Summer Intern Process Engineer Manufacturing

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 Summer Intern will report directly to a Process Engineer and will be responsible for supporting the manufacturing operations team at the Watertown, MA site. They will support several projects focused on new process development, continuous improvement of internal manufacturing processes, and process qualification for vision-saving drug-device combination products.

This position is located at our Watertown, MA site and will begin on Monday, June 3rd and end on Friday, August 9th. 

Responsibilities

Primary responsibilities and projects to be completed include the following:

• Identify and implement process improvements for existing product lines to meet throughput increase objectives
• Author and execute validation protocols (IQ/OQ/PQ) for new and existing equipment
• Source manufacturing equipment, and commission new equipment supporting semi-automated and automated solutions
• Create or revise SOPs and Work Instructions for existing and new processes
• Initiate and execute process change controls, including updates to manufacturing batch record documentation
• Analyze development data and recommend new process development and/or changes to existing manufacturing processes
• Collect and summarize in-process manufacturing data to support trending and statistical process control

Qualifications

Primary skills and knowledge required include, but are not limited to the following:

• Interest in/exposure to the Drug-Device Combination Product Industry
• Excellent communication skills, both written and oral
• Proficiency in the MS Office suite
• Strong foundational engineering and analytical skills
• Familiarity with statistical data analysis
• Detail-oriented and well organized; strong willingness to learn
• Demonstrated ability to be a self-starter and work well on a team
• Working knowledge of current Good Manufacturing Practices (cGMP) and drug-device manufacture regulations, specifically FDA guidelines, is a bonus

Level of Education Required:

• Must be a student in a Bachelor’s degree program at an accredited college/university
• Undergraduate student with a minimum of Rising <Sophomore/Junior/Senior>

Preferred Field(s) of Study:

Mechanical, Biomedical, or Chemical Engineering preferred

Envision Your Future

With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics.

The collective power of our values influences everything we do, and everything we do for you.

• Success begins with our People
• Patients First
• Integrity
• Results-Driven
• Innovation
• Team Focus
• Diversity & Inclusion

EyePoint Pharmaceuticals is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.

#LI-Onsite