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19 часов назад

Document Control Specialist (GMP)

60 000 - 70 000$
Формат работы
onsite
Тип работы
fulltime
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
Document Control Specialist (GMP): Maintaining controlled quality documentation for a beauty contract manufacturing operation with an accent on document lifecycle management, GMP compliance, and audit readiness. Focus on reviewing batch records, coordinating approvals and revisions, and resolving documentation discrepancies before product release.

Location: Onsite at 111 Fieldcrest Ave, Edison, New Jersey, United States

Salary: $60,000–$70,000 annually, based on experience, skills, and qualifications.

Company

THG is a global ecommerce group operating beauty and sports nutrition businesses, while Bentley Labs is its Edison-based beauty contract manufacturing operation producing skincare, haircare, hygiene, and cosmetic products.

What you will do

  • Manage controlled quality documentation, including SOPs, specifications, batch records, testing protocols, forms, and records.
  • Maintain document version control, approval workflows, distribution, archival, and restriction of obsolete documents.
  • Review quality and GMP documentation for accuracy, completeness, compliance, and required approvals.
  • Coordinate with Quality, Production, Laboratory, Regulatory, and other departments on change controls, CAPAs, training records, and periodic reviews.
  • Support internal, customer, and regulatory audits by maintaining traceable, audit-ready records.
  • Review batch records before product release and escalate missing information, discrepancies, or non-compliance issues.

Requirements

  • Experience with electronic document management systems, LIMS, CMS, or similar quality and manufacturing systems.
  • Familiarity with change control and CAPA processes.
  • Experience supporting internal, customer, or regulatory audits.
  • Experience in cosmetics, personal care, pharmaceutical, or contract manufacturing.
  • Working knowledge of ISO, FDA, GMP, or other applicable quality standards.
  • Experience supporting training related to revised procedures or controlled documentation.

Nice to have

  • Bilingual English/Spanish communication skills.

Culture & Benefits

  • Work within a regulated beauty manufacturing environment focused on quality, safety, GMP compliance, and operational efficiency.
  • Collaborate cross-functionally with Quality, Production, Laboratory, and Regulatory teams.
  • Inclusive workplace committed to diversity and reasonable adjustments during the recruitment process.

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