QC Raw Materials Analyst II - cGMP & USP/PhEur

Integrated Resources Inc.; Raleigh (NC); On-site; USD 60,000 - 90,000; Full time

Job summary

A leading staffing firm is seeking a Quality Control Raw Materials Associate II to ensure compliance with industry regulations and support manufacturing processes. The ideal candidate has a strong background in analytical techniques and experience in a cGMP environment, primarily within the pharmaceutical or biotechnology sectors. This role involves performing detailed testing and analysis of raw materials, following stringent quality standards and protocols.

Qualifications

• 3-5 years’ experience in a cGMP environment in the pharmaceutical or biotechnology industry.
• Proficiency in analytical techniques and compliance knowledge.
• Experience in performing compendial analysis.

Responsibilities

• Perform qualification of Raw Materials, protocols and reports.
• Conduct testing such as compendial analysis on raw materials.
• Support manufacturing based on cGMP's and internal procedures.

Skills

Analytical techniques

Problem solving

Communication

Troubleshooting

Organizational skills

Education

B.S. degree in the Sciences, preferably Chemistry

A.S. Degree in Chemistry

Tools

Chromatography

HPLC

GC

Spectroscopy

Karl Fisher

Job description

A leading staffing firm is seeking a Quality Control Raw Materials Associate II to ensure compliance with industry regulations and support manufacturing processes. The ideal candidate has a strong background in analytical techniques and experience in a cGMP environment, primarily within the pharmaceutical or biotechnology sectors. This role involves performing detailed testing and analysis of raw materials, following stringent quality standards and protocols.