📍 Mahwah, New Jersey, United StatesFull time

About this role

The Sr. Quality Manager leads Quality Assurance, Quality Control, and Microbiology for cosmetics, OTC drugs, dietary supplements, partnering with internal teams, external stakeholders and other third-party partners to ensure product quality, compliance, and continuous improvement.

This role leads the quality teams, oversees compliance, supports audits and inspections, and promotes quality excellence. It also ensures effective quality systems and compliant product manufacture, testing, release, and distribution under 21 CFR Parts 210/211, 111, and 820, MoCRA, customer specifications and company procedures, supporting safety, efficacy, and customer satisfaction.

Quality Assurance (QA)

  • Lead and maintain the QMS across all product categories, ensuring compliance with applicable FDA, ISO, and cGMP requirements and effective control of policies, procedures, specifications, records, and other quality documentation.
  • Direct regulatory, certification, customer, supplier, and internal audits, including inspection readiness, responses, and Management Representative responsibilities.
  • Oversee deviations, complaints, change controls, CAPAs, recalls, and major investigations, ensuring timely, scientifically sound root-cause analysis, corrective action, and risk escalation.
  • Provide quality oversight for product development, technology transfer, qualification, validation, laboratory methods and controls, computerized systems, environmental monitoring, water systems, stability, and retain-sample programs.
  • Manage supplier qualification and performance, quality agreements, third-party laboratories, quality metrics, management reviews, product quality reviews, and risks associated with products, processes, facilities, suppliers, and operational changes.
  • Build and develop a qualified, well-resourced Quality team and foster decisions grounded in consumer safety, product quality, scientific evidence, and regulatory compliance.

Quality Control (QC) and Microbiological Functions

  • Oversee in-coming materials (Raw ingredients and components), in-process, bulk, finished product, stability and microbial testing in accordance with regulatory requirements.
  • Ensure laboratory operations follow USP, and compendial methods.
  • Approve specifications, test methods, and analytical results.
  • Maintain calibration and qualification of QC laboratory equipment.
  • Implement effective sampling plans and statistical quality control practices.

Leadership & Cross-Functional Collaboration

  • Lead and mentor the QA/QC team, fostering a culture of accountability, continuous improvement, and compliance.
  • Partner with Manufacturing, R&D, Regulatory, Supply Chain, and Operations to ensure quality is built into all processes.
  • Train and develop employees on cGMPs, ISO standards, and company quality policies.
  • Report key quality metrics and trends to senior leadership.

Education:

  • Bachelor’s degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Engineering, or related field (Master’s degree preferred).

Experience:

  • 8 + years of progressive Quality Management experience in a regulated manufacturing environment (OTC drugs, cosmetics, dietary supplements, or medical devices).
  • Strong working knowledge of 21 CFR 210/211, 111, 820, ISO 13485, and Cosmetic GMPs (ISO 22716 preferred).
  • Experience with FDA inspections, ISO audits, and third-party audits, demonstrated success in investigations, CAPA Management, change control, validation, supplier quality, laboratory controls, product disposition, risk-based quality systems, and continuous improvement initiatives.
  • Proven leadership, coaching, conflict resolution, and team-development abilities.

Skills:

  • Strong knowledge of cGMPs and risk-based quality systems.
  • Sound technical and regulatory judgment in product quality decisions.
  • Clear communicator who effectively conveys quality risks and collaborates at all organizational levels.
  • Organized, accountable, and adaptable in fast-paced environments; proficiency with eQMS, LIMS, or ERP systems is preferred
  • Comprehensive Health Benefits package (Medical, Dental, Vision, Life, AD&D) 
  • Competitive 401(k) match
  • Paid time off (Vacation, Sick, Holiday, Summer Fridays)   
  • Monthly birthday celebrations + other fun activities! 
  • Daily subsidized meals 

iLABS (Innovation Labs) Inc. is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other characteristic protected by federal, state or local laws. All employment is decided on the basis of qualifications, merit, and business need. 

Frequently Asked Questions

Is the salary disclosed for the Sr. Quality Manager position at DC Enterprises (iLABS Inc. and Affiliated Companies:)?
The salary for this Sr. Quality Manager role at DC Enterprises (iLABS Inc. and Affiliated Companies:) is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Sr. Quality Manager position at DC Enterprises (iLABS Inc. and Affiliated Companies:) located?
This Sr. Quality Manager role at DC Enterprises (iLABS Inc. and Affiliated Companies:) is based in Mahwah, New Jersey, United States. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Sr. Quality Manager role at DC Enterprises (iLABS Inc. and Affiliated Companies:) full-time or part-time?
This is listed as a Full time position. It is posted as a Sr. Quality Manager role in the iLABS - Quality department at DC Enterprises (iLABS Inc. and Affiliated Companies:).
Which team or department does the Sr. Quality Manager at DC Enterprises (iLABS Inc. and Affiliated Companies:) belong to?
This Sr. Quality Manager position is part of the iLABS - Quality department at DC Enterprises (iLABS Inc. and Affiliated Companies:). See the full job description for more information about the team structure and responsibilities.
How do I apply for the Sr. Quality Manager position at DC Enterprises (iLABS Inc. and Affiliated Companies:)?
Click the "Apply Now" button on this page. You will be redirected to DC Enterprises (iLABS Inc. and Affiliated Companies:)'s official application portal hosted on workable where you can submit your application directly.
When was the Sr. Quality Manager job at DC Enterprises (iLABS Inc. and Affiliated Companies:) posted?
This Sr. Quality Manager position at DC Enterprises (iLABS Inc. and Affiliated Companies:) was posted on Sep 15, 2026. Apply as soon as possible — early applications are often reviewed first.
Sr. Quality Manager
DC Enterprises (iLABS Inc. and Affiliated Companies:)
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