EyePoint · 16 hours ago
Manufacturing Engineer II/III
Northbridge, MA
Full-time
Onsite
Mid, Senior Level
$85K/yr - $129K/yr
3+ years expEyePoint is an ophthalmology company committed to improving the lives of patients with serious retinal diseases through innovative therapeutics. They are seeking a motivated Manufacturing Engineer II/III responsible for process sustaining and improvement in manufacturing operations, requiring collaboration across various departments and external vendors.
BiotechnologyHealth CareMedicalPharmaceutical
Responsibilities
Ability to identify and lead engineering related projects to continuously review and revise processes in production to enhance quality, yield, and efficiency
Author and execute equipment commissioning and qualification protocols and reports
Apply lean manufacturing methodologies to reduce costs and increase efficiency
Oversee production operations and troubleshoot technical issues in cleanroom environments
Coordinate and communicate engineering related activities with product vendors and suppliers
Support the design, development, and optimization of processes, including upstream and downstream operations
Troubleshoot process-related issues and lead quality investigations and implementation of corrective actions
Create, customize and implement tooling and fixturing to increase efficiency and product quality in manufacturing
Generate and maintain process documentation, including standard operating procedures, work instructions, and batch records
Work in cross-functional teams and work with other departments to implement changes
Serve as subject matter expert from functional area
Ensure compliance with GMP and regulatory standards
Qualification
Required
Strong mathematical and statistical abilities to gather data and calculate optimal output
Proficiency with equipment, facility, and process validations
Analytical skills to analyze process steps and seek optimization
Mechanical skills to oversee the use of equipment used in production
Familiarity with engineering software like AutoCAD and SOLIDWORKS
Proficient in Microsoft Applications (Word, Excel, PowerPoint, Visio)
Strong commitment to compliance and ethical standards
Proficiency with cGMP regulations and quality management systems
Proactive and creative problem solver who is highly organized and detail oriented
Strong listening and communication skills -both written and verbal
Ability to contribute to development of project timelines
Ability to complete tasks within agreed timelines and resources through manager guidance
Adaptability, resiliency, and ability to thrive in fast paced organization
Ability to influence and drive organizational success
Exceptional project management skills; proficiency in tracking processes and projects
A demonstrated willingness to collaborate cross-functionally and build relationships on projects of diverse scope
Ability to lift up to 25 pounds on occasion
Bachelor of Science
A minimum of 3-5 years of experience in the medical device and/or pharmaceuticals industry
Preferred
Experience in life sciences, medical devices, or regulated industry preferred
Preferred Field of Study: Engineering
Company
EyePoint
EyePoint (Nasdaq: EYPT) is a clinical-stage biopharmaceutical company committed to developing and commercializing innovative therapeutics to improve the lives of people with serious retinal diseases.
51-200 employees
H1B Sponsorship
EyePoint has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2024 (4)
2021 (1)
Funding
Current Stage
Public CompanyTotal Funding
$803.8MKey Investors
Silicon Valley BankOcumension TherapeuticsEssex Woodlands Healthcare Partners
2025-10-14Post Ipo Equity· $150M
2023-12-05Post Ipo Equity· $215.9M
2022-03-09Post Ipo Debt· $45M
Leadership Team
Paul Ashton
President, Chief Executive Officer and a Director
D
Diane Shay
Vice President of Quality
Recent News
Longevity.Technology
2026-01-16
Clinical Trials Arena
2026-01-11
2025-12-17
Company data provided by crunchbase