Cynthia Daniel-Wilson
**************@*****.*** 908-***-**** Freehold, NJ
SUMMARY
Quality Control professional with 5 years of experience in the pharmaceutical industry, specializing in compliance with GMP and FDA standards. Proven expertise in conducting chemical, physical, and microbiological inspections, and developing SOPs to enhance product quality. Strong skills in problem-solving, teamwork, and utilizing QMS and LIMS for effective quality assurance. Seeking a Quality Control role to leverage extensive regulatory knowledge and laboratory testing proficiency.
WORK EXPERIENCE
Alpha Apogee LLC Union, NJ
Administrative Officer Dec 2023 - Oct 2024
• Ensured data accuracy by compiling, sorting, and verifying information before entry, and corrected data entry errors as needed.
• Managed office communications, including answering calls, taking messages, and redirecting inquiries to appropriate departments.
• Facilitated efficient office operations by sorting and distributing mail and maintaining logs of completed tasks. Nature's Bounty Leonia, NJ
Quality Control and Special Inspection Mar 2019 - Mar 2023
• Conducted routine testing and inspections of raw materials, in-production processes, and finished goods to ensure compliance with GMP and FDA standards.
• Documented and reviewed non-conformities, deviations from quality standards, and maintained accurate records of all quality control tests and findings.
• Developed and enforced Standard Operating Procedures (SOPs) related to quality control, collaborating with manufacturing, production, and R&D teams for optimal product quality.
• Ensured regular calibration and maintenance of laboratory equipment, managed sample handling, and maintained proper storage conditions to prevent contamination.
• Provided training and support to production and quality control teams, and participated in quality improvement initiatives to enhance operational standards.
EDUCATION
University of Port Harcourt
Bachelor in Technical Science, Medical Laboratory Technology Sep 2012
SKILLS
Experience in Quality Control Within the Pharmaceutical or Biotechnology Industry • Strong Knowledge of Pharmaceutical Regulations (FDA, GMP, ISO) and Quality Assurance Processes • Proficient in Laboratory Testing Techniques, Including Chemical, Physical, and Microbiological Methods • Excellent Attention to Detail and Problem-Solving Skills • Ability to Work in a Fast-Paced Environment and Manage Multiple Tasks Effectively • Strong Communication and Teamwork Skills • Experience With Quality Management Systems (QMS) and Laboratory Information Management Systems (LIMS) • Knowledge of Statistical Process Control (SPC) and Validation Procedures • Familiarity With Analytical Instruments Such as HPLC, GC, and UV/VIS Spectrophotometers • Ensuring That Medication Products Meet the Highest Quality Standards and Regulatory Requirements, Directly Contributing to Patient Safety and Product Reliability