Pamelajoyce Jones

About Pamelajoyce Jones

As a dedicated scientist and quality assurance professional, I have built my career on a foundation of rigorous scientific inquiry, precise quality control, and a passion for driving operational excellence. My unique ability to bridge the worlds of quality control and research development enables me to navigate the complexities of regulatory guidelines while fostering innovation and improvement.Throughout my career, I\'ve specialized in transforming technical and scientific information into clear, actionable insights that align with compliance standards and enhance operational processes. Having worked within Contract Development & Manufacturing Organizations (CDMOs)/Contract Manufacturing Organizations (CMOs), I bring valuable expertise in managing external partnerships while ensuring quality standards are met at every stage of the product lifecycle. My skills encompass molecular and cellular biology techniques, risk mitigation, and the meticulous review of complex documents. I\'m recognized for my analytical mindset, problem-solving capabilities, and unwavering attention to detail.In every role, I strive to make a positive impact by mentoring and leading teams, implementing quality improvement initiatives, and ensuring that products and processes adhere to the highest standards. Whether interfacing with federal and international inspectors or managing high-profile client projects, I am committed to delivering excellence in everything I do.I am passionate about helping others succeed and believe in the power of collaboration to drive transformative change. As a lifelong learner and advocate for continuous improvement, I am always seeking new challenges and opportunities to contribute to the scientific and quality assurance communities.Areas of Expertise:Compliance & Risk MitigationDocument & Analytical Data ReviewTechnical & Scientific WritingMolecular & Cellular Biology TechniquesQuality Systems ManagementChange Control & Deviation InvestigationsMentorship & Leadership DevelopmentOperational ExcellenceTechnical Competencies:Molecular Techniques: RT/PCR, Western Blot, Enzyme ImmunoassayQuality Assurance: GMP, GLP, ISO StandardsInformatics: LIMS, CIMS, SAP, TrackWise, ProCal

Experience

1. Manager

   Eli Lilly and Company

   Jan 2025 — Present · Indianapolis, IN, US

   In my role as a Manager at Eli Lilly and Company, I oversee the strategic leadership and management of PR & D Quality System documents, ensuring compliance and audit readiness. I manage the review, approval, and maintenance of QS documents, collaborate with key business areas, and support Document Owners, Reviewers, and Approvers to communicate process expectations effectively.

Education

• Butler University

  Bachelor of Science - BS, Biology, General

• Cathedral High School

  Diploma

Skills

• • Problem Solver
• Cell Culture
• Root Cause Problem Solving
• Quality Control
• • Microsurgery
• Gmp
• • Critical Thinker
• 21 Cfr Part 11
• Biotechnology
• Mentoring
• Assay Development
• Ich-Gcp
• Laboratory Information Management System (Lims)
• Deviations
• Protein Chemistry
• Document Review
• Communications
• • Technical Analyst
• U.s. Pharmacopeia (Usp)
• Corrective and Preventive Action (Capa)
• Biopharmaceuticals
• • Immunohistochemistry
• Glp
• Leadership
• Cultural Alignment
• Western Blotting
• Change Control
• Pharmaceutical Industry
• Sop
• Fda
• Standard Operating Procedure (Sop)
• Continuous Improvement
• Solutions Specialst
• Validation
• Gxp
• Life Sciences
• Creative Writing
• Trackwise
• Strategist
• Visionary Marketing