Be Seen and Heard at EyePoint Pharmaceuticals

At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for:

• developing therapeutics to improve the lives of patients with serious retinal disease
• advancing best-in-class proprietary drug delivery technologies
• innovative pipeline of sustained delivery products

We See You.

Your wellbeing

Your professional worth

Your future at EyePoint

EyePoint offers robust total rewards in a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected.

Based in Watertown, MA and reporting to the Director, Formulation Development, this position is responsible for the formulation and process development of innovative drug delivery platform/drug product device combination for peptides/small molecules. The individual we are seeking will have a well-established track record of successfully developing peptide/small molecule formulations and processes from concept to late-stage across multiple modalities. In addition, the successful candidate will have demonstrated capabilities in working cross-functionally with internal stake holders and effectively managing development activities at external vendors.

The position holder needs to have a broad range of knowledge across the various functional areas in pharmaceutical development, understand manufacturing technologies, people and organizational structures. The role enables high performing internal and external development teams to successfully develop, commercialize, and file products.

This position is based in Watertown, MA and offers flexible work hours.

Primary responsibilities include, but are not limited to, the following:

Individual responsibilities

• Leads the development of novel extended-release of small molecule drug product formulations and drug-device combinations.
• Ensures drug product development activities and timelines are aligned with project goals
• Designs and executes experiments to evaluate formulation for performance, stability, and manufacturability.
• Manages drug product development activities at external vendors with applicable regulatory and quality requirements including providing input into the design of experiments, managing timelines, reviewing technical and batch manufacturing documentation and ensuring that EyePoint's business needs are met by the vendor
• Identify and implement improvements to existing EyePoint technologies.
• Prepares pharmaceutical development reports and other technical documentation required for regulatory submissions including authoring, review and approval of requisite sections of the IND, CTA, IMPD, and other filings.
• Works collaboratively across internal stakeholder functions such as Project Management, Pre-Clinical and Device development, Manufacturing Operations, Clinical and Regulatory to meet program goals, including representation on CMC development teams
• Ensures that all work is conducted in accordance with applicable policies and procedures, CGMP and regulatory standards and guidelines.
• Maintains an understanding of current laws & regulations applicable to the pharmaceutical/biotechnology industry.