Regulatory Affairs Specialist-V
Artech Information Systems LLC
Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/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 updates, NDA annual reports, PBRERs). With oversight and guidance, contributes to the generation of product regulatory strategy documents (for products in phase 1-3 clinical development), labeling updates for marketed products, generation of FDA meeting requests and corresponding briefing materials, and other tasks as needed. Skills: Working knowledge of FDA and ICH requirements for standard regulatory documents and their maintenance. Excellent written and verbal communication skills, with ability to organize and manage multiple priorities. Proficiency in MS Word, Excel, and PowerPoint. Self-starter with the ability to work independently but seeking out guidance as needed. Technical aptitude to work across multiple information systems and databases with ability to troubleshoot. Sense of urgency and perseverance to achieve results. . QualificationsBachelor s degree and at least 5 years in Regulatory Affairs or relevant industry experience, or Master's, PharmD, PhD degree and 3 years in Regulatory Affairs or relevant industry experienceAdditional Information Sneha ShrivastavaTechnical Recruiter (Clinical/Scientific)Artech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: View phone number on click.appcast.io | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: ResearchExperience level: ExecutiveIndustry: Pharmaceuticals
- ...both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical... ...Master s Degree a plus• 4+ years of pharmaceutical regulatory affairs experience• Strong knowledge of NDA, ANDA, MAA, BLA, CTA, or...SuggestedWork at officeLocal areaImmediate start
- ...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 specify on resume which location candidate is being submitted for....SuggestedWorldwide
- ...Job Title: Regulatory Affairs Specialist Duration: 12 months, potential extension Remote Preferred Ideal Locations: Rochester, NY, Clearwater, FL, St Louis, MO, or Bridgewater, NJ Day shift- Monday to Friday must be available to work EST hours Description:...SuggestedWork at officeRemote workMonday to FridayDay shift
- ...dignity of our employees and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category:... ...searching for the best talent for a Senior Regulatory Affairs Specialist to support our Instrumentation & Accessories team under the...SuggestedFull timeLocal areaImmediate startRemote work
- ...dynamic and growing team 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...SuggestedInternshipWork at officeWorldwide
- ...the strategic priorities that impact the near term and long term priorities of Client's development program.s Alignment with Medical Affairs for global strategic study placement decisions is also expected for phase 3 programs. To better serve some customers experience or...Local areaImmediate startFlexible hours
- ...accountability and commitment.Strong knowledge of international good clinical practices (ICH) and thorough understanding of current regulatory requirements (FDA, EMEA) related/ applicable to the conduct of clinical trials, understanding of FDA Compliance Manual & EMA...Immediate startRemote work2 days per week
$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- ...Regulatory Affairs AssociateAs a Regulatory Affairs Associate you will:Gain experience and exposure to groundbreaking programs and strategies for compounds in development and/or marketing products intended to address unmet medical needs in markets globally. Learn the...
- 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...Full time
- ...& Trade Compliance SpecialistThe Logistics & Trade Compliance Specialist serves as the primary subject matter expert for U.S. and international... ...government agencies such as CBP and the Census Bureau.Monitor regulatory changes and proactively update internal processes, procedures,...Permanent employmentWork at office
$137k - $235.75k
...individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category:ProfessionalAll Job Posting Locations:Raritan, New Jersey, United...Full timeLocal areaImmediate startFlexible hours$137k - $235.75k
...individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category:ProfessionalAll Job Posting Locations:Horsham, Pennsylvania, United...Full timeWork experience placementLocal areaImmediate startWorldwide- Company DescriptionAt the forefront of the staffing industry, Artech is a women-owned business enterprise (WBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured...Work at officeLocal area
$140.5k - $245k
