Aseptic Manufacturing Specialist

6 days ago


Philadelphia, Pennsylvania, United States R&D Partners Full time
Job Overview

R&D Partners is seeking a highly skilled Aseptic Manufacturing Technician to join our team. As a key member of our manufacturing team, you will be responsible for ensuring the quality and integrity of our cell therapy products.

Key Responsibilities
  • Process Execution: Develop a comprehensive understanding of and be able to proficiently execute current cell therapy manufacturing process.
  • Training and Documentation: Complete training sessions and ensure training documentation is maintained.
  • Quality Compliance: Understand and comply with quality standards and requirements as documented.
  • Operational Support: Provides operational support functions including materials stocking, kit preparation, reagent preparation, cleaning activities, and equipment maintenance.
  • Technical Transfer: Supports technical transfer and additional research level testing activities.
  • Regulatory Compliance: Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP). Completes recording of data to comply with regulatory requirements.
  • Documentation Support: Support documentation needs, which may include drafting and approval of SOPs, Batch Records, Deviations, CAPAs, etc. Perform basic revisions as needed to accurately reflect current procedures.
  • Communication: Attends the daily lab meeting and escalates issues/concerns at that forum to Area Management for further investigation.
Requirements
  • Education: B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience.
  • Experience: Experience in biopharmaceutical based GMP manufacturing operations, including experience in cell culture and associated downstream processing.
  • Technical Knowledge: Demonstrated technical knowledge of aseptic processing in cleanroom environments.
  • Quality Mindset: Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA regulations.
  • Schedule Flexibility: Aseptic Manufacturing Technicians are required to work their assigned schedule. This position is currently for regular work week hours (1st shift M-F); however, due to the nature of cell therapy manufacturing schedules, must be willing to work alternative shifts, weekends, evenings, and holidays, as needed. It is also expected that regular work weeks may change once commercial manufacturing commences and may involve shift changes (i.e. Tuesday to Saturday). May be required to work overtime.


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