Senior Manager – Associate Director, CMC Project Management – Process Development & Validation

Artiva Biotherapeutics

Senior Manager / Associate Director in CMC Project Management for biotech company. Leading process characterization and validation workstreams for NK cell therapies.

Posted 6/20/2026full-timeSan Diego • California • 🇺🇸 United StatesSenior💰 $155,000 - $190,000 per yearWebsite

Tech Stack

Tools & technologies

PMP

About the role

Key responsibilities & impact

Own end-to-end project management of the process characterization, PPQ, and Commercial readiness workstreams including planning, sequencing, and execution tracking through to completion
Develop and maintain detailed, bottoms-up workstream timelines and resource planning for process characterization, validation activities, and PPQ campaigns, and ensure they integrate cleanly into the overall CMC program schedule
Translate the strategy into actionable execution plans, milestones, and deliverable trackers
Coordinate the functional contributors to these workstreams—including Technical Operations, internal, and external partners (CDMOs, CROs)—to keep deliverables on track
Coordinate with adjacent PPQ readiness activities—including supplier and raw material qualification and equipment/facility qualification—tracking them as dependencies and ensuring alignment with campaign timelines
Drive alignment on assumptions, deliverables, and timelines specific to process characterization and PPQ execution
Provide clear, structured workstream updates and supporting analysis into existing CMC program governance and decision forums
Proactively identify risks within the process characterization and PPQ workstreams—including validation, batch execution, documentation, and CDMO readiness risks
Develop mitigation options and escalate workstream-level issues with appropriate context and recommended paths forward
Track dependencies that could affect PPQ timing or downstream regulatory and clinical supply needs, and flag them to the CMC project lead for cross-program visibility
Track progress against process characterization and PPQ deliverables, including study execution, engineering and PPQ batch manufacturing, release, stability, and validation activities
Drive PPQ campaign readiness, including coordination of protocols, batch records, documentation, and quality system prerequisites
Build and maintain dashboards, trackers, and status reports for the process characterization and PPQ workstreams, providing clear visibility into progress, milestones, and risks
Report workstream status, key risks, and decision points into existing CMC program governance and leadership forums on a regular cadence
Translate detailed workstream data into concise, decision-ready summaries for the CMC project lead and senior stakeholders
Maintain timely, structured communication with functional contributors and external partners to keep deliverables and timelines aligned
Develop and refine repeatable tools, trackers, and best practices for managing process characterization and PPQ readiness
Identify opportunities to improve execution rigor and efficiency within the workstreams

Requirements

What you’ll need

Bachelor’s degree in life sciences or related field (advanced degree preferred)
6–10+ years of experience in biotechnology or pharmaceutical development
Demonstrated experience supporting or leading process characterization, process validation, and/or PPQ activities
Strong understanding of GMP manufacturing, CDMO operations, and validation/regulatory expectations
Proven ability to manage detailed, cross-functional workstreams with multiple contributors and external partners
Experience working with external partners (e.g., CDMOs)
Ability to manage competing priorities and other tasks as needed
Preferred Direct hands-on experience executing PPQ campaigns or process validation programs
Familiarity with regulatory filings (IND/BLA/MAA) and the CMC/validation content they require
PMP or similar project management certification (a plus, not required)
Small to mid-size Biotech company experience

Benefits

Comp & perks

Comprehensive benefits, including: Medical, Dental, and Vision
Group Life Insurance
Long Term Disability (LTD)
401(k) Retirement Plan
Employee Assistance Program (EAP)
Flexible Spending Account (FSA)
Paid Time Off (PTO)
Company paid holidays, including the year-end holiday week
Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

process characterizationprocess validationPPQ activitiesGMP manufacturingCDMO operationsregulatory filingsproject managementresource planningrisk identificationdata analysis

Soft Skills

communicationcoordinationproblem-solvingtime managementleadershipcollaborationadaptabilityattention to detailstrategic thinkingstakeholder management

Certifications

PMP