Cosmetics & Drug Regulatory Specialist

Englewood Lab, Inc.; Totowa (NJ); On-site; USD 58,000 - 70,000; Full time

Benefits offered by this job

Medical, Dental, and Vision Insurance

Company-paid Life, AD&D, and Disabilty

401(k) Retirement Plan with Employer 6

Paid Time Off and Holidays

Special Paid Leave for Personal Events

Year-End Gift

Employee Referral Program

Additional benefits as outlined in the

Job summary

Englewood Lab, Inc. in Totowa, New Jersey is seeking a Regulatory Affairs Associate to assist the Manager of Regulatory Affairs with inspections, audits, and compliance activities across FDA, EPA, and COSMOS-related standards.

The role involves preparing regulatory documents, coordinating submissions, and ensuring cGMP and global regulatory readiness. You will work cross-functionally with QA/QC, production, and R&D, maintaining product Master Files, DMFs, and statements.

Qualifications

• Bachelor's degree in Life Sciences, Engineering, or related field.
• 2+ years experience in cosmetics regulatory processes.
• Familiarity with FDA regulations under 21 CFR Parts 210 and 211.
• Excellent communication and computer literacy.

Responsibilities

• Assist the Manager of Regulatory Affairs during audits and inspections.
• Prepare and collate Product Master Files (PMFs) and DMFs.
• Generate and review CoCs, CoAs, CoMs, and regulatory statements.
• Coordinate regulatory submissions and compliance with global standards.
• Maintain familiarity with QMS and cGMP requirements.

Skills

Data analysis

Communication

Computer literacy

Education

Bachelor's degree in Life Sciences/Engineering

Job description

Englewood Lab, Inc. in Totowa, New Jersey is seeking a Regulatory Affairs Associate to assist the Manager of Regulatory Affairs with inspections, audits, and compliance activities across FDA, EPA, and COSMOS-related standards.

The role involves preparing regulatory documents, coordinating submissions, and ensuring cGMP and global regulatory readiness. You will work cross-functionally with QA/QC, production, and R&D, maintaining product Master Files, DMFs, and statements.