Quality Assurance Data Entry

Diamond Avila Walker

Demonstrates strong analytical, communication, and teamwork skills, with proven ability to quickly adapt to new environments. Eager to contribute to team success and further develop professional skills. Brings positive attitude and commitment to continuous learning and growth. Skills

Work History

Cleanroom Manufacturing Support

Broadcom, Breinigsville, PA May 2024 - Current

Quality Assurance

Bethlehem, PA 18018 484-***-****

**************@*****.***

PPE compliance

Networking

Collaboration

Remote office availability

Time management

Critical thinking

Recordkeeping

Training & Development

Versatile professional with strong problem-solving skills and history of adapting to diverse challenges. Applies innovative solutions and technical expertise to deliver exceptional results. Committed to streamlining processes and advancing organizational objectives. compliance with GMP and FDA regulations

Demonstrated strong organizational and time management skills while managing multiple projects. Exercised leadership capabilities by successfully motivating and inspiring others. Worked effectively in fast-paced environments.

Skilled at working independently and collaboratively in a team environment. Managed time efficiently in order to complete all tasks within deadlines. Gained extensive knowledge in data entry, analysis and reporting. Proven ability to develop and implement creative solutions to complex problems. Gained strong leadership skills by managing projects from start to finish. ability to operate both manual and computer-controlled equipment CAPS B.Braun Company, Allentown, PA September 2023 - April 2024 Compounding Pharmacy Technician

QuVa Pharma, Bloomsbury, NJ December 2022 - September 2023 Inspection, Labeling and Packaging Technician

QuVa Pharma, Bloomsbury, NJ June 2022 - December 2022 Education

High School Diploma June 2022

Easton High School, Easton, PA

Conduct product QC sampling

Identify and take corrective action when deviations occur Document, monitor and analyze data to drive continuous improvement Maintain a comprehensive understanding of all products Understanding of raw materials, packaging materials, and operations Execute and adhere to GMP's

Compound all required types of sterile preparations accurately and in compliance with master worksheets

Use aseptic practices and procedures to prevent contamination from pathogens Perform process unit operations according to SOP and batch records; record production data and information in a clear, concise format according to GDP Perform cleaning of the clean room areas thoroughly and according to policy without viable particle growth

Pass all initial and ongoing validations and advanced complex media-fill verifications Accurately complete documentation in SOPs, logbooks, and other GMP documents Comply with 503B guidelines, cGMPs, and company standards Conducted labeling and processed production materials as required Completed line and room clearances as per established procedures Completed documents for accountability and traceability of product following GDPs; complied w/ cGMPs and ISO standards

Performed equipment calibration checks and troubleshot equipment as needed Completed documentation activities in accordance with established procedures Attached label specimens and reconciled materials printed with variable data

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