401(K) Jobs in Cambridge
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Looking for 401(K) jobs in Cambridge? Browse our curated listings with transparent salary information to find the perfect 401(K) position in the Cambridge area.
Global Talent Management Specialist
Company: BeiGene
Location: Cambridge
Posted Sep 19, 2023
BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness. All employment is decided on the basis of qualifications, merit, and business need. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. are continuously evolvingStrong proficiency in Microsoft Excel, Word, PowerPoint, Outlook, Teams and Zoom etc. )Work jointly with key stakeholders in Benefits, Equity, IT, Global Security, Legal & Compliance, Corporate Affairs, Quality, and Talent Development departments in order to enhance and support the new colleague experienceExecute reports within Workday HRIS system and partner with HR Operations team to ensure accuracy of new hire start dates, headcount and confidential hiresProvide support on all company surveys; engagement, pulse, exit and onboarding.Create and edit new hire corporate headshotsSupport updates and revisions of Global Talent Management reference guides, trainings and department tools and resourcesExemplify the desired culture and philosophies of BeiGeneMaintain a high degree of confidentiality and discretion on all matters, data and projects. Travel: 0-10%, Flexible schedule to accommodate global meetings Supervisory Responsibilities: NA BeiGene Global Competencies When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Evaluate effectiveness of current programs and provide input on continual improvementServe as key point of contact to the business for Talent Management initiatives and technology, addressing questions and requests in a timely and professional mannerServe as key point of contact for new hires across the Americas, enrich communication channels between new colleagues and other onboarding stakeholders and managementPrepare and execute all project management aspects of running onboarding orientations across Americas, EU and New Markets, including strategic scheduling, invitation distribution and response tracking, agenda and content development, post session follow-up, recording edits, survey administration and slide distributionPresent and host live meetings for new colleagues including interacting with both key presenters/executives and audience, as well as behind the scenes moderation (e.g., monitor chat, manage timing, run breakout rooms, record features, etc. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. As such, the selected applicant must be within commutable distance to either our Cambridge, MA, or San Mateo, CA, offices Qualifications: 1+ years of experience in HR related rolesFamiliarity with employee engagement and talent management programsStrong presentation and public speaking skills, both in person and virtual, with ability to gauge audience engagementStrong technical aptitude, skilled in navigating software and digital programsHighly adaptable and quick-learning professional, who thrives in dynamic environments, excels in navigating ambiguity, and embraces change with enthusiasm and initiativeStrong project management and organizational skills with demonstrated ability to work independently on multiple projects, navigating competing prioritiesProven ability to foster relationships at all levels of the organization, including C-SuiteAbility to collaborate with a team environment across various job functions, regions and time-zonesComfortable working in an environment in which businesses processes, tools, deadlines etc.
Associate Scientist I/II, Process Sciences
Company: Vor Bio
Location: Cambridge
Posted Aug 03, 2023
Vor Bio is seeking a highly motivated Associate Scientist I/II to join the Process Science Team. The successful candidate will have a background in cell/molecular biology, bioengineering, or immunology with experience working with mammalian cell cultures. The role involves establishing the base CAR-T process, evaluating CART phenotype and functionality, and improving the CAR-T platform. The successful candidate will have the opportunity to work in a highly collaborative team in a startup environment.
