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Regulatory Affairs Manager (Santa Clarita, CA)

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Quick Summary

Overview

function googleTranslateElementInit() { new google.translate.TranslateElement({pageLanguage: 'en'}, 'google_translate_element'); } Regulatory Affairs Manager (Santa Clarita, CA)…

Requirements Summary

Knowledge of quality and regulatory requirements, state/federal regulatory requirements concerning the distribution and dispensing of medical device, pharmaceutical and nutritional food products.

Technical Tools
strategic-planning

CEDENT

Client is looking for a Regulatory & Quality Affairs Manager for our Valencia, CA corporate office. The Regulatory & Quality Affairs Manager ensures all facilities and or business entities maintain full compliance with all applicable state & federal regulatory requirements and guidelines for the marketing, sales, warehousing and distribution of the company’s products in their respective target markets.

JOB RESPONSIBILITIES:
  • Interact with business leads at all relevant facilities to partner to maintain compliance standards and foster market expansion and growth.
  • Ensure that known compliance risks (via internal/external audits, changes in regulations, changes in business structure/products) are mitigated via quality/compliance plans.
  • Effectively track and communicate compliance plans with HS/Business Leadership.
  • Ensures the QA/RA organizations fully understand the requirements of all regulatory requirements for the company.
  • Direct and oversee Quality Assurance internal audit schedules (internal and supplier) and programs to ensure effective and timely audits. Facilitate and promote cross audits across businesses.
  • Monitor all corrective and preventive action (CAPA) programs to ensure actions are identified and completed in a timely and risk-based manner.
  • Manage external inspections from Regulatory including developing responses to any inspection findings.
  • Oversee facility practices and conditions related to the safe handling and storage of medical devices, pharmaceutical and food products to ensure the appropriate health and safety standards are being maintained.
  • Plan and execute state licensing applications (DME supplier, distributor, pharmacy), and support the continuous renewal and overall maintenance of the company’s operating licenses.
  • Select, develop, and evaluate staff to ensure the efficient operation of the organization. Provide coaching and guidance to direct reports through regular meetings, on-site visits, and communication.
  • Ensure staff performance review metrics are provided and maintained, and training is provided to meet job qualifications and regulatory compliance.
  • Participate and communicate on regulatory and compliance issues during regularly scheduled management review meetings and ad hoc as required.
  • Participates in special projects and performs other duties as assigned.
QUALIFICATIONS:
  • Knowledge of quality and regulatory requirements, state/federal regulatory requirements concerning the distribution and dispensing of medical device, pharmaceutical and nutritional food products.
  • Strategic planning to ensure Quality and Regulatory systems and processes remain current and compliant.
  • Ability to lead and manage complex projects.
  • Excellent decision-making skills.
  • Excellent analysis and problem-solving skills.
  • Excellent organizational skills and extreme attention to detail.
  • Demonstrated success in negotiations with regulatory bodies and/or notified bodies and other participants.
  • Excellent written and verbal communication skills (including interaction with both internal personnel and external organizations such as regulatory agencies and customers).
  • Ability to read, analyze, and interpret technical journals, legal documents, test reports, clinical and medical terminology, technical product information, and complex documents.
  • Strong PC computer skills with everyday experience working with Microsoft products.
  • Multi-tasking is essential for this position. A high energy level and comfortability performing projects in conjunction with day-to-day activities.
  • Ability to speak effectively before groups of employees, management, and agency representatives.

Visit Careers at CEDENT

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Location & Eligibility

Where is the job
Location terms not specified

Listing Details

First seen
May 6, 2026
Last seen
May 8, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
49%
Scored at
May 6, 2026

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dtRegulatory Affairs Manager (Santa Clarita, CA)