Manufacturing Associate II

Manufacturing & Operations at EyePoint ensures the safe, compliant, and reliable production of innovative therapies for patients with serious retinal diseases. This team oversees end-to-end manufacturing, supply chain, and facilities with a strong focus on regulatory compliance, patient safety, and product integrity. Manufacturing & Operations strives to maintain rigorous standards and efficient processes with the goal of delivering safe, high-quality therapies to patients.

The Manufacturing Associate II is responsible for executing manufacturing, assembly, packaging, inspection, and related production activities for combination products in a GMP-regulated environment. This role requires demonstrated proficiency in manufacturing operations, GMP documentation, and equipment operation. The Manufacturing Associate II serves as a fully trained operator who can work with minimal supervision, support process improvements, assist with training of junior associates, and contribute to achieving production, quality, and compliance objectives.

• Perform manufacturing, assembly, labeling, packaging, and inspection, activities in accordance with approved procedures and production schedules.
• Independently execute manufacturing operations while ensuring compliance with GMP, GDP, and company standards.
• Complete batch records, logbooks, and other production documentation accurately and contemporaneously.
• Set up, operate, troubleshoot, and perform basic maintenance on manufacturing equipment.
• Conduct in-process inspections and verify product quality throughout manufacturing operations.
• Perform line clearances, room preparation, product changeovers, and equipment setup activities.
• Assist with material handling activities, including staging, issuing, and reconciliation of in-process materials and finished goods.
• Identify and elevate process deviations, equipment issues, quality concerns, and safety risks.
• Support deviation investigations, nonconformance activities, corrective and preventive actions (CAPAs), and root cause analyses.
• Participate in process validation, equipment qualification, and manufacturing engineering activities as required.
• Train and mentor junior personnel on procedures, equipment operation, documentation practices, and GMP expectations.
• Support continuous improvement initiatives focused on quality, efficiency, productivity, and compliance.
• Collaborate effectively with Quality Assurance, Quality Control, Engineering, Supply Chain, and other functional teams.
• Maintain production areas and equipment in a state of inspection readiness.
• Comply with all company safety policies, GMP regulations, and training requirements.

• Working knowledge of cGMP regulations, Good Documentation Practices (GDP), and quality system requirements.
• Proficiency in manufacturing documentation and batch record execution.
• Ability to operate and troubleshoot manufacturing and packaging equipment.
• Strong attention to detail and commitment to product quality.
• Ability to identify process issues and recommend practical solutions.
• Effective organizational and problem-solving skills.
• Strong verbal and written communication skills.
• Basic proficiency with electronic quality management systems preferred.
• Ability to train others and effectively transfer knowledge.
• Demonstrated ability to work independently with limited supervision.
• Ability to lift up to 25lbs.
• Ability to wear personal protective equipment (PPE), including cleanroom gowning
• Ability to stand, walk, bend, reach, and perform repetitive motions for extended periods.
• This position requires an eye exam

• 2-5 years of experience in a regulated manufacturing environment.
• Experience in medical device, pharmaceutical, biotechnology, or combination product manufacturing required.
• Experience operating production equipment and documenting manufacturing activities in a GMP environment preferred.

• High School Diploma or GED required.
• Associate degree, technical certification, or coursework in manufacturing, engineering, life sciences, or a related discipline preferred.

EyePoint is committed to fair and equitable compensation practices. The salary offer is commensurate with EyePoint's compensation philosophy and considers factors including but not limited to education, training, experience, market conditions, criticality of the role and internal equity.

The target salary range for this position is listed below:

Salary Range: $32.21 - $41.76 USD

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.

We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning,…