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Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.
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Qualifications: Minimum bachelor’s degree/PhD in Chemistry or related discipline + years working as an R&D Chemist for a pharmaceutical company. Position Details: Position Type: -year contract with additional opportunity contingent upon performance and continued business needJob Location: New Brunswick/Somerset, NJShift: st shiftCompensation: $ per hour (based on experience) The Analytical Research and Development Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.
$35 - $40Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Data science, machine learning, optimization models, PhD in Machine Learning, Computer Science, Information Technology, Operations Research, Statistics, Applied Mathematics, Econometrics, Successful completion of one or more assessments in Python, Spark, Scala, or R, Supervisory experience, Using open source frameworks (for example, scikit learn, tensorflow, torch.
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Intermediate knowledge of pharmaceutical manufacturing and utilities that support cell therapy clinical manufacturing. Location: Warren, New Jersey Type: Contract Job #78973 Our client, a leading pharmaceutical company, is hiring a Commissioning/ Qualification Specialist/ Validation on a contract basis.
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A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs in a pharmaceutical manufacturing facility.
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Master's or PhD degree in Chemistry, Chemical Engineering, Materials Science, or a related discipline. Experience with electrochemistry and materials characterization techniques such as SEM, TEM and XPS.
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Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in above areas with 6 years of experience in a pharmaceutical/biotech QC laboratory.
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Experience in GMP pharmaceutical product testing and knowledge of GDP and GLP requirements. Must have hands-on experience working on laboratory equipment like FTIR, HPLC, GC, AA, or ICP-MS. Certified Chemical Engineer, Certified Quality Engineer, and Certified Six Sigma Green Belt are preferred but not required.
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0 - 2 years of chemical processing experience or batch mixing in the Medical Device or Pharmaceutical manufacturing industry. Responsible for accurately maintaining legible and accurate records, required logs, books, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and Health and Safety requirements.
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Knowledge of cGMP for pharmaceutical and/or vaccine manufacturing, Lean Six Sigma Methodology, Root Cause Analysis, Failure Mode Effects Analysis, knowledge in reliability engineering (including asset life cycle management.
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Doctoral degree which may be a PhD or equivalent in a field such as Cognitive Neuroscience, Psychology/Neuropsychology, Gerontology, Sociology, Epidemiology, Health Economics, or Health Services Research or a clinical doctorate (MD, DO, PharmD, DNP) in Neurology, Psychiatry, Internal Medicine, Family Medicine, Geriatrics, Nursing, Pharmacy, or related fields with advanced research training.
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Required B.S. Chemistry, Biology, Microbiology or relevant discipline Experience/Knowledge: 8 years of relevant work experience required, preferable in a Pharmaceutical environment. Advanced knowledge of Microsoft office applications , LIMS, Quality Management system (e.g. TrackWise or Veeva), Statistics software (e.g. SlimSTAT, JMP.
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Knowledge of analysis of pharmaceutical dosage forms and raw materials utilizing HPLC, GC, ICP-MS, UV, TLC, dissolution testing, spectroscopic and wet chemistry techniques is a plus. The Quality Control (QC) Senior Chemist position supervises a small group of laboratory chemists who are responsible for conducting analysis of pharmaceutical dosage forms (OTC)/ Dietary Supplements and raw materials utilizing HPLC, GC, dissolution testing, spectroscopic and wet chemistry techniques.
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Performs duties as assigned by Pharmacy Manager, Staff Pharmacist and Store Manager including utilizing pharmacy systems to enter patient and drug information, ensuring information is entered correctly, filling prescriptions by retrieving, counting and pouring pharmaceutical drugs, verifying medicine is correct, and checking for possible interactions.
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2+ years or more experience in a chemical/manufacturing plant (or related industry) with a focus on MIQA, reliability, or PSM, preferably in a pharmaceutical or food manufacturing environment. Provides technical, MIQA and reliability support for items such as: vessels, piping, mechanical equipment, rotating equipment, and materials of construction consistent with ASME, API, SAP, DuPont Standards, PSM MIQA requirements, Inspection Briefs, etc.
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pharmaceutical phd jobs Company: Genesis Research in Edison, NJ
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