Director, Technical Centre

AbbVie

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Westport, Ireland
Posted
2 days ago
Freshness
Confirmed live yesterday
Closes
Sep 16, 2126

Market check

Salary context

How this pay compares to similar roles

Similar $228k
$169k most similar roles pay here $286k

This listing doesn't post a salary. Most similar roles pay $195,300–$260,000.

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 340 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 310 roles with salary data.

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At a glance

TL;DR · Director, Technical Centre

The Director, Technical Centre is a strategic leadership role within the manufacturing center of excellence at Westport. This position serves as a critical interface between Research & Development, Pharmaceutical Development Science & Technology, and Manufacturing Engineering & Controls to ensure effective technical transfer activities and sustainable site operations. The successful candidate will manage drug substance introductions, oversee process development and yield improvements, and lead initiatives in process validation, facility requalification, and sterilization qualifications. Day-to-day responsibilities include managing the Biolab process development lab, supporting bioassay teams with bioanalytical investigations, and spearheading NPI introductions for neurotoxin and biologic pipelines. The role requires extensive drug product experience, leadership of leaders, and expertise in end-to-end product transfer and regulatory filings. Key competencies include troubleshooting, problem-solving, and managing technical strategic planning while navigating complex pharmaceutical manufacturing environments.

What you'll do

  • Provide technical support for Unit Dose and Multi Dose process-related issues and investigations.
  • Drive process development and yield improvements across manufacturing operations.
  • Manage Drug Substance introductions and monitor core production processes.
  • Lead initiatives in process validation, facility requalification, and sterilization qualifications.
  • Oversee cleaning and computer system validations to ensure compliance.
  • Spearhead New Product Introduction (NPI) for neurotoxin and biologic pipelines.
  • Collaborate with global CMC teams on product transfers and regulatory filings.
  • Manage the Biolab process development lab and drive digital technical initiatives.

What we're looking for

  • Bachelor's Degree or higher in a relevant discipline.
  • Master's or Ph.D. in Engineering, Science, or Technology (preferred).
  • Over 10 years of experience in pharmaceutical technical or relevant roles.
  • Extensive Drug Product experience is an essential requirement.
  • Proven leadership and people management experience across various levels and departments as a leader of leaders.
  • Experience in end-to-end Product Transfer and launch phases with strong regulatory knowledge.
  • Exceptional collaborative, troubleshooting, and problem-solving skills.
  • Ability to thrive in a dynamic environment and adapt to manage unexpected constraints.

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