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
- ...leading staffing solutions provider in New Jersey is seeking a Regulatory Affairs Associate to prepare and submit annual reports to the FDA. The... ...industry. Key responsibilities include coordinating submissions and maintaining regulatory databases. Strong communication...Suggested
$256.07k - $336.1k
Legend Biotech is a global biotechnology company dedicated to treating and, one day... ...across Research, Clinical Development, Regulatory Affairs, Translational Sciences, Technical... ...and alignment for INDs, CTAs, BLA/MAA submissions, and lifecycle management activities....SuggestedPermanent employmentFull timeTemporary workFor contractorsLocal areaWorldwideFlexible hoursLegend Biotech USA, Inc.
Somerset, NJ11 days ago- ...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
- 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
$166k - $203k
...Position Summary The Associate Director, Regulatory Affairs (Advertising and Promotion) will have accountability... ...will be responsible for all submission types made to OPDP/APLB (FDA). The... ..., Medical Affairs, Legal, Global Regulatory Affairs, Labeling and Compliance...SuggestedWork at officeLocal areaWorldwideBiontech
Berkeley Heights, NJmore than 2 months ago- The Musculoskeletal Transplant Foundation in Edison, NJ, is seeking a Regulatory Affairs Manager to oversee regulatory submissions, inspections, and audits. This role includes managing the Regulatory Affairs team, budget, and compliance with U.S. and international regulations...
$178k - $307.05k
...Johnson MedTech is hiring a Sr. Director, Regulatory Law in New Brunswick, NJ. This role... ...providing expert legal counsel on U.S. and global regulatory law for DePuy Synthes. The position... ...multiple teams to support regulatory submissions and compliance. Candidates should have 1...- Amneal Pharmaceuticals is seeking a Regulatory Affairs Specialist to assist with high-quality regulatory submissions to the FDA, ensuring alignment with timelines and guidelines. The role leads regulatory activity on cross-functional teams across Clinical, CMC, Quality...
$80k - $96k
...Edison, NJ is looking for a dedicated professional to handle FDA regulatory compliance and documentation. In this hybrid role, you will... ..., oversee project compliance, and assist teams in regulatory submissions. A Bachelor’s degree in a science-related field and three...$80k - $96k
Musculoskeletal Transplant Foundation is seeking a Regulatory Affairs Specialist responsible for ensuring compliance with regulatory requirements... ...of regulations and assist in documentation for FDA submissions. This hybrid role requires commuting to NJ and Jessup, PA,...- IEEE and its members rely on robust tax management to sustain its non-profit operations. The Associate Tax Accountant will support the Tax Management team with US and global jurisdictions as they pertain to IEEE's operations. Primary responsibilities include tax reporting...
$86.9k - $121.88k
...patient anatomy.The company has over 1,250 associates around the world with manufacturing... ...products driving the growth of the business globally. Associates are part of a stimulating... ...data collection, validation, and submission, ensuring timely and compliant reporting...Contract workTemporary workLocal areaImmediate startWorldwideFlexible hours- ...and international import/export compliance, managing the full customs clearance lifecycle and ensuring accurate documentation for global shipments. The ideal candidate will have 5-7 years in international logistics or trade compliance, experience with HTS, CBP, EAR, and...
$124k - $174k
...We AreColgate-Palmolive Company is a global consumer products company operating in... ...brighter, healthier future for all.As the Regulatory Affairs Project Manager, you will lead the... ...oversight of complex global regulatory submissions and ensure the rigorous maintenance of...Hourly payLocal areaRelocation$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...Full time$109.6k - $155k
...Jersey, United StatesWho We AreColgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing... ...'s build a brighter, healthier future for all. As the Manager/Associate Manager, Global Commercial Services and Marketing Procurement,...Hourly payContract workLocal areaWorldwideRelocation package$122k - $212.75k
...best talent for a Senior Manager, Health Care Compliance Officer, Global Functions for the Innovative Medicine business with... ...and highly regulated environment, translating evolving legal, regulatory, and policy requirements into clear, practical, and actionable...Local areaImmediate start$117k - $120k
AMNEAL PHARMACEUTICALS Regulatory Affairs Specialist: With minimal supervision assists with the preparation of high-quality regulatory submissions to the Food and Drug Administration (FDA) as required, within company timelines and in accordance with regulatory guidelines...For contractorsLocal area- ...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
- Breckenridge Pharmaceutical, Inc. is seeking a Regulatory Operations professional to oversee FDA eCTD submissions, NDAs, INDs, ANDAs and related documents, ensuring timely, compliant publishing. You will develop and maintain templates, track regulatory records, and collaborate...Flexible hours
- Spectraforce is seeking an Import/Export Specialist in South River, NJ to support domestic and global shipment logistics for RSCR. The role requires coordinating shipping documentation, regulatory paperwork, and end-to-end tracking from initiation to shipment clearance. The...
