GMP QC Analytical Chemist - HPLC & Method Development

Medterials, Inc; San Carlos (CA); On-site; USD 95,000 - 130,000; Full time

Benefits offered by this job

401(k)

Dental insurance

Health insurance

Vision insurance

Job summary

Medterials, Inc. is seeking a QC Analytical Chemist to join its on-site San Carlos, CA facility. The role focuses on analytical testing of GMP drug intermediates within the QC department, with responsibilities spanning HPLC, LCMS, method development, validation, and instrument maintenance.

The ideal candidate will hold a chemistry degree with GMP pharmaceutical experience and will contribute to both QC and R&D efforts in a detail-oriented, compliant laboratory environment.

Qualifications

• Must have a chemistry degree with GMP pharma experience or equivalent. HPLC experience required; LCMS a plus.
• Strong attention to detail, data integrity, and ability to work in a GMP/GLP environment.
• Ability to develop and validate analytical methods and write test methods.

Responsibilities

• Independently perform HPLC and LCMS assays following GMP regulations.
• Develop and validate new analytical methods; refine existing methods.
• Maintain instrument systems and ensure data integrity per ALCOA guidelines.
• Prepare SOPs, test methods and laboratory records; support QC and R&D as needed.
• Manage lab equipment maintenance and hazardous waste in a compliant manner.

Job description

Medterials, Inc. is seeking a QC Analytical Chemist to join its on-site San Carlos, CA facility. The role focuses on analytical testing of GMP drug intermediates within the QC department, with responsibilities spanning HPLC, LCMS, method development, validation, and instrument maintenance.

The ideal candidate will hold a chemistry degree with GMP pharmaceutical experience and will contribute to both QC and R&D efforts in a detail-oriented, compliant laboratory environment.