Be Or Bc Jobs in Cambridge
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Business Development Executive – Research Investment Office
Company: IBM
Location: US Cambridge
Posted Feb 27, 2024
Knowledge of IBM business processes relevant to Intellectual Property Research and M&A transactions is a plus. The candidate will possess core skills like strategic and critical thinking when supporting projects and strong communication skills; prior experience in lab to market venture capital mergers & acquisitions (M&A) private equity or strategy consulting is preferred. Required Technical and Professional Expertise At least 1 year of experience in venture building strategy consulting or deal transaction Prior experience for deal transaction may include but are not limited to roles in corporate mergers & acquisitions (M&A) investment banking private equity venture capital etc. You will also support the development of creative business models monetization strategy and business case in support of key Research programs and/or non-strategic assets. In addition you will support the execution of complex deals from strategy to deal closing. The ability to perform research (primary and secondary) and financial analysis and to transform complex ideas into insights and recommendations is key to success. To collaborate. About you: Achievement of the above goals requires knowledge of strategy development financial modeling and generating market insights. Preferred Technical and Professional Expertise Experience working with emerging technologies that are strategic to IBM (AI Quantum Computing Semiconductors) Knowledge of incubating new businesses and creating business plans for emerging technologies Experience supporting deals from inception to close Experience with agile methodologies and design thinking Familiarity or experience with all stages of the investment lifecycles from deal sourcing to deal execution Skills in supporting acquisitions and investments such as developing financial models featuring discounted cash flows comparable valuations and return on investment (ROI) Strong skills in developing financial models reading and analyzing financial statements High proficiency in translating analysis and business recommendations into storytelling and visual illustrations using tools such as Microsoft Word and PowePpoint Mural etc Demonstrated aptitude for grasping new technologies and performing primary and secondary research Self-motivated independent and proactive; validated creative and critical thinking capabilities; can quickly prioritize.
Scientist, Amplicon-seq Lead
Company: Intellia Therapeutics
Location: Cambridge
Posted Feb 26, 2024
We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. CRISPR) is preferred Experience in managing junior scientists is preferred Strong communications and documentation skills coupled with exceptional time management skills and attention to detail LI-KO2 Covid-19 Vaccination Policy: All Intellia employees, regardless of work location, are expected to follow all applicable federal, state, and local public health regulations and guidelines, and are strongly encouraged to follow all public health recommendations, including being vaccinated for COVID-19. In this role, you will: Lead a team of junior scientists responsible for running a high throughput Illumina amplicon sequencing workflow, as well as smaller scale Pacbio amplicon sequencing workflow Ensure timely data delivery from amplicon sequencing workflow and work with the NGS team and automation team to promptly address run failures Independently and in collaboration with colleagues, apply expertise to troubleshoot and support new project needs Partner with the NGS assay team lead, automation, software engineering, and computational sciences teams, to optimize existing and develop new NGS workflows Communicate amplicon-seq process and schedule updates with submitters from diverse groups across the company Respond to submitter questions about sample submissions, run failures, and data quality Monitor, QC, and analyze data metrics, ensuring the consistent generation of high-data quality Serve as the NGS production assay process subject matter expert Work with program and platform partners to manage project queue ensuring timelines are met Manage and mentor junior-level scientists Present your or the team's work at project and larger team meetings About You: The successful candidate will have demonstrated expertise in Illumina NGS technology, molecular biology, and liquid handling automation PhD in Genomics with 0-3 years with directly relevant experience or MS with 6-9 years equivalent experience (industry experience preferred) Solid hands-on experience with Illumina library construction, quantification, sequencing, and data analysis. EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. Experience with long read PacBio sequencing would be a bonus. The Amp-seq team is central to all research activities, and thereby critical to the development of genome editing programs and platforms. Experience with running and optimizing liquid handling automation (preferably Hamilton) Experience with high throughput workflows and LIMS systems is preferred Experience with genome editing technologies (e.g. Genomics Innovation provides state-of-the-art genomics solutions, ranging from screening different editing modalities to developing and implementing a diverse toolbox of assays to characterize the impact of genome editing. We aren't constrained by typical end rails, and we aren't out to just "treat" people.
