QC Analyst III (Microbiology)
- Employer
- SRG WOOLF
- Location
- Framingham, Massachusetts, US
- Salary
- Competitive
- Closing date
- Oct 19, 2021
View more
- Sector
- Consultancy/Private Sector
- Field
- Conservation science
- Discipline
- Biology
- Salary Type
- Salary
- Employment Type
- Full time
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QC Analyst III (Microbiology)
SRG is in need of a QC Analyst III (Microbiology) for one of our priority clients! Reach out to me if you or anyone you know has interest!
Framingham, MA 6-12 months &
open to Temp to perm
QC Analyst III (Microbiology)
General laboratory procedures in support of microbiological testing. Data analysis, trending, and reporting using MS Word and Excel.
• Conducts microbiology routine and non-routine testing per approved SOPs. This includes analysis of raw materials, in process and finished formulations, microbial identifications, environmental monitoring and water collection/testing including but not limited to Bioburden, Endotoxin, and TOC.
• Development of assays methods for use in QC lab and may participate in validation studies, assay qualifications and special projects as assigned.
• Proficient in writing quality systems records (Deviations, Change Controls, CAPA)
• Troubleshoots assay methods and equipment and assists in troubleshooting and investigations for Alert/Actions, OOS and other non-conforming results.
• Responsible maintenance and calibration of lab equipment
• Proficient in performing aseptic technique for critical biological assays.
• Performs Raw Material Testing and reporting
• Participates in audits and act as technical SME.
• May author design protocols, change control requests, and Quality Technical Reports, as directed. Performs document revisions.
Previous Experience: 4+ years related work experience within a cGMP laboratory.
Skills: Microbiological or bio-analytical techniques, general laboratory skills, computer skills. Working knowledge of microbiological methodologies such as Environmental monitoring, bioburden and endotoxin testing. GMP QC environment experience is preferred. Experience in authoring, SOPs protocols and technical reports.
General knowledge of Lean and 6 Sigma Practices.
#LI-BK1
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
SRG is in need of a QC Analyst III (Microbiology) for one of our priority clients! Reach out to me if you or anyone you know has interest!
Framingham, MA 6-12 months &
open to Temp to perm
QC Analyst III (Microbiology)
General laboratory procedures in support of microbiological testing. Data analysis, trending, and reporting using MS Word and Excel.
• Conducts microbiology routine and non-routine testing per approved SOPs. This includes analysis of raw materials, in process and finished formulations, microbial identifications, environmental monitoring and water collection/testing including but not limited to Bioburden, Endotoxin, and TOC.
• Development of assays methods for use in QC lab and may participate in validation studies, assay qualifications and special projects as assigned.
• Proficient in writing quality systems records (Deviations, Change Controls, CAPA)
• Troubleshoots assay methods and equipment and assists in troubleshooting and investigations for Alert/Actions, OOS and other non-conforming results.
• Responsible maintenance and calibration of lab equipment
• Proficient in performing aseptic technique for critical biological assays.
• Performs Raw Material Testing and reporting
• Participates in audits and act as technical SME.
• May author design protocols, change control requests, and Quality Technical Reports, as directed. Performs document revisions.
Previous Experience: 4+ years related work experience within a cGMP laboratory.
Skills: Microbiological or bio-analytical techniques, general laboratory skills, computer skills. Working knowledge of microbiological methodologies such as Environmental monitoring, bioburden and endotoxin testing. GMP QC environment experience is preferred. Experience in authoring, SOPs protocols and technical reports.
General knowledge of Lean and 6 Sigma Practices.
#LI-BK1
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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