Quality Assurance Specialist
- Employer
- Neurona Therapeutics
- Location
- South San Francisco, CA, United States
- Start date
- Sep 17, 2019
View more
- Discipline
- Clinical, Quality, Quality Assurance
- Required Education
- Bachelors Degree
- Position Type
- Full time
- Hotbed
- Biotech Bay
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Position Summary:
The Research Associate supports activities related to raw material disposition and maintains the inventory for manufacturing. The individual also insures that the documentation accompanying the raw materials conforms with Neurona's procedures. The individual insures that individuals conducting cell activities have completed all the SOP training necessary for manufacturing and testing.
Position Responsibilities:
• Performs receipt, inspection and labeling of raw material as well as prepares documentation for their
release. In addition, maintains up to date the inventory of raw material
• Provide support for execution and maintenance of quality systems (deviations, training and SOPs). This
task involves keeping employee's training records, vendor logbooks, document numbers for SOPs.
• Manage deviations and investigations that occur at the manufacturing site
• Performs project related tasks as assigned
• Receive, control, scan and archive of completed Neurona manufacturing production records
Requirements:
• Bachelor's Degree in chemistry, pharmaceutical science or related field or equivalent; at least 3 years of
pharmaceutical experience, including experience with quality systems.
• Prior experience releasing product in a QC environment.
• Excellent computer skills with knowledge of spreadsheet, word processing and database software.
Attention to detail as applied to data review; excellent analytical skills applied to investigations.
The Research Associate supports activities related to raw material disposition and maintains the inventory for manufacturing. The individual also insures that the documentation accompanying the raw materials conforms with Neurona's procedures. The individual insures that individuals conducting cell activities have completed all the SOP training necessary for manufacturing and testing.
Position Responsibilities:
• Performs receipt, inspection and labeling of raw material as well as prepares documentation for their
release. In addition, maintains up to date the inventory of raw material
• Provide support for execution and maintenance of quality systems (deviations, training and SOPs). This
task involves keeping employee's training records, vendor logbooks, document numbers for SOPs.
• Manage deviations and investigations that occur at the manufacturing site
• Performs project related tasks as assigned
• Receive, control, scan and archive of completed Neurona manufacturing production records
Requirements:
• Bachelor's Degree in chemistry, pharmaceutical science or related field or equivalent; at least 3 years of
pharmaceutical experience, including experience with quality systems.
• Prior experience releasing product in a QC environment.
• Excellent computer skills with knowledge of spreadsheet, word processing and database software.
Attention to detail as applied to data review; excellent analytical skills applied to investigations.
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