Clinical Viral Vector Manufacturing Associate

SLAC

Palo Alto (CA)

On-site

USD 50,000 - 94,000

Full time

9 days ago
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Benefits offered by this job

PTO days
Health benefits
403(b) plan
Tuition assistance

Job summary

Stanford University is seeking a Clinical Process Development & Manufacturing Professional I focused on clinical viral vector products. Work will occur on-site in Stanford, with responsibilities spanning biomanufacturing campaigns, process development, and technology transfer to support Phase I/II clinical trials.

The role requires a Bachelor's degree in a related scientific field, strong biology knowledge, aseptic culture experience, and the ability to work under deadlines with minimal

Qualifications

  • Strong understanding of biological scientific principles.
  • Strong computer skills and ability to learn quickly and master computer programs, databases and scientific applications.
  • Ability to work under deadlines with minimal supervision.
  • Ability to maintain relationships and communicate effectively.
  • Excellent organizational skills and demonstrated ability to complete detailed work.

Responsibilities

  • Plan, prepare for and perform human clinical materials biomanufacturing campaigns.
  • Plan and perform components of process development and technology transfer for manufacturing of clinical materials, scale-up/scale-out and optimization activities.
  • Perform upstream and downstream components of assigned cGMP project(s).
  • Identify, document and report operating excursions and facility deficiencies; make recommendations for process improvements and documentation improvements including SOPs and manufacturing Batch Records (BR).
  • Contribute to detailed manufacturing budget; including sourcing, identifying and ensuring qualified and verified raw materials for manufacturing; outlining overall and per/patient costs for project materials and supplies.
  • Devise and revise methods and/or processes for SOP and Manufacturing Batch Records.
  • Independently track, verify and ensure cGMP grade raw materials for biomanufacturing. Identify and plan for supply chain and raw materials lead times for scheduled campaigns.
  • May prepare abstracts or papers for publication in peer-reviewed journals and/or presentation at scientific conferences. Present results during internal meetings.

Skills

Biology concepts
Computer skills
Deadlines under pressure
Communication
Organization

Education

Bachelor's degree

Job description

Stanford University is seeking a Clinical Process Development & Manufacturing Professional I focused on clinical viral vector products. Work will occur on-site in Stanford, with responsibilities spanning biomanufacturing campaigns, process development, and technology transfer to support Phase I/II clinical trials.

The role requires a Bachelor's degree in a related scientific field, strong biology knowledge, aseptic culture experience, and the ability to work under deadlines with minimal

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