Dremier Williams

Norcross, Ga *****

email: ad4x4b@r.postjobfree.com

Phone: 678-***-****

Objective:

A dynamic pharmaceutical / chemical employee seeking an opportunity to utilize my leadership skills and unique experiences to support the overall growth of organizations in managing manufacturing operation while maintaining quality, yield and provide innovative problem-solving.

Skills and Experiences:

Experienced in leading day to day operations of operational, developing work schedules and assisting in writing department procedures (SOP).

Multiple years of managing employee's quality development which included corrective action and preventive action (CAPA), developing goals adhering to company policy with great success.

Responsibility for organizing department training of 5S and kanban operation.

Great success in working with other departments including but not limited to HR, engineering, quality control. and the safety department.

Experience leading internal and external audits.

Experienced with interviewing, onboarding, and training manufacturing personnel.

Working knowledge of using Microsoft Office Suite, SAP and ability to learn new systems with ease.

Education/Certifications

Emory University Asana CAPM / PMP Project Management

Ashworth College Computer Drafting and Design - Norcross, GA

Ashworth College Computer Drafting and Design - Norcross, GA

ITT Technical Institute-West Covina - West Covina, CA

Kankakee High School - Graduate

I

Work History

Corbion Biomaterials- manufacturing lead/supervisor Tucker, GA May 2021 –Present

Collaborate with the senior supervisor and plant leadership team to establish metrics and goals for operation.

Assist in managing the team in accordance with cleanroom policies, practices, procedures (SOP), and safety programs.

Strong ability to lead and supervise others and solve problems independently.

Assist in training of automatic batch (HMI) operation.

Perform basic mathematical calculations in developing daily batch recipes

Managed the incoming inspection of raw material.

Monitor/ trained employee on safety protocol such as safety showers, eye wash stations, and PPE.

Trained employee on preventive maintenance of equipment operation.

update computerized records and move goods to the appropriate storage locations.

Managed a team of 5 employee is which we reduced deviations by 50% and increase yield output by 10%

Participated in hiring and onboarding of new employees.

Maintain records of all record-related activities, audits, and incidents for reporting and auditing purposes.

Assist in developing quality improvement initiatives by analyzing data from logbooks to identify areas for improvement.

Conduct regular internal audits to identify and address compliance issues, correcting deficiencies as necessary.

TRC STAFFING AGENCY Sienna Corporation

Quality Inspector Suwannee, Ga May 6,2021 -Present

Performed inspections and testing of shipment of customers specifications.

Conduct audits and quality inspection for accuracy of raw materials.

Ensure calibration of inspection tools

Maintain curent (RMA) data base on non-compliance Product.

Worked with engineering to ensure schematics are correct.

Verify incoming materials using SAP database.

Conform blueprints match product produce for quality purposes.

Aerotek

Contractor-production support specialist Immucor Corp Sept. 2020 to Jan 2021

Mixed chemicals per batch sheets for production

Weigh and storage chemicals Production

Conduct audits and quality inspection for accuracy of raw materials.

Ensure calibration and inspection of Lab equipment.

Alcon Laboratories Johns Greeks Dec. 2014 to Aug 2020

Conduct production operation processes per SOPs.

Load, inspection and mixed raw materials for production.

Operate SPC lens inspection.

Knowledge of SAP to track final reviews.

Maintain and operate secondary packaging equipment as needed.

Use calibrated measurement equipment to perform operation

Perform minor repairs on equipment as needed.

Coordinate downtime to ensure efficient use of maintenance, corrective action and cleaning

Worked with validation team to complete validation of new product.

Establish 5s protocol in my department.

Knowledge of ISO/FDA/GDA/GMP and compliance.

Performed in process product quality checks.

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