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Jobs

Research & Development Manager (Nutraceuticals) Keystone & Golden, Inc.

Research & Development Manager (Nutraceuticals)
Los Angeles, CA

The role will support both new product development and existing portfolio optimization , working closely with the VP of R&D and cross-functional partners to move concepts from research through launch. A fast-growing, Los Angeles-based women’s health company is seeking an R&D Manager to help develop and commercialize innovative products across women’s health, wellness, supplements, and personal care.

19 days ago

Clinical Research Coordinator (CRC) Smarter HR Solutions

Clinical Research Coordinator (CRC)
Orange, California

The CRC ensures compliance with California-specific regulatory frameworks, institutional policies, and federal guidelines (FDA, ICH-GCP, HIPAA). This includes FDA-regulated drug and device trials, NIH-funded research, and investigator-initiated protocols.

30+ days ago

Sr Mgr, Program Mgmt BU Evidence Edwards Lifesciences

Sr Mgr, Program Mgmt BU Evidence
Irvine, California

As a Manager in the Clinical, Medical, and Regulatory Affairs Program Management Office, you will lead multiple cross-functional clinical trial programs and teams to plan, execute and drive business objectives. Bachelor's Degree with minimum 10 years hands on experience required in related field, managing mid-to-large scale projects or equivalent work experience based on Edwards criteria.

10 days ago

Senior R&D Project Engineer Katalyst Healthcares & Life Sciences

Senior R&D Project Engineer
Irvine, CA

Job Summary: We are seeking a highly motivated Senior R&D Project Engineer to lead Cost Improvement Projects (CIP), design changes, supplier change initiatives, and product lifecycle management activities within a regulated medical device environment. The ideal candidate will possess strong project management skills, medical device product development experience, regulatory knowledge, and the ability to collaborate effectively with cross-functional teams and external suppliers.

30+ days ago

Principal Quality Engineer Katalyst Healthcares & Life Sciences

Principal Quality Engineer
Irvine, CA

The Principal Quality Engineer serves as a subject matter expert, partnering with cross-functional teams to ensure products meet customer, regulatory, and business requirements while driving continuous improvement and operational excellence. This role provides technical leadership for quality systems, product quality improvements, risk management, CAPA activities, process validation, and compliance programs.

30+ days ago
Pharmavite logo

Manager, Design Quality Pharmavite

Manager, Design Quality
West Hills, CA
  • $117,000–$195,000 / year

Excellent communication skills which foster the ability to lead through influence, living a culture of quality, accountability, and continuous improvement while guiding teams toward sound, risk-based decisions without direct authority. The Manager, Design Quality reports directly to the Director of Design Quality and works closely with cross-functional teams across Pharmavite.

30+ days ago

Associate Director, Communications and Public Relations Pepperdine University

Associate Director, Communications and Public Relations
Calabasas, California

The University conducts such screenings in compliance with applicable laws and with the objectives of evaluating risk and supporting a safe environment for students, faculty, staff, and guests; safeguarding key University assets including people, property, information, and the University’s reputation; and providing comprehensive job-related information to University leaders to enable them to make prudent hiring decisions. Integrated Marketing Communications is directly tasked with supporting the University’s mission and strategic plan by building brand equity, elevating the University’s national reputation, providing strong and consistent institutional message leadership, and implementing effective integrated marketing and communications strategies.

30+ days ago

Regional Director, Medical Science Liaison - West Celldex Therapeutics

Regional Director, Medical Science Liaison - West
Los Angeles, California
  • $176,659–$282,195 / year

Overview: The Regional Medical Science Liaison Director (RMD), Immunology – West is a key leader within Field Medical Affairs, responsible for building, leading, and developing a high-performing team of MSLs across the Eastern/Western U.S. Reporting to the Executive Director of Field Medical Affairs, this leader will translate Medical Affairs strategy into regional execution, this role sits at the forefront of translating Medical Affairs strategy into meaningful scientific engagement, ecosystem influence, and actionable insight generation in preparation for launch. This leader leads a high-performing team of MSLs within a region to deliver strategic, insight-driven engagement across diverse healthcare ecosystems and evolve how Field Medical delivers value through elevated engagement, deeper partnerships across the healthcare ecosystem, and real-time insights that inform enterprise decision-making.

30+ days ago

Sr. Quality Engineer - Medical Manufacturing Freudenberg Group

Sr. Quality Engineer - Medical Manufacturing
Baldwin Park, CA
  • $95,000–$115,000 / year

Lead and mentor Quality Engineers and Technicians, providing technical guidance, developing junior talent, and ensuring effective daily support for production, process improvement, and customer satisfaction. Lead and collaborate cross-functionally with engineering, operations, regulatory, customers and suppliers to ensure all change related items are adequately assessed, documented and tested as required.

