Associate Director, External Manufacturing - Biologics

AbbVie

Confirmed live yesterday High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Worcester, MA
Salary
$141,500–$268,500 / yr
Posted
73 days ago
Freshness
Confirmed live yesterday
Closes
Jun 30, 2126

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $221k
This role $205k
$126k most similar roles pay here $284k

This role pays less than 57% of similar roles. Most pay $182,562–$259,111 — the shaded band above. At the midpoint, this role pays about $205k versus about $221k 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 · Associate Director, External Manufacturing - Biologics

Associate Director, External Manufacturing - Biologics serves as the primary supplier relationship contact for third-party manufacturing operations. This role provides supervision, strategic initiatives, and technical support to manage the supply of designated products while ensuring high-quality manufacturing in compliance with local and international regulations. The individual manages projects to ensure cost-effective, marketable, and manufacturable products throughout their lifecycle. Key responsibilities include negotiating Manufacturing Service Agreements, managing material procurement strategies, coordinating production forecasts, and leading cross-functional teams through matrix management. The role requires expertise in pharmaceutical development, manufacturing processes, and supply activities. Essential skills include project management, risk management, and financial system proficiency. Candidates must possess a broad business perspective to oversee quality systems, conduct audits, and manage performance metrics for subcontracted relationships within the biologics product area to ensure timely delivery and regulatory compliance.

What you'll do

  • Serve as the primary contact for third-party manufacturing suppliers to manage product supply and technical support.
  • Negotiate Manufacturing Service Agreements and ensure compliance with all contract terms.
  • Develop material procurement strategies and coordinate production schedules based on demand forecasts.
  • Manage project lifecycles including scope, cost, time, resource management, and risk mitigation.
  • Oversee the development of financial operating plans and ensure all financial goals are met.
  • Lead virtual operation teams and steering committees to monitor performance and resolve issues.
  • Coordinate with quality units to manage audits, investigate deviations, and ensure regulatory compliance.
  • Review process performance and quality trends to develop and implement improvement plans.

What we're looking for

  • Bachelor’s degree in a science or technical related field (preferred).
  • MSc or MBA degree (preferred).
  • Minimum of 10 years of experience in manufacturing, engineering, project management, quality, or S&T.
  • Experience managing subcontracted relationships (preferred).
  • Proven leadership ability with superior communication skills including listening, verbal, presentation, and written.
  • Strong strategy development and planning skills regarding pharmaceutical development, manufacturing, and supply activities.
  • Strong knowledge of business financial systems and tools.
  • Ability to identify issues and perform strong problem analysis and solution development.

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