Senior Process Development Engineer

Posted Yesterday
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Ivyland, PA, USA
In-Office
Senior level
Biotech
The Role
Leads process development, validation, risk analysis, and continuous improvement for medical device manufacturing. Develops and validates stable production processes, conducts trials and DOE studies, evaluates materials and process changes, establishes acceptance criteria, and authors technical reports. Collaborates with Quality, R&D, engineers, and technicians while supporting manufacturing operations, implementing equipment safety protocols, and leading process improvement initiatives.
Summary Generated by Built In

LifeLens Technologies, Inc. is a medical device developer located in Ivyland, PA. We are pioneering innovative, next-generation treatment devices for personal health monitoring. 

We are seeking to hire a Senior Process Development Engineer. In this role, you will have the opportunity to work on cutting-edge technologies designed to revolutionize wearable health care. You have a collaborative mindset and a passion for developing new technology. You are detail-oriented and goal-driven. You are a capable problem solver with excellent organizational skills and superior verbal and written communication skills.

Your passion and drive will be rewarded with a competitive salary, benefits, and long-term growth opportunities.

This is a full-time, on-site position. 

Summary

The Senior Process Development Engineer is responsible for developing and validating processes to manufacture LifeLens products. This role participates in all phases of product development including research, design, and production. They will work with a team of engineers to ensure the smooth functioning of production lines; to develop new techniques; to modify existing designs; and to coordinate process improvement projects. They will have the technical knowledge and leadership skills to play a vital role in developing products that meet our customer’s needs.

Essential Functions

  • Lead process validation activities including authorship and completion of installation, operational, and performance qualification (IQ/OQ/PQ) protocols and reports. Evaluate process requirements and determine appropriate validation acceptance criteria.
  • Lead and document process risk analysis activities including implementation of statistical sampling plans and testing strategies to ensure process outputs meet product specifications.
  • Establish stable and capable processes meeting company manufacturing and quality goals.
  • Implement process development discipline and best practices.
  • Explore and develop novel processes as designs evolve.
  • Support daily manufacturing activities through process engineering development and continuous improvement projects.
  • Evaluate process changes and material/composition interactions.
  • Conduct process trials with appropriate protocols and documentation.
  • Implement safety protocols for manufacturing equipment.
  • Work with Quality and R&D in process development.
  • Conduct process DOEs and author process reports for studies
  • Other tasks as assigned

Competencies

  • Worked under ISO9001 and/or ISO13485 manufacturing standards.
  • Medical device manufacturing experience required.
  • Experience leading a team of engineers and technicians in a manufacturing environment.
  • Solid understanding of roll-to-roll manufacturing processes.
  • Process validation/verification and FMEA.
  • Experience with DOE, conducting experiments, and analyzing results using statistical analysis software.
  • Must be knowledgeable of polymer materials
  • Must be a versatile, self-starter who can manage several different aspects of the given project
  • Must be detail oriented
  • Must be functional with Microsoft Office, including Word, Power Point, and Excel

Required Experience and Education

  • Advanced degree in Polymer Science, Chemistry, Chemical Engineering or a related technical discipline preferred

Benefits

  • Health Insurance
  • Dental & Vision Insurance
  • Paid Time Off
  • 401(k)
  • Stock option incentive plan
  • FSA & dependent care

Skills Required

  • Medical device manufacturing experience
  • Experience working under ISO 9001 and/or ISO 13485 manufacturing standards
  • Experience leading engineers and technicians in a manufacturing environment
  • Strong understanding of roll-to-roll manufacturing processes
  • Experience with process validation and verification
  • Experience with FMEA
  • Experience conducting design of experiments and analyzing results using statistical analysis software
  • Knowledge of polymer materials
  • Advanced degree in Polymer Science, Chemistry, Chemical Engineering, or a related technical discipline
  • Proficiency with Microsoft Word, PowerPoint, and Excel
  • Strong problem-solving, organizational, communication, and project-management skills
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The Company
HQ: Ivyland, PA
77 Employees
Year Founded: 2014

What We Do

LifeLens was founded in 2014 by Dr. Robert Schwartz, Landy Toth, David Robins, and Dr. Robert Van Tassel. Its mission is to create simple, commercially viable technologies for high fidelity physiologic monitoring.

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