Cell Therapy QA Document Control Specialist
BioSpace
A leading biotechnology firm in Raritan, New Jersey, is seeking a QA Document Control Specialist to support the document management process within its manufacturing facility. The ideal candidate will have a Bachelor's degree in a related field and at least 2 years of experience in quality assurance or aseptic manufacturing. This position offers a competitive salary and comprehensive benefits package including medical, dental, and paid time off. #J-18808-Ljbffr BioSpace
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Cell Therapy QA Document Control Specialist in Raritan, NJ vacancy
$70.67k - $92.76k
QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating life‑threatening diseases. Headquartered in Somerset, New Jersey, we develop advanced cell therapies across multiple technology platforms. Role Overview The QA...SuggestedWork experience placementFlexible hours$38 - $41.8 per hour
Documentation Analyst will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). This individual will be responsible for delivering CMC documentation (dossier and supporting documents...SuggestedHourly payContract workTemporary workWork at officeLocal area- Amneal is hiring a Document Control Assistant to administer processes supporting documentation compliance in a pharmaceutical production facility in New Jersey. You will work with QA, QC and Production to ensure accuracy, quality and integrity of documentation. Responsibilities...Suggested
- ...Documentation Specialist IIIAdministers all aspects of the change controls in TrackWise, Document Change Control (DCC) and management of controlled documentation in the EDMS (Electronic Documentation Management System) in accordance with policies and procedures. Reviews...SuggestedWork experience placement
Artech
Somerville, NJ5 hours ago - A leading pharmaceutical company in Somerville is seeking an Assistant Document Control to support the management of GMP documentation. This role requires 1 to 3 years of experience in the pharmaceutical industry and a BA/BS degree. Responsibilities include document distribution...SuggestedWork at office
- Amneal is seeking a Document Control Assistant to support documentation compliance within a pharmaceutical production facility. You will manage... ...electronic and paper systems. You will collaborate with QA, QC and Production to keep the Document Control System up to date...
- ...regulatory and compendial), and supporting documents for all client drug products, drug... ...will be to perform content review of change controls including global testing standards and test... ...more areas (e.g. research, analytical/QC, QA, stability, supply chain, manufacturing,...
Bristol-Myers Squibb
New Brunswick, NJ1 day ago - ...Documentation Specialist II Provide administrative support to multiple managers within the Contract Development department by submitting requests/entering key information into multiple applications and files, independently manage and maintain trackers, manage mail merge...Contract workWork at office
Hire Talent
Bridgewater, NJ5 days ago - ...Job Title Document Control Assistant Job Description The Document Control Assistant is responsible for administering the processes... ...and practices which support documentation compliance. The Specialist will work in a pharmaceutical production facility and in close...Full timeLocal areaAfternoon shift
- A healthcare solutions company in New Jersey is seeking a candidate to manage document control processes within their production team. Responsibilities include developing production processes, collecting technical documents, and coordinating activities related to document...
- ...manufactures, and markets in-vitro diagnostics (IVD) tests. Responsibilities Develop and implement production processes related to document control and management Collect and register all technical document, such as drawings and blueprints in the Companys system Review and...
- Description The Document Control Assistant is responsible for administering the processes and practices which support documentation compliance. The Specialist will work in a pharmaceutical production facility and in close collaboration with Quality Assurance, Quality Control...Afternoon shift
- ...partners with many of the leading employers across the country. Feel free to check us out at Job Description Responsible for forensic document storage; coordinates storage and retrieval of forensic data from offsite long term storage, including daily packaging & shipping...
