CSV Engineer - Durham, North Carolina, , United States

The resource will not need to travel between sites but will need to be local and able to go on site every day to either location Durham or Elkton VA. · ...

We are looking for a Strong CSV experience. · Strong Computer System Validation Experience  · Quality Assurance experience · ...

The job details are as follows: · Apply specialized knowledge of computer system validation practices including deliverables and risk assessments for enterprise data systems for manufacturing, · purchasing, planning, IT Infrastructure, clinical safety, quality control laboratory, ...

We are seeking a recent engineering graduate with an interest in automation and control systems used in life sciences manufacturing (vaccines, biologics, cell and gene therapy). The ideal candidate will have experience as a Co-Op or Intern in life sciences, chemical or industrial ...

United Therapeutics Corporation seeks a Senior Validation Engineer in Durham, NC to perform job duties including applying computer system validation practices and evaluating operational requirements. · Evaluate operational requirements and develop test plans. · ...

,United Therapeutics Corporation seeks a Senior Validation Engineer to perform duties including deliverables and risk assessments for enterprise data systems. · ,Apply specialized knowledge of computer system validation practices, · Evaluate operational requirements and develop t ...

The QA Data Steward (Contractor) supports the QA-for-QC organization by performing quality-related activities and Computer System Validation (CSV) tasks for QC laboratory computer systems. · ...

Beam is seeking a highly skilled Specialist I/II to join our growing Digital Quality & Data Integrity team and play a pivotal role in shaping the future of digital compliance. · Oversee risk-based Computerized System Validation (CSV)/Computerized Software Assurance (CSA) activiti ...

This is a global position leading and supporting the implementation, migration, validation and ongoing management of key electronic Quality Management Systems (eQMS) and pharmaceutical computerized systems across MedPharm sites in UK and US. · ...

This will be a global position leading and supporting the implementation migration validation and ongoing management of key electronic Quality Management Systems eQMS pharmaceutical computerized systems across MedPharm sites in UK and US ensuring equal support alignment across al ...

Participate in the roll-out/support of a new Lean Systems Development Lifecycle (SDLC) and Quality Management System (QMS). Create procedures or revise existing ones where needed. · ...

The Senior SAP IT Program Manager leads complex global SAP S/4HANA implementation and migration initiatives within a highly regulated pharmaceutical environment. This role ensures successful delivery of SAP enhancements and bug fixes in compliance with FDA GxP SOX and data integr ...

We're hiring a Support Engineer to help customers get fast, accurate answers—and to strengthen the reliability of our platform through great troubleshooting, documentation, and cross-team collaboration. · We'll manage inbound tickets end-to-end, solve Tier 1 issues (and some Tier ...

We're looking for an Enterprise Project Manager to lead complex, multi-system onboarding and integration projects for our largest, most strategic customers. · ...

Lilly is looking for an Associate, QA Compliance to join their team. The successful candidate will have at least 3 years of experience in QA roles, preferably in the pharmaceutical or medical device industry. They will be responsible for providing daily oversight, assistance, and ...

We are seeking a Process Automation Engineer (Associate Specialist, Manufacturing Automation) to join our team at Merck & Co., Inc. · Troubleshoot challenging equipment/automation issues and innovate to improve manufacturing performance · Maintain the automation systems in compli ...

+Job summary · This will be a global position leading and supporting the implementation, migration, validation, and ongoing management of key electronic Quality Management Systems (eQMS) and pharmaceutical computerized systems across MedPharm sites in UK and US. · +To effectively ...

Support implementation of a new MES for drug substance manufacturing operations. · ...

+This will be a global position leading and supporting the implementation, migration, validation, and ongoing management of key electronic Quality Management Systems (eQMS) and pharmaceutical computerized systems across MedPharm sites in UK and US. · +To effectively manage key Ph ...

The Sr.Specialist,LaboratoryInstrumentationresponsibleforinstallations/configurations/troubleshooting/qualificationsoflaboratoryinstrumentationwithintheKriyalaboratories.Thisroleensureslaboratoryequimentoperatesreliablytosupportproducttesting/methodvalidationandqualitycontroloper ...