Martin Solberg

Martin Marty Solberg

President at Medical Analysis Systems , Inc.

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Location:
5300 Adolfo Road, Camarillo, California, United States
HQ Phone:
(805) 987-7891

General Information

Experience

Vice President Regulatory and Quality Assurance  - Sciele Pharma , Inc.

Education

Bachelor of Science  - Biology/Chemistry , University of South Dakota Vermillion

Doctorate  - Regulatory Science , University of Southern California

M.S. MBA  - 

master's degree  - business administration , Pepperdine University

Affiliations

Executive Vice President, Regulatory Affairs and Quality Assurance  - Shionogi Inc.

Active Member  - ISPE

Member  - Association for Manufacturing Excellence

Director  - ZLB Behring LLC

Member  - ABRA

Member  - American Chemical Society

Member  - Plasma Proteins Therapeutic Association

Plant Manager  - Johnson & Johnson

Recent News  

Martin A. Solberg Director of Technical Affairs Martin "Marty" SolbergDirector of Technical Affairs, ZLB Bioplasma Inc. Martin "Marty" Solberg is responsible for providing technical assistance to doctors and pharmacists who have questions about ZLB Bioplasma Inc.'s plasma-based products.He also serves as the regulatoryliaison for the company with the U.S. Food and Drug Administration (FDA). Solberg has more than 20 years of experience in pharmaceutical products.An expert in plasma fractionation, manufacturing and quality systems, Solberg established a ZLB Bioplasma pharmacological group and developed the company's regulatory affairs presence with the FDA.He also designed and implemented a quality assurance system for the company's U.S. operation and created a technical services division for ZLB's Carimune® NF Immune Globulin Intravenous (Human).Prior to joining ZLB Bioplasma Inc., Solberg was the managing director of Medical Analysis Systems Inc., a Camarillo, Calif.-based manufacturer of in vitro diagnostic medical products.While there, Solberg led the company's merger with a leading global healthcare firm.Previously, Solberg worked at Alpha Therapeutics Corp., a biopharmaceutical company in Los Angeles, where he held multiple positions including director of manufacturing, director of quality control and then director of quality assurance and regulatory affairs.At Alpha Therapeutics, Solberg directed the global compliance and quality system improvements process, oversaw the world's largest viral marker testing laboratory and improved quality systems compliance in 50 nationwide facilities.Prior to working for Alpha Therapeutics Corp., Solberg led the fractionation process for Baxter Travenol, Hyland Division, in Glendale, Calif., and was the plant manager of the Johnson & Johnson, Iolab Division, in Claremont, Calif.Solberg earned a bachelor's degree in chemistry from the University of South Dakota and a master's degree in business administration from Pepperdine University (Malibu, Calif.).He is a member of the American Chemical Society, the Association for Manufacturing Excellence, the Plasma Proteins Therapeutic Association and ABRA, the international authority for the source plasma collection industry.

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Martin A. Solberg Director of Technical Affairs Martin "Marty" SolbergDirector of Technical Affairs, ZLB Bioplasma Inc. Martin "Marty" Solberg is responsible for providing technical assistance to doctors and pharmacists who have questions about ZLB Bioplasma Inc.'s plasma-based products.He also serves as the regulatoryliaison for the company with the U.S. Food and Drug Administration (FDA). Solberg has more than 20 years of experience in pharmaceutical products.An expert in plasma fractionation, manufacturing and quality systems, Solberg established a ZLB Bioplasma pharmacological group and developed the company's regulatory affairs presence with the FDA.He also designed and implemented a quality assurance system for the company's U.S. operation and created a technical services division for ZLB's Carimune Immune Globulin Intravenous (Human).Prior to joining ZLB Bioplasma Inc., Solberg was the managing director of Medical Analysis Systems Inc., a Camarillo, Calif.-based manufacturer of in vitro diagnostic medical products.While there, Solberg led the company's merger with a leading global healthcare firm.Previously, Solberg worked at Alpha Therapeutics Corp., a biopharmaceutical company in Los Angeles, where he held multiple positions including director of manufacturing, director of quality control and then director of quality assurance and regulatory affairs.At Alpha Therapeutics, Solberg directed the global compliance and quality system improvements process, oversaw the world's largest viral marker testing laboratory and improved quality systems compliance in 50 nationwide facilities.Prior to working for Alpha Therapeutics Corp., Solberg led the fractionation process for Baxter Travenol, Hyland Division, in Glendale, Calif., and was the plant manager of the Johnson & Johnson, Iolab Division, in Claremont, Calif.Solberg earned a bachelor's degree in chemistry from the University of South Dakota and a master's degree in business administration from Pepperdine University (Malibu, Calif.).He is a member of the American Chemical Society, the Association for Manufacturing Excellence, the Plasma Proteins Therapeutic Association and ABRA, the international authority for the source plasma collection industry.

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