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© All Rights Reserved. ApplyBlast.com
MedPharm
The Computer System Validation (CSV) Specialist is responsible for governing, validating, and managing the lifecycle of GxP-relevant computerized systems to ensure compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, and GAMP5 principles. The role oversees validation activities, assesses system changes, closes compliance gaps, and supports regulatory inspections, collaborating with QA, IT, operations, and external vendors.
Headquarters
Durham, North Carolina, United States
Company Size
51-200 employees
Founded
1999
MedPharm is a contract development and manufacturing organization focused on topical and transdermal products for pharmaceutical, dermatology, and consumer healthcare customers. It provides end-to-end services — formulation development, analytical and stability testing, in vitro skin permeation/bioavailability assays (IVRT/IVPT), clinical study support, and small‑scale GMP manufacturing. MedPharm combines specialized skin‑science labs and regulatory expertise to de‑risk and accelerate topical product programs. Clients choose them for deep technical know‑how, robust testing platforms, and the ability to move formulations from R&D toward commercial supply.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for MedPharm.
MedPharm didn’t post a salary, so this is our estimate from similar listings.
51% below the average for this role
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