Be Or Bc Jobs in Cambridge
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Data Writer
Company: Insurify
Location: Cambridge
Posted Nov 17, 2023
Our team is highly analytical, fast-moving, and focused on one thing: getting more people to compare insurance quotes using Insurify. Join us if you like: $1.3 Trillion market opportunity MIT alumni founders Female-led startup $130M total funding Strong leadership team from Kayak, Amazon, Wayfair, Facebook, Microsoft, Allstate, GEICO, Liberty Mutual, Zillow How you will make an impact: Dive deep into proprietary data sources to find and write the stories that will interest the media and establish Insurify as the leading source of insurance data Gather public data and research from the Census and other public sources to balance topical and tangential content topics Build and nurture relationships with journalists and editors at key media outlets, understanding their interests and how our data, content, studies and reports can resonate with them and their audiences Program survey to gather qualitative and quantitative insights Play a key role in creating a proactive content strategy that drives media attention and builds authority Analyze competitor content and successes to identify opportunities for improvement Drive digital PR strategy for topics including auto and homeownership in relation to insurance Owns the whole process of data insights content creation from ideation to data gathering to writing and to pitching Identify opportunities to collaborate with stakeholders to launch new data content Who you are: A self-starter who has a portfolio of data storytelling You have 1-3 years of data writing and data analysis experience You have some experience with digital PR and are motivated to get your insights reported on by the media You have at least 1 year experience in programming languages R or SQL You already understand or are interested in how links make an impact on SEO You are excited about brainstorming and shipping new data-driven content ideas You are always looking for incremental ways to improve whatever you are working on You love writing and have strong communication skills You are an analytical person who dives deep to understand the “why” behind questions You are a detailed-oriented person who takes time to understand what will engage your audience You consistently strike a writing tone that communicates depth of knowledge and empathy You can accurately employ AP style and active voice within your writing Benefits: Competitive compensation Generous stock options Health, Dental Coverages 401K plan with match Unlimited PTO Generous company holiday calendar Learning & Development Stipends Paid Family Leave Social impact volunteer time and donation matches Catered lunches in the office Free snacks and beverages every day in office We are proud to be an Equal Employment Opportunity and Affirmative Action employer. We’re changing the way millions of people compare and buy insurance with artificial intelligence, technology, and superior product design. Insurify is one of the fastest-growing MIT FinTech startups and has been recognized as a global Top 100 InsurTech company. Do you want to be part of Boston’s hottest up and coming startup?
Senior Scientist, Discovery Toxicology
Company: Biogen
Location: Cambridge
Posted Nov 18, 2023
Biogen is seeking a Toxicologist to join the Discovery Toxicology Group, responsible for developing safety testing strategies, designing and overseeing toxicology studies, and conducting risk assessments. The role involves collaborating with cross-functional teams and presenting toxicology data to peers and senior management. Biogen values a science-based individual with expertise in drug discovery toxicology, strong organizational skills, and excellent communication abilities. Preferred skills include experience with multiple drug modalities and DABT certification. Biogen is committed to fostering a culture of inclusion and belonging.
Program Analyst
Company: Changeis, Inc.
Location: Cambridge
Posted Nov 18, 2023
Changeis, Inc., an award-winning 8(a) certified, woman-owned small business, offers management consulting and engineering services to the public sector. The company has been recognized by Inc. magazine as one of the nation's fastest-growing private companies. Changeis focuses on strategy and transformation management, investment analysis, governance, and innovation management. They provide a comprehensive benefits package. The Program Analyst role involves supporting the Volpe National Transportation Systems Center, offering technical and analytical support for FMCSA's safety programs and systems. Key responsibilities include providing technical support, entering and tracking requests, researching and resolving customer issues, and documenting resolutions. Requirements include a Bachelor's degree, strong communication skills, proficiency in MS Office, detail-oriented work, quality assurance skills, and proven customer service abilities.
