Regulatory Compliance Assistant

Job information Regulatory Compliance Assistant from the Company CurrentBody, this latest Regulatory Compliance Assistant job vacancy is located in the city Remote. This latest job opening is open to job seekers who have the latest education / graduate . Job Vacancies in this Legal field have been opened and published up to the specified time.

Job Description :

CurrentBody is a leading global e-commerce company specialising in beauty tech devices. We are committed to providing our customers with safe and effective products that comply with applicable regulations and industry standards. As part of our dedication to regulatory compliance, we are seeking a detail-oriented and proactive Regulatory Compliance Assistant to join our team.

About the Role

The Regulatory Compliance Assistant will support the Regulator Compliance Manager with managing regulatory strategy development, product registration and listings, regulatory document control and labelling changes to ensure compliance across board.

Responsibilities

Regulatory Strategy Development:

• Conduct regulatory research and provide input on regulatory pathways and timelines.

Product Registration and Listings:

• Manage and maintain accurate records of product registrations and listings with regulatory authorities.
• Ensure timely renewal of licenses, registrations, and certifications.

Document Control:

• Maintain accurate and organized records of all regulatory and compliance documentation.
• Complete and fill in any regulatory forms as necessary.
• Ensure that documentation is readily accessible for internal stakeholders and audits.

Labelling Compliance:

• Ensure that labelling changes are properly documented and necessary changes communicated to relevant stakeholders.

Requirements

• Bachelor's degree in a Law, Pharmacy or Life Sciences subject preferred
• Experience in a regulatory, compliance, or similar administrative role.
• Familiarity with regulatory requirements and compliance processes in the medical device sector including ISO 13485. Knowledge of FDA and EU MDR beneficial as well as other regulatory authorities.
• Strong organisational and multitasking abilities.
• Excellent written and verbal communication skills
• Attention to detail and accuracy
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Ability to work independently and as part of a team.

Benefits

Staff Discount

EAP Scheme

Regular Social Events

We are committed to creating a diverse and inclusive work environment, where all our employees have equal access to opportunities. We strongly encourage applications from all backgrounds, which will be considered regardless of race, colour, religion or belief, gender expression, sexual orientation, national origin, pregnancy and maternity, disability, or age.