Current jobs related to Regulatory Affairs Deputy - Salt Lake City - SentrX Animal Care Inc

  • Global Regulatory Affairs Specialist

    1 month ago

    Salt Lake City, United States USANA Health Sciences Full time

    Who We Are Looking For We are looking for a meticulousindividual to join USANA as a global regulatory affairs specialistto ensure compliance with domestic and international regulations across all assigned markets. In this role, you will be responsible for executing various regulatory affairs functions, maintaining the highest standards of procedural...

  • Regulatory Affairs Manager

    2 weeks ago

    Salt Lake, Utah, United States ICU Medical Full time

    Position Overview The Regulatory Affairs Manager plays a crucial role in providing support and direction related to the global and US registration of medical device products. This position involves analyzing regulatory requirements and monitoring deliverables to ensure compliance. The manager will assist in the development and maintenance of...

  • Director, Regulatory Affairs

    4 days ago

    Redwood City, United States Pulmonx Corporation Full time

    The Director of Regulatory Affairs will support product development, registration, and post market support activities, in addition to managing a small team of Regulatory Affairs Associates and directing their work as it relates to the activities outlined below.Support Product Development & Registration:Provides strategic input and technical guidance on...

  • Senior Manager of Regulatory Affairs

    2 weeks ago

    Salt Lake, Utah, United States ICU Medical Full time

    Position Overview The Regulatory Affairs Manager plays a crucial role in ensuring compliance with global and US regulations related to medical device products. This position involves analyzing regulatory requirements and tracking deliverables to support the registration process. The manager will assist in the development and maintenance of comprehensive...

  • Regulatory Affairs Manager

    5 days ago

    Salt Lake, Utah, United States DSJ Global Full time

    DSJ Global is currently seeking a highly skilled Environmental Compliance Manager to support the growth and success of our industrial composites manufacturing operations in the United States.**Job Summary:**We are looking for an experienced professional to oversee environmental compliance and regulatory affairs for our flagship site in Salt Lake City. The...

  • Product Safety/Regulatory Affairs Specialist

    1 month ago

    Salt Lake City, United States Hexcel Corporation Full time

    With our strong investment in research and development and our culture of continuous improvement, Hexcel is the industry leader in the manufacturing of advance composite materials, including carbon fiber, woven reinforcements, resins, prepregs, honeycombs and additive manufactured parts. We invite you to join the Hexcel team at various manufacturing sites,...

  • Regulatory Affairs Director

    1 day ago

    Redwood City, California, United States Adverum Biotechnologies Full time

    About the RoleWe are seeking a highly experienced and skilled Regulatory Affairs Director to lead our CMC Regulatory strategy for Adverum's gene therapy program/s. As a key member of our team, you will be responsible for developing, executing, and advising on global Regulatory CMC strategies through all phases of our development program/s.Key...

  • Regulatory Affairs Director

    1 week ago

    Redwood City, California, United States Pulmonx Full time

    About PulmonxPulmonx is a leading medical device company dedicated to developing innovative solutions for respiratory health. We are seeking an experienced Regulatory Affairs Director to join our dynamic team.Key ResponsibilitiesRegulatory Strategy Development: Develop and implement comprehensive regulatory strategies that align with company goals and ensure...

  • Director of Regulatory Affairs

    6 hours ago

    Redwood City, United States MFS Talent Full time

    Shift: Days - 8 hours, Monday-Friday, 40hrs/weekLocation: Onsite, Palo Alto, CACompensation: $180k-$230k annually Duties and ResponsibilitiesResponsible for strategic and operational regulatory input and support for collaboration with other project team members, including regulatory team members. Contributes to the development of regulatory plans and...

  • Specialist, Regulatory Affairs

    4 weeks ago

    Oklahoma City, United States Hikma Pharmaceuticals Full time

    Title: Specialist, Regulatory Affairs Founded by Samih Darwazah over 40 years ago in Jordan, Hikma's purpose is to provide affordable, quality medicines to the people who are competent. Based on very solid foundations, we continue to innovate daily and find practical solutions to transform the lives of the millions of people we serve. At the end of the...

