Regulatory Affairs Specialist
$117k - $120kAmneal Pharmaceuticals
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. Full timePosting Date: 2026-07-17
$61.44k - $84.48k
...Job Summary This position will determine the current regulatory requirements and strategies for Terumo's devices and projects... ...Must make a proactive contribution to the overall Regulatory affairs department growth. Participates in project performance team...SuggestedTemporary workWorldwide- ...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
- ...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...SuggestedWork at officeImmediate 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
- ...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...
- ...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...Contract work
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- ...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...Contract workLocal area
- ...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
$80k - $96k
...Regulatory Affairs Specialist MTF Biologics processes tissue grafts from human donors that are used in a growing array of clinical applications – positively affecting lives across the globe. As a global nonprofit organization that saves and heals lives by honoring donated...Temporary workWork at officeLocal areaMonday to FridayFlexible hoursShift work$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$86.9k - $121.88k
...this job. Duties, responsibilities, and activities may change at any time with or without notice.The Senior Healthcare Compliance Specialist supports the development, implementation, and continuous improvement of the Terumo Corporate Compliance Program at Terumo...Contract workTemporary workLocal areaImmediate startWorldwideFlexible hours$60k - $70k
Job Title Essential Duties Reviewing and analyzing system-generated alerts to provide a comprehensive analysis of player transactional activity. Handling alerts from initial trigger through escalation, working cross functionally with other departments to review...Shift work- ...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
- ...Cybersecurity Compliance Specialist Rutgers, The State University of New Jersey, is a leading national research university and the... ...to ensure that the institution's operations comply with legal/regulatory standards, and university procedures and policies. Among the...Full timeTemporary workFlexible hoursShift work
- ...Sr. Regulatory Affairs Specialist 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...
- ...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...
$124k - $174k
...culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.As the Regulatory Affairs Project Manager, you will lead the planning, execution, and oversight of complex global regulatory submissions and ensure the...Hourly payLocal areaRelocation$76k - $125.3k
...providing recommended solutions via research and/or position development. Lead the preparation and review of complex tax/accounting regulatory and tax compliance with limited supervision. Perform research and analysis on related accounting and tax issues. Keep knowledge...Full timeSummer holidayFlexible hours$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- 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...
- 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
$150k - $258.75k
...Management, Project Management Methodology (PMM), Project Management Office (PMO), Project Management Tools, Project Reporting, Regulatory Compliance, Statement of Work (SOW) The anticipated base pay range for this position is : $150,000.00 - $258,750.00 Additional...Full timeFor contractorsLocal areaImmediate startWorldwideFlexible hours- ...Rate: Negotiable Salary: NA $1.00 Responsibilities: Excellent employment opportunity for a Regulatory Affairs Consultant in the Somerville, NJ area. Potenitial Remote Collaborate with cross-functional project team members and...Contract workRemote work
$109.49k
Minimum Education Required Master's degree Compensation $109,491.00 - $109,491.00 / Yearly Hours Per Week 40 Number Of Positions 5 Shift First Shift (Day) Job Description Document and analyze business user requirements. Query Oracle and SQL Server...Full timeShift workDay shift$115k - $135k
...manufactures from around the world. Responsibilities Publishes US Regulatory Submissions to the Food and Drug Administration: NDAs, INDs,... ...Pharmaceutical Industry with 3-4 years’ in drug regulatory affairs operations. Knowledge of eCTD publishing systems and standards...Work at officeFlexible hours- ...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....
$170k - $190k
Kalon Executive Search is seeking a Vice President of E-Commerce to lead digital growth strategies for a consumer products organization. This role involves overseeing the company's e-commerce business, focusing on revenue growth, customer acquisition, and retention. The...
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