Manager, Digital Quality & Data Integrity
Company: Beam Therapeutics
Location: Cambridge
Posted Feb 28, 2024
The Manager, Digital Quality & Data Integrity will lead computer systems validation and qualification activities within the Software/System Development Lifecycle. This role involves overseeing validation on various technology projects, ensuring compliance with regulatory requirements, and managing validation documentation. The individual will collaborate with Global CoE and NC teams, align IT roadmap and strategies, and spearhead risk-based strategies for regulated IT systems. They will also guarantee GxP compliance in all IT policies, processes, and systems, and oversee CSV-related deviations and change control documents.
Senior Specialist, GMP Quality Assurance
Company: Nuvalent, Inc.
Location: Cambridge
Posted Feb 25, 2024
Thank you. Strong knowledge of cGMP regulations, practices, and trends pertaining to pharmaceutical product development, manufacturing, testing, and clinical operations is required. Travel approximately 15% Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Working knowledge of MS Word, MS Teams, Veeva Quality Docs, SharePoint and Smartsheet is preferred. Direct experience working with drug product manufacturing, packaging, and labeling is preferred. Supports associated Investigations, CAPAs, Change Controls, Material Review Boards, OOS, etc. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities. If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Qualifications: Bachelor’s degree in biology, chemistry, life sciences field preferred or related experience. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person.
Supply Chain Associate
Company: Vor Bio
Location: Cambridge
Posted Feb 27, 2024
<div> <p><strong>We engineer stem cell transplants that shield healthy cells from targeted therapies<strong><p> <p>Targeted therapies work by attacking cells that express particular proteins on their surface Unfortunately both diseased and healthy cells often express the same proteins resulting in collateral damage to healthy cells<p> <p>At Vor Bio we engineer hematopoietic stem cells HSCs to lack a biologically redundant target protein then transplant these cells into the patient<p> <p>These eHSCs give rise to generations of new healthy blood cells that are effectively shielded from targeted therapies so that only the remaining cancer cells are killed We are also developing our own CART cell therapy using T cells from the same healthy donor who could potentially provide HSCs for our shielded stem cell transplant and thereby avoid issues of donormismatch We believe our CART cell therapy may enable more potent and durable responses posttransplant<p> <p>Vor Bio is aiming to cure blood cancers through our novel platform combining HSC biology genome engineering and targeted therapies to unlock treatment options previously unavailable to patients Come be a part of a passionate team striving to collaboratively develop a groundbreaking approach to cancer treatment one of medicines greatest challenges<p> <p><strong>What we value in our fellow Voracians<strong><p> <p><strong>Passion<strong> Enthusiastically driving our science toward innovative medicines<p> <p><strong>Fellowship<strong> Fostering genuine bonds of collaboration and mentorship<p> <p><strong>Humility<strong> Acting selflessly by putting the collective mission first<p> <div> <p><strong>Who we are looking for<strong><p> <p>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 The ideal candidate should be detail oriented and a strong team player <p> <p><strong>Key areas of responsibilities<strong><p> <ul><li>Perform material receipts storage cycle counting and distribution activities for VIBE cGMP warehouse<li> <li>Receive and store materials per cGMP guidance amp applicable procedures and ensure accurate inventory is maintained and inventory discrepancies are communicated<li> <li>Perform and document daily warehouse operation and maintenance including cleaning and ensure all warehouse storage areas are inspection and audit ready<li> <li>Ensure timely receipt storage stocking picking issuing and shipping of materials<li> <li>Perform shipments and ensure materials are shipped and received in correct temperature conditions and are handled appropriately along with their required documentation<li> <li>Safely operate all equipment and respond to alarms for the oncall program<li> <li>Support daytoday activities that are related to the maintenance of office administration<li> <li>Ensure compliance and execution against all SOPs related to GMP warehouse operations<li> <ul><p><strong>Skills and requirements<strong><p> <ul><li>High School Diploma or GED required Associate degree or higher education preferred<li> <li>Experience with Microsoft Outlook Word and Excel preferred<li> <li>Experience with WMS or ERP system Oracle preferred<li> <li>Experience working in a GMP regulated manufacturing or distribution environment preferred<li> <li>Proven verbal and written communication skills and ability to interact effectively with other departments and management<li> <li>Ability to stand walk for long periods of time<li> <li>Ability to work flexible schedule to include weekends or holidays as needed<li> <li>Ability to lift 40lbs without assistance while following proper safety lifting techniques<li> <ul><p><br ><br ><p><div> <p>By becoming a team member here at Vor youll have access to competitive health dental and vision coverage as well as life insurance and short term and longterm disability insurance We value work life balance youll benefit from discretionary time off parental leave and an excellent 401k package We also offer a generous transportation stipend to commute as you wish We are conveniently located in Cambridge with easy access to public transportation and ample parking<p> <p>As an equal opportunity employer we at Vor Bio know that diversity inspires innovation inclusiveness and creativity We invite you to come as you are All applicants will be considered for employment agnostic to race age color religion sex sexual orientation gender identity national origin veteran or disability status<p> <p>Please visit our website at httpswwwvorbiocom for more information<p> <div>
