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- Legend Biotech is seeking Document Control Specialist as part of the Quality team based in Raritan, NJ . Role Overview The QA Document Control Specialist role is an exempt level position with responsibilities for supporting the document management process within a cell...SuggestedTemporary workWork experience placementWork at officeWorldwideFlexible hoursShift work
- A biotechnology company in Raritan, NJ, is looking for a Document Control Specialist to manage document compliance and labeling in a GMP environment. The ideal candidate will have a Bachelor’s degree and at least 2 years of relevant experience, especially in a cGMP setting...Suggested
$66.06k - $86.71k
...of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking Document Control Specialist as part of the Quality team based in Raritan, NJ . Role Overview The Quality Assurance Document Control Specialist...SuggestedPermanent employmentFull timeContract workTemporary workWork experience placementWork at officeLocal areaWorldwideFlexible hoursShift workDay shift- A biotechnology company is seeking a QA Document Control Specialist I/II/III in Raritan, NJ to support document management in a GMP environment. The ideal candidate will have a Bachelor's degree in a relevant field and at least 2 years of related experience, preferably...SuggestedAfternoon shift
- A biotechnology company in Raritan, NJ is looking for a Document Control Specialist to manage and support the document management process in a GMP environment. The role involves reconciling GMP documents, creating logbooks, and ensuring the compliance of document storage...Suggested
$66.06k - $86.71k
A biotechnology firm based in Raritan, NJ seeks a Document Control Specialist for its Quality team. This role will support the document management process within a sterile GMP environment, ensuring compliance with procedures and documentation requirements. Candidates should...Suggested- 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
- A biotechnology company in Raritan, NJ is seeking a Document Control Specialist to support document management in a GMP environment. The ideal candidate should have a Bachelor's degree and at least 2 years of experience in a cGMP facility. Responsibilities include ensuring...Suggested
$70.67k - $92.76k
A leading biotechnology company in Raritan, NJ is seeking a QA Document Control Specialist I/II/III to support the document management process within a sterile GMP environment. The specialist will ensure compliance with global and site procedures and manage documentation...SuggestedFull time$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...SuggestedWork experience placementFlexible hours- 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...Suggested
- A global biotechnology company is seeking a QA Document Control Specialist I/II/III in Raritan, NJ. This role involves ensuring compliance with GMP documentation processes, supporting both clinical and commercial activities. Candidates need a Bachelor's degree and at least...SuggestedFull timeShift work
$70.67k - $92.76k
...both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QA Document Control Specialist I/II/III as part of the Quality team based in Raritan, NJ. Role Overview The QA Document Control Specialist role is...SuggestedPermanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaWorldwideFlexible hoursAfternoon shift- A biotechnology company is seeking a QA Document Control Specialist I/II/III in Raritan, NJ. This role involves ensuring compliance within document management in a sterile GMP environment. Candidates should have a Bachelor's degree in a relevant field and a minimum of...SuggestedAfternoon shift
- ...160 countries and regions. As part of our ongoing expansion in North America, we are seeking a meticulous and organized Document Control Specialist to manage our documents to ensure compliance with company policies, industry standards, and legal requirements. The...SuggestedWork experience placementWork at officeFlexible hours
- ...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 work
- ...their fields. This has helped us expand into new sectors and steadily grow. Job Description Job Description: Reporting to the Document Controls Manager, this position has overall responsibility to support all procedures, processes and systems of the administered plan...
- ...following: Creation of PI sheets in the ERP system and obtaining serological test results via email, Fax and tissue portal. The Documentation Coordinator is required to verify and cross-reference applicable TRP paperwork and labels against the ERP system and RFID label....Work experience placementRelocation
- ...About the job Document Controller Company Overview The Company develops, manufactures, and markets in-vitro diagnostics (IVD) tests. Responsibilities Develop and implement production processes related to document control and management Collect...Relocation package
$24 - $28 per hour
Overview Document Specialist - must have banking experience Base pay range: $24.00/hr - $... ...Description Summary Reporting to the Credit Control Unit - Unit Head, the staff member is... ...to time. Job Details Seniority level: Associate Employment type: Temporary Job function:...Temporary workWork at officeRemote workWork from homeMonday to Friday$24 - $28 per hour
A financial institution in New Jersey is seeking a Document Specialist to monitor daily operations in the Credit Control Unit. Candidates must have a Bachelor's degree and 5-10 years of experience in corporate banking documentation. The role involves supporting Vault Custody...Remote work$21.5 - $24 per hour
...Job Summary: The Document Workflow & Mailing Operations Specialist is a key operational role responsible for coordinating daily... ...status/risk updates to leadership. Familiarity with SLA/quality controlled operations and regulated environments. Education and...Hourly pay- ...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...
- ...Job Description: Implement, control and coordinate changes in documentation. Facilitates the updating and routing of controlled documents, including, but not limited to, Governance and Procedure documents, Master Forms and Master Batch Records within the eDMS....
- ...seeking an Executive Recruiter for a 12-month contract primarily remote, based in Princeton, NJ. The role involves supporting GxP document management initiatives, facilitating project plans, and providing audit support. Ideal candidates will have a bachelor’s degree in...Remote jobContract work
- A medical technology company in New Jersey is seeking a Document Control Specialist to manage company documents and ensure compliance with policies and regulatory standards. The ideal candidate will possess strong organizational skills, attention to detail, and experience...
- 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...
- Job Title Are you open to look at candidates willing to relocate at their own expense? No Onsite - 100% What are the top 3-5 skills, experience or education required for this position? High school graduate, bachelors preferred. At least 1 to 3 years work experience ...Work experience placementRelocation
- A leading global staffing firm is seeking a Coordinator in Pennington, NJ. The role involves supporting teams with administrative and organizational tasks, including managing travel reports, tracking purchase orders, and preparing reports. Ideal candidates will have a strong...
- ...working 8 hours per day. Education: HS/GED. Experience: Knowledge of filling systems. We are looking for an organized, detail-oriented Documentation professional to perform file management (hard copy files and electronic files), data entry,... Abacus Service CorporationFlexible hoursShift work

