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Nivagen Pharmaceuticals

Develops, acquires, and markets generic drugs

Laboratory Technician - Analytical Method Development

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeSacramento, CA, USA

About the Job

Requirements

  • A bachelor's degree in chemistry, pharmaceutical sciences, biochemistry, or a related scientific discipline is required.
  • Zero to three years of experience in a pharmaceutical, biotechnology, contract laboratory, or academic laboratory environment is required; internship or laboratory coursework experience may qualify entry-level candidates.
  • A basic understanding of analytical chemistry principles is required.
  • Knowledge of laboratory documentation practices and data recording is required.
  • Applicants must live in or be willing to move to the Sacramento Metropolitan Region, approximately a 40-mile radius.
  • Applicants must be able to stand for extended periods while performing laboratory activities, lift up to 25 pounds, and work safely with chemicals and laboratory equipment.

Responsibilities

  • Assist with analytical method development and validation for pharmaceutical drug substances and drug products.
  • Prepare reagents, mobile phases, standards, and sample solutions according to approved procedures.
  • Perform analytical testing using HPLC, UPLC, UV-Vis spectrophotometers, dissolution systems, pH meters, balances, and other laboratory instruments.
  • Support troubleshooting and optimization of analytical methods under the guidance of senior scientists.
  • Maintain accurate laboratory notebooks, worksheets, and electronic data records.
  • Assist with stability studies, sample management, and laboratory inventory control.
  • Perform routine instrument maintenance, calibration, and qualification activities.
  • Ensure compliance with GMP, GDP, data integrity, laboratory safety, and company procedures.
  • Participate in laboratory investigations, deviations, and corrective actions as assigned.
  • Maintain laboratory cleanliness and organization to support inspection readiness.

Desired Qualifications

  • Familiarity with HPLC, UPLC, UV-Vis, FTIR, dissolution, or related analytical techniques is preferred.
  • Experience with Microsoft Office applications, including Excel and Word.
  • Familiarity with GMP regulations is a plus.

About the Company

Nivagen Pharmaceuticals

Develops, acquires, and markets generic drugs

Nivagen Pharmaceuticals develops, acquires, and sells generic prescription drugs and OTC products for the North American market. It leverages global partnerships with FDA-approved manufacturing facilities to deliver high-quality, affordable products and collaborates with the world’s best CROs and CRAMs to develop and manufacture niche generics. The company supports small FDA-qualified manufacturers entering the U.S. market and differentiates itself through its ability to launch new generic products and its strong sales and marketing team, rather than relying on a single manufacturing or development approach. Revenue comes from product development, co-development, acquisitions, in-licensing, and providing sales and marketing services. Nivagen aims to grow its portfolio by forging CRO/CRAM partnerships, acquiring existing products, and expanding its product lineup to capture a larger share of the evolving generic and OTC market in North America.

Company size
51-200
Company stage
Growth Equity (Venture Capital)
Total funding
$26M
Headquarters
Rancho Cordova, CA
Founded
2009

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