{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/kincellbio/jobs/5118982007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4623433007,"location":{"name":"Durham, NC"},"metadata":null,"id":5118982007,"updated_at":"2026-04-23T19:02:47-04:00","requisition_id":"91","title":"Environmental Health and Safety Specialist II","company_name":"Kincell Bio, LLC ","first_published":"2026-04-23T19:02:47-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Kincell Bio\u0026amp;nbsp;\u0026lt;em\u0026gt;engineers cells into therapies\u0026lt;/em\u0026gt;. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. \u0026amp;nbsp;Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For more information, please visit our website at www.kincellbio.com.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Essential Duties\u0026lt;/strong\u0026gt; \u0026lt;strong\u0026gt;and Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.\u0026lt;/em\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt;This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for developing and deploying Environmental Health \u0026amp;amp; Safety programs \u0026amp;amp; policies to mitigate risk, drive regulatory compliance and promote a positive EHS culture.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compliance with GMP/GDP/FDA/EH\u0026amp;amp;S requirements and regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify, monitor, and own key EHS performance indicators. Use data to develop strategies to improve site safety and reduce environmental impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reinforce and sustain safety-first culture.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ownership of EHS component for existing facilities (2) and involvement in construction of future facilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participation in project meetings, anticipate outcome of decisions and monitor site construction activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical expertise and guidance to solve site hazards (chemical, biological, physical, electrical, slip/trip/fall, confined space, ergonomic, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead EHS compliance and program audits of the manufacturing site and service operations. Provide follow-up and support post audits to ensure execution to action plan, risk mitigation \u0026amp;amp; program improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate facility EHS conditions, assess risks and develop appropriate corrective-action plans and budgets to address deficiencies in comparison to regulations and internal policy/protocol.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide EHS guidance and compliance support to site managers in addressing government inquiries, violations and to ensure compliance with program requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leads accident response, reporting, and corrective actions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently manages the good catch program\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently manages the first aid training program\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently manages the bloodborne pathogen program\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently manages the HEP-B program\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides guidance for best Laboratory safety practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides guidance for best Manufacturing safety practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinates and leads multi-discipline Site Safety Team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently manages the sites EHS policies, procedures and programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently manages the sites safety shoe and glasses programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages multiple sites permits pertaining to EHS (Biosafety Permit, Fire Permit, Hazardous Waste, Etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversight (Administrator) of the Alert Media notification program\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages EHS budget with Engineering Lead\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attends and actively participates in cross functional meetings to ensure EHS/ENG site- and company-wide deliverables are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully. \u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Required:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Associate’s degree in occupational / industrial safety, industrial hygiene, environmental science or in a physical science with 2 years of progressive EH\u0026amp;amp;S experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in occupational / industrial safety, industrial hygiene, environmental science or in a physical science with 2 years of progressive EH\u0026amp;amp;S experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of three years of related experience in mixed use (office, manufacturing, and lab) environment required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An equivalent combination of education and experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge and experience with Confined Space Entry, LOTO implementation/training, respirator implementation/training and health programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated understanding of key regulatory requirements (e.g. Hazmat/RCRA, NFPA and OSHA rules and regulations) and their application to a laboratory and manufacturing environment, particularly in the following key areas: Environment (ex. waste management, lab safety, energy efficiency, and sustainability) \u0026amp;amp; EHS management systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive knowledge of technical specialty, applicable laws, applicable licensure, applicable permitting, regulations, and guidelines related to area of expertise.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled in the standards, concepts, practices, and procedures within the health, safety, and environmental fields.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to quickly assess situations through demonstrated problem-solving skills and knowledge of state-of the-art technology related to their EHS discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Computer software skills, organization, record keeping and planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must have excellent communication skills and ability to work in a team-oriented environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The individual must be capable of independent work required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Business setting and acumen required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible, proficient in technical writing, strong interpersonal and communication skills required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to quickly assess situations through demonstrated problem-solving skills and knowledge of state-of the-art technology related to their EHS discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works well in a team environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of current industry trends and the ability to use the latest technologies is beneficial.