Archive-Submittals Coordinator
Company: SMMA
Location: Cambridge
Posted Sep 22, 2023
We are guided by a shared pursuit of design excellence, sustainability, and social responsibility. Company Perks Employee-owned firm with Employee Stock Ownership Program Hybrid work-from-home policy Competitive benefits including paid time-off, company-funded MA Paid Family and Medical Leave, company-paid dental plan, company-paid life insurance, and 401(K) matching Employee Assistance Program (includes confidential emotional support, legal guidance, and financial resources) Mentor/protégé program Educational reimbursement Licensure and membership reimbursement “Lunch and Learns” with internal and external speakers Today, we remain dedicated to this flexible, integrated approach. Our work straddles seven markets—K-12, Higher Education, Corporate, Commercial, Life Science, Federal Government, and Advanced Technology—with the opportunity to work across a wide range of projects and specialisms. Cambridge-based since our incorporation in 1955, we offer an integrated, multidisciplinary environment driven by collaboration between architects, interior designers, engineers, technologists, researchers, and industry experts. We offer a fast-paced, team-oriented environment that promotes intellectual and creative growth. SMMA was founded by MIT and Rensselaer alumni who believed that the balance of architecture, engineering, interiors, and site design afforded clients the agility of a single source of creative and technical expertise. Key Archive Responsibilities Assist with digital asset management, records management, and project close-out activities Organize and inventory drawings and project documentation Preserve and rehouse archival material in various formats Assist with the preparation of archival materials for transfer to off-site storage and clients Key Submittals Responsibilities Process and track shop drawings and samples with respective trades (Ex: architectural, structural, MEP, specialist consultants) Coordinate with respective trades, contractors, and consultants during construction phase Prepare shop drawing status reports Respond to technical and coordination issues related to tracking of shop drawings Set up QC reviews and coordinate with project managers, consultants, and clients Secondary Responsibilities As needed additional support for administrative team members to cover vacations and absences. Print Room services: Printing, coordinate delivery services, travel arrangements, and mail distribution Administrative services: catering requests, meeting arrangements, and occasional reception coverage Key Competencies Proficient with Bluebeam, Acrobat, and MS Office including Word, Excel, Teams, and Outlook Ability to work in a team environment and on an individual basis Ability to communicate both verbally and in writing Good interpersonal skills and attention to detail Ability to work well under pressure Well-organized and flexible, with the ability to prioritize tasks in a fast-paced environment Strong organizational, interpersonal, and communication skills Minimum Qualifications Current college student actively pursuing a degree in Architecture, Engineering, or Interior Design Technical knowledge of the AE industry or experience as a librarian Two years of general office experience Ability to lift and carry boxes weighing up to 40 pounds and move furniture Ability to stand, stoop, bend, and work in tight spaces About the Firm SMMA is one of New England’s most unique design firms due to our composition, reputation, and focus. We focus on building lasting relationships with strategic partners in both the public and private markets. As an employee-owned firm, we believe that good ideas are welcome from anywhere. The primary responsibility of the Archive/Submittals Coordinator will be to maintain control over project archives and shop drawings through a computerized database and to ensure proper filing, storage, and retrieval of documents. The secondary responsibility will be to provide print room and administrative support. SMMA is seeking an Archive/Submittals Coordinator to handle project document archiving maintaining control over a computerized database of historic project information, and to manage project submissions and approve shop drawings and samples from consultants.
Senior IP Counsel
Company: BeiGene
Location: Cambridge
Posted Aug 22, 2023
BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness. All employment is decided on the basis of qualifications, merit, and business need. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. BeiGene Global Competencies When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. Adaptability - Able to adapt to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events. Project Management - Communicates changes and progress; Completes projects on time and within budget. Computer Skills: Proficiency in the Microsoft Office Suite, Outlook, Word, Excel, SharePoint Other Qualifications: Advanced degree in organic chemistry, medicinal chemistry or other chemical sciences required. Analytical - Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data.
Principal Associate Scientist/Scientist I: Antibody Immunologist
Company: Vor Bio
Location: Cambridge
Posted Aug 17, 2023
The text describes a company, Vor Bio, that is developing a targeted immunotherapy approach to treat diseases. They are looking for a Principal Associate Scientist/Scientist I: Antibody Immunologist to contribute to this effort. The position involves working in a team environment to execute experimental plans, including generating, isolating, and analyzing monoclonal antibodies in vitro. The company offers competitive benefits and values diversity and work-life balance.
