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Opportunity to join Graybug Vision, a clinical stage biopharmaceutical company focused on developing transformative medicines to treat diseases of the retina and optic nerve. Graybug’s lead product candidate, GB-102, a microparticle depot formulation of the pan-VEGF inhibitor targeting a six-month or longer dosing regimen, is in phase 2 clinical development for wet age-related macular degeneration. Two additional compounds are in pre-clinical development.

As the Senior Director, Human Resources, reporting to the Chief People Officer, you ensure that all human resources (HR) operations are carried on smoothly and effectively. You will be responsible for developing HR strategies and providing sound advice to senior management on all related subjects.

As an experienced professional with deep knowledge of all HR matters, you have a strategic mindset paired with strong operational skills to deliver results in alignment with our corporate business objectives.

The ideal candidate thrives working in a fast-paced, innovation-driven environment, and is flexible, pro-active, resourceful and efficient. Excellent interpersonal and leadership skills, as well as organization and execution skills are critical as well as the ability to handle complex issues and develop and implement relevant plans and programs.

Opportunity to join Graybug Vision, a clinical stage biopharmaceutical company focused on developing transformative medicines to treat diseases of the retina and optic nerve. Graybug’s lead product candidate, GB-102, a microparticle depot formulation of the pan-VEGF inhibitor targeting a six-month or longer dosing regimen, is in phase 2 clinical development for wet age-related macular degeneration. Two additional compounds are in pre-clinical development.

As the Senior Director, Quality Assurance, reporting to the Chief Operations Officer, you are an innovative leader with a mission to improve the standard of care in ophthalmology by working with external and internal experts on innovative approaches to improve disease management, reduce healthcare burdens and ultimately deliver better clinical outcomes.

The Clinical Development Medical Director will lead and provide medical strategic input for clinical program level activities (e.g. submission activities, clinical data review, safety updates, health authority responses, investigator brochure, briefing books etc.) for our clinical trials. The location for this job is flexible between our headquarters in Redwood City, CA, and our lab in Baltimore, MD.

Opportunity to join Graybug Vision, a clinical stage biopharmaceutical company focused on developing transformative medicines to treat diseases of the retina and optic nerve. Graybug’s lead product candidate, GB-102, a microparticle depot formulation of the pan-VEGF inhibitor targeting a six-month or longer dosing regimen, is in phase 2 clinical development for wet age-related macular degeneration. Two additional compounds are in pre-clinical development.

The Senior Analytical Chemist will play a key role in the development of lead products, the advancement of R&D programs, and preparation for commercialization. He/she will be responsible for developing and validating analytical methods for small-molecule APIs and formulations, transferring established methods to CROs/CMOs, and establishing GMP-compliant lab systems and procedures. Responsibilities also include collaborating with R&D team members to determine appropriate testing and specifications for lead compounds and formulations as well as providing analytical support and testing of ingredients, candidate compounds, and formulations for research, development, clinical, and commercial stages. Other duties of the job include working closely and collaboratively with business partners, consultants, company employees, external vendors, and suppliers to provide