1,508 Results for

Regulatory Affairs Jobs in Roosevelt Island, NY

Jobs

Quality Assurance and Regulatory Affairs Associate Canfield Scientific, Inc.

Parsippany-Troy Hills, NJ

Full time

The Quality Assurance and Regulatory Affairs Lead is responsible for assisting the Quality Assurance team with day-to-day activities in support of companywide quality assurance procedures. The right candidate will have excellent written/verbal communication skills, strong attention to detail, and work well in fast paced environment.

13 days ago

Regulatory Affairs Specialist System One

Lyndhurst, NJ

$28–$35 / hour
Quick Apply

Respond to internal and external compliance inquiries regarding TSCA, PFAS, RoHS, Conflict Minerals, and related requirements. Partner with R&D, Procurement, Product Management, Operations, EHS, Legal, Marketing, and Sales teams to ensure compliance.

11 days ago

Regulatory Affairs Strategist Aquestive Therapeutics Inc.

Warren, NJ

This role serves as a key liaison between the company and regulatory agencies, ensuring compliance with applicable regulations while facilitating timely submissions for clinical trials, marketing authorizations, and post-approval changes. Working cross-functionally with R&D, Clinical, Quality, CMC, and Commercial teams, the strategist provides regulatory guidance throughout all phases of product development.

30+ days ago

EHS, QMS & Regulatory Specialist Synerfac Technical Staffing

Carlstadt, NJ

Quick Apply

Nice to have: direct experience with ChemStewards or a comparable EHS&S system (Responsible Care®, RC14001); experience in dispersion, emulsion, or polymer manufacturing; prior work at a growing or newly acquired manufacturer where systems were being built, not inherited. You'll spend time in production areas requiring PPE (safety glasses, footwear, gloves, and periodic respiratory protection), and should be comfortable standing/walking for extended periods, climbing stairs and ladders, and occasionally lifting up to 50 lbs.

2 days ago

Specialty Pharmaceutical Sales Representative Takeda Pharmaceutical

New York, NY

Remote

$63.51–$87.31 / hour
Quick Apply

Establish professional working relationships with Health Care Providers decision makers, support staff, and other stakeholders within assigned customers, to support the safe and effective use of the company's products - through developing and applying clinical and business expertise, and effective selling skills. Utilize discretion and judgment to execute the franchise and company brand strategy and tactics within the assigned customer segment, which may include physicians within specialty medical practices and their staff, specialists within local hospitals, clinics, and support staff as well as pharmacists within a specific geographic area.

5 days ago

Engr 2, Product Development /R&D Engineer Kaygen Inc.

Franklin Lakes, NJ

$40–$47 / hour
Temporary
Contractor
Full time
Quick Apply

The MDVC platform depends on a steady flow of well-vetted design changes, including material, component, packaging, and supplier changes, to offset cost pressure while protecting quality on high-volume products such as syringes, needles, and flush. We specialize in providing high-volume contingent staffing, direct hire staffing and project-based solutions to companies worldwide ranging from startups to Fortune 500 and Managed Service Providers (MSP) across a wide variety of industries.

13 days ago

Director, Healthcare Compliance Aquestive Therapeutics Inc.

Warren, NJ

Reporting to the Chief Legal Officer & Chief Compliance Officer, this position serves as the Company's primary healthcare compliance leader and strategic advisor to Commercial, Medical Affairs, Market Access, Patient Services, Regulatory Affairs, and other business functions. Key Internal Partners: Legal, Commercial, Medical Affairs, Market Access, Regulatory Affairs, Finance, Human Resources, Quality, Patient Services, and Executive Leadership.

30+ days ago

Senior Director Community Finance - Underwriting & Portfolio Management Discover Financial Services

New York, NY

$245,100–$279,800 / year

Our ideal candidate possesses critical thinking skills, demonstrates the willingness and ability to provide effective challenge, strong risk orientation, strong analytical skills, concise verbal and written communication skills, high level of attention to detail, ability to manage internal and external relationship, ability to work independently and as part of a team, problem solving skills, risk management skills, as well as a high level of attention to detail and the ability to work independently and as part of a team. You will be responsible for defining the overarching governance frameworks, managing emerging and current portfolio risks, driving commercial and business growth, and cultivating deep, long-term relationships with key internal and external stakeholders across the affordable housing ecosystem.

8 days ago

Pharmaceutical Sales Specialist Takeda Pharmaceutical

New York, NY

Remote

$63.51–$87.31 / hour
Quick Apply

5 days ago

Pharmaceutical Account Manager Takeda Pharmaceutical

Bronx, NY

Remote

$63.51–$87.31 / hour
Quick Apply

5 days ago

Dermatology Specialty Account Manager Takeda Pharmaceutical

New York, NY

Remote

$63.51–$87.31 / hour
Quick Apply

5 days ago

Specialty Business Manager, Derm - Bronx, NY Takeda Pharmaceutical

Bronx, NY

Remote

$63.51–$87.31 / hour
Quick Apply

5 days ago

Medical Director/Senior Medical Director, Clinical Development - Remote Agios Pharmaceuticals

New York, NY

Remote

$277,140–$461,900 / year

The current base salary range for this position at the Medical Director is expected to be between $221,600 and $369,333 annualized and the current base salary range for this position at the Senior Medical Director is expected to be between $277,140 and $461,900 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Follow important developments and relevant trends in scientific literature and develop/maintain contracts with external experts to support understanding of the candidate drug effects and to gain strategic insights to the further development and placement of study and overall program.

