Search Results: 5,957 vacancies
...Job Description
Job Description Overview:
A boutique bankruptcy litigation firm is seeking a temporary Document Reviewer in the tri-state area for contract work. The ideal candidate must have at least one year of experience coding and document review in Relativity...
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The Opportunity
Description
We're looking for an eTMF Reviewer I , working in Pharmaceuticals and Medical Products industry... ..., New Jersey, United States .
Job description:
Reviewing documents for quality review that are in company's eTMF system in the Functional...
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...Title - Documentation Specialist
Duration - 6 months
Location: Branchburg, NJ 08876
Description:
Anywhere b/w 6:30am -8:00pm M... ...the consent, Medical Director decision and final serological review. This is inclusive of but not limited to assessing the chart and...
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Work experience placement
...The Opportunity
Description
We're looking for a Document Control , working in Biotechnology/Medical Devices industry... ...may include filing, copying, and scanning.
Work may include review of documents and the document control flow in the Master Control...
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JOB DESCRIPTION
As the Underwriting Support Coordinator on the Compliance Review Team, you will be assisting the Underwriting Centers by reviewing and managing critical requirement documents relating to home inspections for compliance. The team delivers personalized service...
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Local area
Assistant Document Control needs 1 to 3 years of relevant experience in the pharmaceutical/biopharmaceutical industry
Assistant Document Control requires:
BA/BS degree or equivalent experience is preferred.
1 to 3 years of relevant experience in the pharmaceutical...
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...with the CEO of Gan & Lee Pharmaceuticals USA. The Sr. Manager, Document Management supports all Controlled Document Management at the... ...Policies, Forms and Work Instructions
Knowledge/Regulation:
Review SOPs, Policies, and Work Instructions for compliance with GCP...
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...Job Description:
Job Title Rheumatology Review Group (RRG) Eligibility Liaison
Division R&D / Global Drug Development
Functional Area Description: The RRG Eligibility Liaison (REL) employs scientific and technical expertise to track, coordinate and enforce the...
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Permanent employment
Remote job
Flexible hours
Shift work
...of multiple myeloma.
Legend Biotech is seeking a QC Data Reviewer as part of the Quality team based in Raritan, NJ.
Role... ...•Utilization of electronic systems (LIMS) for execution and documentation.
•Create, review, and approve relevant QC documents, SOP's...
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Work experience placement
Immediate start
Shift work
Night shift
Afternoon shift
Top Skills:
- 2+ years of Document Control & Reporting Experience,
- Veeva experience preferred
- Technical troubleshooting
- Self motivated... ...document approvals, document change control process, periodic review and system reporting.
Duties/Responsibilities:
Primary...
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...of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in Raritan, NJ.
Role Overview
The Quality Assurance Document Control Specialist...
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Work experience placement
Flexible hours
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...Guidance & Assistance, Inc., (SGA), is searching for a
Sr. Documentation Specialist
for a
Contract assignment with one of our premier... ...clients in
Madison, NJ .
Responsibilities :
Review document folders in boxes and sort documents, log/track files,...
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Permanent employment
Full time
Contract work
...Responsibilities
Role and Responsibilities
The Contract Quality Assurance Documentation Associate is responsible for specializing in record keeping.... ...requested
Assist with the site record retention activities:
Review records in storage to identify what needs to be discarded...
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Contract work
...We are offering a contract to hire employment opportunity for a Document Controller in Bridgewater, New Jersey. This role is crucial in... ...entry tasks and manage tasks efficiently
• Compile documents, review them for accuracy, and carry out document scanning activities...
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Contract work
...dedicated individual committed to work under the highest ethics standards for the following position:
* Project Manager for CQV Documentation Project
Qualifications:
* Bachelor's Degree in Science or Engineering.
* Minimum of 5 years of experience in Project...
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Holiday work
Immediate start
Weekend work
Director, Material Review Board and Disposition page is loaded Director, Material Review Board and Disposition Apply locations Summit West - NJ - US time type Full time posted on Posted Yesterday job requisition id R1580665 Working with Us
Challenging. Meaningful. Life...
Full time
Remote job
Flexible hours
Shift work
Monday to Friday
...Job Description
Job Description Job Title: Document Coordinator II
Pay Range: $20-$22/hr
Contract: 6-month W2 contract (potential... ...the consent, Medical Director decision and final serological review.
This is inclusive of but not limited to assessing the chart...
Holiday work
Contract work
Temporary work
Work experience placement
Monday to Friday
Sr. Manager, Global Document Control and Records Management - Just Evotec Biologics (Field Based)
Just-Evotec Biologics (JEB) is seeking... ...process owners (BPOs) and Subject Matter Experts (SMEs) to review written procedures in order to create document management structure...
Remote job
Holiday work
Temporary work
Flexible hours
...Registry Cards. Working with other departmental personnel, the document coordinator will maintain and file records, as well as... ...Quality Assurance, and Quality Control, to complete the process of reviewing, logging, and filing documents.
· Ensure accurate entry of the...
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Contract work
Local area
...performance of the QA team that coordinates and leads the Material Review Board (MRB) meetings for commercial and clinical products... ...of any risks or delays to product release.
Approves post MRB documentation in the Quality Management System.
Oversees and approves procedures...
Remote job
Flexible hours
Shift work
Monday to Friday
