📑 Job Description:POSITION OVERVIEW :Rust Developer - MuleSoft Flex Gateway Specialist- Solid experience in Rust programming language, with a focus on developing policies for MuleSoft Flex Gateway.- Proficiency in integrating external endpoints and ensuring secure, efficient communication. - Strong unde ...
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📑 Role: Mulesoft API Developer with Data Privacy & Security ExperienceWork Location: Iselin, NJExperience: 10+ yearsResponsibilities:Design, develop, and implement API integrations using Mulesoft Anypoint Platform.Collaborate with cross-functional teams to gather requirements and design technical solutions.Perform security assessments and vulnerabili ...
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📑 Title: Oracle Technical Developer Location: Remote Duration: 6 months Job Description: As a technical developer on a project to implement the Oracle Retail Xstore Point of Service solution, participate in the development and evolution of the required integrations. The Oracle Technical Developer will be responsible for developing and evolving applic ...
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📑 Job Type Full-timeDescriptionCambrae Business Strategies, Inc., recognized for consistently providing excellent results for its federal government and private sector clients, is seeking a remote, highly motivated, and experienced Senior Software/System Architect with Java and PL/SQL development experience to join our team to support our government ...
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📑 New Billing/ Non- Exclusive/ StrategicSenior Mulesoft DeveloperSkills: MulesoftLead the System Integration platform team.Manage and evolve the System Integration platform governance.Manage the System Integration platform and use case demands.Onboard and guide the System Integration use case team (on-demand basis).Participate and assess the System I ...
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📑 Associate Director/Director, Regulatory Affairs (Oncology)Remote - East Coast CandidatesMeet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director or Director of Regulatory Strategy to join their team. This role will be reporting into the VP ...
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📑 Vice President or Senior Vice President, Regulatory Affairs & Quality AssuranceHybrid Role - San Francisco Bay AreaMeet has engaged on a search for a confidential search for a VP/SVP of Regulatory and Quality with one of our biotech clients. Our client is focused in the Heme/Onc space - you'll be reporting into C-Suite and will be heading up Reg an ...
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📑 Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - will work partly in office and partly remote. Looking for a Regulatory Affairs Specialist with at least 2 years of regulatory experience along with submissions. Will work on IND submissions (publishing and structure of the IND, not ...
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📑 Clinical Development Leader (Medical Director to Senior Director level)San Francisco (remote/hybrid) **MUST reside on the West Coast or willing to relocate**Full-timeSciPro is working with one of the most exciting names in Oncology. This position holds high visability and will report directly to the CMO.My client is on the verge of going public due ...
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📑 Clinical Development Leader (Medical Director to Senior Director level)San Francisco (remote/hybrid) **MUST reside on the West Coast or willing to relocate**Full-timeSciPro is working with one of the most exciting names in Oncology. This position holds high visability and will report directly to the CMO.My client is on the verge of going public due ...
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📑 Position Summary: As the Pharma Commercial Data Management Lead at Chryselys, you will be pivotal in driving the growth and success of our MDM and data management practice within the pharmaceutical industry. You will be responsible for overseeing the client relationships, successful delivery of client projects, and overall capabilities development. ...
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📑 Reporting to our Senior Director, Drug Product, Process Development, we are seeking an Associate Director to join our team. This position is predominantly a lab-based role and will be responsible for developing scalable processes for LNP delivery of gene-editing RNA cargos. This position will play a critical role in successfully developing manufact ...
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📑 A California-based biopharmaceutical company is looking to add an experienced professional to their CMC Quality Control Department as a Writer / Reviewer. In this role, the CMC Quality Control Writer / Reviewer will be responsible for authoring, drafting. reviewing, and approving the Regulatory QC CMC sections of the company's IND/IMPD and BLA/NDA ...
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📑 ** Assoc Dir RA, Boston ** Working on rare diseases, obesity, liver in early and mid-phase compounds for a smaller and stable company with higher visibility from an exclusive leadership teamDo you want to be autonomous in your work and interact closely with the leadership team, to have higher visibility and more opportunities to grow …… then this c ...
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📑 To get the best candidate experience, please consider applying for a maximum of 3 roles within 12 months to ensure you are not duplicating efforts.Job CategorySalesJob DetailsAbout SalesforceWe’re Salesforce, the Customer Company, inspiring the future of business with AI+ Data +CRM. Leading with our core values, we help companies across every indus ...
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📑 To get the best candidate experience, please consider applying for a maximum of 3 roles within 12 months to ensure you are not duplicating efforts.Job CategorySalesJob DetailsAbout SalesforceWe’re Salesforce, the Customer Company, inspiring the future of business with AI+ Data +CRM. Leading with our core values, we help companies across every indus ...
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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...
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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...
