Hasante Johnson

Managed daily on-floor tasks according to established production schedule to optimize workflow efficiency.

Executed aseptic filling operations with a strong understanding of first air dynamics to maintain sterile environments.

Engaged in team discussions to generate and polish ideas for strategic campaign initiatives.

Executed standard operating procedures and good documentation practices to enhance operational efficiency and accuracy.

Monitored and evaluated manufacturing processes in accordance with current good manufacturing regulations to maintain industry standards.

Achieved operational readiness by effectively washing and sterilizing vials, contributing to seamless production processes. Facilitated the preparation of components through thorough washing and sterilization of vials, enhancing workflow efficiency. Delivered operational support by maintaining high standards in washing and sterilizing vials, ensuring components were primed for use.

Achieved streamlined production operations that improved overall efficiency. Delivered consistent operational results by optimizing production workflows. Facilitated effective communication within teams to enhance production outcomes.

Conducted thorough cleaning and integrity assessments of equipment and rooms to maintain operational standards.

Conducted thorough testing to ensure quality and functionality during pre- and post-production stages.

Developed and implemented training programs to enhance team collaboration and staff competencies.

Documented and prioritized project requirements to ensure alignment with business objectives.

Improved batch records and standard operating procedures, resulting in streamlined operations. Championed regular enhancements to processes, leading to increased efficiency.

Analyzed completed batch records and logbooks regularly to identify discrepancies and uphold documentation standards.

Directed execution of corrective measures to enhance operational efficiency.

· Generates Purchase requisitions and service receipts for consumables items within the

Achieved timely project completions within the manufacturing department through effective collaboration. Enhanced production outcomes by implementing process improvements. Maintained high safety standards that resulted in a reduction of workplace incidents.

Managed production tasks autonomously, ensuring adherence to regulations and operational guidelines.

schedule.

Delivered timely updates to management regarding project milestones and data transfer efficiency. Optimized information flow on project statuses and data processing activities.

Collaborated with management to recommend ongoing process improvements aimed at increasing efficiency.

Maintained meticulous records and documentation practices to align with compliance protocols.

Recorded detailed task procedures to maintain comprehensive documentation.

Facilitated successful project outcomes by providing operational support to validation and maintenance teams. Contributed to improved operational efficiency through dedicated assistance to validation and maintenance staff.

Achieved successful project completions by leading collaborative efforts among engineering teams. Delivered high-quality engineering solutions through effective project management. Optimized project workflows to maximize team productivity and performance.

Developed and executed training sessions aimed at elevating the technical capabilities of novice technicians.

Implemented quality control measures to guarantee effectiveness and quality during production operations.

Managed routine housekeeping and maintenance operations, focusing on cleanliness and hygiene across the facility.

Achieved operational readiness in production areas by maintaining cleanliness standards. Optimized equipment sterilization processes to enhance routine aseptic operations. Strengthened gowning compliance for restricted access barrier systems, contributing to efficient ISO 5/6 area management and effective terminal sterilization.

• Executed monitoring and preparation of automated cell processing and fill-and-finish equipment, ensuring compliance with protocols for autologous stem cell transplants.
• Oversaw cultivation and maintenance of human cells, specifically T cells, ensuring optimal growth conditions.
• Executed comprehensive filter testing procedures to ensure product quality.
• Managed preparation of filtration media and performed cell counting.
• Maintained rigorous BSC aseptic and sterile techniques while operating within Grade A and B clean room environments to uphold product integrity.
• Executed precise documentation practices in alignment with SOPs and CGMP regulations to support efficient commercial manufacturing operations.
• Applied analytical expertise to evaluate situations critically and enhance decision-making processes.
• Achieved operational efficiency by effectively utilizing MES, PAS-X, SAP, Oracle EBS, HMI, MS Word, Excel, TrackWise, Microsoft Outlook, and Blue Mountain software. Streamlined processes through proficient application of various software tools.
• Managed communication channels with various departments, addressing escalations related to MSAT, QA, QC, facilities, and document control.

• Executed operation of various scales, maintaining precision and reliability in production processes.
• Managed daily production schedule, ensuring timely execution of tasks to maintain workflow efficiency.
• Executed weight checks to ensure precision in inventory management.
• Demonstrated proficiency in aseptic techniques while operating biosafety cabinets to safeguard sample integrity.
• Operated washers and autoclaves to maintain cleanliness and safety standards. Assisted in the assembly of solution preparation tanks for efficient production. Supported daily operations through effective handling of equipment.
• Configured and sanitized process equipment to ensure operational efficiency.
• Conducted thorough monitoring of processes while implementing SIP, CIP, and manual cleaning techniques to maintain operational standards.
• Executed production record completion and upheld clean room standards to ensure regulatory compliance.
• Diagnosed and addressed basic technical problems to maintain operational continuity.
• Assisted with the use of PASX, SAP, GQC, LIMS, HMI, Microsoft Office, and SharePoint systems. Supported team members in utilizing various software tools for project tasks. Provided help in navigating SAP and SharePoint systems to enhance workflow efficiency.
• Maintained accurate and thorough documentation in accordance with GMP and ISO standards while working in a high-volume manufacturing facility.

• Managed operation of fluid bed equipment for both wet and dry granulation processes.
• Conducted thorough verification of raw materials, confirming product names and weights prior to processing to support production efficiency.
• Executed formulation adjustments by incorporating API and excipient into wet granulation protocols.
• Managed equipment set-up, adjustment, and disassembly processes to support seamless production and thorough cleaning.
• Executed detailed visual assessments of products for defects and quality assurance, facilitating seamless discharge processes.
• Maintained accurate records of fluid bed readings in alignment with CGMP guidelines and standard operating procedures.
• Performed operational maintenance and setup of Fette 3090, Fette 3100, Kikusui, Gemini 855, and Sejong P2105 to support production efficiency.
• Monitored tablet production to identify and address physical defects such as sticking, chipping, and capping during compression processes.
• Conducted in-process checks to ensure compliance with weight, thickness, and hardness specifications.
• Performed detailed assessments of logos during compression to confirm compliance with design specifications.

• Operate solid dose equipment
• Routinely performed line-specific duties including line inspection and release
• Assisted with the work center changeovers and product movements
• Set up and adjusted equipment including tablet fillers, capers, induction sealers, bottle labelers, check weighers, cartons, and palletizers as needed
• Examined products to detect defects or other visual problems
• Trained and certified in SAP and MES systems

• Operated Fluid bed for wet and dry granulation
• Verify raw materials for product names and weights prior to processing
• Add API and Excipient for wet granulation
• Set-ups adjust and disassemble equipment for production and cleaning
• Visually inspect products for defects and quality prior to discharge
• Document fluid bed readings in accordance with GMP and SOP