Systems Analyst - G&A Applications (IT)
Company: Amylyx
Location: Cambridge
Posted Nov 17, 2023
We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical matters), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. Preferred Qualifications Knowledge of FDA regulations, GDPR, SOX and/or HIPPA compliance is a plus. To stay connected with us, follow Amylyx Pharmaceuticals on LinkedIn. 2+ years of experience in working with NetSuite, Concur, Adaptive, Sage, Achievers and/or other ERPs and HRIS platforms. If you need an accommodation, please let your Amylyx Talent Acquisition contact know. Strong customer service orientation. Support audit activities. Able and willing to travel to our offices in Cambridge, MA 1-2 days per week. Develop and foster effective relationships between the business, partners, and Amylyx IT. Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.
Director, DMPK
Company: Atavistik Bio
Location: Cambridge
Posted Nov 17, 2023
Solid understanding of drug metabolism, bioanalysis, pharmacokinetics, preclinical pharmacology, PK/PD modeling and clinical study designs. Expertise managing CROs, GLP, and other regulated activities. D., or equivalent training in pharmacokinetics, pharmaceutical sciences, or related disciplines. Required Qualifications: Ph.D., Pharm. Author DMPK, nonclinical toxicology, and biomarker sections of regulatory documents. Contribute to candidate selection, development strategy, and coordinate IND-enabling study reports. Minimum 10 years of experience in bio/pharmaceutical industry, combined with drug development Excellent communication and collaborative skills to work on project teams with chemists, biologists, and platform scientists. Experience in nonclinical toxicology is a plus. Must be able to work on multiple projects simultaneously. Review preclinical study reports, in conjunction with Pharmacokinetics/DMPK and prepare regulatory submission documentation.
Aerospace Algorithms Engineer
Company: MORSE Corp
Location: Cambridge
Posted Nov 17, 2023
MORSE is a tech company in Cambridge, MA, specializing in solving complex problems for the US National Security Ecosystem. They are seeking an Aerospace Algorithms Engineer with a strong background in physics, math, and statistics to develop mission planning algorithms. The ideal candidate will have experience in Python development, algorithm and simulation development, and presenting technical work. MORSE values work-life balance and offers a comprehensive benefits package.
Research Associate, Process Development
Company: Vizgen
Location: Cambridge
Posted Nov 17, 2023
Demonstrated knowledge of molecular biology, cell biology and imaging protocols (fluorescent in situ hybridization (FISH), immunofluorescence, immunohistochemistry, fluorescent microscopy, single-molecule imaging, flow cytometry, cell culture, tissue sectioning, NGS library construction, RNA-seq, cell transfection, antibody-labeling, etc.) WE ARE AN EQUAL OPPORTUNITY/AFFIRMATIVE ACTION EMPLOYER Vizgen affords equal employment opportunity to all qualified persons regardless of race, color, religious creed, national origin, age, military status, sexual orientation, disability, genetic information, gender identity, gender expression or gender unless based upon a bona fide occupational qualification. All pre-employment checks will comply with all applicable federal, state, and local laws. We offer a competitive salary, meaningful stock ownership, 401K, health benefits, a great work environment and the opportunity to enter a high-growth startup company. Experience in enzyme kinetics, qPCR, antibody-oligo conjugation is a plus. Knowledge and/or experience in process characterization, process optimization is a plus. Experience and/or familiarity of correct operation of basic laboratory equipment: pH meters, DO probes, lab scales, centrifuges, chemical fume hoods is required. in Chemical Engineering, Biological Engineering, or equivalent degree in life sciences. Experience and/or familiarity in the use of analytical equipment such as spectrophotometers, microscopes, plate readers, and flow cytometers is preferred. This position may be subject to pre-employment checks, including driving history check, drug screening and a background check for any convictions directly related to its duties and responsibilities.
