Hengrui USA is hiring : Regulatory Publishing Specialist — 恒瑞-全球精英计划 in Princeton
MediabistroPrinceton, NJ, United States
30+ days ago
Job type
Full-time
Job description
HR Management Trainee | Talent Acquisition at Hengrui Pharmaceuticals
Job Responsibilities
Assist Regulatory Affairs personnel in the preparation and submission of INDs / BLAs / NDAs and life cycle management.
Electronically format and publish electronic documents; builds Regulatory submission deliverables. Ensures quality, accuracy, and submission-readiness per Regulatory agency guidance and specifications, and internal procedures.
Provides guidance on good documentation and submission practices to project teams.
Provides input on submission timelines and eCTD content plans.
Reviews documents to ensure compliance with electronic requirements.
Support archiving (categorizing and classifying information) of Regulatory records pertaining to multiple Regulatory Applications (e.g., IND, BLA, MAA, Annual Reports, AEs), maintaining Regulatory Application indexes, tracking of regulatory submission documents, and special projects as needed.
Identifies and communicates regulatory system enhancement needs or technical issues.
Assist with maintaining Document Authoring Template Library and Template development.
Contribute to miscellaneous regulatory operational activities and special projects as assigned.
Qualifications
BA / BS degree in Life Sciences or related field
1 – 3 years of experience in Regulatory Operations, Regulatory Affairs, or related publishing / technical documentation role
Basic knowledge of regulatory practices, electronic submission guidelines and requirements.
Familiarity with electronic Common Technical Document submission requirements during development, registration and commercialization
Experience working in a cross-functional environment and supporting submission deliverables.
Strong attention to detail, good organization, and collaboration skills.
Ability to manage multiple tasks simultaneously and meet deadlines.
Familiarity with applicable FDA, EMA and ICH guidelines related to regulatory submissions, clinical trials and marketing applications.
Familiarity with eCTD publishing systems, EDMS technology (Veeva Vault preferred), and document authoring tools and templates.
Proficiency in Microsoft Office Suite, Adobe, Excel.
Understanding of regulatory submission content and format requirements.
Understanding of applicable FDA and ICH guidelines related to regulatory submissions.
Clear understanding of regulatory submission content and format requirements.
Experienced in lifecycle management eCTD submissions including but not limited to, IND Safety, IND Investigator submissions and post marketing LCM.
Ability to work both independently and collaboratively in a fast-paced environment.
Detail-oriented with strong organizational and time-management skills.
Strong written and verbal communication skills.
Mandarin language skills a plus; East Coast (U.S.) location strongly preferred for time zone alignment.
Seniority level
Entry level
Employment type
Full-time
Job function
Writing / Editing
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr
Create a job alert for this search
Is Hiring Publishing • Princeton, NJ, United States
Related jobs
Promoted
Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor
Syneos Health / inVentiv Health Commercial LLCBridgewater, NJ, United States
Full-time
Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor.Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.We...Show moreLast updated: 11 days ago
New!
Senior Regulatory Affairs Specialist
Tap Growth aiPhiladelphia, Pennsylvania, US
Full-time
We're Hiring : Senior Regulatory Specialist! 🌟.We are seeking an experienced Senior Regulatory Specialist to ensure compliance with regulatory requirements and guide strategic regulatory decisions....Show moreLast updated: 14 hours ago
Promoted
Senior Manager Regulatory Affairs
VirtualVocationsHamilton, New Jersey, United States
Full-time
A company is looking for a Senior Manager, Regulatory Affairs US Advertising and Promotion - Immunology (Remote).Key Responsibilities Proactively monitors and communicates changes in pharmaceutic...Show moreLast updated: 30+ days ago
Promoted
Regulatory Publishing Manager I
AequorPiscataway, NJ, US
Full-time
Two new Regulatory Manager requisitions are about to go live in the system; one based in Princeton, NJ, and the other in San Diego, CA.
Job Title : Regulatory Publishing Manager I Duties The Manager / ...Show moreLast updated: 30+ days ago
Promoted
Regulatory Affairs Specialist (Hybrid)
Spectrum VascularBridgewater, NJ, US
Full-time
Spectrum Vascular is an innovative medical device company focused on vascular access and medication management.Our mission is to improve the lives of patients worldwide by providing caregivers with...Show moreLast updated: 4 days ago
Promoted
Regulatory & Medical Affairs - Project Manager
Tech DigitalLawrence Township, NJ, US
Full-time
Innovation And Digital Health, Project Manager - Digital Optimization Initiatives.The Innovation Lab team partners with R&D stakeholders to design and deliver innovative analytics solutions that he...Show moreLast updated: 30+ days ago
NantWorks (the "Company") is the parentcompany of various private and public entities that are changinghow we work, live and play.
