Biology jobs in Durham, North CarolinaCrear alertas

Job DescriptionJob Title: QC Analyst I Duration: 06 months with possible extension Office: Durham, NC, 27709 Pay rate: $30.48/hr. on W2 Position Summary The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories. Job Responsibilities · Perform routine analytical testing including but not limited to cell-based potency assays, ddPCR, qPCR, ELISAs, limit tests using HPLC techniques. · Prepare solutions and maintain cell lines for various clinical programs · Prepares laboratory solutions, maintains cell lines, and other day to day laboratory activities. · Maintains laboratory documentation including logbooks, test forms, LIMS data, and electronic data. · Assist with revisions of work instructions, SOPs, forms, reports, and electronic laboratory notebook analytical records. · Assist with management analytical test method supplies and samples as needed. · Ensure lab areas are clean, organized, maintain equipment and consumables. · Work closely with Analytical Development, Quality Control, Quality Assurance, Production staff and any other relevant departments. · Strictly adheres to all applicable written Standard Operating Procedures (SOPs), company policies, and technical guidance documents, both internal and external. · Participates in continuous improvement projects in the AD and QC labs. · Support revisions to work instructions, SOPs, forms, protocols, and reports Minimum Requirements · Bachelor's degree in biology or related field. Powered by JazzHR JeL3Ea75Cc

Title: Laboratory Technician (Lab Technician) Location: 100% Onsite Role in Durham, NC Local Candidates ONLY Interview Process - Onsite Interview MUST ROLE AND RESPONSIBILITIES: Reporting to the LC/MS group lead, the Research Associate, Vapor Lab will support the Chemistry and Regulatory Testing and regulatory submissions. The Research Associate is a hands-on, laboratory-based role in Durham, NC that will be responsible in helping to test products for regulatory submissions. The Research Associate is highly motivated, nimble at navigating complex challenges, a skilled multitasker, is adaptable and works effectively in a fast-paced environment and works collaboratively with the teams in the laboratory. • Perform routine collection of aerosol samples from ENDS devices., • Perform preparation of aerosol samples for analysis., • Perform preparation of reagents for lab usage., • Perform routine maintenance on vapor machines., • Cleaning of laboratory glassware., • Write and review scientific documents in a timely manner (SOPs, VOPs, and Work Instructions)., • Manage the regulatory documents systematically in a highly organized fashion., • Perform other related duties as assigned. A successful Research Associate will be able to successfully complete assigned tasks in a timely manner. They need to be readily adaptable to change while following established standard operating procedures. PERSONAL AND PROFESSIONAL QUALIFICATIONS: Experience with vaping machines and collection techniques is preferred. Strong mechanical skills. Strong weighing skills. Ability to prepare clear and concise written documents. Ability to communicate issues in a succinct and logical manner. Strong problem-solving skills. High motivation and flexibility. ENDS or nicotine-related products experience is preferred. Experience in a regulated laboratory environment such as ISO 17025 is preferred but not required. EDUCATION: Associate degree in biology, chemistry, or related field with a focus in aerosol sample collection and preparation.

Job Description Company Overview Are you a results-driven problem-solver, eager to positively change the world? Do you believe that climate change is the biggest issue facing us today? Then the Biomason team needs you! Biomason is leading the global transition to plant-friendly construction by employing biology to produce cement. Since 2012, we have used microorganisms to grow sustainable, structural biocement® in ambient temperatures, harnessing the power of biotechnology to reinvent traditional cement and offer a planet-friendly alternative. We are seeking dedicated, passionate, and hardworking individuals to become part of our ever-growing team. Join Biomason and help us end the world's dependence on carbon-emitting construction materials. Let’s change the way we build. Biomason is privately held and headquartered in Research Triangle Park, North Carolina. For additional information, please visit . We offer a competitive benefits package including medical, dental, vision, and more! Position Summary We are seeking a highly motivated and experienced Human Resources Generalist to join our growing team and serve as the primary point of contact for all HR-related matters in the U.S. and assisting with supporting Danish employees. This role plays a vital part in supporting our people and sustaining a positive, compliant, and high-performing workplace culture across our organization. The ideal candidate will have a strong foundation in HR operations, employee relations, and compliance, with the ability to work independently while collaborating closely with leadership. This role is well-suited for a results-oriented HR professional who is eager to grow with the company and contribute directly to Biomason’s mission and culture. This position will report to the CFO (or CEO in the interim) and will be based in Durham, NC. Responsibilities • Serve as the primary HR contact for all U.S.-based employees and managers, • Serve as a supporting HR contact for all Danish-based employees and managers, • Manage full-cycle recruiting, onboarding, and offboarding processes to ensure a seamless employee experience, • Support employee relations by providing guidance, maintaining documentation, and promoting consistent communication, • Partner with ADP and other providers to administer benefits, coordinate payroll inputs, and manage leaves of absence, • Ensure compliance with federal, state, and local employment regulations (including OSHA, FMLA, and EEO), • Maintain and update HR systems and records to ensure accuracy, confidentiality, and compliance, • Support performance and development processes, including review cycles and goal-setting, • Collaborate with leadership to drive employee engagement, culture, and wellness initiatives, • Provide light office and safety committee support, and assist Danish HR counterparts as needed for cross-site coordination, • Bachelor’s degree in Human Resources, Business Administration, or related field required, • Minimum of 5 years of combined professional experience, including at least 1–2 years in direct HR work, • Solid understanding of U.S. employment laws and HR compliance practices, • Demonstrated ability to manage multiple HR functions independently with high attention to detail, • Strong communication, organization, and interpersonal skills, • Experience using ADP Workforce Now or a similar HRIS system (preferred), • Highly organized and possess excellent attention to detail, • Creative, flexible, proactive, punctual, persistent, • Self-driven with a track record of networking and successful project completion, • Comfortable with a demanding, fast-paced work environment, • Remain stationary or walking for periods of time, often standing or sitting for prolonged periods, • Prolonged use of computer and digital screens, • Moving about to accomplish tasks or moving from one space to another, • Typical office environment, • Seldom exposure to odors and sounds Biomason is an Equal Opportunity Employer. We celebrate diversity and are committed to providing an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. If you need assistance completing the application process, please contact

