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QC Chemist I

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Somerset, NJ

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TitleQC Chemist IJob DescriptionSUMMARY: The Quality Control Chemists perform the testing on raw materials, bulk formulations, finished products, stability samples, and any other samples from plant operations which require chemical analysis.  ESSENTIAL FUNCTIONS:Include the following. Other duties may be assigned.  Sampling and testing of raw materials.Physical and chemical testing of bulk and (pre-fill, finished product, and stability) product.Maintaining laboratory notebook and checking the work of others.Maintaining the work area in an orderly manner.Keeps current with all SOP’s dealing with their job assignments.Reports any problems with assays or components to the QC Lab Supervisor.Responsible for preparing and standardizing any reagents or standard materials required for analysis. Reports any supply needs to the QC Lab Supervisor.Disposes of unused samples and laboratory waste in appropriate containers.Performs calibration of lab instruments.Cleaning of laboratory glassware.   ADDITIONAL RESPONSIBILITIES: Other duties will be assigned as required.   Auto req ID915BRStateNew Jersey CitySomersetQualificationsQUALIFICATIONS:To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION AND EXPERIENCE:  BA or BS in chemistry. Minimum two years of experience in a the lab performing chemistry related duties Experience with High Pressure Liquid Chromatography, Infra-Red (IR), Gas Chromatograph (GC), Ultra Violet/Visible, Particle Size Analysis, KF Titration and wet chemistry skills are required.  Familiarity with HPLC/GC analytical software.Familiarity with GLP/GMP guidelines.Good Communication and writing skills.Familiarity with out-of-specification (OOS) and out-of-trend (OOT) investigation.Computer literate.Experience with USP/EP monographs.  JOB PREREQUISITES:  Ability to meet attendance standards.  All full-time employees are required to work a 40-hr week.  At times it may be necessary to work additional hours in order to get the required tasks accomplished to meet deadlines. Must be detail oriented. Must have GMP experience in an FDA related environment, inclusive of 21 CFR Part 11 compliance criteria. Must have a team work attitude.   Company Overview**MEMBERS ONLY**SIGN UP NOW***. is a niche pharmaceutical company that develops, manufactures and markets generic and branded prescription pharmaceuticals as well as animal and consumer health products. We specialize in difficult-to-manufacture sterile and non-sterile dosage forms including: ophthalmics, injectables, oral liquids, topicals, inhalants, and nasal sprays. Akorn markets its products to retail pharmacies, ophthalmologists, optometrists, physicians, veterinarians, hospitals, clinics, wholesalers, distributors, group purchasing organizations, and government agencies.EEO Statement**MEMBERS ONLY**SIGN UP NOW***. is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.,skills:null,hiringOrganization:{@type:Organization,name:**MEMBERS ONLY**SIGN UP NOW***.,logo:null},identifier:{@type:PropertyValue,name:**MEMBERS ONLY**SIGN UP NOW***.,value:496238},url:****usadvertisehelpprivacytermsprotect yourself© 1999-2018 Jobing.com, LLC.All rights reserved.•••

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