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Director of Quality

Remote / Online - Candidates ideally in
Raleigh, Wake County, North Carolina, 27601, USA
Listing for: Euromed Pharma Us Inc
Remote/Work from Home position
Listed on 2026-07-16
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 130000 - 200000 USD Yearly USD 130000.00 200000.00 YEAR
Job Description & How to Apply Below
Position: Director of Quality US

Benefits:

  • 401(k)
  • Health insurance
  • Paid time off
  • 401(k) matching
  • Bonus based on performance
  • Competitive salary
  • Dental insurance
  • Training & development
  • Vision insurance
  • Wellness resources
About the Role:

Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and champion quality assurance initiatives. This is a high-impact leadership role where you'll shape the quality culture of a growing pharmaceutical organization. If you're passionate about compliance & regulatory, excellence, and making a difference in the pharma industry, we want to hear from you.

Key Responsibilities 1. Quality Assurance & QMS Oversight
  • Maintain and develop the company’s Quality Management System to support third party logistics activities in compliance with all state, federal and international regulations as applicable
  • Own and manage key QMS processes, including CAPA, Change Control, Deviations, Complaints, Document Control, Data Integrity, Recalls and Internal Audits
  • Lead Management Reviews and promote a culture of continuous improvement
  • Ensure alignment between quality processes and operational functions, including warehousing, logistics, and commercial supply chain activities
  • Provide input into strategic business initiatives, driving process efficiency and compliance
  • Serve as the primary point of contact for regulatory inspections, audits, and agency communications
  • Represent the company during regulatory inspections (Authority and customer audits
2. Responsible Person (RP)
  • Ensure compliance with FDA, cGDP requirements and applicable regulations for wholesale distribution acting as Responsible Person
  • Maintain compliance with the Drug Supply Chain Security Act (DSCSA), including serialization, verification, and transaction documentation
  • Maintain and approve supplier and customer bona fides; ensure all third-party licenses are verified and current
  • Oversee recall, returns, complaints, and falsified product investigations
  • Approve training programs and verify competence of all staff involved in distribution activities
  • Authorize return to saleable stock decisions and oversee product storage, temperature excursions, and transport records
  • Approve contracts and SOPs related to distribution and outsourced activities
  • Ensure records for the minimum period required by the law
  • Participate in senior-level decisions relating to quarantine, disposal, or recall of medicines
  • Fulfil the obligations required for importation of medicinal products
  • Ensure products are only imported from authorized sites and meet all local quality requirements before release
  • Verify that products imported under the WDA(H) are fully compliant
  • Work closely with supply chain partners and import/export authorities to ensure compliance at all touchpoints
  • Represent the company during FDA, customer, and state inspections
Additional Responsibilities
  • Maintain inspection readiness at all times across facilities and systems
  • Ensure full compliance with internal policies, including Health & Safety, Pharmacovigilance, Falsified Medicines legislation and corporate governance
  • Safeguard company reputation by promoting ethical, compliant, and customer focused business practices
  • Provide training, mentorship, and leadership to quality and operational staff
  • Perform delegated duties in the absence of colleagues where appropriate
  • Other duties which may be reasonably required from time to time by company managers, including delegated duties during the absence of colleague.
Requirements:
  • Bachelor's degree or higher in Pharmacy, Life Sciences, Chemistry, or a related field
  • 7+ years of quality assurance experience in the pharmaceutical industry
  • Familiarity with federal and state regulatory frameworks (e.g. FDA, DSCSA, State Boards of Pharmacy) Preferred: completion of certified training in Good Distribution Practice
  • Strong understanding of US, EU, UK and international regulatory frameworks (e.g. FDA, EMA, MHRA)
  • Auditing experience (internal and external) of suppliers, vendors, and contractors
  • Familiarity with ISO
    9001 QMS and Controlled Drug regulations (US DEA)
  • Knowledge of US Customs and Border Protection requirements
  • Knowledge of COSHH and hazardous goods transportation
  • Excellent interpersonal, written and verbal communication skills
  • Strong leadership, communication, and cross-functional collaboration skills
  • Team oriented with leadership, training, and delegation capabilities
  • Customer focused, innovative, and process-improvement minded
  • Detail-oriented, decisive, and committed to a culture of continuous improvement
About Us:

Euromed Pharma US Inc is part of the 60-year strong Petrone Group, dedicated to delivering high-quality, innovative healthcare and pharmaceutical solutions globally. Our team is driven by a shared commitment to patient safety, regulatory excellence, and scientific integrity. We offer a collaborative and forward-thinking work environment where talented professionals can grow and make a meaningful impact in the pharmaceutical industry.

Flexible work from home options available.

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