Director Process Development and Manufacturing, CMC

Job Title: Di rector Process Development and Manufacturing, CMC

Department: CMC

Reports to: Chief Technical Officer

Opus Genetics is committed to building an innovative, efficient and sustainable science based and commercial ophthalmic biopharmaceutical company leading the development of transformative gene therapies for the treatment of inherited retinal diseases (IRDs) and therapies to treat patients with other retinal and refractive disorders.

The Director of Process Development and Manufacturing will be the technical lead for development and manufacturing of assigned assets within the Opus gene therapy programs focusing on technical transfer and process development and execution supporting product development and manufacturing to achieve company goals and strategies.

This includes working collaboratively with external partners (i.e. CDMOs, contract labs, suppliers) to develop technical studies, analyze complex data, make data driven decisions, and author, review, and approve technical and regulatory documents.

The ideal candidate will have a deep technical understanding of AAV gene therapy upstream and downstream development and process optimization. This role will directly interact with the CDMO/contract partners and be responsible for building and maintaining excellent working relationships. Knowledge of manufacturing platforms, consistent with AAV technology, at scales ranging from process development through GMP and PPQ activities.

The candidate will be hands-on and expected to provide content to all these areas.

• Work with Opus CDMO/contract manufacturing and laboratory partners to develop a phase appropriate robust manufacturing program to support the process development and engineering of pre commercial and commercial cGMP material to support pre-clinical studies, clinical trials, and commercial supply.
• Support, author, and review/approve manufacturing plans and documentation including technical transfer, batch records and documentation, product specifications, stability programs, bridging and comparability studies, and other reports utilizing phase appropriate QbD best practices.
• Support, author, and review/approve manufacturing documentation including testing records, certificates of testing/analysis, campaign summary reports, investigations, etc.
• Support, author, and review/approve regulatory documentation including pINDs, INDs, agency responses, CMC meeting requests and briefing packages, and BLAs.
• Ensure proper reference standard material is in place, tested, and released for each product.
  
  Lead technology transfer between sites.
• Ensure regulatory requirements are in place to support manufacturing campaigns with respect to Master Cell Banks, Plasmids, Drug Substances, Drug Products, and Diluents, to prevent developmental delays and or interruptions to clinical programs or regulatory filings.
• Perform the role of person in plant as needed at the Opus CDMO/contract manufacturing partner’s sites.
  
  Act as the CMC expert during audits and interactions with regulatory agencies.
• Manage work to project plans for multiple gene therapy programs in the preclinical, pre-IND, IND/clinical, and commercial stages.
• Identify and lead the resolution of operational and functional level challenges, work with program and/or function managers to elevate issues to senior management.
• Hands on resolution to issues/content generation.
  
  Design effective and high-quality presentations and progress reports, as requested.

• Master’s degree (minimum) from an accredited institution in a science or health-related field with minimum of 7-10 years of experience in the pharmaceutical or biotechnology industry.
  
  Ophthalmology experience is preferred.
• Additionally, a minimum of 5 years of direct manufacturing experience for biopharmaceuticals.
  
  Preference will be given for direct AAV gene therapy experience.
  
  Previous CDMO/contract lab experience also preferred.
• Experience designing and executing technical transfer and scale up campaigns and associated documentation.
• Experience in writing and reviewing regulatory submissions including…