GMP Manufacturing Associate II: Skilled Ops & Trainer

EyePoint; Watertown (MA); On-site; USD 44,372 - 57,528; Full time

Job summary

EyePoint is seeking a Manufacturing Associate II in Watertown, MA to execute manufacturing, assembly, labeling, packaging, and inspection for combination products in a GMP environment. The role requires proficiency in GMP documentation and equipment operation.

You will train junior associates, support CAPAs, deviations, and process improvements, and work with QA, QC, Engineering, and Supply Chain to maintain inspection readiness and product quality.

Qualifications

• High school diploma or equivalent required.
• Experience in regulated manufacturing environment (2–5 years) preferred.
• Strong GMP/GDP/documentation and equipment operation skills.
• Ability to work with limited supervision and train others.

Responsibilities

• Perform manufacturing, assembly, labeling, packaging, and inspection per approved procedures and schedules.
• Independently execute manufacturing operations ensuring GMP/GDP compliance.
• Complete batch records and production documentation accurately.
• Set up, operate, troubleshoot, and perform basic maintenance on manufacturing equipment.
• Conduct in-process inspections and verify product quality throughout manufacturing processes.
• Assist with material handling such as staging, issuing, and reconciliation of materials.
• Identify deviations and safety risks; support CAPAs and root-cause analyses.
• Train junior personnel and participate in process improvements.

Skills

GMP documentation

Equipment operation

Attention to detail

Problem solving

Training others

Independent work

PPE gowning

Lifting 25 lbs

Education

High School Diploma or GED

Associate degree or relevant coursework

Tools

Electronic quality management systems

Job description

EyePoint is seeking a Manufacturing Associate II in Watertown, MA to execute manufacturing, assembly, labeling, packaging, and inspection for combination products in a GMP environment. The role requires proficiency in GMP documentation and equipment operation.

You will train junior associates, support CAPAs, deviations, and process improvements, and work with QA, QC, Engineering, and Supply Chain to maintain inspection readiness and product quality.