QC Documentation Analyst — GLP/SOP & Data Review

Noven Pharmaceuticals; Miami (FL); On-site; USD 50,000 - 70,000; Full time

Job summary

A pharmaceutical company in Miami is looking for a QC Document Reviewer to carry out sample analysis and ensure compliance with quality standards. The ideal candidate will have a degree in chemistry or a related scientific field and experience with chromatographic analysis. Strong organizational and communication skills are essential. This full-time position requires a high level of detail and the ability to work under pressure in a laboratory environment.

Qualifications

• Minimum four years experience with a bachelor’s degree in chemistry required or equivalent experience.
• Broad knowledge in scientific methods and chromatographic analysis.
• Good written English and verbal communication skills.

Responsibilities

• Responsible for sample analysis and data processing.
• Review test results for compliance with GLP and internal SOPs.
• Compile and maintain review records according to best practices.

Skills

Chromatographic analysis

Analytical methods (HPLC, GC)

Wet chemistry techniques

Communication skills

Organizational skills

Interpersonal skills

Microsoft applications

Education

Bachelor’s degree in chemistry or related field

Master’s degree in chemistry or related field

PhD in chemistry or related field

Tools

Waters Corp. Empower

LIMS

Job description

A pharmaceutical company in Miami is looking for a QC Document Reviewer to carry out sample analysis and ensure compliance with quality standards. The ideal candidate will have a degree in chemistry or a related scientific field and experience with chromatographic analysis. Strong organizational and communication skills are essential. This full-time position requires a high level of detail and the ability to work under pressure in a laboratory environment.