Regulatory Affairs Specialist
$117k - $120kMerck & Co. Inc
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 and applicable federal laws. This includes, but is not limited, to New Drug Application (NDA), Investigational New Drug Application (IND), Biologics License Applications (BLA), Post-Approval Supplements, Annual Reports (AR), and Periodic Adverse Drug Experience Reports (PADERs). The incumbent serves as regulatory lead on cross functional teams including Clinical, CMC, Quality, and Marketing. Assists in tracking project timeliness and follows up cross functionally for required documents. Coordinates with external vendors, contractors and consultants for project support activities. Assists in organizing meetings with FDA including compilation of meeting requests and briefing packages with cross functional contributors. Must have at least a Bachelor's degree in Pharmacy Administration or Chemistry or Pharmaceutical Manufacturing, or related field . Must have at least 60 months of experience in the advertised position or in a related position. Salary: $117K - $120K per annum. Hours: 40 hrs/wk 8:30am - 5:30pm Location: Piscataway, NJ Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at View email address on click.appcast.io . Requests will be handled confidentially and in accordance with applicable laws. #J-18808-Ljbffr
$61.44k - $84.48k
...Job Summary This position will determine the current regulatory requirements and strategies for Terumo’s devices and projects and define... ...Must make a proactive contribution to the overall Regulatory affairs department growth. Participates in project performance team meetings...SuggestedTemporary workWorldwide- ...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...Suggested
- ...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...SuggestedLong term contract
$80k - $96k
...is simple–do what's right for patients, surgeons, tissue donors, and their families through our guiding principles. The Regulatory Affairs Specialist is responsible for working with product development and manufacturing management to ensure that the product development...SuggestedTemporary workWork at officeLocal areaMonday to FridayFlexible hoursShift work- ...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
- ...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
$75k - $90k
...chemicals/supplies transactions in compliance to local/state/federal regulations, including documentation screening and review, regulatory data entry in customer file, licensing, data reporting to various regulatory agencies, product review and setup. ESSENTIAL DUTIES...Work experience placementWork at officeLocal areaWork from home- ...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
$60k - $70k
Overview Responsibilities and duties include reviewing and analyzing system-generated alerts to provide a comprehensive analysis of player transactional activity. This includes reviewing customer profiles, account documentation, prior reviews, past investigations, and ...Shift work- ...University of New Jersey is seeking a Cybersecurity Compliance Specialist for the Office of Information Technology, department of... ...to ensure that the institution's operations comply with legal/regulatory standards, and university procedures and policies. Responsibilities...
- ...Recruitment/Posting Title Cybersecurity Compliance Specialist Job Category Staff & Executive - Information Technology... ...to ensure that the institution's operations comply with legal/regulatory standards, and university procedures and policies. Among the...Full timeTemporary workSeasonal workFlexible hoursShift work
- Rutgers University is seeking an Information Security Risk Analyst to facilitate and evaluate internal and third-party information security risk assessments. You will provide remediation recommendations and maintain a formal risk register while collaborating with campus...
$124k - $174k
...experience, constant challenge, and development opportunities in an environment that respects work/life effectiveness. Job Title: Regulatory Affairs Project Manager Travel Required?: Travel - up to 10% of time Posting Start Date: 6/22/26 Hybrid No Relocation Assistance...Hourly payLocal areaWorldwideRelocation- Pharmaceutical Role: Financial Data Analyst Location: New Brunswick, NJ Duration: 6 Months+ No: of Positions: 3 Responsibilities: Partner with Planning & Reporting GPOs to collect the data required for the Enterprise planning workstream Partner closely...Work experience placement
$94.49k - $144.72k
Position Details Title: Financial Reporting Analyst Department: UFA Financial Planning & Analysis Location: Rutgers University‑New Brunswick (Piscataway, NJ) Employment Type: Full Time Salary: $94,492 - $144,715 annually Work Hours: 37.5 hours per week Grade: 07 Overview...Full time3 days per week- ...emerging trends and technologies, foster a culture of impactful innovation and scientific excellence, and ensure compliance with regulatory standards. The ideal candidate should have a strong background in scientific research, preferably with a Ph.D. in a relevant field...Permanent employmentFull timeTemporary workFor contractorsLocal areaWorldwideFlexible hours
- ...support in the interpretation of regulations and the Bank's policies and procedures and disseminate information on matters affecting regulatory compliance, including consultation with management and teammates on compliance-related issues. Maintain knowledge of consumer...
