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| Department: | Field - LL |
| Location: | Chaska, MN |
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
Location: Remote (preferred near Minnesota – Chaska area)
Travel: Occasional travel (Miami, Cincinnati/Kentucky area, and vendor sites)
Duration: 6–12 months (Contract)
Reports To: Sr. Director, Project Management
Industry: Biotechnology / Diagnostics
The Project Consultant will support the transition of diagnostic equipment, processes, and reagent filling operations within a leading biotechnology diagnostics organization. This role focuses on lab automation assets, operational readiness, and risk assessment related to equipment deployment, relocation, and qualification.
The consultant will work cross-functionally with engineering, operations, quality, and supplier stakeholders to ensure seamless integration of systems and processes across multiple sites.
Lead and coordinate projects for equipment and process transfers across diagnostic labs and operations.
Support transition of lab automation equipment.
Oversee filler and reagent equipment readiness, integration, and operational qualification planning.
Conduct risk assessments and mitigation planning for equipment relocation and manufacturing continuity.
Support development and execution of transition schedules, RACI, and communication plans.
Track and report project progress, risks, and critical decisions to the Sr. Director and leadership teams.
Coordinate with supplier partners on technical interfaces, upgrades, and delivery timelines.
Ensure alignment with quality, validation, and safety requirements throughout transition activities.
Prepare and maintain project documentation (status reports, dashboards, meeting minutes, action logs).
5+ years’ experience in biotech/diagnostics or life sciences manufacturing environments.
Experience with equipment transitions, lab automation, or reagent/filler equipment strongly preferred.
Knowledge of risk assessment methodologies and change management best practices.
Ability to work effectively in virtual/remote cross-functional teams.
Strong communication, leadership, and vendor coordination skills.
Flexibility to travel as required (15–25%).
Familiarity with regulated environments (GMP/ISO 13485).
Project coordination or project management experience.
Remote with visits to Minnesota (Chaska) and Cincinnati/Kentucky/Miami as needed