Jobs: katalyst healthcares life sciences

Senior Financial AnalystKatalyst Group is recruiting for a Senior Financial Analyst on behalf of a non-profit delivering tremendous impact to the communities it serves through the delivery of healthcare and education-based services.Job Overview:The Senior Financial Analyst will play a vital role in performing financial planning and analysis activities for...

Responsibilities: Collaborate with project team members to architect solutions per Business Requirements. Perform analysis and design (functional/non-functional) activities to create clinical/Regulatory solution landscapes for our Life Sciences Clients. Take complex concepts and articulate them to an audience of varying levels of expertise and subject matter...

Responsibilities: Should have solid validation lead experience working for pharmaceutical companies as Val lead/SME. Should have Validation Lead and LIMS advisory experience to guide the entire program/project teams. Should have great communication and coordination skills between internal team and customers across shores. Should have great stakeholder...

Responsibilities: Minimum 7 years' Experience in the Validating IT software systems like Quality Management System in Life Sciences industry Experience in FDA and/or Global regulated environment with good understanding of GxP standards like CFR 820 and Risk based validation. Experience in validating Global Risk and Compliance modules Provides consultation...

Responsibilities: Minimum 7 years' Experience in the Validating IT software systems like Quality Management System in Life Sciences industry Experience in FDA and/or Global regulated environment with good understanding of GxP standards like CFR 820 and Risk based validation. Experience in validating Global Risk and Compliance modules. ...

Responsibilities: Conduct single or multi-center medical device clinical studies. Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items. Participate in study start up activities. Responsible for shipping study devices and supplies to clinical sites and performing study device...

Responsibilities:Conduct single or multi-center medical device clinical studies. Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items. Participate in study start up activities. Responsible for shipping study devices and supplies to clinical sites and performing study device accountability....

Responsibilities: Conduct single or multi-center medical device clinical studies. Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items. Participate in study start up activities. Responsible for shipping study devices and supplies to clinical sites and performing study device...

Responsibilities: A statistical programmer consultant provides timely support to the study team on all programming matters according to the project strategies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent implements and executes the...

Responsibilities: The candidate should have expertise in (verification) testing, systems and methods qualification & validation, and maintenance of Laboratory Equipment Experience designing validation protocols for Equipment Validation, including IQ/OQ/PQ and reports is required. Experience qualifying analytical laboratory equipment and/or...

Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis, CMC comparison and validation for the quality reports Experienced in authoring of assessment reports and Part2/ Expert reports for Dossiers Experience in reviewing of quality documents such as Reformulation studies, process validations, particle size method...

Responsibilities: Supports delivery of projects involving implementation and/or management of Regulatory Information Supports Data & Content Migration into Regulatory Information Management System, involves. Source to target data model mapping. Data quality assessment Recommend / identify / facilitate agreeing on data standards for new RIMS and data...

Responsibilities: Lead the design, development, implementation, and execution of test scripts/test plans to identify software problems and their causes. Coordinate and execute performance and functional testing associated with multiple concurrent development and/or infrastructure projects. Perform testing of the entire SDLC, including version/change control...

Responsibilities: Primarily responsible for the support and execution of laboratory equipment qualification and associated computer system validation activities in compliance with current cGMP regulations and client's corporate principles, quality policies, standards, and core values. You will work closely with instrument vendors, facilities, IT, and lab...

Responsibilities: Provide support and enhancements for the administration of benchtop instrumentation applications, PC hardware, and IT administrative tools within a GxP environment. Support would encompass various instrument types such as cellometers, plate readers, and flow cytometers throughout the site which include laboratory and manufacturing...

At Katalyst we believe satellite owners and operators shouldn't be stuck with outdated capabilities as they try to adapt to a rapidly changing environment. We are building the upgrade economy where satellites are reconfigured on orbit rapidly, routinely, and regularly. We do this by adding new capabilities to satellites post-launch with in-space servicing,...

Responsibilities: This position is responsible for leading and performing activities in support of creating and maintaining GxP (GMP, GCP, and GLP) quality and compliance environment for SAP S/4 HANA. This position is also responsible for monitoring Computer System validation (CSV) as well as compliance with GxP regulations and 21 CFR Part 11. Leads the...

**Responsibilities**: - Develop global regulatory strategies for medical device products to meet business objectives and collaborates across a matrixed organization to ensure global success of products\' registration. - Participate on product development teams, providing regulatory strategies, timelines, and direction. Reviews and approves technical...

The Scoop As an On-Camera Fitness Instructor with Katalyst, you will have the opportunity to bring your passion for Health and Fitness to a large audience and be their guide to EMS, helping them reach their fitness goals.  We are looking for people that are comfortable being on camera, have experience in the world of Health and Fitness, and are able to...

Responsibilities: B.A. or B.S. degree (preferably in Engineering or Life Science) and at least two years of experience in the pharmaceutical or biopharmaceutical industry, or an equivalent combination of education and experience. Basic knowledge of engineering principles and concepts applicable to Process as they relate to system performance, regulatory...