Quality Assurance - Computer System Validation (CSV) As the Quality Assurance - Computer System Validation (CSV) , you will be part of the Quality organization supporting Clinton Manufacturing ...
Quality Assurance - Computer System Validation (CSV) As the Quality Assurance - Computer System Validation (CSV) , you will be part of the Quality organization supporting Clinton Manufacturing ...
Quality Assurance - Computer System Validation (CSV)
Clinton, IN · On-site
$18.25 - $24/hr
Quality Assurance - Computer System Validation (CSV) As the Quality Assurance - Computer System Validation (CSV) , you will be part of the Quality organization supporting Clinton Manufacturing ...
Quality Assurance - Computer System Validation (CSV)
Clinton, IN · On-site
$18.25 - $24/hr
Quality Assurance - Computer System Validation (CSV) As the Quality Assurance - Computer System Validation (CSV) , you will be part of the Quality organization supporting Clinton Manufacturing ...
We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation ...
Quick apply
We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation ...
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
Quick apply
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
CSV Lead - (Delta-V and Rockwell)
Indianapolis, IN · On-site
$98K - $129K/yr
We are looking for an experienced Computer System Validation (CSV) Lead to oversee automation systems validation for utilities at a large-scale greenfield pharmaceutical manufacturing facility. This ...
Quick apply
CSV Lead - (Delta-V and Rockwell)
Indianapolis, IN · On-site
$98K - $129K/yr
We are looking for an experienced Computer System Validation (CSV) Lead to oversee automation systems validation for utilities at a large-scale greenfield pharmaceutical manufacturing facility. This ...
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
Demonstrated experience in computer systems validation (CSV) for building management or automation and control systems in a pharmaceutical/GMP-regulated environment. * Strong knowledge of GAMP 5 ...
Demonstrated experience in computer systems validation (CSV) for building management or automation and control systems in a pharmaceutical/GMP-regulated environment. * Strong knowledge of GAMP 5 ...
Advise on validation strategy for future automation system upgrades and expansions. * Demonstrated experience in computer systems validation (CSV) for automation and control systems in a ...
Advise on validation strategy for future automation system upgrades and expansions. * Demonstrated experience in computer systems validation (CSV) for automation and control systems in a ...
Senior MES Engineer
$97.80K - $134.30K/yr
Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Provide technical support to Computer System Validation (CSV) activities, including MES ...
Senior MES Engineer
$97.80K - $134.30K/yr
Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Provide technical support to Computer System Validation (CSV) activities, including MES ...
Senior MES Engineer
Fishers, IN · On-site
$97.80K - $134.30K/yr
Description Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...
Senior MES Engineer
Fishers, IN · On-site
$97.80K - $134.30K/yr
Description Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...
Senior MES Engineer
$94.10K - $129.20K/yr
Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...
Quick apply
Senior MES Engineer
$94.10K - $129.20K/yr
Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...
Senior MES Engineer
Fishers, IN · On-site
$94.10K - $129.20K/yr
Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...
Senior MES Engineer
Fishers, IN · On-site
$94.10K - $129.20K/yr
Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...
Manager - Validation Lead - Technical Support & Operations - Global Services
Indianapolis, IN · On-site
Manager - Validation Lead - Technical Support & Operations - Global Services As a Senior Consultant - Validation, you will be responsible for driving Computer System Validation (CSV)/Computer ...
Manager - Validation Lead - Technical Support & Operations - Global Services
Indianapolis, IN · On-site
Manager - Validation Lead - Technical Support & Operations - Global Services As a Senior Consultant - Validation, you will be responsible for driving Computer System Validation (CSV)/Computer ...
Manager - Validation Lead - Technical Support & Operations - Global Services As a Senior Consultant - Validation, you will be responsible for driving Computer System Validation (CSV)/Computer ...
Manager - Validation Lead - Technical Support & Operations - Global Services As a Senior Consultant - Validation, you will be responsible for driving Computer System Validation (CSV)/Computer ...
Requirements * 3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience ...
Quick apply
Requirements * 3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience ...
The Senior Computer Systems Validation Specialist focused on Building Management Systems to support a regulated pharmaceutical manufacturing environment. The specialist will support a Site Automation ...