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📑 OverviewJoin a growing Clinical Science team where you will work directly with the VP, Clinical Science. You will support Celldex’s clinical development programs by contributing to the design, data collection, and reporting of clinical studies in a manner consistent with industry standards, applicable regulations and clinical development strate ...
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📑 This is an opportunity to work with an innovative biotechnology company working on the development and manufacturing of small molecules for a diverse portfolio of therapeutic targets. To support the continued growth of the pipeline, we are looking for an experienced Senior/Executive Director of CMC to guide strategy.Responsibilities:Oversee vendors ...
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📑 This is an opportunity to work with an innovative biotechnology company working on the development and manufacturing of small molecules for a diverse portfolio of therapeutic targets. To support the continued growth of the pipeline, we are looking for an experienced Senior/Executive Director of CMC to guide strategy.Responsibilities:Oversee vendors ...
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📑 Data Power AdminDuration: 12 months (likely extension) Location: Southern CaliforniaSummary: Perform administration responsibilities for the GDC Data Power instances including project and operational support and maintenance for the GMS/ADMS interfaces passing through Data Power. Specifically, this position will have operational responsibility to co ...
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📑 Associate Director, Regulatory AffairsThis position will serve as the company US Agent and a contact point between the FDA and company sites. Responsible to communicate with FDA for all regulatory issues/questions and provide regulatory guidance to internal constituents. It will lead a team of Regulatory Associates and Senior Regulatory Associates ...
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📑 Director, Clinical Development - Immunology*Remote for East Coast Candidates*Meet has partnered with a well-established pharma based on the East Coast! They are looking for a Director of Clinical Development to join their immunology department. This position will be reporting into a Senior MD and will be supporting multiple global clinical programs ...
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📑 GeneCoda has been retained to identify and evaluate candidates for a Chief Medical Officer (CMO) to onboard in late Q2 or early Q3 of 2023 and to be located in the Research Triangle Park, NC. Some relocation assistance can be provided for candidates not already located in the region. Learn why the RTP, NC area as a global life sciences leader m ...
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📑 A clinical-stage biotechnology company based in San Francisco, backed by Third Rock Ventures, is harnessing the power of adipocyte biology and the latest advances in human genetics to develop first-in-class, next-generation medicines for cardiometabolic diseases. The company is building a pipeline of therapies that target rare and common cardiometa ...
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📑 About Firefly Bio:Firefly specializes in Degrader Antibody Conjugates (DACs) which combine the unique strengths of ADCs with selective protein degraders. Our state-of-the-art platform results in highly specific delivery of degraders to target tissue. Our mission is to realize the full potential of ADCs by unlocking new classes of payloads. Our comp ...
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📑 About Firefly Bio:Firefly specializes in Degrader Antibody Conjugates (DACs) which combine the unique strengths of ADCs with selective protein degraders. Our state-of-the-art platform results in highly specific delivery of degraders to target tissue. Our mission is to realize the full potential of ADCs by unlocking new classes of payloads. Our comp ...
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📑 About this Opportunity: As a Salesforce Developer and Data Integration Specialist, you will be responsible for helping the sales team to grow revenue by bringing our sales processes to life through automation, data connection, and insights. This individual will be essential to ensuring data accuracy, optimizing workflow efficiency ...
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📑 RBW is partnering with an innovative clinical-stage, Biotech in their search for a newly created position - (Sr.) Director, R&D Quality Assurance. Our client is focused on discovering and developing medicines for the treatment of Crohn's and other inflammatory diseases.The candidate will report directly to the Head of QA, and this role will be resp ...
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📑 Our innovative Oncology ADC Pre-IPO biotech client is seeking a Medical Director / Senior Medical Director with strong Oncology Clinical Development experience to cover development programs spanning phases I, II, III.Responsibilities:Providing clinical leadership; from early-stage clinical trial design for novel cancer drugs through to CoP stageWor ...
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📑 About Firefly Biologics:Firefly Biologics is a Bay Area venture-backed company currently operating in stealth mode. Our mission is to unlock the full potential of bioconjugates and develop medicines with long-lasting benefits for patients. We are establishing an expert team to build state-of-the-art platform capabilities for the invention and devel ...
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📑 A clinical-stage biotech focused on Rare Diseases. This company utilizes antibodies to harness the bodies immune system to fight off disease.The RoleThis person ill serve as the GRL for the company's early stage proprietary pipeline as well as supporting partnered programs with large pharma , reporting into the SVP of Regulatory Affairs.Main Respon ...
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📑 RBW is partnering with an innovative clinical-stage, Biotech in their search for a newly created position - (Sr.) Director, R&D Quality Assurance. Our client is focused on discovering and developing medicines for the treatment of Crohn's and other inflammatory diseases.The candidate will report directly to the Head of QA, and this role will be resp ...
