Be Or Bc Jobs in Waltham
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Looking for Be Or Bc jobs in Waltham? Browse our curated listings with transparent salary information to find the perfect Be Or Bc position in the Waltham area.
Senior Payroll Specialist
Company: connectRN
Location: Waltham
Posted Oct 11, 2023
As Connectors, we embrace humans of every background, appearance, race, religion, color, national origin, gender, gender identity, sexual orientation, age, marital status, veteran status, and disability status. If this role would make you excited to come to work every day, please apply! We look forward to connecting. connectRN is an equal opportunity employer. The ideal candidate is meticulous, knowledgeable about payroll processes and regulations, and able to work in a fast-paced environment.Note: This is a full-time, in-office, exempt position stemming from company growth. You will…Assist with preparing and processing daily / weekly payments to deliver a world-class pay experience to cliniciansEnsure compliance with federal, state, and local payroll regulations and tax laws.Resolve payroll discrepancies and answer employee inquiries related to payroll matters.Maintain and update employee payroll records, including changes in status, tax withholdings, and direct deposit information.Assist with special payroll projects and process improvements as needed.Create accurate and timely reporting to back up all payroll/Next Day Pay dataPrepare ad hoc reports as requested by the Payroll Manager and Director of Payroll OperationsCollaborate with the HR department to ensure accurate processing of new hires, terminations, and other personnel changes.Generate payroll reports and assist in reconciling payroll accounts You have…Minimum of 5 years of progressive experience in payroll processing.Strong proficiency in payroll software ADO workforce now and Microsoft Office, especially Excel.Exceptional attention to detail and accuracy.Excellent communication and interpersonal skills.You’ll get…100% employer-paid premiums for your (and your family's) Health, Dental, Vision, Short Term Disability, Long Term Disability, Life and AD&D insuranceHealth Savings Account with contributions from connectRN of up to $2,000 annuallyFree gym and parking on-siteFlexible time off policy401k with matchPlease note that we are only able to hire permanent residents (green card holders) or U.S. citizens at this time. To better serve the daily payroll needs of our nurses and aides, this Payroll Specialist's schedule will be from Monday - Friday. connectRN is headquartered in Waltham, Massachusetts and serves clinicians across the U.S. To learn more about connectRN, please visit www.connectrn.com.We are looking to hire a Senior Payroll Specialist to ensure accurate processing and recording of the ConnectRN’s daily STATcash and weekly payments. As the Senior Payroll Specialist, you will play a pivotal role in overseeing payroll processes, compliance, and continuous improvement. The Senior Payroll Specialist will also deliver support to the clinician community by answering all payroll-related questions, and ensuring all clinicians receive the correct compensation in a timely manner. The platform offers career development resources and flexible shift offerings for nurses, while alleviating staffing shortages at healthcare facilities. By leveraging technology, connectRN connects the nursing community to flexible work opportunities and each other to build a supportive and thriving network. connectRN is the leading nurse-centric platform that is reinventing the way nurses and other healthcare professionals are finding work.
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.
IT Audit Manager
Company: Evolv Technology
Location: Waltham
Posted Oct 14, 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. 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]. Please note that the compensation details listed in role posting reflect the base salary only, and do not include commission, equity, or benefits.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. If you are inspired by invention and gain satisfaction from seeing how your work impacts the bigger picture, Evolv will be a great fit. We are passionate, knowing that what we do and how we do it can affect life or death situations for our customers.
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.
Senior Accountant
Company: Evolv Technology
Location: Waltham
Posted Oct 13, 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. 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. What is the structure and culture of the team?You will be joining the Accounting team and reporting directly to the Assistant Controller.The team culture is one based on building trust, collaboration, on-going development through kindness, authenticity, courage, drive, and fun!Where is the role located? 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. Evolv will not tolerate discrimination or harassment based on any of these characteristics.
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, Neuromuscular Research
Company: Dyne Therapeutics
Location: Waltham
Posted Oct 05, 2023
All Employees are expected to adhere to all company policies and act as a role model for company values.Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. Applicants must be able to relocate to the area.Primary Responsibilities Include:Design, execute, and analyze in vitro and in vivo studies to profile candidates for proof of mechanism and proof of concept.Evaluate and validate models of rare genetic disorders.Utilize creativity and resources to design, evaluate, and develop new assays to answer key scientific questions to drive programs towards clinical development.Work effectively with other functions including Platform Development and Preclinical Development to collectively build the preclinical data package to support clinical development.Build high-quality presentations and effectively communicate research to senior scientific leadership and at cross-functional opportunities.Contribute to a culture of strong scientific curiosity and build a positive, team-oriented environment.Education and Skills Requirements:PhD in molecular biology, pharmacology or related life sciences and 2+ years of hands-on post-doctoral experience or BSc/MSc with 5+ years of relevant industry experience is required.Experience in providing scientific and technical leadership applied to novel assay development, advancing challenging drug discovery programs, and mentoring junior colleagues.Strong hands-on experience working with disease models including primary cell culture and rodent models.Experience with established molecular techniques including qPCR, western blotting, ELISA, immunohistochemistry/immunofluorescence, fluorescence in-situ hybridization, flow cytometry, and confocal microscopy.Strong written and oral communication skills, organization, and multitasking, and working in a highly collaborative and cross-functional research environment.Proven ability to work independently and to facilitate interactions with academic labs to ensure project progression is desirable.Strong track record of scientific accomplishments with relevant peer-reviewed publications and presentations.LI-OnsiteThe statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This role requires substantial commitment to the bench and is based in Waltham, MA without the possibility of being remote. For more information, please visit https://www.dyne-tx.com/, and follow us on Twitter, LinkedIn and Facebook.Role Summary:The Scientist, Neuromuscular Research plays a critical role in developing new therapies for genetic disorders, with a focus on neuromuscular diseases. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned. This role is involved in all aspects of in vitro and in vivo exploration of disease biology and in the evaluation of mechanisms of action, efficacy, pharmacodynamics, and pharmacokinetics of our therapeutic molecules. As part of the Dyne research team, this individual is an innovative and collaborative team player who enjoys working in a fast-paced team setting driven by aggressive timelines. The person in this role brings key strategic thinking and provides core scientific leadership to cross-functional teams. Dyne has a broad pipeline for serious muscle diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and a preclinical program for facioscapulohumeral muscular dystrophy (FSHD). This role leads from the bench and conducts the development and implementation of patient cell and animal disease models that support ongoing projects.
Sr Technical Accountant
Company: Excelitas Technologies
Location: Waltham
Posted Sep 30, 2023
The Senior Technical Accountant at Excelitas Technologies is responsible for technical accounting research and external reporting. Key responsibilities include drafting memos on complex transactions, preparing financial statements, coordinating with external auditors, and providing research on non-standard accounting matters. The role requires strong US GAAP knowledge, excellent communication skills, and at least 3 years of accounting experience. Public accounting experience is preferred. The position involves coordinating with various stakeholders, assessing the impact of new accounting pronouncements, and drafting technical accounting memos. The candidate must be a US citizen or green card holder due to ITAR regulations.
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.