Summary
Overview
Work History
Education
Skills
Certification
Timeline
Generic

CHARLES PELLA

Davie

Summary

Pharmaceutical, manufacturing professional with more than 10+ years' experience driving revenue and improving Industrial operations within Warehouses, Technological, Manufacturer and maintenance environments. Proven ability in building profitable organizations by achieving the highest standards in service, employee development, and expense control. Expertise in monitoring quality, containing costs, warehousing skills, Training, hiring, management, improving customer satisfaction. Reputation for resolving problems on first contact and improving operations through diligence and determination. Proficient in Microsoft Office. Revenue Growth, Budget Management, Inventory Control, Quality Assurance, Training & Development, Manufacturing supervisor successful at exceeding production, revenue and quality standards through effective leadership and cross- training. Well-qualified Quality Control Inspector proficient in documentation, reporting and compliance standards. Meticulous and methodical professional with a deep understanding of manufacturing and production operations. Expert at testing products using specialized tools and instruments. Fully compliant with safety rules and processes. Experience in Pharmaceutical/Manufacturing environments. Motivates employees to align performance with company objectives in fast-paced production environments. Superior competency in resource allocation, production scheduling and workflow management. Authorized to work in the US for any employer.

Overview

21
21
years of professional experience
1
1
Certification

Work History

Production Manager

Sofie
04.2025 - Current
  • Supervise and coordinate all production activities at the site.
  • Perform normal Production/QC technologist duties plus added management tasks.
  • Act as liaison with RCM group and contract partners.
  • Oversee synthesis unit operations, setup, documentation, and maintenance.
  • Ensure completion of training for synthesis unit operation.
  • Manage and maintain inventory (supplies, spare parts, critical materials).
  • Assist with routine and emergency maintenance of equipment and cyclotron.
  • Operate particle accelerator and support cyclotron engineer.
  • Perform QC testing on batches and support basic QC activities.
  • Enforce compliance with cGMP, SOPs, radiation safety, and ALARA principles.
  • Ensure cleanliness and sanitization of production and QC areas.
  • Track and report manufacturing metrics and production performance.
  • Manage production staff scheduling, PTO approvals, training, and performance reviews.
  • Handle deviation reports, daily logs, and weekly reporting tasks.
  • Participate in weekly production manager calls and cross-department communication.
  • Stay within production budget and identify cost-reduction opportunities.
  • Provide 24/7 technical and administrative support via company-issued phone.
  • Communicate clearly with pharmacists and resolve production delays or issues.
  • Ensure acceptance of incoming inventory per SOP.
  • Perform other duties as assigned.

Director of operations

Sanitas Medical center
02.2024 - Current
  • Direct supervision of all personnel and ensure adequate staffing levels.
  • Ensures that work schedules and staffing patterns are implemented and recognizes and promotes teamwork orientation and training of personnel on center policies and procedures.
  • Evaluate supervision personnel, employee performance and makes recommendations accordingly to the administrator.
  • Counsel and discipline employees when necessary; monitor productivity levels of personnel.
  • Assist in developing and updating policy and procedure manuals. Process daily cash reconciliation/ deposits and other reports as necessary and ensures petty cash is accounted and safeguarded.
  • Collects and summits monthly statistical reports to Upper Management for all center services and departments.
  • Develops progressive departmental goals and appropriate measures to ensure timely effective results.
  • Responsible for and will recommend procurement of supplies, equipment and modifications necessary for practical economical operations.
  • Responsible to comply with on call rotation, Analyze and develop productivity of departments, analyze data related to physicians' productivity and member services, Works closely with the Marketing Dept. in developing strategies to increase and retain membership, Handle member complaints, ensures that referrals are being issued in a timely manner.
  • Maintain updated documentation of licenses and in-services to comply with regulatory procedures, maintain open communication with assistant administrator on daily operational issues, responsible to comply with on call rotation, schedule supervision and staff meetings, ensures customer satisfaction with all members.
  • Manages all employees of the department and is responsible for the performance management and hiring of the employees within that department.

