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
- ...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...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...SuggestedLocal 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...SuggestedImmediate startRemote work2 days per week
$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- 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
- 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
- ...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
$86.58k - $123.3k
...and consumers. POSITION OVERVIEW: The Senior Regulatory Operations Specialist is an experienced individual contributor who plans,... ...global regulatory submissions. The role works with Regulatory Affairs, content owners, technology teams, and external providers...Remote work$116.3k - $155.1k
General Information LocationNew York, New York Alternative Location(s) Posting Location:Bridgewater, New JerseyPosting Location:St Louis, Missouri Working Schedule Full-Time Work Arrangement Hybrid Relocation Assistance Available No Grade 12C ...Full timeTemporary workWork at officeLocal areaRelocation package3 days per week$35 - $40 per hour
...or a related field (or equivalent experience). 2 to 5 years of corporate experience with solid Excel and Office skills, including v look ups and pivot tables Excellent communication skills (both written and oral), as the role involves communicating with senior managers...Hourly payLong term contractContract workTemporary workWork experience placementWork at officeImmediate start$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- Clinical Data Analyst IIIClient: Direct ClientLocation: Raritan, NJJob Title: Clinical Data Analyst III/Clinical Data Manager III PositionDuration: 1 year+Job responsibilities:• Clinical Data Analyst is responsible for CTMS and Grants Manager study build, maintenance, ...
- 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
$25 - $30 per hour
Job Description Job Description We are looking for a Crew Chief for an immediate hire opportunity in Bridgewater, NJ! A well established water damage restoration company is seeking an experienced Crew Chief/Water Restoration Tech. If you are looking to continue your...Live inLocal areaImmediate startMonday to Friday$154.38k - $193.13k
Job DescriptionPrincipal - Business Consulting (SAP Program Manager)About UsDo you want to boost your career and collaborate with expert, talented colleagues to solve and deliver against our clients' most important challenges? We are growing and are looking for people to...Full timeTemporary workLocal areaRemote work$15.92 per hour
...Description Yoh Life Sciences is hiring a Shipping And Receiving Specialist in Bridgewater, NJ. The individual will perform daily... ...Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. Place of Work On-site Requisition ID 1652196 Job...Hourly payFull timeContract workShift workWeekend workDay shift$110k - $146k
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...Full timeTemporary workFor contractors$135k - $180k
...tracking schedule to complete on time.• Provide a quality project while minimizing unbudgeted change orders.• Manage interface with regulatory agencies to ensure compliance with adopted environmental, life safety and technical code references.• Organize required internal...Full timeContract workTemporary workFor contractors$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$134k - $148k
...Johnson & Johnson Health Care Systems Inc. Job Title: Compliance Specialist IV Job Code: A011.7404.7 Job Location: New Brunswick , NJ Job... ...remediation activities. Ensure the Quality program maintains regulatory compliance. Provide quality support for existing and new...Full timeLocal areaImmediate startRemote work$150k - $258.75k
...lab to life while championing patients every step of the way.Learn more at are searching for the best talent for Director, Site Regulatory Compliance to be located in Raritan, NJ; Horsham, PA or Malvern, PA. Purpose: The Director, Regulatory Compliance is the senior Site...Full timeLocal areaImmediate start$199k - $343.85k
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise...Full timeWork at officeImmediate start- ...creates it—where your skills and values drive our collective progress and impact.The Senior Director of Advertising & Promotion- Regulatory Affairs drug and device products manages and, if required participates in, the reviews and approvals of advertising and promotional...Temporary workWork at officeFlexible hours
$150k - $258.75k
...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 Product Submissions and RegistrationJob Category:People LeaderAll Job Posting Locations:...Full timeWork at officeLocal areaImmediate start- ...employees. Including lab draws and vaccinations.Ensures delivery of integrated services in accordance with Health & Wellness and regulatory guidelines and in alignment with the business needs of our customers.Conduct medical surveillance procedures as directed to ensure...
- Our client is currently seeking a Data Analyst II The CX Insights and Engagement Team designs and implements a best-in-class Voice of the Customer (VOC) program to drive customer-centric decision-making. This role requires strong communication, interpersonal, presentation...Work experience placement
- Clinical Data AnalystA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 19...
$122k - $212.75k
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise...Full timeTemporary workFor contractorsWork at officeLocal areaImmediate startRemote work
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