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Job Description

We are seeking a skilled consultant to support our client's Device Product & Process Development Team. The team designs, develops, and commercializes innovative intravitreal drug-device combination products to enable safe, effective, and targeted delivery of biologics to the retina and other ocular tissues. These products are critical to advancing treatment for ophthalmic conditions such as age-related macular degeneration, diabetic retinopathy, and retinal vein occlusion.

Key Responsibilities:

Collaborate with cross-functional teams (including ophthalmology clinical development, regulatory, quality, and device engineering) to support technical and engineering leads in developing and maintaining timelines for intravitreal combination product programs.

Track milestones, deliverables, and risks specific to intravitreal delivery systems, including preparation of dashboards and risk registers tailored to ophthalmic device development.

Support execution of strategic plans for assigned intravitreal projects, ensuring risk management plans are robust and aligned with ocular safety and usability standards.

Lead scenario planning to evaluate trade-offs in device design and provide updated timelines based on clinical and technical constraints.

Ensure accurate reporting of project data in systems used to manage ophthalmic device development, including cost, schedule, and resource planning.

Facilitate structured team meetings focused on intravitreal product development, issuing clear minutes and action items to internal and external stakeholders.

Integrate timelines from clinical, regulatory, and commercial teams with device development milestones, especially for ophthalmic trials and launch readiness.

Coordinate with external partners and suppliers to ensure availability of materials needed for intravitreal product development and scale-up.

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Skills and Requirements

5+ years in combination device development project management, including 3+ years in ophthalmic or intravitreal product development.

Strong understanding of intravitreal drug delivery systems, ocular anatomy, and device design controls.

Ability to harmonize complex and independent project plans into a succinct and comprehensive plan

Excellent communication and interpersonal skills, with proven ability to manage cross-functional teams and external partners.

Strong conflict resolution and consensus-building skills to align diverse stakeholders around intravitreal product goals.

Ability to work independently and lead task forces focused on ophthalmic device development.

Strategic thinking to align project details with broader ophthalmology portfolio and corporate objectives.

Demonstrated agility and creativity in solving challenges unique to intravitreal delivery

Proactive in raising issues and driving resolution in a regulated and patient-focused environment. PMP or equivalent