  • Regulatory Affairs Director

    23 hours ago

    Redwood City, California, United States HealthCare Recruiters International Full time

    **About the Role**HealthCare Recruiters International is seeking a highly qualified Director of Regulatory Affairs to join our team. As a key member of our R&D team, you will play a critical role in the development and commercialization of innovative robotic systems for the diagnosis and treatment of patients with advanced surgical interventions.**Key...

  • Regulatory Affairs Specialist

    2 weeks ago

    Oklahoma City, Oklahoma, United States Hikma Pharmaceuticals Full time

    Position: Regulatory Affairs SpecialistHikma Pharmaceuticals, a leader in the pharmaceutical industry, is dedicated to delivering accessible and high-quality medications to those in need. With a rich history spanning over four decades, we pride ourselves on our commitment to innovation and excellence in healthcare.As we expand our operations, we are seeking...

  • International Regulatory Affairs Manager

    2 weeks ago

    Redwood City, California, United States Pulmonx Corporation Full time

    Manager, Regulatory Affairs, InternationalPulmonx is a leading entity in the field of Interventional Pulmonology, specializing in innovative tools and therapies for Obstructive Lung Disease. Our commitment to excellence is exemplified by our flagship product, the Zephyr Valve, which has been recognized for its groundbreaking technology in the realm of...

  • Regulatory Affairs Manager, International

    1 week ago

    Redwood City, California, United States Pulmonx Full time

    Company OverviewPulmonx is a leading innovator in Interventional Pulmonology, Planning Tools, and Treatments for Obstructive Lung Disease. Based in the United States and Switzerland, Pulmonx is the manufacturer of the Zephyr Valve. The Zephyr Valve was granted breakthrough status and approved by the FDA in 2018, as it represents a breakthrough technology...

  • Regulatory Affairs Specialist

    2 weeks ago

    Oklahoma City, Oklahoma, United States Hikma Pharmaceuticals Full time

    Position: Regulatory Affairs SpecialistHikma Pharmaceuticals, established over four decades ago, is dedicated to delivering accessible, high-quality medications to those in need.With a strong foundation, we strive for daily innovation and practical solutions to enhance the lives of millions globally.In the late 1980s, we expanded our operations beyond the...

  • International Regulatory Affairs Manager

    7 days ago

    Redwood City, California, United States Pulmonx Corporation Full time

    Manager, Regulatory Affairs, InternationalPulmonx is a leading innovator in the field of Interventional Pulmonology, specializing in advanced tools and therapies for Obstructive Lung Disease. The company is recognized for its groundbreaking Zephyr Valve, which received breakthrough designation from the FDA due to its significant clinical advantages in lung...

  • Manager, Regulatory Affairs, International

    4 days ago

    Redwood City, United States Pulmonx Corporation Full time

    Manager, Regulatory Affairs, InternationalPulmonx is a Global Leader in Interventional Pulmonology, Planning Tools, and Treatments for Obstructive Lung Disease. Based in Redwood City, California, and Neuchâtel, Switzerland, Pulmonx is the maker of the Zephyr Valve. The Zephyr Valve was granted breakthrough status and approved by the FDA in June 2018,...

  • Lead Manager of Regulatory Affairs

    2 weeks ago

    Lake George, United States COV Covidien LP Full time

    Position OverviewAs a key member of the team at COV Covidien LP, you will embark on a fulfilling career dedicated to advancing healthcare solutions and ensuring equitable access to medical innovations.Role ResponsibilitiesIn the capacity of Senior Regulatory Affairs Manager, your primary focus will be to devise and implement strategies for global product...

  • International Regulatory Affairs Manager

    2 weeks ago

    Redwood City, California, United States Pulmonx Corporation Full time

    Manager, Regulatory Affairs, InternationalPulmonx is a recognized leader in the field of Interventional Pulmonology, specializing in innovative tools and therapies for obstructive lung diseases. Our flagship product, the Zephyr Valve, has received significant accolades, including breakthrough designation from the FDA due to its unique approach to lung volume...

