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
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
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
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),
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
Clinical Lab Technologist Staff Position Location: New York, NY 10036 Duration: Full Time Shift: 9 AM to 5 PM Salary Range: $140,000 - $140,689/year Chemistry Lab Supervisory Experience is required. Licensed/qualified CLT. + 4 years of
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
Facility Solutions Associate II - OFCI Coordinator The Facility Solutions Associate II role focuses on conducting processes and completing deliverables associated with facility services and operations. They will have advanced involvement with drawings, specifications and submittal
Role Descriptions: • Demonstratable Experience in Computer System Validation (CSV) • Experience in software development processes (SDLC) and software testing life cycle (STLC) • Experience in drafting, reviewing, revising, and maintaining validation documents (CSV), including Compliance Analysis, Compliance Plan,
Validation Engineer Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Location: Ridgefield, New Jersey – Sterile Fill-Finish & Packaging Site Our state-of-the-art sterile fill-finish and packaging facility in Ridgefield, NJ, is dedicated to meeting the growing needs of biotech