1,003 Results for

Spanish Jobs in Littleton, CO

Jobs

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).

7 days ago

Associate Director, Regulatory Affairs - Power Platform Solutions Specialist Merck & Co Inc

Rahway, NJ

$129,000–$203,100 / year

Required Skills: Business Applications Development, Change Controls, Data Engineering, Defects Management, Microsoft Dataverse, Microsoft Power Apps, Microsoft Power Automate, Microsoft Power Platform Copilot, Problem Solving, Release Management, Root Cause Analysis (RCA), Software Testing, Technical Troubleshooting. Identify opportunities to improve the current system, bring innovative enhancement ideas, remain versed in new and emerging Power Platform tools, design capabilities, and user-interface development approaches supporting modernized Power Apps UI and usability, efficiency, and long-term platform value.

23 days ago

Senior Manager, Regulatory Affairs, CMC Shionogi Inc.

Florham Park, New Jersey

$140,000–$170,000 / year

Demonstrated ability to collaborate effectively with cross-functional teams, including R&D, Quality Assurance, Manufacturing, and Commercial teams, to achieve regulatory milestones and drive product development initiatives forward. Work closely with cross-functional teams, including R&D, Quality Assurance, Manufacturing, and Commercial teams, to ensure alignment of CMC regulatory requirements with overall product development plans and timelines.

30+ days ago

Associate Director, Regulatory Affairs - Biosimilars (US) Sandoz Group AG

Princeton, NJ

$145,600–$279,400 / year

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

30+ days ago

Manager Rates and Regulatory Affairs - NJ Finance & Regulatory FirstEnergy Corp

Morristown, NJ

$157,590–$222,480 / year

Given the complexity of New Jersey''s regulatory environment, the frequency and significance of ongoing regulatory proceedings, and the need to protect both customer and shareholder interests, backfilling this position is necessary to maintain continuity of expertise, preserve key stakeholder relationships, support critical business initiatives, and ensure successful execution of JCP&L''s regulatory and financial objectives. We are committed to rewarding individual and team efforts through our total rewards philosophy which includes competitive pay plus incentive compensation, a company-sponsored pension plan, 401 (k) savings plan with matching employer contribution, a choice of medical, prescription drug, dental, vision, and life insurance programs, as well as skills development training with tuition reimbursement.

10 days ago

Regulatory Affairs Specialist OrganOx

Madison, NJ

$120,000–$135,000 / year
Quick Apply

The role works closely with Regulatory Affairs team members responsible for software, hardware, disposable products, labelling, and other regulatory disciplines to support submission activities, maintain accurate regulatory records, and ensure alignment across product areas and markets. It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant.

30+ days ago

Senior Specialist, Regulatory Affairs ImmunityBio

Summit, NJ

Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response. ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.

30+ days ago

Senior Manager, Regulatory Affairs, CMC Shionogi & Co Ltd

Florham Park, NJ

$140,000–$170,000 / year

30+ days ago

Associate Director, Regulatory Affairs Legend Biotech US

Somerset, New Jersey

Serves as regulatory representative in global cross-functional development teams for pipeline programs; work closely with other line functions to ensure efficient execution of regulatory strategies. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases.

19 days ago

Regulatory Affairs Associate - Cosmetics SGS

Fairfield, New Jersey

$61,500–$75,000
Full time

With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services. For C&H: Knowledge / experience in cosmetics, personal care or household care related testing services (microbiological, chemical, etc.) desirable (Preferred).

5 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

Associate Director, Regulatory Affairs Legend Biotech Corp

Somerset, NJ

$168,372–$220,988 / year

18 days ago

Regulatory Affairs Strategist, Digitalization - Advertising & Promotion Becton Dickinson and Co

Franklin Lakes, NJ

$135,500–$216,800 / year

Manage Platform Roadmap and Continuous Improvement: Manage the business platform roadmap by identifying, evaluating, prioritizing, and advancing platform capabilities and improvements, including opportunities related to workflow, AI-enabled capabilities, automation, reporting, integration, data quality, and user experience, in alignment with the broader Regulatory Affairs digital roadmap. Manage Global Ad/Promo Digital Platforms: Serve as the Regulatory Affairs business owner for digital platforms supporting Advertising & Promotion, providing business leadership for platform operations, lifecycle management, enhancements, releases, and continuous improvement.