Data Scientist, Translational Data Science (Principal Scientist)
Company: HiFiBio Therapeutics
Location: Cambridge
Posted Feb 25, 2024
Examples include: Best practices for single cell methods including data imputation and normalization, bulk deconvolution, cell type/state analysis, cell-cell interaction/trajectory inference, reconstruction of cell type specific interactomes – cellphoneDB and spatial transcriptomic analysis and visualization Pipelines for data processing and QC including visualization and integrative analysis (e.g., Nextflow, Python, shell scripts) including but not limited to quality control, alignment, variant calling, annotation, deconvolution, etc. All full-time employees are eligible for our comprehensive benefits package: Medical, Dental, and Vision insurance (Company covers 80% of the premium cost) Life, AD&D, Short-term, and Long-term Disability Insurance (100% company covers) Health Savings Account & Flexible Spending Account Telehealth Service (100% company covers) Dependent Care Pre-tax Account Parking and Commuter Pre-tax Account Unlimited PTO (Paid Time Off) 10 Paid Holidays and Sick Time (40 hours per year) 401(K) Plan Demonstrated ability to lead projects of moderate scope, mapping-out critical path, milestones and timelines, as well as manage expectations with minimal supervision. Identification and qualification of biomarkers (e.g., selection, PD, efficacy biomarkers) and analysis of data from both our clinical and research effects Assessment of treatment effects from both RNA (e.g., bulk, single cell, TCR/BCR, and spatial) and protein modalities (e.g., CITE/REAP-Seq, mIF, and high dimensional flow cytometry Develop and apply computational, AI/ML methods to analyze our multi-modal data. For example, multivariate analysis; dimensionality reduction methods; parametric and non-parametric statistical methods; Bayesian statistics; pattern recognition or classification methods Expert level fluency in statistical programming using Python, R/bioconductor or equivalents. Generative AI models to integrate and to analyze multi-modal molecular as well as patient clinical data Interactive dashboards for data visualization and interpretation What you will bring: Ph.D. in a computational, statistical, biophysics, or bioinformatics related fields A minimum of 5-years research (academia or industry) experience First-hand experience in single cell sequencing analysis and data generation methods as well as the computing infrastructure and data management methods First-hand multi-parametric data mining experience for disease endotyping, target identification and biomarker analysis. This is an on-site position in Cambridge, MA. Demonstrated experience in deep learning and generative AI model assessment is a differentiator. What you will do: Synthesize our data into actionable insights by supplying to the Translational teams any needed computational, statistical, machine learning or modeling capabilities needed to advance our clinical programs. Curiosity to dive below the surface and proactively identify critical issues including their tactical and strategic resolutions.
Director, Senior Director Genome Engineering (Vector Genome)
Company: Voyager Therapeutics
Location: Cambridge
Posted Feb 25, 2024
Sophisticated scientific management skills and business judgment with an ability to evaluate alternatives, establish priorities, and apply resources effectively. Must be highly motivated, and will derive motivation from working in a small, entrepreneurial biotech environment, accepting the challenge of broad responsibilities and opportunities within a fast-paced, matrix-focused can-do culture. Must have intellectual and scientific curiosity and integrity; must be scientifically rigorous and creative; committed to patient-centricity, transparency, and ethical research values. Can-do team-oriented attitude which is consistent with Voyager core values. Qualifications A Ph.D. or MD/Ph.D. Track record of driving innovative ways of thinking and/or innovative ways of using data. Enthusiasm for operating effectively within an entrepreneurial and science-driven company environment. Participate in the process of selecting, prioritizing, and accelerating the development of assets. Responsible for interrogation of candidate sequences, and reduction-to-practice of sequences intended for clinical application, for numerous gene therapy initiatives. Support the continued protection, creation, and expansion of the company’s intellectual property.
Account Executive, City Growth
Company: Soofa
Location: Cambridge
Posted Feb 27, 2024
Soofa is seeking a City Growth Account Executive to acquire new customers and expand existing relationships across the United States. The role involves selling Soofa's signs to municipal stakeholders, managing an opportunity pipeline, and collaborating with internal teams. The ideal candidate should have 2-3+ years of government, city planning, or full-cycle sales experience, and a proven track record of achieving sales quotas. Soofa values diversity and encourages BIPOC and minority applicants. The role offers a range of benefits, including flexible work arrangements and comprehensive healthcare plans.
