Tech Jobs in Waltham
2,284 open positions · Updated daily
Waltham is emerging as a high‑growth tech hub within the Greater Boston corridor. With 6,396 openings across software, fintech, health‑tech, and data‑analytics sectors, the city is attracting talent from across New England. The mix of established companies and fast‑moving startups keeps the job market vibrant and competitive.
Key players include Verint Systems, a leader in customer engagement software; Acuity Insurance, which blends underwriting with AI; and Verifone, a global payment‑technology pioneer. In addition, dozens of fintech firms, health‑tech innovators, and cybersecurity vendors have set up shop in Waltham’s tech corridor, creating a diverse range of roles from software engineering to product management.
Living costs in Waltham are high—median house prices hover around $700,000 and average rents exceed $2,400/month—so knowing the exact pay range is crucial. Salary transparency lets candidates negotiate confidently and ensures they can afford the local lifestyle, from dining in the historic downtown to enjoying nearby parks and public transit.
Sales Engineer - Spot
Company: Boston Dynamics
Location: Waltham
Posted Sep 22, 2023
However, we are not able to sponsor visas for this position. To thrive in this role, you must provide the necessary depth and breadth of knowledge to gain trust from our customers and prospects, and to serve as their voice to product management, engineering, and operations teams. Day to day activities: Execute on an established scalable and repeatable customer evaluation processWork within a quickly growing team to support our strategic enterprise engagementsConduct engaging but technically-focused in-person demonstrations of our robots' capabilities to a wide variety of audiencesBecome the customer's trusted advisor, providing a realistic perspective on what is possible with mobile autonomy without sacrificing the momentum of excitement that our robots bringInterface with our customers' Operations, Innovation, Information Technology and Information Security teams to address their questions and requirements for incorporating Spot into their workflows and enterprise networksLeverage ecosystem knowledge to recommend any appropriate actions, pre-requisites, or 3rd-party additions to the sum total of a solution that provides valueFulfill requests for information (RFIs) from customers,, and draft SOWs and proposalsInterface with product management, engineering, and operations teams to provide constructive customer feedback, addressing common blockers to widespread adoption Required Skills: Bachelor's degree in a technical discipline is preferredMinimum 5 years experience in a customer facing technical roleFamiliarity with industrial inspection and manufacturing workflowsStrong public speaking skills and experience with presenting to audiences of mixed technical backgroundsAbility to accommodate 50% travelExperience with some variety of wireless digital communication systems such as WiFi deployment, mesh radio networks, or cellular systemsValid driver's license with a good driving recordAmbulatory movement with the ability to lift 70lbsValid Passport Beneficial Skills: Proficient knowledge of Linux-based operating systemsExperience with predictive maintenance systemsKnowledge and/or experience with information security strategies, standards, and policies We are interested in every qualified candidate who is eligible to work in the United States. You'll accomplish this by aligning our robot's capabilities, any relevant sensors, communications, software, and services into a defined workflow, with an SOW, to map out how our customers will get value out of the solution. You'll need to communicate effectively with a broad spectrum of stakeholders, both internally and externally, explore use cases with operators of Spot and guide them on the path that brings the fastest value from our solutions. You and your team will partner with the Sales team by being the technical subject matter experts in Spot, assisting with cross-functional customer team alignment, and be able to collect the relevant information to appropriately issue proposals and ROI analysis to prospects and customers. As a Sales Engineer supporting the Sales organization for Spot, our quadruped robot, you will help highlight the "art of the possible," guide customers on the journey of making mobile autonomous robots part of their day-to-day operations, and execute on your team's process to ensure our customers find value from Spot. LI-JM1 You will also enable your team and our salespeople to showcase all the best capabilities that Boston Dynamics has to offer. For years, our awe-inspiring viral videos on YouTube have shown the world what remarkably capable robots can do.