...and play by connecting them to what brings them joy. We do what we love — driving innovation, creativity, and impact in the world. Our V Team is a community of people who anticipate, lead, and believe that listening is where learning begins. In crisis and in celebration,...Full timeContract workTemporary workPart timeWork experience placementWork at officeWork from homeShift work3 days per week- Why Messer? Messer is the world’s largest privately held industrial gases company and what we do matters because it is woven into every part of life, from the medical gases that patients rely on to the essential elements needed to safely and sustainably produce the goods...Permanent employmentFull timeTemporary work
- About Us:We are brand builders who focus our passion and creativity to build Calvin Klein and TOMMY HILFIGER into the most desirable lifestyle brands in the world and at the same time position PVH as one of the best-performing brand groups in our sector. Guided by our values...Full timeSeasonal workLocal areaFlexible hours
$137k - $235.75k
...individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category:ProfessionalAll Job Posting Locations:Raritan, New Jersey, United...Full timeLocal areaImmediate start$83.71k - $109.87k
...Legend Biotech is seeking a QA Laboratory Compliance Specialist III as part of the Quality team based in Raritan, NJ . Role Overview The... ..., compliance, and adherence to global standards as well as regulatory requirements. Support Level I/II QALC by overseeing the completion...Permanent employmentFull timeTemporary workFor contractorsWork experience placementWork at officeLocal areaImmediate startFlexible hours- ...performance, this is an exciting opportunity to support the growth of the captive reinsurance business, become an expert in the Bermuda regulatory framework, and gain exposure across a variety of risks and markets.Location: This role will be based in Hamilton, Bermuda....Full timeWork at officeRelocation package3 days per week
- Amneal Pharmaceuticals in Piscataway, NJ, seeks a Regulatory Affairs Specialist to lead and support high-quality regulatory submissions to the FDA, including NDA, IND, BLA, PADERs, and post-approval reports. The role collaborates with Clinical, CMC, Quality, and Marketing...
$18 - $20 per hour
Credentialing and Provider Enrollment Specialist Job Category : Human Resources Requisition Number : CREDE003404 Posted : August 3, 2026 Full-Time On-site Locations Showing 1 location Pay or shift range: $18 USD to $20 USD The estimated range is the budgeted amount for...Full timeShift work$61.4k - $76.9k
Job Title: Credentialing Specialist Location: RWJUH Somerset Facility: RWJ Somerset Department: Medical Affairs Address: 110 Rehill Ave, Somerville, NJ 08876 Req #: 0000... ...Evaluation (FPPE) processes in accordance with regulatory standards Handles with discretion issues...Temporary workWork experience placementWork at officeLocal areaFlexible hoursShift work- ...OR Spring House, PA (2-3 times onsite per week) ASAP start The Regulatory Program Manager (RPM) will be an asset-level operational... ...Regulatory Leader (GRL) and partners across Global Regulatory Affairs as well as Project Management, Medical Writing, Clinical and other...Contract workImmediate startWorldwideFlexible hours
$72k - $141k
...oversight capabilities, advancing key compliance programs, enhancing regulatory responsiveness, and facilitating compliance assessment and... ...7 years of experience in insurance, compliance, regulatory affairs, or audit.Demonstrated ability to analyze and interpret state...Full timeWork experience placementWork at office- Job ID: c4cgc8Location: Bridgewater, NJPosting Date: 2026-08-18Pay: $30/HRPosted by: Global Channel Management, IncWe are looking for a highly motivated, detail-oriented Pricing Data Analyst to support our global product portfolio activities across their full lifecycle....Work at office
- ...UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent. Job Description Description: The Regulatory Affairs Associate, with minimal guidance prepares, reviews and submits high quality annual reports with FDA within Annual report timelines...
- ...Role: Regulatory Affairs Associate Location: United States Duration: Long Term contract Position Summary We are seeking a detail-oriented Regulatory Affairs Associate to support regulatory activities for medical devices, pharmaceuticals, biotechnology products, or combination...Long term contract
$117k - $201.25k
...Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function: Regulatory ScienceJob Category:Scientific/TechnologyAll Job Posting... ...best talent for Principal Scientist (Manager), Global Regulatory Affairs, CMC.Purpose: The Principal Scientist of Global Regulatory Affairs...Full timeLocal areaImmediate start$82.5k - $117.1k
Senior Analyst, Decision Support - Retail InsightsThe Senior Analyst, Decision Support - Retail Insights supports the Manager of Retail Insights in the creation and oversight of vision for advanced analytics across PVH brands. As part of the Business Intelligence and Strategic...Seasonal workLocal areaFlexible hours
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