MDI Production Supervisor — Onsite in Fall River

Merck & Co.

Fall River (MA)

On-site

USD 90,000 - 115,000

Full time

14 days+

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Job summary

Merck & Co. in Fall River, MA is seeking a Manufacturing Supervisor for Metered-Dose Inhaler production. This onsite, full-time role focuses on ensuring cGMP compliance, adherence to SOPs, and FDA requirements while supporting packaging operations and quality investigations.

The supervisor will lead a production team, manage schedules, and uphold safety and documentation standards. The ideal candidate holds a Bachelor's in pharmaceutical engineering or related field, with 1–3 years of pharma

Qualifications

  • Bachelor's degree in pharmaceutical engineering, Pharmaceutical Sciences or related field.
  • One to three years of direct work experience in pharmaceutical manufacturing.
  • Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field preferred.

Responsibilities

  • Schedule the production process and set targets for production phases.
  • Delegate responsibilities and create team leadership roles.
  • Manage performance and train assigned employees to meet standards and targets.
  • Perform material reviews, weight checks, and ensure correct labeling and inspection.
  • Follow Master Batch Records and SOPs for packaging MDIs and ensure cGMP compliance.
  • Prepare documentation and support quality investigations.

Skills

English proficiency
Teamwork
Leadership
Safety awareness
Documentation
Basic math

Education

Bachelor's degree in pharmaceutical engineering, Pharmaceutical Sciences or related field
Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field

Tools

SAP

Job description

Merck & Co. in Fall River, MA is seeking a Manufacturing Supervisor for Metered-Dose Inhaler production. This onsite, full-time role focuses on ensuring cGMP compliance, adherence to SOPs, and FDA requirements while supporting packaging operations and quality investigations.

The supervisor will lead a production team, manage schedules, and uphold safety and documentation standards. The ideal candidate holds a Bachelor's in pharmaceutical engineering or related field, with 1–3 years of pharma

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