Senior Manager, Quality Systems , NY

Hi, we’re Supergoop! Since 2005, we’ve been changing the way the world thinks about sunscreen. Today, we’re as committed as ever to creating feel-good sunscreen that you’ll really want to wear. Because protecting your skin’s health is what we’re all about. Every. Single. Day.™

Supergoop! is seeking a strategic and hands‑on Senior Manager, Quality Systems to build, implement, and lead a robust, scalable Quality Management System (QMS) across our product lifecycle. This role will oversee both QA and QC functions, ensuring our products consistently meet regulatory requirements, internal standards, and customer expectations.

The ideal candidate brings deep experience in cosmetic, OTC, or personal care manufacturing and thrives in a fast‑paced, high‑growth environment. This role will partner cross‑functionally with Innovation (Product Development and Packaging), Regulatory, Operations, Supply Chain, and external manufacturing partners to embed quality at every stage from formula development to finished goods release.

• Design, implement, and continuously improve a comprehensive Quality Management System aligned with FDA OTC requirements, cosmetic GMPs (21 CFR Parts 210/211 where applicable), ISO 22716, and other relevant global standards.
• Establish and maintain quality policies, procedures, SOPs, and work instructions across the organization.
• Develop quality metrics and KPIs to monitor performance and drive continuous improvement.
• Lead management review processes and quality reporting.
• Champion a culture of quality and accountability across internal teams and external partners.
• Qualify, audit, and monitor raw material suppliers, packaging vendors, and contract manufacturers.
• Establish supplier quality agreements and performance scorecards.
• Conduct routine GMP audits (domestic and international) and ensure corrective actions are implemented.

• Verify raw material and packaging component specifications are consistently met.
• Ensure Certificates of Analysis (COAs) are reviewed and verified.
• Define in process testing requirements for contract manufacturers.
• Review batch records for accuracy and completeness.
• Monitor critical quality attributes (CQAs) and critical process parameters (CPPs).
• Review batch documentation and approve finished product testing results prior to release.
• Establish bulk review and retain sample program.
• Monitor product performance and quality trends post‑launch.

• Oversee third‑party testing laboratories and ensure validated methods are used.
• Ensure stability, microbiological, and preservative efficacy testing meet regulatory and brand standards; serving as primary liaison for the execution of method validation and micro‑suitability.
• Review and sign off on SPF testing results in partnership with Regulatory.
• Evaluate and approve test methods and specifications.

• Implement and manage document control systems (SOPs, specifications, batch records).
• Own product documentation, including but not limited to analytical, efficacy, safety, and OTC drug stability performed by third‑party manufacturers and labs. Track reporting dates and keep internal teams apprised of results. Assist with quality investigations related to COAs and batch records.
• Collaborate with Regulatory on NHP/DIN registrations in Canada by supplying mandatory quality related documents.
• Interface with international consultants (e.g.: Canadian consultant) and provide all necessary documentation to ensure goods are imported and released without delay.
• Lead change control processes for formulations, packaging, suppliers, and manufacturing processes.
• Ensure appropriate risk assessments (FMEA or equivalent)…