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
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.
The Process Improvement Coordinator is responsible for identifying, developing, and implementing process improvement initiatives that enhance operational efficiency, product quality, productivity, and customer satisfaction. This position analyzes manufacturing and business processes, monitors performance metrics, supports continuous improvement initiatives,
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,
Computer System Validation Specialist Computer System Validation, CSV, GxP, 21 CFR part 11, Risk Based Approach Roles and Responsibilities 10+ yrs. of experience in Computer System Validation Senior Level individual with GxP experience Ability to lead, fully knowledgeable of
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
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
Training Specialist Location: Summit West, NJ (HYBRID) Position Summary: The Training Specialist, Instructional Design & Systems Training is a full-time role. The primary focus for this role is to lead and manage the instructional design, the
Process Improvement Coordinator The Process Improvement Coordinator is responsible for identifying, developing, and implementing process improvement initiatives that enhance operational efficiency, product quality, productivity, and customer satisfaction. This position analyzes manufacturing and business processes, monitors performance metrics, supports continuous
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
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
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
CSV for SAP Systems/Projects To create, assign, and track the project module work plans for delivery and also provide technical guidance for work completion. (1.) To ensure process improvement and compliance in the assigned module and participate
Senior Quality Validation Specialist We are seeking an innovative and highly motivated Senior Quality Validation Specialist, who will contribute significantly to the growth of the Cellares team. The Quality Validation team at our IDMO Bridgewater facility will be responsible
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,
Job Description The Pharmaceutical Analytical Sciences (PAS) group has an exciting opportunity for an Associate Principal Scientist based in Rahway, NJ. Join us and experience our culture firsthand - one of strong ethics & integrity, diversified
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
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.