Ronkonkoma, NY, 11779
TEVA PHARMACEUTICAL COMPANY,
At present working at incoming packaging components.
Review and reconciliation of quality assurance batch records.
Master batch records, SOP, monographs, APRs, change control.
Certificates of analysis, Logbooks, complaints, deviations and CAPA.
AQL inspections: Packaging in process/ research and development.
Control of rejected material.
Labeling: Release, rejection, approval, quarantine hold.
Line clearance for the next component.
Inspection of blaster card, checking the barcode and shipper labeling.
Performing inspections of all packaging areas (including equipment, components prior to start, during and after operation.
Performing first checks and second checks.
Inspects filling/packaging/labeling and other manufacturing operations to assure compliance with S.O.P.’s and cGMP’s.
Performs visual inspections of packaging lines and equipment for cleanliness.
Pulls samples of finished product according to sampling plan for analytical testing.
Assist with the performance of CGMP training for packaging and related groups personnel based upon written procedures in the CFR and standard operating procedures.
Review/modifying manufacturing and packaging record.
Duties, activity and responsibilities for QA assurance.
Plan, organize and supervise daily activity and scheduling of employees who are engaged in packaging.
Conducting training, development and performance.
Reviewing and modifying master compliance with GMP guideline and company SOP coordinates.
Preparing and issuing clearance and maintenance log book.
Institute of technology, diploma in mechanical technology.
University of Karachi, Bachelor of Science in Physics, Chemistry and Mathematics.