Media Sales Appointment Setter
Company: Soofa
Location: Cambridge
Posted Nov 17, 2023
Soofa is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities, and general treatment during employment. Exceed quotas, on a monthly, quarterly, and annual basis. Ability to work independently, set priorities, and meet sales targets. Candidate Characteristics Transitions well from independent work to collaborating with a team Tenacious and resilient when faced with challenges Highly coachable and seeks improvement/feedback Great relationship builder Excited by trying new things Benefits Best of both worlds: Soofa’s Cambridge HQ is open, safe, and compliant for anyone who wants to use it; or, work from anywhere Potential to move to a full time position Virtual and in-person team events Company culture focused on community, inclusion, and talent development Soofa is an Equal Opportunity Employer that does not discriminate on the basis of race, creed, color, religion, national origin, ancestry, citizenship status, age, disability or handicap, sex, marital status, veteran status, sexual orientation, gender identity, pregnancy or pregnancy-related condition, genetic information, arrest record, or any other characteristic protected by applicable federal, state, or local laws. Resilient and goal-oriented, with a focus on achieving and exceeding sales targets. Excellent communication and interpersonal skills. Highly organized with strong time management skills. Requirements Lead Generation: Actively prospect and generate leads through outbound calls, emails, and other communication channels. We're a woman-founded MIT startup with a mission to make cities smart, social, and sustainable. Qualifications Proven track record in lead generation and sales.
Sr. Administrative Assistant/Project Coordinator
Company: Biogen
Location: Cambridge
Posted Nov 18, 2023
The Sr. Administrative Assistant/Project Coordinator role at Biogen involves providing administrative support to the VP of the Gene Therapy Accelerator Unit. Key responsibilities include managing calendars, coordinating meetings, handling expenses, travel arrangements, and creating written materials. The ideal candidate should be proactive, organized, collaborative, and have excellent communication skills. A Bachelor's degree and proficiency in MS Office Suite are required. Biogen values diversity and inclusion, offering equal employment opportunities to all qualified applicants.
Senior Development Scientist, Antibody Lead
Company: Vizgen
Location: Cambridge
Posted Nov 17, 2023
WE ARE AN EQUAL OPPORTUNITY/AFFIRMATIVE ACTION EMPLOYER Vizgen affords equal employment opportunity to all qualified persons regardless of race, color, religious creed, national origin, age, military status, sexual orientation, disability, genetic information, gender identity, gender expression or gender unless based upon a bona fide occupational qualification. All pre-employment checks will comply with all applicable federal, state, and local laws. Demonstrated knowledge of molecular biology, cell biology, fluorescent imaging(fluorescent in situ hybridization (FISH), immunofluorescence, immunohistochemistry, fluorescent microscopy, single-molecule imaging, molecular/cell biology assays, etc.) We offer a competitive salary, meaningful stock ownership, 401K, health benefits, a great work environment and the opportunity to enter a high-growth startup company. This position may be subject to pre-employment checks, including driving history check, drug screening and a background check for any convictions directly related to its duties and responsibilities. 8 years relevant experience. Hands-on experience with in-situ molecular biology protocols (immunohistochemistry or FISH) and multiplexed protein imaging experience is a plus Experience in product/process development and/or NPI (New product Introduction) with experience commercializing products in a fast-paced environment Experience with formulation, filling, assembly, and/or packaging of consumables is preferred Familiarity with quality management systems such as ISO:9001 A high level of commitment and a track record of quality work, with attention to detail. Above all, we're looking for the right person with skills and talent to grow the company together all while enriching your professional and scientific experience. We believe diversity drives innovation. Key Responsibilities: Lead projects in the reagent product development area to support the commercialization of the kits and consumables for the latest spatial transcriptomic platform and accompanying workflows Lead the product development for multiplexed protein imaging and spatial multi-omics measurement, oversee the design of experiments; driving execution, data analysis, and presentation of outcomes, making recommendations based on data Design, plan and execute experiments within the reagent development process that involve commercialization of benchtop methods and techniques for Vizgen's MERFISH technology Design, plan, and execute product and process optimization and characterization experiments Bring consumable technology from research concepts to production for commercial release Lead the design, develop, and execution of test procedures for verification and validation studies as well as standardizing and establishing quality control assays for the consumables Contribute to the company's intellectual property portfolio by documenting results and filing for IP protection Requirements and Qualifications: PhD with 4 years relevant experience or B.Sc./M.Sc.
