Objective:
 

I bring 20+ years in a CGMP manufacturing environment that


Work Desired:Full Time - Permanent
Citizenship:US Citizen
Resident Of:State: New York - Area Code: 631
Willing To Relocate:No
Posted By Candidate:1+ Year Ago
Experience:More than 3 years of work-experience
Technical Skills:, Project Management
Work Experience:
JOSEPH S. POSANTI
P.O. Box 293 * Holtsville, New York 11742
 [Send email to request phone number] 77.7932 * 

QA SUPERVISOR / MANAGER ~ PRODUCTION SUPERVISOR / MANAGER

20+ years of experience managing Quality, Production, Safety and Cost Control
for multimillion dollar pharmaceutical and chemical manufacturing corporations.
Verifiable strengths in pioneering new quality control techniques and improving
work procedures in support of continuous improvement programs. Practiced in
executing Lean Management and 5S methodologies within fast-paced CGMP
environments. Well-versed in all aspects of quality assurance, production
management, and FDA regulations. A strong supervisor; able to train and motivate
teams to peak performance.

QA Management * Production Planning/Management * Performance Management * SAP
SOP Development/Implementation * KPI Development/Management * Plant Management
HPLC, GC, UV, FTIR, Wet Chem Testing * Testing Validation * Cost
Reduction/Avoidance

PROFESSIONAL EXPERIENCE

SULZER METCO, Westbury, New York * 2007-Present
Manufacturer of thermal spray powders for global aircraft and automotive
industry clients; 200 employees.

Production Supervisor
Oversee all manufacturing processes and production operations encompassing
chemical manufacture of metal oxide powders. Coordinate all production phases,
from job acquisition through material procurement and product manufacture,
finishing, and shipping; maintaining compliance with CGMPs and OSHA/EPA
regulatory guidelines. Supervise, train, and motivate 7 team members while
optimizing daily productivity, quality assurance, and annual budget/financial
performance. Conduct safety and environmental inspections.
 * Implemented quality improvement program including spot audits, root-cause
analysis, and implementation of corrective actions.
 * Instituted standard operating procedures, process improvements, Lean
principles, and 5S practices.
 * Generated $75,000 annual savings by developing and deploying internal waste
removal process.
 * Optimized staff productivity and lean manufacturing by cross training all
personnel.
 * Launched performance improvement initiative, 'First Time Right Manufacture',
including intensive operator training and KPI analysis; significantly reducing
reworked product rates.

EIGHT IN ONE PRODUCTS, Haupaugge, New York * 2003-2006
Manufacturer of FDA regulated pharmaceutical products for animals; 75
employees.

QC Chemist / QA, Pharmaceutical
Planned and executed chemical testing of all raw materials and final
manufactured products including FDA regulated tablets, creams, lotions and
ointments. Provided decisive leadership and direction for quality assurance
workforce, ensuring compliance with CGMPs and FDA regulations.
 * Incorporated HPLC, GC, UV, FTIR and wet chem testing methods.
 * Supported and trained QA inspectors in CGMP compliance, including in-depth
review of batch and packaging records, line clearances, equipment cleaning and
documentation, and hourly line checks for product conformance.

DEL LABS, Farmingdale,N.Y * 2000-2002
Manufacturer of pharmaceutical and cosmetic products;280+ employees and $100
million annual sales.

Production Supervisor
Planned and executed daily production strategy, expertly coordinating the
filling, labeling and the packaging of cosmetic and pharmaceutical products.
Supervised, trained, and motivated production line employees. Monitored and
maintained production schedule, ensuring on-time delivery, quality control, and
customer satisfaction.
 * Introduced Lean and 5S methodologies to improve quality, reduce waste/cost,
and increase production.
 * Drove overall improvements in performance efficiency through cost cutting
process improvements, capacity planning, and production schedule management.

ADDITIONAL EXPERIENCE:

Pharmaceutical Recruiter, Michael McGregory & Associates (2002-2003): Screened
and interviewed potential candidates for employment with top tier pharmaceutical
companies.

Assistant Plant Manager, Poly Research Corp./Tangram Corp. (1995-2000): Planned,
coordinated, and monitored all manufacturing and production phases, from initial
receipt of customer orders and raw materials through final product shipping.
Implemented and managed SAP system. Developed recrystallization process,
resulting in $100,000 in new product revenue.

Note: Early career history includes roles as Assistant QC Chemist for Nature's
Bounty and Environmental Lab Technician for Ecotest Labs.

EDUCATION

Associate of Science, Liberal Arts / Science
Suffolk Community College

Wilson Technical Certificate, Medical Lab Technology

P.O. Box 293 * Holtsville, New York 11742
 [Send email to request phone number] 77.7932 * 

Dear Sir / Dear Madam:

If your organization is in need of a QA or Production Manager with a proven
track record of impacting corporate performance and profitability through
leading-edge Quality, Production, Safety and Cost Control solutions; please
review the enclosed resume. With extensive skills honed over 20+ years of
maximizing resources and streamlining production for multimillion dollar chemical
and pharmaceutical corporations; I feel confident in my ability to generate
superior results for your team.

My ability to lead, train, and motivate top performing teams should prove highly
beneficial to your company. I am a creative problem solver and strategic planner
with a strong work ethic and consistent commitment to both personal and
professional integrity.

Some of my most notable accomplishments include:
 * Implemented quality improvement program including spot audits, root-cause
analysis, and implementation of corrective actions for Sulzer Metco.
 * Generated $75,000 annual savings by developing and deploying internal waste
removal process.
 * Launched performance improvement initiative, 'First Time Right Manufacture',
including intensive operator training and KPI analysis; significantly reducing
reworked product rates.
 * Planned and executed chemical testing of all raw materials and final
manufactured products for Eight in One Products, including FDA regulated tablets,
creams, lotions and ointments.

Seeking to provide your company with the same high quality services as those
mentioned above, I would like to speak with you to further discuss the
possibility of contributing to your organization's success. Please contact me at
your convenience to arrange an interview. Thank you for your time and
consideration. I look forward to conversing with you soon.

Sincerely,

Joseph S. Posanti

 

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