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in occupational / industrial safety, industrial hygiene, environmental science or in a physical science, with 5 years of progressive EH\u0026amp;amp;S experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An equivalent combination of education and experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in Safety, Industrial Hygiene, Environmental Sciences or related field preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of GMP, FDA and EMA regulatory requirements applicable to Biologics including Cell/Gene/Viral therapy products as they pertain to EH\u0026amp;amp;S is beneficial.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Demands\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Adjusting or moving objects weighing up to 25lbs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;lt;25%\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Required to travel to alternate sites at least once a quarter\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This position is 100% on-site in Raleigh, North Carolina, with quarterly trips to Gainesville, FL.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;#LI-Onsite\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;NOTE TO EMPLOYMENT AGENCIES\u0026lt;/strong\u0026gt;: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023268007,"name":"Facilities and Engineering","child_ids":[],"parent_id":null}],"offices":[{"id":4037887007,"name":"Research Triangle Park, NC","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/kincellbio/jobs/5137219007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4632160007,"location":{"name":"Gainesville, FL"},"metadata":null,"id":5137219007,"updated_at":"2026-05-15T09:50:44-04:00","requisition_id":"94","title":"Quality Assurance Associate II, Contingent Worker","company_name":"Kincell Bio, LLC ","first_published":"2026-05-15T09:50:44-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Kincell Bio\u0026amp;nbsp;\u0026lt;em\u0026gt;engineers cells into therapies\u0026lt;/em\u0026gt;. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. \u0026amp;nbsp;Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For more information, please visit our website at www.kincellbio.com.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The contingent staff member for Quality Assurance will primarily be responsible for supporting quality operation activities. This highly motivated member of the Quality Unit will promote a culture of compliance throughout the organization by reviewing all production-related documents and assisting with quality oversight of quality events. The Associate II oversees the generation and revision of product-related master documents to support GMP manufacturing of drug substances and drug products. Mature professional capable of working independently and in a team setting. Continually evaluate opportunities for improvement to increase efficiency while ensuring compliance with applicable regulatory requirements and standards. Requires the ability to produce results in a fast-paced environment to meet client deadlines and to prioritize based on criticality effectively.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Essential Duties\u0026lt;/strong\u0026gt; \u0026lt;strong\u0026gt;and Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.\u0026lt;/em\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt;This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Actively participates in fostering a positive, collaborative work\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensuring adherence to cGMPs across the\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Addresses all quality and compliance matters in an open and timely\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluating standard operating procedures, master batch records, and test methods for alignment with GMPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs review of all product-related documents such as production batch records, testing forms, logbooks, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports raw material and finish product release\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports deviation, CAPA, and change control\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Will work directly with all departments and across sites to review and track executed documents to meet timelines. Provide status updates and reminders when necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains databases used for tracking various lot disposition\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support regulatory (FDA, EMA) and client audits/inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;HS Diploma With 7+ years of relevant industry experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree preferred in life sciences with 2+ Years of relevant industry experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prefer experience with FDA Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDP) in the pharmaceutical, biologic, medical device, or human tissue industries in a Document Control position, including the revision, issuance, and tracking of batch records, Standard Operating Procedures (SOP), Specifications, etc. Microsoft Word and Microsoft Excel experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An equivalent combination of education and experience may be\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to 21 CFR Parts 210 \u0026amp;amp; 211, 21 CFR 820, and/or 21 CFR 1270, biotechnology, and electronic computer systems is desired\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills, written and\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team player with the ability to influence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented, excellent written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively manages cross-functional communication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Multitasks strategically and tactically in a fast-paced work\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills; able to prioritize and manage complex processes/projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to define problems, collect data, establish facts, and draw valid conclusions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in a rapidly changing environment and balance multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Demands\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Adjusting or moving objects weighing up to 25lbs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;N/A\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is a site-based temporary position located in Gainesville, FL, and it will require some non-standard working hours, including early morning or late evening.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;#LI-Onsite\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;NOTE TO EMPLOYMENT AGENCIES\u0026lt;/strong\u0026gt;: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023276007,"name":"Quality Assurance","child_ids":[],"parent_id":null}],"offices":[{"id":4023400007,"name":"Gainesville, FL","location":"Gainesville, FL","child_ids":[],"parent_id":null}]}],"meta":{"total":2}}