Job DescriptionCompany Description Syngenta Seeds is a global leader in developing and producing high-quality seeds that improve crop yields and resilience. Our advanced seed technologies help farmers mitigate risks from disease and drought while using less land, water, and inputs. We deliver innovative hybrid varieties and biotech crops, including more vigorous, resistant plants that thrive even in challenging conditions. Headquartered in the United States, Syngenta Seeds is committed to sustainable agriculture and feeding the world. Job Description At Syngenta, every employee plays a role in safely feeding the world and caring for our planet. Our Bioinformatics group in Durham, North Carolina is seeking a Functional Genomics Intern to analyze next gen omics datasets and use artificial intelligence prediction tools to solve biological problems. You will develop cutting-edge skills in computational approaches to genomics data analysis and contribute to innovations in agricultural biotechnology. The scope and complexity of the project will be adjusted based on the intern’s experience level and academic background. Role Purpose • Gain valuable experience supporting bioinformatics scientists with high throughput genomics data analysis, • Learn to use cutting edge AI tools for gene expression inference, • Work in a diverse team of computational biologists developing new innovations for agricultural biotechnology, • Contribute to written reports and presentations Accountabilities • Evaluate and compare high throughput analytical methods for genomics data analysis, • Leverage Deep Learning models to optimize gene expression in crops, • Document methods, workflows, and code in a reproducible manner, • Create clear visualizations and summaries of analytical results, • Collaborate with team members and communicate findings in group meetingsQualifications Requirements • Education, • Pursuing MS or PhD in Bioinformatics, Molecular Biology, Genetics, Computer Science, or related fields, • Technical, • Experience with Linux/Unix command line environments and shell scripting, • Analytical coding languages such as Python or R, • Knowledge of molecular biology and genetics, • Experience using git for version control, • Analytical, • Ability to work with large datasets and implement reproducible computational workflows, • Strong problem-solving skills and attention to detail, • Effective written and verbal communication skills Preferred Requirements • Experience with high throughput omics data analysis (e.g., RNAseq analysis), • Experience with high-performance computing job schedulers (SLURM, etc.) and/or cloud computing (AWS, etc.), • Self-motivated with ability to work independently and collaboratively, • Enthusiasm for learning new computational methods and tools, • Experience presenting technical work to diverse audiences Additional Information Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here:

Job Description Office Administrator Location: On-site in Durham, NC (RTP area) Company: Avalo Compensation: $50 - $65k annually + full benefits, PTO, retirement About Avalo At Avalo, we’re reinventing crop development to build a climate-resilient, equitable, and sustainable future for agriculture. Our mission is to accelerate crop evolution using AI and evolutionary biology—cutting development time from decades to just a few years while dramatically reducing environmental impact. From low-input cotton to sugarcane, we work with nature’s complexity, not against it, to deliver high-performance crops without harmful externalities. Join us in transforming agriculture from the seed up. About this opportunity: We’re seeking a highly organized, detail-oriented, and proactive Office Administrator to ensure the smooth and efficient operation of Avalo’s Durham office. This role is central to maintaining day-to-day administrative excellence, supporting financial workflows, coordinating vendors, and reinforcing our collaborative culture. The ideal candidate will thrive in a fast-moving startup environment, demonstrate exceptional communication and problem-solving skills, and play a key role in supporting operational accuracy, compliance, and team success across the company. Key Responsibilities: Financial & Administrative Support • Support vendor setup, W-9 collection, invoice routing, and payment documentation., • Assist with credit card reconciliation by collecting receipts and verifying coding., • Maintain organized financial and administrative records to ensure audit readiness.Office & Facilities Management, • Oversee daily office operations, vendor coordination, and supply inventory., • Manage shipping and receiving for materials, equipment, and samples., • Assist with safety documentation, required trainings, and compliance recordkeeping., • Serve as the first point of contact for employees and guests, maintaining a welcoming environment., • Contribute to company culture initiatives and cross-team collaboration., • Coordinate onsite meetings, catering, office meals, and general logistics.Travel & Coordination, • Arrange domestic and international travel; track expenses and documentation., • Maintain administrative trackers, shared files, and compliance documentation., • Support planning and logistics for company-wide meetings and events.HR & Onboarding Support, • Assist with interview scheduling, candidate communication, and reference checks., • Coordinate new-hire onboarding, workspace setup, and documentation tracking., • Bachelor’s degree in Business Administration, Accounting, or a related field OR equivalent professional experience in office administration, bookkeeping, or operations., • 3–5 years of experience in office administration, financial coordination, or similar support roles., • Experience supporting financial processes (vendor documentation, invoice routing, expense tracking) preferred., • Strong written and verbal communication skills with excellent attention to detail and accuracy., • Proven organizational skills with the ability to manage multiple priorities and shifting tasks., • Ability to maintain confidentiality and handle sensitive financial or personnel information., • Experience coordinating interviews, onboarding logistics, or HR administration is a plus., • Proficiency with Microsoft and Google applications (Word, Excel, PowerPoint, Google Workspace, • Familiarity with Bill.com, DocuSign, Adobe Acrobat, Slack, and Canva is helpful., • Highly proactive, dependable, and comfortable working independently in a fast-paced startup environment., • Passion for Avalo’s mission and a collaborative, service-oriented mindset. Powered by JazzHR WMJm1inU7y

