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Pharmaceutical Manufacturing

Administrative Assistant; QA Document Control

Hauppauge, NYOnsiteFull Time$19–$21 /hrPosted 7 days agoVisa sponsorship available

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Required skills

  • GMP records
  • filing
  • scanning
  • organizing
  • reviewing
  • retrieval
  • document logs
  • filing system
  • accuracy
  • compliance

Nice to have

  • some college coursework
  • strategic-thinking skills

Role summary

The Administrative Assistant; QA Document Control supports Quality Assurance Document Control functions by managing GMP records. Responsibilities include filing, scanning, organizing, and reviewing these records for accuracy and compliance with SOPs. The role also involves maintaining document logs and filing systems, and assisting with intercompany communication and document retrieval requests. Proficiency in MS Office and ERP systems like Aurantium is required, along with knowledge of cGMPs related to the US FDA and manufacturing environments. Previous experience in an FDA-regulated industry is preferred.

Description

Position Summary:

Support Quality Assurance Document Control functions, with a specific focus on filing, scanning, organizing, and reviewing GMP records. 

Requirements

Responsibilities: Including but not limited to:

  • 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. 

Education and Experience:

  • High school diploma; some college coursework or an associate degree is a plus.
  • Previous work experience, preferably in an FDA-regulated industry.

Skills, Abilities and Knowledge:

  • 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

Physical Demands:

  • While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear.
  • May be required to lift up to 50lbs, stand, bend, climb stairs. 
  • Specific vision abilities required include close vision, ability to focus. 
  • Requires the ability to climb stairs as part of regular duties, including accessing multi-level facilities or transporting documents between floors. 

Work Environment:

  • Required to be present in the office to collaborate with peers and supervisors. 
  • Work/Travel schedule must be adhered to and/or changed as needed to meet business requirements. 
  • Potential ongoing travel throughout geographic areas on a continual basis as normal scope of role.

Supervisory Responsibilities:

  • None

Personnel Protective Equipment or Attire Required for Position:

  • As needed
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