Manufacturing Supervisor III

AbbVie

Quick summary

Work type
On-site
Location
Worcester, MA
Posted
2 days ago
Closes
Jun 25, 2126

Market check

Salary context

How this pay compares to similar roles

Similar $152k
$122k most similar roles pay here $198k

This listing doesn't post a salary. Most similar roles pay $135,000–$170,000.

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 36 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 5 roles with salary data.

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At a glance

TL;DR · Manufacturing Supervisor III

The Manufacturing Supervisor III role at AbbVie is a senior position within the operations team, requiring advanced expertise in manufacturing processes and safety protocols. This individual will oversee daily production activities, ensuring adherence to all safety, quality, and regulatory standards while fostering a culture of continuous improvement. Key responsibilities include managing a team’s deployment, conducting regular performance reviews, and driving engagement through effective communication and training initiatives. The supervisor must also coordinate shift operations seamlessly, manage compliance issues proactively, and lead process improvement projects. Proficiency in Microsoft Office and manufacturing systems like SAP is essential, along with familiarity with industrial automation technologies. Ideal candidates will have a bachelor’s degree, preferably in sciences or engineering, and at least four years of supervisory experience in the pharmaceutical industry.

What you'll do

  • Manage production safety programs and promote zero incidents.
  • Delegate tasks effectively to meet daily production schedules.
  • Train team members to required standards and conduct performance reviews.
  • Coordinate shift activities to ensure safe and efficient operations.
  • Implement proactive compliance management processes and address issues promptly.

What we're looking for

  • Bachelor’s degree required, preferably in sciences or engineering.
  • Minimum 4 years of experience supervising or leading a functional team.
  • Proficient in Microsoft Office and manufacturing systems like SAP.
  • Working knowledge of safety, quality systems, and cGMPs.
  • Experience in regulated pharmaceutical industry strongly preferred.
  • Leads process improvement initiatives and obtains ideas from the team.

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