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3 дня назад

Incoming QC Supervisor (Pharmaceutical Quality)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Incoming QC Supervisor (Pharmaceutical Quality): Oversees incoming quality control for raw materials, components, and supplies at a 503A compounding facility with an accent on USP compliance, supplier quality, and material disposition. Focus on supervising IQC personnel, managing deviations and OOS results, supporting audits, and improving quality systems for sterile compounded medications.

Location: New Albany, Ohio, United States; on-site

Company

Hims & Hers is a public health and wellness platform providing personalized access to diagnosis, treatment, and delivery.

What you will do

  • Supervise, mentor, train, and provide performance feedback to incoming quality control personnel.
  • Schedule and prioritize inspections, documentation reviews, testing, and material disposition.
  • Review and approve Certificates of Analysis, Certificates of Conformance, and vendor documentation.
  • Manage deviations, nonconformances, and out-of-specification results related to incoming materials.
  • Support supplier qualification, audits, vendor monitoring, internal audits, external inspections, and regulatory interactions.
  • Identify process improvements and collaborate with Procurement, Quality Control, and Compounding teams to resolve quality issues.

Requirements

  • Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, or a related field.
  • 3–5 years of QA/QC experience in a 503A, 503B, or cGMP-regulated environment.
  • Strong understanding of cGMP and USP <795>, <797>, and <800> requirements.
  • Knowledge of raw material testing, supplier quality, and risk-based quality management.
  • Strong communication, leadership, organizational, and problem-solving skills.
  • Ability to work in office, laboratory, and cleanroom environments, including gowning and handling hazardous drugs with required PPE; medical approval is required for respirator use.

Nice to have

  • Experience in sterile compounding or pharmaceutical manufacturing.
  • 1–2 years of supervisory or team leadership experience.
  • Proficiency with quality management systems, electronic documentation systems, Google Workspace, and Microsoft Office.

Culture & Benefits

  • Competitive salary and equity compensation for full-time roles.
  • Unlimited PTO, company holidays, and quarterly mental health days.
  • Medical, dental, and vision coverage with parental leave.
  • Employee Stock Purchase Program and 401(k) with employer matching.
  • Physical work may include extended standing, walking, lifting, squatting, bending, and lifting up to 50 lbs during shifts of up to twelve hours.

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