Biomanufacturing Specialist at Planet Phar in Warrendale, Pennsylvania

Posted in Other about 4 hours ago.

Type: full-time





Job Description:

Key Responsibilities and Duties:

  • Primary responsibility for:
  • Manufacturing operations to support production from start-to-finish of device and biologic products:
  • Processing upstream raw materials (porcine tissue)
  • Manufacturing downstream final device
  • Manufacturing downstream final biologic
  • Aseptic fill & finish
  • Filtration
  • Set-up and operate specialty equipment
  • Preparation of reagents
  • Tissue inspection and handling
  • Assist in the setup, breakdown, and cleaning of equipment and manufacturing areas before and after production runs
  • Collaborate with manufacturing and quality teams to ensure that facilities are prepared and ready for production activities as per schedule
  • Follow and document all procedures, including batch records, cleaning logs, and any other required documentation accurately and in a timely manner
  • Support a standard 40-hour work week with flexibility to support occasional off-shift hours and/or weekends
  • Sterilization - Autoclave
  • Lyophilization
  • In-process testing
  • Release testing
  • Secondary responsibility for:
  • Manufacturing process improvement
  • Inventory management, ensure adequate supply of raw materials, components, processing aids, etc.
  • Ordering supplies (electronically)
  • Perform routine environmental monitoring sampling. Coordinate with external lab for sample analysis. Perform evaluation of EM data.
  • Equipment logs
  • Laboratory management

  • Additional Responsibilities:Assist with ongoing product research and development projects
  • Work with team to investigate and qualify equipment needed for developed products and/or products in research and development stage
  • Assist with preparation of large-scale raw materials for processing and purification
  • Assist with maintaining laboratory equipment and instrumentation required for processing of material, or process control.
  • Become familiar with equipment and the overall processes in order to make recommendations based on results.
  • Assist Quality in preparation and completion of documentation, following cGMP practices
  • Follow GMP requirements and procedures.
  • Work with a team to provide consistent quality product at high efficiency
  • Perform other tasks, as assigned

Qualifications:
  • (Required)Bachelor's degree or higher with experience in biochemistry, molecular biology, biology, or engineering principles preferred but not required, with equivalent past experience.
  • Ability to work in a cleanroom for 1-2 hours at a time
  • Experience with a broad range of production and test/inspection equipment and ability to do minor maintenance on equipment
  • Ability to work independently, and also collaborate as part of a multi-disciplinary team
  • Demonstrated ability to be highly organized and manage multiple priorities
  • Effective communication skills, both verbally and written
  • Good work ethic, reliable, and punctual
  • Strict adherence to established protocols
  • Flexibility to handle new and changing process steps / tests as they evolve[LS1] , and changing assignments
  • Proficiency in general laboratory techniques (e.g., pipette, sterile technique, weigh, titrate, reagent preparation)
  • Must have a desire to be part of a fast-paced and dynamic environment.
  • Ability to lift 15-25 pounds and stand for prolonged periods.

  • (Preferred, not required):cGMP/GLP experience
  • Experience with plate-based assays (e.g., colorimetric, ELISA)
  • Experience with mechanical testing

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