Quality Assurance Manager

Octapharma Plasma
10.2021 - 02.2024
  • Perform daily donor record reviews for approval and deferred activities.
  • Perform final quality control review and release for all shipments to ensure it meets customer specifications.
  • Review medical incidents reports and documentations.
  • Perform other job-related duties, as assigned.
  • Responsible for initiating, investigating, and reporting any supplies that have not met quality specifications promptly.
  • Assisting all quality with compliance of all procedures, Current Good Manufacturing (cGMP), FDA approved Standards Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), and other regulations.
  • Conduct root cause analysis for deviations and customer complaints to determine the need for corrective action, ensure appropriate documentation, and assess the effectiveness of the action.
  • Perform QKPI in a monthly basis, go over improvements or errors in the center monthly meetings.
  • Perform QISM meeting with all management team to discuss center procedures, deviations, employee development, new employee training process.
  • Identify employees who need training, disciplinary actions, budget control, hiring process, NPS score, google reviews.
  • Perform employee observations, employee assessments.
  • Performed minor, major deviations and CAPAS.

Production Manager

Sun Distribution
10.2021 - 10.2022
  • Resolved issues quickly to maintain productivity goals.
  • Managed continuous improvement initiatives to drive gains in quality, flow and output.
  • Reviewed work for quality and compliance with company standards and design specifications.
  • Standardized production procedures, job roles and quality assurance guidelines.
  • Assessed manufacturing processes and recommended improvements to increase productivity.
  • Use Finale for inventory control.
  • Addressed personnel issues and scheduling conflicts promptly.
  • Training process.

Quality Control Inspector/ Physical Lab

ANTHEM SOUTH
06.2020 - 09.2021
  • Quality and manufacturing departments to ensure the quality of production and products produced meet company standards, Responsible for monitoring and providing support to the weighing, blending, production and lab areas of manufacturing.
  • Performed visual inspections and non-destructive tests where appropriate.
  • Evaluated components and final products against quality standards and manufacturing specifications.
  • Monitored performance and generated reports detailing quality of product and defect rates.
  • Communicated with production team members about quality issues.
  • Created and deployed best practices to improve efficiency and reduce defects.
  • Verify sampling and PH testing of blend through documentation.
  • Performed PH, conductivity and Quat testing for Clorox and other products from PC lab.
  • Review batch records and release for product information against production schedule.
  • Discarded and rejected products, materials and equipment not conforming with specifications.
  • Supervised production workers to identify areas in need of improvement for high-quality production.
  • Training process for all new employees.
  • Inspected outbound shipments and conducted random sampling of product quality.
  • Identified and helped resolve non-conforming product issues.
  • Validation process expert.

Technician II Manufacturing

BIOTEST PHARMACEUTICAL
02.2016 - 02.2020
  • Maintained and communicated daily productivity and shipment reports for all departments.
  • Verified that all process control parameters were being documented and always followed.
  • Defined manufacturing performance standards and reviewed the outcome of performance goals to set future targets.
  • Created and updated department work instructions and reports on a regular basis.
  • Addressed all personnel issues promptly and professionally.
  • Responsible for the manufacture of plasma receipt, plasma pooling and protein separation.
  • Cleans and sanitizes equipment before and after use responsible for plasma receipt operations make and verify connections on flow panels.
  • Perform HP and conductivity measurements.
  • Operation of filter press and CUNO filter.
  • Initiate product processes on the process automated system.
  • Harvest of product precipitates, take and prepare samples, order and maintain raw material inventories.
  • Complete batch records, assist group leader.
  • Deviation Process forms, minor deviations.
  • PLC basic technical skills and knowledge necessary to work with programmable logic control systems.
  • Calibration, repair, adjustment and replacement of components.

SKY CAP, SWISS CAPS USA
10.2012 - 02.2016
  • Adhere to batch record specifications and keep the encapsulation process in control.
  • Assure applicable SOPs are followed and production is performed in accordance with GMPs.
  • Team environment by promoting a teamwork atmosphere with spreaders and inspection employees and covering co-workers' machines during breaks.
  • Provide 'hand-on' training to new encapsulation employees.
  • Document activities in logbooks incorporating good documentation practices.
  • Disassemble and clean encapsulation machines and equipment.
  • Assemble and set-up encapsulation machines and equipment.
  • Clean tumblers, working area, and gelatin tank covers.
  • Perform Encapsulation start-up activities, check seam percentage and fill material mixing.
  • Perform in-process checks for fill-weight variation, temperature variation, gelatin ribbon thickness and capsule length.
  • In charge of making sure product was ready to be run into machines.
  • Release product, put product on hold for further investigation or deviation process.
  • Made sure Batch records were properly filled out and singed before releasing the batch.

