This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Responsible for building and leading cross-functional quality assurance systems across Loyal teams with an emphasis on FDA-CVM regulatory compliance for drug submissions and products. The work will ensure that all aspects of drug development, manufacturing and clinical operations are high quality, and that any deviations from this are investigated and understood. The Quality Compliance Officer is responsible for maintaining and continuously improving the company’s Quality Management System (QMS) to ensure compliance with applicable regulations, standards, and internal policies. This role oversees the development, implementation, and management of Standard Operating Procedures (SOPs), company-wide training programs, and quality compliance activities that support operational excellence and regulatory readiness.
Job Responsibility:
Maintain, monitor, and continuously improve the company’s eQMS in alignment with GxP and ISO quality principles
Ensure eQMS documentation is current, compliant, and effectively implemented across departments
Oversee document control processes, including drafting, reviewing, approving, and archiving quality documents
Lead periodic reviews and revisions of quality documents
Identify gaps or new operational areas requiring formalized procedures
Author, review, and approve SOPs in collaboration with functional area leaders
Manage the SOP lifecycle
Administer the company’s training management system
Develop and implement training programs for onboarding, GxP, SOPs, and compliance topics
Track and report training completion metrics
Support internal and external audits
Coordinate corrective and preventive actions (CAPA)
Monitor quality metrics and generate compliance reports
Promote a culture of quality, integrity, and continuous improvement
Requirements:
Bachelor’s degree in STEM or related field or equivalent work experience
Minimum 5-10+ years of experience in quality assurance, compliance, or document control (animal health strongly preferred)
Strong working knowledge of QMS principles, GxP requirements (especially GCP/GLP and GMP), and relevant regulatory standards (FDA, EMA, ISO 9001, VICH)
Experience with electronic Quality Management Systems (eQMS) and learning management systems (LMS)
Track record of success and a broad understanding of current QA practices as they apply to animal health and quality assurance
In-depth knowledge of FDA-CVM and other international clinical research regulations
Proven experience in managing audits, inspections, and CAPA systems
Exceptional writing, organizational, and communication skills
Proven ability to manage multiple projects and deadlines in a regulated environment
Ability to influence cross-functional teams and drive a culture of quality and compliance
Nice to have:
Animal Health pharmaceutical industry GXP experience
What we offer:
Full-coverage health insurance — medical, dental and vision — for you and your dependents
$1,000 home office equipment stipend
$1,200/year learning budget for books, courses, etc.
$250/month wellness budget for gym, cleaners, spa, food, etc.
All 3-day weekends are turned into 4-day weekends
Unlimited vacation and paid holidays
Paw-ternity leave — adopt a dog and get a day off with your new family member
Welcome to CrawlJobs.com – Your Global Job Discovery Platform
At CrawlJobs.com, we simplify finding your next career opportunity by bringing job listings directly to you from all corners of the web. Using cutting-edge AI and web-crawling technologies, we gather and curate job offers from various sources across the globe, ensuring you have access to the most up-to-date job listings in one place.
We use cookies to enhance your experience, analyze traffic, and serve personalized content. By clicking “Accept”, you agree to the use of cookies.