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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:
- preventing blindness through vision-saving medications
- delivering best-in-class proprietary pharmaceutical technologies
- transforming ocular drug delivery
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.
Regional Medical Director/Sr. MSL/MSL-West Coast
This is a field-based position requiring interested candidates to live in the Western part of the country.
This position is supporting the West Region, and reporting to our Vice President, Market Strategy. You will serve as a key scientific resource for clinical trial investigators, key opinion leaders, and medical meetings.
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:
- preventing blindness through vision-saving medications
- delivering best-in-class proprietary pharmaceutical technologies
- transforming ocular drug delivery
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.
Regional Medical Director/Sr. MSL/MSL-East Coast
This is a field-based position requiring interested candidates to live in the Eastern part of the country.
This position is supporting the East Region, and reporting to our Vice President, Market Strategy. You will serve as a key scientific resource for clinical trial investigators, key opinion leaders, and medical meetings.
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:
- preventing blindness through vision-saving medications
- delivering best-in-class proprietary pharmaceutical technologies
- transforming ocular drug delivery
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.
An exciting opportunity is available for a Sr. Scientist II to join the in vivo ocularpharmacology team at EyePoint Pharmaceuticals. We are seeking a highly skilled, self-motivated and talented scientist to lead and execute in vivo preclinical research and biomarker discovery activities supporting portfolio progression. The successful candidate will work collaboratively across functions within clinical, regulatory and R&D to think strategically, lead and execute preclinical research to generate decisional data packages in support of our ocular drug discovery and development projects.
The ideal candidate will bring extensive knowledge of a wide variety of in vivo and ex vivo research methodologies and analyses and a track record of successful scientific impact in the biotechnology or pharmaceutical industry with demonstrated experience in leading and managing scientific projects from conceptualization through execution and analysis. This includes setting project goals, designing and executing on experimental strategies, managing timelines, thinking creatively of opportunities to leverage cutting-edge technologies, and coordinating with cross-functional teams to achieve milestones and deliverables.
This position is located at our Watertown, MA site.
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:
- preventing blindness through vision-saving medications
- delivering best-in-class proprietary pharmaceutical technologies
- transforming ocular drug delivery
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.
We are seeking a Vice President, Head of Biometrics and will be responsible for creating and implementing both the near-term and long-term strategic direction for EyePoint clinical program. This includes all areas and phases of development while ensuring systems, capabilities, and resources are in place to optimize the design/ conduct and analysis/interpretation of clinical trials and clinical data, respectively. This person will report to the Chief Medical Officer.
This position is fully remote. The base annual salary range for this position is $355 up to $395.
This person should have a positive attitude and be adaptable to a dynamic startup environment.
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:
- preventing blindness through vision-saving medications
- delivering best-in-class proprietary pharmaceutical technologies
- transforming ocular drug delivery
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.
The Associate Director/Senior Manager of Financial Planning and Analysis will report to the Head of Financial Planning and Analysis and Financial Systems. This role will provide financial support and partner with leaders to manage EyePoint’s overall FP&A processes to optimize month-end close activities, internal management reporting, planning, and ad-hoc analysis. This role will be responsible for generating business insights and analysis along with managing the budgeting and forecasting processes, working collaboratively across the organization.
This position is located at our Watertown, MA site. We offer a hybrid work schedule.
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:
- preventing blindness through vision-saving medications
- delivering best-in-class proprietary pharmaceutical technologies
- transforming ocular drug delivery
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.
We are seeking to attract an exceptional Senior Director of External Reporting and Technical Accounting to join our growing Finance organization. Reporting to the VP, Finance & Head of Accounting, the Sr. Director of External Reporting and Technical Accounting plays a crucial role in leading EyePoint's external financial reporting processes, ensuring compliance with SEC regulations, and upholding the integrity of our financial reporting. This role will interact closely with members of the finance, corporate development and legal teams, along with independent auditors to ensure accurate reporting and full compliance with all external standards. This individual will also have the opportunity to assist in special projects and process improvements. We expect successful candidates to have a sense of ownership in their career development and a commitment to excellence.
This position is located at our Watertown, MA site. We offer a hybrid work schedule.
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:
- preventing blindness through vision-saving medications
- delivering best-in-class proprietary pharmaceutical technologies
- transforming ocular drug delivery
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.
This person will report directly to the quality control manager and will be responsible for all aspects of quality control in respect to clinical trial materials and commercial products as required. This position provides production support for analytical quality control testing of pharmaceutical raw materials and drug products.
The individual will work in the QC laboratory located in Watertown, MA with potential to relocate to the Northbridge, MA QC laboratory when appropriate. The individual will ensure that all products are tested,in accordance with all applicable GxP regulations and guidelines (e.g. 21CFR Parts 11, 210/211, 820, (USP/EP/JP), ICH Guidelines), as well as internal company procedures.