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📑 Job role and responsibility :Work closely with AI strategists and analysts to understand their immediate and long-term needsDefine the end-to-end architecture to leverage data assets from multiple data lakesUnderstand the global/enterprise architecture and define solutions that comply with global standardsRepresent local business groups in the glob ...
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📑 The Integration & Hyperautomation Architect is responsible for designing, delivering, and sustaining integration and automation solutions and services. You’ll collaborate with cross-functional teams, contribute to architectural standards, and drive the adoption of best practices. Additionally, you’ll lead efforts to optimize processes, improve data ...
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📑 Job Summary:Under general guidance, the Middleware Administrator is responsible for designing and configuring the company's middleware and integration infrastructure and platforms, enabling communication between multiple enterprise applications. They are accountable for design, development, configuration, problem analysis, deployment, and continuou ...
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📑 The Integration & Hyperautomation Architect is responsible for designing, delivering, and sustaining integration and automation solutions and services. You’ll collaborate with cross-functional teams, contribute to architectural standards, and drive the adoption of best practices. Additionally, you’ll lead efforts to optimize processes, improve data ...
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📑 Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and se ...
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📑 Title: Director/Senior Director of Regulatory Salary: $200,000 to $270,000Summary: An Oncology based biotech client of ours is looking to fill their Director/Senior Director role based out of their facility in the San Francisco Bay Area. They are looking for very committed and passionate candidates who can collaborate with their colleagues to help ...
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📑 Title: Director/Senior Director of Regulatory Salary: $200,000 to $270,000Summary: An Oncology based biotech client of ours is looking to fill their Director/Senior Director role based out of their facility in the San Francisco Bay Area. They are looking for very committed and passionate candidates who can collaborate with their colleagues to help ...
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📑 Fantastic new opportunity for an experienced toxicologist at a brilliant biotech company!My client is looking for a highly knowledgeable, competent and detail-oriented Toxicology Consultant with extensive responsibility for designing, monitoring and reporting results of in vitro and in vivo preclinical pharmacology and toxicology studies. Experienc ...
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📑 We are recruitng for a full-time, direct, hybrid IT Delivery- Workday Integrations Specialist as our compay is embarking on its Workday journey. We’re seeking a top-tier individual with technical experience in Workday. This position, IT Delivery- Workday Integrations Specialist, will be primarily responsible for development and sustainment of integ ...
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📑 Position: Java Developer Duration: Yearly Renewing Contract (ongoing) Client Location: Remote or Hybrid (Downtown Indianapolis) Objective: The Java Developer will work closely with our client’s four stream-aligned teams, enablement team, and system team to carry out complex application development projects including enhancement features and modern ...
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📑 Job Title: Head of Biology & Translational ScienceLocation: San DiegoBackgroundRayzeBio is a dynamic biotechnology company headquartered in San Diego, CA. Launched in late 2020 and recently acquired by Bristol Myers Squibb (BMS) as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power ...
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📑 Munkebo Seafood tilbyder et job i en mindre produktionsvirksomhed, hvor den rette person vil få stor indflydelse på opgaverne indenfor sit ansvarsområde og få mulighed for at præge beslutningerne og fremtiden. Hos Munkebo Seafood A/S er der ikke langt til beslutningerne, og de deltager alle aktivt i hverdagens udfordringer og hjælper hinanden, hvis ...
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📑 Job Title: Head of Biology & Translational ScienceLocation: San DiegoBackgroundRayzeBio is a dynamic biotechnology company headquartered in San Diego, CA. Launched in late 2020 and recently acquired by Bristol Myers Squibb (BMS) as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power ...
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📑 JOB INFORMATIONJob Title: Mulesoft ArchitectLocation: Boston, MARole: Long Term ContractThis is Hybrid Mode onsite position.Required skillset:1. MuleSoft Platform, OpenShift AWS, MuleSoft Application Network, MuleSoft API Lifecycle, MuleSoft Integration,2. MuleSoft API-Led Connectivity ...
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📑 Required skillset:1. MuleSoft Platform, OpenShift AWS, MuleSoft Application Network, MuleSoft API Lifecycle, MuleSoft Integration,2. MuleSoft API-Led Connectivity, MuleSoft Flow Design, MuleSoft Catalyst Knowledge.3. MuleSoft Catalyst Playbooks, MuleSoft Platform Admin.Job Summary:• 10 - 15 years of Integrati ...
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📑 I'm partnered with an SF Bay Area-based clinical staged biopharmaceutical company focused on the treatment of liver and cardio-metabolic diseases. This position will be reporting to the VP of CMC and will support the drug development and manufacturing activities for phase 3 and commercialization at CDMOs and CTLs for Biologic programs.Responsibilit ...
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