Research Chemist

Nivagen Pharmaceuticals; Sacramento (CA); On-site; USD 65,000 - 95,000; Full time

Job summary

Nivagen Pharmaceuticals is seeking a chemist to perform analytical testing on pharmaceutical products to ensure regulatory compliance with FDA/ICH guidelines. The role involves working with GC, LC-MS, HPLC, and related detectors in a GMP/GDP environment.

The candidate should have 1–5 years of experience in a pharmaceutical QC laboratory, a chemistry-related degree, and strong documentation skills. The position emphasizes accuracy, traceability, and collaboration with R&D, production, and QA

Qualifications

• Bachelor’s or Master’s degree in Chemistry or related field.
• 1-5 years of experience in a pharmaceutical quality control laboratory.
• Experience with GMP, GLP, and GDP requirements.

Responsibilities

• Operate and maintain analytical instruments (GC, LC-MS, HPLC, etc.).
• Calibrate and maintain lab equipment to ensure accuracy.
• Develop and validate analytical methods per ICH and FDA guidelines.
• Perform qualitative and quantitative analyses on raw materials and finished products.
• Conduct stability studies following ICH guidelines.
• Investigate deviations and implement CAPA.
• Ensure GLP, GMP, GDP compliance.
• Assist in regulatory inspections and audits.
• Collaborate with R&D, production, and QA.

Skills

Pharma regulations

Troubleshooting

Documentation

Attention to detail

Lab safety

Education

Bachelor’s or Master’s in Chemistry or related field

Tools

GC

GC-MS

LC-MS

UPLC

HPLC

UV-Vis

PDA

CAD detectors

Job description

Job Summary: As a chemist atNivagenyou willbe responsible forconducting analytical tests on pharmaceutical products, ensuring that they meet regulatory standards such as those set by the FDA and ICH. This role involves performing tests on raw materials, intermediates, and finished dosage forms to guarantee product safety, efficacy, and quality in compliance with Good Manufacturing Practices (GMP) and other regulatory standards.

Responsibilities:

• Operate andmaintainanalytical instruments such as GC, GC-MS, LC-MS, UPLC, and HPLC, which are equippedwith UV-Vis, PDA, and CAD detectors.
• Ensure proper calibration and regular maintenance of laboratory equipment to guarantee accuracy and precision inresults.
• Assistin developing andvalidatinganalytical methods for new products, ensuring compliance with regulatoryguidelines, including those from ICH and FDA.
• Perform qualitative and quantitative analyses on raw materials, in-process materials, and finished products usingvalidated methods to ensure compliance with required specifications.
• Conduct stability studies on products following ICH guidelines, adhering to stability protocols, and documentingresults for regulatory submissions.
• Investigate deviations and out-of-specification (OOS) results, conduct root cause analysis, and implementcorrective and preventive actions (CAPA) to address and prevent recurrence.
• Ensure all testing adheres strictly to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), GoodDistribution Practices (GDP), and other relevant regulatory standards.
• Implement ICH Q2 (R1) guidelines for method validation andparticipatein internal and external audits tomaintainlaboratory compliance.
• Collaborate with R&D, production, and quality assurance teams to support product development andcommercializationefforts, andprovide assistanceduring regulatory inspections.
• Perform anyadditionaltasks as assigned by the Chief Scientific Officer (CSO)

Required Skills/Abilities:

• Strong understanding of pharmaceutical regulations (FDA and ICH).
• Ability to troubleshoot analytical issues and conduct root cause analysis.
• Strong communicationand documentation skills.
• Excellent attention to detail and organizational skills.
• Familiarity with FDA, ICH guidelines, including ICH Q7 (Good Manufacturing Practice for Active PharmaceuticalIngredients) and ICH Q10 (Pharmaceutical Quality System).
• Knowledge of stability testing guidelines, including ICH Q1A.
• Ability to stand and work for extended periods in a laboratory environment.
• Comfortable handling chemicals and pharmaceuticalsubstances.

Education and Experience:

• Bachelor’s orMaster’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry, ora relatedfield.
• 1-5 years of experience in a pharmaceutical quality controllaboratory.
• Experience with GMP, GLP, and GDP requirements.

Physical Requirements/ Working Conditions:

To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. Nivagen is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, Nivagen will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer. Nivagen uses E-Verify.

Nivagenis a nicotine-free campus , meaning the use of nicotine products—including cigarettes, vaping, chewing tobacco, and any other nicotine-containing substances isstrictly prohibitedon company property. All employees should be able to complete their full shift without the need to use nicotine . By joiningNivagen, you agree to adhere to our nicotine-free workplace policy, which supports a healthier environment for all employees.