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Document Control Specialist

1 month ago

Elkridge, United States Piper Companies Full time

Piper Health Sciences is seeking a QA Document Control Specialist to join a clinical-stage biotech company located in Elkridge, MD. The QA Document Control Specialist will be responsible for filing and archiving GMP documents.

Responsibilities of the QA Document Control Specialist include:

Create and update documents by writing, formatting, and editingUtilize electronic document systems for all documentationInitiate new SOPs and revise existing SOPsCollaborate with various teams to facilitate document review, approval, and distribution processesFollow SOPs (Standard Operating Procedure) to support the document approval process

Qualifications for the QA Document Control Specialist include:

2-5 years of experience in a GMP environmentPrevious document control experience, handling batch records, and performing batch record reviewsExperience using electronic document control systemsAssociate degree or Bachelor's degree

Compensation for the QA Document Control Specialist include:

Rate Range: $25 - $35 Per Hour **depending on experience**Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401k

Keywords: QA, quality assurance, doc control, document control, biotechnology, pharmaceutical, GMP, SOP, eDMS, electronic document control system, document approval, editing, Mastercontrol, master control, batch records, Veeva, Compliance Wire, Agile, QMS Systems, document filing, batch review, batch release, electronic document management system, Quality Systems fundamentals, quality systems, batch disposition, quality compliance, biotech, pharma, pharmaceuticals, document specialist, document control specialist, trackwise, 21 CFR, EU regulations, Quality control, training records, document updating, document editing, document formatting, biopharmaceutical

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