Sr Sales Development Representative
Company: Thermo Fisher Scientific
Location: Cambridge
Posted Sep 01, 2023
For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response. A one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. We offer a comprehensive Total Rewards package that our US colleagues and their families can count on, which generally includes: A choice of national medical and dental plans, and a national vision planA wellness program, and valuable health incentive opportunities for company contributions to a Health Reimbursement Account (HRA) or Health Savings Account (HSA)Tax-advantaged savings and spending accounts and commuter benefitsEmployee assistance programAt least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer time off in accordance with company policyRetirement and savings programs, such as our competitive 401(k) U.S. retirement savings planEmployees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Compensation & Benefits. Please contact us to request accommodation. Knowledge, Skills, Abilities Ability to communicate account objectives and action plans to management via weekly calls and reports as well as other communication methods.Ability to collaborate with, and nurture strong partnerships with, multi-national and cross-functional matrix teamsAbility to generate pipeline and business opportunity leadsAbility to sell strategic and new products to existing and new customersAbility to increase our market share by generating new business leadsAbility to synthesize and integrate customer insights, draw conclusions/implications, and translate information into product requirements, portfolio strategies, and business recommendations.Demonstrate authentic leader that holds themselves and others accountableDemonstrated success meeting or exceeding bookings targetsStrong negotiation, communication, presentation and resolution skills.Financial competence and self-leadership with a focus on analysis, planning, organization, execution and follow-up.Work remotely, to flexible patterns, and ability to travel up to 50%.Position may require Covid-19 vaccination and/or routing testing, per client discretion. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
R&D Scientist
Company: Generation Bio
Location: Cambridge
Posted Aug 02, 2023
We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race (to include traits historically associated with race including, but not limited to, hair texture, hair type, hair length, and protective hairstyles such as braids, locks, twists, hair coverings, and Bantu knots), color, gender, religion, national origin, gender identity, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Generation Bio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. To see additional roles, please also check out https://generationbio.com/careers/ Job Location: 301 Binney Street, Suite 401, Cambridge, MA 02142 (Telecommuting is available up to one day per week)Approximately 10% domestic and approximately 10% international travel required.This position qualifies for Generation Bio Co.’s employee referral incentive program.The R&D Scientists will be responsible for the following duties:Lead, design, and execute laboratory experiments to develop the manufacturing process for pharmaceutical substances used in gene therapy treatments;Perform in-house experiments and supervise efforts related to the purification process development;Perform experiments and collaborate efforts related to the development of process steps including cell lysis, enzyme-based synthesis of DNA drugs, chemical precipitation, depth filtration, tangential flow filtration, sterile filtration, viral filtration, and column chromatography;Perform testing and analysis of process intermediates and final drug substance;Lead tech transfer of small-scale process(es) to the MST (Manufacturing science and technology) and GMP groups for large scale manufacturing at contract manufacturing organization (CMO);Provide technical resources for recent technologies in drug development;Write and review protocols, reports, and manufacturing batch records; andPrepare, analyze, and present data to cross functional teams.Job Requirements:Employer requires a Master’s degree in Pharmaceutical Sciences, Biotechnology, Bioengineering, or closely related field and at least two (2) years of work experience as a Research Scientist (or related occupation) performing downstream process development in a pharmaceutical manufacturing or industrial environment.In addition, the employer requires the following:Demonstrated ability testing and analyzing process intermediate and final drug substance samples gained through two (2) years of work experience;Demonstrated ability designing, executing, and troubleshooting experiments to develop downstream processes for the purification of drugs gained through two (2) years of work experience;Demonstrated ability authoring and executing protocols, interpretating data, and generating final reports gained through two (2) years of work experience; andDemonstrated ability optimizing scalable purification processes and manufacturing activities in a GMP environment gained through one (1) year of work experience.All years of experience may be gained concurrently.EEOC Statement: Generation Bio believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. RES has the potential to expand Generation Bio’s manufacturing scale to hundreds of millions of doses to support its mission to extend the reach of genetic medicine to more people, living with more diseases, around the world.We are a thriving, collaborative, creative community of 165 people with diverse talents, beliefs, and experiences headquartered in Cambridge, Massachusetts. Delve further. Please visit www.generationbio.com or follow @generationbio. The platform is designed to enable multi-year durability from a single dose, to deliver large genetic payloads, including multiple genes, to specific tissues, and to allow titration and redosing to adjust or extend expression levels in each patient. The company’s non-viral platform incorporates a novel DNA construct called closed-ended DNA, or ceDNA; a unique cell-targeted lipid nanoparticle delivery system, or ctLNP; and a highly scalable capsid-free manufacturing process that uses its proprietary cell-free rapid enzymatic synthesis, or RES, to produce ceDNA. Generation Bio is innovating genetic medicines to provide durable, redosable treatments for people living with rare and prevalent diseases.
