QA Compliance Specialist, Qunol

Opella Healthcare Group SAS

$86K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a technical field or equivalent experience
  • 3+ years of quality compliance experience in regulated industries
  • Knowledge of FDA, cGMP/GDP, and Dietary Supplement regulations under CFR 111 preferred
  • Experience with deviations, investigations, and OOS reports
  • Strong analytical and problem-solving skills
  • Ability to work independently and manage competing priorities
  • Excellent communication skills for collaboration across teams

Responsibilities

  • Manage the product complaint process from intake to closure
  • Investigate quality issues with internal teams and suppliers
  • Lead investigations for deviations and out-of-specification issues
  • Collaborate with suppliers and stakeholders for compliance and improvement
  • Deliver quality training programs and track requirements
  • Develop and maintain quality documentation for compliance
  • Support regulatory audits and manage change control activities

Benefits

  • Participation in employee benefit programs
  • Opportunity to lead change in the self-care industry
  • Collaboration-centric workplace culture
  • Chance to contribute to continuous improvement initiatives
  • Hybrid work environment flexibility
Full Job Description
Quality Assurance Compliance Specialist, Qunol

Location: Pine Brook, NJ

Main Responsibilities:
  • Manage the end-to-end product complaint process, including complaint intake, evaluation, investigation coordination, supplier corrective actions (ECARs), and timely closure of complaint cases.
  • Partner with internal teams, suppliers, and customer service to investigate quality issues, facilitate customer communications, assess supplier responses, and drive effective corrective and preventive actions.
  • Lead deviation and out-of-specification (OOS) investigations by initiating documentation, conducting root cause analyses using methodologies such as Fishbone and 5 Whys, and ensuring thorough resolution and closure.
  • Collaborate with suppliers and cross-functional stakeholders to ensure timely investigations, regulatory compliance, and continuous improvement of quality systems and processes.
  • Administer and deliver quality training programs, assign and track employee training requirements, conduct instructor-led sessions, and serve as a Quality Champion promoting a culture of quality throughout the organization.
  • Develop, review, and maintain quality documentation, including SOPs, specifications, and other controlled documents, ensuring alignment with supplier requirements and regulatory standards.
  • Support regulatory and external audits while managing change control activities, including initiation, implementation, tracking, and timely completion of all required actions throughout the change lifecycle.


About You:
  • Bachelor's degree in a technical discipline or equivalent professional experience, with 3+ years of quality compliance experience in a regulated industry.
  • Working knowledge of FDA, cGMP/GDP, and other regulatory requirements, with familiarity with Dietary Supplement regulations under CFR 111 preferred.
  • Experience conducting and documenting deviations, investigations, root cause analyses, and Out-of-Specification (OOS) reports to support quality system compliance.
  • Strong analytical, critical thinking, and problem-solving skills, with the ability to balance quality standards and business objectives while driving continuous improvement initiatives.
  • Proven ability to work independently, manage competing priorities with minimal supervision, and deliver results in a fast-paced environment.
  • Excellent written and verbal communication skills, with demonstrated success building collaborative relationships across internal teams, suppliers, and external partners.
  • Highly organized and detail-oriented team player with proficiency in Microsoft Office and experience using quality management and documentation systems.


This is more than the next step in your career, it's a chance to lead change and help reinvent self-care for the world. If you're ready to challenge, inspire and deliver impact that matters, we're ready for you.

North America Applicants Only

The salary range for this position is: $86,000.00 - $120,000.00

All Compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs.

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