24 days ago

Sr. Director/Executive Director, Regulatory Affairs Systimmune

Princeton, NJ

$220,000–$300,000 / year

The Regulatory Affairs (Clinical/Nonclinical) role will drive regulatory strategy and execution within SI Project development teams and the RA Department in all aspects of global regulatory affairs related to development of novel oncology therapeutics (multiple modalities such as ADCs, bispecific antibodies and T-cell engagers etc.). Own/drive the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: BLA/INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator’s Brochure.

3 days ago

Director/Sr. Director/Executive Director, Clinical Regulatory Affairs Systimmune

Princeton, NJ

$200,000–$300,000 / year

30+ days ago

Associate Director/Director, Regulatory Affairs Advertising & Promotions Tris Pharma

Monmouth Junction, NJ

$160,000–$180,000 / year

Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned US biopharmaceutical company focused on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. Associate Director- PhD or PharmD in life sciences, pharmacy, medicine or a related discipline and minimum 3 years' experience as a regulatory reviewer of advertising and promotional materials in the pharmaceutical, biotechnology or related industry REQUIRED.

30+ days ago

Staff Regulatory Affairs Specialist, Advertising & Promotion Becton Dickinson and Co

Franklin Lakes, NJ

$135,500–$216,800 / year

Our Staff Regulatory Affairs Specialist position is primarily focused on compliant advertising and promotion of our existing Specimen Acquisition and Lab Specimen Management product portfolios, in addition to opportunities to provide regulatory support for new product claims. This role ensures claims and communications are truthful, non-misleading, appropriately substantiated, aligned to approved indications/intended use, and compliant with applicable US, EU, and global medical device/IVD requirements.

30+ days ago

Senior Manager / Associate Director, Regulatory Affairs CMC Shionogi Inc.

Florham Park, New Jersey

$140,000–$200,000 / year

Serve as the primary CMC regulatory liaison with Health Authorities for designated assets, which involves guiding agency communications, creating briefing documents, handling information requests, and ensuring alignment with management on strategic or high‑risk issues before making commitments. Excellent verbal communication skills, with demonstrated ability to act as a regulatory CMC spokesperson and effectively communicate aligned regulatory CMC strategies and positions across working teams, cross‑functional forums, and senior leadership.

30+ days ago

Senior International Regulatory Affairs Specialist Becton Dickinson and Co

Franklin Lakes, NJ

$110,200–$176,400 / year

Proactively identifies regulatory risks, assesses potential business impact, develops mitigation plans, and escalates critical issues in a timely manner to enable effective decision-making and maintain project timelines. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance.

23 days ago

See More Jobs

Browse All Spanish Locations

Browse Jobs Near Littleton, CO

Get noticed by top employers!

Upload your resume to let employers know you're open to Spanish job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Spanish Jobs in Littleton, CO

Regulatory Affairs Associate I IntelliPro Group Inc.

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

Associate Director, Regulatory Affairs - Power Platform Solutions Specialist Merck & Co Inc

Senior Manager, Regulatory Affairs, CMC Shionogi Inc.

Associate Director, Regulatory Affairs - Biosimilars (US) Sandoz Group AG

Manager Rates and Regulatory Affairs - NJ Finance & Regulatory FirstEnergy Corp

Regulatory Affairs Specialist OrganOx

Senior Specialist, Regulatory Affairs ImmunityBio

Senior Manager, Regulatory Affairs, CMC Shionogi & Co Ltd

Associate Director, Regulatory Affairs Legend Biotech US

Regulatory Affairs Associate - Cosmetics SGS

Regulatory Affairs Strategist Aquestive Therapeutics Inc.

Associate Director, Regulatory Affairs Legend Biotech Corp

Regulatory Affairs Strategist, Digitalization - Advertising & Promotion Becton Dickinson and Co

Sr. Director/Executive Director, Regulatory Affairs Systimmune

Director/Sr. Director/Executive Director, Clinical Regulatory Affairs Systimmune

Associate Director/Director, Regulatory Affairs Advertising & Promotions Tris Pharma

Staff Regulatory Affairs Specialist, Advertising & Promotion Becton Dickinson and Co

Senior Manager / Associate Director, Regulatory Affairs CMC Shionogi Inc.

Senior International Regulatory Affairs Specialist Becton Dickinson and Co

Similar Job Searches

See More Jobs