Regulatory Relations Specialist jobs in Pasadena, CA

Regulatory Relations Specialist files applications and interacts with governmental officials during the regulation and certification process for a plant or other facility. Assists in developing procedures to ensure regulatory compliance. Being a Regulatory Relations Specialist gathers data pertaining to organizational projects and their impact on the regulation process. May require a bachelor's degree. Additionally, Regulatory Relations Specialist typically reports to a supervisor or manager. To be a Regulatory Relations Specialist typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. (Copyright 2024 Salary.com)

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Senior Regulatory Operations Specialist
  • 5TA US Quintiles Laboratories
  • Valencia, CA FULL_TIME
  • We are seeking a Senior Regulatory Operations Specialist to join Q² Solutions, IQVIA’s laboratory business in Valencia, CA.

    We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

    As the Regulatory Operations Specialist, you will be acting as a liaison between lab operations and the sponsor to ensure coordination of study logistics. You will be responsible for ensuring the study documentation is accurate, complete, and well organized in accordance with internal and regulatory standards.

    What you’ll be doing:

    • Coordinating with internal and external stakeholders to ensure study set up and site initiation is as detailed in the protocol documentation and qualification visits are scheduled.
    • Organizing documentation from lab analysis in study binder and ensuring study documentation is complete and accurate.
    • Planning and hosting monitoring visits with sponsors.
    • Filing deviation documentation, as needed and may participate in investigation and resolution.
    • Attending study calls to stay abreast of study needs and ensures follow up on assigned actions.
    • Ensuring adequate inventory of reagents for training and sample analysis.
    • Partnering with management to ensure training records for lab staff dedicated to the study are up to date and ensuring sample analysis in accordance with study timelines.
    • Identifying opportunities for process improvement, supporting six sigma, and suggests best practices for effectiveness.

    What We Are Looking For:

    • Bachelor's Degree.
    • 3 years of experience in a regulated laboratory environment.
    • Or other equivalent combination of education, training, and experience

    The Knowledge, Skills and Abilities needed for this role:

    • Sound knowledge of good documentation practices.
    • Strong interpersonal, communication, organizational, and time management skills.
    • Working knowledge of laboratory workflows.
    • Knowledge of Six Sigma principles a plus.

    What We Offer You:

    We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental, and emotional, financial, and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

    To learn more about our benefits, visit https://jobs.iqvia.com/benefits.

    If you’re looking to unleash your potential, join Q² Solutions, IQVIA’s laboratory business, to help make the extraordinary possible!

    Q² Solutions, IQVIA’s laboratory business, creates connected intelligence by combining our expertise, technology and analytics - this fuels unparalleled research & development solutions. We uphold a deep commitment to patients, sites, customers, and each other. https://www.q2labsolutions.com/careers 

    We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/q2-solutions-eoe

    Q² Solutions’ ability to operate and provide certain services to customers and partners necessitates Q² Solutions and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/q2-solutions-covid-19-vaccine-status

    The potential base pay range for this role, when annualized, is $82,900.00 - $124,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
  • 13 Days Ago

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Principal Regulatory Affairs Specialist
  • Kindeva Drug Delivery
  • Los Angeles, CA FULL_TIME
  • Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our cus...
  • 5 Days Ago

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Regulatory Affairs Specialist
  • PureTek Corporation
  • Panorama, CA FULL_TIME
  • We are currently seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be pivotal in ensuring compliance with regu...
  • 6 Days Ago

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Principal Specialist, Regulatory Affairs
  • Advanced Bionics, LLC
  • Valencia, CA FULL_TIME
  • Who we areYou enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: We...
  • 19 Days Ago

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Principal Regulatory Affairs Specialist
  • Kindeva Drug Delivery Careers
  • Los Angeles, CA FULL_TIME
  • Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our cus...
  • 20 Days Ago

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Principal Specialist, Regulatory Affairs
  • Sonova
  • Valencia, CA FULL_TIME
  • Who we are You enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: W...
  • 22 Days Ago

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0 Regulatory Relations Specialist jobs found in Pasadena, CA area

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Regulatory Affairs Specialist
  • Medtronic, plc
  • Northridge, CA
  • Partner with Geography RA to plan, develop and execute global regulatory activities necessary to obtain and maintain reg...
  • 4/18/2024 12:00:00 AM

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Senior Regulatory Affairs Specialist
  • NeuroVasc Technologies, Inc.
  • Irvine, CA
  • We are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world....
  • 4/18/2024 12:00:00 AM

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Regulatory Affairs Specialist II - Neuromodulation
  • Boston Scientific
  • Valencia, CA
  • Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II - Neuromodulation About the role: Support the regulator...
  • 4/18/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Cypress HCM
  • Irvine, CA
  • Regulatory Affairs Specialist This is an exciting opportunity to join an industry leading biotech company leading. The R...
  • 4/17/2024 12:00:00 AM

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Regulatory Affairs Specialist (IVD)
  • Nelson Connects
  • Irvine, CA
  • Location: Irvine, CA Shift: 8am-5pm (hybrid) Type: 12 month assignment (Temporary) Industry: Life Science Pay Range: $40...
  • 4/17/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Tucker Parker Smith Group (TPS Group)
  • Irvine, CA
  • Regulatory Affairs Specialist Location: Irvine, CA Schedule: Hybrid M-F 8-5, 3 days on site T,TH and tbd 1 year, No full...
  • 4/17/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Nihon Kohden America
  • Irvine, CA
  • The Regulatory Affairs Specialist temp is responsible for developing and influencing regulatory policy and determining a...
  • 4/16/2024 12:00:00 AM

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Senior Regulatory Affairs Specialist
  • Neurovasc Technologies Inc.
  • Irvine, CA
  • We are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world....
  • 4/16/2024 12:00:00 AM

Pasadena is a city in Los Angeles County, California, United States, located 10 miles (16 kilometers) northeast of Downtown Los Angeles. The estimated population of Pasadena was 142,647 in 2017, making it the 183rd-largest city in the United States. Pasadena is the ninth-largest city in Los Angeles County. Pasadena was incorporated on June 19, 1886, becoming one of the first cities to be incorporated in what is now Los Angeles County, following the city of Los Angeles (April 4, 1850). It is one of the primary cultural centers of the San Gabriel Valley. The city is known for hosting the annua...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Relations Specialist jobs
$82,692 to $113,522
Pasadena, California area prices
were up 3.2% from a year ago

Regulatory Relations Specialist in Albany, GA
The Regulatory Relations Specialist is responsible for the execution of the overall strategy for regulatory engagement and enterprise-wide standards.  This includes assisting with the management of regulatory examinations, inquiries and meetings.  Additional responsibilities include.
December 09, 2019
Regulatory Relations Specialist in Monroe, LA
We are looking for a Marketing Specialist to plan, coordinate and manage marketing campaigns and activities across marketing channels.
February 06, 2020