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Analytical and globally minded professional with a strong foundation in neuroscience and chemical engineering. Skilled in interpreting and communicating complex scientific data, with proven ability to collaborate effectively across cross-functional teams. Adept at building scientific dialogue with diverse stakeholders, supported by advanced English communication skills and academic experience. Passionate about bridging cutting-edge science with clinical application to improve patient outcomes as a Medical Science Liaison.

Clinical Research Professional with expertise in clinical trial management, safety management, and protocol development. Proven ability to ensure adherence to Good Clinical Practices and mentor teams to achieve high standards in clinical research.
Highly-motivated employee with desire to take on new challenges. Strong work ethic, adaptability, and exceptional interpersonal skills. Adept at working effectively unsupervised and quickly mastering new skills.


  ~Lean Six Sigma~Quality Systems & Compliance~Leadership~Team Building~Process Improvement Expertise

1.) Merck Pharmaceuticals, Jaffrey NH~Lean Six Sigma Black Belt-QC Associate
2.) DuPont Pharmaceuticals, Billerica MA~Microbiology Associate Scientist
3.) Bayer Pharmaceuticals, Fitchburg MA~Quality Control/Quality Assurance
4.) Lonza Biologic, Special Modalities (LSA), Portsmouth NN QA Systems Manager
~Completed 40 Lean Six Sigma Projects with total ROI exceeding $25 Million, including a Process Capability Study on Viresolve Pro, saving over a $1,000,000 on each batch.
~Trained in teaching complete DMAIC methodology including LEAN to include a full day and half day agenda.
~Played a key role in implementing the Total QMS at Merck in the Membrane Analytical Laboratory in 2022, working with five different shifts
~Trained and Experienced in External Manufacturing as well as API/Drug Substance (Active Pharmaceutical Ingredient) to include Cardiolite and Aspirin.
~Trained and Experienced in Small Molecule Production and Manufacturing as well as Contract Development and Manufacturing Organization (CDMO) with DuPont Pharmaceuticals
~Highly trained, with over 30 years of experience, in all aspects of cGMP, cGDP and cGLP
~Applied Quality Control Tools and Techniques, Six Sigma and Lean framework at Dupont and Merck
~Proven Time Tested Team building experience, promoting daily, a Culture of Quality and Continuous Improvement, motivating, mentoring and managing team members using process and performance metrics to drive change and continuously grow each and every day.
~Strong knowledge base in Project Management, both waterfall and agile, with an applicable understanding of corporate alignment and strategic planning.
~Deployed Project Charters at both Dupont Pharmaceuticals and Merck using standard deployment technique-Performance, Cost and Time, reducing variation, defects and money ($294,000 Projected for 2023)
~Skilled, refined and battle tested in creating a Culture of Quality, Value-Added, Voice of the Customer, Right the first time working environment with 29 years of experience.
~Skilled in Value Stream Mapping, Process Mapping and Standardizing Procedural and Process improvements with proven track record at Merck, DuPont and Bayer Pharmaceuticals
~Highly developed written and verbal communication skills, communicating with both internal and external customers as well as upper management
~Would interface with multiple functional areas and staff members on a daily basis, serving as the Voice of The Customer (VOC), Quality Control SME, Project Manager and the Continuous Improvement Specialist.
~Reported monthly and quarterly Quality Control metrics to Director of Corporate Quality Operations
~Initiated and verified Change Control documentation to include TrackWise for Deviations, investigations and CAPA
~Used Excel, MiniTab, Smartsheets, Power BI and Microsoft Projects to manage and oversee all Quality records and various performance metrics for accuracy and compliance at Merck in 2021 and 2022
~As the Continuous Improvement/Lean Six Sigma Black Belt regularly met with Customers to discuss possible changes, metrics of concern, projects or any deviations, CAPA, investigations or other relevant issues
~Cross Functionally facilitated all Quality Control Project Meetings as well as Process Improvement meetings in 2022 and 2023 as the Lean Six Sigma Black Belt.
~An empathetic and experienced agent of change, equipped to generate value and customer satisfaction in any process.
~A dedicated Leader with a foundational gift to listen and relate on a personal level.
~A Detail oriented self starter with strong organizational skills
~Ability to handle multiple issues cross functionally with a high degree of accuracy (problems, projects, personnel, equipment, etc.)
~Supported department leaders in Lean deployment and implementation, problem solving methodology and change management-very analytical and data driven
~Partner with Functional leadership to help orientation and training regarding policies, regulations, procedure, clinical record structure and documentation standards applicable for pre-clinical and clinical GXP activities.
~Direct and facilitate strong cross-functional communication by building working relationships across the organization.
~Directed growing Quality department programs by serving as the Key Subject Matter Expert and implementing fit for purpose standardized processes.
~Oversaw and drove a Culture of achievement and accountability with DuPont and Merck.
~Oversaw collaborations with finance, functional heads and team representatives to develop and manage program budgets and scenario planning at DuPont.
~Cross-functional support for all relevant Quality GXP activities in adherence to applicable regulations (FDA, EU, etc.) and standards (ICH, ISO).
~Oversaw development and maintenance of Quality documentation, coordinated document development, assuring proper reviews, approvals and training programs.
~Developed, tracked and routinely published Key Quality System metrics and data at both DuPont and Merck.
~Directed Continuous improvement of Quality Systems to assure quality and adherence with GMP and inspection readiness.
~Directed and supervised employees to ensure daily performance was appropriate to department and organizational goals and objectives.
~Created assignments for employees in an efficient and equitable manner to achieve quality performance and align with company and department goals and objectives.
~Provided instructions, explanations and performance evaluations
~Directed and advised employees of performance requirements and review work status progress for individual and group basis.

Highly-motivated employee with desire to take on new challenges. Strong worth ethic, adaptability and exceptional interpersonal skills. Adept at working effectively unsupervised and quickly mastering new skills.

Logan Vélez

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Quality Control Associate

Side-by-Side Assembly Production Worker

VARIED POSITIONS

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Quality Control Associate

Side-by-Side Assembly Production Worker

VARIED POSITIONS

HIGH SCHOOL GRADUATE -

STUDENT -

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