We are seeking Biology tutors and teachers in Durham.

Do you have a Master's Degree or a Doctoral Degree in Biology or a related field with at least 18 graduate semester hours in biological sciences?. Yes, I have a Master's Degree in Biology or a related field with at least 18 graduate semester hours in biological sciences, or I am enrolled in a PhD pr

Agricultural Solutions Professional Development Program - Biology. As a Biology program participant, you will:.

Application Process** - Submit your resume or CV highlighting biology background and relevant achievements - Complete a brief interview (20–30 minutes) - Submit a short form detailing your experience writing problems and competing in biology competitions - Selected applicants will be contacted wit

Job DescriptionJob Title: Quality Control Analyst I Duration: 12 months with possible extension Office: Research Triangle Park, NC 27709 Shift: 09:00 am to 05:30 pm Pay rate: $30/hr. on W2 Job Description: The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories. Job Responsibilities: • Perform routine analytical testing including but not limited to cell-based potency assays, ddPCR, qPCR, ELISAs, limit tests using HPLC techniques., • Prepare solutions and maintain cell lines for various clinical programs, • Prepares laboratory solutions, maintains cell lines, and other day to day laboratory activities., • Maintains laboratory documentation including logbooks, test forms, LIMS data, and electronic data., • Assist with revisions of work instructions, SOPs, forms, reports, and electronic laboratory notebook analytical records., • Assist with management analytical test method supplies and samples as needed., • Ensure lab areas are clean, organized, maintain equipment and consumables., • Work closely with Analytical Development, Quality Control, Quality Assurance, Production staff and any other relevant departments., • Strictly adheres to all applicable written Standard Operating Procedures (SOPs), company policies, and technical guidance documents, both internal and external., • Participates in continuous improvement projects in the AD and QC labs., • Bachelor's degree in biology or related field. About Us: Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU. IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at . Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility. Powered by JazzHR kKQOeiqNmh

Job Description Summary The Director of Clinical Operations will lead and oversee the planning, execution, and management of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. This role is pivotal in driving operational excellence across multiple clinical programs, coordinating cross-functional teams, and optimizing resource allocation to meet project timelines and objectives. The Director will serve as a strategic partner to senior leadership, providing insights and recommendations to enhance clinical development strategies and improve patient outcomes. They will also be responsible for fostering a culture of continuous improvement, quality assurance, and adherence to Good Clinical Practice (GCP) guidelines. Ultimately, this position ensures that clinical operations contribute effectively to the successful development and approval of new therapies within the United States and potentially global markets. Responsibilities • Lead the design, implementation, and management of clinical trial operations from study start-up through close-out., • Provide primary oversight for the CRO, ensuring that CRO activities are executed per study timelines. Maintain frequent and meaningful contact with the CRO to assess performance and provide oversight and guidance as needed., • Collaborate with cross-functional departments such as Regulatory Affairs, Data Management, and Clinical Development, to ensure alignment and compliance., • Ensure adherence to all regulatory requirements, company policies, and industry standards including FDA regulations and ICH-GCP guidelines., • Identify and mitigate operational risks, implementing corrective actions as necessary to maintain study integrity and patient safety., • Drive process improvements and implement best practices to enhance clinical trial efficiency and data quality., • Contribute to review of other study documents such as protocols/amendments, eCRFs, clinical study reports, IBs, DSURs, conference presentations, publications, etc., • In coordination with the cross-functional team, participate in the RFP process and ultimately select CROs, and other vendors for clinical trials., • Participate in the selection of investigational sites with input from relevant stakeholders. Lead the study and site feasibility process in association with the CRO. Assess site and investigator performance and enrollment on a regular basis., • Develop and oversee clinical operations budgets, timelines, and resource plans to ensure project milestones are met., • Work closely with Clinical team members to ensure investigational product needs for clinical studies are available and managed appropriately., • Partner closely with internal functional areas to operationalize the procurement and analysis of biological samples for the study, including contributing to lab manuals, identifying vendors for lab kitting and sample management, and providing regular training and feedback to sites regarding completeness and quality of sample collection., • Oversee the creation and maintenance of all trial files, including the trial master file. Work with quality assurance to ensure inspection readiness of sites and implement risk-based quality management of the clinical study., • Mentor clinical operations team members to promote professional growth and high performance. Qualifications and skills • Bachelor’s or Masters degree in science or healthcare with a minimum of 10+ years of Clinical Operations experience, including at least 8 years in direct management of clinical trials., • Knowledge of clinical drug development, with experience in Phases I-III, CRO/vendor oversight, global clinical trials, and budget/timeline management., • Thorough understanding of ICH GCP and FDA guidelines., • Strong interpersonal skills with demonstrated ability to effectively work with internal cross- functional as well as external groups., • Good communication and interpersonal skills and ability to work with cross-functional teams., • Self-starter with an entrepreneurial spirit and a good team player. Shattuckians are a diverse group of physicians, scientists, drug developers and protein engineers that are linked through our shared desire to build transformative medicines for patients suffering from life-altering diseases. We are experts in the biology of TNF receptors, including DR3, and have assembled one of the most experienced teams in the industry with regard to understanding the immuno-biology of TNF receptor agonists and antagonists. Employee Benefits • Competitive salary and health benefits, 401k., • Opportunities for training and career advancement., • Collaborative and inclusive work environment., • Access to cutting-edge research and technology. Note to External Recruiters Our Human Resources department manages all open positions and candidate recruitment. We ask that recruiters not contact employees or hiring managers directly to present candidates or solicit business. We will consider failure to comply with this request when determining whether to enter a professional relationship with a recruiting agency. The submission of unsolicited resumes does not create any obligations for Shattuck Labs, implied or otherwise.

