Manufacturing Microsoft Office

JAMIE ESTIMÉ

*** ***** ****** *** * Quincy, MA **169

1-781-***-**** *****.******@*****.***

SUMMARY

Biochemist with 8 years of experience within a cGMP environment.

Auditor of manufacturing and testing batch records with a focus on adhering to cGMP and cGLP practices.

Previous roles included the execution of manufacturing and quality control evaluation of products used for immunoassay testing on the ADVIA Centaur line platforms.

Excellent multitasker, communicator, and leader overseeing the work of technicians in a manufacturing department.

WORK EXPERIENCE

Siemens Healthcare, Biochemist 11/2007- present

Audit manufacturing and testing batch records for in process products to verify Good Documentation Practices have been followed.

Delegate weekly manufacturing schedule and assignments to technicians, ensuring daily lab tasks are completed,

Train lab technicians on manufacturing processes, safety procedures, as well as Good Documentation Practices and Good Manufacturing Practices.

Implement continuous improvement and lean activities within the lab in order to improve daily processes.

Carry out monthly lab safety audits

Assist product development groups with test method transfers and validations for new and enhanced assays

Tufts Medical Center, Unit Coordinator 06/2005 – 07/2012

Transcribed of doctors’ orders

Processed applicable data into hospital’s internal system

Performed office tasks such as answering phones, faxing, and copying

EDUCATION

2012-2014 MBA, Endicott College, Beverly MA

2003-2007 BS Stonehill College, North Easton MA

TECHNICAL SKILLS AND QUALIFICATIONS

Excellent analytical and problem solving skills

Extensive knowledge of GDP, cGMP and cGLP practices

Excellent interpersonal skills with the ability to work in either a team or individual environment

Experienced in Microsoft Office applications, UPLC, and UV-Vis Spectrophotometry

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