Summary
Overview
Work History
Education
Skills
Timeline
Generic

Jacob Nail

Lithia Springs

Summary

Results-driven professional ready to excel in Production Coordination, and/or all aspects of supporting an effective production site. Extensive experience ensuring smooth operations and meeting tight deadlines. Known for effective teamwork and adaptability, consistently contributing to successful project completions.

Overview

7
7
years of professional experience

Work History

Production Coordinator

Deerland Probiotics and Enzymes/ADM
11.2022 - Current
  • PRODUCTION LIASION:
  • Assist in material transfers, issues, returns, inventory adjustments and stock conversions.
  • Collaborate with Quality for any unplanned deviations and production process errors.
  • Support logistics process with physical material movements, and forklift operations.
  • JOB CREATION, JOB RELEASE, AND FOLDER CREATION:
  • Assemble comprehensive job folders for pilot/production runs, ensuring inclusion of all relevant documentation (e.g., QR/RM case transfers, development job tickets, and customized Work Instructions for new processes or formulations).
  • While managing the production schedule, evaluate/ensure the cleaning procedures between each product are performed correctly, and forward to QA for approval.
  • Assist in printing all Production Specifications and alert QA or Customer Service of any issues; along with following up on Production Specifications that are pending for changes that may affect upcoming SKUs.
  • Collaborate with R&D, QA, and inventory teams to review and assign appropriate lots for Raw Materials (RM) and Work In Progress (WIP) items used in Production.
  • Monitor and confirm that all stability testing samples are incorporated and submitted to lab for New Product Jobs.
  • Amend job details as needed to meet product-specific testing or customer requirements.
  • DEVIATION AND JOB AMENDING MANAGEMENT:
  • Keep an up-to-date inventory of specific deviations from standard quality parameters.
  • Review the production and Product Development pipeline to identify potential applications for QR RM.
  • For Productions / BI for which QR RM can be used, perform the calculations to determine the revised quantities for each recipe.
  • Work with R&D and Formulation teams to model the impact of QR RM on product performance, safety, and quality.
  • MANAGING RAW MATERIAL NEEDS:
  • Coordinate with the Purchasing/Procurement team to review open Material Purchase Orders and explore the possibility of expediting order fulfillment.
  • Collaborate with the Customer Service team to assess the status of open purchase orders for Customer Supplied Components and verify their on-time delivery.

Bottling Lead Operator

Deerland Probiotics and Enzymes
06.2020 - 11.2022
  • Monitor Workers on site during production activities to ensure adherence to ethics and safety procedures.
  • Motivate workers to enhance production quantity and at the same time maintain high production standards.
  • Train and mentor existing and new Deerland associates in all processes defined in the bottling area including but not limited to procedures, equipment operation, changeovers, cleanings, paperwork, and properly entering data into the VORNE system.
  • Act in a supervisory capacity in the absence of the supervisor/or manager on occasion.
  • Perform machine changeovers and cleaning as specified by the production schedule in accordance with appropriate SOPs.
  • Learn the operator roles, responsibilities and SOPs specific to the assigned area and equipment.
  • Set-up and perform adjustments on machines to ensure bottling line runs productively and efficiently.
  • Ensure efficiency is maintained using the VORN system and track/evaluate any opportunities to improve efficiency.

Operator - Manufacturing, Packaging Lead

Osmotica Pharmaceuticals
03.2018 - 06.2020
  • Ensure the proper set-up and operation of standard pharmaceutical process equipment in Packaging.
  • Ensure proper execution of Master Batch Records, standard operating procedures and validation protocols.
  • Ensures accurate completion of equipment logs and logbooks.
  • Ensures cleanliness and proper assembly of manufacturing equipment per approved procedures (SOP's).
  • Interfaces and consults with Analytical Sciences and Quality Assurance personnel.
  • Understands and adheres to all cGMP and FDA regulations.
  • Set – up room for specific batch referring to Master Batch Records.

Education

Diploma -

Lithia Springs High School
Lithia Springs, GA
05.2013

Skills

  • Analytical problem solving
  • Adaptable learner
  • Openness to tackling new responsibilities
  • Team-focused contributor
  • Proficient in task prioritization
  • Maintain composure under challenging circumstances
  • Strong focus on accuracy
  • Proficient in cGMP practices
  • Workflow coordination

Timeline

Production Coordinator

Deerland Probiotics and Enzymes/ADM
11.2022 - Current

Bottling Lead Operator

Deerland Probiotics and Enzymes
06.2020 - 11.2022

Operator - Manufacturing, Packaging Lead

Osmotica Pharmaceuticals
03.2018 - 06.2020

Diploma -

Lithia Springs High School

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Jacob Nail