Stryker Corporation
Cambrex
Associate Analytical Scientist I (QC)
US-CO-Longmont
Job ID:
2026-4606 Type:
Regular Full-Time # of Openings:
1 Category:
Analytical - Quality Control Cambrex - Longmont
Overview Quality control chemist capable of executing analytical methods and provide general analytical support. Able to organize routine work with supervision and evaluate and interpret generated data. Exercise judgment within defined procedures and practices to determine appropriate action.
Responsibilities
Maintain working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
Responsible for ensuring compliance with cGMP and other regulatory guidelines.
Perform assigned tasks carefully, safely, and on schedule according to SOPs and supervisor instructions.
Perform calibrations and verifications of instrumentation according to procedures with little to no supervision.
Execute analytical methods for release and stability monitoring of bulk drug substances and drug products under cGMP requirements.
Generate hand‑written records of actions accurately and legibly on appropriate documentation with minimal errors.
Compile, maintain, interpret and
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Job ID:
2026-4606 Type:
Regular Full-Time # of Openings:
1 Category:
Analytical - Quality Control Cambrex - Longmont
Overview Quality control chemist capable of executing analytical methods and provide general analytical support. Able to organize routine work with supervision and evaluate and interpret generated data. Exercise judgment within defined procedures and practices to determine appropriate action.
Responsibilities
Maintain working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
Responsible for ensuring compliance with cGMP and other regulatory guidelines.
Perform assigned tasks carefully, safely, and on schedule according to SOPs and supervisor instructions.
Perform calibrations and verifications of instrumentation according to procedures with little to no supervision.
Execute analytical methods for release and stability monitoring of bulk drug substances and drug products under cGMP requirements.
Generate hand‑written records of actions accurately and legibly on appropriate documentation with minimal errors.
Compile, maintain, interpret and
#J-18808-Ljbffr