Product Integrity Scientist

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    "description": "<div>\r\n<div>\r\n<p style=\"margin-left:7px;margin-right:44px;text-align:justify;\"><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><strong>Position Summary: </strong>The Product Integrity Scientist will support product safety/integrity related to regulatory affairs for product development, raw materials or finished products. They will provide product integrity support for Swiss American Contract Development and Manufacturing (SA). The person in this role will support sound product safety strategy and follow-through implementation for product, finished good and product compliance in different skin health categories across global regions. As the product integrity personnel in the organization, this role is responsible for supporting product safety and compliance.</span></span></p>\r\n\r\n<p style=\"margin-left:7px;\"><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><strong>Essential Duties and Responsibilities:</strong></span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for managing product safety and compliance intelligence, policies, and programs of diverse scope across the business for raw materials, bulk products, finished and commercialized goods</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for creation of cosmetic ingredient declaration, quantitative and qualitative formulas</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Review and assess changes to safety and global regulatory requirements and industry best practices and facilitate implementation through new or revised processes.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for evaluating and assessing safety and regulatory compliance of raw materials used at SA</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for safety and regulatory documentation for compliance requested by clients on SA formulations</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for safety assessments and compliance evaluations for skincare, OTC and medical device products across global regions including but not limited to prop 65, impurities, EU allergens etc.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for working with other employees to ensure adherence to compliance of products, resolve compliance issues, as appropriate, and communicate as required to clients.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Develop, plan, oversee and generate clinical, in vitro, in silico studies, and/or technical reviews which will insure the efficacy and safety of Swiss American products or Swiss American contracted formulations</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Expertise in methodologies used to assess the safety and efficacy of OTC, cosmetic and medical devices</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Manage client meetings and responses for ingredient and regulatory compliance</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for owning and maintaining current formulation system (Formulator Pro) to manage ingredient entry, ingredient compliance etc.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Oversee the creation and/or maintenance of technical files as necessary to obtain and sustain product approval.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Determine and communicate submission and approval requirements early in the product lifecycle to assure that projects plans are aligned to meet safety and regulatory guidelines.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Participate in multidisciplinary project teams with the Client.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for RID product safety compliance metrics for Quality Management Reviews.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Responsible for SA quarterly newsletter on compliance based on research and interpretation of compliance guidelines</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Other duties may be assigned.</span></span></li>\r\n</ul>\r\n</div>\r\n</div>\r\n",
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    "qualifications": "<h1 style=\"margin-left:7px; text-align:left\"><strong><span style=\"font-family:Arial,Helvetica,sans-serif\">Essential Skills and Qualifications:</span></strong></h1>\n\n<ul>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Experienced in leading cross-functional interactions related to product safety matters</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Bachelor&#39;s Degree in Life Sciences or related field.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Preferred: Advanced Degree (e.g., Master&#39;s, PhD) in a relevant field.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Minimum 4+ years of relevant experience in the skincare, pharmaceutical, or OTC industry.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Minimum 3 years of experience in a Product Safety/Regulatory function.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Proven experience in skincare OTC and medical device product safety and compliance, with a history in clinical studies preferred.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Experience interacting with regulatory agencies (e.g., FDA, EMA, Health Canada).</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Strong understanding of pharmaceutical and medical device R&amp;D, product development, and regulatory environments.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">In-depth knowledge of global product safety and regulatory requirements for skincare, OTC, and medical devices.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Proven ability to lead cross-functional teams and manage complex projects.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Excellent analytical, problem-solving, and decision-making skills.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Strong written and verbal communication and interpersonal skills.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Proficiency in Microsoft Office Suite.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Experience with process management and continuous improvement.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Demonstrated knowledge of global regulations and compliance requirements.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ability to analyze complex situations, identify risks, and develop effective strategies.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ability to lead teams, build relationships, and effectively collaborate with cross-functional partners.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Proven ability to manage multiple projects with aggressive timelines and deliver high-quality results.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">A proactive approach to identifying and implementing process improvements.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">May be responsible for supervising a team of 3-6 personnel.</span></li>\n</ul>\n\n<h1 style=\"margin-left:7px; text-align:justify\"><strong><span style=\"font-family:Arial,Helvetica,sans-serif\">Work Environment:</span></strong></h1>\n\n<p style=\"margin-left:48px; margin-right:7px; text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment Is usually moderate.</span></p>\n\n<h1 style=\"margin-left:7px; text-align:justify\"><strong><span style=\"font-family:Arial,Helvetica,sans-serif\">Physical Demands:</span></strong></h1>\n\n<p style=\"margin-left:48px; margin-right:7px; text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</span></p>\n\n<p style=\"margin-left:7px; margin-right:7px; text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.</span></p>\n\n<p style=\"margin-left:7px; margin-right:7px; text-align:justify\"><u><strong>Candidates selected for employment will be required to complete a pre-employment screening, including a drug test, employment verification, and education verification.</strong></u></p>\n",
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