We focus on three main categories : lifesciences; energy & renewable...Show moreLast updated: 24 days ago
Senior Regulatory and Compliance Specialist
ArdenaSomerset, New Jersey, US
Full-time
Quick Apply
As a leading Contract Development and Manufacturing Organization (CDMO), Ardena partners with pharmaceutical companies of all sizes—from emerging biotech to global industry leaders—united by the mi...Show moreLast updated: 25 days ago
Sanofi is hiring : Global Regulatory Affairs-Advertising and Promotion Excellence
MediabistroConvent Station, NJ, United States
Full-time
Global Regulatory Affairs-Advertising and Promotion Excellence Head page is loaded Global Regulatory Affairs-Advertising and Promotion Excellence Head Job Title : GRA-Advertising and Promotion Ex...Show moreLast updated: 30+ days ago
Promoted
Regulatory Affairs Specialist
VirtualVocationsElizabeth, New Jersey, United States
Full-time
A company is looking for a Regulatory CMC Author.Key Responsibilities Lead the preparation, submission, and maintenance of regulatory documents for clinical trials and drug registration Provide ...Show moreLast updated: 30+ days ago
Promoted
Senior Regulatory Affairs Specialist
VirtualVocationsNewark, New Jersey, United States
Full-time
A company is looking for a Senior Regulatory Affairs Specialist (Remote).Key Responsibilities Author and compile CMC sections of regulatory applications, including INDs, IMPDs, CTAs, amendments, ...Show moreLast updated: 30+ days ago
Novartis Group CompaniesEast Hanover, NJ, United States
Full-time
Novartis has an incredible opportunity for a talented individual to join our team as the Director, Regulatory Affairs Advertising & Promotion.
You will provide strategic regulatory advice on.US orga...Show moreLast updated: 30+ days ago
Promoted
Regulatory Affairs Specialist
Cynet SystemsPiscataway, NJ, US
Full-time
Responsibilities : Utilizing multiple software systems (SAP, Veeva, Excel) to find and record packaging data to place all findings into one document for reference.
Calling out differences from existi...Show moreLast updated: 30+ days ago
At Nestle Health Science, we believe that nutrition, science, and wellness must merge, not collide.Here, we embrace the intrinsic connections of these three pillars, harnessing their collective str...Show moreLast updated: 11 days ago
Promoted
Regulatory Affairs Specialist II
Katalyst Healthcares & Life SciencesNewark, NJ, US
Full-time
Responsibilities : This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.
Europe, support of international product registrations ...Show moreLast updated: 30+ days ago
Promoted
Principal Regulatory Affairs Specialist - Ad Promo
Bausch + LombBound Brook, NJ, US
Full-time
Principal Regulatory Affairs Specialist - Ad Promo.Bausch + Lomb is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the wor...Show moreLast updated: 30+ days ago
Promoted
Regulatory Affairs Specialist III
HireTalentBound Brook, NJ, US
Full-time
Regulatory Affairs Specialist III.Location : Bridgewater, NJ Duration : 9 Months.Manager will consider candidates to be based in either Bridgewater, New Jersey or Cambridge, Massachusetts.Please spec...Show moreLast updated: 30+ days ago
Promoted
Regulatory Specialist
ChubbPhiladelphia, PA, US
Full-time
Chubb’s activities in the United States, and .This role can sit in our Philadelphia, PA or New York, NY offices.Major Duties and Responsibilities : .
Assist in the planning and coordination of adminis...Show moreLast updated: 2 days ago
Promoted
Regulatory Assurance Specialist
ArxadaMorristown, NJ, US
Full-time
A member of a world-class regulatory team focused on regulatory excellence to support and manage supplemental registrations for Arxada and affiliated organizations.
This team member will be ensuring...Show moreLast updated: 13 days ago
Promoted
Regulatory and Medical affairs - Medical Promotional Review Advisor
Tech DigitalMadison, NJ, US
Full-time
Top 3-5 skills you are looking for : Advanced degree experience in medical and / or regulatory affairs clinical background strong organizational and communication skills.
This position reports to the M...Show moreLast updated: 30+ days ago