This role pays less than
77%
of similar roles. Most pay
$127,196–$192,587
— the shaded band above.
At the midpoint, this role pays about
$123k
versus about
$160k
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.
The Cleaning Validation & Commissioning Specialist is an engineering role focused on the commissioning, qualification, and validation of new and modified equipment, facilities, utilities, products, and processes. Working with project owners and designers, the individual will develop and execute test protocols, manage risk assessments including FMEA, and oversee sampling for cleaning validation to ensure high-quality results that meet regulatory requirements. The role involves coordinating change requests, supervising contract resources, and managing multiple complex projects simultaneously. Key competencies include expertise in risk management principles, quality and compliance management, and technical knowledge of manufacturing environments such as pharmaceuticals or medical devices. Candidates should possess strong communication skills and the ability to lead special projects while ensuring all activities align with established safety protocols and operational standards for robust product delivery.
Develop and execute commissioning, qualification, and validation test protocols for equipment, facilities, and processes.
Lead risk management activities including FMEA facilitation and periodic updates to the Validation Master Plan.
Coordinate and execute sampling related to cleaning validation and document results in summary reports.
Manage and process change requests according to established procedures and regulatory requirements.
Supervise contract resources and internal team members to ensure timely completion of validation activities.
Lead special projects specifically related to the cleaning validation area.
Develop operational procedures and provide training for staff on new equipment or processes.
Ensure all operations comply with environmental, health, and safety (EH&S) systems and policies.
What we're looking for
Bachelor’s Degree in Engineering, science, or a related field (preferred) or equivalent technical experience with 3+ years of engineering/operational experience (preferred).
Experience developing commissioning, qualification, and validation deliverables that meet regulatory scrutiny.
6+ years of experience in Manufacturing, Quality, or Engineering including 4 major validation subjects (preferred).
Technical background in healthcare, nutritional products, laboratory diagnostics, medical devices, or pharmaceuticals (preferred).
Knowledge of quality/compliance management and regulations affecting API, Bulk Drug, or Finished goods manufacturing (preferred).
Ability to manage complex projects and more than five projects simultaneously.
Strong interpersonal, communication, and negotiation skills within a team environment.
Ability to supervise junior or contract team members (prior supervisory experience preferred).