807 Job openings in Cgxpserve
Job Description: The Hillsboro Innovative Therapies (HIT) team at the client site is at the forefront of bringing new medical advancements from development stages to commercial manufacturing. We work with cutting-edge technologies such as individualized DNA/RNA therapies cell therapi More...
Responsibilities: Provide leadership strategic planning direction and implementation of clinical systems for data collection which may include vendor selection budgeting resource planning vendor oversight EDC build and study timelines etc. Perform or provide oversight to staff for al More...
Job Description: The scientist will be responsible to run in vitro primary cell culture in 96-well plate format perform serial dilutions of drug molecules perform ELISA for cytokine analysis and perform FACS flow cytometry analysis to look at cell populations changes and cell phenotyp More...
Responsibilities: Lead projects in manufacturing process areas to achieve process efficiencies such as increase in process yield quality improvements cycle time/throughput and cost reduction initiatives. Gather and analyse process data using statistical process control methodology. D More...
Roles & Responsibilities: Mechanical Engineering Degree. Quality Control exposure. ISO 13485 awareness (not mandatory). College Graduate (freshers) to (less than) 10 years of experience. Experience with relevant Supplier Quality requirements is added advantage. Management of supplier More...
Responsibilities: Performing data manipulation analysis and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming. Generating and validating SDTM and Adam datasets/analysis files and tables listings and figures (TLFs). Production and QC More...
Job Description: Strong written and verbal communication skills. Possess strong analytical and problem-solving skills. Familiarity with one of SAS JMP or Minitab is strongly desired. Working knowledge of MS Office including Office Project software. Six Sigma Process Improvement Exper More...
Job Description: The Medical Imaging Specialist is responsible for providing CT and MR imaging expertise for the Intuitive 3D modelling service and operation team. This includes performing initial inspection of CT and MR scans received for 3D model segmentation providing in-process co More...
Job description: This position will play a key role in the development of complex in vitro models to support late-stage internal programs. The ideal candidate will have extensive experience with primary cell culture and complex in vitro models and the potential of applying these model More...
Responsibilities: Position leads complex studies in study design statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health More...
Roles & Responsibilities: Process non-conformances and CAPAs following approved procedures. Perform investigations and assist in problem solving following approved methodologies. Partners with engineering production maintenance etc. to maintain/increase the quality level within the o More...
Responsibilities: Collect enter and manage clinical trial data using electronic data capture (EDC) systems. Perform data validation and query management to ensure data quality and compliance with study protocols. Assist in the development of case report forms (CRFs) and data manageme More...
Position Overview: This position is responsible for reviewing and verifying documentation related to the Initial Sample Inspection Report (ISIR) process to ensure compliance with internal and industry standards. This role works closely with Engineering Quality Sourcing and suppliers. More...
Responsibilities: Provide leadership strategic planning direction and implementation of clinical systems for data collection which may include vendor selection budgeting resource planning vendor oversight EDC build and study timelines etc. Perform or provide oversight to staff for al More...
Job Description: Client is seeking a Verification and Validation SR Engineer to help with formal verification and validation of complex medical devices under the regulations of the FDA. The individual will be part of an engineering team that is responsible for requirements based manu More...
Responsibilities: Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Creates revises and implements quality standards as well as procedures i.e. Standard Operating Procedures (SOPs) etc. for Erbe USAs Quality Management Sy More...
Responsibilities: Leads the statistical programming activities for projects with lower complexity. Leads the statistical programming activities for studies. Develop SAS programs for the creation of Adam data sets following CDISC standards. Develop SAS programs for the creation of Tab More...
Job Description: We are seeking a highly skilled Bioinformatics Data Analyst to join our team. The ideal candidate will be responsible for retrieving managing and visualizing large datasets while developing custom applications and the integration of laboratory equipment. Responsibilit More...
Responsibilities: In this role you will perform specialized level work assignments and/or analyses evaluation preparation and submission of documentation for regulatory registration ensuring products and procedures comply with regulatory agency specifications. Supports necessary regu More...
Responsibilities: Provides leadership/expertise in day-to-day statistical programming in support of ongoing projects. Develops and/or validates SAS programs to generate SDTM/ADaM datasets following industry standards regulatory requirements and statistical instructions. Develops and/ More...
