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
- ...Rate: Negotiable Salary: NA $1.00 Responsibilities: Excellent employment opportunity for a Regulatory Affairs Specialist in the Raritan, NJ area. Input in development, post-approval and life cycle management Participate in Working...SuggestedContract workLocal area
- ...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
- ...Rate: Negotiable Salary: NA, $1.00 Responsibilities : Excellent employment opportunity for a Regulatory Affairs Specialist II in the Somerville, NJ area. Ensure compliance with regulatory agency regulations and interpretations. Prepare...SuggestedContract work
- ...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
- ...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
$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$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 timeLocal areaImmediate start3 days per week- ...Regulatory Affairs Associate As 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....
- ...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...InternshipWork at officeWorldwide
$47k - $78k
...departmental guidelines: Through coordination with others, implements compliance mechanisms and protocols, internal controls and regulatory compliance policies and procedures and methodology to measure and monitor compliance to internal controls and regulatory requirements...Full timeWork experience placementWork at office- 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
$122k - $212.75k
...submission.We are searching for the best talent for Senior Manager, Regulatory Program Management, Immunology.Purpose:The Regulatory Program... ...Regulatory Leader (GRL) and partners across Global Regulatory Affairs as well as Project Management, Medical Writing, Clinical and...Full timeLocal areaImmediate startWorldwide- 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
- ...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 timeFor contractorsWork experience placementWork at officeLocal areaImmediate 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 timeTemporary workLocal areaImmediate start$83.71k - $109.87k
...immunotherapy for multiple myeloma. QA Laboratory Compliance Specialist III – Location: Raritan, NJ Role Overview The QA Lab Compliance... ...ensure quality, compliance, and adherence to global standards and regulatory requirements. Support Level I/II QALC by overseeing spot‑check...Temporary workWork experience placementWork at officeWorldwideFlexible 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
$130.91k - $192.01k
Job SummaryMesser Americas runs a strong project management system for implementation of our capital projects. The Project Manager is accountable for executing the assigned projects, safely, to specification, on time and on budget. Our Project Managers lead multi-discipline...Full timeContract workTemporary workFor contractorsLocal area$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- Responsibilities: Excellent employment opportunity for a Clinical Data Analyst in the Raritan, NJ area. The Data Entry Analyst is needed to support re-creation of clinical trial data into Medidata CTMS system. Knowledge of the Clinical Trial Management...Monday to Friday
- Clinical Data Analyst A 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 ...
$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- ...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
- ...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...
- • Responsible for the timely, efficient and accurate coordination, creation and maintenance of various master data elements (e.g. Material Master, BOM/Recipes, Production Versions, etc.) in SAP/ECC directly and/or through automated workflow system(s). • Execute the data...Local areaRemote work
$94k - $151.8k
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 workLocal areaImmediate start$116k - $139.74k
Title: Actuarial Analyst Company: Everest Global Services, Inc. Job Category: Analytics Job Description: About Everest: Everest is a global leader in risk management, rooted in a rich, 50+ year heritage of enabling businesses to survive and thrive, and economies...Full timeWork at officeHome office$165k - $218k
Description and Requirements The Team You Will Join Join our Global Risk Management Group, where you’ll play a key role in safeguarding the company, ensuring we deliver on our commitments to customers and stakeholders, and driving responsible growth. As part of our...Temporary workWork at officeLocal areaShift work3 days per week
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