Manager, IT Service Desk
Company: CarGurus
Location: Cambridge
Posted Nov 17, 2023
CarGurus is a leading automotive marketplace, offering a comprehensive online journey for car shopping, including selling old cars, financing, purchasing, and delivering new ones. The company fosters a people-first culture, emphasizing kindness, collaboration, and innovation. The Global IT Service Desk Manager role involves leading the Service Desk team, planning daily operations, managing budgets, and ensuring high-quality customer service. Qualifications include a bachelor's degree, 4 years of end-user support experience, and advanced knowledge of Service Desk operations using Jira Service Management or Zendesk.
Senior Director, QA (QMS)
Company: BlueRock Therapeutics
Location: Cambridge
Posted Nov 17, 2023
quality polices, manuals, etc. SOPs, WI, JA etc.) Must demonstrate strategic thinking, excellent organizational skills and be able to drive project teams forward while having a willingness to do hands on work to achieve goals Must be adaptable, flexible and able to work under high pressure and fast moving environment, Demonstrates calmness and decisiveness under pressure, with the ability to bring others along Strong technical writing skills (procedures, policies) with working knowledge of MS office programs, such as Word, Excel, SharePoint, and Adobe Acrobat professional are required Must be self-motivated with the demonstrated ability to work effectively with people from multiple departments, ensure deadlines are met, and manage multiple, potentially changing, priorities. ), documentation, including metrics, dashboards, readouts in support of Quality Oversight, including an overall picture of the health of BlueRock's overall Quality management System in collaboration with the SVP, Quality Assurance Grow & lead a team of quality professionals responsible for managing our process related to documentation and training and providing high levels of support for the enterprise as it relates to achieving documentation and training deliverables. Previous experience with analytics for use in managing quality issues enabling a risk-based approach Experience with implementation of electronic quality management systems is desired, Veeva experience preferred. Collaboration with a highly-motivated, world-class team of scientists, engineers, as well as quality & compliance professionals dedicated to enabling our teams to deliver on bringing life changing medicines to patients, promises an exciting and engaging work environment for a motivated, self-starting candidates, that can strategically design, build, implement and adapt processes and approaches as the organization evolves. Check us out on Comparably: https://www.comparably.com/companies/bluerock-therapeutics Follow us on Linkedin: https://www.linkedin.com/company/bluerocktx/ Equal Opportunity Workplace: At BlueRock, we welcome and support differences and diversity and we are proud to be an equal opportunity workplace. This includes the ownership of technologies and vendors that support these areas as well as defining measurable outcomes to indicate that the processes are delivering as needed Serve as the lead on development of programs to drive a risk-based and outcomes focused Quality Management System, supporting compatibility and integration of quality processes driven core principles, Data Integrity, Scientific Integrity, Patient safety and Product Integrity Support the development of Governance related processes (e.g. Influence and guide in a collaborative fashion, across all aspects of the quality organization partnering with peers to enable quality processes within their space as well as establishing supportive partnership across the organization where appropriate Other duties as assigned Minimum Requirements: Minimum of a Bachelor’s degree in Biology or relevant scientific or engineering discipline Minimum of 10-12+ years of experience in a quality role, preferably implementing and overseeing QMS within a broader quality organization for a life sciences organization supporting development programs (biotechnology, cell & gene therapy) Minimum 10 years in a personnel managing role with demonstrated ability to mentor and develop staff and achieve goals through empowering teams. The Quality System applies to the development, production and testing of cell therapies and medical devices under current Good Manufacturing Practices (cGMP) as well as preclinical (GLP), clinical activities (GCP), and compliance as well as support a broader GVP ecosystem through our parent company Bayer at the enterprise level.