MDI Manufacturing Operator II — Night Shift

Merck & Co.

Fall River (MA)

On-site

USD 29,000 - 39,000

Full time

14 days+
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Job summary

Cipla is seeking a Manufacturing Operator II to support the production of metered dose inhalation products in Fall River, MA. This full-time, non-exempt role operates on the third shift (11:00 PM–7:30 AM) and reports to the Production Supervisor.

You will follow cGMP and SOPs, perform batch execution, material handling, equipment maintenance, calibration, and ensure proper documentation while collaborating with QA, QC, packaging, and engineering.

Qualifications

  • High school diploma or equivalent required.
  • Accredited college certificate or degree preferred.
  • Minimum 2–3 years of manufacturing experience with MDI or aerosol products.
  • English language proficiency required.
  • Knowledge of cGMP and regulatory requirements preferred.

Responsibilities

  • Dispensing raw materials and primary packing materials per work order.
  • Ensure proper planning and execution of batches.
  • Monitor cleaning and sanitation of production area and machinery per SOP.
  • Record production materials and lines daily and conduct process checks.
  • Coordinate with QA/QC for sampling and changeovers.
  • Maintain inventory of machine parts, tools and accessories.
  • Operate and maintain equipment; ensure line clearance during batch changes.
  • Collaborate with packaging, engineering, QA and QC for planning and execution.

Skills

English proficiency
Team player
Attention to detail
Safety awareness
Problem solving

Education

High school diploma or equivalent
College certificate or university degree preferred

Job description

Cipla is seeking a Manufacturing Operator II to support the production of metered dose inhalation products in Fall River, MA. This full-time, non-exempt role operates on the third shift (11:00 PM–7:30 AM) and reports to the Production Supervisor.

You will follow cGMP and SOPs, perform batch execution, material handling, equipment maintenance, calibration, and ensure proper documentation while collaborating with QA, QC, packaging, and engineering.

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