Job Description Company Overview Are you a results-driven problem-solver, eager to positively change the world? Do you believe that climate change is the biggest issue facing us today? Then the Biomason team needs you! Biomason is leading the global transition to plant-friendly construction by employing biology to produce cement. Since 2012, we have used microorganisms to grow sustainable, structural biocement® in ambient temperatures, harnessing the power of biotechnology to reinvent traditional cement and offer a planet-friendly alternative. We are seeking dedicated, passionate, and hardworking individuals to become part of our ever-growing team. Join Biomason and help us end the world's dependence on carbon-emitting construction materials. Let’s change the way we build. Biomason is privately held and headquartered in Research Triangle Park, North Carolina. For additional information, please visit . We offer a competitive benefits package including medical, dental, vision, and more! Position Summary The IT Manager plays a critical role in ensuring the stability, security, and scalability of Biomason’s global technology environment. This position oversees all aspects of IT operations—including infrastructure, cybersecurity, enterprise systems, and digital collaboration tools—across both U.S. and Denmark locations. As a strategic and hands-on leader, the IT Manager will drive innovation in support of Biomason’s mission to revolutionize construction through biotechnology. The role involves managing IT staff and vendors, leading technology initiatives, and ensuring compliance, reliability, and business continuity across all functional areas,including R&D, Manufacturing, Finance, and Operations. Responsibilities • Lead and manage day-to-day IT operations, including system administration, helpdesk support, infrastructure,and cybersecurity, • Develop and implement IT strategies that align with business goals and ensure reliability and scalability, • Develop and lead IT team, setting priorities, tracking performance, and fostering continuous improvement, • Oversee IT infrastructure, including networks, servers, cloud services, and hardware lifecycle management, • Manage cybersecurity programs, audits, and compliance with data privacy and security standards, • Support enterprise systems such as ERP, databases, and automation tools in the US and Denmark, • Identify and implement technology solutions that improve processes and data integrity, • Develop and manage vendor relationships, budgets, and technology procurement, • Bachelor’s degree in Computer Science, Information Systems, or related field, • 5–7 years of experience in IT management or systems administration, including supervisory roles, • Experience in manufacturing or production environments is preferred, • Strong knowledge of IT infrastructure, networks, cloud services, and cybersecurity, • Experience with ERP systems, business applications, and systems integration, • Familiarity with IT compliance, data privacy, and business continuity, • Excellent communication, project management, and problem-solving skills, • Strategic and hands-on leadership, • Organized, analytical, and proactive, • Strong collaboration and communication skills, • Customer-focused and responsive to team needs, • Adaptable and effective in a fast-paced environment, • Ability to lift 15 pounds, • Remain stationary for long periods of time, often standing or sitting for prolonged periods, • Able to work on computer up to 8 hours per day, • Typical office environment majority of working hours, • Seldom exposed to excessive noise, • Seldom exposure to odors Biomason is an Equal Opportunity Employer. We celebrate diversity and are committed to providing an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. If you need assistance completing the application process, please contact

