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Packaging Manager

Job in Fall River, Bristol County, Massachusetts, 02720, USA
Listing for: Pharmaceutical Manufacturing
Full Time, Per diem position
Listed on 2026-01-20
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Packaging Engineer, Production Manager, Pharmaceutical Manufacturing
Job Description & How to Apply Below

Job Title:
Packaging Manager – Inhalation / MDI (Pharmaceutical Manufacturing)

Location:
Fall River, Massachusetts, USA (Onsite)

Work Schedule: General: 8:30 AM – 5:00 PM (May vary based on business needs; shift flexibility required)

Employment Type: Full-Time | Exempt (Professional)

Salary Range: (Based on Experience) (Relocation support may be available)

Position Overview

We are seeking an experienced Packaging Manager – Inhalation/MDI to lead and manage pharmaceutical packaging operations in a cGMP-regulated manufacturing environment
. This role is critical in ensuring safe, compliant, and on-time packaging of Metered Dose Inhaler (MDI) products
, while driving operational excellence, team development, and continuous improvement.

This is a hands-on people manager role
, not a desk-based position.

Key Responsibilities
  • Plan, monitor, and control daily packaging activities to meet production targets, quality standards, and timelines
  • Review planned vs. actual production and adjust schedules as required
  • Ensure availability of packaging materials, components, consumables, and spare parts across all shifts
  • Drive execution of new product introductions and technology transfers through gap analysis
  • Optimize utilization of packaging equipment, consumables, and manpower
  • Ensure all packaging activities comply with cGMP, safety, and regulatory requirements
  • Review in-process controls and packaging documentation to ensure right-first-time execution
  • Lead and support investigations including deviations, OOS, OOT, complaints, and CAPAs
  • Prepare, review, and maintain SOPs, BMRs, APQRs, validation, and qualification documents
  • Support internal, external, and regulatory audits (including USFDA inspections)
  • Coordinate with Engineering and Maintenance for preventive maintenance and breakdown resolution
  • Monitor OEE / OOE data and implement PDCA-based improvements
  • Drive packaging excellence initiatives to improve yield, reduce downtime, and minimize losses
  • Identify bottlenecks and develop capacity utilization plans
  • Lead, train, and manage packaging teams across multiple shifts (15 direct / ~45 total staff)
  • Ensure adequate staffing, shift planning, and effective manpower utilization
  • Train teams on SOPs, GMP, safety, and new processes
  • Promote a strong safety culture; ensure PPE compliance and safe work practices
  • Bachelor’s degree in Pharmaceutical Manufacturing, Industrial Engineering, or related discipline preferred
  • 5–9 years of pharmaceutical packaging experience in a cGMP environment
  • Minimum 3+ years in a supervisory or managerial role
  • Hands-on experience with MDI (Inhalation) packaging lines is required
  • Direct exposure to USFDA and regulatory audits
  • Experience with SAP and manufacturing systems is a plus
  • Strong knowledge of pharmaceutical packaging operations and MDI products
  • Expertise in GMP documentation and compliance
  • Proven troubleshooting, investigation, and root cause analysis skills
  • Effective leadership, communication, and cross-functional collaboration
  • Comfortable working in a fast-paced, regulated manufacturing environment
Working Conditions
  • Onsite role in a pharmaceutical manufacturing environment
  • PPE required (gowning, safety equipment, respiratory protection as applicable)
  • Shift flexibility, including occasional weekends or holidays based on business needs
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