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Internal Title: Expert Science & Technology. We are currently looking for an Expert Science & Technology to join our team and help us deliver high-quality solutions that supports the management of data, analytical equipment and computerized system specialist. Your Role: As the Expert Science & Techn

The Project Specialist provides project management support ensuring projects are executed within established quality metrics, budgets, and timelines.

PURPOSE AND SCOPE OF POSITION (Position Summary): The Quality Assurance Specialist position plays a key role in supporting the cGMP quality operations for the Vector External Manufacturing.

Position summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP document control operations for the Client Cell Therapy Above. Quality Assurance Document Control Associate Specialist. Top skills: 2+ years of document control and reporting experience, Veeva expe

The Global Supplier Quality, External QC - Vector will process external deviation and change records from our Contract Test Laboratories (CTL).

Actual Position Title: Onboarding Specialist, CAR T.Location: Cell Therapy Operations Summit, New Jersey.Purpose And Scope Of Position: This role is responsible for working on New Hire Orientation Program (NHOP) for the Summit West Cell Therapy Operations organization, as well as the accurate and ti

Normal business hours Quality Systems support within Quality Operations, External Manufacturing.Client specifications and the principles of Client directives.In addition ensure effective management of change controls, prod.

We are seeking a skilled and compassionate Part-Time Psychiatric Specialist to join our committed healthcare team. Sun River Health is dedicated to providing high-quality, affordable healthcare to underserved communities. Become part of our award-winning network of care committed to improving the he

Job Title: CTO QA Label Specialist Job Description: The Specialist Quality Assurance Label Control supports the cGMP Label Control operations for the client site, including the coordination, issuance, reconciliation, and management of production labels and records.

Specialist R&D Quality & Compliance.The Specialist R&D Quality & Compliance (R&D Q&C) is responsible for the administration of integrated and comprehensive quality systems and controls that are appropriate, effective, efficient and continuously improving in order to ensure that R&D functions.

Medical Information Specialist is responsible for meeting the medical information needs of internal and external Eisai customers as it relates to the companys products. Medical Information Specialist. The incumbent will contribute to the development of high-quality Medical Information deliverables w

Responsibilities: Review QS (Quality Systems) records in Track wise to ensure completion and compliance with internal procedures and applicable regulatory requirements.Monitor On-Time Closure of QS records.Follow up timely closure of QS records due for the week.Serve as a point of contact for QS rec

Global Product Quality Specialist. Position Summary: The Global Product Quality Specialist will be responsible for managing and owning documentation and change controls associated with key deliverables to clinical and commercial documentation across multiple programs.

Purpose And Scope Of Position: Individual contributor to packaging and labeling materials project management, strategic and tactical change planning and forecasting of new product markets and indications launches to ensure the Cell Therapy Operations organization meets its performance goals. Special

Associate Specialist, Quality Product Release-Disposition.

Ultrasound Specialist, Per Diem. The compensation offered to the candidate selected for the position will depend on several factors, including the candidate's educational background, skills and professional experience. In addition, the individual must be prepared to render quality patient care by ex

In addition, you will lead regional quality programs; share best practices among manufacturing sites through quality benchmarking; manage special situations and early warnings with respect to plant investigations, root-cause analysis, and follow-up to protect Mondel?z International and our consumers

Specialist R&D Quality & Compliance.The Specialist R&D Quality & Compliance is responsible for the administration of integrated and comprehensive quality systems and controls that are appropriate, effective, efficient and continuously improving in order to ensure that R&D functions are operating in

The Specialist R&D Quality & Compliance is responsible for the administration of integrated and comprehensive quality systems and controls that are appropriate, effective, efficient and continuously improving in order to ensure that R&D functions are operating in full compliance with sound scientifi

The Food Safety & Regulatory Compliance Specialist in the food industry is responsible for policy creation and implementation of the programs for food safety, and to ensure compliance of regulatory standards and 3rd party certifications. Food Quality/Safety/Regulatory space (food manufacturing highl

Quality Assurance Label Control Specialist.The Quality Assurance Label Control Specialist at the S-12 Cell Therapy manufacturing facility is responsible for supporting site Label Control activities at S-12 in accordance with client policies, standards, procedures, and global cGMPs.Functional respons

Training Specialist, Instructional Design & Systems Training.Important Note: We might need to open this up for Hybrid/remote workers (if approved for exception, waiting for it from management), so please go ahead and submit candidates for Hybrid/remote as well.Initial review would be given to on-sit

Join a Global Leader in Workforce Solutions.Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+.Our mission? To bridge the talent gap with precision.

The QA Shop Floor Specialist is responsible for quality oversight of Manufacturing Operations in accordance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP.

Specialist, QA Shop Floor - Summit, NJ. The QA Shop Floor Specialist is responsible for quality oversight of Manufacturing Operations in accordance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP.

Establishing data entry standards by continually updating filing systems to improve data quality. We are looking to hire a dynamic data entry specialist to join our company's administrative department. At least 1 year of experience working as a data entry specialist.

We have an opening for a talented Costco Inventory Control Specialist to work collaboratively across teams and departments, coordinate tasks to ensure deadlines are met, and manage daily responsibilities with a focus on quality and efficiency.

Senior Specialist, Quality Engineer. Ability to work effectively on a team yet maintain professional Quality independence. AS 9100/ISO 9001 quality system experience.

The Life Science Quality Assurance Specialist Ii is a mid-level quality professional responsible in maintaining, quality system processes and programs to include: Supplier Quality, Investigation Systems, Quality Event Reporting (Deviations, Nonconformance, Change Management, Capa) management, traini