Job Description Title: Project Support Coordinator (Part-time) Location: Durham, NC Status: Part-Time Travel: may be required Position Summary: The National Institute of Environmental Health Sciences (NIEHS) is one of 27 institutes and centers of the National Institutes of Health (NIH), which is a component of the U.S. Department of Health and Human Services (HHS). NIEHS's broad focus on the environmental causes of disease makes the institute a unique part of the NIH. NIEHS is home to the National Toxicology Program (NTP), the nation's premier program for testing and evaluation of agents in our environment. The focus of the NIEHS research is to discover how the environment affects people to promote healthier lives. The Animal Husbandry Support Contract for the National Institute of Environmental Health Sciences provides care, maintenance, and technical services for laboratory animals, seven (7) days per week, including weekends and holidays, for 72,447 square feet of laboratory animal facility space (which includes ancillary support areas outside of the main facility, including a separate facility located approximately one mile from the main facility). The contractor is responsible for the care and maintenance of the animals, the sanitation of equipment, technical training, and the general maintenance of the facilities in such a manner as to maintain the highest level of Accreditation from the Association for Assessment and Accreditation of Laboratory Animal Care, International (AAALAC, Intl.) The services provided by this contract are considered mission critical. The Project Support Coordinator will report directly to the Project Manager/Assistant Project Manager. The Project Support Coordinator assists both CMB and NIEHS researchers in the performance of both one time and ongoing projects. The incumbent assists CMB and NIEHS researchers in the design, implementation, and interpretation of research studies. The incumbent also supports, coordinates, and implements CMB improvement projects, including the integration of technology to enhance efficiency and workflow to include, but not limited to, animal census, reporting, tracking and documentation of clinical cases, and genotyping and rodent colony management activities. The incumbent works with both CMB personnel and external vendors to facilitate implementation, training, and troubleshooting of associated devices and programs. The ideal candidate will have great communication skills and works well with a team, is adaptable, acts in a positive, professional, and helpful manner, and demonstrates a strong work ethic. This position is pending contract award. Duties/Responsibilities: • Assists CMB and NIEHS researchers in the design, implementation, and interpretation of research studies., • Supports, coordinates, and implements CMB improvement projects, including the integration of technology to enhance efficiency and workflow to include, but not limited to, animal census, reporting, tracking and documentation of clinical cases, and genotyping and rodent colony management activities., • Works with both CMB personnel and external vendors to facilitate implementation, training, and troubleshooting of associated devices and programs., • Shall be certified by the American Association for Laboratory Animal Science (AALAS) as Laboratory Animal Technologist (LATG), • Additional experience in the performance of experimental/study activities in a biomedical research setting is required., • Experience with rodent colony management, • Formal education must include a minimum of a B.S. degree in the animal or other biological sciences, e.g. zoology, biology, microbiology, veterinary science (MS preferred)., • Employees are subject to adverse variables of environmental conditions, both inside and outside. Work areas are often hot, humid, and noisy due to operation of cage washing machines and autoclaves. Employees are potentially exposed to minor injuries such as cuts, bites, scrapes, pulled muscles, burns and unpleasant odors, and the possibility of exposure to hazardous materials including radioisotopes. Employees are exposed to animals and animal urine, feces, and dander that can act as allergens or as potential sources of zoonotic disease., • Animal care personnel are required to wear a contractor supplied, washable cotton/polyester two-piece uniform of scrub pants and a long sleeve, snap-front shirt (a one piece cotton coverall may be substituted), safety shoes, disposable shoe cover, head cover, surgical mask), and gloves when working in the animal rooms., • Protective clothing is required to be worn by ALL personnel entering an animal room from the return corridors. The disposable PPE identified above is furnished by the Government. The contractor is responsible for an annual fit test of all personnel required to wear an N95 respirator KIC offers a comprehensive benefits package to eligible full-time employees including Medical, Dental, and Vision Insurance, 401k with Match, Life and ADD Coverage, Short and Long Term Disability, Paid Time Off and Holidays, Education Assistance/Tuition Reimbursement, Employee Assistance Program, Employee Discount Program, and more! Apply online at our website: Disclaimer: This is not to be an exclusive list of all responsibilities, duties, and skills required of the person in this job. KIC is an Equal Opportunity Employer as to all protected groups, including protected veterans and individuals with disabilities. Pursuant to The Alaska Native Claims Settlement Act 43 U.S.C. Sec. 1601 et seq., and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders, and their Descendants. Successful candidates must adhere to KIC's Drug and Alcohol policy/testing requirements and may be required to pass a background and/or Motor Vehicle Records check. The salary range for this position is based on several factors, including relevant experience, education, skills, and current market conditions.

Job DescriptionCompany Description Syngenta Seeds is one of the world’s largest developers and producers of seed for farmers, commercial growers, retailers and small seed companies. Syngenta seeds improve the quality and yields of crops. High-quality seeds ensure better and more productive crops, which is why farmers invest in them. Advanced seeds help mitigate risks such as disease and drought and allow farmers to grow food using less land, less water and fewer inputs. Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions. Syngenta Seeds is headquartered in the United States. Job Description At Syngenta, we believe every employee has a role to play in safely feeding the world and taking care of our planet. To support that challenge, the Syngenta Seeds team is currently seeking a Digital Platform Product Owner. Role Purpose: The Digital Platform Product Owner will lead product ownership for the Trialing Process ecosystem, and collaborate with other product owners to ensure platform features meet the needs of all product teams and deliver cohesive, integrated solutions. Accountabilities: • Serve as a decision-maker for scope and prioritization., • Stakeholder mapping and drive platform product lifecycle from ideation to launch, ensuring timely delivery and iterative improvement based on user feedback and KPIs., • Develop and maintain a comprehensive product roadmap for the Trialing Process ecosystem, • Advocate for platform usability, to foster internal adoption and reduce time to market for new products., • Ensure effective prioritization of features and enhancements across all related systems, • Collaborate with stakeholders to define and refine product requirements, • Coordinate with IT, analytics, and data science teams to implement technical solutions, • Drive continuous improvement in Seeds Material Management and Inventory processes Qualifications, • Bachelor’s degree in Biology, Agriculture, Computer Science, Information Systems, or related field, • Minimum 5 years of experience in product management or program ownership, • 5+ years of experience in agricultural technology or related field, • Advanced knowledge of product management methodologies and best practices, • Understanding of agricultural research processes, particularly in seed trialing, • Familiarity with inventory management systems and practices, • Knowledge of data collection tools and technologies, • Strong project management skills, including resource allocation and timeline management, • Proven track record of successful stakeholder management and cross-functional leadership Additional Information What We Offer: • A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs., • Full Benefit Package (Medical, Dental & Vision) that starts your first day., • 401k plan with company match, Profit Sharing & Retirement Savings Contribution. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. WL:5B #LI-NL2 #LI-remote

