
Compsciprep LLC
Hybrid in Chicago, Illinois • Today
Easy Apply
Contract, Third Party
Depends on Experience
9 results (2 new)

Compsciprep LLC
Hybrid in Chicago, Illinois • Today
Easy Apply
Contract, Third Party
Depends on Experience

RAVIN IT SOLUTIONS, Inc
Remote or Hybrid in Fort Worth, Texas • Today
Easy Apply
Contract
Depends on Experience





Hi,
👾 Reticulating splines...
Chicago, Illinois
•
Today
Job Description: The Senior Computer System Validation (CSV) Engineer is responsible for leading validation activities for computerized systems used in regulated environments such as pharmaceutical, biotechnology, or medical device manufacturing. This role ensures that systems including LIMS, ERP, MES, and laboratory applications are validated in compliance with FDA, EU, and global regulatory requirements. The Senior CSV Engineer will act as a subject matter expert (SME), providing guidance on
Full-time
Round Lake, Illinois
•
Today
Job Summary: We are seeking an experienced Validation Engineer to support system-level Verification & Validation (V&V) activities for medical device products. The role involves planning and executing V&V activities, developing and executing validation protocols, supporting design verification, and ensuring compliance with FDA, ISO 13485, and internal quality system requirements. Experience with infusion pump systems or similar electromechanical medical devices is preferred. Roles & Responsibilit
Full-time
New Jersey
•
Today
Job Description: We are seeking a Computer System Validation (CSV) Engineer with experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical or biotechnology environment. The ideal candidate will have expertise in GAMP 5, 21 CFR Part 11, validation lifecycle documentation, and QC laboratory or manufacturing systems validation, while collaborating with cross-functional teams to ensure regulatory compliance. Roles & Responsibilities: Develop, execute, and maintain Computer
Full-time
Remote
•
Today
Job Summary Responsible for the validation of facility utilities, equipment processes and cleaning for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Assist in authoring and executing protocols to demonstrate that manufacturing and cleaning processes are executed with consistent quality and results within a controlled environment. Responsible for managing and or performing reval
Full-time
USD 73,000.00 - 110,000.00 per year