Merck & Co. / Schering Plough Research Institute (Summit, NJ) 2003 — 2004 Scientist I • Managed quality control,
batch record review, compliance audits, and data automation • Identified batch errors and instigated corrective measures while increasing efficiency • Oversaw national and international legal compliance ensuring professional operations • Designed, developed, and implemented electronic specification application • Utilized data automation which enhanced compliance and cut calculation time by 70 %
Perform
batch record review for shipping approval.
Supervised 6 Manufacturing QA Inspectors conducting the in - process testing and inspections, line clearances,
batch record review and final batch releases in coordination with other QA sections performing the chemical, biological and physical controls of each lot produced
Quality at the source utilizing on the floor real time
batch record review, disposition
batch record review, disposition and in process auditing.
QA experience with quality management systems (QMS) and documentation,
batch record reviews, annual product reviews, SOP drafting, review and approve, investigate deviation, change and document control.
Not exact matches
Be aware that while most of the customers are very happy with these healthy dog treats by themselves, there's a lot of
recorded proof of poor
batches of these dog treats being sent out with white worms infesting the bag, with the last
review coming from May, 2015.
Review batch records and... more
Responsible for
reviewing batch production
records to assure that no deviations have occurred.
Strong interpersonal and communication (both oral and written) skills; interact with various departments; able to work independently and as part of a team; proficient computer skills;
review of documentation, protocols, and
batch records; initiate and
review of change control
records, initiate and
review of investigation reports.
Responsible for the
review, encoding, scanning and filling of manufactured drugs
batch records.
Conduct internal audits, supplier / contract (3rd party) manufacturer audits, and allograft (
batch record) file
reviews.
Reviewed all laboratory
batch records and test results at 100 % for completeness and accuracy with no erroneous release of product as a result of a QC
review failure.
Reviewed and approved Equipment Cleaning Logs, Work Orders, Manufacturing
Batch Records and SOPs.
Documents all entries required within
Batch Record and
reviews Batch End paperwork for accuracy and completeness.
Review batch records (BR), Standard Work Instructions (SWI) Client Work Instruction and Standard Operation Procedure.