Materials Management Associate (I, II, III / Sr.)

Neurona Therapeutics

South San Francisco, CA, US
  • Job Type: Full-Time
  • Function: Operations
  • Post Date: 03/23/2021
  • Website: neuronatherapeutics.com
  • Company Address: 650 Gateway Blvd Suite 125 South, San Francisco, CA, 94080

About Neurona Therapeutics

Neurona Therapeutics is a pre-clinical stage biotechnology company that was founded by four leading-edge neuroscientists and stem cell pioneers at The University of California, San Francisco. We are focused on the discovery and development of cell-based therapies to treat intractable neurological disease. Our initial aim is to generate therapeutic compositions of a specific type of nerve cell (or neuron) for targeted delivery into the injured nervous system. Based on nearly two decades of research, we believe that particular subpopulations of neurons have the unique ability to integrate and repair dysregulated neural circuits. Our talented team of scientists, scientific advisors, and board directors is working to accelerate breakthrough treatments for patients with significant unmet medical needs.

Job Description

Neurona Therapeutics is an early stage biotechnology company based in South San Francisco focused on the development of neuronal cell-based therapies for neurological diseases. Our ideal candidate is a self-motivated individual who has a passion for excellence. This is a fantastic opportunity to join a small team, work on transformative science, and take part in building an exciting, science-driven company.
 
Responsibilities:
·Manage inventory of raw materials and supplies
·Receive and inspect raw materials, supplies and equipment. Provide support with disposition and release. Support the archival of all associated documentation.
·Ensure compliance with SOPs
·Coordinate and assist with cleanroom kit preparation and planning of activities
·Preparation of SOPs for material and supply management
·Assist with maintaining laboratories (equipment maintenance, calibration, cleaning and related documentation).
·Ensure all safety and compliance procedures are always followed.
·Participate in and drive raw material and vendor qualifications
·Participate in and coordinate with vendors and suppliers on supply agreements
·Write and revise controlled documentation (SOPs, Manufacturing Procedures (MPs), Forms, Technical Reports, etc.)
·Lead resolution of Non-Conformances/Process Deviations and execution of Corrective and Preventive Actions (CAPA).
·Collaborate with Quality and other functional groups internally to resolve discrepancies in a timely manner.
·Assure appropriate escalation to various levels of management when personnel and environmental safety, equipment functionality, product supply, or quality are at risk.
·Collaborate with Quality, Manufacturing, and Regulatory Compliance staff in cross-functional teams.
·Must possess the ability to work independently or as a team.
 
Required Qualifications:
·Bachelor’s degree in science or engineering with 2+ years of industrial experience or equivalent.
 
Preferred Qualifications:
·2+ years of industrial experience in cGMP operations.
·Knowledge of inventory management systems
·Knowledge of CFRs and cGMP requirements and ability to interpret and apply the knowledge
·Ability to independently collaborate with outside vendors
·Possess excellent troubleshooting skills, presentation and interpersonal skills
·Able to take initiative to improve work processes, develop innovative methodologies and approaches to enhance process productivity.
 
 
For immediate consideration, please visit our website at www.neuronatherapeutics.com.
 
Neurona is proud to be an equal opportunity employer and will consider all qualified applicants for employment.

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Disclaimer: Local Candidates Only
This company does NOT accept candidates from outside recruiting firms. Agency contacts are not welcome.