Regulatory Affairs Associate — Streamline Global Submissions
Stark Pharma Solutions Inc
Stark Pharma is looking for a detail-oriented Regulatory Affairs Associate to support regulatory activities for medical devices and pharmaceuticals. You will prepare and submit regulatory documentation, maintain compliance, and assist with FDA submissions to ensure adherence to regulatory standards. The ideal candidate will have 1-3 years of experience in Regulatory Affairs and a Bachelor's degree in a related field. Strong communication skills and project management abilities are essential. #J-18808-Ljbffr Stark Pharma Solutions Inc
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Regulatory Affairs Associate — Streamline Global Submissions in Piscataway, NJ vacancy
- Role: Regulatory Affairs Associate Location: United States Duration: Long Term contract Position Summary... ...will assist in preparing regulatory submissions, maintaining regulatory documentation... ...to ensure adherence to FDA and global regulatory standards. Key Responsibilities...SuggestedLong term contract
- ...complex service level expectations. Our global presence with offices in USA (NJ, PA,... .... Job Description Description: The Regulatory Affairs Associate, with minimal guidance prepares,... ...obtaining documents for annual report submissions. Archive and maintain all post approval...Suggested
$168.1k - $268.7k
...As an Associate Director in Regulatory Affairs, Advertising and Promotion at BioNTech,... ...therapies that improve global health. You’ll lead interactions... ...and accurate FDA 2253 submissions for U.S. promotional... ...regulatory inquiries. Develop streamlined processes for...SuggestedHourly payWork at office$193.04k - $289.56k
...to "be an innovative global healthcare company contributing... ...Job SummaryThe Global Regulatory Lead (GRL) is... ...representing Global Regulatory Affairs on the Global Project... ...regulatory activities associated with the registration... ...and health authority submission documents.Serves as...SuggestedDaiichi Sankyo
Basking Ridge, NJ2 days ago$344k - $400k
Title:Chief Pricing Actuary - Global Wholesale and SpecialtyCompany:Everest Reinsurance CompanyJob Category:AnalyticsJob Description:... ...optimization.Monitor emerging market, social inflation, legal, economic, regulatory, and competitive trends and incorporate insights into pricing...SuggestedFull timeEverest Re Group
Warren, NJ1 day ago- ...with large CPA firm experience. The role focuses on corporate tax provisions, ASC 740, and related tax compliance for multi-state and global entities. The ideal candidate will hold an Active CPA (NY) or JD with a law license, bring 4-7 years of progressive tax experience,...
- ...DescriptionResponsibilities:• Author Module 3 submission documentation according to... ...project teams.• The Regulatory CMC Technical Associate may be called upon to... ...to adhere to local and global SOPs to meet pre-... ...pharmaceutical regulatory affairs experience• Strong knowledge...Work at officeLocal areaImmediate start
Artech
Bridgewater, NJ2 days ago - ...looking for a Quality Assurance & Compliance Associate to join our Supply Chain Quality &... ...checks Review test reports, factory submissions, and inspection documents for accuracy... ...Collaboration Coordinate with FOCO’s global offices, including China-based QA teams,...Work at officeWorldwide
FOCO
Piscataway, NJ4 hours ago $124k - $160k
...Regulatory Affairs Project ManagerEstablished in 1806 as a small soap and candle business in New... ..., Colgate-Palmolive is now a truly global company with products sold in over 200... ...oversight of complex global regulatory submissions and ensure the rigorous maintenance of...Hourly payLocal areaWorldwideColgate-Palmolive
Piscataway, NJ2 days ago- ...in the Company's Incentive Plan.BENEFITS INFORMATION:For information on Sysco’s Benefits, please visit We Are:Guest Worldwide is a global collective of dynamic, industry-leading companies with more than 40 years of unparalleled experience serving the unique needs of...Full timeLocal areaWorldwide
Sysco
Somerset, NJ3 days ago - Daiichi Sankyo, Inc. in New Jersey, is seeking a Project Manager for Regulatory Affairs CMC to lead global dossier activities, manage schedules, resources, and risk mitigation across development and commercial products. The role emphasizes collaboration across functions...
- Daiichi Sankyo US in New Jersey seeks a Global Regulatory Lead to shape regulatory strategy for... ...in GPT meetings. You will guide submissions, align regional plans, and ensure Health... ...programs. Required: 7+ years in regulatory affairs with NDA/BLA experience including the...
$141.9k - $284.9k
...leading provider of professional services to the middle market globally, our purpose is to instill confidence in a world of change,... ...excluding internships, you may be eligible for hire as an experienced associate.RSM will consider for employment qualified applicants with...Full timeWork experience placementInternshipWork at officeLocal areaOverseasRSM International
New Brunswick, NJ3 days ago$140.4k - $210.6k
...our 2030 vision to "be an innovative global healthcare company contributing to the... ...Provides insights and/or recommendations to streamline data management information flow,... ...integrity, and timelines with respect to regulatory submissions.Builds business relationships with...Daiichi Sankyo
Basking Ridge, NJ5 days ago- ...Director, Regulatory CMC Legend Biotech is a global biotechnology company dedicated to treating and, one day,... ...Regulatory CMC as part of the Regulatory Affairs team based in Somerset, NJ. Key... ...CMC planning, preparation of submissions, and interaction with Health...Worldwide
Legend Biotech
Somerset, NJ1 day ago $30 - $36 per hour
...Job Description Job Description Job Title: Regulatory Affairs Associate I Position Type: Contract (12+ Months) Location: Clark, NJ 0... ...experience About Us Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment...Contract workWork experience placementIntelliPro Group Inc.
