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Employment Type:
Full time
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(This job is no longer available)
Frontage Laboratories | Exton, PA
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Job Description


For a contract research organization (Frontage Laboratories, Inc. – Exton, PA): perform method validation, development and transfer for drug products and substances; perform release and stability sample analyses; perform extractable and leachable studies; API and finished product release testing; commercial product stability testing and storage and GLP dosing sample analysis; draft pharmaceutical sample reports all under current Good Manufacturing Practices (cGMP), GLP and all applicable requirements.


  1. Master of Science or foreign equivalent degree in Pharmacy, Pharmaceutical Chemistry or a related field.
  2. 6 months experience in job offered or 6 months experience as an Analytical Chemist in regulated environment. This required experience must include 6 months experience in stability and release test, method development and validation for pharmaceutical products, analysis of zeta potential and particle size of Nano-emulsion, optimization of water soluble molecules, USP testing such as viscosity, loss on drying, residue on ignition, heavy metal, spectrophotometric identification, water determination and thin-layer chromatographic identification.
  3. Proficient with High Performance Liquid Chromatography (HPLC), Ultra Performance Liquid Chromatography (UPLC), Gas Chromatography (GC), Ultraviolet-Visible Spectroscopy (UV) and Fourier Transform Infra-red Spectroscopy (FTIR), Karl Fisher, LC-MS and HPLC-CAD.

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About Frontage Laboratories

Frontage Laboratories, Inc. is more than a contract laboratory ... we're a collaborative R & D company dedicated to advancing the development efforts of pharmaceutical companies around the world. We specialize in assisting our partners to resolve complex product development issues through our combined expertise in pharmaceutical analysis, bioanalytical testing and method development, and custom synthesis of investigational compounds. Frontage Laboratories, Inc. has a passion for detail and is committed to following Good Laboratory and Manufacturing P ractices (GLP and GMP). We have an experienced management team and scientific staff (over 75 years of combined technical experience), most of whom have received their training and expertise from such notable companies as Wyeth, Merck, Pharmacia, and Aventis. We have incorporated these experiences into establishing robust laboratory quality systems. Our current clientele range from drug discovery companies, large pharma companies to generic pharmaceutical companies in the US and abroad. Frontage Laboratories, Inc. is fully compliant with cGMP/GLP regulations. We offer quality services, rapid turnaround and competitive pricing.