Astrix Technology
QC Analyst II
Manufacturing
Chicago, IL, US
Pay Rate Low: 30 | Pay Rate High: 33.65
Added - 14/04/2025
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Our client, a global leader in biopharma R&D and manufacturing, is seeking an experienced
QC Analyst II
to support upstream/downstream manufacturing operations. QC Analyst II Pay
: $29-33/hr
Hours:
1st shift M-F
Terms:
6 month contract-to-hire
Key Responsibilities: Perform analytical testing for in-process, release, and stability studies.
Support OOS investigations, deviations, CAPAs, and audits.
Collaborate with cross-functional teams on projects and equipment maintenance.
Author and revise SOPs, QC methods, and reports.
Train junior analysts and support regulatory inspection readiness.
Qualifications: BS in biotech, biochem, or related field + 5 yrs QC lab exp.(MS + 3 yrs or PhD + 2 yrs also considered)
cGMP lab experience required.
Strong background in protein chemistry and analytical troubleshooting.
Technical Skills: Proficient with HPLC, SDS-PAGE, ELISA, CE, bioassays, and compendial methods.
Experience with regulatory filings and inspection prep (e.g., PAI).
Additional Info: Office/lab split; some travel may be required.
Fast-paced environment; must meet tight deadlines.
This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-DNP: We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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QC Analyst II
to support upstream/downstream manufacturing operations. QC Analyst II Pay
: $29-33/hr
Hours:
1st shift M-F
Terms:
6 month contract-to-hire
Key Responsibilities: Perform analytical testing for in-process, release, and stability studies.
Support OOS investigations, deviations, CAPAs, and audits.
Collaborate with cross-functional teams on projects and equipment maintenance.
Author and revise SOPs, QC methods, and reports.
Train junior analysts and support regulatory inspection readiness.
Qualifications: BS in biotech, biochem, or related field + 5 yrs QC lab exp.(MS + 3 yrs or PhD + 2 yrs also considered)
cGMP lab experience required.
Strong background in protein chemistry and analytical troubleshooting.
Technical Skills: Proficient with HPLC, SDS-PAGE, ELISA, CE, bioassays, and compendial methods.
Experience with regulatory filings and inspection prep (e.g., PAI).
Additional Info: Office/lab split; some travel may be required.
Fast-paced environment; must meet tight deadlines.
This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-DNP: We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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