Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Manager of DRG Coding & Clinical Validation Audit Manager of DRG Coding Audit-Program/Project Locations: The selected candidate must reside within a reasonable commuting distance of the designated posting location(s): Virginia, Indiana, Georgia, Ohio, Maryland; New Jersey, New
Director, Business Systems Validation External / Automation The Director, Business Systems Validation External / Automation provides strategic leadership and direction to validation teams within an assigned geography. They oversee performance management, organizational capability building and process optimization. They partner with
Project Manager, Validation You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is
Manager, IT Validation Services Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day,
Computerized System Validation Specialist Experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. Experience of CSV Validation in any one of the Lab systems is must. Should have worked
Computer System Validation Specialist 10+ years experience in computer system validation or quality management or business analysis in GxP application area Has working experience in any one or two of the following domains - clinical development and supply
Overview We are seeking an experienced and innovative Associate Principal Scientist to join the Process Analytical Technologies (PAT) team within Analytical Enabling Capabilities. In this role, you will collaborate with a cross-functional, highly engaged team to advance
Job Summary The QA Process Control Engineer is responsible for ensuring that all sterilization processes and microbiological testing meet the highest regulatory and quality standards. This role involves managing sterilization cycle validations, maintenance, and evaluations, overseeing product release
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Responsibilities & Qualifications Contract position for a Validation Engineer supporting quality-system remediation at a medical device manufacturer. Assess product and process risk and drive corrective action tied to regulatory findings and open quality records. Perform or refresh hazard
IT Quality Compliance Specialist/Analyst Hybrid role-Local Candidates Only Work Schedule: Mon - Fri, Business HoursMust haves: Ideal candidate would have prior experience of Labelling system (Esko - Web Center, Bonitasoft BPM) Quality assurance mindset for computer
Provide strategic leadership and direction to validation teams within an assigned geography Oversee performance management, organizational capability building and process optimization Partner with other leaders on workforce strategy, talent development, and alignment on enterprise Business Validation goals Define and
Onkos Surgical is seeking a QA Process Control Engineer in New Jersey to ensure sterilization and microbiological testing meet top regulatory and quality standards. You will manage sterilization cycle validations, maintenance, and product release procedures related to cleaning
Project Manager, Validation page is loaded# Project Manager, Validationlocations: East Brunswick, NJtime type: Full timeposted on: Posted Todayjob requisition id: R020999BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Director of Compliance & Validation, Life Sciences Location: East Brunswick, New JerseyWho You’ll Work With You will join our East Brunswick, New Jersey office, be part of a committed organization of over 1,500 professionals, and work in
Who You’ll Work With You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work