GMP Operations Associate
Company: Vor Bio
Location: Cambridge
Posted Feb 26, 2024
<div> <p><strong>We engineer stem cell transplants that shield healthy cells from targeted therapies<strong><p> <p>Targeted therapies work by attacking cells that express particular proteins on their surface Unfortunately both diseased and healthy cells often express the same proteins resulting in collateral damage to healthy cells<p> <p>At Vor Bio we engineer hematopoietic stem cells HSCs to lack a biologically redundant target protein then transplant these cells into the patient<p> <p>These eHSCs give rise to generations of new healthy blood cells that are effectively shielded from targeted therapies so that only the remaining cancer cells are killed We are also developing our own CART cell therapy using T cells from the same healthy donor who could potentially provide HSCs for our shielded stem cell transplant and thereby avoid issues of donormismatch We believe our CART cell therapy may enable more potent and durable responses posttransplant<p> <p>Vor Bio is aiming to cure blood cancers through our novel platform combining HSC biology genome engineering and targeted therapies to unlock treatment options previously unavailable to patients Come be a part of a passionate team striving to collaboratively develop a groundbreaking approach to cancer treatment one of medicines greatest challenges<p> <p><strong>What we value in our fellow Voracians<strong><p> <p><strong>Passion<strong> Enthusiastically driving our science toward innovative medicines<p> <p><strong>Fellowship<strong> Fostering genuine bonds of collaboration and mentorship<p> <p><strong>Humility<strong> Acting selflessly by putting the collective mission first<p> <div> <p><strong>Who we are looking for <strong><p> <p>Vor Bio is seeking a GMP Operations Associate who is an enthusiastic and driven individual to support cGMP manufacturing for clinical phase cell therapy manufacturing facility The candidate will be responsible for providing assistance in the support area for the manufacturing of Vors geneedited cell therapies and maintaining compliance of cGMPs in manufacturing areas <p> <p><strong>Key areas of responsibility<strong><p> <ul><li>Support and perform cleanroom operations such as cleaning specialized equipment restocking materials sample transfer and document management<li> <li>Work with internal and external partners to track equipment preventative maintenance and calibration events and support equipment management in a computerized maintenance management system CMMS<li> <li>Coordinate with appropriate groups Supply Chain Safety and Facilities for material management safety equipment checks and facility maintenance<li> <li>Responsible for material management in and out of the cleanrooms to support clinical production<li> <li>Responsible for waste management and working with internal partners for waste removal<li> <li>Strict adherence to current good manufacturing practices standard operating procedures and manufacturing documentation<li> <li>Must be able to lift up to 50lbs<li> <ul><p><strong>Qualifications<strong><p> <ul><li>HS diploma or BS in Biology or related field<li> <li>1 3 years of handson experience with supporting manufacturing facility<li> <li>Cell therapy production support and aseptic manufacturing technique preferred<li> <ul><p><br ><br ><p><div> <p>By becoming a team member here at Vor youll have access to competitive health dental and vision coverage as well as life insurance and short term and longterm disability insurance We value work life balance youll benefit from discretionary time off parental leave and an excellent 401k package We also offer a generous transportation stipend to commute as you wish We are conveniently located in Cambridge with easy access to public transportation and ample parking<p> <p>As an equal opportunity employer we at Vor Bio know that diversity inspires innovation inclusiveness and creativity We invite you to come as you are All applicants will be considered for employment agnostic to race age color religion sex sexual orientation gender identity national origin veteran or disability status<p> <p>Please visit our website at httpswwwvorbiocom for more information<p> <div>
Machine Learning Engineer
Company: Kensho Technologies
Location: Cambridge
Posted Feb 28, 2024
Kensho Technologies, a subsidiary of S&P Global, is seeking a mid-level ML Engineer to join their Catalyst team. The role involves designing and developing Large Language Model (LLM)-based systems, integrating structured and unstructured data, and collaborating with various teams to build ML-based solutions. The ideal candidate should have a degree in Computer Science or a related field, 3+ years of industry experience in ML and NLP, strong Python skills, and proficiency in ML libraries/frameworks. Kensho offers competitive benefits including top-of-market insurance, unlimited PTO, parental leave, 401(k) matching, tuition assistance, and a dynamic work environment.
