Astrix Technology
QC Associate Scientist - Analytical Chemistry
Laboratory
Cleveland, OH, US
Pay Rate Low: 85000 | Pay Rate High: 95000
Apply for Job
We’re hiring an Associate Scientist with analytical chemistry experience to join a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO partners and generic drugs. This is a great opportunity to work with an industry leader that focuses on their expertise and competence in all of the companies processes!
Salary:
85K-95K
Schedule:
M-F 8a-5p
Location:
Cleveland, OH
Responsibilities
Perform routine HPLC, GC, and other analytical testing (e.g., FTIR, KF, NMR)
Support GMP method transfers, including protocol/report preparation
Conduct release testing for raw materials, intermediates, and APIs
Investigate out-of-specification (OOS) results and document findings
Ensure timely and compliant data generation to meet project timelines
Review analytical data for accuracy and GDP compliance
Qualifications
B.S. in Chemistry with 5+ years of relevant experience in a GMP pharmaceutical lab
Experience with HPLC and GC analysis in a regulated environment
Strong knowledge of GLP/GMP, quality control, and lab documentation practices
Proficient with lab equipment, Microsoft Excel and Word
* 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!
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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Cleveland, OH, US
Pay Rate Low: 85000 | Pay Rate High: 95000
Apply for Job
We’re hiring an Associate Scientist with analytical chemistry experience to join a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO partners and generic drugs. This is a great opportunity to work with an industry leader that focuses on their expertise and competence in all of the companies processes!
Salary:
85K-95K
Schedule:
M-F 8a-5p
Location:
Cleveland, OH
Responsibilities
Perform routine HPLC, GC, and other analytical testing (e.g., FTIR, KF, NMR)
Support GMP method transfers, including protocol/report preparation
Conduct release testing for raw materials, intermediates, and APIs
Investigate out-of-specification (OOS) results and document findings
Ensure timely and compliant data generation to meet project timelines
Review analytical data for accuracy and GDP compliance
Qualifications
B.S. in Chemistry with 5+ years of relevant experience in a GMP pharmaceutical lab
Experience with HPLC and GC analysis in a regulated environment
Strong knowledge of GLP/GMP, quality control, and lab documentation practices
Proficient with lab equipment, Microsoft Excel and Word
* 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!
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.
#J-18808-Ljbffr