MDI Packaging Specialist – Generic Pharmaceuticals

MDI Packaging Specialist – Generic Pharmaceuticals

1 day ago Be among the first 25 applicants

Location: Fall River, MA (927 Currant Rd.) – Full‑Time, 2nd Shift: 3:00 PM – 11:30 PM (may vary)

Work Type: Permanent

Experience

Required:

5 – 10 Years (preference for pharmaceutical MDI packaging)

Compensation: USD 72,800 – 93,600 + Comprehensive Benefits (401k match, medical/dental/vision, PTO, holidays, etc.)

The Packaging Specialist (2nd Shift) coordinates daily packaging activities ensuring production schedules are met while adhering to cGMP, FDA, and company quality standards. The role focuses on process monitoring, documentation, efficiency improvements, and cross‑functional collaboration in a generic pharmaceuticals manufacturing environment specializing in metered dose inhalers (MDI).

• Coordinate daily packaging operations to meet production schedules, material needsmouth, and project timelines.
• Monitor packaging processes for cGMP/FDA compliance and quality standards; identify and resolve inefficiencies.
• Ensure accurate documentation of batch records, logs, deviations verständlich, and related cGMP records.
• Assist in deviation investigations, non‑conformances, and CAPA (Corrective and Preventive Actions).
• Collaborate with QA, Supply Chain, Project Management, Engineering, and R&D to address bottlenecks and optimize resources.
• Create and manage purchase requisitions (PR) in SAP for services, equipment, consumables, and vendor coordination.
• Support training on SOPs and implement process improvements to reduce waste and enhance productivity.
• Monitor operational metrics (efficiency, compliance, resource utilization) and contribute to performance reviews.
• Participate in safety programs, maintain clean work areas, and enforce safety regulations/PPE usage.
• Perform other duties as assigned by management.

• 5–10 years of experience in pharmaceutical packaging, operations, or team management (MDI packaging preferred).
• Strong understanding of cGMP, FDA regulations, and pharmaceutical packaging processes.
• Experience with SAP system and packaging data analysis tools.
• Excellent problem‑solving, attention to detail, and ability to work in a fast‑paced, regulated environment.
• Strong communication skills with internal/external stakeholders.
• Proficient in Microsoft Office suite.
• Knowledge of SOP creation/revision and quality system compliance.
• Ability to handle compliance/regulatory audits.