Manufacturing Supervisor III

AbbVie

Confirmed live yesterday High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Worcester, MA
Salary
$96,500–$183,500 / yr
Posted
78 days ago
Freshness
Confirmed live yesterday
Closes
Jun 25, 2126

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $144k
This role $140k
$86k most similar roles pay here $194k

This role pays less than 58% of similar roles. Most pay $117,500–$170,000 — the shaded band above. At the midpoint, this role pays about $140k versus about $144k for comparable roles.

Based on 240 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 297 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 271 roles with salary data.

Most-posted roles

View all roles at AbbVie

At a glance

TL;DR · Manufacturing Supervisor III

The Manufacturing Supervisor III serves as a technical subject matter expert within the operations team, where they lead and facilitate safe production activities while ensuring compliance with all regulatory requirements. This individual manages the daily deployment of team members, oversees training, conducts performance reviews, and coordinates shift activities to meet production schedules. They are responsible for cycle time management, change-over improvements, and leading operational excellence initiatives to enhance quality and safety. The role requires proficiency in Microsoft Office, SAP, and industrial automation systems like distributed control and PLC-based systems. Candidates must possess a working knowledge of safety, quality systems, and cGMPs within the regulated pharmaceutical industry. Experience in an aseptic production environment is preferred for this role, which focuses on maintaining high standards in a highly regulated manufacturing environment.

What you'll do

  • Manage production safety programs and conduct routine safety gembas to ensure a zero-incident environment.
  • Coordinate daily shift activities and manage transitions between shifts to meet production schedules.
  • Oversee team deployment, task delegation, and the training of staff to required standards.
  • Conduct performance reviews, 1:1 meetings, and development planning for direct reports.
  • Ensure compliance with regulatory agencies through routine material checks, line clearances, and spot checks.
  • Manage cycle times and change-over durations while identifying opportunities for process improvements.
  • Lead operational excellence initiatives to improve quality, productivity, and safety across the area.

What we're looking for

  • Bachelor’s degree required.
  • Degree in sciences or engineering (preferred).
  • Minimum 4 years of experience supervising or leading a functional team.
  • Experience in the regulated pharmaceutical industry (preferred).
  • Proficiency in Microsoft Office and manufacturing systems like SAP.
  • Familiarity with industrial automation, including distributed control and PLC based systems.
  • Working knowledge of safety, quality systems, and cGMPs.
  • Experience working in an aseptic production environment (preferred).

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