MILINKA DJURICH

** *** ******, *******, ** ***** 973-***-**** acve2n@r.postjobfree.com

SUMMARY OF QUALIFICATION

Confident, motivated, and highly qualified quality professional with 24 years of experience in the medical device industry. Broad-based background includes exceptional work ethic and commitment to organizational objectives within a highly competitive work force. Supervisory experience managing a product line to ensure customers is served on time.

PROFESSIONAL EXPERIENCE

CareFusion (formerly GE Healthcare & Vital Signs, Inc.) – Totowa, NJ Jan 1992 - Present

Provide support to manufacturing facilities to ensure safety, quality, and productivity. Manage the $2M product line by coordinating all Production and Quality activities.

Advisor Manufacturing Operations (Enflow Coordinator): Apr 2010 – Present

* Work with Supply Chain Manager to plan weekly production schedule

* Coordinate all activities from receiving quality inspection assembly shipping ensuring product are shipped out on time, every time.

* Schedule QC personnel to complete inspections and if needed, request help from QC Supervisor.

* Manage and execute trainings with QC Inspectors for different types of inspections

* Enflow product line makes up $2M of the Vital Signs business with 60 different part numbers

* Communicate on a weekly basis with Enflow supplier in China to receive Certificate of Sterility, Certificate of Conformance, and Toxicon Reports for product shipped to us.

* Initiate and support Engineering change request for any internal Enflow documentation that requires update.

* Review and work with Quality Manager to approve COS

QC Inspector (Incoming, In-process, MRB Coordinator): Oct 1995 – Apr 2010

* Executed part inspections based on QF-1 Component History Record

* Reviewed test procedures and engineering drawings to ensure that the inspection process is followed in accordance to the plans.

* Reported any quality issues and part discrepancies to the Quality Supervisor.

* Initiated nonconformance reports for any failures that are noticed during inspections.

* Coordinated rework activities with production team to ensure proper execution following rework procedure

* Completed in-process inspections following C=0 sampling plan for finished medical devices ensuring component assemblies

* Inspected medical hoses and breathing bags following inspection record (QF-2) performing thickness, leak, distensibility, weight, & concentricity tests

Production Team Leader: 1992 – Oct 1995

* Motivated the team to achieve high standards and meet quality targets.

* Reviewed and assisted team members in product assembly per device history record.

* Led a team of 5 with product assemblies

TECHNICAL SKILLS AND CERTIFICATIONS

* Environmental Health & Safety Element Owner – Accident Investigation

* CPR Certified 2014

* Knowledgeable in AS400 / JD Edwards and Oracle

* MS Office (Excel, Outlook, Word)

* Expert in reading ANSI ASQ and C=0 Sampling Plans

* Proficient in using all inspection instruments: Caliper, Manometer, Temperature probes, Micrometers, Instron machine, Snap gage, flowmeter

EDUCATION

* Economic High School Diploma – Smederevo, Serbia

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