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CAMRIS · 10 hours ago

CQV Project Manager

Silver Spring, MD

Full-time

Onsite

Senior Level

$110K/yr - $130K/yr

5+ years exp

CAMRIS is a dynamic medical research and development firm that provides innovative solutions to health and development challenges. They are seeking a CQV Project Manager to support the Pilot Bioproduction Facility at the Walter Reed Army Institute of Research, focusing on managing project scope, teams, and regulatory compliance throughout the project lifecycle.

BiotechnologyInformation Technology

Comp. & Benefits

No H1B

Responsibilities

Solution project challenges with multi-disciplinary teams tracking and reporting metrics

Manage project actuals vs. forecast and update status with program leadership

Facilitate project team meetings, including scheduling, planning, and tracking

Experience scheduling and executing GMP equipment design, testing and qualification

Project planning and project lifecycle management from conception to completion

Track qualification and operational readiness of equipment and systems, as necessary

Leverage dependency matrices, diagrams, and gap assessments to define project scope

Communicate and coordinate with PBF stakeholders to define scope and budget

Grow and maintain relationships with WRAIR staff, customers, and vendors

Organize and participate in customer and potential customer visits

Manage project submittals, change control processes and project management artifacts

Actively communicate customer project and facility constraints

Evaluate schedule constraints, risk, and feasibility of performing CDMO projects

Assist managers with subcontractor schedule development and maintenance

Support shutdown planning and execution and update capacity utilization metrics

Optimize and scale the Project Management function as capacity grows

Perform other duties as assigned

Qualification

GMP KnowledgeBiologics ExperienceProject ManagementMS ProjectPMP CertificationCost AnalysisSmartSheet ExperienceLeadershipCommunication Skills

Required

BS/BA in business, engineering, life sciences, or a related field

5+ years of biologics development or manufacturing industry experience

MS Project proficiency, including resource planning

MS Excel, MS Word, MS SharePoint, and MS Teams familiarity

Familiarity with implementing operational excellence

Excellent written and verbal communication skills

Must be currently eligible to work in the United States without visa sponsorship and have lived in the United States for three of the past five years if a non-US citizen