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Manufacturing Supervisor III (Onsite)

AbbVie
Full-time
On-site
Worcester, MA
$94,000 - $178,500 USD yearly
Operations

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Role Summary

The Manufacturing Supervisor III is a technical SME with advanced expertise in operations. Lead and facilitate safe operations, ensure quality and regulatory compliance, drive cost efficiency, and foster a high-performance culture within the team.

Responsibilities

  • Safety: Manage production safety program, promote a culture of zero incidents, and ensure compliance with EHS requirements.
  • People: Deploy team members effectively, delegate tasks to meet production schedule, train staff to required standards, conduct regular performance reviews, development planning, and ensure accurate time and attendance.
  • People: Communicate effectively with the team, act as advisor/coach to units, mentor junior peers, and supervise production support personnel.
  • Operational: Coordinate shift activities to meet production schedule and ensure smooth handovers for safe, planned operations.
  • Compliance: Ensure regulatory compliance, perform proactive material checks, line clearances, and spot checks; manage compliance issues impacting lot completion.
  • Performance: Manage cycle times, optimize change-overs, lead process improvement projects, monitor site metrics, and support area targets.
  • Development: Develop direct reports with training and challenging tasks; focus on key talent and growth opportunities; pursue personal development.
  • Operational Excellence (OpEx): Lead process improvement initiatives and solicit ideas from the team to improve culture, quality, productivity, and safety.

Qualifications

  • Bachelorβ€šΓ„Γ΄s degree required; sciences or engineering preferred.
  • Minimum 4 years of experience supervising or leading a functional team; regulated pharmaceutical industry experience strongly preferred.
  • Systems: Proficient in Microsoft Office and manufacturing systems (e.g., SAP); familiarity with industrial automation (DCS/PLC).
  • Regulatory: Working knowledge of safety, quality systems, and cGMPs required.
  • Aseptic: Experience in aseptic production environment preferred (if applicable).
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