Principal Device Development Engineer - CONTRACT

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Not verified last checked Jun 13, 2026

Salary

Not verified not verified - source not recorded; timestamp not recorded

401(k) match

Listed Source: EMPLR_CONTRIB_INCOME_AMT. source Last checked Jun 13, 2026.

Was this benefit information wrong? Tell us.

Schedule

Shift type

Not verified

Weekend work

Not verified

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Principal Device Development Engineer - CONTRACT Bedford, MA Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space. Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity. Position Summary : The Principal Medical Device Engineer is a highly experienced and strategic leader in coordinating the ideation, assessment, and development of drug delivery technologies and medical devices. This role focuses on long-term technical vision, innovation, and team leadership while also remaining hands-on with complex technical challenges. The engineer is responsible for managing projects, ensuring compliance, and contributing to the overall success of the company's medical device portfolio. Principal Duties and Responsibilities include the following : - Leads the design and development of new or improved medical devices, ensuring they meet regulatory requirements, quality standards, and user needs. - Ensure high-quality science, technology, and deliverables while ensuring compliance with global regulatory and quality requirements to support development and lifecycle management of Ocular drug delivery systems. - Oversees design verification testing

Read the full description at www.ocutx.com. FewerJobs shows a source-linked preview and links to the original posting.