QA Document Control Associate - Summit, United States - Piper Companies

Description

Piper Companies

is currently seeking a

QA Document Control Associate

for an opportunity in

Summit, New Jersey (NJ),

to join a global biopharmaceutical company delivering life-saving medicines to patients with serious diseases.

Responsibilities of the QA Document Control Associate
Manage electronic document system, including document change control and release
Develop and update document control procedures and tools
Support document approval process, training workflows, and document archiving
Assist with cross-training, generate system reports, support audits, and communicate with stakeholders

Qualifications of the QA Document Control Associate
2+ years of document control and reporting experience in cGMP/FDA regulated setting
Experience with technical troubleshooting and working cross-functionally
Proficient in technical writing, MS Office, Document Management Systems, and Quality Management Systems; experience with Veeva Vault is preferred
Bachelor's degree or equivalent is required

Compensation for the QA Document Control Associate
Salary Range
:
$24 - $26 / hour
Benefits
:
Medical, Dental, Vision, 401k match, Paid Holidays, and PTO

Keywords :
QA, quality assurance, document control, associate, specialist, QADC, veeva, veeva vault, document reporting, cGMP, current good manufacturing practice, GMP, technical writing, quality systems, quality, cross functional, document approvals, document change control process, review, change control, EDC, electronic document system, change requests, document release, SOP, standard operating procedure, audit, internal audit, external audit, regulatory, FDA, PM, project management, manufacturing quality, manufacturing, packaging, facility, facilities, critical systems, validation

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