Respiratory Manufacturing Technician (2nd/3rd Shift)

Merck & Co.; Fall River (MA); On-site; USD 34,000 - 55,000; Full time

Benefits offered by this job

Weekly pay

Health insurance

401k with matching

Bonuses

Paid time off

Job summary

Merck & Co. is hiring a Manufacturing Technical Associate for 2nd or 3rd shift in Fall River, MA. The role focuses on operating and maintaining MDI manufacturing equipment in a highly regulated respiratory pharmaceutical environment.

Responsibilities include equipment setup, troubleshooting, changeovers, and ensuring production documentation complies with cGMP. Requires a bachelor’s in a related field and 7+ years in pharma manufacturing. Competitive benefits and overtime opportunities offered.

Qualifications

• Bachelor's degree in engineering or related field as listed.
• Minimum seven (7+) years of experience in pharmaceutical manufacturing or related regulated environments.
• Demonstrated 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

• Operate, set up, adjust, monitor and troubleshoot MDI manufacturing and packaging equipment.
• Perform routine manufacturing activities while achieving production, quality, and safety targets.
• Prepare rooms and equipment for manufacturing operations and verify calibration status.
• Maintain line clearance documentation and ensure compliance with cGMP requirements.
• Assist with equipment qualification, validation, and commissioning activities.

Skills

Machine operation

Education

Bachelor's degree in engineering, Industrial Technology, Pharmaceutical Sciences, Chemistry, Biology, Manufacturing Technology, or a related scientific or technical discipline

Job description

Merck & Co. is hiring a Manufacturing Technical Associate for 2nd or 3rd shift in Fall River, MA. The role focuses on operating and maintaining MDI manufacturing equipment in a highly regulated respiratory pharmaceutical environment.

Responsibilities include equipment setup, troubleshooting, changeovers, and ensuring production documentation complies with cGMP. Requires a bachelor’s in a related field and 7+ years in pharma manufacturing. Competitive benefits and overtime opportunities offered.