MDI Manufacturing Technician — 2nd Shift

Cipla; Fall River (MA); On-site; USD 62,000 - 83,000; Full time

Benefits offered by this job

401(k) matching

Health insurance (medical/dental/vison

PTO/paid time off

HSA/FSA

Job summary

InvaGen Pharmaceuticals, Inc. in Fall River, MA is seeking a Manufacturing Technical Associate for the 2nd shift to support Respiratory MDI production.

Responsibilities include operating and maintaining packaging lines, performing changeovers, and ensuring compliance with cGMP and safety standards. The ideal candidate will have 7+ years in pharmaceutical manufacturing, strong mechanical skills, and experience with documentation and SOPs.

Qualifications

• Bachelor’s degree in engineering, Industrial Technology, Pharmaceutical Sciences, Chemistry, Biology, Manufacturing Technology, or a related discipline.
• 7+ years of experience in pharmaceutical/manufacturing environments.
• Experience operating, setting up, troubleshooting, and minor repairs on automated manufacturing equipment.
• Experience performing equipment changeovers, startup activities, line clearances, and production documentation in a cGMP environment.

Responsibilities

• Work in pharmaceutical manufacturing settings including controlled environments for MDI production.
• Operate, set up, monitor, troubleshoot and adjust manufacturing equipment per BMRs and SOPs.
• Perform line setup, changeovers, and cleaning per approved procedures to ensure readiness.
• Document production and equipment data legibly and contemporaneously per cGMP.

Skills

Mechanical aptitude

Troubleshooting

Documentation

SOPs reading

Education

Bachelor’s degree in engineering / related field

Job description

InvaGen Pharmaceuticals, Inc. in Fall River, MA is seeking a Manufacturing Technical Associate for the 2nd shift to support Respiratory MDI production.

Responsibilities include operating and maintaining packaging lines, performing changeovers, and ensuring compliance with cGMP and safety standards. The ideal candidate will have 7+ years in pharmaceutical manufacturing, strong mechanical skills, and experience with documentation and SOPs.