DSR Global
Please note we can only consider candidates living in a commutable distance from Fort Worth.
Our client is currently looking for a consultant with experience in CSV/CSA validation and GxP compliance to support a medical client of ours in the US.
Start: ASAP
Duration: 12+ Months
Location: Hybrid – remote with flexibility to be onsite in Dallas-Fort Worth 1-2 times per month
Type: Contract/Freelance
Utilization: 50% - this can be 2/3 full days or part time 5 days per week
Role/Responsibilities
Proven experience in CSV/CSA validation and GxP compliance within pharmaceutical, biotech, or medical device industries, preferably in an international setting.
Specialist in managing enterprise system validation projects, including ERP, QMS, and cloud/SaaS solutions.
Strong expertise in SAP S/4HANA.
Proficient with relevant standards and documentation (FDA 21 CFR required; GAMP5 and EU Annex 11 desirable).
Excellent management, communication, and adaptability skills in complex, multi-site project environments.
Willingness and flexibility to work onsite in Dallas-Fort Worth as required.
Seniority Level Mid-Senior level
Employment Type Contract
Job Function Information Technology
Industries IT Services and IT Consulting, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing
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Our client is currently looking for a consultant with experience in CSV/CSA validation and GxP compliance to support a medical client of ours in the US.
Start: ASAP
Duration: 12+ Months
Location: Hybrid – remote with flexibility to be onsite in Dallas-Fort Worth 1-2 times per month
Type: Contract/Freelance
Utilization: 50% - this can be 2/3 full days or part time 5 days per week
Role/Responsibilities
Proven experience in CSV/CSA validation and GxP compliance within pharmaceutical, biotech, or medical device industries, preferably in an international setting.
Specialist in managing enterprise system validation projects, including ERP, QMS, and cloud/SaaS solutions.
Strong expertise in SAP S/4HANA.
Proficient with relevant standards and documentation (FDA 21 CFR required; GAMP5 and EU Annex 11 desirable).
Excellent management, communication, and adaptability skills in complex, multi-site project environments.
Willingness and flexibility to work onsite in Dallas-Fort Worth as required.
Seniority Level Mid-Senior level
Employment Type Contract
Job Function Information Technology
Industries IT Services and IT Consulting, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing
#J-18808-Ljbffr