(Senior) Facilities Engineer

EyePoint Pharmaceuticals, Inc. • Watertown, MA

5d • Onsite

About The Position

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:
focus on science and innovation, we aim to offer a lifetime of clearer vision
commitment to developing and commercializing innovative therapeutics to improve the lives of patients with serious retinal diseases
Delivery of innovative therapeutics to protect vision, specializing in sustained-release treatments for serious retinal diseases.
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 position will report to the Sr. Director, Facilities & Engineering and be located at our Watertown, MA site at first, after 6-9 months, will transition to our Northbridge, MA facility.

Requirements

• Experience in life sciences, medical devices, or regulated industry.
• Exceptional project management skills, the ability to track and manage complex processes, projects, and budgets.
• Analytical skills to analyze process steps and seek optimization.
• Mechanical skills to oversee the use of equipment used in production.
• Experience with commissioning and qualification of equipment and utilities in a GMP facility.
• Familiar with engineering software like Bluebeam, AutoCAD and/or SOLIDWORKS.
• Experience owning and supporting management of Quality Systems such as Deviations, Change Controls, and CAPA.
• Proactive and creative problem solver who is highly organized and detail oriented.
• Excellent listening and communication skills - both written and verbal.
• Demonstrated adaptability, resiliency, and ability to thrive in fast-paced organization.
• Proven ability to influence and drive organizational success.
• A demonstrated track record of successful cross-functional leadership, collaboration, and relationship building.
• Bachelor of Science, preferably in Chemical or Mechanical Engineering
• A minimum of 5-8 years of experience in medical device and/or pharmaceuticals industry

Responsibilities

• Lead engineering aspects of projects through all phases of engineering projects including design, equipment procurement, construction, installation, startup, commissioning, qualification, and validation.
• Lead or collaborate for project planning and implementation activities to reduce operating costs and increase efficiency.
• Drive results by owning and completing complex projects to implement new manufacturing and utility equipment to support new manufacturing processes and increase operational efficiency.
• Maintain Engineering Turnover Packages, including specifications, component lists, operating manuals, and drawings for GMP equipment and update as required.
• Coordinate and communicate engineering related activities with equipment vendors and internal stakeholders.
• Provide direct engineering support and Subject Matter Expertise for process and utility equipment in use at all Eyepoint facilities as needed.
• Write and execute project execution plans, test protocols, validation protocols, and final reports.
• Work in cross-functional teams and coordinate activities with various departments for implementing new equipment and operational improvements.
• Provide support to Facilities Operations with troubleshooting equipment issues, reviewing maintenance plans/activities, reviewing and revising SOP’s and improving efficiencies within Facilities and Engineering.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level