QA Specialist II job vacancy

Vacancy expired!

Piper Life Sciences is seeking a

QA Specialist II (Document Control) to join one of the top biotechnology companies in the

Silver Spring, MD area. The company offers great culture and many perks and bonuses! (Note: this role requires on-site work )

Responsibilities for the QA Specialist II include:

Processing and managing the full life cycle of documents from initiation to release in the eDMS system
Ensuring adherence to regulatory requirements and current site practices in support of clinical and commercial manufacturing
Issuing batch records, worksheets, logbooks, and other requested documents to support QC, Manufacturing, and Quality Assurance
Scanning and physically filing documents and/or records to their designated locations
Maintaining the document archive rooms to ensure records are preserved, organized, structured, and accessible in a timely manner

Qualifications for the QA Specialist II include:

Bachelor's Degree in Science, Technical, or related degree is required
2+ years of experience in using an electronic document management system (eDMS) within a GMP regulated environment
Knowledge of the Microsoft suite (i.e. Word, Excel, Visio, PowerPoint, etc.) and Adobe is preferred

Compensation for the QA Specialist II includes:

Salary Range: approximately $62,000 - $73,000 annually, commensurate with experience
Benefits: Medical, Dental, Vision, 401k, Annual bonus