GMP Document Control Specialist

Contract Pharmacal Corp

Hauppauge (NY)

Vor Ort

USD 45.000 - 65.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Contract Pharmacal Corp. is seeking a detail-oriented QA Document Control Assistant to support filing, scanning, and organizing GMP records.

You will ensure SOP compliance, retrieve documents for departments, maintain accurate logs, and collaborate with cross-functional teams in an FDA-regulated manufacturing environment.

This role requires strong communication, proficiency with MS Office and ERP systems, and the ability to multitask and prioritize in a fast-paced setting.

Qualifikationen

  • Strong communication and strategic-thinking skills.
  • Proficient in using MS Office programs and ERP systems such as Aurantium, and other document management and business communication tools.
  • Ability to multitask, prioritize and manage time effectively.
  • Some knowledge of cGMPs related to US FDA and manufacturing environments.

Aufgaben

  • Assist with the retention and organization of all GMP documents.
  • File, scan, and index related GMP documentation.
  • Retrieve GMP documents in response to requests from all departments.
  • Maintain and improve document logs and the filing system.
  • Support intercompany communication and document retrieval requests.
  • Review GMP records for accuracy and compliance with Standard Operating Procedures (SOPs).
  • Other responsibilities as assigned by senior leadership team.

Kenntnisse

Communication
Strategic thinking
MS Office
ERP systems
Time management
cGMP knowledge

Ausbildung

High school diploma

Tools

Aurantium

Jobbeschreibung

Contract Pharmacal Corp. is seeking a detail-oriented QA Document Control Assistant to support filing, scanning, and organizing GMP records.

You will ensure SOP compliance, retrieve documents for departments, maintain accurate logs, and collaborate with cross-functional teams in an FDA-regulated manufacturing environment.

This role requires strong communication, proficiency with MS Office and ERP systems, and the ability to multitask and prioritize in a fast-paced setting.

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