Manager, CMC Quality Assurance
Company: Vor Bio
Location: Cambridge
Posted Aug 31, 2023
All applicants will be considered for employment agnostic to race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.Please visit our website at https://www.vorbio.com/ for more information. We value work life balance, you'll benefit from discretionary time off, parental leave, and an excellent 401(k) package. We are conveniently located in Cambridge with easy access to public transportation and ample parking.As an equal opportunity employer, we at Vor Bio know that diversity inspires innovation, inclusiveness, and creativity. Review batch data, including batch records, deviations, QC Analytical release testing, and other quality systems as applicable to determine acceptability of product dispositionResponsible for review and assisting in development of MBRs as neededPerform batch release and disposition of Vor investigational productsSupport of Process Development and Analytical Development studies and reportsEnsure documentation aligns with regulatory standards and Vor expectationsReview and approval of product and materials stabilityReview drug product temperature excursions for Clinical Trial MaterialReview and approve SOPs and specifications as neededProvide on-the-floor QA support for manufacturing activitiesPerform technical review of QC analytical testing (including raw test data) to ensure compliance with established protocols and governing procedures Draft quality assurance SOPs Skills and requirements: BA/BS and a minimum of 8-10 years' experience in a Quality Assurance position within a GMP environment.Strong knowledge of GMP regulations and quality systemsAbility to support a risk-based approach to QMS with knowledge of and experience with Quality Risk Management principles.Must be able to work collaboratively with cross-functional groups to ensure compliance and adherence to regulations and established procedures.Should be highly motivated, flexible, and have excellent organizational and communication skills.Experience with cell and gene therapy products is a plusMust be able to work both independently and as part of a multi-disciplinary teamMust be able to work onsite at our Cambridge facility on a regular basisExperienced, self-motivated individual who can handle multiple priorities to meet project team goals and timelines Experience in managing relationships with internal departments and external vendors in a collaborative, constructive manner By becoming a team member here at Vor, you’ll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. The successful candidate will engage with and support Process Development and Analytical Development, review production data including batch records, QC reports, manage deviations and other quality system records, and perform batch release and disposition. These responsibilities include assisting in and driving risk management activities, and reviewing and approving CMC SOPs, as necessary.Key areas of responsibility:Responsible for clinical batch review, and quality oversight of CMC operations. This process potentially broadens the therapeutic window and improves the utility of complementary targeted therapies.What we value in our fellow VoraciansPassion: Enthusiastically driving our science toward innovative medicinesFellowship: Fostering genuine bonds of collaboration and mentorshipHumility: Acting selflessly by putting the collective mission first Who we are looking for: Vor Bio is seeking a Manager, CMC Quality Assurance who will be responsible for providing Quality support for CMC Operations at Vor’s internal manufacturing facility and external manufacturing partners. We invite you to come as you are. We also offer a generous transportation stipend to commute as you wish. Unfortunately, both diseased and healthy cells often express the same proteins, resulting in collateral damage to healthy cells.At Vor Bio, we engineer hematopoietic stem cells (HSCs) to lack a biologically redundant target protein, then transplant these cells into the patient.These eHSCs give rise to generations of new healthy blood cells that are effectively invisible to targeted therapies.
Associate Scientist I/II, Process Development
Company: Vor Bio
Location: Cambridge
Posted Aug 02, 2023
Vor Bio is seeking an Associate Scientist I/II to join their Process Development team. The role involves developing the manufacturing process for cell therapy products, focusing on gene-edited hematopoietic stem cells. The candidate will perform primary human cell isolation, gene-editing, and culture, write SOPs, analyze data, and present results. Experience in mammalian cell culture, analytical software, and cell therapy product manufacturing is preferred. Vor Bio offers competitive benefits, work-life balance, and a diverse, inclusive environment.
Supply Chain Associate
Company: Vor Bio
Location: Cambridge
Posted Aug 30, 2023
All applicants will be considered for employment agnostic to race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.Please visit our website at https://www.vorbio.com/ for more information. We value work life balance, you'll benefit from discretionary time off, parental leave, and an excellent 401(k) package. We are conveniently located in Cambridge with easy access to public transportation and ample parking.As an equal opportunity employer, we at Vor Bio know that diversity inspires innovation, inclusiveness, and creativity. without assistance while following proper safety lifting techniques.Ability to be on call on a rotating basis.By becoming a team member here at Vor, you’ll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. We invite you to come as you are. The ideal candidate should be detail oriented and a strong team player.Key areas of responsibilities:Perform material receipts, storage, cycle counting and distribution activities for cGMP warehouse.Receive and store materials per cGMP guidance & applicable procedures and ensure accurate inventory is maintained and inventory discrepancies are communicated.Perform and document daily warehouse operation and maintenance including cleaning and ensure all warehouse storage areas are inspection and audit ready.Ensure timely receipt, storage, stocking, picking, issuing, and shipping of materials.Perform shipments and ensure materials are shipped and received in correct temperature conditions and are handled appropriately along with their required documentations.Safely operate all equipment and respond to alarms for the on-call program.Support day-to-day activities that are related to the maintenance of office administration.Ensure compliance and execution against all SOPs related to GMP warehouse operations.Skills and requirements:High School Diploma or GED required. We also offer a generous transportation stipend to commute as you wish. This process potentially broadens the therapeutic window and improves the utility of complementary targeted therapies.What we value in our fellow VoraciansPassion: Enthusiastically driving our science toward innovative medicinesFellowship: Fostering genuine bonds of collaboration and mentorshipHumility: Acting selflessly by putting the collective mission first Who we are looking for:Vor Bio is seeking a Supply Chain Associate who will be responsible for fulfilling the logistics behind receiving, processing, storing, and shipping inventory according to GMP processes. (Associate Degree or higher education preferred)Experience with Microsoft Outlook, Word and Excel preferred.Experience with WMS or ERP system preferred.Experience working in a biotech/pharmaceutical GMP regulated manufacturing or distribution environment preferred.Proven verbal and written communication skill and ability to interact effectively with other departments and management.Ability to stand walk for long periods of timeAbility to work flexible schedule to include weekends or holidays as needed.Ability to lift 40lbs. Unfortunately, both diseased and healthy cells often express the same proteins, resulting in collateral damage to healthy cells.At Vor Bio, we engineer hematopoietic stem cells (HSCs) to lack a biologically redundant target protein, then transplant these cells into the patient.These eHSCs give rise to generations of new healthy blood cells that are effectively invisible to targeted therapies.
