Randstad USA
Job Summary
We are seeking a highly motivated
Chemist
to join our Quality Control (QC) team in Cleveland, OH. The successful candidate will be a key contributor to a project focused on the testing and verification of 14 amino acids used in the manufacturing of high-purity biopharmaceutical and/or life science products. This role requires a strong foundation in analytical chemistry and a working knowledge of compendial standards (e.g., USP, EP, JP) within a cGMP/GLP environment. Location:
Cleveland, Ohio Job Type:
Contract Salary:
$25.50 - 30.50 per hour Work Hours:
9 to 5 Education:
Bachelor's degree
Responsibilities
Compendial Testing: Perform complex and routine analytical testing on amino acids and raw materials in accordance with established compendial monographs (USP, EP, JP) and internal SOPs.
Analytical Instrumentation: Operate, maintain, and troubleshoot analytical instrumentation such as HPLC, UV-Vis, FT-IR, titration, and other wet chemistry techniques.
Data Analysis and Documentation: Accurately document all laboratory work, including raw data, calculations, and results in notebooks, LIMS, and/or worksheets, adhering to GDP.
Quality & Compliance: Ensure all work is performed in compliance with cGMP, company quality systems, and safety protocols (EH&S).
Method Support: Participate in laboratory investigations (e.g., OOS, OOT), method verifications, and method transfers as needed.
Lab Operations: Maintain an audit-ready laboratory, manage inventory of chemicals and standards, and perform equipment calibrations and performance checks.
Qualifications
Education: Bachelor’s degree (B.S.) in Chemistry, Analytical Chemistry, Biochemistry, or a closely related scientific discipline.
Experience: 1 to 3 years of relevant analytical laboratory experience, preferably in a Quality Control or cGMP/regulated industry setting (e.g., pharmaceutical, biotechnology, or chemical manufacturing). Relevant internship or academic research experience will be considered.
Skills: Chemistry, Good Laboratory Practices (GLP).
Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. We welcome people of all abilities and are committed to providing reasonable accommodations during the application and interview process. If you require an accommodation, please contact HRsupport@randstadusa.com.
Note:
This posting is open for thirty (30) days and reflects current information about this role.
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We are seeking a highly motivated
Chemist
to join our Quality Control (QC) team in Cleveland, OH. The successful candidate will be a key contributor to a project focused on the testing and verification of 14 amino acids used in the manufacturing of high-purity biopharmaceutical and/or life science products. This role requires a strong foundation in analytical chemistry and a working knowledge of compendial standards (e.g., USP, EP, JP) within a cGMP/GLP environment. Location:
Cleveland, Ohio Job Type:
Contract Salary:
$25.50 - 30.50 per hour Work Hours:
9 to 5 Education:
Bachelor's degree
Responsibilities
Compendial Testing: Perform complex and routine analytical testing on amino acids and raw materials in accordance with established compendial monographs (USP, EP, JP) and internal SOPs.
Analytical Instrumentation: Operate, maintain, and troubleshoot analytical instrumentation such as HPLC, UV-Vis, FT-IR, titration, and other wet chemistry techniques.
Data Analysis and Documentation: Accurately document all laboratory work, including raw data, calculations, and results in notebooks, LIMS, and/or worksheets, adhering to GDP.
Quality & Compliance: Ensure all work is performed in compliance with cGMP, company quality systems, and safety protocols (EH&S).
Method Support: Participate in laboratory investigations (e.g., OOS, OOT), method verifications, and method transfers as needed.
Lab Operations: Maintain an audit-ready laboratory, manage inventory of chemicals and standards, and perform equipment calibrations and performance checks.
Qualifications
Education: Bachelor’s degree (B.S.) in Chemistry, Analytical Chemistry, Biochemistry, or a closely related scientific discipline.
Experience: 1 to 3 years of relevant analytical laboratory experience, preferably in a Quality Control or cGMP/regulated industry setting (e.g., pharmaceutical, biotechnology, or chemical manufacturing). Relevant internship or academic research experience will be considered.
Skills: Chemistry, Good Laboratory Practices (GLP).
Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. We welcome people of all abilities and are committed to providing reasonable accommodations during the application and interview process. If you require an accommodation, please contact HRsupport@randstadusa.com.
Note:
This posting is open for thirty (30) days and reflects current information about this role.
#J-18808-Ljbffr