Packaging Machine Operator

Packaging Machine Operator

Location: Onsite in Fall River, MA Shifts available: 2nd shift: 3:00pm - 11:30pm or 3rd shift 11:30pm - 7:30am (flex based on production needs) Classification: Full-Time Reports To: Packaging Supervisor Required: Automated packaging line experience in a pharmaceutical company or from a food or cosmetic company. Power the Final Step in Life-Changing Inhalation Medicines Join a team where precision packaging isn't just a process—it's the final quality checkpoint before critical respiratory therapies reach patients. As a Packaging Operator supporting Metered Dose Inhalers (MDIs), you'll work hands-on with highly specialized aerosol drug delivery systems, ensuring every inhaler meets strict regulatory, safety, and performance standards. This role goes beyond basic packaging—you'll be part of a high-speed, high-precision manufacturing environment where accuracy, compliance, and teamwork drive success.

What You'll Do

• Operate and monitor automated and semi-automated packaging lines for MDI inhalation products
• Ensure consistent dose delivery system integrity through accurate assembly, labeling, and packaging
• Drive maximum output with minimal rejects, maintaining strict quality thresholds

Equipment & Technical Execution

• Understand and operate mechanical systems, conveyor lines, and control panels supporting MDI packaging
• Perform line setup, changeovers (batch-to-batch / product-to-product), and cleaning activities
• Execute routine preventative maintenance and basic troubleshooting to keep operations running smoothly

Quality, Compliance & cGMP Excellence

• Maintain full adherence to cGMP regulations, SOPs, and data integrity practices
• Perform and document line clearance before each batch start
• Ensure correct status labeling and documentation at every stage of the packaging process
• Support calibration checks and documentation accuracy to maintain audit readiness

Problem Solving & Continuous Improvement

• Identify packaging defects or deviations and support corrective actions in real-time
• Escalate issues promptly and collaborate cross-functionally to resolve them
• Contribute to maintaining 100% compliance during all operational hours

What Makes You a Strong Candidate

Basic Qualifications

• High school diploma or equivalent (required)
• 1+ year experience in pharmaceutical or regulated packaging/manufacturing (preferred)
• Comfortable working fully onsite in a structured, SOP-driven environment

Technical & Functional Skills

• Hands-on experience with packaging equipment, mechanical systems, or production lines
• Basic understanding of cGMP, FDA regulations, and documentation practices
• Ability to follow detailed written and verbal instructions with precision
• Strong math, accuracy, and attention to detail

Work Style & Mindset

• Team-oriented but able to work independently in a fast-paced environment
• Strong accountability for quality, compliance, and safety
• Willingness to support extended hours or schedule adjustments when production demands increase

Work Environment & Safety

• Operate in a regulated pharmaceutical manufacturing setting focused on MDI production
• Work around packaging machinery, aerosol components, and pharmaceutical materials
• Required PPE includes: lab coats, gloves, safety glasses, respiratory protection (APR/SAR systems depending on area)
• Strict adherence to OSHA, EHS, and company safety protocols is mandatory

Physical Requirements

• Frequent standing, bending, and movement throughout shift
• Lift/carry: up to 25 lbs regularly, up to 50 lbs occasionally (assisted if needed)
• Ability to safely operate within a manufacturing line environment

Why This Role Stands Out

Specialized MDI Experience

– Gain exposure to one of the most technically complex pharmaceutical dosage forms

Hands-On Impact

– Play a direct role in delivering respiratory therapies patients depend on

Career Growth

– Build in-demand experience in pharma manufacturing & inhalation systems

Quality-Driven Culture

– Work in an environment where precision and compliance are everything

Important Notes

• Local applicants only (not open to global/internal transfer requests)
• No remote work – fully onsite role
• Candidates must be authorized to work in the U.S. (no sponsorship available)