MAJOR DUTIES AND RESPONSIBILITIES:
to all company procedures/SOPs (Standard Operating
Good Documentation Practices (GDP)/Good Manufacturing Practices
finished product inspections on all the products using measuring
(calipers, crimp gauges, pressure gauges, etc.); scales; visual
review of in-process checks
pre and post clearance activities during production runs.
daily verification of instrumentation (scales, gauges, etc.)
monitoring and verification of monthly logbooks (temperature,
differential, equipment logs, etc.)
Accurately reviews and records data.
Accurately collects retain samples and samples
for Analytical and Micro Lab
Performs audits of the batch records
as a liaison between Quality and Production
proficiency in quality finished product inspections on at least
different production machine lines
support to all other departments in an overall quality capacity
(lab, warehouse, etc.)
continuous improvement and customer satisfaction
in other activities as required by Quality Management
knowledge of FDA regulations for drugs and/or medical
of inspecting critical parameters for following products:
School diploma or equivalent.
CRITICAL SKILLS AND ABILITIES:
to use a personal computer and measuring devices.
to detail, thorough and accurate
to establish priorities, work independently, productively, and
objectives without supervision.
to perform effectively under conditions of fluctuating
to handle and resolve recurring problems.
with others clearly and concisely.
to work in a fast paced environment sometimes rapidly shifting
Ability to concentrate in such an environment and perform
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IPQA Manager and/or IPQA Supervisor
to chemicals and/or other potential hazards