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Keywords: Katalyst Healthcares & Life Sciences, Location: Boston, MA

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Quality Assurance (QA) Specialist

guidelines and company quality policies. Requirements: Bachelor's degree in Pharmaceutical Sciences, Life Sciences, Chemistry...

Posted Date: 21 Dec 2024

SW QMS Specialist

multiple priorities. Requirements: Bachelor's degree in quality management, Regulatory Affairs, Life Sciences, or a related...

Posted Date: 05 Dec 2024

Senior Validation Consultant

and continuous improvement. Extensive CSV expertise in life sciences, especially patient safety. Proficiency in Argus Safety, Veeva...

Posted Date: 20 Nov 2024

Validation Engineer – APS

as needed. Qualifications: Bachelor's degree in engineering, Life Sciences, or a related field. 5-8 years of experience in validation...

Posted Date: 17 Nov 2024

IT Quality Lead (CSV)

Qualifications: - Providing the validation strategy for different computer systems in life sciences industry...

Posted Date: 27 Oct 2024

Data Integrity Lead

life cycle (SLC) activities for Vertex GxP systems. Managing and Facilitating Data Mapping initiatives for programs level...

Posted Date: 11 Jan 2025

Clinical Quality Compliance

Responsibilities: Lead development and implementation of the GCP supplier audit and compliance strategy for clinical development programs, GMA and MPG studies. Serve as primary point person for key GCP strategic partners; lead key suppli...

Posted Date: 15 Jan 2025

Scientist II

Responsibilities: Establish strong scientific and technical initiatives and hands-on implementation for new in vitro models. Execution of in vitro experiments to create cellular models in immortalized cell lines, primary neurons and/or i...

Posted Date: 12 Jan 2025

GCP Supplier Quality

Responsibilities: Lead development and implementation of the GCP supplier audit and compliance strategy for clinical development programs, GMA and MPG studies. Serve as primary point person for key GCP strategic partners; lead key suppli...

Posted Date: 12 Jan 2025

Equipment Engineer

Responsibilities: Authoring and reviewing of SOP's (both new and existing). Authoring and reviewing Equipment Requirements Specifications. Document calibration and maintenance requirements, generate procedures. Supporting Equipment Man...

Posted Date: 08 Jan 2025

Scientist II

Responsibilities: Request and handle human and monkey donor blood samples. Isolate primary cells from peripheral blood using sterile techniques. Set up, maintain, and monitor cell cultures with isolated blood cells. Perform cell stimul...

Posted Date: 05 Jan 2025

Scientist II

Responsibilities: Establish strong scientific and technical initiatives and hands-on implementation for new in vitro models. Execution of in vitro experiments to create cellular models in immortalized cell lines, primary neurons and/or i...

Posted Date: 01 Jan 2025

CSV Engineer

Responsibilities: Draft and implement Quality System documentation designed to establish good validation practices within the organization. Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and intern...

Posted Date: 20 Dec 2024

Medical Device Senior Manufacturing Engineer

Responsibilities: Developed and optimized efficient, cost-effective, and validated manufacturing processes for medical devices, focusing on capital and/or disposable devices, including assembly, lot release testing, sterilization, and pac...

Posted Date: 04 Dec 2024

Scientist III

Roles & Responsibilities: Bachelor of Science in Lifesciences or master's Preferred. 3-5-year experience level. In vitro primary cell culture (human PBMC, Cyno PBMC and mouse splenocyte). Serial dilutions of drug molecules and applicat...

Posted Date: 22 Nov 2024

CMC Regulatory Affairs Program Manager

Responsibilities: Lead the strategic efforts in the interpretation of relevant and new quality guidelines to ensure that the current and phase appropriate requirements and standards are properly and timely implemented. Provide support to...

Posted Date: 20 Nov 2024

Senior Word Processing Coordinator II

Responsibilities: Processes, proofreads, verifies and manages various clinical regulatory documents, ensuring they are submission-ready for publishing with an appropriate level of accuracy and consistency. Communicates regularly with col...

Posted Date: 15 Nov 2024

Bioinformatics Operation Engineer

Overview: The Genomics Research Canter (GRC) is a centre of excellence for genetics and genomics that supports both Discovery and Development. The GRC plays an integral role towards our goal of developing extraordinary genetics and genom...

Posted Date: 15 Nov 2024

GMP Validation

Responsibilities: Strong Windows Desktop Support Experience. Hands-on experience in handling the Parma LAB devices and instruments. Desktop Hardware and troubleshooting at L2 + (Window 10, 7). Experience in handling IT Desktop ...

Posted Date: 13 Nov 2024

Sr. CSV Lead

Roles & Responsibilities: The ideal candidate will have 7-8 years of validation experience and at least 3 in Salesforce Validation. Seeking a CSV resource who has experience specifically with Salesforce. They are currently seeking a Sr....

Posted Date: 09 Nov 2024