GMP Manufacturing Associate II – Process & Quality

BioSpace; Northbridge (MA); On-site; USD 44,372 - 57,528; Full time

Job summary

EyePoint is seeking a Manufacturing Associate II to perform manufacturing, assembly, labeling, packaging, and inspection of combination products in a GMP-regulated environment. You will execute operations, complete batch records, set up and troubleshoot equipment, and participate in process improvements to support quality, efficiency, and compliance goals.

The role requires 2–5 years in a regulated manufacturing setting, strong attention to detail, and ability to work with minimal supervision

Qualifications

• Requires 2–5 years in a regulated manufacturing environment.

Responsibilities

• Perform manufacturing, assembly, labeling, packaging, and inspection in accordance with procedures and schedules.
• Independently execute operations while maintaining GMP, GDP, and company standards.
• Complete batch records, logbooks, and production documentation accurately and contemporaneously.
• Set up, operate, troubleshoot, and perform basic maintenance on manufacturing equipment.
• Assist with material handling including staging, issuing, and reconciliation of materials and finished goods.
• Identify and raise process deviations, equipment issues, quality concerns, and safety risks.
• Support deviation investigations, CAPAs, and root cause analyses as needed.
• Train and mentor junior personnel on procedures, equipment operation, and GMP expectations.

Skills

GMP compliance

Batch record execution

Equipment operation

Attention to detail

Training others

Problem solving

Education

High School Diploma or GED

Associate degree or coursework in related field

Tools

eQMS

Job description

EyePoint is seeking a Manufacturing Associate II to perform manufacturing, assembly, labeling, packaging, and inspection of combination products in a GMP-regulated environment. You will execute operations, complete batch records, set up and troubleshoot equipment, and participate in process improvements to support quality, efficiency, and compliance goals.

The role requires 2–5 years in a regulated manufacturing setting, strong attention to detail, and ability to work with minimal supervision