Regulatory Document Control Specialist
ClinLab Solutions Group
ClinLab Solutions Group is seeking a Document Control Coordinator to support documentation processes, maintain document systems, and ensure regulatory compliance for document control and written procedures. The role involves managing archival and destruction of regulated documents and digitizing records in a fast-paced setting. The ideal candidate has a High School Diploma or GED (degree preferred) and 1–2 years of experience in pharmaceutical or FDA-regulated industries, with strong MS Office #J-18808-Ljbffr ClinLab Solutions Group
- ...steadily grow. Job Description Job Description: Reporting to the Document Controls Manager, this position has overall responsibility to support... ...all project standards · Assist in overseeing archiving of regulatory documents in a central repository and ensure/monitor...Regulatory
- ...Document Control SpecialistReporting to the Document Controls Manager, this position has overall responsibility to support all processes... ...systemHelp to develop processes to help ensure archiving of regulatory documents in a central repository and required access and distribution...RegulatoryFor contractorsWork at office
- ...Job Title Document Control Assistant Job Description The Document Control Assistant... ...support documentation compliance. The Specialist will work in a pharmaceutical production... .../audits. Assist validation and regulatory department for documentation and for their...RegulatoryFull timeLocal areaAfternoon shift
- Description The Document Control Assistant is responsible for administering the processes and... ...support documentation compliance. The Specialist will work in a pharmaceutical production... .../audits. Assist validation and regulatory department with documentation and various...RegulatoryAfternoon shift
- ...specifications and methods (internal release, stability, regulatory and compendial), and supporting documents for all client drug products, drug substances,... ...candidate will be to perform content review of change controls including global testing standards and test method...Regulatory
- Amneal Pharmaceuticals LLC in New Jersey seeks a Document Control Assistant to support documentation compliance within a pharmaceutical production facility. You will manage controlled documents, distribute approvals, and maintain training records in collaboration with...
- ...Documentation Specialist III Administers all aspects of the change controls in TrackWise, Document Change Control (DCC) and management of controlled documentation in... ...Quality Documentation and Change Control during regulatory audits. As team lead provides guidance and...RegulatoryWork experience placement
- Merck & Co. is seeking a Document Control Assistant to administer documentation processes in a pharmaceutical production facility, collaborating with QA, QC and Production to ensure accuracy and integrity. You will manage electronic and paper systems, distribute approved...
- Amneal is seeking a Document Control Assistant to support documentation compliance within a pharmaceutical production facility. You will manage document control processes, distribute approved docs, and maintain training records, ensuring accuracy and integrity across electronic...
- ...specifications and methods (internal release, stability, regulatory and compendial) and to support related documents for drug products, substances, intermediates,... .... The role focuses on content review of change controls and associated global testing standards and test method...Regulatory
$38 - $41.8 per hour
Documentation Analyst will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline... ...(dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage...RegulatoryHourly payContract workTemporary workWork at officeLocal area- ...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...
- 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...
$24 - $28 per hour
Overview Document Specialist - must have banking experience Base pay range: $24.00/hr - $28.00/hr Bill Rate: $39.48/hr Work location: Iselin... ...: 1/14/2026 Job Description Summary Reporting to the Credit Control Unit - Unit Head, the staff member is responsible for monitoring...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- ...Summary: Supervise the development, creation, and revision of controlled documentation in accordance with client policies and procedures, current... ...for Quality Documentation and Change Control during regulatory audits. Fulfill the responsibilities and tasks of the Change...RegulatoryContract workLocal areaShift work
- ...disciplinary teams, manages nuclear quality and regulatory expectations, and partners with clients... ..., environmental, licensing, project controls, procurement support, construction/... ...Appendix B, NQA-1, configuration management, document control, records retention) as required...RegulatoryContract workFor subcontractorWork at officeLocal areaRemote workWorldwideFlexible 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...
$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...Work experience placementFlexible hours$63k - $93k
Innophos is hiring a Quality Assurance Documentation Specialist- Supplier Quality in our Cranbury, NJ... ...requirements from a quality or regulatory standpoint. The ideal candidate is a... ...FSMA/FSVP, Food Defense. Preventative Controls Qualified Individual (PCQI) certification...RegulatoryWork at officeLocal areaRemote work- 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...Work at office
- ...supporting regional operations in the areas of Document Management, Quality, Compliance, and SOX... ...managing departmental/Regional Change Control documentation and deliverables to ensure... ...or concentration in Quality Management, Regulatory Affairs, or Operations. Experience and...RegulatoryWork experience placementWork at officeLocal areaImmediate startRemote work
- ...QMS) of Micro. This role ensures compliance with applicable regulatory requirements, industry standards, customer requirements, and... ...target and act on systemic improvements after issues occur. Document Control & Training Maintain document control processes that keep...Regulatory
- Work Location: Middlesex County, Massachusetts Summary: The Document Control Coordinator is responsible for supporting documentation... ...maintaining document systems, and ensuring compliance with regulatory standards for document control and written procedures. Responsibilities...RegulatoryWork at office
- ...Position Summary: We are seeking an experienced Senior Regulatory Affairs Quality Systems Manager to lead FDA 510(k) and CLIA... ...485. Harmonize U.S. and China quality systems. Manage document control, CAPA, training, and audits. Cross-Border Manufacturing...RegulatoryOverseas
$96.8k - $137k
...results.Create/maintain all required R&D documentation to ensure flawless, high quality... ..., registration documents, NODs, change control documents and technical justifications.... ...including those for product development, regulatory and safety.Deliver effective presentations...RegulatoryHourly payLocal areaRelocation$137k - $210k
...consulting, architecture, engineering, project controls, procurement, construction management,... ...and in compliance with the contract documents and project schedule.Additional... ...ensuringcompliance of project activities with legal and regulatory requirements.Oversees startup activities...RegulatoryFull timeContract workFor subcontractorWork at officeVisa sponsorshipWork visaFlexible hoursNight shiftWeekend workDay shiftAfternoon shift$38.55 - $50.53 per hour
...expertise, quality assurance practices, and regulatory compliance standards while... ...Follow proper procedures for reporting and documenting test results, including timely communication... ...values, Perform and document quality control testing according to established protocols...RegulatoryHourly payFull timeTemporary workFlexible hoursShift workDay shift$21 - $26 per hour
...of surplus lines taxes in all states. Key Responsibilities Timely and accurately complete state regulatory surplus lines tax filings Ensure proper documents are received and reviewed from client submission Conduct compliance and quality review on documents,...RegulatoryFull timeRemote work- ...critical in-depth review of all scientific data for Quality Control laboratory documents under general supervision. Area Of Responsibility... ...approved SOP’s, compendia (USP, BP, and EP), ICH, FDA and other regulatory guidances. Ensures that all documents are in compliance...RegulatoryWeekly payFull timeContract workFlexible hours
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