Job Description Position Summary To perform experiments, ensuring that projects are completed to plan, while complying with all quality and safety regulations. Assist with study plan writing, data analysis and interpretation, and report writing. Essential Functions: • Assist or act as the lead scientist on assigned studies., • Draft study plans and contribute to the preparation of reports for sponsors., • Review literature and appropriate guidances (FDA and/or EMA) in preparation for studies and to regularly update knowledge by reviewing appropriate literature., • Perform experiments (with supervision as needed) in line with in vitro testing such as in vitro permeation and penetration studies, in vitro release testing studies, extractions, stability studies, etc., • Assist with data analysis for studies related to in vitro testing., • Confer with scientists, study managers, and management to conduct analyses of research projects, interpret test results, or develop nonstandard tests., • Crosstrain and assist with research biology activities (e.g. PCR, PK/PD, etc.) as needed., • Report any amendments or deviations from Study Plans/SOPs to Lead Scientist and/or Study Director, as appropriate., • Maintain laboratory instruments to ensure proper working order and troubleshoot malfunctions with scientists when needed., • Adhere to MedPharm Standard Operating Procedures (SOPs) and guidance documents, where applicable., • Contribute to the preparation and review of SOPs and Forms where applicable., • Where applicable, promptly record all data according to Good Documentation Practices., • Adhere to MedPharm Health & Safety Policy and OSHA regulations at all times and to ensure the safety of others in any procedures or tasks performed., • Ensure that all documentation, computer data, and records are stored appropriately. CgdzTtjodV

Job DescriptionRegulatory & Quality SpecialistLocation: Durham, NC (On-site) Department: Product Development Reports to: Head of Product Development Employment Type: Full-TimePlease email directly your resume, and a non chat-GPT paragraph as to why you would be a good fit for this role to be considered. About CarpeCarpe is the fastest-growing deodorant brand in the US. Our team is composed of ~25 insanely smart people working together in-person in downtown Durham, NC. Our office is rather open with many private niches, and our energy level is HIGH.About the RoleWe’re looking for a proactive, detail-driven, and organized teammate to join our Product Development group. In this role, you’ll work across Regulatory, Quality, and Product Development to ensure every Carpe product meets our high standards from concept to launch. You’ll be hands-on in every step of the process: managing testing, documentation, and regulatory compliance submissions that keep each formula safe, effective, and ready for market. If you love connecting details to big-picture outcomes and want to be part of every step of bringing innovative products to life, this role is for you.What You’ll DoRegulatory & Compliance • Work directly with our external regulatory partners to identify regulatory requirements for every Carpe product, • Maintain regulatory submissions and renewals (MoCRA, NDC, WERCS, EPR), • Ensure labels, ingredients, and packaging meet U.S., Canadian, and EU/UK cosmetic and OTC requirements, • Prepare and manage SDS, product technical files, and retailer documentation (Target, Amazon, CVS, etc.), • Track and organize regulatory deliverables across consultants, legal, and internal teams, • Support claims, substantiation documentation, and filing Quality Systems • Conduct or coordinate onsite quality audits with contract manufacturers (CMs), • Manage incoming lot inspections, supplier documentation, and CAPA follow-ups, • Support annual product reviews, deviation logs, and supplier quality programs, • Maintain audit readiness and document control for all quality and regulatory filesProduct Development, • Support the regulatory and quality steps for each product launch from formula review through production, • Track product timelines, testing schedules, and sample status across multiple projects, • Maintain formulation, artwork, and testing documentation in shared systems, • Partner cross-functionally with Marketing, Operations, and Creative to ensure smooth, compliant launchesPartner Coordination, • Serve as the main contact for regulatory consultants and external testing partners, • Track deliverables and provide regular updates on project milestones to leadership, • Support internal knowledge and process documentation as Carpe builds internal capability at increasing scale, • Approximately 10-15% travel for on-site visits to contract manufacturers or testing partnersWho You Are, • Bachelor’s degree in a STEM field (Cosmetic Science, Chemistry, Biology, or Toxicology preferred)., • 2–3 years of experience in Regulatory Affairs, Quality Assurance, or Research & Development in cosmetics, OTC, or personal care (or if you lack this experience, explain why you believe you have equivalent experience), • Working knowledge of FDA regulations [e.g., The Food Drug and Cosmetic Act (FD&C Act), Modernization of Cosmetics Regulation Act (MOCRA)], global regulatory frameworks (including European Union, Canada and Asia markets), and OTC drug regulations/monographs, • Strong organizational and project management skills, • Excellent attention to detail and accuracy, • Clear communication and cross-functional collaboration skills, • Must have hands-on experience owning regulatory compliance for consumer cosmetic and/or OTC personal care products (including labeling, claims review, and U.S. market readiness); pharma, medical device, and clinical regulatory experience alone is not sufficient.Bonus If You Have, • Hands-on experience managing regulatory or quality documentation, • Exposure to global regulatory documentation, such as EU or Health Canada registrations, • Experience with quality audits What You’ll Get, • Competitive salary based on experience, • Health, vision, and dental benefits, with Carpe covering a portion, • Flexible PTO, • A front-row seat to the growth of one of the most disruptive brands in body careWhy You’ll Love It Here, • You’ll be part of every Carpe launch, seeing products through from idea to shelf., • You’ll collaborate directly with leadership, consultants, and labs., • You’ll help shape the systems and standards that build Carpe’s next stage of growth., • You’ll work on products that genuinely improve people’s confidence and comfort. Please email directly your resume, and a non chat-GPT paragraph as to why you would be a good fit for this role to be considered. Powered by JazzHR jqHQ4NZDEh

