Qa jobs in Summit

<p>50% onsite<br/>Work Schedule: M-F (normal business hours)</p><br/><p>The primary responsibility of the Global QA Patients Operations Specialist is to support the Onboarding and Maintenance of Apheresis Centers in Client systems and tools.</p><ol><li&gt

Global QA Patients Operations SpecialistThe primary responsibility of the Global QA Patients Operations Specialist is to support the Onboarding and Maintenance of Apheresis Centers in Client systems and tools.• Provide Global Patient Services (GPS) system general support, data configuration approval

Label Control Specialist (Manufacturing Facility) Responsible for supporting site Label Control activities in accordance with BMS policies, standards, procedures and Global cGMPs. Functional responsibilities include performing in‑process and drug product label printing activities; ensuring accurate

1 00% onsite Job Title: CTO QA Label Specialist Shift: This position is scheduled for Wed- Sat (1 pm to 11 pm). The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the client site, including the coordination, issuance, reconciliation, a

An established industry player is seeking a Global QA Patients Operations Specialist to enhance the onboarding and maintenance of Apheresis Centers. This role involves supporting systems and tools, ensuring compliance, and facilitating effective communication with technical departments across the gl

<h3>Top Skills:</h3><ul><li>2+ years of Document Control & Reporting Experience</li><li>Veeva experience preferred</li><li>Technical troubleshooting</li><li>Self motivated, independent, great communication</li><li>Experience

<p>Hosokawa Micron Powder Systems in Summit, NJ, seeks a Quality Assurance Supervisor to lead quality and process improvements in manufacturing. You will oversee quality systems, ensure ISO 9001 compliance, and support ESG initiatives while driving efficiency.</p><p>The role requir

An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role involves managing an electronic document system, ensuring compliance with policies and procedures, and supporting audits and inspections. The ide

CTO QA Label Control SpecialistThe 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 responsibilities in

Quality Assurance Document Control Associate SpecialistThe Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic rev

An established industry player is seeking a Senior Training Specialist to lead instructional design and training development for computer-based training courses. This full-time role focuses on enhancing the Supply Chain Capabilities portfolio and requires expertise in SAP S4/HANA. The ideal candidat

Quality Systems Support100% onsite 1st shift- Normal business hours Quality Systems support within Quality Operations, External Manufacturing. Ensure that Client Co. products manufactured at external contract manufacturers are manufactured, tested and released according to established Client specifi

Label Control SpecialistThis is a 100% onsite position scheduled for Sun-Wed (6:30 am -4:30 pm). The Label Control Specialist at the S-12 Cell Therapy manufacturing facility supports site Label Control activities in accordance with client policies, standards, procedures, and Global cGMPs. Functional

An established industry player is seeking a meticulous Quality Assurance Label Specialist to support critical document control operations. This role involves ensuring compliance with cGMP regulations and managing the issuance of production labels. You will work collaboratively with production teams

A technology firm in New Jersey is seeking a Data Migration Manager to oversee the data migration product backlog, collaborating with cross-functional teams and utilizing strong expertise in Veeva Vault. The role requires in-depth knowledge of data migration strategies and ETL processes, leadership

Global QA Patients Operations SpecialistThe primary responsibility of the Global QA Patients Operations Specialist is to support the Onboarding and Maintenance of Apheresis Centers in Client systems and tools.• Provide Global Patient Services (GPS) system general support, data configuration approval

Quality Assurance Label Control SpecialistThe 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 responsi

CTO QA Label Control SpecialistThe 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 responsibilities in

Omni Inclusive

Top Skills: - 2+ years of Document Control & Reporting Experience, - Veeva experience preferred - Technical troubleshooting - Self motivated, independent, great communication - Experience working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist

Omni Inclusive

Quality Systems Support 100% onsite 1st shift- Normal business hours Quality Systems support within Quality Operations, External Manufacturing. Ensure that Client Co. products manufactured at external contract manufacturers are manufactured, tested and released according to established Client specif