical Device Manufacturing

SUMMARY

Connect and engage with company leads to establish and cultivate professional partnerships by focusing on business development and inside sales objectives.

REQUIREMENTS

1+ years' experience with outbound/cold calling. Must be a US Citizen or Permanent Resident. Must be physically located in the Eastern or Central Timezone. Must have reliable and secure access to a computer and internet during 8AM to 5PM EST M-F.

Process Development Engineer

CALIFORNIA

Medical Devices

Perm/Full-Time

Catheter Development; R&D

SUMMARY

Develop and optimize process parameters for manufacturing. Evaluate specifications and decide on needed equipment to support product line. Train technicians, operators, and engineers in assembly techniques, inspections methods, and documentation. 

REQUIREMENTS

5+ years of hands-on experience with a variety of catheter production equipment, such as: hot boxes, die-bonders, braiders, coil winders, laminators, ovens, UV adhesive light welders, laser welders, and others. Strong understanding of materials typical to catheter production: Pebax, Nylon, Polyurethanes, PEEK, PTFE, FEP, CA and UV adhesives, Stainless steel, NiTi, etc. Strong Solidworks skills.

Sr. Electrical Engineer

VIRGINA

Medical Devices

Perm/Full-Time

Embedded Software

SUMMARY

Design Embedded System electronics and software for electrical / electronic Medical Devices. Work with NPD project teams. Develop specifications for components and assemblies. Build and test prototypes. Write test protocols and reports.

REQUIREMENTS

Engineering degree. 10+ years' experience technical design and debug of analog and digital controls and embedded software applications within a highly regulated manufacturing environment.

Project Manager

CALIFORNIA

Medical Devices

Perm/Full-Time

Project Management

SUMMARY

Define and manage project scope across the product development life cycle. Lead teams through a systematic stage-gate product development process. Responsible for project planning, budget, tracking, scheduling, and risk management.

REQUIREMENTS

5+ years' in medical device manufacturing. 2+ years' of regulated project management experience.

Regulatory Affairs Manager

CALIFORNIA

Medical Devices

Perm/Full-Time

Regulatory Affairs; Compliance

SUMMARY

Manage audits, inspections, and recalls. Develop strategies and solutions with available resources. Advise others on legal/RA matters.

REQUIREMENTS

10+ years' of quality/regulatory experience in a medical device manufacturing environment.