QC Analytical Chemist

Sacbar; San Carlos, Northern (CA, KY); On-site; USD 90,000 - 115,000; Full time

Job summary

Medterials is seeking a QC Analytical Chemist to join a small, specialty pharmaceutical manufacturing and development company. The role focuses on GMP-compliant analytical testing of drug intermediates, mainly by HPLC, with involvement in method development and validation.

The candidate will contribute to equipment and laboratory maintenance and support both QC and R&D initiatives, requiring a chemistry degree and GMP experience; advanced degrees are welcomed for entry-level opportunities.

Qualifications

• Bachelor's degree in Chemistry with at least four years GMP industry experience or Master's degree with at least two years GMP industry experience.
• PhD in Analytical/Physical/Organic/Medicinal/Pharmaceutical Chemistry welcomed for entry-level.
• HPLC experience is required; LCMS experience is a plus.

Responsibilities

• Perform analytical testing of GMP drug intermediates within the QC department.
• Develop, refine, and validate analytical methods.
• Participate in equipment and laboratory maintenance for the analytical department.

Skills

Attention to detail

Time management

Team communication

Troubleshooting

Analytical thinking

Education

Bachelor's degree in Chemistry

Master's degree in Analytical Chemistry

PhD in Analytical/Physical/Organic/Medicinal Chemistry

Tools

HPLC

LCMS

Microsoft Office

HPLC data software

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.