$110.71k - $145.3k
Legend Biotech is a global biotechnology company dedicated to treating... ...is seeking a Manager, Regulatory Project Management as part of... ...Research, CMC, Quality, Regulatory Affairs, Clinical Operations, and... ...New Drug (IND) submissions and other regulatory filings....Permanent employmentFull timeContract workTemporary workFor contractorsWork at officeLocal areaWorldwideFlexible hoursLegend Biotech USA, Inc.
Somerset, NJ12 days ago$79k - $127.65k
...Jersey, United States of AmericaJob Description:The Johnson & Johnson Family of Companies is recruiting for a Senior Financial Analyst Global Finance, to join the team in New Brunswick, NJ.At Johnson & Johnson, we believe health is everything. Our strength in healthcare...Full timeLocal areaImmediate start- ...Pharmaceutical, Inc. in Berkeley Heights, NJ, seeks a Senior Associate, Regulatory Operations to lead US regulatory submissions to the FDA, maintain eCTD templates, and ensure... ...skills and 5+ years in pharma regulatory affairs, with 3-4 years in regulatory operations....
- Colgate-Palmolive, a global consumer products company, is seeking a Manager Global Apps M&A to translate executive strategy into IT integration execution. You will oversee day-to-day IT integration projects for mergers and acquisitions, liaise with Global M&A teams, and...
$124k - $174k
...United States Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing... ...projects to drive savings and validate network changes. Streamline operations by evaluating requests, refining business value, and...Hourly payLocal areaRelocation packageColgate-Palmolive Company
Piscataway, NJa month ago- ...firm is seeking a Product Manager with extensive experience in regulatory submission processes and health authority queries. The role requires... ...will be preferred, especially those familiar with TransPerfect Global Link Enterprise. This position offers the chance to support...
$102k - $177.1k
...life while championing patients every step of the way. Learn more at We are searching for the best talent for a Finance Manager - Global HR, located in New Brunswick, NJ. Purpose: The Finance Manager serves as a strategic finance business partner supporting Global...Work at officeLocal areaImmediate startFlexible hours3 days per weekJohnson & Johnson Innovative Medicine
New Brunswick, NJ1 day ago$124k - $155k
...We Are Colgate-Palmolive Company is a global consumer products company operating in... ...offers an exciting opportunity to drive regulatory compliance, technical excellence, and data... ...technical documentation prepared for submission to external regulatory agencies Partner...Hourly payLocal areaWorldwideRelocationColgate-Palmolive Company
Piscataway, NJa month ago$80k - $96k
...Regulatory Affairs Specialist MTF Biologics processes tissue grafts from human donors that... ...affecting lives across the globe. As a global nonprofit organization that saves and... ...will be incorporated into regulatory submissions to assure scientific rigor, accuracy,...Temporary workWork at officeLocal areaMonday to FridayFlexible hoursShift workMTF Biologics
Edison, NJ17 hours ago
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
- compliance coordinator Piscataway, NJ
- regulatory specialist Piscataway, NJ
- compliance associate Piscataway, NJ
- risk and compliance analyst Piscataway, NJ
- regulatory officer Piscataway, NJ
- compliance specialist Piscataway, NJ
- compliance officer Piscataway, NJ
- regulatory affairs specialist Piscataway, NJ
- coding compliance specialist Piscataway, NJ
- healthcare compliance officer Piscataway, NJ