CSV Engineer (INTRL - India)

Insight Global
Danvers, United States of America
1 month ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English
Experience level
Intermediate
Compensation
$ 73K

Job location

Remote
Danvers, United States of America

Tech stack

Software Applications
Systems Development Life Cycle
System Testing
Information Technology
Meditech
Mdsap
GXP

Job description

Insight Global is hiring for a CSV Engineer for our medical device client in Danvers, MA. This role will sit fully remote and offshore in India. We are seeking a Computer System Validation (CSV) Engineer to ensure that all computer systems and software applications comply with industry standards and regulatory requirements. This role involves collaborating with cross-functional teams, executing validation activities, maintaining documentation, and supporting compliance initiatives. Hours will be roughly 12-8pm IST daily, based on project needs., Develop and execute remediation activities for CSV processes to assess, plan, and enhance validation practices.

-Create and implement validation plans for new and existing GxP computer systems and digital solutions.

-Lead and/or support SDLC and Software V&V activities, including requirements analysis, validation planning, testing, qualification, and related deliverables.

-Prepare and maintain validation documentation such as test protocols, reports, and risk/compliance assessments.

-Conduct assessments and periodic reviews of validated systems to ensure ongoing compliance with regulatory standards.

-Provide subject matter expertise (SME) in CSV to system owners and users.

Collaborate with QA team members to support quality improvement initiatives.

Requirements

Bachelor's degree or equivalent in a relevant field (Computer Science, Engineering, Life Sciences, Data Science, or similar).

-4-6 years of related experience in computer system validation.

-Hands-on experience with CSV in regulated environments such as MedTech or Pharma.

-Strong knowledge of regulatory requirements, including: 21 CFR Part 11 ,EU Annex 11, ISO 13485, IEC 82304, FDA CSA, MDSAP

Benefits & conditions

$30-35/hr.

Exact compensation may vary based on several factors, including skills, experience, and education.

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