Fathom Life Sciences welcomes to join our team, we always look for self-motivated, highly enthusiastic team players. Please send your information with your job interest our team will reach out to you.

Full Time
New York
Posted 4 months ago

Location: Rensselaer, NY Interview: Phone/Skype Start date: 10/01 Category : Full Time Qualify equipment based on cGMP (Good Manufacturing Practices) standards. Author and execute validation protocols for IQ, OQ, and PQ for the equipment as well as utilities, HVAC’s and facility. Review the Installation & Operational Qualification procedure of the newly installed Air Handling Unit (AHU)…

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Full Time
California
Posted 6 months ago

Location: Fremont, CA Interview: Phone/Skype Start date: 10/01 Category : Full Time Involve in documentation of different stages of validation life cycle in compliance with 21 CFR Part 11. Responsible in analyzing business requirements, development of  validation plans (VP),Validation Protocols (Installation Qualification, Operational Qualification and Performance Qualification), Requirement Traceability Matrix (RTM) and Summary Reports (validation and Test…

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Full Time
Kansas
Posted 9 months ago

Location: McPherson, KS Interview: Phone/Skype Start date: 10/01 Category : Full Time Perform Chemical assessment to determine the storage conditions of the finished, semi-finished products, work in progress chemical, active pharmaceutical ingredients (API’s), other chemicals and manufacturing components (eg: vials, ampoules) of pharma products. Develop and Execute Validation life cycle deliverables which include Validation plans, requirement…

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Full Time
New York
Posted 9 months ago

Location: Tarrytown, NY Interview: Phone/Skype Start date: 10/01 Category : Full Time Perform, record, troubleshoot and analyze temperature mapping of manufacturing equipment using Kaye Validator 2000, Advanced systems (AVS), Data loggers and data traces using Val-suite Pro and track sense Pro. Assist in project management by updating equipment information, calibration schedule, preventive maintenance schedule, re-qualification…

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Full Time
Kansas
Posted 9 months ago

Location: McPherson, KSInterview: Phone/Skype Start date: 10/01 Category : Full Time Author and execute validation protocols for IQ, OQ, and PQ for the equipment as well as utilities, HVAC’s and facility. Ensure that the development and maintenance process are adequate in order, for the system to meet its objective. Responsible for document preparation and execution…

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Contract
California
Posted 1 year ago

Start: 9/25 Interview: Phone, Skype Length: 1 year plus Type: Contract Prerequisites: Minimum of BS/BA degree in science (Masters or PhD preferred) with at least 5 years of regulatory writing and submission experience Recent experience writing regulatory submission documents, eg, CSRs, CTD summaries or clinical overview, briefing books Experience in oncology, hematology, and/or inflammation and…

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Contract
Maryland
Posted 1 year ago

The Medical Affairs Manager, Hematology, is a member of the Oncology brand Core Medical Teams, and supports the development and execution of the Brand Medical Plans. Responsibilities include

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