Associate Scientist - Virology QC
- Employer
- Actalent
- Location
- Alachua County, Florida, US
- Salary
- Competitive
- Closing date
- Jan 15, 2022
View more
- Sector
- Consultancy/Private Sector
- Field
- Conservation science
- Discipline
- Other
- Salary Type
- Salary
- Employment Type
- Full time
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Description:
QC Associate Scientist in Virology lab reports to Principal Scientist, QC and will be responsible for development, validation and performing various in vitro assays to support drugs and clinical product development BSL-3 Clean Room developing viral technologies. Will be responsible for QC duties in Virology lab. Responsibilities include: qPCR, ddPCR analysis and development in virology lab ? Working in QC GLP and/or cGMP BSL-2, and BSL 3 laboratory facilities and operations. ? Develop and validate in vitro assays. ? Transfer client-developed methods. ? Perform QC release and in-process tests on large number of samples. ? Perform QC tests in support of Viral banking. ? Prepare and review virology SOPs, protocols and reports. ? Routine operation and management of BSL2 and BSL3 labs. • Working in QC GLP and/or GMP BSL-2, and BSL 3 laboratory facilities and operations • Develop and validate in vitro, lives virus assays • Transfer client-developed virology methods • Perform QC release and in-process tests on large number of samples • Perform QC tests in support of Viral banking • Provide technical support for biosafety and adventitious agent risk assessments activities • Prepare and review virology SOPs, protocols and reports. • Routine operation and management of BSL2 and BSL3 labs
Skills:
Virology, Virologist, Virus, Cell Culture, cGMP, Vaccine Manufacutring, Assay Development, i vitro, live virus, Molecular Biology, Cell Production, Vector, Scientist, CDMO, cGMP
Top Skills Details:
Virology, Virologist, Virus, Cell Culture, cGMP, Vaccine Manufacutring, Assay Development, i vitro, live virus, Molecular Biology, Cell Production, Vector, Scientist, CDMO, cGMP
Additional Skills & Qualifications:
Minimum qualifications for AVERAGE candidate: -Bachelor Degree in Virology, Microbiology, Molecular Biology or relative field -2 years of QC experience in GMP specifically with qPCR, ddPCR experience a PLUS Preferred qualifications for BEST candidate: - 5+ years of GMP Vaccine experience - Virology experience in BSL-3 level clean room - 5+ years of Assay Development experience in Vaccine development/manufacturing environment - Bachelor or higher specifically in Virology
Experience Level:
Expert Level
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
QC Associate Scientist in Virology lab reports to Principal Scientist, QC and will be responsible for development, validation and performing various in vitro assays to support drugs and clinical product development BSL-3 Clean Room developing viral technologies. Will be responsible for QC duties in Virology lab. Responsibilities include: qPCR, ddPCR analysis and development in virology lab ? Working in QC GLP and/or cGMP BSL-2, and BSL 3 laboratory facilities and operations. ? Develop and validate in vitro assays. ? Transfer client-developed methods. ? Perform QC release and in-process tests on large number of samples. ? Perform QC tests in support of Viral banking. ? Prepare and review virology SOPs, protocols and reports. ? Routine operation and management of BSL2 and BSL3 labs. • Working in QC GLP and/or GMP BSL-2, and BSL 3 laboratory facilities and operations • Develop and validate in vitro, lives virus assays • Transfer client-developed virology methods • Perform QC release and in-process tests on large number of samples • Perform QC tests in support of Viral banking • Provide technical support for biosafety and adventitious agent risk assessments activities • Prepare and review virology SOPs, protocols and reports. • Routine operation and management of BSL2 and BSL3 labs
Skills:
Virology, Virologist, Virus, Cell Culture, cGMP, Vaccine Manufacutring, Assay Development, i vitro, live virus, Molecular Biology, Cell Production, Vector, Scientist, CDMO, cGMP
Top Skills Details:
Virology, Virologist, Virus, Cell Culture, cGMP, Vaccine Manufacutring, Assay Development, i vitro, live virus, Molecular Biology, Cell Production, Vector, Scientist, CDMO, cGMP
Additional Skills & Qualifications:
Minimum qualifications for AVERAGE candidate: -Bachelor Degree in Virology, Microbiology, Molecular Biology or relative field -2 years of QC experience in GMP specifically with qPCR, ddPCR experience a PLUS Preferred qualifications for BEST candidate: - 5+ years of GMP Vaccine experience - Virology experience in BSL-3 level clean room - 5+ years of Assay Development experience in Vaccine development/manufacturing environment - Bachelor or higher specifically in Virology
Experience Level:
Expert Level
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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