Cell Therapy Process Validation Scientist - Innovative Gene Therapies - Menlo Park


Full-time

Menlo Park, California, United States

Cell Therapy Operations

Reporting To: Senior Scientist, Cell Therapy Operations

Location: Menlo Park, Ca

Orchard Therapeutics, Ltd. is a biotechnology company incorporated in September 2015 and dedicated to bringing transformative gene therapies to patients with serious and life-threatening rare diseases. This an exciting opportunity for a well-qualified candidate to join a rapidly growing international company focused on transforming the lives of patients through innovative gene therapies.

Job Summary

The Cell Therapy Process Validation Scientist will lead activities for development, scale up, optimization, and validation of Orchard Therapeutics’ innovative gene-modified cell-based therapeutic products. Such activities will include process and assay development, cell therapy intermediate and final drug product formulation and stability evaluation, raw material evaluation, process scale-up / scale-out, and validation of manufacturing processes and controls to support company’s product programs from pre-clinical research through to commercial.

RESPONSIBILITIES:

  • Lead development, scale-up, optimization, and validation of cell isolation, cell culture, cell transduction and cell cryopreservation processes to include:
    • Process and assay development, cell therapy intermediate and final drug product formulation and stability evaluation, raw material evaluation, process scale-up / scale-out, and validation of manufacturing processes and controls
    • Compile, review and edit master production records, standard operating procedures, development/validation protocols and reports
    • Perform FMEA risk assessments for cell therapy manufacturing processes
    • Provide SME review of executed batch, records, test records and associated documentation for release of gene-modified cell therapy products. Support investigations.
    • Co-ordinate activities with the research, pre-clinical development, QA, QC, clinical development and commercial departments to ensure the successful achievement of company timelines and milestones
    • Prepare protocols and reports for prospective qualification and validation activities
    • Ensure the successful execution of activities performed between departments and company designated collaborators and CMO’s
    • Prepare CMC / CTD documents for regulatory filings with US and EU regulatory agencies
  • Other activities as may be assigned

Requirements

The ideal candidate for this position must have experience in the development, manufacture and delivery of cell-based therapy products with significant applied experience in the biotechnology industry. Candidate must possess:

  • Experience designing and executing process validation experiments using statistical multi-parameter design methods such as DOE
  • Experience performing FMEA risk assessments
  • Experience managing process and assay development and validation in support of GMP operations
  • Experience preparing documentation for regulatory filings with US and EU regulatory agencies
  • Experience with the set-up and technology transfer of manufacturing processes and controls at international CMOs
  • In-depth knowledge of FDA, EMA, GMP and ICH regulatory requirements

EDUCATION & SKILL REQUIREMENTS:

  • PhD in Biomedical Engineering or equivalent with at least 5 years of postdoctoral industry experience in bio-processing, medical technology, or biological sciences with a primary focus on the development, manufacture, distribution and delivery of cell-based therapy products. Experience in lieu of advanced degree will be considered
  • Proven personnel and project management skills
  • Outstanding organizational skills
  • Excellent written and oral communication skills
  • Ability to operate in a fast-paced, multi-disciplinary industrial environment
  • Experience of GMP cell processing production equipment operation and validation, including IQ, OQ & PQ a plus

Benefits

The successful candidate will enjoy a competitive base salary and the opportunity to participate in incentive compensation programs, including a stock option plans. Orchard Therapeutics, Ltd. offers a comprehensive benefits program, including: medical, dental and vision care; paid vacation and holiday time; access to a voluntary 401(k). Orchard Therapeutics is an equal opportunity employer.

Notice to All Applicants: Orchard Therapeutics participates in E-Verify

Notice to RECRUITERS: All employment offers and CV’s are managed through our Human Resources Department and all candidates are presented through this avenue. Therefore, the Human Resources Department at Orchard Therapeutics requests that recruiters are not to contact Orchard Therapeutics employees directly to present candidates. Complying with this request will be a factor in determining future professional relationships with Orchard Therapeutics. Orchard Therapeutics will not accept unsolicited resumes from any source other than directly from candidates for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the recruiter does not create any implied obligation on the part of Orchard Therapeutics.