cGxPServe

Responsibilities: The Clinical Data Manager (CDM) is responsible for the oversight integrity and quality of clinical trial data from collection through database lock. The CDM ensures that data is accurate consistent and meets regulatory and protocolspecific requirements. This role c المزيد...

Job Description: Reporting directly to the Quality Engineering Supervisor this position involves product team support for the manufacturing operations provides quality guidance product resolution decisions and statistical problemsolving techniques to manufacturing operations and proj المزيد...

Roles & Responsibilities: Ensures that the divisions Approved Supplier List is maintained and accurate. Assesses potential new suppliers and service providers for quality and quality system capabilities through the of onsite or desk top audits and review of other objective evidence المزيد...

Responsibilities: Responsible for providing guidance to ensure that all regulatory submissions are planned communicated and performed per regulatory and business requirements. In addition this position serves as a subject matter expert on various regulations coordinating regulatory i المزيد...

Job Description: The Project Manager Combination Products Development is accountable for leading the cross functional team (Engineering Quality Supply Chain Marketing Operations Human Factors and External Partners) in the of a portfolio of projects focused on the delivery system cons المزيد...

Responsibilities: You will work within the Scientific Programming team to provide support to the analysis and management of our clinical trials and have the opportunity to significantly contribute to special projects that will revolutionize some of our key ways of working. Develop an المزيد...

Position Overview: The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment and computerized systems at multiuse sites through interaction with internal customers and external service providers. The incumbent in this role contributes to the com المزيد...

Responsibilities: We are seeking a highly skilled Statistical Programmer to generate and produce programming deliverables such as datasets tables figures and listings for study reports and integrated summaries using statistical analysis systems (i.e. SAS . The ideal candidate will s المزيد...

Responsibilities: Ensure departmental or functional training plans in place and appropriate. Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget. Generate validate and/ المزيد...

Responsibilities: Under direction of supervisor or the sterility assurance focal point contributes to the design development or enhancement of new products and processes. Effectively contribute solid technical knowledge to a variety of projects within the sterility assurance discipli المزيد...

Job Description: The role involves scanning of histological slides processing slides using digital pathology applications generating and analyzing precise data and ensuring timely and reliable delivery of results. Responsibilities include quality assurance data storage management and المزيد...

Job description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes follow written procedures (SOPs) monitor equipment and processes perform basic laboratory tasks inc المزيد...

Responsibilities: We are seeking a highly skilled Statistical Programmer to generate and produce programming deliverables such as datasets tables figures and listings for study reports and integrated summaries using statistical analysis systems (i.e. SAS . The ideal candidate will s المزيد...

Job Description: The Project Manager Combination Products Development is accountable for leading the cross functional team (Engineering Quality Supply Chain Marketing Operations Human Factors and External Partners) in the of a portfolio of projects focused on the delivery system cons المزيد...

Job description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes follow written procedures (SOPs) monitor equipment and processes perform basic laboratory tasks inc المزيد...

Responsibilities: Serve as the main contact for servicerelated inquiries from recruitment managers employees and other HR team members. Ensure the complete resolution of HR requests including tracking and tracing. Offer outstanding customer service by promptly resolving queries and i المزيد...

Responsibilities: Regulatory Affairs Specialist* This position assists the Director of Quality Operations (DQO) in maintaining an effective Quality Operations and Regulatory Program which consistently delivers high quality EZIP products on time. Handles regulatory submissions CAPAs c المزيد...

Roles & Responsibilities: Must have deep experience in Lab Vantage LIMS experience including ELN and the Stability Module. At least 5 years of experience. Experience in process of transitioning to Lab Vantage Stability LIMS. Experience in implementing ELN.

Responsibilities: Candidate must be able to answer questions in the STAR format (Situation Task Action Result). If they cannot formulate a response this way please coach or whittle down the resume. Note answers should pull from multiple projects and not the same one over and over. C المزيد...

Responsibilities: Serve as the main contact for servicerelated inquiries from recruitment managers employees and other HR team members. Ensure the complete resolution of HR requests including tracking and tracing. Offer outstanding customer service by promptly resolving queries and i المزيد...