CMC Program Lead: Process Characterization & PPQ

Artiva Biotherapeutics; San Diego (CA); On-site; USD 155,000 - 190,000; Full time

Benefits offered by this job

Medical, Dental, and Vision

401(k) Retirement Plan

Paid Time Off (PTO)

Job summary

Artiva Biotherapeutics, located in San Diego, CA, is looking for a CMC Project Management professional to lead the planning and execution of process characterization and PPQ workstreams. The role requires strong project management skills, collaboration, and a solid understanding of GMP manufacturing.

Candidate must have 6–10+ years in biotech and experience with external partners, plus a bachelor’s degree in a related field. Artiva offers a competitive salary along with comprehensive benefits.

Qualifications

• 6–10+ years of experience in biotechnology or pharmaceutical development.
• Demonstrated experience in process characterization, validation, and/or PPQ activities.
• Experience with external partners like CDMOs.

Responsibilities

• Lead end-to-end project management of process characterization and PPQ workstreams.
• Develop and maintain detailed workstream timelines and resource planning.
• Track deliverables and manage risks proactively.

Skills

Project management

GMP manufacturing knowledge

Collaboration skills

Attention to detail

Education

Bachelor’s degree in life sciences or related field

Job description

Artiva Biotherapeutics, located in San Diego, CA, is looking for a CMC Project Management professional to lead the planning and execution of process characterization and PPQ workstreams. The role requires strong project management skills, collaboration, and a solid understanding of GMP manufacturing.

Candidate must have 6–10+ years in biotech and experience with external partners, plus a bachelor’s degree in a related field. Artiva offers a competitive salary along with comprehensive benefits.