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Operator Machine

Location:
Newark, New Jersey, United States
Posted:
October 11, 2016

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Carmen S. Velez

* ***** ******

Plainfield, NJ **060

(908) ***-****

acw0a9@r.postjobfree.com

OBJECTIVE: To secure a position in a manufacturing environment where I can contribute my skills and abilities

SKILLS: • Skilled working from drawings, specifications, and verbal instructions

• Experienced with precision hand tools, microscopes, and soldering

• Familiar with mechanical, optical, chemical, x-ray and electronic test equipment

• Bilingual – Spanish/English

EDUCATION:

• Plainfield High / Diploma. Union County College

• AIG Technical School- South Plainfield, NJ- completed course for medical assistance

PROFESSIONAL EXPERIENCE:

Laboratory Technician 04/2016- present

Compunnel Software Group Plainsboro, NJ

Assigned to Roche Molecular Systems

• Laboratory in a tube (LIAT) department

• Filler operator- Run and operate equipment through an HMI (human machine interface)

• Labeler operator- Watch labels for expiration dates and batch numbers

• Pouch operator- Operate equipment through HMI

• Work with volumetric flask and various glassware in a laboratory setting

• Packaging Operator

• Collect Samples/Inspect finish product

• Measure and weigh reagents

Level 1 Tech 02/2013-07/2014

Sunny Delight Beverages, East Brunswick, NJ

• Unload, inspect and verify new bottle receipts for aseptic co-packing line

• Transfer bottles to depalletizer for loading onto lanfrancis bottle unscrambler

• Ensure continuous empty bottle flow to krones filler

• Maintain area up to GMP/SQF and 5s standards

• Changeover equipment as needed

• Records results on packaging inspection report to ensure accurate batch records reconciliation

• Weigh and inspect finish produdcts

Pharmaceutical Packaging Operator 11/2009 – 04/2012

Merck, Kenilworth, NJ

• Follow Line Leaders directions in the operation of various types of equipment, such as die cut and pouch machines, fillers, inserters, cartoners, banders, case packers and cappers while ensuring efficient and effective packaging of goods

• Performs line-related checks and records results on inspection record. Checks include component verification, equipment challenges, seal integrity, oxygen analysis, fill weights, immediate removal torques, functionality tests, etc., to ensure guidelines are maintained

• Communicates quality issues to the line leader/supervisor in charge of the line, to ensure product quality and minimize rework

• Monitors component availability and replenishes as required, following first in-first out (FIFO) inventory control guidelines. Notifies Line Leader when additional components are needed

• Segregates rejected material during shift production.

• Records results on packaging inspection report to ensure accurate batch records reconciliation

• Clears equipment as assigned to adhere to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs)

Production/Lab Technician 11/2008 – 5/2009

GE Healthcare, Piscataway, NJ

• Clears jams quickly and safely

• Maintained, cleaned, and sterilized laboratory instruments and equipment

• Records results on packaging inspection report to ensure accurate batch records reconciliation

• Inspected, tested, or measured materials, products, installations, and work for conformance to specifications

• Notified supervisors and other personnel of production problems and assisted in identifying and correcting these problems

• Recorded inspection or test data, such as weights, temperatures, grades, or moisture content, and quantities inspected or graded

Machine Operator 2/2007 – 12/2007

Kelly Services (Assigned to Ortho-Clinical Diagnostics, Raritan, NJ)

• Downloaded job specifications, labels, tracking, and evaluation forms for each job order

• Gathered and staged raw materials and maintained inventory records

• Filled, sealed, labeled, packaged, inspected and maintained batch records for production of BioVue cassettes

• Moved finished product to designated locations in warehouse

• Monitored environmental conditions in clean room and notified engineer for adjustments, as needed

• Strictly followed all regulations and requirements including GMP’s OSHA, and Universal and Product License requirements



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