Cambrex

Scientist III (QC) or Sr. Scientist I (QC)

US-CO-Longmont

Job ID: 2024-3910 Type: Regular Full-Time

of Openings: 1

Category: Analytical - Quality Control Cambrex - Longmont

Overview

An experienced quality control chemist capable of testing and troubleshooting all common analytical methodologies. This role is expected to understand all aspects of Quality Control processes. This individual will have the ability to execute difficult analytical methods as needed and provide leadership and training to junior Chemists. Able to organize routine work with minimal instruction from management and accurately evaluate and interpret generated data. This individual will demonstrate a strong understanding of compliance as related to the analytical laboratory.

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 written procedures with no supervision.
• Executes all test methods required for quality control for the release of novel drug products, drug substances, in-process monitoring, and stability.
• Generate hand-written record of actions accurately and legibly on appropriate documentation with minimal errors.
• Compile, maintain, interpret and extrapolate results of analysis and communicate these results to supervisor.
• Utilize Laboratory Information Management System (LIMS) according to procedure for inventory management and data entry.
• Participate in group and project meetings as required.
• Maintain a clean and safe workspace.
• Maintain laboratory equipment and testing supplies as directed.
• May support laboratory investigations process with assistance.
• May assist with writing technical documentation for quality events such as OOS, atypical investigations, deviations and CAPAs.
• Enter project hours promptly and update project status on appropriate tracking and/or timekeeping systems.
• Attend and apply new training as required.
• Participate in and comply with all current safety, health and environmental programs.
• Communicate issues or challenges to senior staff and/or laboratory management and shares ideas of process improvements.
• Performs other related duties as assigned.

Qualifications * BS/MS in chemistry or similar science-related fields and 10+ years industry experience. Chemistry or Biochemistry degree preferred. PhD in Chemistry or Analytical Chemistry and 6+ years industry experience.

Apply Here: https://www.click2apply.net/KLQNPpIadNYGNtRmVc5NDn

PI249524729