$17 - $21 per hour
A leading consulting firm is seeking an entry-level Data Information / Input Assistant to support their team from home. The role involves updating and verifying data, organizing digital files, and ensuring data privacy. The ideal candidate is detail-oriented and willing...Remote jobHourly pay$52.5k - $84.53k
...administrative support to the Vice President, Quality, Advanced Therapies, as well as the Quality Platform – Advanced Therapies... ...such as SharePoint, Teams, and other collaboration tools for document management and communication. Prepare high‑quality presentations...Work at officeLocal areaImmediate startShift work6062-Janssen Pharmaceuticals, Inc. Legal Entity
Raritan, NJ1 day ago$52.5k - $84.53k
...administrative support to the Vice President, Quality, Advanced Therapies, as well as the Quality Platform Advanced Therapies leadership... ...such as SharePoint, Teams, and other collaboration tools for document management and communication. Prepare high-quality...Work at officeLocal areaImmediate startShift workJ&J Family of Companies
Raritan, NJ3 days ago- ...Documentation Coordinator High school graduate, bachelor's preferred. At least 1 to 3 years work experience in the GmP industry. 1 to 3 year medical/pharmaceutical industry preferred. Data Entry. Medical Terminology. Daily Work Schedule Expectations M-F 7:30 4pm....Work experience placement
Mindlance
Neshanic Station, NJ1 day ago - ...Position Title: Documentation Specialist III Work Location: Branchburg, NJ 08876 Assignment Duration: 3 Months (Possible extension) Work Arrangement... ...: Supervise the development, creation, and revision of controlled documentation in accordance with our organization policies...Local areaShift work
Spectraforce Technologies
Branchburg, NJ4 days ago - Contract QA Data Reviewer job at ProStaff Solutions Inc. New Brunswick, NJ. Are you looking to be a part of a growing pharmaceutical... ...in-depth review of all scientific data for Quality Control laboratory documents under general supervision. Area Of Responsibility Performs...Weekly payFull timeContract workFlexible hours
$22 - $32 per hour
This QA Auditing Reviewer role is responsible for thoroughly auditing production records, determining batch disposition (Release, Hold... ...like JDE while ensuring held or rejected batches are properly controlled and stored. It also logs and loads batch data into required...Hourly payTemporary workLocal areaFlexible hours$790 per week
Get paid for your opinion, one survey at a time. Focus Group Panel matches you with paid online surveys and remote studies from brands you already use. Active members earn up to $790 a week on the studies they qualify for — from home, on their own schedule. No experience...Full timePart timeRemote workFocus Group Panel
Bound Brook, NJ3 days ago- College Achieve Public Schools is seeking an Office Manager Assistant to support the Office Manager, Principal, and leadership team in a 12-month role. The position handles student records, attendance, communications, and front-office operations while delivering exceptional...Work at office
$57k - $82k
...accurate and responsive service while maintaining strong operational controls. This role is part of Everest's Operations organization and... ...ensure that submissions, bind requests, endorsements, policy documents, and related records are processed accurately and within...Full timeShift work- Amneal Pharmaceuticals is seeking a QA Auditing Reviewer to thoroughly audit production records and determine batch disposition (Release, Hold, Reject). The role involves executing decisions in JDE, ensuring proper storage of held/rejected batches, and logging data into...
- ...QA Documentation Clerk We are seeking an organized and detail-oriented QA Documentation Clerk to support our Quality Assurance department... ...lifecycle of standard operating procedures (SOPs) and change controls for required manager approvals and signatures. Audit...Work at office
- ...telephone calls Correspond with customer clearly and effectively, via phone and email Draft correspondences and other formal documents Plan and schedule appointments and events Greet and assist onsite guests Perform all other office tasks Qualifications...Full timePart timeWork at officeMonday to FridayShift work
SC Engineering
Hillsborough, NJ15 days ago - ...administrative support to attorneys in a professional office environment. This is an entry-level opportunity involving data entry, document handling, and general office support. Responsibilities Enter attorney time records accurately and efficiently. Type...Work at office
A great organization!
Bridgewater, NJ4 days ago $55k - $90k
...exposures, loss information, driver information, financials, loss control reports, etc.). Communicates and follows up with broker for... ...all systems accurately reflect updated account information/documentation in accordance with company underwriting guidelines. Interpret...Temporary workLocal areaFlexible hoursMSIG Holdings Inc
Warren, NJ1 day ago$100 per hour
...Committee archives. Role description: Organize and maintain the Co‑op's digital files, including Google Drive materials, historical documents, and organizational records. Volunteers are eligible to receive Co‑op discounts according to volunteer hours, upon receipt of $100...Remote workGeorge Street Co-op
New Brunswick, NJ3 days ago$17.3 - $19.63 per hour
...Secretary, or in a hospital or medical office setting is preferred. Knowledge of medical terminology, electronic medical records, physician order entry, and healthcare documentation is also preferred. RWJBarnabas Health is an Equal Opportunity Employer #J-18808-Ljbffr...Hourly payDaily paidWork at officeShift workAfternoon shiftRWJBarnabas Health
Somerville, NJ2 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Cell Therapy QA Document Control Specialist. Be the first to apply!
Related searches
- quality assurance associate Raritan, NJ
- qa specialist Raritan, NJ
- qa associate Raritan, NJ
- quality assurance specialist Raritan, NJ
- document manager Raritan, NJ
- document analyst Raritan, NJ
- document processing Raritan, NJ
- document Raritan, NJ
- therapy technician Raritan, NJ
- preferred therapy solutions Raritan, NJ