QC Data Review Scientist for Analytical Excellence

Cambrex Corp.; Charles City, Northern (IA, KY); Hybrid; USD 70,000 - 90,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

Cambrex Charles City is seeking a Data Review Scientist to review laboratory data and ensure compliance with SOPs, compendial and CGMP requirements. The role requires knowledge of instrument theory to vet data and draw conclusions from collected results.

You will review raw data from technicians and scientists, identify inaccuracies, verify conclusions, and maintain cGMP records and systems. A bachelor’s degree in chemistry with several years in pharma/cGMP, plus experience with analytical

Qualifications

• Bachelor’s degree in chemistry with three years’ experience in a pharmaceutical and cGMP environment highly preferred.
• Experience in a laboratory environment highly preferred.
• Knowledge of analytical instrumentation (GC, HPLC, FTIR, UV-VIS, etc.) required.

Responsibilities

• Reviews raw technical data provided by technicians, chemists and laboratory supervision to ensure accuracy, completeness and correct scientific conclusions have been drawn.
• Identifies data inaccuracies, incomplete inferences and works directly with laboratory staff to provide guidance and direction on the correction of laboratory data packages.
• Verifies and ensures that conclusions drawn on laboratory data are sound and accurate and representative of materials under examination.
• Maintains and manages cGMP and controlled substance systems in all QC/PSG labs at defined levels of compliance in accordance with site approved procedures and protocols.
• Maintains open communication within and across departments to ensure timely delivery and approval of laboratory documents.

Skills

Chemistry knowledge

Education

Bachelor's in chemistry

3 years pharma/cGMP experience

Tools

GC

HPLC

FTIR

UV-VIS

Job description

Cambrex Charles City is seeking a Data Review Scientist to review laboratory data and ensure compliance with SOPs, compendial and CGMP requirements. The role requires knowledge of instrument theory to vet data and draw conclusions from collected results.

You will review raw data from technicians and scientists, identify inaccuracies, verify conclusions, and maintain cGMP records and systems. A bachelor’s degree in chemistry with several years in pharma/cGMP, plus experience with analytical