Manager, Deal Desk
Company: Imprivata
Location: Waltham
Posted Sep 22, 2023
Imprivata provides equal employment opportunities, regardless of race, religion, age, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. At Imprivata, we have a top-notch work environment, developmental opportunities, a competitive total rewards package, and the desire to have fun. Actual salaries will vary and may be above or below the range based on various factors, such as a candidate's location, skills, experience, and qualifications. Partners, and internal stakeholders during the deal process. In addition, more information about Imprivata's benefit offerings can be found here . Duties and Responsibilities Responsible for the entire upfront deal cycle, including collaboration with Field and Renewal Sales, Legal, and Finance within the deal cycle to improve deal velocity, drive pricing discipline and increase transparency. The Manager will identify process gaps, help with solutioning the improvements, and facilitate training as needed. You will be responsible for leading the team that manages Deal Structuring, Discounting, Co-terming, and all aspects of the deal cycle. Manage a team of Deal Desk analysts Assist with complex contract negotiation and provide pricing options, deal construct alternatives and business analysis to help facilitate the deal process. You should have a proven success with customers and internal stakeholders (e.g., Sales, Finance, Legal, and Customer Success) to ensure that value is realized for the customer and commercial objectives are aligned with the growth of our business.
Implementation Engineer - IDG
Company: Imprivata
Location: Waltham
Posted Sep 24, 2023
Imprivata provides equal employment opportunities, regardless of race, religion, age, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.LI-Remote At Imprivata, we have a top-notch work environment, developmental opportunities, a competitive total rewards package, and the desire to have fun. Actual salaries will vary and may be above or below the range based on various factors , such as a candidate's location, skills, experience, and qualifications. In addition, more information about Imprivata's benefit offerings can be found here . A basic understanding of Operating Systems Knowledge of common information technologies deployed with enterprise-class solutions including, but not limited to, networks, Microsoft Windows-based workstation platforms, wireless client devices, terminal servers, directory services, RDBMS servers, and automated software distribution software. Clinical healthcare IT experience a plus. Demonstrated success working in a team environment. Required Qualifications Hands-on experience either with the following technologies or equivalents: JavaScript Java Java BeanShell SQL Active Directory (knowledge of basic attributes, user and group management) Knowledge of Networking, TCP/IP protocols, DHCP, SMS, Active Directory, Certificate Authorities, Exchange and IIS as it pertains to server configuration and maintenance is a plus. Preferred BS in Computer Science or other technical discipline. Working knowledge of server administration and setup.
Data Acquisition Specialist
Company: Affectiva
Location: Waltham
Posted Sep 28, 2023
Smart Eye, a global leader in Human Insight AI, is seeking a Data Acquisition team member to assist in executing data collection protocols. The role involves designing, installing, and maintaining systems for in-lab and in-vehicle data collection, as well as facilitating studies with participants. The ideal candidate is a problem solver with strong technical skills, excellent communication, and attention to detail. Responsibilities include recording environment setups, building custom cables, designing data collection protocols, and troubleshooting hardware and software issues. The role requires independence, a passion for building stuff, and a valid driver's license.
Associate Scientist I/II -- Protein Production
Company: Dragonfly Therapeutics
Location: Waltham
Posted Sep 23, 2023
We offer a unique opportunity to learn, grow professionally and be part of a fun, dedicated and goal-oriented team.Responsibilities:Manual and automated mammalian protein production (upstream and downstream)Bench-scale mammalian protein purification using column chromatography (Affinity, IEX, SEC, HIC) and FPLC/liquid chromatography (AKTA Pure, AKTA Avant)Molecular biology techniques including cloning, PCR, and plasmid DNA prepMammalian cell culture (Expi293, ExpiCHO) utilizing strong aseptic techniqueTecan liquid handler method development, optimization, validation, and execution for automated high-throughput (HTP) protein production (DNA cloning, mammalian protein expression (Expi293, ExpiCHO), and mammalian protein purification)Design of Experiments (DOE) applied statistical approach to upstream and downstream process development activities to expand existing HTP protein production capabilities and related QC activitiesPerform assorted analytical biochemistry techniques (Octet titer, SDS-PAGE, SEC-HPLC, protein quantification, LAL endotoxin, etc)Work closely with Biologics and Biology leadership teams to ensure that program timelines and milestones are met for the production processesDocument observations and data in electronic labAnalyze and present data at group meetingsQualifications:S. in relevant field with 2+ years of industry experience or M.S. with 0-1+ years of industry experienceFamiliarity with liquid handler platforms (Opentrons, Tecan) is preferredExperience with mammalian cell culture, molecular biology, protein purification, and analytical biochemistry techniquesExperience in method development, optimization, and troubleshootingCapable of operating independently with high level critical thinking and problem-solving