E

Edgewise Therapeutics

Develops therapies for rare muscular disorders

Associate Director - Technical Operations

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeUnited States

About the Job

Requirements

  • A bachelor's degree in chemistry, pharmaceutical sciences, engineering, biology, or a related scientific discipline is required.
  • At least 7 years of biotechnology or pharmaceutical development experience and at least 5 years of CMC small-molecule development experience are required.
  • Demonstrated end-to-end knowledge of the CMC drug development lifecycle, from early development through commercialization.
  • Experience supporting and integrating drug substance development, process validation, and manufacturing; drug product development, process validation, and manufacturing; and analytical development, testing, validation, and lifecycle management.
  • Significant experience within CMC organizations, including R&D development, technical operations, manufacturing, and supply chain.
  • Direct experience leading or coordinating GMP change controls, including cross-functional impact assessments and implementation planning.
  • Experience collaborating with Quality Assurance, Regulatory Affairs, Manufacturing, Supply Chain, and external partners.
  • Experience supporting shipping coordination, logistics planning, shipment execution, and preparation of shipping reports.
  • Deep understanding of pharmaceutical Quality Management Systems and GMP requirements.
  • Hands-on experience with electronic Quality Management Systems such as Veeva Vault QMS, TrackWise, MasterControl, or equivalent platforms.
  • Experience managing change controls, deviations, CAPAs, risk assessments, and related quality records within a QMS environment.
  • Working knowledge of cGMP regulations, ICH guidelines, FDA, EMA, and global regulatory expectations.
  • Strong understanding of change management principles and regulatory impact assessments throughout the product lifecycle.
  • Strong project management, communication, and stakeholder management skills.
  • Ability to read, understand, and comply with workplace health and safety policies, safe work practices, and company policies and procedures.
  • Willingness to travel 25%, including all company retreats.

Responsibilities

  • Serve as the change owner and lead all CMC-related change controls.
  • Initiate, develop, coordinate, and track change controls from inception through closure.
  • Ensure appropriate assessment of CMC technical, quality, regulatory, manufacturing, supply chain, and validation impacts.
  • Partner with QA while maintaining CMC ownership of technical change strategy and implementation.
  • Establish processes that improve consistency, compliance, and efficiency of change control management.
  • Identify proactively activities requiring change controls through participation in forums and team meetings.
  • Provide guidance to functional teams regarding change control requirements and expected documentation.
  • Collaborate with QA to monitor change control metrics, timelines, and risks and provide visibility to leadership.
  • Provide operational leadership for CMC shipment planning and coordination.
  • Prepare and review shipping reports and associated documentation.
  • Coordinate shipment activities involving CMOs, CROs, testing laboratories, and distribution partners.
  • Coordinate shipment-related activities to ensure appropriate planning, documentation, and alignment with project objectives.
  • Identify opportunities to improve shipment planning, reporting, and logistics workflows.
  • Support broader MS&T operational priorities and special projects as needed.
  • Represent CMC Change Control at project team and Change Control Review Board meetings.
  • Serve as a key point of contact between CMC and QA regarding change implementation.
  • Escalate risks, delays, and compliance issues to senior leadership.
  • Drive continuous improvement initiatives related to change control and logistics management.
  • Perform other duties as assigned by the supervisor.

Desired Qualifications

  • Advanced degree (MS, PharmD, or PhD) is preferred.

About the Company

Edgewise Therapeutics

Develops therapies for rare muscular disorders

Edgewise Therapeutics develops therapies for rare muscle disorders using a proprietary drug discovery platform. Its lead molecule, sevasemten (EDG 5506), targets the muscle motor protein myosin to reduce stress in fast skeletal muscle fibers, aiming to improve muscle health without affecting other muscle types. The company owns global development and commercialization rights to its programs and pursues strategic collaborations and asset acquisitions to accelerate its pipeline. Its focus is precision medicine for conditions like Duchenne muscular dystrophy, Becker muscular dystrophy, Limb Girdle muscular dystrophies, and McArdle disease. Overall, Edgewise seeks to deliver targeted treatments that protect and improve muscle health for patients and families affected by these rare diseases.

Company size
51-200
Company stage
IPO
Headquarters
Boulder, CO
Founded
2017

Recently Posted Jobs

Explore more opportunities at Edgewise Therapeutics

See more jobs