ELISA / HPLC / qPCR Biologist
- Employer
- Eurofins USA PSS Insourcing Solutions
- Location
- Lexington, Massachusetts, US
- Salary
- Competitive
- Closing date
- Nov 7, 2021
View more
- Sector
- Consultancy/Private Sector
- Field
- Conservation science
- Discipline
- Other
- Salary Type
- Salary
- Employment Type
- Full time
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Job Description
* Contributes as part of a team of AD scientists towards execution and development of various analytical methods to support of biological therapeutic product release and characterization testing in a compliance-based environment
* Independently performs routine testing using established Test Methods, including associated protocol/report documentation and presentations
* Experience in high throughput technologies and automated liquid handling systems (Tecan, Janus, etc.) a plus
* Background in technology transfers, qualifications and validation activities for regulatory support a plus
* Demonstrated hands-on trouble-shooting capabilities using HPLC and UPLC systems a must
* Independently executes method for: elucidation and monitoring of functional properties of protein therapeutics and the quantitation of process- and product-related impurities
* Understands and applies advanced scientific principles, theories, concepts, practices and standards for product development
* Experience with sterile cell culture and execution of cell-based assays a plus.
* Conducts work in compliance with cGMP/GLP, safety and regulatory requirements
* Demonstrates independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives
* Contributes as part of a team of AD scientists towards execution and development of various analytical methods to support of biological therapeutic product release and characterization testing in a compliance-based environment
* Independently performs routine testing using established Test Methods, including associated protocol/report documentation and presentations
* Experience in high throughput technologies and automated liquid handling systems (Tecan, Janus, etc.) a plus
* Background in technology transfers, qualifications and validation activities for regulatory support a plus
* Demonstrated hands-on trouble-shooting capabilities using HPLC and UPLC systems a must
* Independently executes method for: elucidation and monitoring of functional properties of protein therapeutics and the quantitation of process- and product-related impurities
* Understands and applies advanced scientific principles, theories, concepts, practices and standards for product development
* Experience with sterile cell culture and execution of cell-based assays a plus.
* Conducts work in compliance with cGMP/GLP, safety and regulatory requirements
* Demonstrates independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives
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