Senior Materials Engineer - Med Device, GMP & Scale-Up

LifeLens Technologies, LLC.; Ivyland (PA); On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Health Insurance

Dental & Vision Insurance

Paid Time Off

401(k)

Stock option incentive plan

FSA & dependent care

Job summary

LifeLens Technologies, Inc. in Ivyland, PA seeks a Senior Materials Engineer to lead development and application of materials for SAC technology, including formulations for manufacturing scale-up and process validation, with emphasis on FDA compliance and GMP.

Responsibilities include strategic direction in formulation, prototype materials, data-driven process improvements, supplier qualification, and cross-functional collaboration to scale production for healthcare devices.

Qualifications

• Master’s or PhD in Polymer Science, Chemistry, or a related technical discipline.
• 5+ years in material development for healthcare or medical devices.
• Experience with FDA, QSR, cGMP, ISO13485.
• Strong data analysis and problem-solving skills.
• Excellent communication and teamwork in cross-functional settings.

Responsibilities

• Lead development and application of materials and formulations for SAC technology.
• Research available materials and evaluate impact on product design.
• Develop formulations and processes to support manufacturing scale-up and process validation.
• Lead material selection, testing, and failure analysis; prepare specifications and reports.
• Ensure GMP/cGMP alignment and FDA-compliant in-house manufacturing plans.

Skills

Polymer chemistry

Soft materials

Composite development

Quality engineering concepts

FDA compliance knowledge

MS Office proficiency

Analytical skills

Communication skills

Education

Master’s degree or PhD in Polymer Science, Chemistry or related discipline

Job description

LifeLens Technologies, Inc. in Ivyland, PA seeks a Senior Materials Engineer to lead development and application of materials for SAC technology, including formulations for manufacturing scale-up and process validation, with emphasis on FDA compliance and GMP.

Responsibilities include strategic direction in formulation, prototype materials, data-driven process improvements, supplier qualification, and cross-functional collaboration to scale production for healthcare devices.