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
- 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
$150k - $258.75k
...Director, Health Care Compliance Officer, Global Functions, for the Innovative Medicine... ...informed guidance. Assess emerging risks associated with strategic growth initiatives,... ...required. 5+ years of compliance experience (Regulatory, Quality, Compliance, Legal). 2+ years of...SuggestedFull timeLocal areaImmediate start$96.5k
...remarkable impact on people's lives. As a Global Trade Compliance organization, we are... ...classification requests for government submissions, ensuring accuracy and thoroughness.... ...tracking, interpreting, and communicating regulatory and legislative updates to GTC stakeholders...SuggestedTemporary workLocal areaWorldwide- brobstongroup.com - Jobboard is seeking a Specialist, Customs Compliance to manage U.S. import/export and customs regulatory compliance in Piscataway, NJ. This hybrid role requires collaboration with legal and supply chain teams, focusing on compliance for fashion and...Suggested
$122k - $212.75k
...Overview Senior Manager, Global Transparency Reporting... ..., industry, and regulatory disclosure requirements... ...generation, and timely submission. Ensure adherence to all... ...and industry/trade association codes. Collaborate with Legal, Government Affairs, and HCC leadership to...Local areaWorldwide- A leading luxury brand is seeking a Customs Compliance Specialist in Piscataway, NJ. This role involves ensuring regulatory compliance across various divisions and requires a minimum of three years of experience in customs compliance. The ideal candidate should possess...Work at officeRemote work3 days per week
- ...Legend Biotech is a global biotechnology company dedicated... ...safety, efficacy, and regulatory compliance of the... ...trials, regulatory submissions, and product commercialization... ...with Regulatory Affairs to interact with... ...regulatory complexities associated with the commercial stage...Permanent employmentFull timeTemporary workFor contractorsLocal areaWorldwideFlexible hours
$184.09k - $223.08k
Director, Global Customs & Trade Compliance (New Brunswick, NJ) Responsibilities Strategic Leadership: Influence and execute the strategic direction for global customs compliance. Process Optimization: Standardize and optimize global trade activities, policies, and procedures...$95k - $143k
...A publicly traded global specialty chemicals and advanced materials manufacturer is adding an Engineering Project Manager to drive its engineering, scale-up, and capital projects across North America and Europe. You own projects end to end, on scope, on schedule, and...- ...is seeking a Director, Technology Product Group Leader for Submission Excellence. This role involves overseeing the development, engineering, and global operationalization of solutions to accelerate regulatory submissions. The ideal candidate will have extensive experience...
$184.09k - $223.08k
Scorpion Therapeutics is seeking a Director of Global Customs & Trade Compliance in New Brunswick, NJ. This role requires 10+ years of progressive experience in global trade compliance, preferably within the biopharma industry. The successful candidate will oversee the...- Hobbsnews is seeking a Director, Commercial Technology to lead the global CRM strategy and implement sales planning technologies. This position will oversee critical technology strategies ensuring data-driven decision-making and operational efficiency across the commercial...
- ...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...
$109.6k - $155k
...Associate Manager/Manager, Global Commercial Services and Marketing Procurement Established in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries and territories under such...Hourly payContract workLocal areaWorldwideRelocation package- ...instructional design, facilitation, and project management. Responsibilities include managing logistics for learning events and supporting AI-related initiatives. IEEE offers an opportunity to influence the professional growth of a global organization. #J-18808-Ljbffr IEEETemporary work
$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 placement- ...with established products and an entrepreneurial mindset. Role Description: dThe Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory submissions and compliance activities to ensure medical device products meet applicable regulatory...InternshipWork at officeWorldwide
$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...Work at officeLocal areaWorldwide$54 - $80 per hour
Manager - Securities Compliance QA (Global Banking ) We are the leading provider of professional... ..., and surveillance programs. Validate regulatory compliance with SEC, FINRA, Reg BI, Form... ...be eligible for hire as an experienced associate. RSM will consider for employment...Hourly payTemporary workWork experience placementInternshipLocal area- ...looking for a Quality Assurance & Compliance Associate to join our Supply Chain Quality &... ...quality checks Review test reports, factory submissions, and inspection documents for accuracy... ...reviews Coordinate with FOCO’s global offices, including China-based QA teams,...Work at officeWorldwide
- Vita Global Sciences, a Kelly Company, is seeking a full-time Program Manager for a long-term engagement in New Brunswick, New Jersey... ...across various teams, leading program delivery within Clinical Affairs, and managing stakeholder relationships. The ideal candidate has...Full time
- ...Myers Squibb is seeking a Manager for CMC Documentation & Specifications in New Brunswick, NJ. This role entails authoring CMC regulatory submissions, collaborating closely with various departments to ensure timely filings. The ideal candidate will have a degree in a...Flexible hours
$94k - $151.8k
...Description: Johnson & Johnson is recruiting for a Sr. Analyst Global Strategic Insights to join our MedTech Surgery business... ...functional collaboration and alignment on projects, resulting in streamlined workflows, improved communication, and timely project delivery...Temporary workLocal area$165k - $220k
...NYSE/TSX: BLCO) is a leading global eye health company... ...the globe. We have long been associated with many of the most significant... ...future. The Director, Regulatory Affairs leads global regulatory strategy... ..., ensure highquality submissions, and manage regulatory risk...Temporary workWork visa$174.73k - $262.1k
Element Solutions seeks a Director of Engineering Project Management to lead global teams in driving key engineering projects across multiple business units. The role requires over 8 years of leadership experience in project management and a deep understanding of the electronics...$72k - $118k
...in the governance of this data and the associated processes and procedures around its creation... ...initiatives both in the Americas and globally, playing an active role with... ...any source other than candidates. The submission of unsolicited resumes by recruitment or...$50k - $60k
Job Description Job Description Position Description: The position requires that you learn and completely understand all company policies, as well as state and federal laws relating to employers in the state of New Jersey. You will be responsible for the safety knowledge...Temporary workWork at officeLocal area- ...is seeking a Manager for CMC Documentation in New Brunswick, NJ. The role involves compiling and authoring CMC sections of regulatory submissions, coordinating with various teams to ensure timely document delivery. Ideal candidates will have a degree in organic chemistry...Flexible hours
$172k - $250k
...of Information Security Audit & Compliance to lead and scale a global audit and compliance practice. This role will be responsible for... ...NIST 800-53. The ideal candidate combines deep audit and regulatory expertise with strong operational leadership, enabling the organization...InternshipSeasonal workWork at officeLocal areaFlexible hours3 days per week
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