Translational Reseach Scientist I/II
Company: Vor Bio
Location: Cambridge
Posted Jul 20, 2023
Vor Bio is seeking a highly motivated scientist to join their Pre-Clinical and Translational Biology team. The Translational Research Scientist will lead clinical assay development, perform data analysis, and review data from third-party labs. The ideal candidate should have a Ph.D. in life science with 1-2 years of relevant experience, wet-lab experience, and proficiency in flow cytometry and LBA assays. The role involves working in a cross-functional environment, collaborating with the Clinical team, and assisting with the selection of specialty labs and biobanking facilities. Vor Bio offers competitive benefits, including health insurance, life insurance, disability insurance, and a generous 401(k) package. The company values diversity and innovation, and requires all employees to be fully vaccinated against COVID-19.
Principal Architect
Company: Inari
Location: Cambridge
Posted Aug 14, 2023
This is the first architect role at Inari Agriculture.What you’ll do• Design and build cloud computing and event-driven architectures with high availabilityat global scale.• Evaluate, review, and assess different designs that different engineering squads areproposing.• Collaborate and partner with various organizational levels to ensure timely delivery oftechnology driven business solutions aligned with company strategies, defined businesspriorities, and regulatory mandates• Work with our science and product development divisions to propose solutions thataddress genomic, imagery, greenhouse, and field level digital needs.• Work with division leaders to understand the implications to changes across theenterprise.• Work with partners such as AWS to do architecture assessment workshops with changesin technological landscape.You Bring• Bachelors/Master’s in Computer Science, Biotechnology, Bioinformatics, Mathematics orrelated STEM fields.• Previous SW Development experience preferred10+ years of software/data engineering experience, building data heavy systems andmicroservice oriented applications• 3+ year in architecting systems with a passion for robust architecture that lasts.• Track record of technical leadership via collaboration, mentorship, and leveling upteams• A strong commitment to our team’s values: learn from every decision, noheroes/heroines, thoughtful inclusion, and fail fast.• Knowledge of application modeling languages/techniques (e.g., UML, OML, entityrelationship modeling, DFDs) including the ability to create and read the associateddiagrams.Extras:• Previous Experience in software or architecture in biotech or agtech preferred.• Designing architecture around high performance and scientific computing FOR U.S. Any discrepancies or inaccuracies found during the background check may impact your candidacy for the position. CANDIDATES: Please note that we use the resume you submit with your application during our background check process. To ensure an efficient and accurate background verification, we kindly ask that you carefully review and accurately represent your work history, education and other relevant information on your resume. This role would be responsible in creating wellarchitected systems and platforms that support Inari’s mission of unlocking the full potential ofseeds. If you want to be part of a diverse and inclusive team developing unique solutions to feed the world while protecting our planet’s natural resources, we’d love to hear from you!About Inari... Inari is the SEEDesign™ company. As we scale our various platforms, we are looking for an architect that can help assessand build scalable architectures. Through our unrivaled technology platform, Inari uses predictive design andadvanced multiplex gene editing to develop step-change products. And we've intentionally combined experience with potential, bringing agriculture industry experts with the desire to innovate together with bright minds from academia, human therapeutics, software, and consulting. We’ve deliberately built a team that brings diversity of thought to all aspects of our business, to generate new ideas, approaches, and ways of operating.