Biopharmaceutical CQV Manager / Project Manager

Job overview

The Biopharmaceutical CQV Manager / Project Manager role is onsite at client facilities in Portland, OR. Compensation is not specified. MMR Consulting is an engineering and consulting firm serving pharmaceutical and biotechnology industries; the listing location is San Francisco, CA, while the described work site is Portland, OR. The role leads commissioning, qualification, and validation activities for sterile and aseptic filling and packaging operations. It coordinates project plans, technical teams, vendors, and client stakeholders to support compliant equipment and processes, reduce contamination and process risks, and improve packaging operations.

What you'll do

• Lead or participate in packaging design and operations
• manage project execution, CQV strategies, schedules, budgets, and resources
• develop user, design, and functional specifications
• assess packaging operations and improvement opportunities
• conduct reliability and optimization studies
• support factory and site acceptance testing, commissioning, and qualification
• coordinate cross-functional meetings and project updates.

What we're looking for

Skills & competencies

biopharmaceutical cqv manager

project management

mmr consulting

portland or client site

san francisco ca listing

pharmaceutical

biotechnology

commissioning

qualification

validation

aseptic manufacturing

packaging operations

Work arrangement

• Weekend coverage required

Benefits & perks

• Relocation packages or travel packages are available.

Why this role

Pharmaceutical or biotech experience is mandatory; relocation or travel packages are available. Occasional travel or off-hours work may be required.

About the employer

MMR Consulting is hiring for this role. Industry: Engineering Services. Sector: 54.