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
About Us:BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from
Job Description The Pharmaceutical Analysis & Digital Technologies (PADT) Analytical Capabilities & Operations (ACO) department of our Research and Development Division is seeking applicants for a Metrology and Validation Specialist position available at the Rahway, New Jersey
Job Description The Pharmaceutical Analysis & Digital Technologies (PADT) External Capabilities, Validation, and Compliance (ECVC) department of our company Research Laboratories Division is seeking applicants for a Validation Specialist position available at either the Rahway, New Jersey research
Graver Technologies LLC As a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway—you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making
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
Bristol Myers Squibb in New Brunswick, NJ, is seeking a Process Development Engineer for Device and Packaging Development to advance fill-finish and device assembly processes for sterile drug products. The role requires collaboration with Clinical and Commercial
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.
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.
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
Payroll - Validation Professional Location: 126 E. Lincoln Avenue Rahway, NJ Qualifications: Education: Bachelors Degree with a minimum of 8+yrs of applicable experience Required: Knowledge of ADP Technology ev6, Workday, MS Office Candidate would need to be
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
Director, Compliance and Validation You will join our East Brunswick, New Jersey office, be part of a committed organization of over 1,500 professionals, and work in teams and directly with our clients doing work that is shaping
Validation Analyst We are seeking a Validation Analyst to support validation of our Quality Management System (MasterControl) and SAP implementation (QM, Materials Management, Production modules). This role works under the direction of a senior validation lead and partners with Quality,
Manager AI Assisted Process, Risks and Controls Transformation Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect, and transform their organization. Join
Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager Johnson and Johnson is recruiting for an Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager, located in either Horsham, PA; Raritan, NJ; Beerse, Belgium or Allschwil, Switzerland. The
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
Director of Compliance & Validation, Life Sciences Location: East Brunswick, New Jersey Who 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