Quick apply
The Senior Computer Systems Validation Specialist focused on Building Management Systems to support a regulated pharmaceutical manufacturing environment. The specialist will support a Site Automation ...
Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks. * Ensure systems ...
Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks. * Ensure systems ...
Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks. * Ensure systems ...
Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks. * Ensure systems ...
Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks. * Ensure systems ...
Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks. * Ensure systems ...
Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks. * Ensure systems ...
Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks. * Ensure systems ...
Senior Computer System Validation Csv information
What are the key skills and qualifications needed to thrive as a Senior Computer System Validation (CSV) professional, and why are they important?
What are some common challenges Senior Computer System Validation (CSV) professionals face when working on large-scale projects?
What is a Senior Computer System Validation (CSV) specialist?
What is the difference between Senior Computer System Validation Csv vs Computer System Validation Specialist?
| Aspect | Senior Computer System Validation Csv | Computer System Validation Specialist |
|---|---|---|
| Certifications | GxP, 21 CFR Part 11, CSV certifications | GxP, 21 CFR Part 11, CSV certifications |
| Work Environment | Regulated industries like pharma, biotech, medical devices | Regulated industries like pharma, biotech, medical devices |
| Responsibilities | Leading validation projects, ensuring compliance, mentoring | Executing validation activities, documentation, testing |
While both roles require similar certifications and work in regulated environments, the Senior Computer System Validation Csv typically involves leading projects and overseeing compliance efforts, whereas the Computer System Validation Specialist focuses on executing validation tasks and documentation. The senior role often requires more experience and leadership responsibilities.
$18.25 - $24/hr
Full-time
Retirement, PTO
Posted 20 days ago
Elanco rating
7.8
Based on 25 frontline employees who took The Breakroom Quiz
39th of 70 rated pharmaceutical
Job description
At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Your Role:Quality Assurance - Computer System Validation (CSV)
As theQuality Assurance - Computer System Validation (CSV), you will be part of the Quality organization supporting Clinton Manufacturing Operations. In this role, you will provide quality oversight for computerized systems used in GxP operations, ensuring compliance with global regulatory requirements and data integrity standards. You will partner with IT, Automation, Engineering, and Production teams to maintain validated systems and integrate compliant digital solutions across the site.
Your Responsibilities:
Provide quality oversight for the lifecycle of computerized systems, ensuring compliance with GAMP 5, 21 CFR Part 11, and Data Integrity standards
Review and approve Computer System Validation (CSV) documentation including Validation Plans, IQ/OQ/PQ protocols, and summary reports
Lead investigations for CSV-related deviations, system failures, and data integrity issues, including root cause analysis
Partner cross-functionally with IT, Engineering, Automation, and Operations to implement and maintain compliant computerized systems
Support continuous improvement of site Quality Systems through SOP development, training, coaching, and change control management
What You Need to Succeed (minimum qualifications):
Education: Bachelor's Degree in Science, Technology, Engineering, Computer Science, or a related technical discipline (or equivalent experience)
Required Experience: Minimum 10 years of experience in a GxP regulated environment (Pharmaceutical, Biotech, or Medical Device), including at least 3-5 years of experience in Computer System Validation (CSV) or Computer System Quality Assurance (CSQA)
Top 2 Skills: Strong knowledge of Data Integrity and computerized system validation regulations (21 CFR Part 11, Annex 11, ALCOA++), and ability to influence and coach cross-functional technical teams on compliance requirements
What will give you a competitive edge (preferred qualifications):
Professional certifications such as CISA (Certified Information Systems Auditor) or CSQE (Certified Software Quality Engineer)
Experience supporting Data Integrity audits and regulatory inspections
Experience with regulated system platforms such as SAP, Veeva, MES, or LIMS
Experience implementing risk-based validation approaches aligned with GAMP 5
Experience supporting manufacturing or laboratory systems in regulated environments
Additional Information:
Location: Clinton, IN - Onsite Manufacturing Facility
Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
Multiple relocation packages
Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
8-week parental leave
9 Employee Resource Groups
Annual bonus offering
Flexible work arrangements
Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against jobrelated criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
About Elanco
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
5,001 - 10,000 Employees
Headquarters location
Greenfield, IN, US
Year founded
1954