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Seasoned director with a robust background in business development, technical services, and customer support, notably at Grace Davison and Santai Science Inc. Excelled in enhancing client relations across NA and Europe, spearheading product development, and leading skilled teams. Experienced in flash chromatography and prep HPLC.

To be associated with a challenging & innovative environment where my knowledge, idea & potency can be implemented as well as enhanced and to be part of a team that dynamically work towards the growth of organization.
I have consistent academic and extra-curricular track record. I possess excellent analytical and leadership skills. I would like to work with an organization, which gives me complete business prospect

Experienced director of chemistry process research, scale-up, development, and production with expertise in project planning and management. Implemented supply chain management processes for just-in-time inventory, resulting in annual savings of over 500k. Skilled in DNA/RNA solid phase synthesis, high and low pressure chromatography, conjugation, ultrafiltration, and lyophilization. Proficient in HPLC, UPLC, LC/MS, TLC, and other analytical methods. Implemented quality systems and tracking from raw material control through finished goods for approved therapeutic and materials for Laboratory Developed Tests. Familiar with 21 CFR parts 210 and 820. Strong problem-solving skills. Proficient in MS Office suite, MS Project, and Visio.

Quality Assurance, Quality Control, Quality Systems/Compliance, Sterility Assurance and Sterilization executive with over 14 years of extensive experience in designing, enhancing, restructuring and remediating compliance related issues within the Biologics, Pharmaceutical, Biotechnology and Medical Device industries.
Quality Assurance, Quality Control, Quality Systems/Compliance, Sterility Assurance and Sterilization executive with over 14+ years of extensive experience in designing, enhancing, restructuring and remediating compliance related issues within the Biologics, Pharmaceutical, Biotechnology and Medical Device industries. Quality Systems Subject Matter Expert (SME) with a proven and successful track record and skills in handling routine or difficult and complex quality related compliance issues and remediation, FDA Form 483’s, Warning Letters and Consent Decree issues.

JOSHUA N. NELSON

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Assistant Director

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B.S. - Chemistry, ACS-Certified

Associate of Science - Biochemistry & Chemistry

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Laboratory Instrumentation Experience

Assistant Director

Associate of Science - Biochemistry & Chemistry

B.S. - Chemistry, ACS-Certified

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