Job Description Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our sales team as a Senior Sales Representative. As a Senior Sales Representative, you will be responsible for driving sales growth within the academic sector, government agencies, and emerging biotech companies in your assigned territory. You will focus on building and nurturing relationships with R&D professionals in academic institutions and smaller biotech firms, positioning our solutions as essential tools for advancing mRNA modalities. A successful candidate will thrive in a dynamic environment, leveraging their strong scientific background, sales expertise, and strategic acumen to identify opportunities, expand market share, and deliver innovative solutions that meet the evolving needs of our customers. Description of Duties: • Sales strategy and execution: Develop and implement effective sales strategies and tactics to drive new customer acquisition and product adoption while maintaining and expanding relationships with existing customers., • Customer relationship management: be an extension of the Maravai and TriLink brand by building and maintaining strong relationships with key decision makers that align with research and development objectives., • Product and scientific knowledge: maintain deep understanding of our product portfolio including reagents and services that support making mRNA. Effectively communicate product features, benefits and applications to customers., • Conduct presentations that demonstrate our offering and value to specific customer applications., • Stay informed about industry trends, competitor activities and emerging technologies. Utilize this knowledge to develop and adapt sales strategies., • Track sales activities, opportunity and pipeline in SFDC and use dashboards, metrics and KPIs to provide reports and forecasts that demonstrate progression to goals., • Work closely with Senior Business Development manager and director as well as marketing, product development and customer support teams., • Bachelor's degree in Life Sciences, Biology, Chemistry, or a related field with 5 years of experience in sales or business development within the life sciences or academic research sectors. An advanced degree or certification is a preferred., • Proven track record of meeting or exceeding sales targets., • Strong knowledge of life sciences products and research methodologies, mRNA and enzymes is the focus., • Excellent communication, presentation, and negotiation skills., • Ability to build and maintain relationships with researchers and institutions., • Self-motivated with a strong drive for results and a proactive approach to sales., • You have the potential to change, improve, and save lives around the world., • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans., • We offer comprehensive medical plans and HSA/FSA options., • Fertility & family planning assistance., • A variety of additional optional benefits and insurance options, including pet insurance., • Retirement contributions. To view more opportunities to become a #MiracleMaker, visit our career site at Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.), • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment., • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at . If you believe you have been a victim of fraud, you can report this activity at: or .

Job Description Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our sales team as a Senior Sales Representative. As a Senior Sales Representative, you will be responsible for driving sales growth within the academic sector, government agencies, and emerging biotech companies in your assigned territory. You will focus on building and nurturing relationships with R&D professionals in academic institutions and smaller biotech firms, positioning our solutions as essential tools for advancing mRNA modalities. A successful candidate will thrive in a dynamic environment, leveraging their strong scientific background, sales expertise, and strategic acumen to identify opportunities, expand market share, and deliver innovative solutions that meet the evolving needs of our customers. Description of Duties: • Sales strategy and execution: Develop and implement effective sales strategies and tactics to drive new customer acquisition and product adoption while maintaining and expanding relationships with existing customers., • Customer relationship management: be an extension of the Maravai and TriLink brand by building and maintaining strong relationships with key decision makers that align with research and development objectives., • Product and scientific knowledge: maintain deep understanding of our product portfolio including reagents and services that support making mRNA. Effectively communicate product features, benefits and applications to customers., • Conduct presentations that demonstrate our offering and value to specific customer applications., • Stay informed about industry trends, competitor activities and emerging technologies. Utilize this knowledge to develop and adapt sales strategies., • Track sales activities, opportunity and pipeline in SFDC and use dashboards, metrics and KPIs to provide reports and forecasts that demonstrate progression to goals., • Work closely with Senior Business Development manager and director as well as marketing, product development and customer support teams., • Bachelor's degree in Life Sciences, Biology, Chemistry, or a related field with 5 years of experience in sales or business development within the life sciences or academic research sectors. An advanced degree or certification is a preferred., • Proven track record of meeting or exceeding sales targets., • Strong knowledge of life sciences products and research methodologies, mRNA and enzymes is the focus., • Excellent communication, presentation, and negotiation skills., • Ability to build and maintain relationships with researchers and institutions., • Self-motivated with a strong drive for results and a proactive approach to sales., • You have the potential to change, improve, and save lives around the world., • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans., • We offer comprehensive medical plans and HSA/FSA options., • Fertility & family planning assistance., • A variety of additional optional benefits and insurance options, including pet insurance., • Retirement contributions. To view more opportunities to become a #MiracleMaker, visit our career site at Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.), • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment., • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at . If you believe you have been a victim of fraud, you can report this activity at: or .

