Project Manager � CQV Biotech Project LL06-250822

Veg Group; Juncos (PR); On-site; USD 85,000 - 110,000; Full time

Job summary

A leading engineering services provider is seeking a Project Manager for CQV activities in Juncos, Puerto Rico. The ideal candidate will have over 8 years in the biopharma industry and experience in managing CQV projects. You will oversee project planning, compliance, and stakeholder communication. Strong knowledge of cGMP operations is required, along with leadership skills. A degree in Engineering or Life Sciences is essential.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or related technical field.
• 8+ years of experience in the biopharma or biotech industry, with 4+ years in CQV project leadership roles.
• Strong knowledge of cGMP manufacturing operations and validation lifecycle requirements.
• Demonstrated experience managing complex CQV projects from design through operational readiness.
• Familiarity with scheduling software (e.g., MS Project, Primavera P6) and project management tools.

Responsibilities

• Develop and maintain the integrated CQV project schedule for commissioning and qualification activities.
• Define project scope, milestones, deliverables, and resource requirements.
• Track progress against the CQV schedule; report status to stakeholders.
• Act as the primary point of contact for CQV-related activities.
• Ensure all CQV activities meet regulatory expectations.

Job description

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Project Manager – CQV Biotech Project LL06-250822

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 Manager

The CQV Project Manager is responsible for leading the successful planning, execution, and delivery of Commissioning, Qualification, and Validation (CQV) activities for a biotechnology manufacturing project. This role requires coordination across functional teams—including QA, Engineering, Automation, Operations, and external vendors—to ensure the project achieves compliance with cGMP standards, adheres to schedule and budget constraints, and is aligned with the project’s strategic objectives. The ideal candidate has a strong background in CQV delivery within biotech/pharmaceutical environments and experience managing multiple systems or project streams.

Key Responsibilities:

Project Planning & Execution

• Develop and maintain the integrated CQV project schedule, including commissioning and qualification activities for process, utility, and facility systems.
• Define project scope, milestones, deliverables, and resource requirements across upstream, downstream, and support systems.
• Coordinate and lead CQV planning meetings, system handoffs, and readiness reviews.
• Track progress against the CQV schedule; report status to stakeholders and leadership.
• Drive alignment with construction turnover and engineering deliverables (e.g., URS, design docs, P&IDs, FAT/SAT plans).
• Manage CQV team members and third-party contractors/consultants.
• Assign workstreams, ensure accountability, and monitor deliverable quality.
• Support onboarding and training of new team members and ensure safety and compliance awareness.

Stakeholder Communication & Reporting

• Act as the primary point of contact for CQV-related activities, issues, and updates.
• Interface with QA, Facilities, Engineering, Manufacturing, and Automation to align schedules and priorities.
• Generate weekly/monthly progress reports, risk logs, and executive summaries.

Compliance & Quality Oversight

• Ensure all CQV activities meet regulatory expectations (FDA, EMA), ASTM E2500, ISPE Baseline Guides, and internal procedures.
• Facilitate deviation management, change control impact assessments, and documentation reviews.
• Ensure that commissioning and qualification documentation supports future inspection readiness and PPQ requirements.

Systems in Scope:

• Upstream and Downstream Biotech Process Equipment
• Clean Utilities (WFI, Clean Steam, Process Gases)
• Black Utilities (HVAC, Electrical, Water, Compressed Air)
• Laboratory and QC Equipment

Qualifications:

• Bachelor’s degree in Engineering, Life Sciences, or related technical field.
• 8+ years of experience in the biopharma or biotech industry, with 4+ years in CQV project leadership roles.
• Strong knowledge of cGMP manufacturing operations and validation lifecycle requirements.
• Demonstrated experience managing complex CQV projects from design through operational readiness.
• Familiarity with scheduling software (e.g., MS Project, Primavera P6) and project management tools.

Preferred Skills:

• PMP or equivalent project management certification.
• Experience with electronic validation systems (e.g., Valgenesis, Kneat).
• Experience supporting greenfield or large capital expansion projects.
• Strong interpersonal, organizational, and communication skills.