Specialist, MSEO Manufacturing Systems Validation

Minimum 50% onsite required every week (Candidate is supposed to align the onsite days with the manager and be available onsite when a manager requests) Bachelor's degree required in Life Science or Engineering Duration: 6 months (Possibility of extension for the right candidate) Job Description: The Specialist works cross-functionally to execute...

Job Description: Minimum 50% onsite required every week (Candidate is supposed to align the onsite days with manager and be available onsite when manager requests) REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE) and Recipe Authoring/Validation. Ability to work...

Job Description: Minimum 50% onsite required every week(Candidate is supposed to align the onsite days with manager and be available onsite when manager requests) The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy...

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading Pharmaceutical company is hiring a MES Validation Specialist.Rate type: W2 only CommentsMinimum 50% onsite required every week(Candidate is supposed to align the onsite days with manager and be available onsite when manager requests)Bachelor's...

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading Pharmaceutical company is hiring a MES Validation Specialist.Rate type: W2 only CommentsMinimum 50% onsite required every week(Candidate is supposed to align the onsite days with manager and be available onsite when manager requests)Bachelor's...

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading Pharmaceutical company is hiring a MES Validation Specialist.Rate type: W2 only CommentsMinimum 50% onsite required every week(Candidate is supposed to align the onsite days with manager and be available onsite when manager requests)Bachelor's...

Responsibilities: Responsible for providing quality oversight for the qualification and validation activities for equipment, utilities, and facilities. This role will be responsible for drafting, reviewing and approving qualification protocols/reports and any associated documentation in support of CQV activities for a new facility. The Role also needs to...

100% onsite Job Responsibilities: Supports Cell Therapy External Manufacturing with facilitation of service contracts, agreements, purchase orders, approvals and payments as needed, vendor monitoring, and oversight executed from Client ERP systems. Create contract review and approval request in Icertis, contract management system. Create Oracle & Ariba...

Hybrid Role-minimum 50% onsite required Purpose and Scope of Position: This job is part of an organization established to manage our rapidly evolving Cell Therapy business. The Business System Analyst Operational Support will work alongside the Global Business Process Owner (BPO) for Cell Therapy Warehouse & Inventory Management, to support cross-site...

**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. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Piper Companies is currently seeking a QA Document Control Associate for an opportunity in Summit, New Jersey (NJ), to join a global biopharmaceutical company delivering life-saving medicines to patients with serious diseases. Responsibilities of the QA Document Control Associate Manage electronic document system, including document change control and...

Job Description: Quality Systems support within Quality Operations, External Manufacturing. Ensure that Client. products manufactured at external contract manufacturers are manufactured, tested and released according to established Client specifications and the principles of Client directives. In addition ensure effective management of change controls,...

Job DescriptionJob DescriptionIPL is a global leading sustainable packaging solutions provider that manufactures specialty rigid packaging products used in the food, consumer, agricultural, logistics and environmental markets. We shape the future of plastics packaging. We invest in protecting our people, developing future talent, and enabling greater...

At Client, we are inspired by a single vision transforming patients' lives through science. In oncology, hematology, immunology, and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we...

Job Description: The Scientist/Engineer is responsible for leading manufacturing and QC investigation reports in support of S12 CAR T operations. This includes execution of thorough root cause investigations, interviewing personnel, hypothesis testing and interpretation of results, authoring investigation reports, identifying corrective and preventive...

**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. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Position: - Quality-Business Systems AnalystLocation: - Summit , NJ 07901 (50% hybrid)Duration: - 12 MonthsPurpose and Scope of Position:This job is part of an organization established to manage our rapidly evolving Cell Therapy business.The Business System Analyst Operational Support will work alongside the Global Business Process Owner (BPO) for Cell...

Hybrid Role- minimum 50% onsite required Bachelor's degree required Job Description: Hybrid Role-minimum 50% onsite required Purpose and Scope of Position: This job is part of an organization established to manage our rapidly evolving Cell Therapy business. The Business System Analyst Operational Support will work alongside the Global Business Process...

Title: Equipment Commissioning & Qualification (ECQ) Engineer/Equipment Validation Engineer Location: Summit NJ 07901 Duration: 06 Months Comments: 100 % onsite Must Haves: BS in Engineering or Science related discipline required Minimum of 5 years experience performing/supporting activities in a GMP environment. Minimum of 3 years experience in equipment,...

Job DescriptionJob DescriptionIPL is a global leading sustainable packaging solutions provider that manufactures specialty rigid packaging products used in the food, consumer, agricultural, logistics and environmental markets. We shape the future of plastics packaging. We invest in protecting our people, developing future talent, and enabling greater...