experienceMust be detail-oriented with excellent organizational skills; diligent documentation and highly efficient time management are requiredPrevious success operating in a fast-paced, dynamic work environmentExcellent communication and interpersonal skillsAbout DragonflyDragonfly Therapeutics is a clinical-stage biopharmaceutical company committed to discovering, developing and commercializing therapies that use its novel multispecific antibody technology to harness the body's immune system to bring breakthrough treatments to patients. In addition to its wholly owned clinical assets, Dragonfly has a deep pipeline of wholly owned preclinical candidates discovered using its proprietary platform, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas. Our mission is to revolutionize disease treatment by inventing natural killer cell-based therapies for vastly improved patient outcomes. The candidate would be responsible for optimization, and expansion of DNA cloning, protein expression and protein purification platforms in coordination with downstream functional teams. We believe in a small team with a big impact. Associate Scientist I/II, Protein ProductionDragonfly Therapeutics is seeking a highly motivated scientist with a strong focus in Molecular Biology and Protein expression and purification to join the Biologics team. The successful candidate will play a pivotal role in the DNA cloning and rapid generation of antibodies and multi-specifics at various scales to streamline discovery efforts.
Senior Director of Channel
Company: Evolv Technology
Location: Waltham
Posted Sep 27, 2023
We welcome and encourage diversity in the workplace, and all employment decisions are made without regard to race, color, religion, national, social or ethnic origin, sex (including pregnancy), age, disability, HIV Status, sexual orientation, gender identity and/or expression, veteran status, or any other status protected by law in the locations where we operate. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Our salary ranges are determined by role, level, and location. Please note that the compensation details listed in role posting reflect the base salary only, and do not include commission, equity, or benefits. The team culture is one based on building trust, collaboration, on-going development through kindness, authenticity, courage, drive and fun! Evolv is committed to offering an inclusive and accessible experience for all job seekers, including individuals with disabilities. At Evolv, you will have unparalleled exposure to all aspects of our business, working with a talented team that shares our vision for a safer world. If you need a reasonable accommodation as part of the job application process, please connect with us at [email protected]. If you are inspired by invention and gain satisfaction from seeing how your work impacts the bigger picture, Evolv will be a great fit. The location of this&8239;role is remote, with an expectation to connect with your team in the field, approximately 50% of the time.
Director of IT Business Applications and Data
Company: Evolv Technology
Location: Waltham
Posted Sep 23, 2023
We welcome and encourage diversity in the workplace, and all employment decisions are made without regard to race, color, religion, national, social or ethnic origin, sex (including pregnancy), age, disability, HIV Status, sexual orientation, gender identity and/or expression, veteran status, or any other status protected by law in the locations where we operate. Our salary ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Please note that the compensation details listed in role posting reflect the base salary only, and do not include commission, equity, or benefits. The team culture is one based on building trust, collaboration, and ongoing development through kindness, authenticity, courage, drive, and fun! Evolv is committed to offering an inclusive and accessible experience for all job seekers, including individuals with disabilities. At Evolv, you will have unparalleled exposure to all aspects of our business, working with a talented team that shares our vision for a safer world. If you need a reasonable accommodation as part of the job application process, please connect with us at [email protected]. If you are inspired by invention and gain satisfaction from seeing how your work impacts the bigger picture, Evolv will be a great fit. BenefitsIf you want to solve one of the most difficult issues of our time and save lives doing it, you want to work at Evolv.
Senior Product Manager
Company: Thermo Fisher Scientific
Location: Waltham
Posted Sep 27, 2023
For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. http://jobs.thermofisher.com 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. 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. As 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*. Experience 5+ years' professional experience in life science product management, marketing, application, sales, applications, or customer support function.Experience working with customers, commercial teams and multifaceted sales channels and direct - strongly preferred.Strong technical capabilities consistent with market segment and product category (equipment, software, consumables).Experience in developing and launching new products. MBA desired. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Experienced working in a matrixed organization.Global mentality, excellent communication, and presentation skills, including significant active listening skills.Results and proactive solution driven, the ability to think critically to overcome potential business hurdles to complete tasks.Demonstrated ability to question the status quo and motivate change successfully.Requires up to 25% travel including international.
