Quality Engineer

• Brand New Position Reporting into Global Director of Quality!
• Growing Clinical Skincare Brand! Hybrid Role in NYC!

About Our Client

Join a growing, global clinical skincare brand!

Job Description

* Develop, implement, and maintain quality assurance processes and procedures in alignment with industry standards and regulations.


* Ensure all manufacturing processes comply with relevant regulations, including but not limited to FDA, EMA, ICH, and GMP guidelines.


* Review batch records, validation documentation, and quality control data to ensure compliance and product quality as needed.


* Review and trend costumer complaints and ensure issuance and closure of nonconformance reports when applicable.

* Prepare detailed CAPA (Corrective and Preventive Actions) reports, and other documentation as required.


* Maintain thorough and accurate records of quality assurance activities, audits, and regulatory communications.


* Participate in the preparation and review of SOPs, work instructions, and other quality-related documents.


* Lead or participate in continuous improvement initiatives, focusing on quality and operational efficiency.


* Assist suppliers in understanding and implementing Client product specifications.

* Support line trials and startups and contract manufacturers as needed. MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.


The Successful Applicant

* Bachelor's degree in engineering or related technical field.


* Minimum of 3-4 years of experience in quality assurance within the cosmetic industry.


* Experience with regulatory bodies such as the FDA, EMA, and other international regulatory agencies.


* Familiarity with Quality Management Systems (QMS), CAPA, deviation management, and risk management.


* Strong understanding of GMP regulations, FDA guidelines, and other applicable industry standards.


* Excellent analytical and problem-solving skills.


* Exceptional attention to detail and ability to identify potential areas of risk and non-compliance.


* Strong verbal and written communication skills, with the ability to prepare clear and concise reports.


* Ability to travel domestically and internationally up to 25% of the time.

What's on Offer

• Competitive salary ranging from $90,000 to $105,000 annually, depending on experience.
• Comprehensive benefits package.
• Opportunities for professional growth and development.
• Collaborative and supportive work environment with exposure to C-Suite
• HYBRID working structure - 3 days/week on-site in Midtown Manhattan & 2 days/week remote

Contact

Brooke Gautier

Quote job ref

JN-052026-7025642