Maintenance Manager

FRISCO INDEPENDENT SCHOOL DISTRICT
02.2008 - 01.2012
  • Plan, manage, and provide leadership for Custodial and school district, worked for almost 3 years having Successful years of work and experience.
  • Maintained areas cleaned, make sure all light bulbs were in good condition, paint any walls or doors from classrooms as need it.
  • Help in any activities from the school and Saturdays as well, help Teachers and students, setting up events for students and parents.
  • Computer Skills, Able to change light bulbs, make sure all Air Conditioning filters are changed.
  • Scrubbing floors, waxing and sealer installation, as well as, operating Scrubbing Machines, Buffers, Wet.
  • E hiring process, training, delivering supplies.
  • The Essential duties of cleaning, supervised and managed 30+ employees, Inventory of supply, budgeting control, Bilingual fluently.
  • Highly organized coordination of meetings and events, including preparing all materials and setting up equipment.
  • Able to Follow directions and instructions.
  • Team Player Championed quality initiatives.
  • Immediately addressed all expired product Dispositions.
  • Recommended and executed quality improvements for production and product Quality Addressed all personnel issues promptly and professionally.

Semiconductor Technician

TEXAS INSTRUMENTS
06.2009 - 06.2010
  • Worked with WAFERS, Microchips.
  • Build components with the necessary electrical structure to rapidly switch and transfer signals for computational purposes.

Floor Supervisor Shipping and Receiving

CNS Wholesale food
03.2004 - 12.2007
  • Started as a selector consisting of operate electrical pallet jacket, forklift, upload and download trucks, Data entry, supervising packages and trucks, controlled inventory.
  • Verified that all process control parameters were being documented and always followed.
  • Managed Documentation of and training on production procedures and work instructions.
  • Recommended and executed quality improvements for production and product quality.
  • Data Entry Computer processing and inventory management skills.

Education

High School Diploma -

Miami Dade High School
Miami, FL

Skills

  • Manual and Finger Dexterity
  • Decision Making
  • Sample Collection
  • Performance Monitoring
  • Equipment Function Testing
  • Inspection and Testing Reports
  • Documentation and Recordkeeping
  • Information Ordering
  • Problem Anticipation and Resolution
  • Quality Control
  • Attention to Detail
  • Processing Operations Review
  • Product Planning
  • Production Schedule Review
  • Inventory Control Programs
  • Spanish: Native or Bilingual
  • English: Native or Bilingual
  • Leadership
  • Supervising experience
  • Budgeting
  • Manufacturing
  • Quality control
  • CGMP
  • Assembly
  • Laboratory experience
  • Production planning
  • Customer service
  • Quality assurance
  • Continuous improvement
  • Program management
  • Warehouse management system

Certification

Forklift Certification

Timeline

Production Manager

Sofie
04.2025 - Current

Director of operations

Sanitas Medical center
02.2024 - Current

Quality Assurance Manager

Octapharma Plasma
10.2021 - 02.2024

Production Manager

Sun Distribution
10.2021 - 10.2022

Quality Control Inspector/ Physical Lab

ANTHEM SOUTH
06.2020 - 09.2021

Technician II Manufacturing

BIOTEST PHARMACEUTICAL
02.2016 - 02.2020

SKY CAP, SWISS CAPS USA
10.2012 - 02.2016

Semiconductor Technician

TEXAS INSTRUMENTS
06.2009 - 06.2010

Maintenance Manager

FRISCO INDEPENDENT SCHOOL DISTRICT
02.2008 - 01.2012

Floor Supervisor Shipping and Receiving

CNS Wholesale food
03.2004 - 12.2007

High School Diploma -

Miami Dade High School

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