Senior Manager, Financial Planning & Analysis
Company: Imprivata
Location: Waltham
Posted Sep 27, 2023
Imprivata provides equal employment opportunities, regardless of race, religion, age, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. At Imprivata, we have a top-notch work environment, developmental opportunities, a competitive total rewards package, and the desire to have fun. Actual salaries will vary and may be above or below the range based on various factors, such as a candidate's location, skills, experience, and qualifications. Required Qualifications Bachelor's degree in business, Accounting or Finance. Advanced MS Excel skills is required. Perform ad hoc analysis as required. In addition, more information about Imprivata's benefit offerings can be found here . Minimum of 5-7 years in financial planning and analysis roles. Provide benchmarking data in assisting management with strategic decisions. Experience in software company and/or PE backed company is desirable but not required.
Scientist
Company: Alkermes
Location: Waltham
Posted Sep 23, 2023
For more information, please visit Alkermes' website at www.alkermes.com Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law. Headquartered in Dublin, Ireland, Alkermes has an R&D center in Waltham, Massachusetts; a research and manufacturing facility in Athlone, Ireland; and a manufacturing facility in Wilmington, Ohio. Alkermes is an E-Verify employer. The company has a portfolio of proprietary commercial products focused on alcohol dependence, opioid dependence, schizophrenia and bipolar I disorder, and a pipeline of product candidates in development for neurodegenerative disorders and cancer. About Us Alkermes plc is a fully-integrated, global biopharmaceutical company developing innovative medicines in the fields of neuroscience and oncology. An established track record of solving complex technical problems, creativity, excellent communication skills, and an ability to thrive in a cross-functional environment are necessary for success. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Collaboration is critical to effectively moving projects forward in this role. The successful candidate will have a strong laboratory presence and provide technical excellence in the areas of drug substance form selection, crystallization, and preformulation within a highly integrated pharmaceutical development environment. This individual should maintain and hone state-of-the-art technical knowledge and champion ideas for new and ongoing projects.
Engineer/Sr. Engineer, Upstream Process Development
Company: Dragonfly Therapeutics
Location: Waltham
Posted Sep 27, 2023
Candidate must be independent, goal-oriented, flexible, and able to work efficiently across multiple projects. The successful candidate will contribute and drive our upstream cell culture process development, while interacting regularly with other CMC functions. Responsibilities:Lead development of robust and scalable upstream processes for biologics in different stages of clinical development, including design, execution, analysis, and documentation of all stages of cell-culture process developmentSupport external manufacturing with technology transfer for implementation of new processes and provide person-in-plan support as requiredSupport process change controls, deviations, impact assessments, and perform batch record reviewImprove upstream processes through research and innovation, while assessing technologies and industry best practicesReview, collect and trend data from manufacturing batches to help identify trends, assess performance, build process understanding, and enable improvement activitiesChampion compliance and safety; promote a culture of diversity, inclusion, and equityMaintain good communication and collaborate with cross-functional colleagues and external partners for successful execution/completion of projectsAuthor and contribute to IND/IMPD/BLA submissionQualifications:BS/MS with 10+ years, or PhD with 2+ years of industry experience and background in Chemical/Biochemical engineering, or a related fieldStrong fundamental knowledge and subject matter expertise in cell-culture process development, fed-batch cell culture, bioreactors across scales, as well as recent advances, and challenges in the fieldExperience and aptitude to lead, work and collaborate in internal and external cross-functional, matrixed teamsWorking knowledge of cGMP and quality systemsAction-oriented mindset, ability to take initiative, innovate, iterate and problem solveExperience with cell culture and predictive modeling (omics, metabolic flux analysis); statistics, data-science, machine learning, artificial intelligence a plusAbility and willingness for approximately 10% domestic travel consistent with project needsAbout DragonflyDragonfly Therapeutics is a clinical-stage biopharmaceutical company committed to discovering, developing and commercializing therapies that use its novel multispecific antibody technology to harness the body's immune system to bring breakthrough treatments to patients. In addition to its wholly owned clinical assets, Dragonfly has a deep pipeline of wholly owned preclinical candidates discovered using its proprietary platform, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas. Our mission is to revolutionize disease treatment by inventing natural killer cell-based therapies for vastly improved patient outcomes. Engineer, Upstream Process DevelopmentDragonfly Therapeutics seeks an upstream process development engineer who brings enthusiasm, intellectual curiosity, scientific rigor and a desire to help deliver novel immunotherapy programs. We believe in a small team with a big impact. Engineer/Sr. The successful candidate will excel in a highly collaborative work environment with a multi-disciplinary and diverse team focusing on multiple programs in parallel.
