Quality - Quality Records Specialist

Job Title: Quality Records Specialist Duration: 12 Month Contract (Possible extension based on work performance) Location: Summit, NJ 07901 Onsite Position Work Schedule: Mon - Fri, Business Hours ABOUT ROLE: Must Haves: - 1+ years in Cell Therapy - 1+ years in biomanufacturing - 1+ years in biotherapeutics - 1+ years in QA/QC PURPOSE AND SCOPE OF POSITION:...

Quality Assurance Specialist50% onsite 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. Primary responsibilities include the review of cGMP controlled documents such as SOPs, specifications, completed batch records,...

50% onsitePURPOSE 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. Primary Responsibilities include the review of cGMP Controlled Documents such as SOPs, specifications, completed batch records, material disposition, and manages...

Specialist R&D Quality & ComplianceThe 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 scientific practice, Current Good...

Job Description: 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 are operating in full compliance with sound scientific practice, Current Good...

CTO QA Label SpecialistThis position is scheduled for Sun-Wed (5:45am to 3:45pm). This is a 100% onsite position. The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the client site, including the coordination, issuance, reconciliation, and management of production labels and records. To support...

CTO QA Label Specialist100% Onsite Job Title: CTO QA Label Specialist Number of Positions: 2 Shift: This position is scheduled for Wed-Sat (8 pm - 6 am) Location: US-NJ-Summit West, S12PURPOSE AND SCOPE OF POSITION: The Quality Assurance Label Control Specialist at the S-12 Cell Therapy manufacturing facility is responsible for supporting site Label Control...

Job Description: This is a 100% onsite position.This position is scheduled for Sun-Wed (6:30 am -4:30 pm).PURPOSE AND SCOPE OF POSITION:The 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....

An established industry player is seeking a Project Management Specialist to support a cutting-edge cell therapy facility. This role involves executing project activities, collaborating with various departments, and ensuring projects are completed within quality metrics and timelines. The ideal candidate will have a strong background in project management,...

CompensationAverage weekly gross $1600.00 Run DetailsMulti-run positionHometime varies from multiple times a week to home weekly for a restartWork week can consist of: Local Chicagoland, Regional, Dedicated, and Intermodal Up to a 6-day work week to maximize your 70 hoursOut and back runs along with reloading back to the Chicago MarketLanes of operation...