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Qualifications:PhD or MS in Analytical Chemistry, Chemistry, Biochemistry, or another relevant field. Overview Within the Translational Bioanalytical Sciences (TBS) group of Clinical Development, the role focuses on LC-MS/MS of small and large molecule quantitative assay development of biological samples.
$140,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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EXPERIENCE/EDUCATION: · B.S. in Science Field or related discipline is required (Chemistry or Bio Chemistry is preferred) · Knowledge in oligonucleotide synthesis and PCR technology is desirable · Knowledge in lab equipment automation and programming · Ability to work under cGMP guidelines, and coordinate/implement production schedule is necessary If interested, please share your updated resume at.
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Minimum of a Bachelors in a Science degree including but not limited to biology, chemistry, physics, chemical, mechanical or materials science engineering. Assists PLM’s and applications with in-house (e.g., Raman Boot Camp) and outside events (e.g., workshops/seminars at customer sites.
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Proven track record meeting aggressive targets as related to safe, timely and successful synthetic organic chemistry projects. Coordinate analytical chemistry methodology to process and/or catalysis discovery, development optimization and problem solving.
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Minimum of Bachelor's Degree in Chemistry, Chemical Engineering, or Biology. Perform GC and GC-MS analysis for quality control samples, fragrance compounds, essential oils, and chemical compounds.
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Ph. D./M.S. degree in chemistry, biochemistry, or related field with 5 to 8 years of relevant industry experience (10+ for M.S.) with applied knowledge in plant-based carbohydrate polymer processing, development, commercialization.
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Basic understanding of fundamental principles of physics, mathematics, AC and DC electrical theory, heat transfer and fluid flow, thermodynamics, chemistry, and metallurgy. The purpose of the Control Room Operator is to control, operate and maintain generation and auxiliary equipment in a manner that will ensure safety of personnel and equipment, promote high plant reliability, produce power economically and operate the generation facility in a manner to maintain the Landfill Gas Collection System goals and remain within environmental and regulatory compliance.
$36 - $46.65 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Applicants must have received a Ph. D. (or foreign equivalent) in experimental or computational structural biology, biochemistry, chemistry, physics, computer science, statistics, or related field; made outstanding contributions in basic/applied research; acted as a persuasive advocate for the open data movement and the FAIR and FACT Principles emblematic of responsible data stewardship; and successfully led large multidisciplinary teams engaged in national/international collaborations.
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Chemistry : We foster and nurture an entrepreneurial spirit throughout the Triple-S family. The position requires working in accordance with Triple-S Steel job requirements and Safe Methods of Work. Overtime hours may be required to meet our customers’ needs.
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Must possess Chemistry, Manufacturing and Controls (CMC) experience and have some knowledge of CTD. Job Title: CMC Regulatory Technical Writer II. Expertise with MS Office, Word, Excel and document management systems such as Veeva or Documentum is a plus.
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Bachelor's degree required; scientific field (chemistry, biology) or professional medical required (MD, PharmD, RN, etc. The successful candidate will provide quality expertise to manage and improve processes across Aquestive's development program, ensuring compliance with Good Clinical Practices (GCP), Good Laboratory Practice (GLP), Preclinical stage and GMP for clinical manufacturing oversight.
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Intermediate knowledge of Microsoft Word, Microsoft Excel and Adobe AcrobatKnowledge of cGMP/GDP regulations, ICH Guidelines, and CMC (Chemistry and Manufacturing Controls) recommendedExcellent communication, organizational, interpersonal and computer skillsExcellent Oral/Written Communication SkillsDemonstrated ability to manage multiple competing prioritiesSolid organizational skills and attention to detail.
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Experience with Veeva (Quality Docs, QMS and Training modules) a plus. Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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Create, route and track controlled records within documents management system, Veeva. This includes documentation control, change control, deviation management, and CAPA (Corrective and Preventive Action) systems.
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Master's Degree or PhD in relevant Life Science field (biology, biochemistry, chemistry) Bachelor's degree in relevant Life Science field (biology, biochemistry, chemistry, etc.) This position is part of the Sales Team located in the United States of America and will be fully remote.
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chemistry job in Piscataway, NJ
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