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:
- preventing blindness through vision-saving medications
- delivering best-in-class proprietary pharmaceutical technologies
- transforming ocular drug delivery
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.
This person will report directly to the quality control manager and will be responsible for all aspects of quality control in respect to clinical trial materials and commercial products as required. This position provides production support for analytical quality control testing of pharmaceutical raw materials and drug products.
The individual will work in the QC laboratory located in Watertown, MA with potential to relocate to the Northbridge, MA QC laboratory when appropriate. The individual will ensure that all products are tested, in accordance with all applicable GxP regulations and guidelines (e.g. 21CFR Parts 11, 210/211, 820, (USP/EP/JP), ICH Guidelines), as well as internal company procedures.
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.
EyePoint is seeking an experienced Sr. CMC Program Manager to manage multiple projects at various stages of the drug development lifecycle. This position will report directly to the Sr Director, Portfolio Management.
The Senior CMC Program Manager is responsible project related activities including project plans, dashboards, timelines, budgets, decisions, critical path items, and milestones for the Watertown site. In this position, the Senior Program Manager will work across all departments to ensure successful progress towards EyePoint’s goal to help improve the lives of patients with serious eye disorders.
This position is located at our Watertown, MA facility. We offer a hybrid work schedule.
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.
This person will report directly to the VP, Quality and be responsible for the Clinical Quality activities including responsible for creating/monitoring and maintaining phase appropriate ICH levels of compliance in all of our CROs, as well as within EyePoint. The scope of this role includes working with Clinical Development / Operations and CROs on the review / approval of clinical activities and associated documentation.
This position is located at our Watertown, MA facility. We offer a hybrid work schedule.
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.
Eyepoint Pharmaceuticals is seeking a talented formulator to join our Development group in Watertown MA. Our department works closely with Operations and Regulatory affairs department to formulate and manufacture innovative ocular formulations.
Ideal candidate should have a strong background in advanced physical chemistry, the use of polymers in Ocular Delivery. The selected scientist will design and conduct experiments to develop ocular formulations as well as designing and conducting robust analytical experiments for the designed formulations. The qualified candidate will interact with other departments, CMOs, participate in cross functional teams, contribute to the product development plans, and authorship of publications and pertinent sections of regulatory submissions, as needed.
Additionally, the candidate must be a strong team player with excellent communication skills working in a complex cross-functional environment. The candidate must be able to work independently and take initiative by providing input on multiple projects. The candidate must be able to think critically, intellectually curious, and shows resilience and courage to resolve complex formulation and manufacturing problems.
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 leading late-stage ocular drug product development, from Phase III through early commercialization. The individual we are seeking will have a strong laboratory presence and well-established technical excellence in drug product development in, authoring technical report, and overseeing the tech transfer at scale. 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.
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.
Reporting directly to the Senior Director CMC of Regulatory Affairs, the (Associate) Director of Regulatory CMC will be responsible for the development of regulatory CMC submissions. In this position, you will be responsible for driving the development of optimal CMC regulatory strategies and the preparation and submission of high-quality CMC sections of INDs, IMPDs, CTAs, and original marketing applications (NDAs/BLAs/MAAs), in close collaboration with our in-house CMC and Quality teams, contract manufacturing organizations, external experts, collaborators, strategic partners, and health authorities.
This position is in Watertown, MA. We offer a hybrid work schedule.
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.
The Senior Manager, Regulatory submissions will be working closely with Regulatory Project Lead(s) develop regulatory submission plans and regulatory affairs systems and tools to further the company’s goals. You will be responsible for timely planning and coordination of regulatory submissions. Create and maintain submission content plans (trackers), ensure administrative forms and documents are current and new guidance is disseminated within the Regulatory Operations group. Final review and sign off of eCTD documents for publishing to health authorities. You will also be expected to remain current in regulatory guidance in the US and select ex-US countries, procedures and practices. You will provide guidance and some oversight to the publishing and submission teams.
This role will report to the Senior Director, Regulatory Affairs. This position will be remote and be required to come to our Watertown, MA on an as needed basis.
The salary range for this position is from $145,000 up to $180,000 based upon experience level.
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.
Our team is growing, and we are currently seeking an experienced solid-state characterization scientist to provide support for the Analytical Development Department. Reporting to the Director of Analytical Development, the ideal candidate will be a collaborative team player with experience in a regulated analytical testing environment. Our department works closely with Formulations, Operations, Regulatory Affairs, and Quality control to formulate and manufacture innovative ocular formulations.
This position is based in Watertown, MA.