Job ID: JOB_ID_845
Position Summary: Senior Decommissioning Engineer
Verito Solutions is urgently hiring a Senior Decommissioning Engineer for a critical project based in North Chicago, IL. This role is strictly for local candidates who can provide on-site support for large-scale capital and facility projects within the pharmaceutical and biotech manufacturing sectors. As a Senior Engineer, you will be responsible for the technical oversight of decommissioning activities, ensuring that all processes align with global SOPs and stringent GMP requirements. This is a high-impact role requiring a blend of technical expertise, regulatory knowledge, and project management skills.
Core Responsibilities
- Technical Review: Perform comprehensive technical reviews and approvals of all decommissioning documentation to ensure accuracy and compliance.
- Strategy Development: Provide expert guidance on change control strategies and documentation approaches for complex engineering projects.
- Compliance Oversight: Ensure all activities remain in strict compliance with site-specific and global Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).
- Deviation Management: Lead and support deviation investigations, identifying root causes and implementing effective resolution strategies.
- Workflow Management: Oversee documentation workflows within specialized systems such as AbbVie document systems, KNEAT, OneVault, and OneTrack.
- Cross-Functional Leadership: Coordinate with diverse teams to drive project milestones, participating in Validation Review Boards and high-level project meetings.
- Reporting and Mentorship: Provide detailed weekly reporting on project progress, risks, and resource utilization while mentoring junior staff to support knowledge transfer.
Qualifications and Preferred Skills
Candidates must have a minimum of 7 years of experience in Commissioning, Qualification, and Validation (CQV), validation, or decommissioning within highly regulated industries. A deep understanding of the validation lifecycle and GMP compliance is mandatory. We are looking for a professional with a proven ability to lead project documentation strategies and communicate effectively across various organizational levels. Experience in pharmaceutical or biotech manufacturing is highly desirable, particularly with familiarity in KNEAT or similar electronic validation platforms. This position offers a unique opportunity to lead decommissioning efforts for a major industry player in the Chicago region.
Special Requirements
Local Candidate Only; Pharmaceutical/Biotech domain; Requires experience with AbbVie systems (KNEAT, OneVault, OneTrack).
Compensation & Location
Salary: $135,000 – $175,000 per year (Estimated)
Location: North Chicago, IL
Recruiter / Company – Contact Information
Recruiter / Employer: Verito Solutions
Email: govind@veritosolutions.com
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