Katalyst Healthcares & Life Sciences

Job Description: The primary role of Manufacturing Quality function is to design implement and monitoring quality control programs. Key deliverables include but not limited to recommending changes to methods procedures and standards to improve quality of output based on analysis of da More...

Responsibilities :You will provide technical expertise as an experienced R programmer to develop process methodology ensuring the department meets the needs of both internal and external clients.Responsibilities include planning and coordinating the development of integrated programm More...

Responsibilities:Develop and execute comprehensive SOPs to ensure strict adherence to protocol requirements and maintain the highest standards of practice while guaranteeing full compliance with Good Clinical Practice (GCP) standards.Formulate and implement robust training programs fo More...

Job Description:We are seeking an experienced Lead Clinical Data Manager to oversee and manage all aspects of clinical data management activities for multiple clinical studies. The ideal candidate will ensure the accuracy integrity and quality of clinical trial data while collaboratin More...

job Description:The Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products.The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clini More...

Job Description:The main function of a supplier quality engineer is to research and test and develop quality standards for components. A typical quality engineer has the ability to read and interpret blueprints and evaluate component integrity and standards.We are NPD Supplier Quality More...

Job Description:Join a leading biomedical software development project and provide Quality Assurance oversight throughout the Software Development Life Cycle (SDLC) ensuring compliance with regulatory standards (FDA/GMP). Youll act as a QA subject matter expert on cross-functional tea More...

Job Summary:The Pharmaceutical Technician will efficiently effectively and safely clean set-up and operate machinery in the manufacturing area while adhering to applicable cGMPs SOPs FDA and DEA guidelines.Responsibilities:Follow Master Batch Records for the manufacturing of controlle More...

Job Description:This role supports the Market Research (MR) Compliance and Operations Team under direction and guidance from the MR Compliance Lead. The coordinator works cross-functionally supporting Analytics activities related to Market Research and GVP Activities to ensure that in More...

Roles & Responsibilities:Bs degree with 9 years experience in Supplier quality from aerospace / automobile / medical.Experience in PPAP / APQP and new product development and CAPA.Supplier audits and new supplier onboard.Knowledge of quality tools such as 7 QC tools MSA SPC and ot More...

Job Description:This role is responsible for executing microbiological testing environmental monitoring and method validation in a GMP-regulated laboratory. The candidate supports quality control functions including method development troubleshooting and test execution for raw materia More...

Job Description:The Equipment Validation Specialist is responsible for ensuring that all critical GMP equipment and systems used in manufacturing are validated maintained and compliant with regulatory requirements. This role supports manufacturing operations by providing documented ev More...

Job Description:The Lead HR Generalist reporting to the Sr. HR Manager is responsible for delivering the end-to-end Human Resources agenda for assigned departments and functions at the site. The role involves implementing and maintaining procedures and programs for site employees in a More...

Job description:The Biologics CMC Developability team is an integral part of the Biologics CMC Drug Product Development Org. The Biologics CMC Developability team is responsible for- (1) the identification of biophysical- and chemical liabilities in discovery-stage biologic drug candi More...

Responsibilities:Lead the development and implementation of submission-ready SDTM datasets in accordance with regulatory requirements (e.g. FDA EMA PMDA).Collaborate with regulatory affairs and quality assurance teams to ensure compliance with submission guidelines and standards.Perfo More...

Roles & Responsibilities:Lead design configuration and commissioning of DeltaV and Client-X automation systems for GMP-critical manufacturing equipment and process controls.Support change controls deviations and CAPAs involving DeltaV and Client-X logic batch strategies and alarm More...

Job Description:Will be responsible to work in a team atmosphere on production of medical equipment spare parts and accessories in accordance with quality specifications.Works within clearly defined SOPs and adheres to quality guidelines.High school diploma or equivalent.Zero (0) to o More...

Responsibilities:Support the plant manufacturing effort with ability to identify problems and specific focus will be in areas of improving quality waste and equipment efficiencies.Application of Transfer functions during troubleshooting and production support (i.e. Statistical Toleran More...

Responsibilities:Maintains all qualified and validated equipment and systems in compliance with policies guidelines and procedures.Develops protocols and associated reports while adhering to a change management process.Supports the execution of equipment qualifications and validation More...

Job Description:The position of Warehouse Team Member performs activities related to the receipt shipment movement manufacture or control of raw materials product recyclable materials and waste. Operates equipment/machinery when necessary.Responsibilities:Performs activities related t More...