Mervin Williams, Jr., Ph.D.

Mervin Williams, Jr., Ph.D. Email and Phone Number

Senior Research and Development Formulation Scientist @ Nephron Pharmaceuticals
Columbia, SC, US
Mervin Williams, Jr., Ph.D.'s Location
Columbia, South Carolina Metropolitan Area, United States, United States
Mervin Williams, Jr., Ph.D.'s Contact Details

Mervin Williams, Jr., Ph.D. work email

Mervin Williams, Jr., Ph.D. personal email

About Mervin Williams, Jr., Ph.D.

Product Development technical support and project team leader with 20+ years of experience in Research and Development. Focused on formulation and process development optimization from lab scale to commercialization in pharmaceutical industry. Expertise in documentation review, soft gelatin capsule technology, sterile drug products and technical writing. Prior experience in controlled-release solid dosage formulations. Detail oriented and thorough in job responsibilities. U.S. Patent for Liquisoft Capsules (9,867,779).Specialties: Organizational skills, documentation review, technical writing, DEA (Drug Enforcement Agency) authorized, cGMP training (anually), technical support, statistical design of experiments (DOE) training, Six Sigma Green Belt training, Minitab training, team-oriented, operational excellence, customer projects, soft gelatin capsule technology and safety audits

Mervin Williams, Jr., Ph.D.'s Current Company Details
Nephron Pharmaceuticals

Nephron Pharmaceuticals

View
Senior Research and Development Formulation Scientist
Columbia, SC, US
Website:
nephronpharm.com
Employees:
886
Mervin Williams, Jr., Ph.D. Work Experience Details
  • Nephron Pharmaceuticals
    Senior Research And Development Formulation Scientist
    Nephron Pharmaceuticals
    Columbia, Sc, Us
  • Nephron Pharmaceuticals
    Sr. Research And Development (R&D) Formulation Scientist
    Nephron Pharmaceuticals Jul 2018 - Present
    West Columbia, South Carolina, Us
  • Banner Pharmacaps
    Pharmaceutical Sr. Scientist
    Banner Pharmacaps Sep 2009 - Jul 2018
    Integral and valued member of the Product Development Group in Research and Development at Banner Life Sciences (formerly Banner Pharmacaps, Inc.), Division of Patheon. Project technical team leader on several high profile customer ventures in addition to my own internal projects. Responsible for formulation and process development of internal and external projects from lab scale to commercial scale. Provide guidance and expertise to colleagues on their respective assignments. Accountable for formal reports (i.e. development, process scale-up), protocols, batch production records, and other forms of documention to support product advancement from early development to commercialization. Source and purchase API (Active Pharmaceutical Ingredient) and other excipients for GMP and non-GMP process batches. Implement statistical DOE as part of Quality by Design (QbD) during product development. Primary formulator/technical lead on several ANDA submissions and approvals to the FDA (including First to File application/approval); in addition, provided support to other ANDA and NDA submissions/approvals. Responsible for safety audits and awareness as a member of the Banner Safety Committee.
  • Banner Pharmacaps
    Certified Green Belt
    Banner Pharmacaps Jun 2010 - 2018
    Responsible for process and formulation improvements utilizing Six Sigma tools that are helpful in the reduction of development time, and therefore resulting in significant cost and time savings.
  • Banner Pharmacaps
    Pharmaceutical Scientist
    Banner Pharmacaps Sep 2003 - Sep 2009
    Integral and valued member of the Product Development Group in Research and Development at Banner Pharmacaps. Project technical team leader on several high profile customer ventures. Responsible for formulation and process development of internal and external projects from lab scale to commercial scale. Provide guidance and expertise to colleagues on their respective assignments. Accountable for formal reports (i.e. development, process scale-up), protocols, batch production records, and other forms of documention to support product advancement from early development to commercialization. Source and purchase API (Active Pharmaceutical Ingredient) and other excipients for GMP and non-GMP process batches. Implement statistical DoE as part of Quality by Design (QbD) during product development.
  • Panac
    Member Board Of Directors
    Panac Feb 2013 - Feb 2018
    Pi Alpha National Alumni Coalition (PANAC) of Alpha Phi Alpha Fraternity, Inc.
  • University Of Georgia, College Of Pharmacy
    Graduate Teaching Assistant
    University Of Georgia, College Of Pharmacy Aug 1998 - Aug 2003
    Provided instruction and guidance in pharmacy labs in addition to grading responsibilities during my tenure in graduate school. Also responsible for proctoring of examinations.

Mervin Williams, Jr., Ph.D. Skills

Gmp Formulation Fda Pharmaceutical Industry Pharmaceutics Quality By Design Validation Anda R&d Drug Delivery Process Improvement Six Sigma Dissolution Technology Transfer Glp Product Development Drug Development Capa Sop Hplc Pharmaceutical Research V&v Change Control Cgmp Manufacturing Technical Writing Nda Team Oriented Capsules Usp Gxp Technical Support Uv/vis Andas Dissolution Testing Uv Trackwise Document Review Stability Studies Formulation Development Private Investigations Soft Gelatin Capsules Technology Projects Cmc Business Process Improvement Scale Up/optimization Investigations Customer Projects Documentation Review Atlas

Mervin Williams, Jr., Ph.D. Education Details

  • Clemson University
    Clemson University
    Biological Sciences
  • The University Of Georgia
    The University Of Georgia
    Pharmaceutics
  • North Carolina State University
    North Carolina State University
    Green Belt Certification
  • Richland Northeast High School
    Richland Northeast High School
    Academic And High School Diplomas

Frequently Asked Questions about Mervin Williams, Jr., Ph.D.

What company does Mervin Williams, Jr., Ph.D. work for?

Mervin Williams, Jr., Ph.D. works for Nephron Pharmaceuticals

What is Mervin Williams, Jr., Ph.D.'s role at the current company?

Mervin Williams, Jr., Ph.D.'s current role is Senior Research and Development Formulation Scientist.

What is Mervin Williams, Jr., Ph.D.'s email address?

Mervin Williams, Jr., Ph.D.'s email address is me****@****hoo.com

What schools did Mervin Williams, Jr., Ph.D. attend?

Mervin Williams, Jr., Ph.D. attended Clemson University, The University Of Georgia, North Carolina State University, Richland Northeast High School.

What skills is Mervin Williams, Jr., Ph.D. known for?

Mervin Williams, Jr., Ph.D. has skills like Gmp, Formulation, Fda, Pharmaceutical Industry, Pharmaceutics, Quality By Design, Validation, Anda, R&d, Drug Delivery, Process Improvement, Six Sigma.

Who are Mervin Williams, Jr., Ph.D.'s colleagues?

Mervin Williams, Jr., Ph.D.'s colleagues are Flynn Bowie Mba [803-467-6968], Nancy Whitmore, Danielle Skomurski, Jennifer Crawford, Melissa Kennerly, Brian Greene, Jared Crowetipton.

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