Quality - Technical writer - TechDigital
Libertyville, IL
About the Job
MSAT Technical Writer, Cell Therapy Vector Engineering Support (CTES), Manufacturing Science and Technology (MSAT)
The focus of the MSAT Technical Writer is to investigate and write root cause analyses of in-process and end-of-process testing results outside of the specified range during and after drug product manufacturing. The MSAT Tech Writer:
- Compiles and interprets manufacturing process data to identify possible failure modes
- Learns complex cell biology concepts & applies them to root cause investigations
- Works independently and with Process Engineer(s) to understand different failure modes
- Works with GMP Quality Systems to deliver completed Root Cause Analysis investigation reports
Education:
- BS in Bio/Chem Science/Engineering or related field
- Immunology education preferred
Experience:
Required experience:
• 3+ years relevant experience in drug product biopharmaceutical or equivalent industry
• Deviation writing
• cGMP/cGDP
• Ability to prioritize multiple investigations in order to meet deadlines
• Strong scientific and technical acumen including technical writing skills
Preferred experience:
• Quality management system
• Complex problem-solving skills, including root cause investigation
• Cross-functional collaboration with engineering and quality partners
• Biologics or cell therapy manufacturing
• Trained in Kepner Tregoe Problem Solving
Duties and Responsibilities:
• Facilitates deviation closure through working with quality partners and site quality systems
• Analyzes and summarizes manufacturing data to support root cause investigations
• Analyzes and summarizes characterization data to write root cause investigations
• Utilizes root cause analysis tools such as Kepner Tregoe Problem Solving to identify root cause
• Writes technical and thorough investigation reports
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The focus of the MSAT Technical Writer is to investigate and write root cause analyses of in-process and end-of-process testing results outside of the specified range during and after drug product manufacturing. The MSAT Tech Writer:
- Compiles and interprets manufacturing process data to identify possible failure modes
- Learns complex cell biology concepts & applies them to root cause investigations
- Works independently and with Process Engineer(s) to understand different failure modes
- Works with GMP Quality Systems to deliver completed Root Cause Analysis investigation reports
Education:
- BS in Bio/Chem Science/Engineering or related field
- Immunology education preferred
Experience:
Required experience:
• 3+ years relevant experience in drug product biopharmaceutical or equivalent industry
• Deviation writing
• cGMP/cGDP
• Ability to prioritize multiple investigations in order to meet deadlines
• Strong scientific and technical acumen including technical writing skills
Preferred experience:
• Quality management system
• Complex problem-solving skills, including root cause investigation
• Cross-functional collaboration with engineering and quality partners
• Biologics or cell therapy manufacturing
• Trained in Kepner Tregoe Problem Solving
Duties and Responsibilities:
• Facilitates deviation closure through working with quality partners and site quality systems
• Analyzes and summarizes manufacturing data to support root cause investigations
• Analyzes and summarizes characterization data to write root cause investigations
• Utilizes root cause analysis tools such as Kepner Tregoe Problem Solving to identify root cause
• Writes technical and thorough investigation reports
has context menu
Source : TechDigital
