Summary
Overview
Work History
Education
Skills
Milestones
Timeline
Generic

Cedric Slade

Houston,TX

Summary

Progressive and seasoned management professional with expertise in pharmaceutical and distribution operations. Implemented initiatives, influenced by lean methodology, resulting in measurable improvements to the bottom-line. Oversees deviation management to expedite QA batch disposition. Quality-centric resource who enforces adherence to cGMP and Federal compliance regulations. Proven leader who champions employee development through pragmatic mentorship. Engaging communicator who builds cohesive teams while fostering staff retention.

Overview

18
18
years of professional experience

Work History

Manufacturing Manager

Lonza
03.2022 - Current
    • Applied lean principles to improve workflow, operational quality and reduce waste.
    • Set, enforced and optimized internal policies to maintain responsiveness to demands.
    • Ensure right first time execution of manufacturing activities through identifying continuous improvement initiatives
    • Supervised team of 6 supervisors and 40 technicians, keeping production schedules on track to meet tight deadlines.
    • Assisted business units with existing functioning projects by implementing set strategies to improve process productivity.
    • Leveraged on-site observation and personal interviews to identify team and individual strengths.

Supervisor

Catalent
08.2021 - 03.2022
  • Manufacturing lead for both Allogeneic and Autologous cell and gene based t therapies outside clients
  • Designed and implement Process flow diagrams and value stream mapping maps to optimize to optimize project planning and execution
  • Provided expertise for equipment installation and Qualification, Grade B room qualification, qualification, and Batch record and SOP creation
  • Negotiated purchasing agreements with vendors for new Capital Expenditures equipment equipment as well as ongoing consumable materials
  • Lead technology transfer from Client to onsite manufacturing team
  • Partnered with Analytical analytical and process development to generate and implement project timeline with with quantifiable deliverables.

Operations Manager

Merck
01.2017 - 07.2021
  • Responsible for all processes for the VAQTA vaccine, Cell side, Bioreactor, and Purification
  • Developed internal mentorship program for new area people leaders
  • Created weekly production schedule and ensures all essential deliverables are achieved to produce quality product on time and in the right quantity.
  • Conducts departmental audits with Regulatory agencies.
  • Partner with other function areas to ensure timely and effective completion and installation of production equipment as well as work initiatives
  • Liaison with plant committee, adroitly navigated dynamic between management and union affairs.
  • Supports continuous improvement for Quality and production through participations in QRA's and continuous learning using Kata and Kaizen
  • Plans and coordinates external and inter-departmental services for HVAC, utility, and process equipment
  • Leads collaborative teams to decrease hourly overtime spend, not to exceed yearly forecast
  • Utilize Leader Standard of Work to increase operational efficiency and task prioritization.

Senior Production Supervisor

Allergan
04.2012 - 01.2017
  • Enforces cGMP compliance by reviewing production batch records with QA and escalates discrepancies to senior management as required
  • Ensure regulatory compliance for multiple MOH both foreign and domestic
  • Root cause analysis: executes investigations and troubleshoots automation and control systems
  • Hold employees accountable to support the Value Stream initiatives
  • Analyze production and quality control to detect and correct problems
  • Identify areas of improvement, synergize value added activities
  • Ensure cross functional collaboration and coordination between relevant departments including Filling, Packaging, and Quality Assurance
  • Develop system to ensure financial metrics and performance KPI's are achieved such as OEE, Right the First time, labor and material variances.

Production Supervisor

Hospira/ Pfizer
04.2008 - 04.2012
  • Ensured cGMPs are followed for all regulatory agencies: OSHA, FDA, DEA, and EPA
  • Provided leadership to the technicians in the Aseptic Filling and Inspection Packaging
  • Prepared and maintained production reports and personnel records
  • Drove the continuous improvement agenda in area of responsibility through teamwork, skills and capability development
  • Created and revised control documentation such as SOP, Protocols, and controlled forms.

Shipping Supervisor

QVC
06.2007 - 04.2008
  • Supervised and coached a shipping operation of 30+ employees
  • Improved area's cycle time to 97% during peak business season
  • Managed multiple production areas sorter, LNC, Automation, and shipping
  • Performed 5S reorganization of the shipping department
  • Coordinated delivery schedules with Transportation department to meet customer agreed delivery date

Operation Coach

Lowes
06.2005 - 06.2007
  • Coordinated and delegated responsibilities of 20-40 team members Decreased cycle time ranking from 12 out of 14 to 2 out of 14
  • Reviewed/audited receiving purchase orders and bills of lading
  • Fostered interdepartmental communication and cooperation
  • Taught new E2 practices, standards, and processes
  • Implemented Pick schedule in building department to increase daily demand turns
  • Utilized computerized inventory management system to predict trends in inventory levels.

Education

Bachelor of Science - Operations/ Supply Chain Management

North Carolina State University

Skills

  • DMAIC guided Process Improvement
  • Risk Mitigation Analysis for Non-Conforming events
  • Benchmarking best practices
  • Data driven analysis and decision-making
  • Safety Protocols
  • Change Management Process
  • Training and Development
  • Comprehensive Preparedness for Internal/External audits
  • Technical Support for Proprietary and 3rd Party
  • Employee Performance Management

Milestones

•Spearheaded shift Lean transformation production increase of 23% in OEE Achieved OSHA recordable rate of 0.
•Soaring Eagle award recipient (for best plant safety team) Led and implemented 5S process for packaging lines.
•Leader of Six Sigma Green Belt cost reduction team responsible for cost reductions of 100k per year.
•SME for separation of filling and packaging lines; increased annual product throughput yield of 6+ million units
•Led Kaizen events for reduction in line turn times and MUV reduction annualized savings of 50K production line.
•Completed greenbelt project for alternative packaging component savings 15k annually.
•Partnered with QA to create robust defect classification matrix to increase transparency between departments.

•Led QRA and PRA for End to End processing unit using failure mode analysis to identity and mitigate potential process risk.

•Collaborated with support groups to reduce material utilization and reduced scrap by 10% annually.

•Rolled out new GMP compliance training software for audit. Provided better transparency and retrieve for records during audits and investigation.

• Led IPT, benchmarked and implemented best practices for operations areas sitewide.

• Implemented visual factory concepts to foster timely and effective communicate of alarm and alert condition to reduce machine downtime by 15%.

•Introduced GEMBA walks to Packaging department to increase employee engagement and cultivate skip level information exchange.

Timeline

Manufacturing Manager

Lonza
03.2022 - Current

Supervisor

Catalent
08.2021 - 03.2022

Operations Manager

Merck
01.2017 - 07.2021

Senior Production Supervisor

Allergan
04.2012 - 01.2017

Production Supervisor

Hospira/ Pfizer
04.2008 - 04.2012

Shipping Supervisor

QVC
06.2007 - 04.2008

Operation Coach

Lowes
06.2005 - 06.2007

Bachelor of Science - Operations/ Supply Chain Management

North Carolina State University
Cedric Slade