Clark, NJ21 days ago- ...Job Description Role Summary: Responsible for global coordination and preparation of regulatory submission documents/packages for Baxter medical devices. The... ...with medical devices / healthcare regulatory affairs. Knowledge of U.S. and OUS device regulations,...
Katalyst Healthcares & Life Sciences
Avenel, NJ3 days ago - ...worldwide, reporting to the Senior Manager - Capital Projects. This role focuses on safety, quality and innovation while coordinating with global teams. Responsibilities include FEL through Start-Up, front-end loading, budget control, scheduling, and contractor oversight....For contractorsWorldwide
$150k - $258.75k
...searching for the best talent for a **Director, Global Prostate Portfolio Commercial Lead** to... ..., Global Strategic Analytics, Medical Affairs, R&D, Market Access, Operations,... ...competitive implications of technical/clinical/regulatory data.This individual will interact with...Work experience placementLocal areaBiopharma Careers
Raritan, NJ3 days ago$127.28k - $190.92k
...vision to "be an innovative global healthcare company contributing... ...with technical and regulatory standards. This role involves... ...regulatory dossier generation and submission activities as a project manager... ...of experience in regulatory affairs required Project Management knowledge...Daiichi Sankyo
Basking Ridge, NJ3 days ago$90k - $125k
...through strategic partnerships with manufactures from around the world. About the Role The Regulatory Affairs Senior Associate is responsible for managing key regulatory submission activities (e.g., ANDAs and post-approval changes), supporting commercial product...Flexible hours- ...in the Company's Incentive Plan.BENEFITS INFORMATION:For information on Sysco’s Benefits, please visit We Are:Guest Worldwide is a global collective of dynamic, industry-leading companies with more than 40 years of unparalleled experience serving the unique needs of...Full timeContract workWork at officeLocal areaWorldwide
Sysco
Somerset, NJ4 days ago $166.72k - $250.08k
Associate Director, Regulatory Affairs Advertising and Promotion Job Requisition ID: 1826 Posting Start Date... ...2030 vision to \"be an innovative global healthcare company contributing to... ...Guide and support required promotional submissions, including Form FDA 2253, Subpart E...Work at office- RSM US LLP is seeking a Tax Senior Manager for our Global Family Enterprise (GFE) practice. You will manage cross-jurisdiction tax engagements, lead staff, and implement efficient processes to ensure high-quality service. The role emphasizes international tax planning...Work at office
- .../financial flexibility by offering contingent labor as a variable cost.Job DescriptionThis individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual...Work at officeImmediate start
Artech
Bridgewater, NJ4 days ago - DePuy Synthes, a global orthopaedics leader and part of Johnson & Johnson, seeks a Senior Tax Counsel to lead the Tax Counsel group in New Brunswick, NJ. You will report to the Global Head of Tax and guide cross-border and domestic tax strategies during the planned separation...
- ...find your future at Fiserv.We're Fiserv, a global leader in Fintech and payments, and we... ...as a veteran.For incentive eligible associates, the successful candidate is eligible for... ...agencies:Fiserv does not accept resume submissions from agencies outside of existing agreements...Full timeTemporary workH1bWork at officeMonday to Friday
Fiserv
Berkeley Heights, NJ3 days ago - Johnson & Johnson Innovative Medicine seeks a Director, Global Commercial Strategy, Precision Medicine in Raritan, NJ. You... ...influence while aligning with brand teams, Medical Affairs, Market Access, Regulatory and R&D. 20% travel expected. #J-18808-Ljbffr Johnson &...
$140k - $235k
...advisory services. This group is a specialized team within the Global Commercial Bank which serves public and private healthcare companies... ..., facilitating, leading and negotiating with a team of bank associates to solve client problems. Securities Industry Essentials (SIE)...Work experience placementWork at officeLocal areaFlexible hoursShift workDay shift- Johnson & Johnson is seeking a Director, Global Commercial Strategy, Precision Medicine, based in Raritan, NJ. This role leads the design and execution of the global PM strategy in collaboration with cross-functional teams across R&D, Global Brand, and Regions. The ideal...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Associate — Streamline Global Submissions. Be the first to apply!
Related searches
- regulatory contract Piscataway, NJ
- regulatory law Piscataway, NJ
- regulatory scientist Piscataway, NJ
- food regulatory Piscataway, NJ
- regulatory Piscataway, NJ
- medical compliance Piscataway, NJ
- compliance technician Piscataway, NJ
- customs compliance Piscataway, NJ
- compliance team leader Piscataway, NJ
- regulatory affairs assistant Piscataway, NJ