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Internship Computer System Validation Csv Jobs in California

Supermicro

System Validation Engineer

San Jose, CA · On-site

$100K - $113K/yr

Come join R&D Lab in Super Micro Computer. We strive to ensure the product quality and reliability ... Manages standard system environmental and reliability validations with AI approaches during the ...

Supermicro

System Validation Engineer

San Jose, CA · On-site

$90K - $115K/yr

Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Information Systems, or a related field. * 3+ years of experience in systems validation, firmware validation, or ...

Supermicro

System Validation Engineer

San Jose, CA · On-site

$100K - $113K/yr

Supermicro Computer is currently looking for talented System Validation Engineer to partner with Hardware Designing team to validate in-house servers and workstation platforms, troubleshoot and ...

Creo Inc

Consultant (CSV SAP S/4HANA)

San Francisco, CA · On-site

$140 - $190/hr

This includes Computer Systems Validation (CSV) and, importantly, applying modern approaches to Computer Software Assurance (CSA). * Lead technical discussions, document key compliance decisions, and ...

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Internship Computer System Validation Csv information

What is an internship in computer system validation (CSV)?

An Internship in Computer System Validation (CSV) is a temporary position, typically for students or recent graduates, that provides hands-on experience in ensuring that computer systems used in regulated industries (like pharmaceuticals or healthcare) meet required standards and regulations. Interns assist with validating software and hardware, documenting processes, and ensuring compliance with industry guidelines such as FDA 21 CFR Part 11 or EU Annex 11. This role helps interns understand the lifecycle of computer systems in a regulated environment and prepares them for careers in quality assurance, compliance, or IT within highly regulated sectors.

What is the difference between Internship Computer System Validation Csv vs Computer System Validation Specialist?

AspectInternship Computer System Validation CsvComputer System Validation Specialist
CredentialsTypically pursuing or recent graduate, basic understanding of validationRelevant certifications (e.g., GAMP, ISPE), experience preferred
Work EnvironmentInternship setting, supervised, entry-level tasksFull-time role, independent responsibilities in regulated industries
Industry UsageUsed in pharmaceutical, biotech, and medical device companies for trainingUsed for maintaining compliance, validating systems in regulated environments

In summary, the Internship Computer System Validation Csv is an entry-level position focused on learning and supporting validation tasks, while the Computer System Validation Specialist is a more experienced role responsible for ensuring system compliance and validation in regulated industries.

What are the key skills and qualifications needed for an internship in computer system validation (CSV)?

To thrive as an Internship Computer System Validation CSV specialist, you need foundational knowledge in computer science, life sciences, or engineering, along with an understanding of regulatory standards like GxP or FDA 21 CFR Part 11. Familiarity with validation documentation, software testing tools, and quality management systems is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting requirements and collaborating with cross-functional teams. These skills ensure compliance, data integrity, and the successful validation of computerized systems in regulated environments.

What are the typical responsibilities of an intern in computer system validation (CSV)?

As a Computer System Validation (CSV) intern, you can expect to assist with tasks such as reviewing and drafting validation documentation, executing test scripts, and collecting evidence to ensure compliance with regulatory requirements. You may also support the maintenance of validation records and participate in team meetings to discuss project progress or findings. These responsibilities are crucial in ensuring that computer systems used in regulated industries, like pharmaceuticals or healthcare, function as intended and meet quality standards. Working closely with senior validation specialists, you'll gain hands-on experience with industry guidelines and learn how cross-functional teams collaborate to achieve compliance.
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Internship Computer System Validation Csv jobs near you

Delta-V Automation Project Manager

Stark Pharma Solutions Inc

San Diego, CA • On-site

Contractor

Re-posted 9 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Delta-V Automation Project Manager position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Role: Delta-V Automation Project Manager / Automation Engineer (Life Sciences)

Location: San Diego, CA - Onsite
Duration: Long-Term Contract
 

We are seeking an experienced Automation Project Manager / Automation Engineer to lead automation projects for pharmaceutical and biopharmaceutical manufacturing facilities. This role will oversee automation system design, project execution, validation, and commissioning while ensuring compliance with cGMP and regulatory requirements.

Key Responsibilities

  • Lead automation projects from concept through design, implementation, commissioning, qualification, and operational readiness.
  • Manage project scope, schedules, budgets, risks, and vendor deliverables.
  • Collaborate with Engineering, Manufacturing, Validation, Quality, and Facilities teams.
  • Develop and review automation documentation including URS, FRS, SDS, control narratives, and system architecture.
  • Support FAT, SAT, commissioning, startup, and CQV activities.
  • Oversee PLC, DCS, SCADA, HMI, instrumentation, and control system implementation.
  • Manage automation-related deviations, change controls, and Computer System Validation (CSV) activities.
  • Ensure compliance with cGMP, GAMP 5, ASTM E2500, 21 CFR Part 11, and Data Integrity requirements.
  • Serve as the technical lead for system integrators, contractors, and cross-functional project teams.

Required Qualifications

  • Bachelor's degree in Electrical, Chemical, Mechanical, Computer Engineering, or related field.
  • 8+ years of automation engineering or automation project management experience in pharmaceutical, biotech, or life sciences.
  • Strong knowledge of PLC, DCS, SCADA, HMI, instrumentation, VFDs, and industrial control systems.
  • Experience with CSV, CQV, change control, FAT/SAT, commissioning, and GMP compliance.
  • Proven experience managing automation projects, vendors, and cross-functional teams.
  • Excellent communication, documentation, and stakeholder management skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com