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Manager Assistant

Location:
Dover, DE
Posted:
May 12, 2020

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Resume:

JOHN SHERIDAN adc6xx@r.postjobfree.com

*** ****** ***** ****, *********, NY 11803 516-***-****

SUMMARY

Production Manager for a supplement manufacturer.Production Supervisor in cosmetic manufacturing working with LEAN manufacturing practices. Production Manager in the shading industry. Nineteen years of pharmaceutical/nutraceutical manufacturing experience. Eight years experience as Supervisor, Assistant Manager then Manager for Inspection and Packaging. Over six years as a QA Inspector. I have excellent knowledge for both 21 CFR 211 Current cGMP’s For Finished Pharmaceuticals and 21 CFR 111 Current cGMP’s For Dietary Supplements and ISO 9000. EXPERIENCE

Production Manager, Custom Nutraceutical

Bohemia, New York (03/18-07/18)

● Created an environment that increased monthly billable Finished Goods up to 40%

● Increased first time through to 85% on batch record accuracy

● Team Lead procuring machinery to increase production

● Lead for advancing compliance (GMP, OSHA)

● Performed daily and weekly cost analysis

● Deal with vendors to ensure all material was available

● Ensure KPI’s are met

Production Supervisor, Estee-Lauder (Contract)

Melville, New York (06/17-03/18)

● Use LEAN manufacturing practices to schedule daily work to employees ensuring efficiency in labor and machine hours are favorable

● Team Lead to evaluate practices to strengthen compliance and instill longevity

● Team member showing downtime at startup and giving suggestions to correct behaviors

● Run production meetings coaching employees and going over the KPI’s

● Evaluate employee performance for potential raise or job transfer

● Create SOP’s to strengthen compliance

● Ensure employees comply to all SOP’s

Production Manager, Windowtex Inc (Contract)

Garden City Park, New York (01/16-3/16)

● Schedule daily work orders according to ship date or need

● Run production floor to meet schedule and quality standards

● Institute quality measures to create better production flow

● Create Job descriptions for all current production/warehouse positions

● Evaluate current employees for potential raise and interviewees for potential hire

● Member of team to adjust current pay scale and raise compensation

● Hire and Terminate employees

Inspection Manager, Tishcon Corp

Westbury, New York (06/07- 12/15)

Manager 08/15- 12/15

Assistant Manager 08/11-08/15

Supervisor 06/07- 08/11

● Increase inspection by 30% by streamlining functions

● Assure production schedules are met. Work with other departments to ensure the timeliest receipt of product is made.

● Write or revise SOP’s to assure accuracy and completeness to FDA standards 21 CFR 111

● Train employees ensuring they understand job duties and policies

● Coach and develop employees in areas of responsibilities and developing of employee skill. I have promoted 5 workers to leads as they demonstrated ability to understand training and guidance

● Review product batch records for accuracy of entries

● Conduct internal investigation for returned product from packaging facility or customer. I have reduced returned product issues by 20% due to staff training and practices QA Inspector II, Watson Laboratories

Copiague, New York (03/02-11/06)

● Responsible for in-process checks for production

● Sample, test and release incoming raw material and packaging components with a 100% first time through metric

● Committee member for the creation of new packaging component specifications and test sheets with accompanying SOP according to 21 CFR 211

● Committee member for reviewing procedure to evaluate non mixed material in product. This group saved money from wasting materials by not having to throw product away and by not having to have the lab work to see what this material was

● Train new employees on sampling and inspection procedures. Trained a new hire on job functions that they eventually became a supervisor

● Inspect and release manufacturing and packaging rooms prior to production

● Audit batch records for accuracy and compliance to cGMP’s

● Coordinate scheduling of sampling and material status changes with various operational departments

EDUCATION

2012 Bachelor of Science with Honors

State University of New York College at Old Westbury Business Administration



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