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MDI Packaging Operator - 2nd​/3rd Shift; On-Site

Job in Fall River, Bristol County, Massachusetts, 02720, USA
Listing for: Cipla
Full Time position
Listed on 2026-05-26
Job specializations:
  • Manufacturing / Production
    Packaging Engineer, Manufacturing Production, Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 20 - 22 USD Hourly USD 20.00 22.00 HOUR
Job Description & How to Apply Below
Position: MDI Packaging Operator - 2nd/3rd Shift (On-Site)

Packaging Machine Operator - 2nd & 3rd shift available

Posting Date:
May 22, 2026

Country:
United states

State:
Massachusetts

Location:

Fall River

Location: Fall River, MA (On-site – Local Candidates Only)
Shifts available: 2nd shift: 3:00pm - 11:30pm or 3rd shift 11:30pm - 7:30am (flex based on production needs)
Pay Range: $20 – $22/hour
Classification: Full-Time

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 MDI Packaging Line Operations
  • 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
  • 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

  • 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)

EEO Statement

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

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