Tamela Williams
Florence,SC
Summary
Methodical Quality Control Analyst skilled in developing protocols to positively impact manufacturing quality. Practiced at completing exhaustive tests of incoming materials, components and finished products. Proven experience within the manufacturing industry performing direct hands-on work in QA and QC functions with strong familiarity of general practices. Hardworking Quality Technician experienced in documenting results, modeling trends and comparing findings to specifications. Excellent organizational and problem-solving abilities developed over 18 years. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
Overview
20
20
years of professional experience
8
8
years of post-secondary education
1
1
Certification
Work History
Research and Development Scientist II
Thermo Fisher Scientific, Patheon
Florence , SC
06.2021 - Current
- Maintained detailed journals of all methods used in testing and research conducted by laboratory scientists.
- Wrote and updated reports on compiled material test data gleaned from experiments and shared results with fellow scientists.
- Exceeded goals through effective task prioritization and great work ethic.
- Created spreadsheets using Microsoft Excel for daily, weekly and monthly reporting.
- Delivered reports and updated SOPs to customer locations within specific time frames.
- Carried out day-day-day duties accurately and efficiently.
- Used Microsoft Word and other software tools to create documents and other communications.
- Executed degradation studies, method validation, and method transfers.
- Created corrective actions for continuous improvement for SOPs.
- Authored GMP documentation (methods, reports, deviations).
- Mentored junior scientists, fostering collaborative, productive work environment.
- Met and collaborated with clients to ascertain desired results and laboratory testing objectives.
- Planned laboratory experiments to confirm feasibility of processes and techniques to produce materials with special characteristics.
- Protected confidentiality and data integrity in work-related tasks as depicted in company regulations and protocols.
- Coordinated project management efforts to meet deliverables and deadlines.
- Evaluated competitor products to identify potential areas for differentiation and improvements in our own offerings
Quality Engineer/Quality Documentation Specialist
Clarios (Johnson Controls
06.2020 - 03.2021
- Developed traceability of produced lead alloy to aid in investigating faults and defects.
- Demonstrated product and quality expertise in product inspections.
- Developed training protocols in alignment with company quality standards and ISO 9000 regulations.
- Coordinated with quality control staff to complete inspections.
- Escalated concerns about project and process quality, referring discovered issues to engineering manager for correction.
- Contributed to root cause analysis to determine core reason for failures and errors.
- Supported quality team members during corrective action updates.
- Evaluated components and final products against quality standards and manufacturing specifications.
- Performed visual inspections and non-destructive tests where appropriate.
- Reported repeated issues to supervisors and other departments, collaborating to identify issue roots and rectify problems.
- Communicated with production team members about quality issues.
- Inspected quality of products, taking note of functionality, appearance and other specifications.
- Conducted investigations into questionable test results.
- Used Sharepoint for routing document revisions for approval.
- Lead Quality Assurance onboarding.
- Reported on non-compliance issues and other negative factors discovered during production.
- Reviewed issues, analyzed and interpreted data and determined corrective action.
- Conducted data review and followed standard practices to find solutions.
- Located and defined new process improvement opportunities.
- Supported team members in achieving department goals through effective collaboration on complex cases.
- Troubleshot problems with equipment and recalibrated devices or brought serious concerns to supervisor for handling.
- Played integral role in preparing for ISO certification audits, demonstrating compliance with international quality management systems.
- Ensured timely resolution of non-conformance issues by effectively communicating findings to relevant departments and recommending corrective actions.
- Performed thorough inspections of incoming materials and outgoing products.
- Fixed identified issues to increase productivity and boost workflows.
- Implemented process improvements to increase productivity in quality assurance operations.
- Cultivated interpersonal skills by building positive relationships with others.
- Skilled at working independently and collaboratively in a team environment.
Quality Technician
Johnson Controls (Clarios)
Florence, SC
11.2012 - 06.2020
- Sampled materials and products to conduct in-depth measurements and tests
- Made recommendations on ways to improve testing procedures, production processes and training
- Performed preventative maintenance to maintain optimal productivity
- Developed training schedules and trained new employees
- Developed inventory control system and reduced monthly consumables spending
- Developed Standard Operating Systems for daily testing
- Scheduled meetings with potential vendors to lower spending.
- Developed system to reduce cost on laboratory consumables.
- Helped uncover and fix production problems in order to reduce overall defect rates
- Performed raw materials testing
- Adhered to safety and clean area procedures to comply with agency and regulatory mandates
- Conducted data review and followed standard practices to find solutions
- Contributed to continuous improvement initiatives by actively participating in regular team meetings and sharing insights about potential areas of improvement.
- Conducted routine internal audits, ensuring that all departments adhered to established company policies and procedures related to product quality.
- Provided training on quality assurance best practices for new employees, fostering culture of excellence within organization.
Quality Control Scientist
IRIX Pharmaceuticals Inc
05.2004 - 11.2012
- Maintained compliance with safety and clean area procedures
- Performed testing per FDA guidelines on raw materials and in process materials for pharmaceutical drugs
- Developed methods for raw materials and active pharmaceutical ingredients
- Coordinated weekend and after hour support with project chemist Identified and reported potential safety hazards to management and/or EHS
- Designated work to subordinates in absence of supervisors
- Evaluated employee performance and training progress.
- Testing APIs using HPLC and GC.
- Performed raw materials testing using KF, pH meter, Metrohm potentiometric titrator, Nicolet FTIR, and wet chemistry.
- Developed training materials for new staff members to ensure consistent application of quality control procedures
- Presented findings from audits and inspections to senior management, providing actionable insights for continuous improvement efforts
- Mentored junior staff members and provided guidance on best practices in quality control, fostering an environment of continuous learning and professional growth
- Evaluated components and final products against quality standards and manufacturing specifications
- Monitored inventory levels to restock materials and maintain consistent supply
Education
M.D. - Business Administration and Management
University of Phoenix
Tempe, AZ 01.2010 - 05.2012
Bachelor's - Chemistry
Francis Marion University
Florence, SC 08.2003 - 06.2005
Bachelor's - Biology
Francis Marion University
Florence, SC 08.1999 - 05.2003
Skills
Testing procedures
Specifications understanding
Materials handling
Reporting skills
Process monitoring
Documentation expertise
Equipment calibration
Technical troubleshooting
Data interpretation
Materials inspections
Affiliations
SIgma Gamma Rho Sorority Inc.
Certification
IATF Auditor
Baking
Baking is my favorite pass time. It is something I enjoy doing that brings me joy. I love when other enjoy my baked goods and it makes them feel good. It is a great stress reliever.
Timeline
Research and Development Scientist II
Thermo Fisher Scientific, Patheon
06.2021 - Current
IATF Auditor
02-2021
Quality Engineer/Quality Documentation Specialist
Clarios (Johnson Controls
06.2020 - 03.2021
Quality Technician
Johnson Controls (Clarios)
11.2012 - 06.2020
M.D. - Business Administration and Management
University of Phoenix
01.2010 - 05.2012
Quality Control Scientist
IRIX Pharmaceuticals Inc
05.2004 - 11.2012
Bachelor's - Chemistry
Francis Marion University
08.2003 - 06.2005
Bachelor's - Biology
Francis Marion University
08.1999 - 05.2003