Senior QC Analyst - cGMP & Protein Chemistry

AL Solutions; New Jersey; On-site; USD 70,000 - 90,000; Full time

Job summary

A pharmaceutical manufacturing company is seeking a QC Analyst to support clinical and commercial programs by conducting analytical testing in compliance with regulatory standards. The ideal candidate will have at least 3 years of experience in a GMP environment and expertise in techniques like HPLC and ELISA. This full-time position requires a bachelor's degree in a related field and offers a dynamic work environment.

Qualifications

• Minimum of 3 years of hands-on experience in a GMP-compliant QC laboratory environment.
• Proficient in key analytical techniques including HPLC, SDS-PAGE, ELISA, and Capillary Electrophoresis.

Responsibilities

• Conduct analytical testing for in-process, raw materials, release, and stability programs.
• Ensure compliance with cGMP, ICH guidelines, and internal Quality Systems.
• Participate in investigations related to Out-of-Specification results.

Skills

Analytical Testing

Protein Chemistry

HPLC

SDS-PAGE

ELISA

Capillary Electrophoresis

Education

Bachelor’s degree in Biotechnology, Biochemistry, Chemistry, or related field

Job description

A pharmaceutical manufacturing company is seeking a QC Analyst to support clinical and commercial programs by conducting analytical testing in compliance with regulatory standards. The ideal candidate will have at least 3 years of experience in a GMP environment and expertise in techniques like HPLC and ELISA. This full-time position requires a bachelor's degree in a related field and offers a dynamic work environment.