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 Scientist - Exton, Pennsylvania, United States

   
Job information
Posted by: frontage laboratories 
Hiring entity type: Other 
Work authorization: Existing work authorization required for United States
Position type: Direct Hire, Full-Time 
Compensation: ******
Benefits: See below
Relocation: Not specified 
Position functions: Science
 
Travel: Unspecified 
Accept candidates: from anywhere 
Languages: English - Fluent
 
Minimum education: See below 
Minimum years experience: See below 
Resumes accepted in: English
Cover letter: No cover letter requested
Job code: 23Onx64xycqbDj7yMXwlOqjm8fcHIO / Latpro-3774397 
Date posted: Feb-21-2021
State, Zip: Pennsylvania, 19341

Description

Scientist For Frontage Laboratories, Inc. - Exton, PA, perform biological method development, validation, transfer, quantitation and bioanalytical sample analysis in SOPs and Good Laboratory Practice (GLP) environments; provide high-quality analytical testing of finished products, raw materials, Active Pharmaceutical Ingredient (API), in-process products and stability samples in Good Manufacturing Practice (GMP) environment; conduct biologics and bioanalytical assays using High and Ultra Pressure Liquid Chromatography (HPLC/UPLC), Gas Chromatography Mass Spectrometry (GC-MS), Malvern Mastersizer, dissolution apparatus, SpectraMax, SIMOA,  Meso Scale Discovery, ELLA, Scanning Electron Microscopy (SEM) and Phase Contrast Microscopy; perform data analysis quality control (QC) and interpretation for biologics per GLP or CLIA guidelines using Watson; perform assay, impurities and elemental analysis for drug products under GMP using EMPOWER; write and review protocols, laboratory notebooks, reports, deviations and analytical documents for method validation and ANDA submissions.

Requirements:

  1. Master of Science or foreign equivalent degree in Pharmacology, Pharmaceutical Sciences or a related field.
  2. 2 years experience in job offered or 2 years experience as a Research and Development Scientist. This required experience must include evaluation of toxicity of nanoparticles using instruments and techniques, including cell culture, Scanning Electron Microscopy (SEM), Phase Contrast Microscopy, MTT Cytotoxicity Assay, Lactate Dehydrogenase (LDH) Assay, ELISA, TUNEL Assay, method development, transfer, validation, qualification and sample analysis using High and Ultra Pressure Liquid Chromatography (HPLC/UPLC), Gas Chromatography Mass Spectrometry (GC-MS), Malvern Mastersizer, dissolution apparatus, SpectraMax, SIMOA,  Meso Scale Discovery, ELLA in SOPs, GLP, GMP environment or under ICH and CLIA guidelines.
  3. Proficiency in cell culturing, Scanning Electron Microscopy (SEM), Phase Contrast Microscopy, MTT Cytotoxicity Assay, Lactate Dehydrogenase (LDH) Assay, TUNEL Assay, ELISA, HPLC, UPLC, GC, Malvern Mastersizer, dissolution apparatus, SpectraMax, SIMOA, Meso Scale Discovery Assay, ELLA, GC-MS, Watson and Empower software.

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Requirements

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