Job Description We are seeking a Scientific Content Marketing Manager to help shape how EpiCypher’s epigenetic technologies are communicated to the global research community. This role bridges deep scientific expertise with strategic marketing, translating complex chromatin biology and genomics into clear, compelling, and accurate content across digital, campaign, and go-to-market channels. The Scientific Content Marketing Manager will lead scientific messaging, product positioning, and cross-functional alignment—working closely with R&D, Applications, Sales, and Marketing to ensure a consistent, credible voice that drives customer engagement and product adoption. Position Responsibilities: Scientific Communication & Content Strategy • Translate complex science and market insights into strategic messaging that guides campaigns, launches, and customer engagement., • Develop scientific content across digital, print, and campaign channels., • Elevate EpiCypher's thought leadership through compelling storytelling of real-world product applications. Market & Product Positioning • Define and refine product positioning, value propositions, and customer segments., • Conduct customer and market research to inform messaging and strategy., • Analyze competitive landscape and market trends to assist in shaping long-term marketing direction. Go-to-Market & Cross-Functional Leadership • Drive cross-functional alignment for product launches, • Lead lifecycle marketing efforts for launch through adoption., • Partner with Sales, Product Applications, R&D, and design teams. Sales Enablement & Customer Engagement • Develop sales enablement tools and messaging frameworks., • Gather customer insights, testimonials, and feedback., • Support customer education through webinars and training materials. Credentials and Experience: • Ph.D. in biology, biochemistry, other life science, or equivalent relevant background., • Minimum two or more years scientific writing experience and strong background in chromatin biology or genomics preferred. Knowledge and Skills: • Proven experience developing scientific content for diverse audiences is required., • Ability to manage multiple priorities, deadlines, and stakeholders., • Ability to analyze data and metrics to evaluate marketing effectiveness and guide decisions., • Proficiency in design and creative tools (Adobe Creative Suite - Illustrator, InDesign, Photoshop; Canva; PowerPoint; Premiere), or willingness to master them quickly, is strongly desired., • Experience with project management platforms (e.g., Workflowy, ClickUp), digital marketing and social tools (e.g., Hootsuite, Buffer), and website CMS (WordPress) is a plus. Compensation: • Competitive salary commensurate with experience., • Generous benefits package includes subsidized health, dental, and vision; paid vacation, sick leave, and parental leave; federal and floating holidays, mental health day; 401k matching up to 6%; professional development reimbursement; paid life insurance, and stock options. EpiCypher’s mission is to lead the epigenetics field in developing high-quality products and services that accelerate chromatin science to improve and extend human life. In this mission, we hold our core values in high regard: mutual respect, fairness, commitment to excellence, customer success, scientific advancement, effective communication, integrity, and teamwork. EpiCypher is committed to providing a work environment that is free from all forms of harassment, discrimination, and inequality. We provide equal employment opportunities to all employees and applications for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: The role of the Sales Account Manager is to drive and support sales efforts in a given territory by implementing the sales and marketing strategies for GenScript's custom life science services. The Sales Account Manager will use his/her knowledge of science and business including corporate contacts to develop and deliver profitable initiatives and build sales. This role will support the Research Triangle Park territory and requires the candidate to reside ideally within the Durham, NC area. The estimated salary range is $80,000 - $95,000, based on experience level. Key Responsibilities: The Sales Account Manager will work with the District Sales Lead (DSL) and Technical Account Managers (TAMs) to grow and develop an assigned sales territory. They will promote GenScript's custom life science service lines and will be responsible for achieving the sales goals for the assigned territory. The Sales Account Manager will also work with their DSL, TAM and Sales teams to build the GenScript brand. The Sales Account Manager will work 50% of the time doing account management, quote and lead follow-up, and 50% of the time traveling in the field making customer visits and attending virtual meetings. These customer engagements are crucial for building relationships to achieve the agreed monthly/quarterly/yearly sales goals. • Work with DSL to develop and implement territory sales strategies for services, new markets and applications, • Work together with the DSL, TAMs and Regional Manager to ensure all possible actions have been taken to secure business in a competitive environment, • Responsible for understanding the customer's research applications and matching GenScript's custom life science services with their project requirements, • Share market knowledge with Sales, TAM and Marketing teams through weekly field feedback reports, • Strong scientific background- either a Bachelor's degree or above majoring in life science area or equivalent experience, • Minimum of 2 years of experience in scientific or life science sales, • Knowledge of the Biological and CRO or CDMO market or general biotech industry. Emphasis on Gene Synthesis, Protein, Peptide, Bioassays, Antibody and Cell Line Products/Services preferred, • Experience in the lab is preferred, • Ability to operate effectively in an international business environment #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Research experience in epigenetics and chromatin biology is preferred but not required.

Application Process** - Submit your resume or CV highlighting biology background and relevant achievements - Complete a brief interview (20–30 minutes) - Submit a short form detailing your experience writing problems and competing in biology competitions - Selected applicants will be contacted wit

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