Manufacturing Supervisor III

AbbVie

Confirmed live 2 days ago High trust

Quick summary

Work type
On-site
Location
Worcester, MA
Salary
$96,500–$183,500 / yr
Posted
36 days ago
Freshness
Confirmed live 2 days ago
Closes
Aug 6, 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.

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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 manufacturing operations team, where they lead and facilitate safe production activities in compliance with regulatory requirements. This role involves managing the production safety program, coordinating shift activities to meet schedules, and overseeing cycle time and change-over improvements. The supervisor is responsible for team development through coaching, performance reviews, and training, while also managing waste disposal according to federal regulations. Key technical competencies include proficiency in Microsoft Office, SAP, and industrial automation systems such as distributed control and PLC-based systems. Candidates must possess a working knowledge of safety, quality systems, and cGMPs. The role operates within the pharmaceutical industry, specifically addressing production challenges in potentially aseptic environments while ensuring high levels of product quality and operational excellence through proactive process improvement initiatives.

What you'll do

  • Manage the production safety program and conduct routine safety gembas to ensure a zero-incident environment.
  • Coordinate shift activities and manage handovers to ensure the production schedule is met safely.
  • Oversee team deployment, task delegation, and training to meet operational standards.
  • Conduct performance reviews, 1:1 meetings, and development planning for all direct reports.
  • Ensure compliance with regulatory agencies through routine material checks, line clearances, and spot checks.
  • Manage cycle times and change-over times while identifying opportunities for process improvements.
  • Lead Operational Excellence initiatives to improve quality, productivity, and safety within the department.
  • Manage hazardous and non-hazardous waste in compliance with internal procedures and federal regulations.

What we're looking for

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

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