Head of Drug Safety
Company: AlloVir
Location: Waltham
Posted Sep 29, 2023
AlloVir is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. With a company vision of “ImmUnity for all”, we place special emphasis on unity, on equality, and on inclusion for all employees, patients, and partners. AlloVir will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. This includes all aspects of safety data evaluation, including assessing safety from a variety of sources, e.g. Join a team committed to scientific excellence, focused on passionate engagement, and united in purpose to treat and defeat viral diseases.At AlloVir, we are committed to fostering and expanding diversity in the workplace. Provide support for safety sections of clinical documents, including the review and approval of the safety portion of protocols, annual reports, final study reports, IB, and other documents Support the operations of a global function supporting the company pipeline from early Phase development, through BLA/MAA filings, to approval and post marketing Coordinate design development and implementation Risk Evaluation and Mitigation Strategies (REMS) among multiple stakeholdersAdvisement on the design of post-approval safety studiesDevelop and align processes to support safety and pharmacovigilance in the post marketing settingQUALIFICATIONSREQUIREDMD, DO or equivalentMinimum 8 years employment working in a clinical practice, clinical research, or product developmentMinimum 4 years’ experience in clinical safety including activities related to post marketing surveillance and pharmacovigilanceExpert knowledge within global regulatory landscapesDirect experience interfacing with relevant global regulatory authoritiesExperience in interpretation of global regulations, guidelines, and reg policy mattersAbility to thrive in a fast-paced environment Strong leader, and team player who demonstrates initiative, willingness to roll-up his/her sleeves, and problem solve Strong writing skills is a must, including ability to author documents Ability to communicate effectively and represent the Regulatory and Safety organization PREFERREDCell and gene therapy experienceInfectious disease experienceBoard certification in a medical field or medical specialtyActive US state license to practice medicine or surgeryWhy join AlloVir?AlloVir is the global leader in developing novel cell therapies that restore natural immunity against life-threatening viral diseases for immunocompromised patients.We have an innovative pipeline of allogeneic, off-the-shelf, T-cell therapies that treat and prevent many devastating and life-threatening viral diseases. Ensure ongoing evaluation of the overall safety profile for AlloVir’s investigational products, serving as the product safety expert, working in partnership with medical monitors to bring potential safety issues to the attention of the Clinical Team and upper management. clinical trials, literature, and pre- and, in the future, post-approval use. This senior role works closely with Company leadership to implement the evolving direction for the risk management and safety function of the department, as well as leading the effort to develop and align processes to support safety and pharmacovigilance in the post marketing setting.RESPONSIBILITIESLead and drive safety strategy for the development of assigned productsCollaborate with appropriate cross-functional company department, and the therapeutic area heads, to ensure efforts are aligned to meet global risk management strategies Define the strategic Drug Safety plans and policies including leadership in product safety surveillance strategy and management of evolving safety profile for clinical development programsLead all interactions regarding product safety issues with our governance committees and regulatory agenciesProvide oversight for the medical review of serious adverse event reports to ensure accuracy, integrity and completeness of safety information, and to ensure consistency of medical coding of safety data. Our proprietary technology platform delivers commercially scalable, “ready-to-administer” solutions by leveraging off-the-shelf, allogeneic, multi-virus specific T-cells, designed to treat or prevent multiple devastating virus-associated diseases. Under the general direction of the Senior Vice President of Clinical Research and Safety, the Head of Drug Safety will be responsible for overall clinical risk management and safety surveillance of assigned investigational products.