Функция: Разработка нового продукта

Тип занятости: Полный рабочий день

Место расположения: New Jersey - Jersey City

Страна: USA

Job Title: It Cosmetics Regulatory Coordinator

 Function: Regulatory

 Supervisor Title: Mgr Regulatory Product Development


Job Summary

Will provide assistance and support to the Regulatory team with an emphasis on the administrative, organizational, and coordination task to optimize efficiency of the Regulatory team. Candidate must be highly organized, detail-oriented, trustworthy with sensitive confidential information, productive, self-motivated, and interested in growing in a regulatory career.

 Job Requirements

 - Bachelor’s degree, science background preferred.

- Proficient in Microsoft Office – Word, Excel, Outlook, OneDrive, Adobe Acrobat DC, and ability to learn internal software/systems

- High level of organization

- Able to be trusted with sensitive confidential information

- Ability to thrive in a fast-paced, constantly changing environment

- Strong verbal communication, writing and interpersonal skills

- Desire to grow in regulatory knowledge and responsibilities.

 Section 4: Judgment and Decision Making

Close supervision required for judgment or decision making associated with this position. This position is not responsible for judgment or decision making,

 Essential Physical

 Ability to lift up to 15lbs.

 Essential Duties and Responsibilities:

 Product Information File (PIF) Management

• Collect documents for Product Information File (PIF) including raw material information, stability reports, manufacturing process information, etc.

• Follow up communication with manufacturer on outstanding items.

• File sharing with consultant and internal counterparts as needed.

• Organization of internal and shared files

• Preparing product registration documents as needed

 Study Coordination

• Labeling, packing, and shipping product samples for analytical, microbiological, in vitro, and clinical testing.

• Preparation of sample submission paperwork for analytical, microbiological, in vitro, and clinical testing.

• PO generation and invoice processing through internal software systems to ensure timely vendor payment.

 Data and Reporting

• Updating master database with regulatory information.

• Data entry into internal software systems.

We are an Equal Opportunity Employer and take pride in a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.