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We realize that your privacy is important to you. That is why we developed our site to be confidential. However, more and more of our Employers and Recruiters want to see a full resume as opposed to an anonymous profile.
You can still put your best foot forward and protect your privacy by coding your resume to remove your personal contact information. If you are not concerned with privacy issues, simply cut/paste your resume into the Resume section.
Please remember that the more information you give our subscribers the better your chances of garnering their interest. Please take a few moments to enter a coded resume to best display your experience and expertise. Your search results will improve dramatically with this small investment of your time.
We Suggest…..
A coded resume should have the person’s name and contact information removed and replaced with a code name (for instance Candidate 1602).
A coded resume should have the employer names and locations removed and replaced with a general description (For instance, 3M plant in Champaign, IL. could be Midwest manufacture).
Read through the job descriptions and eliminate or replace any specific references to your employer.
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UnCoded Resume |
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Coded Resume |
William Smith
1602 S. Newton Ave.
Champaign, IL 64112
smithwilliam@cs.rr.com
EDUCATION:
B.S. Microbiology, Northeast Missouri State University, May 1990.
Major: Microbiology,
G.P.A: 3.54
EXPERIENCE:
5/2001 to Present
BAXTER HEALTHCARE - Round Lake, IL.
Production Supervisor - Report to Production Manager in a 300 person, nonunion medical device production facility. Have responsibility for managing up to 25 hourly associates over three high speed production lines. Duties include training, safety of crews, employee relations, maintaining product quality, troubleshooting technical and production issues and disciplinary actions when necessary. Have significantly increased productivity and efficiencies within department in the last twelve months while decreasing downtime.
5/1990 to 5/2001
KMI / PAREXELL - St. Louis, MO.
Senior Compliance Consultant - Report to General Manager. Industry Compliance Consultant specializing in pharmaceutical, medical device, and software cGMP compliance issues. Considered to be an industry leader and expert in computerized systems validation and 21 CFR Part 11, Electronic Records and Electronic Signatures. Lead pharmaceutical and medical device manufactures to design and implement programs that meet cGMP requirements and expectations of the FDA. Responsible for employee output and quality of work. Maintained morale, motivation, and positive employee relations.
REFERENCES: Will be furnished upon request. |
CANDIDATE 1602
EDUCATION:
B.S. Microbiology, Northeast Missouri State University, May 1990.
Major: Microbiology,
G.P.A: 3.54
EXPERIENCE:
5/2001 to Present
MIDWEST BIOTECHNOLOGY / PHARMACEUTICAL MANUFACTURER
Production Supervisor - Report to Production Manager in a 300 person, nonunion medical device production facility. Have responsibility for managing up to 25 hourly associates over three high speed production lines. Duties include training, safety of crews, employee relations, maintaining product quality, troubleshooting technical and production issues and disciplinary actions when necessary. Have significantly increased productivity and efficiencies within department in the last twelve months while decreasing downtime.
5/1990 to 5/2001
MIDWEST COMPLIANCE CONSULTING COMPANY.
Senior Compliance Consultant - Report to General Manager. Industry Compliance Consultant specializing in pharmaceutical, medical device, and software cGMP compliance issues. Considered to be an industry leader and expert in computerized systems validation and 21 CFR Part 11, Electronic Records and Electronic Signatures. Lead pharmaceutical and medical device manufactures to design and implement programs that meet cGMP requirements and expectations of the FDA. Responsible for employee output and quality of work. Maintained morale, motivation, and positive employee relations.
REFERENCES: Will be furnished upon request.
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