30+ days ago

R&D Lab Technical Specialist II Envista Dentistry

R&D Lab Technical Specialist II
Pomona, California

Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.

8 days ago

Director, Organizational Learning & Development Arrowhead Pharmaceuticals

Director, Organizational Learning & Development
Los Angeles, CA
  • $190,000–$230,000 / year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. This role ensures employees across R&D, Manufacturing, Quality, Regulatory Affairs, and Commercial functions are equipped with the knowledge and skills needed to perform their roles safely, compliantly, and effectively.

23 days ago
The Walt Disney Company logo

Operations Analyst, Supply Chain Visibility The Walt Disney Company

Operations Analyst, Supply Chain Visibility
Glendale, California

This includes collaborating with Corporate and Business partners to operationalize new regulatory requirements, analyzing internal and external supply chain data to evaluate compliance, developing tools and methodologies to conduct due diligence in support of regulatory requirements, and partnering with internal Sourcing teams to gather and evaluate information from Disney’s vendors. The role works closely with the SCV Operations Team, the SCV Program Team, and other cross‑functional partners to support due diligence reviews, operational documentation, stakeholder engagement, and program development initiatives across various internal and external supply chain compliance programs.

30+ days ago
Lancesoft logo

Chemist II Lancesoft

Chemist II
Northridge, CA
  • $40

In this role, you will support analytical testing, method development, validation, and troubleshooting activities for pharmaceutical and/or medical device products. Required Qualifications Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.

29 days ago
Freudenberg logo

Sr. Quality Engineer - Medical Manufacturing Freudenberg

Sr. Quality Engineer - Medical Manufacturing
Baldwin Park, California
  • $95,000–$115,000 / year

Lead and mentor Quality Engineers and Technicians, providing technical guidance, developing junior talent, and ensuring effective daily support for production, process improvement, and customer satisfaction. Lead and collaborate cross-functionally with engineering, operations, regulatory, customers and suppliers to ensure all change related items are adequately assessed, documented and tested as required.

30+ days ago

Treasury Governance East West Bank

Treasury Governance
Pasadena, California
  • Full time

Our teams of experienced, multi-cultural professionals help guide businesses and community members on both sides of the Pacific looking to explore new markets and create new opportunities, and our sustained growth and expertise in industries like real estate, entertainment and media, private equity and venture capital, and high-tech help build sustainable businesses and expand our associates’ potential for career advancement. The ideal candidate will bring deep expertise, strategic vision, and a results-oriented mindset to help Treasury achieve best-in-class governance, operational efficiency, and regulatory alignment as we navigate this exciting phase in our continued growth and evolution.

30+ days ago

Sr. Quality Assurance Engineer (ISO 13485) Glidewell Dental

Sr. Quality Assurance Engineer (ISO 13485)
Irvine, California

Minimum of 5 years of experience in Quality Assurance or Quality Engineering within the medical device industry, or equivalent education and experience demonstrating comparable skills and knowledge. Own and continuously improve elements of the Quality Management System (QMS), including document control, internal audits, supplier quality, and change control.

11 days ago

Specialist, Quality Compliance (Label) Herbalife

Specialist, Quality Compliance (Label)
Torrance, California
  • Full time

Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D; Short-Term and Long-Term Disability, and an Employee Assistance Program (EAP). US Benefits Statement: Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off.

30 days ago
New

Research and Development Manager Kalon Search

Research and Development Manager
Los Angeles, CA
  • $130,000–$155,000 / year

This individual will support the development and launch of innovative products, as well as ongoing portfolio maintenance and reformulation initiatives, across a growing line of supplements and wellness offerings. Bachelor’s degree in Food Science, Biochemistry, Chemical Engineering, Pharmaceutical Science, or another relevant scientific discipline; equivalent relevant experience may be considered.

3 days ago
New

Med Supp (Medigap) Compliance Program Manager SCAN Health Plan

Med Supp (Medigap) Compliance Program Manager
Long Beach, California

The Med Supp (Medigap) Compliance Program Manager provides independent oversight of assigned components of the Medicare Advantage and Prescription Drug (MAPD) compliance program, with primary responsibility for compliance oversight of the Medigap product and state Department of Insurance regulatory requirements. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

4 days ago

Research & Development Manager O Positiv

Research & Development Manager
Santa Monica, California

Our growing portfolio spans PMS & hormone balance, vaginal & urinary health, digestion, menopause, and conception support—offering vitamins, supplements, and personal care products that women trust. Since launching in 2018, O Positiv has reshaped the women’s health space, tackling long-overlooked issues with innovative, science-backed products and boldly breaking taboos along the way.

30+ days ago
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