•Independently manage and create product data setup for new items in SAP Recipe Management (PDM), from project scoping through tech transfer and ensures data accuracy.•Review sterility, purification, and composition results of raw materials. •Ensure all raw material, and packaging certifications are accurate and current. •Review technical documents of packaging components for accuracy and comply to FDA Standards. •Anticipate and communicate potential timing issues and collaborate… Show more •Independently manage and create product data setup for new items in SAP Recipe Management (PDM), from project scoping through tech transfer and ensures data accuracy.•Review sterility, purification, and composition results of raw materials. •Ensure all raw material, and packaging certifications are accurate and current. •Review technical documents of packaging components for accuracy and comply to FDA Standards. •Anticipate and communicate potential timing issues and collaborate solutions with process, packaging, and operations teams. •Conduct PDM scoping discussions enabling R&D to plan projects accordingly. •Ensure adequate scopings have occurred prior work execution. •Convey the fundamental connections between Recipe Management (PDM) and the Clorox Production environment (SAP R3) and its impact on new projects to all division teams. •Manage expectations with R&D partners and collaborated solutions to Recipe management set-ups.•Participates on PDM Steering Team and ensures R&D community is adhering to latest business processes during PDM project work, including Gold Standards, routings, and FDA qualifications. •Identify data accuracy issues and work with other COE members to determine the best solution to ensure consistency. •SAP Recipe Management authoring knowledge and in-depth searching.•Develop and implement manufacturing standards in SAP-PDM (or similar system) with a thorough understanding of product data management in alignment with ERP systems and compliance.•Track project requirements (data and timing) and communicate potential issues (missing data, slipping timelines) to all divisions. •Manage shifting project priorities and the fluctuating project load. Show less

TASKS: -Conduct Batch Record Review and product specs analysis trending -Inspection, sampling, material specification review, and release of Raw Materials -Update and creation of Raw Materials Specification forms-Review of Document Change Request (DCR) of new and updated batch records. -Support implementation and maintenance of an efficient system for reviewing and releasing pharmaceutical products-Communicate with manufacturing personnel /managers to correct and… Show more TASKS: -Conduct Batch Record Review and product specs analysis trending -Inspection, sampling, material specification review, and release of Raw Materials -Update and creation of Raw Materials Specification forms-Review of Document Change Request (DCR) of new and updated batch records. -Support implementation and maintenance of an efficient system for reviewing and releasing pharmaceutical products-Communicate with manufacturing personnel /managers to correct and improve deficiencies in data collection, analysis, and reporting-Investigate deviations and systematic problems to identify root cause and effective corrective and preventative actions (CAPAs)-Perform validation testing to support the release of raw materials, in-process materials, and finished products-Provide QA support to execute protocols for validation of new equipment and product lines-Provide in-process QA support in compounding, filling, visual inspection, and packaging of pharmaceutical products-Perform internal Audits per FDA 21 CFR 820 and FDA 21 CFR 211-Perform QA testing on all applicable Pharmaceutical, FDA, USP, NF, and CFR products-Support QA complaint system by receipt and investigation of customer complaints and ensure product is produced according to customer specifications and immediate customer requests-Provide QA support for engineering runs. -Inspect and audit product lines to ensure pharmaceutical products meet customer specifications-Inform customers of production line change and time adjustments.-Construct Annual Product Reviews for commercial drug products. -Train new hires on batch record reviews, manufacturing audits, line release, and inspection of raw materials Show less

AWARDS: • Clinical Care Extender Exemplary Service Certificate: 2012 Rotations C and D 2013 Rotations A and B• Clinical Care Extender Outstanding Dedication: 2013 Rotations A and B TASKS: -archived, maintained, patient charts - Prepare patient charts for nurse and doctor examinations - Prepare examination rooms for Rehab, Maternity, and Psych wards - Feed patient and ambulated patients - Assist nurses in… Show more AWARDS: • Clinical Care Extender Exemplary Service Certificate: 2012 Rotations C and D 2013 Rotations A and B• Clinical Care Extender Outstanding Dedication: 2013 Rotations A and B TASKS: -archived, maintained, patient charts - Prepare patient charts for nurse and doctor examinations - Prepare examination rooms for Rehab, Maternity, and Psych wards - Feed patient and ambulated patients - Assist nurses in changing and dressing patients - Transport specimens to lab- Supervise patients group therapy - Assessed Patient comfort and reported health status to nurse - Patient check-in and discharge - Responsible for tracking, reordering, and maintaining medical supplies Show less

- Conducted extensive sanitation of culinary equipment
- Actively engaged with guests providing optimal guest satisfaction

- Coordinated multi-floor seating for a high flow 1500 capacity restaurant. - Provided guided tours and ensured proper sanitation techniques.
- Trained new hires

- Constructed and repaired customized stuffed toys
- Provided private guided tours through customized stuffed animal production for large groups.-Customer Service -Inventory and Stock-Sales/Cashier