Adekunle Adekuebi
Laurel,MD
Summary
Resourceful Associate dedicated to mentoring and educating new team members. Thorough resource on internal company policies and procedures. Driven attitude toward providing customer care within business environment. Motivated Team Lead possessing excellent leadership and planning abilities. Focused on delivering high-quality products on tight schedules. Monitors, trains and encourages employees to improve skills and meet demanding targets. History of successfully developing and managing strong teams through proactive training and issue management.
Overview
9
9
years of professional experience
1
1
Certification
Work History
Senior Manufacturing Associate III
Catalent Pharma Solutions
HARMAS, MD
12.2023 - Current
- Lead daily manufacturing activities
- Daily review of GMP Batch records
- Collaborate with other team members to improve production processes while ensuring safety protocols are followed at all times.
- Train new manufacturing associate and existing employees
- Troubleshoot problems in the manufacturing process by identifying root causes and proposing solutions.
- Perform adherent cell Harvest and downstream using TFF and ultrafiltration techniques
- Understand and determine maintenance requirement ,preventative and calibration of equipment and work with vendor to resolve issues
- operate and use of single use bioreactor and all accompanying materials
Manufacturing Associate II/Qualified Trainer
Catalent Pharma Solutions
Harmas , MD
03.2023 - 12.2023
- Leverages knowledge and application of the theories and principals utilized to solve operational, as well as routine tasks in the operation of microbial or cell culture processes (media/buffer prep, cell passaging , bioreactor production, harvesting operation
- Adhered to current good manufacturing practices to support proper design, monitoring and control of manufacturing processes and facilities.
- Completed and reviewed GMP documentation, driving traceability of development, manufacturing and testing activities.
- Generate operational protocols internal or external document including SOPs, Deviations and summary report
- Ability to successfully trained operators on all upstream process
- Escalated manufacturing issues to management and quality assurance to identify solutions.
- Monitor critical process parameters on manufacturing equipment and perform first line troubleshooting of equipment
- Perform RTRs of batch record after process step and complete any assigned special project as require
Maufacturing Associate I/Qualified Trainer
Catalent Pharma Solutions
Harmas, MD
06.2022 - 03.2023
- Completes Batch Production Records under cGMP, and documents in detail through the use of SOPs and BPRs for the processes and manufacturing steps.
- Documents/Records cGMP data and information for processing steps and/or equipment activities, following standard operating procedures. Key documentation includes batch records and equipment logbooks.
- Built and maintained relationships with peers and upper management to drive team success.
- Execute biomanufacturing processes per Master Batch Record as well as respond to alarms and trouble shoot bioreactors and other manufacturing equipment.
- Setup KTF and POD filters to execute TFF process as well as the inoculation of bioreactor, perfusion, 1st and 2nd Transfection, batching of tanks, charging of bioreactor. Experienced with various manufacturing equipment such as 20L WAVE, pH/Conductivity meter, incubators, Vi-Cell, as well as the Nova Flex2.
- Execute Gamba walk to provide feedback on process as well as to identify any possible safety hazard or provide feedback for consistent improvement of processes as well as document any abnormalities of equipment
- Trained newly hired top talent to fill key positions and maximize productivity.
- Monitor critical process parameters and performs first-line troubleshooting of equipment and processing and generate shift report.
- Perform RTRs on batch records after process step and complete any assigned special projects as required as well as training new associates on processes and equipment.
Team Lead
Nestle
Laurel, MD
08.2015 - 06.2022
- Delegated daily tasks to team members to optimize group productivity.
- Created and distributed monthly, quarterly and annual reports to management regarding performance.
- Implemented performance, quality and efficiency measures to achieve aggressive production goals.
- Kept work areas clean, neat and free of safety hazards to maximize efficiency.
- Completed daily quality assurance duties to provide feedback for improvements.
- Worked closely with shipping, warehouse and other personnel to coordinate movements and keep workflows smooth.
Education
Associate of Arts - BANKING AND FINANCE
FEDERAL POLYTECHNIC
ADO EKITI,NIGERIA10.2012
High School Diploma -
Unity High School
Ikire ,Nigeria 06.2006
Skills
- Biotechnology Industry
- cell culture
- problem solving
- Manufacturing processes
- Communication
- Documentation
- Training Delivery
- TrackWise
Certification
- Certified security+, comptia - Nov 2021
- Certified certified Ethical Hacker, EC- Council - Nov 2022
- lean six sigma white belt certification -Mar 2023
- six sigma yellow belt certification -Mar 2023
Timeline
Senior Manufacturing Associate III
Catalent Pharma Solutions
12.2023 - Current
Manufacturing Associate II/Qualified Trainer
Catalent Pharma Solutions
03.2023 - 12.2023
Maufacturing Associate I/Qualified Trainer
Catalent Pharma Solutions
06.2022 - 03.2023
Team Lead
Nestle
08.2015 - 06.2022
Associate of Arts - BANKING AND FINANCE
FEDERAL POLYTECHNIC
High School Diploma -
Unity High School