R&D CHEMIST I

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    "description_html": "<p>&nbsp;&nbsp;</p><p><strong>Job Purpose:&nbsp;</strong></p><p>This role is to Perform research and development projects for established products and new products including but not limited to analytical test method validation/transfer/verification, reformulation, procedures, investigations, and other non-specified projects or initiatives.&nbsp;</p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</p><p><strong>Essential Duties and Responsibilities:&nbsp;</strong></p><ul><li>Plans, organizes, and manages resources on projects to assure technical quality and schedule adherence</li><li>Capable of working in a GMP environment and responsible for generating GMP data.&nbsp;</li><li>Capable of working with different analytical techniques including but not limited to HPLC, UPLC, GC, Automatic Titrator, IR, DSC, ICP, and Mass Spectrometry.&nbsp;</li><li>Responsible for performing different analytical tests for R&amp;D and QC as needed.&nbsp;</li><li>Responsible for executing research and development projects for established products and new product development with respect to formulation, laboratory &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;investigations, and early process development.&nbsp;</li><li>Responsible for evaluating new raw materials and components for quality and safety prior to implementation into exhibit batches and GMP production.&nbsp;</li><li>Responsible for conducting the development and validation of analytical methods for pharmaceutical ingredients and dosage forms, including establishment of specifications.&nbsp;</li><li>Assist in drafting R&amp;D and QC protocols and report.&nbsp;</li><li>Performs research and development stability testing as necessary.&nbsp;</li><li>Participates in the development and implementation of associated programs (e.g. cleaning validation, process validation, GMP compliance, equipment validation, maintenance and use, etc.)</li><li>Oversee and ensure reports, submission documentation, and development summaries documenting the product &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;development process are available for clients, partners, and health authorities (i.e. FDA)</li></ul><p><strong>Supplemental Functions:&nbsp;</strong></p><ul><li>Performs other similar duties as required.</li></ul><p>&nbsp;<strong>Job Specifications and Qualifications:&nbsp;</strong></p><p><br></p><p><strong>Knowledge &amp; Skills:&nbsp;</strong></p><p>· Strong interpersonal, verbal, and written communication skills. Effective organization, multi-tasking, and problem-solving skills</p><p>· Computer experience (Microsoft Word, Excel, Power Point, Project)</p><p>· Specific expertise, skills and knowledge within research, product development, gained through education and/or experience</p><p>· The ability and willingness to change direction and focus to meet shifting organizational and business demands</p><p>· The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals</p><p>· Possesses the initiative and follow through to implement, track and achieve on-time completion of projects, as assigned by management.&nbsp;</p><p>· Must strive for continuous improvement in all work activities.&nbsp;</p><p>· The ability to take strategic objectives and accept accountability, motivate and influence others thinks globally and leverages diversity</p><p><strong>Education/Experience:&nbsp;</strong></p><p>· Regionally accredited Master’s Degree in Chemistry and/or a minimum of 8 - 10 years of previous experience in cGMP related environment</p><ul><li>Highly skilled in conducting analysis by HPLC, UPLC, GC, FT-IR, UV/Vis spectroscopy as well as wet chemistry techniques, needing little or no guidance</li></ul><p><strong>Working Conditions / Physical Requirements:&nbsp;</strong></p><p>· Position requires typing, climbing, lifting, reaching, standing, sitting, walking, and hearing.&nbsp;</p>",
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