QC Analytical Chemist

Califesciences; San Carlos, Northern (CA, KY); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Medterials is seeking a QC Analytical Chemist to perform analytical testing of GMP drug intermediates within a small, specialty pharmaceutical manufacturing and development company.

The role focuses on method development, validation, and routine QC analysis using HPLC, with involvement in documentation, troubleshooting, and collaboration with QC and R&D teams. Strong GMP/GLP practices and data reporting are essential.

Qualifications

• Bachelor’s in Chemistry required; 4+ years GMP industry experience or Master’s in Analytical Chemistry with 2+ years GMP experience.
• PhD candidates may apply with relevant analytical chemistry focus.
• HPLC experience is required; LC-MS is a plus; strong documentation and data analysis skills expected.

Responsibilities

• Perform analytical testing of GMP drug intermediates in QC as part of a small specialty pharma team.
• Develop and refine analytical methods; validate and transfer methods to QC; support R&D efforts as needed.
• Assist in equipment and laboratory maintenance; generate technical reports and troubleshooting documentation.

Skills

Detail oriented

Time management

Troubleshooting

Written technical reports

Education

Bachelor's in Chemistry

Master's in Analytical Chemistry

PhD in Analytical/Pharmaceutical Chemistry

Tools

HPLC

LC-MS

MS Office

Job description

Medterials is seeking a QC Analytical Chemist with chemistry education and experience to work in a small, specialty pharmaceutical manufacturing and development company. This person’s primary responsibility is to work within the QC department to perform analytical testing of GMP drug intermediates. The person will also work in development of new analytical methods, refinement of existing analytical methods, and perform method validations. The person will also participate in equipment and laboratory maintenance for the analytical department. We are looking for a committed, detail-oriented individual who can carry out routine analytical tests compliant to GMP/GLP practices primarily using HPLC but can also contribute to assay development and problem solving to support both QC and R&D efforts.

Qualifications:

To perform this job successfully, an individual must be able to perform each essential duty independently and satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

Education/Experience:

Chemistry degree is required. Minimum requirements are a Bachelor’s degree (BS) in Chemistry with at least four years GMP industry experience or a Master’s degree (MS) in Analytical Chemistry or other Chemistry field with at least two years GMP industry experience. Entry level with no experience will be considered for candidates with a Doctor of Philosophy (PhD) in Analytical Chemistry, Physical Chemistry, Organic Chemistry, or Medicinal/Pharmaceutical Chemistry. HPLC experience is required; LCMS experience is a plus.

General Skills:

Must be organized and detail oriented. Must be able to manage time efficiently. Must be able to work effectively with staff members of different backgrounds. Able to troubleshoot problems associated with assays and equipment that are being used.

Language Ability:

Must be able to follow verbal instructions and written protocols. Must be able to communicate any issue or problem with Supervisor and laboratory staff in a timely manner. Most be able to assimilate data and produce comprehensive technical reports.

Software Skills:

To perform this job successfully, candidates must have a working knowledge of Microsoft Office Suite (Word and Excel), HPLC Analysis Software, and basic internet tools. Statistical analysis software experience is a plus.