What are the responsibilities and job description for the Product Development Engineer position at LifeLens Technologies Inc.?
LifeLens Technologies, Inc. is a medical device developer located in beautiful Bucks County, PA. We are pioneering innovative, next-generation treatment devices for personal health monitoring.
We are seeking to hire a Product Development Engineer. The ideal candidate is a collaborative, detail-oriented, and goal-driven self-starter. You excel at developing concepts, resolving technical issues, and supporting others in a dynamic environment. You will participate in the development of electro-chemical, medical devices. You will play an important role in all phases of device development and designing for manufacturability. Your role includes the identification and evaluation of design options, the definition of product/performance specifications, design verification/validation activities, the creation of technical data; and the generation of documentation for the product’s Design History File. 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.
Responsibilities:
- Generate product concepts/prototypes/designs to meet customer needs.
- Produce design prototypes and conduct performance evaluations to drive design selection and design freeze.
- Support risk management activities such as hazard analysis, dFMEA, pFMEA, etc.
- Collaborate with cross-functional teams (Mfg., QA, RA, etc) to optimize overall design solutions.
- Define and document design output documentation including specifications and drawings.
- Develop and execute design verification and design validation testing strategies.
- Write testing protocols and reports in support of design verification and design validation.
- Communicate relevant information regarding project status, design details, and deliverable content to peer collaborators and management stakeholders.
- Provide technical support to cross-functional team members including technical review of marketing collateral, providing product information for regulatory submissions, etc.
Qualifications:
- Bachelor’s Degree in Engineering or related discipline (e.g. Physical or Life Science) with an advanced degree preferred.
- Minimum 5 years of experience in medical device product development utilizing Design Controls and stage-gate development processes for Class II or III devices.
- Demonstrated ability to bring products from concept through regulatory clearance and to market.
- Experience in electro-mechanical devices, including software/firmware, is strongly preferred.
- Demonstrated ability in applying DOE and other experimental techniques when evaluating new or changes to existing products and processes, and materials/compositions
- Experience in prototyping, 3D printing, mechanical testing, and material characterization.
- Define and document engineering specifications and process documentation used in the manufacturing process.
- Working knowledge of and experience in applying Design Controls and international standards (e.g. CFR820, ISO 13485, ISO 14971, IEC 60601, GMP, etc.).
- Experience in installation qualifications of manufacturing equipment and associated processes (IQ/OQ/PQ).
- Must be able to communicate effectively, both verbally and written. Comfortable presenting information to team members and stakeholders.
- Ability to travel 5-10%
Benefits:
- Health Insurance
- Dental & Vision Insurance
- Paid Time Off
