QA Document Control Associate

2 weeks ago


Summit, United States Piper Companies Full time

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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