Director, Site Lead Combination Product Development, R&D

AbbVie

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
North Chicago, IL
Salary
$182,000–$346,000 / yr
Posted
84 days ago
Freshness
Confirmed live yesterday
Closes
Jun 18, 2126

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $243k
This role $264k
$162k most similar roles pay here $366k

This role pays more than 68% of similar roles. Most pay $202,496–$283,212 — the shaded band above. At the midpoint, this role pays about $264k versus about $243k 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 · Director, Site Lead Combination Product Development, R&D

The Director, Site Lead Combination Product Development, R&D leads the Lake County team and serves as the site lead for combination product development activities within the R&D organization. This role provides strategic and operational leadership to a multidisciplinary team of engineers, scientists, and technical specialists to drive the clinical development of drug-device systems including prefilled syringes, autoinjectors, on-body injectors, and subcutaneous ambulatory infusion pumps. The individual will oversee the full product lifecycle from feasibility and design analysis through verification testing and transition to operations. Key responsibilities include managing resource allocation, overseeing lab capabilities, and coordinating with global cross-functional partners in regulatory, quality, and supply functions. The role requires expertise in medical device design, lean development methodologies, and knowledge of standards like 21 CFR 820.30 and ISO 13485 to solve complex drug delivery challenges.

What you'll do

  • Lead the Lake County site as the primary head for all combination product development activities in R&D.
  • Drive the clinical development of drug delivery systems including prefilled syringes, autoinjectors, and infusion pumps.
  • Oversee the full product lifecycle from initial feasibility and design analysis through verification and transition to operations.
  • Manage a multidisciplinary team of engineers and technical specialists across mechanical, electrical, software, and materials science disciplines.
  • Coordinate with global cross-functional partners in Regulatory, Quality, and Supply to ensure products meet all requirements.
  • Manage resource allocation, staffing plans, and the selection of external contract manufacturing partners.
  • Oversee laboratory operations and design verification teams to support testing and development of new technologies.
  • Represent the site in global forums to contribute to organizational strategy for combination products.

What we're looking for

  • Advanced degree (MS/PhD) in a pharmaceutical or engineering discipline.
  • Minimum 15 years of relevant industry experience in medical devices and/or the pharmaceutical industry.
  • At least 8 years of experience leading product development teams.
  • Experience with subcutaneous injection devices and electromechanical devices (preferred).
  • Expertise in combination product design, development, verification/validation, and technology transfer.
  • Experience leading product development to commercial launch (preferred).
  • Strong working knowledge of global regulatory requirements and industry standards such as 21 CFR 820.30 and ISO 13485.
  • Proven ability to lead multidisciplinary teams and communicate effectively with senior and global stakeholders.

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