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Our Vision

To save sight through transformative science.

Our Mission

We create practical solutions to treat vision-threatening diseases that improve quality of life and care for all involved.

Our Purpose

To help people live fuller lives through healthier vision.

Our Beliefs
  • No patient should have to settle for good enough.
  • There are no limits to what we can achieve together.
  • We are the best when the challenges are big.
  • We embrace diversity to enable our success.
“We believe that no patient should have to settle for good enough. We are curious and focused on finding practical solutions that make a real difference.”
Fred Guerard, PharmD, CEO
Our Employee Benefits
We offer a comprehensive benefits package in addition to competitive compensation:
  • Medical Coverage (Options for HMO, PPO)
  • Dental and Vision Coverage
  • Life and AD&D Coverage
  • Long-Term Disability Coverage
  • Short-Term Disability Coverage
  • Flexible Spending Account (FSA)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Additional Life and AD&D Coverage
  • Bonus Compensation
  • Paid Time Off
  • Paid Holidays
Benefits subject to change
We're Hiring

Senior Director, Quality Assurance

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.

Vice President, Medical Affairs

Incredible opportunity to develop and implement the Medical Affairs strategy for 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 Vice President of Medical Affairs, reporting to the Chief Medical 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.

Laboratory Technician

The Laboratory Technician will be an integral part of the Research and CMC Department.  They will be responsible for the support of the CMC and Research Team to produce R&D to GMP batches.  The ideal candidate will clean, setup, operate, and breakdown manufacturing equipment according to established protocols. They will be responsible for organizing and keeping inventory, cleaning laboratory supplies, handling and storing waste, and communicating with management on the needs of the laboratory. The ideal candidate will be expected to know general laboratory practices and be able work independently in the laboratory. A degree in science or engineering related fields is a required and previous experience is a plus.

Research Associate

The Research Associate will be an integral part of the Research and Development Department. The successful candidate will be expected to perform research studies and prepare scientific reports to support product development activities. Previous experience in formulation development, micro- and/or nano-particles or other drug delivery systems is strongly preferred.Previous experience in process development/manufacturing is a plus.  A B.S. or M.S. in chemical engineering, biomedical engineering, pharmacology and pharmaceutical sciences, chemistry, materials science, or other related fields is required.

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