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    "requisitionDescription": "<div><div><div><div><div><div><div><div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;' data-pasted=\"true\"><strong><span style=\"font-size:15px;\">PRIMARY DUTIES AND RESPONSIBILITIES:</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong>&nbsp;</strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Write method validation protocols/reports and perform method development/validation/ verification for API and finished drug products.&nbsp;</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Familiar with analytical testing of raw materials, in-process samples, finished products, and analytical laboratory instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, dissolution apparatus, etc.</span></li><li><span style=\"font-size:15px;\">Supervise the daily activities of the QC laboratory by establishing testing priorities and schedules, and assignments of staff based on company priorities and objectives.&nbsp;</span></li><li><span style=\"font-size:15px;\">Provide daily direction, guidance, and feedback to staff based on work priorities and schedules.</span></li><li>Serves as scientific liaison to other facilities and departments and scientific/quality control member of the Material Review Board.</li><li><span style=\"font-size:15px;\">Assists with appropriate review of analytical results of completed raw material, stability samples, and finished product testing.&nbsp;</span></li><li><span style=\"font-size:15px;\">Reviews and approves laboratory investigations, corrective and preventive actions, change requests, and deviations as necessary.</span></li><li><span style=\"font-size:15px;\">Maintain equipment calibration schedule and ensure that all required calibrations and maintenance are completed in a timely fashion.</span></li><li><span style=\"font-size:15px;\">Author standard operating procedures and assist with the revision process of current procedures.</span></li><li><span style=\"font-size:15px;\">Ensure laboratory compliance with applicable regulations.&nbsp;</span></li><li><span style=\"font-size:15px;\">Assist with procedural, cGMP, and safety training of laboratory staff.</span></li><li><span style=\"font-size:15px;\">Assist with preparations for internal and external (including FDA) laboratory audits and inspections.</span></li><li><span style=\"font-size:15px;\">Administers annual laboratory budget and other related duties as required.</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong><span style=\"font-size:15px;\">REQUIRED SKILLS, ABILITIES, AND QUALIFICATIONS:</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong>&nbsp;</strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Bachelor&#39;s or higher degree in Chemistry or related discipline.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">10+ years of experience in a QC or Analytical chemistry laboratory.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Experience with semi-solid and liquid pharmaceutical environment.&nbsp;&nbsp;</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">3+ years of experience in GLP or GMP (preferred) environment.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Demonstrated ability to act in a Lead capacity and provide direction to others.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Strong communication with the ability to build relationships at all levels of the organization.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Ability to organize, prioritize, and effectively perform concurrent tasks with minimal supervision.</span></li></ul></div><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><p><br></p><p><span style=\"font-size:15px;\"><span style=\"color: rgb(36, 36, 36); font-family: Aptos, sans-serif; font-size: 14.6667px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; display: inline !important; float: none;\" data-pasted=\"true\">At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.</span><br></span></p></div></div></div></div></div></div></div></div></div>\n",
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