CMC Operations Lead: Cross-Program Biotech Ops

Crispr Therapeutics AG; Boston, Northern (MA, KY); Hybrid; USD 110,000 - 120,000; Full time

Benefits offered by this job

Bonus

Equity

Benefits

Job summary

CRISPR Therapeutics is seeking an Associate Manager, CMC Operations in South Boston, MA. This full-time role requires coordinating cross-program timelines and risk management across CMC, Regulatory, QA, and CDMO partners, with hands-on oversight of tech transfer and manufacturing deliverables.

The successful candidate will have a Bachelor’s degree in a scientific or engineering field with 5–7+ years of related experience, familiarity with GMP milestones, and strong cross-functional communication

Qualifications

• Bachelor's degree and 5-7+ years of relevant experience in a scientific/engineering field.
• Experience supporting biologics, cell/gene therapy, or LNP-based drug product programs.
• Familiarity with project management tools for multi-program tracking.

Responsibilities

• Build and maintain integrated cross-program timelines spanning tech transfer, process development, manufacturing campaigns, and regulatory-supporting deliverables.
• Own program-level risk and action logs; identify dependencies, conflicts, and timeline risks across active programs.
• Coordinate deliverables across CMC, Regulatory, QA, and external CDMO partners, driving accountability without formal authority.
• Track CDMO batch scheduling, tech transfer milestones, and manufacturing deliverables; flag scheduling conflicts early.
• Prepare status reports, dashboards, and meeting materials for governance reviews.

Skills

Cross-functional communication

Project management

CMC terminology

Biologics knowledge

Education

Bachelor's degree in a scientific or engineering field

Advanced degree a plus

Tools

Smartsheet

MS Project

Job description

CRISPR Therapeutics is seeking an Associate Manager, CMC Operations in South Boston, MA. This full-time role requires coordinating cross-program timelines and risk management across CMC, Regulatory, QA, and CDMO partners, with hands-on oversight of tech transfer and manufacturing deliverables.

The successful candidate will have a Bachelor’s degree in a scientific or engineering field with 5–7+ years of related experience, familiarity with GMP milestones, and strong cross-functional communication