- Job Description Job Description Sprinkler Project Manager - Fire Protection and Sprinkler Systems - Base Salary to 100k/year - Somerset, NJ Our client is an established provider of commercial fire protection services serving customers throughout New Jersey, New ...Contract workFor contractorsFor subcontractorWork at officeMonday to Friday
$28.07 - $35.66 per hour
The Project Coordinator will provide administrative and project support to senior leaders within a multi-site biologics development organization. This role supports leadership across Global Upstream and Cell Line Development, Analytical Development and Attribute Sciences...Hourly payContract workMonday to Friday- ...A leading regulatory compliance firm is seeking a detail-oriented Regulatory Affairs Associate I to support compliance activities for products distributed in the United States and Canada. The role involves reviewing product formulas and artwork for regulatory compliance...Contract work
$30 - $36 per hour
...Job Description Job Description Job Title: Regulatory Affairs Associate I Position Type: Contract (12+ Months) Location: Clark, NJ 07066 Salary Rate: $30–36/hour Job Description We are seeking a detail-oriented Regulatory Affairs Associate I to support...Contract workWork experience placement$45k - $83.5k
...USD to $83,500 USD Locations Showing 1 location NJE Non Clinical CBO New Providence, NJ 07974, USA Description The Credentialing Specialist reports to the Credentialing Manager and is responsible for timely submission and follow-up of payer enrollment applications and...Full timeShift work- ...Job Description Job Description [Job Summary] The General Affairs Associate ensures smooth day-to-day office operations by managing facilities, procurement, assets, vendors, and administrative services. This role maintains a safe, efficient, and compliant workplace...Contract workWork at officeLocal areaRelocation
- ...Job Description Job Description Position Overview: The Customs Compliance Specialist will be a part of our Corporate Logistics team and has extensive knowledge of HTS codes. This position is responsible for classification of arts and crafts products under the harmonized...Work at officeOverseas
- ...area of expertise.We are looking for an Environmental & Safety Specialist interested in starting a SWEET career as part of our team at... ...by supporting identifying and mitigating risk and assisting in regulatory matters.Support monitoring and maintaining compliance with all...Work at officeLocal areaImmediate startAll shifts
- ...A healthcare company in New Jersey is seeking a Credentialing Specialist to manage payer enrollment and credentialing applications. The ideal candidate will have 3-5 years of relevant experience in the medical field, strong organizational and communication skills, and...
$71.25k - $116k
...and solutions in a way that drives business value while ensuring alignment with GxP requirements, data integrity principles and regulatory expectations. The IT Compliance analyst helps enable business effectiveness by identifying opportunities across business areas for...Temporary workWork experience placementRelocation packageFlexible hoursShift work$56 - $59.44 per hour
Project Manager – Manufacturing Sciences and Technology The Project Manager will join the Manufacturing Sciences and Technology (MS&T) group and support the Technical Project Management Team. The role involves ensuring projects are properly chartered, resourced, and budgeted...Hourly payLocal area$122k - $151k
Employment Type: Full-Time FSLA: Salary/Exempt Division: Project Management Department: Project Management Reports to: Project Executive Supervisory Duties: Yes Salary Range: $122,000 - $151,000 The Project Manager (PM) will serve as a main point of contact and corporate...Full timeFor contractorsFor subcontractor$170k - $250k
Legal Entity: AECOM Technical Services Inc Business Line: Transportation Work Location Model: Hybrid Primary Location: US - Piscataway, NJ - 30 Knightsbrid Compensation: USD 170,000 - USD 250,000 - yearly Job Description AECOM is seeking a Senior Project Manager to focus...Contract workRelocation packageFlexible hours
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