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 Agile based System development
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
Director, Software Validation At Slipstream we work to streamline IT Support and provide managed solutions with a strategic consulting and global leadership management approach. Our solutions are designed exclusively for emerging pharma and biotech organizations. Slipstreams industry-leading
Validation Lead Raritan, NJ OR New Brunswick, NJ (Onsite Hybrid Model ( 3 days a week) ) Long Term Contract Job Responsibility: Must be able to work out of Raritan or New Brunswick Office at least 3
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.
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
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
Job Description Position Summary The Technical Project Manager (TPM) is responsible for delivering digital, automation, and data integration scope across capital projects within the Digital Manufacturing Division Manufacturing Value Team portfolio. This role ensures the reliable,
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.
Job Description Non-Sterile Specialist, Engineering Position Summary This Engineer position provides on-site engineering support for the Rahway, NJ FLEx (Formulation, Laboratory & Experimentation) center, supporting non-sterile operations within Our Companys Research Labs Pharmaceutical Sciences (Pharm Sci),
Senior Manager, GxP IT Quality Assurance & E-Compliance 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
Metrology Specialist I On-site in Rahway, NJ Summary: Manage equipment assets at multiple locations Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or communicate with the vendor/ service engineer to identify resolutions Participate
Lead, Complaints / Adverse Events Enterprise Quality is a comprehensive organization within J&J that focuses on ensuring the highest standards of quality & compliance. It encompasses a Quality Operations division that handles Computer System Validation (CSV), QMS Management,
GMP Senior Facilities Mechanic For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently
Job Title Provides direct patient care, coordinates treatment plans, and collaborates with interdisciplinary teams to ensure quality outcomes. Maintains clinical documentation, adheres to safety protocols, and supports patient education and advocacy. Perform systematic, comprehensive, and accurate
Manager, Csv Cell Therapy 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
remote type Hybrid Work locations Raritan, New Jersey, United States of America Irving, Texas, United States of America Irvine, California, United States of America Horsham, Pennsylvania, United States of America time type Full time posted on
Manager, R&D Quality Risk Management V Position Summary: Responsible for planning, writing, implementing and reviewing computer system validation (CSV) protocols of GxP computerized systems. Serve as the CSV subject matter expert and provide guidance on and interpretation of global GxP
Sr. Mgr Technology Quality - Security, Data & Digital Core Technology Quality Operations (TQ) manages the Quality and Compliance strategy for Technology systems including applications, infrastructure and digital health solutions for J&J. TQ is the subject matter