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A growing pharmaceutical company located in Beverly, MA is looking for a quality assurance
associate to join their team for a 6 month contract-to-hire opportunity.
Our client is looking for a qualified quality assurance associate to join their team under the
direction of the QA Global Director and QA Manager. Qualified candidates will be maintaining
approved QA controlled documents files and assisting in tithe distribution of documents for
controlled document binders in production, QC and other departments. Will be assisting with
development and maintenance of quality assurance programs including documentation control,
change control, materials control, facilities and equipment in production and QC. Other
duties include: assist in the implementation and training of GMP related policies and SOPs as
required; auditing laboratory raw data and other source documents; assisting with batch record
reviews and with performance of periodic self inspections per QA policy; assign numbering
system to new controlled documents and maintain version control on all existing and new
controlled documents as per policy of the company.
Requirements: BS in life sciences with 2 years experience in pharmaceutical environment,
experience with document control, knowledge of FDA, ICH and other guidelines and regulations