QC Specialist, Microbiology
- Employer
- Randstad Life Sciences
- Location
- Arcadia, California, US
- Salary
- Competitive
- Closing date
- May 30, 2022
View more
- Sector
- Academic / Research
- Field
- Conservation science
- Discipline
- Biology
- Salary Type
- Salary
- Employment Type
- Full time
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Job Description
A CDMO whose mission is to translate research concepts to scalable, manufacturable therapies for patients is seeking a QC Specialist, Microbiology.
This is a temporary to permanent position
Job Summary:
Minimum of 5 years of experience in QC - microbiology alone in Biotech or Pharma. Experience in risk assessment, environmental monitoring, and method validation of endotoxins and bioburden required. Ability tp work with minimum supervision.
Education and Professional Experience:
Bachelor's degree in Microbiology, Molecular and Cell biology, Biology or related field required. In lieu of this requirement, work experience may be considered
Minimum of 5 years of work experience in the Pharmaceutical, Life Sciences industry with cGMP, GLP
A strong background in method development, qualification and validation is highly desired. A background in quality control testing related to Biopharmaceuticals is required.
Experience with problem solving methods such as DMAIC or other similar Root Cause Analysis Tools
Strong knowledge of cGMP and ICH guidelines. Other regulatory agencies experiences preferred
A CDMO whose mission is to translate research concepts to scalable, manufacturable therapies for patients is seeking a QC Specialist, Microbiology.
This is a temporary to permanent position
Job Summary:
Minimum of 5 years of experience in QC - microbiology alone in Biotech or Pharma. Experience in risk assessment, environmental monitoring, and method validation of endotoxins and bioburden required. Ability tp work with minimum supervision.
Education and Professional Experience:
Bachelor's degree in Microbiology, Molecular and Cell biology, Biology or related field required. In lieu of this requirement, work experience may be considered
Minimum of 5 years of work experience in the Pharmaceutical, Life Sciences industry with cGMP, GLP
A strong background in method development, qualification and validation is highly desired. A background in quality control testing related to Biopharmaceuticals is required.
Experience with problem solving methods such as DMAIC or other similar Root Cause Analysis Tools
Strong knowledge of cGMP and ICH guidelines. Other regulatory agencies experiences preferred
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