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Melissa S.
Quality Assurance Technical Associate
Posted: 08/29/2024
2024-08-29
2024-10-20
Employment Type:
Permanent
Industry: Technical & Professional
Job Number: MS268573826
Pay Rate: $45000-55000 / year
Job Description
Quality Assurance Technical Associate
Candidates must have:
-Quality Assurance experience in the pharmaceutical industry or laboratory environment PREFERRED
-Excellent cGMP knowledge
-Strong organizational skills
-Microsoft Word and Excel proficiency
-Technical writing skills (be able to provide sample on request)
-Ability to work independently and as part of the team
-Bachelor’s degree in a science discipline – strong science background, chemistry preferred.
Responsibilities may include:
-Analytical support/product development, formulation review, protocol approvals
-Familiarity with CMC sections of abbreviated new drug applications
-Document activation and distribution: SOPs, specifications, protocols, etc.
-Analytical review: Must be able to review, interpret, and approve analytical reports
-Stability data: Interpret results, trend analysis, and approval of stability data
-Issuance and control of preventative maintenance documentation
-Lab audits
-Batch record maintenance and issuance
-Final batch record review, release, and pedigree issuance
-Support in various specialized software systems, such as Calibration program, documentation software, temperature monitoring, etc.
-Incident and investigation writing
-Technical support as needed.
For more details, please call Melissa @ 815-997-1442
Candidates must have:
-Quality Assurance experience in the pharmaceutical industry or laboratory environment PREFERRED
-Excellent cGMP knowledge
-Strong organizational skills
-Microsoft Word and Excel proficiency
-Technical writing skills (be able to provide sample on request)
-Ability to work independently and as part of the team
-Bachelor’s degree in a science discipline – strong science background, chemistry preferred.
Responsibilities may include:
-Analytical support/product development, formulation review, protocol approvals
-Familiarity with CMC sections of abbreviated new drug applications
-Document activation and distribution: SOPs, specifications, protocols, etc.
-Analytical review: Must be able to review, interpret, and approve analytical reports
-Stability data: Interpret results, trend analysis, and approval of stability data
-Issuance and control of preventative maintenance documentation
-Lab audits
-Batch record maintenance and issuance
-Final batch record review, release, and pedigree issuance
-Support in various specialized software systems, such as Calibration program, documentation software, temperature monitoring, etc.
-Incident and investigation writing
-Technical support as needed.
For more details, please call Melissa @ 815-997-1442
Meet Your Recruiter
Melissa S.
Technical Recruiter
Year Started: 2020
I wanted to be an elementary school art teacher when I grew up.
Favorite Quote:
“Not all of us can do great things. But we can do small things with great love.” – Mother Theresa
What do you enjoy most about your work?
I enjoy matching the right people with the best opportunities.
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