Lead Business Development Rep
Company: Proton.ai
Location: Cambridge
Posted Feb 25, 2024
Proton, a tech startup specializing in AI-powered CRM software for the wholesale distribution industry, is seeking a passionate and resilient Business Development Representative. The role involves cold outreach, lead qualification, and nurturing prospects to fuel the sales pipeline. The ideal candidate will have a proven track record in business development or outbound sales, excellent communication skills, and a curious, resilient, and creative mindset. Proton offers competitive salaries, company stock options, unlimited PTO, medical benefits, and more. The role is based in the greater Boston area (Kendall Square) and is a hybrid position.
Sales Manager
Company: Watershed Informatics
Location: Cambridge
Posted Feb 28, 2024
<p><strong>About Watershed <strong><p> <p>Our vision is to become the leading biocomputing platform The future of biology is in big data analysis and we are on a mission to accelerate digital drug discovery with the Watershed platform Watershed enables scientists to conduct all essential analysis from lab data to plot with a single software platform <p> <p>We have attracted some of the best bioinformatics engineering and commercial talent and we are growing Join a team thats intellectually curious with a bias for action headquartered in Cambridge Massachusetts composed of people who have come together to enable outcomes while empowering the research of all those committed to changing lives all while bringing transformational change to a $40 billion industry <p> <p><br ><p><p><strong>Sales Manager Role<strong> <p> <p>Watershed is hiring a Sales Manager The ideal candidate is a dynamic individual who has experience and drive working in a fastpaced biotech environment and a track record of execution and teamwork You should be someone who has experience managing strong relationships with biotech companies <p> <p><br ><p><p><strong>Responsibilities <strong><p> <ul><li>Serve as the primary point of contact for existing and new accounts in your region<li> <li>Manage multiple biopharma accounts in the US territory at various stages of the cycle from prospecting through to value delivery<li> <li>Develop and implement a strategic sales plan to achieve Watersheds goals and revenue targets in your region<li> <li>Build and maintain strong relationships with key opinion leaders key customers and stakeholders in the industry<li> <li>Analyze sales data and market trends to make informed decisions and adjust the sales strategy as necessary<li> <li>Ensure that you are trained and equipped with the necessary tools to effectively sell the companys products and solutions<li> <li>Represent Watershed at industry events conferences and trade shows and build a strong brand presence in the market<li> <li>Own the endtoend process of tracking the sales funnel and operational metrics providing regular updates to leadership <li> <ul><ul><li>Collaborate with sales marketing and finance to become a performance enhancement partner and to synchronize key business functions <li> <ul><p><br ><p><p><strong>Required Qualifications <strong><p> <ul><li>Bachelors Degree in the Life Sciences or related field MBA MS or PhD is a plus<li> <li>Minimum of 3+ years of Sales experience in the life science industry<li> <li>A demonstrated successful track record in pitching and completing deals with biotech and academia<li> <li>Demonstrated ability to manage client engagements at all levels to ensure delivery of value and to expand use of a technology or service deeply and broadly throughout accounts<li> <li>Experience managing negotiations and communications on multiple contracts simultaneously or interfacing with highly matrixed multidisciplinary teams to complete contract terms<li> <li>Ability to develop and implement effective sales strategies and adjust them as necessary in response to market changes<li> <li>Strong analytical and problemsolving skills with the ability to analyze sales data and market trends to inform decisionmaking<li> <li>Excellent communication and interpersonal skills with the ability to build relationships with customers stakeholders and internal teams<li> <li>Strong presentation and public speaking skills with the ability to deliver compelling sales presentations<li> <li>Ability to travel as necessary to meet with customers and attend industry events and trade shows<li> <li>Driven to be successful in a commercial and salesoriented career<li> <ul><p><br ><p><p><strong>Desirable Qualifications<strong><p> <ul><li>MSPhD or equivalent experience in a biotechnology or life sciences field BioinformaticsComputational Bio or similar experience preferred<li> <li>Deep knowledge of the biopharma life cycle from drug discovery through drug development and understanding of pain points such that they can be addressed with an applicable technology<li> <li>Experience in a drug discovery biopharmaceutical or biotech environment<li> <li>Demonstrated ability to work independently and take initiative with a high level of selfmotivation and selfdiscipline<li> <li>Ability to adapt to a fastpaced and dynamic work environment with the ability to prioritize and manage multiple projects and tasks simultaneously<li> <ul>