9 days ago

Records and Information Specialist ECLARO

White Plains, NY

Quick Apply

Position Overview: The Records Assistant role supports the Corporate Records team by reviewing, preparing, digitizing, and classifying hardcopy documents for inclusion in the Organization's Records Management System. Work in accordance with Client's records and content management policies under the supervision of Digital warehouse and the Law department, assist in the creation of a digital collection for archived hard copy law cases.

Today

QA Product Manager (Sterile Products) System One

Florham Park, NJ

Quick Apply

Lead and coordinate end-to-end technology transfer projects for drug substance and/or drug product between R&D, manufacturing sites, and external partners (CMOs/CDMOs) including review of all technical documentation (gap assessments, comparability protocols, equipment qualification, and validation protocols/reports.). Lead the Quality Assurance activities for sterile pharmaceutical products manufactured by third-party manufacturers including change controls, product quality incidents, deviations, non-conformances, out of specification/out of trend investigations, product complaints and CAPAs.

14 days ago

Senior Director, Chemical Development & Manufacturing, CMC - Remote Agios Pharmaceuticals

New York, NY

Remote

$229,562–$344,342 / year

The successful candidate will combine deep small-molecule API expertise with meaningful experience in, or strong technical fluency across, nucleic acid therapeutics and will translate that breadth into reliable supply, sound decisions, and high-performing partnerships. The current base salary range for this position is expected to be between $229,562 and $344,342 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.

9 days ago

Accounting and General Affairs Manager Page Group

Manhattan, NY

$140,000–$160,000 / year
Full time

Following the successful establishment of their US entity, they are now expanding operations across North America with plans to launch retail stores and e-commerce operations over the coming years. The successful candidate will play a key role in building scalable finance processes, implementing accounting policies, and supporting the next stage of the company's expansion.

4 days ago

Sr. Director, Global Brand & Portfolio Management CSL

Summit, NJ

$287,000–$352,000 / year

Oversees and guides continued global launch planning for aTIVc, including maximizing the portfolio opportunity across Fluad and aTIVc, refining the launch sequencing strategy, advancing business cases for key investments, and leveraging the Glocal brand marketing model (global to local division of activities) to drive efficiencies. Working in close partnership with R&D and cross-functional stakeholders, the role ensures alignment from research through commercialization, advances high-value strategic investments, and drives portfolio decisions that maximize mid- to long-term growth, value creation, and public health impact.

30+ days ago

Regulatory Affairs Associate I IntelliPro Group Inc.

Clark, NJ

$30–$36 / hour

This role will focus on reviewing product formulas and artwork for regulatory compliance, supporting product notification and registration processes, and maintaining documentation related to regulatory requirements. Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more.

30+ days ago

Regulatory Affairs Senior Manager, Regulatory Information & Content Management Becton Dickinson and Co

Franklin Lakes, NJ

$172,000–$275,200 / year

Primary Responsibilities: Lead Global Regulatory Information and Content Management: Provide strategic and operational leadership for global regulatory information, regulatory content, digital capabilities supporting document and submission management, and assigned digital platforms, ensuring alignment with regulatory strategy, business needs, and the broader Digital RA roadmap. The Senior Manager, Regulatory Information & Content Management is responsible for developing, executing, and maintaining the global Regulatory Affairs strategy and roadmap for regulatory information, regulatory content, and the digital platforms that support their management across Business Units and Regions, in alignment with the broader Digital RA strategy and with specific responsibility for the Regulatory Information Management System (RIM).

17 days ago

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Regulatory Affairs Jobs in Roosevelt Island, NY

Quality Assurance and Regulatory Affairs Associate Canfield Scientific, Inc.

Regulatory Affairs Specialist System One

Regulatory Affairs Strategist Aquestive Therapeutics Inc.

EHS, QMS & Regulatory Specialist Synerfac Technical Staffing

Specialty Pharmaceutical Sales Representative Takeda Pharmaceutical

Engr 2, Product Development /R&D Engineer Kaygen Inc.

Director, Healthcare Compliance Aquestive Therapeutics Inc.

Senior Director Community Finance - Underwriting & Portfolio Management Discover Financial Services

Pharmaceutical Sales Specialist Takeda Pharmaceutical

Pharmaceutical Account Manager Takeda Pharmaceutical

Dermatology Specialty Account Manager Takeda Pharmaceutical

Specialty Business Manager, Derm - Bronx, NY Takeda Pharmaceutical

Medical Director/Senior Medical Director, Clinical Development - Remote Agios Pharmaceuticals

Records and Information Specialist ECLARO

QA Product Manager (Sterile Products) System One

Senior Director, Chemical Development & Manufacturing, CMC - Remote Agios Pharmaceuticals

Accounting and General Affairs Manager Page Group

Sr. Director, Global Brand & Portfolio Management CSL

Regulatory Affairs Associate I IntelliPro Group Inc.

Regulatory Affairs Senior Manager, Regulatory Information & Content Management Becton Dickinson and Co

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