  • Head of Regulatory Affairs for Advertising

    1 week ago

    Foster City, California, United States Milestone Technologies, Inc. Full time

    Position OverviewThe Senior Director of Regulatory Affairs for Advertising & Promotion will lead, guide, and provide strategic direction on all advertising and promotional initiatives, ensuring adherence to regulations, alignment with approved product registrations, and compliance with company policies throughout the product lifecycle. This role will...

Regulatory Affairs Deputy

2 months ago

Salt Lake City, United States SentrX Animal Care Inc Full time

Company: Sentrx Animal Care Position Title: Regulatory Affairs Deputy Position Type: Full-time, Experienced Wage: Commensurate with Experience + Benefits and Bonus Opportunity Location: 570 W 1700 S, Suite 1400, SLC, UT 84115 Summary Sentrx Animal Care, Inc., located in Salt Lake City, Utah, has been recently acquired by Domes Pharma, a leading pharmaceutical company located in France. Sentrx and Domes Pharma manufacture products with primary focus on the animal health industry. SentrX is looking for a Regulatory Affairs Deputy. Under the responsibility of the VP of Quality and Product Development and in collaboration with Group Head of Regulatory Affairs, manage all regulatory aspects for the registration and marketing of the veterinary medicines of the Group in the USA and Ensure that the regulatory activities are compliant to the regulatory requirements for the concerned products category. Key Responsibilities Be the Interface with internal and external (consultants, competent authorities) resources, to understand US (FDA, USDA) regulatory approval requirements Prepare and submit, in collaboration with Group regulatory team (either directly or through direct supervision of others) the regulatory documents/applications for new/existing products and determines acceptability of data, procedures, and other product-related documentation presented in support of product registration/variation. Responsible, in collaboration with the Dômes Pharma Group regulatory team, for compliance with post-market approval regulatory obligations and maintenance of authorizations for existing products, Develop and maintain current regulatory knowledge and keeps abreast of regulatory procedures and changes, interprets regulations, shares regulatory insight, advice and support to other departments. Assist the Group regulatory team in analysing US product data, regulatory legislation and providing US specific information. Ensure product labelling for all products comply with product dossiers and relevant regulations. Key Attributes of the Successful Candidate Degree in Pharmacy, Chemistry or veterinary Medicine – BS or higher – preferred background in Ophthalmology Experience working in Regulatory & Medical Affairs function in Pharmaceutical industry. Versed in medical devices, registered drug products and over the counter authorizations Experience in Regulatory Affairs for medications. Knowledge of CMC activities and requirements. Strong communication, organizational, negotiation and interpersonal skills. Salary commensurate with experience and skills Full benefits package including medical/dental/vision/HSA with generous employer contribution Duration

Description cookielawinfo-checkbox-analytics

11 months

This cookie is set by GDPR Cookie Consent plugin. The cookie is used to store the user consent for the cookies in the category "Analytics". cookielawinfo-checkbox-functional

11 months

The cookie is set by GDPR cookie consent to record the user consent for the cookies in the category "Functional". cookielawinfo-checkbox-necessary

11 months

This cookie is set by GDPR Cookie Consent plugin. The cookies is used to store the user consent for the cookies in the category "Necessary". cookielawinfo-checkbox-others

11 months

This cookie is set by GDPR Cookie Consent plugin. The cookie is used to store the user consent for the cookies in the category "Other. cookielawinfo-checkbox-performance

11 months

This cookie is set by GDPR Cookie Consent plugin. The cookie is used to store the user consent for the cookies in the category "Performance". viewed_cookie_policy

11 months

The cookie is set by the GDPR Cookie Consent plugin and is used to store whether or not user has consented to the use of cookies. It does not store any personal data.

#J-18808-Ljbffr