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LL01-120325 CQV Project Scheduler

Validation & Engineering Group
United Statesfull_timeVerifiedPosted 3 Dec 2025

About the role

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:

  • CQV Project Scheduler – Biotech Facility

Position Summary

The CQV Project Scheduler will coordinate, and oversee all Commissioning, Qualification, and Validation (CQV) activities for a biotechnology manufacturing site in Norwood, MA. This role blends technical CQV expertise with project scheduling, resource planning, and cross-functional coordination. The ideal candidate has strong startup experience, deep understanding of GMP requirements, and proven ability to build and maintain integrated CQV schedules using industry tools—including Smartsheet.

Key Responsibilities

CQV Project Scheduler

  • Schedule CQV activities for utilities, equipment, automation, and process systems.

  • Develop, manage and schedule CQV execution strategies, resource plans, and deliverables.

  • Follow up CQV documentation status (URS, DQ, IQ/OQ/PQ protocols, summary reports).

  • Schedule activities for CQV risk assessments, deviations, change controls, and CAPAs.

Scheduling & Project Controls

  • Develop, maintain, and optimize integrated CQV schedules using Primavera P6, MS Project, and Smartsheet.

  • Create weekly and monthly look-ahead schedules and critical-path analyses.

  • Track schedule progress, identify constraints, and implement mitigation plans.

  • Coordinate schedule inputs across construction, automation, engineering, and manufacturing.

  • Prepare dashboards, milestone reports, and schedule updates for stakeholders.

Cross-Functional Coordination

  • Facilitate daily and weekly CQV coordination meetings.

  • Manage TOP (Turnover Package) completions, FAT/SAT readiness, and commissioning interfaces.

  • Align CQV milestones with mechanical completion, automation readiness, and process tech transfer.

  • Communicate risks, impacts, and timeline strategies to leadership teams.

Vendor & Contractor Management

  • Coordinate vendor documentation, FAT/SAT execution, and punch list closeout.

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Company

Validation & Engineering Group

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