Recursion

Recursion is a technology company focused on advanced solutions in artificial intelligence and high-performance computing, emphasizing innovation in storage engineering.

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📍 Salt Lake City, London, Toronto, Montreal, San Francisco Bay Area

🧭 Contract

🔍 Biotechnology, pharmaceutical

  • Bachelor's or Master's Degree in a scientific or technical discipline.
  • 7+ years of relevant Record Management experience in a biotech/pharmaceutical setting.
  • Hands-on experience with controlled/regulated record lifecycle management.
  • Strong project management skills and ability to manage multiple projects.
  • In-depth knowledge of relevant regulations like FDA 21 CFR and ISO 9001.
  • Excellent cross-functional collaboration and communication skills.
  • Experience managing audits and regulatory inspections.
  • Demonstrated analytical and problem-solving abilities.
  • Familiarity with Content Management Systems and similar business tools.
  • Ability to thrive in a dynamic, fast-growing biotech environment.

  • Build world-class infrastructure to enable the management of records across the enterprise.
  • Lead the implementation, ownership, oversight, maintenance, and execution of record management systems and strategies.
  • Collaborate with various departments to foster a quality-minded culture and identify innovative technologies for the records program.

Project ManagementGCPQAContent managementCommunication SkillsCollaborationMicrosoft OfficeWritten communicationComplianceMicrosoft Office Suite

Posted 2024-11-13
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📍 Salt Lake City, US, London, UK, Toronto, Canada, Montreal, Canada, San Francisco Bay Area, US

🧭 Full-Time

💸 152000 - 186000 USD per year

🔍 Pharmaceutical / TechBio

  • A minimum of 10 years in the pharmaceutical industry.
  • A minimum of 8 years in Global Regulatory Affairs.
  • Experience with major Health Authorities (US FDA, Health Canada, UK MHRA, EMA) is mandatory.
  • Minimum of 6 years experience with regulatory submissions including INDs, NDAs, post marketing measures, pediatric submissions.
  • Strong understanding of regulatory strategy and operational activities.
  • Outstanding management, interpersonal, communication, negotiation, and problem-solving skills.

  • Build relationships and collaborate in a global team environment for regulatory strategy management.
  • Manage complex issues and coordinate multiple projects simultaneously.
  • Create procedures for regulatory execution and support program leads.
  • Collaborate with other functions to provide regulatory insight.
  • Serve as point of contact with Health Authorities and lead interactions.
  • Review regulatory guidelines and communicate impact assessments.

LeadershipStrategyNegotiationDocumentation

Posted 2024-11-09
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📍 US, UK, EU

🧭 Full-Time

💸 117500 - 143000 USD per year

🔍 TechBio / Drug discovery

  • Bachelor's degree (BS/BA) in a scientific discipline preferred; equivalent work experience will be considered.
  • 5+ years of industry-related experience in a regulatory publishing function.
  • 2+ years of experience working with specialized regulatory submission systems.
  • Experience in FDA regulatory submissions for drugs, with familiarity with FDA's electronic submission gateway.
  • Knowledge of regulatory requirements related to submissions, particularly in CTD/eCTD format.
  • Experience with technical writing is a plus.
  • Proficient in software for document formatting and publishing.

  • Collaborate with Regulatory Leads on submission plans and timelines.
  • Perform critical reviews of documents for quality and consistency.
  • Format and publish regulatory documents per health authority requirements.
  • Maintain regulatory records in controlled systems.
  • Contribute to new internal processes for submissions.
  • Oversee data migration activities in Regulatory Affairs.
  • Stay updated on regulatory submission requirements.
  • Support training for end users of regulatory systems.

Project ManagementCommunication SkillsAnalytical SkillsCollaboration

Posted 2024-11-07
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📍 Salt Lake City, Utah, United States

🧭 Contract

🔍 TechBio, drug discovery

  • Direct experience with HRIS platforms.
  • Understanding of HR processes such as payroll and benefits administration.
  • Experience with tools like Workato.
  • Proficiency in working with RESTful and SOAP APIs.
  • Knowledge of data formats like XML, JSON, and CSV.
  • Experience in data transformation and mapping.
  • SQL proficiency for querying and manipulating databases.
  • Understanding of relational database structures.
  • Ability to customize HRIS for integration points.
  • Experience in troubleshooting data flows and integration issues.
  • Hands-on experience in identifying and resolving system problems.
  • Experience in creating test plans and conducting User Acceptance Testing.
  • Experience in cross-functional collaboration with HR, IT, and vendors.

  • Design, implement, and maintain integrations between HRIS and other HR-related systems.
  • Ensure seamless data exchange and resolve data integrity issues.
  • Configure integration settings based on organizational needs.
  • Collaborate with HR, IT, and vendors for gathering requirements and managing timelines.
  • Conduct troubleshooting and technical issue resolution.
  • Develop and execute test plans for systems.
  • Maintain detailed documentation of systems and integrations.
  • Ensure compliance with security standards and data protection laws.
  • Provide support for ongoing upgrades and enhancements.
  • Identify opportunities for process efficiencies.

Project ManagementSQLData AnalysisData analysisCommunication SkillsAnalytical SkillsCollaboration

Posted 2024-10-25
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📍 United States, Canada, United Kingdom

🧭 Full-Time

💸 $160,000 - $182,000 per year

🔍 TechBio

  • A minimum of 7 years of experience in managing data storage infrastructure, preferably within global BioPharma organizations.
  • In-depth knowledge of distributed/parallel file systems (IBM Storage Scale GPFS), multi-tier file (NAS), hybrid object storage (MinIO), and storage access and data transfer networking protocols.
  • Extensive experience designing, deploying, testing, supporting, and troubleshooting complex Linux-based computing and data storage environments.
  • Python programming and Bash scripting experience.
  • In-depth hands-on experience in provisioning, configuring, and managing infrastructure through modern CI/CD techniques, GitOps, Infrastructure as Code (IaC) and cloud automation principles.
  • Solid experience with software-defined infrastructure and cloud computing platforms, including Kubernetes, GCP, AWS, and others.
  • Practical knowledge of resource management and job scheduling using Slurm and Kubernetes. Knowledge of container technologies like Apptainer and Docker.
  • Strong verbal and written communication skills for effective documentation and collaboration.
  • Prior experience mentoring, guiding, and cross-training team members.

  • You will be responsible for designing, implementing, testing, maintaining, and optimizing our data storage infrastructure and services, utilizing an Infrastructure as Code approach across both on-premises and public cloud environments.
  • You will drive innovation across all storage tiers within our AI/HPC infrastructure, ensuring we deliver a scalable and effective data platform to support our mission.
  • By developing scripts and workflows, you will automate and verify storage infrastructure provisioning and dynamic reconfiguration, enhancing support for our AI/HPC storage environments.
  • Your role also includes researching, deploying, and optimizing accessibility, performance, security, and data lifecycle management policies.
  • Regular assessments of our storage platforms' health and operational performance against established metrics will be part of your responsibilities, with a focus on meeting and exceeding operational service level objectives.

AWSDockerLeadershipPythonBashCloud ComputingGCPKubernetesCommunication SkillsCollaborationCI/CD

Posted 2024-10-12
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