Regulatory Documentation Specialist
Ipsen Group
Ipsen Group is seeking a Document Specialist in Cambridge, MA to support regulatory submissions and ensure documents are submitted in a Ready For Submission (RFS) format. You will be responsible for training authors and managing eDMS properties. The ideal candidate has over 5 years' experience in a pharmaceutical environment, proficiency with eDMS tools like Veeva Vault, and is fluent in English. The role offers a competitive salary and a comprehensive benefits package. #J-18808-Ljbffr
$91.5k - $134.2k
Ipsen Innovation (SAS) seeks a Document Specialist in Cambridge, MA, to support Regulatory and submission teams in electronic regulatory submissions globally. The role involves ensuring documents are completed to high standards and mentoring authors on compliance with standard...Suggested- ...cost. Job Description Tracking and reviewing change control documentation. Assist with the editing of quality documents (SOP's, guidelines... ..., validation master plans, etc.) to ensure compliance with regulatory requirements. Must be able to work quickly with a high degree...SuggestedWork at officeImmediate start
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$36.06 - $40.87 per hour
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Senior Global Custody Registration Market Specialist The Senior Global Custody Registration Market Specialist is a member of the CAP... ...for markets that require foreign investor registration and/or documentation requirements to open cash and securities accounts. You will liaise...Work experience placementLocal area- ...cost. Job Description Tracking and reviewing change control documentation. Assist with the editing of quality documents (SOP's, guidelines... ..., validation master plans, etc.) to ensure compliance with regulatory requirements. Must be able to work quickly with a high...Work at officeImmediate start
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Tufts Medicine in Boston is seeking a Medical Scribe to support physicians by documenting patient histories, physical exams, and medical procedures in real time. This role is essential for maintaining accurate medical records and improving the efficiency of patient care...$94k - $150k
...Senior Regulatory Affairs Specialist The Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and authorities... ...include coordinating and preparing regulatory submission documents for agencies such as the FDA, Health Canada, EU Competent...Full timeWork at officeImmediate startWork visaRelocation package3 days per week- ...Boston, United States | Posted on 05/20/2026 ATS+Partners is seeking a GDI / Document Intelligence & NLP Specialist who brings verifiable, multi-year experience implementing Intelligent Document Processing and Generative Document Intelligence solutions—ideally for government...Contract workFor contractorsFlexible hours
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...Job Description Job Description Senior International Regulatory Affairs Specialist Company Description Butterfly Network, Inc. (NYSE:... ...participating countries Prepare and manage regulatory submission documentation, integrating cross-functional inputs and supporting...Work at officeImmediate startWork visaFlexible hours2 days per week- ...Responsibilities Create mechanical component and electromechanical assembly drawings with supporting documentation such as component specs and BOMs. Create new drawings in SolidWorks Create BOM in PLM system Create OST item specifications Support ECOs Implement drawing...Contract work
- ...Document Specialist Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic... ...patients and society! The Document Specialist will support Regulatory and submission teams to enable electronic regulatory...Work at officeLocal areaWorldwideFlexible hours
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...bringing deep expertise and a commitment to excellence to every project. Join us to do the best work of your career as a Document Control Specialist at our headquarters in Boston, MA (hybrid schedule - Seaport District with 4-minute walk from South Station). As a...Hourly payFor contractorsWork at officeRemote workFlexible hours2 days per week- ...Role: Document Control Coordinator Work Location: Burlington, MA (Onsite) Schedule: Mon-Fri, 8 AM-5 PM (flexible 7-4 or 9-6) Target Start Date: Immediate Assignment Length: 6 months with possible extension Rate: $22/hr on w2 Managing the archival...Immediate startFlexible hours
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The Principal Specialist of Regulatory Affairs & Compliance provides regulatory expertise on labeling, claims, legal matters, recalls, audits... ..., CFIA audits), packaging and labeling requirements, and documentation to ensure smooth global trade. Monitor and evaluate...$63k - $105k
...hybrid, 2 days a week in the office.POSITION SUMMARYThe Regulatory Affairs Specialist supports MegaFood compliance with U.S. and international... ...considerations).Support development and maintenance of regulatory documentation for ingredients and finished goods.Prepare, submit, and...Fixed term contractWork at officeLocal areaRemote workWork from home2 days per week- Summary This position has responsibility for ensuring regulatory compliance within the areas of the animal care and use program that fall under the responsibility of the IACUC office. Responsible for supporting the implementation and maintenance of the compliance program...Work at officeLocal area
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