ZipRecruiter

Log In

1

Senior Computer System Validation Csv Jobs in Decatur, MI

Flowserve

Controls Engineer, Senior

Kalamazoo, MI · On-site

$91K - $120K/yr

The Mechatronics Controls Engineer, Senior will work closely with electrical engineers, mechanical ... Validation and Testing - Perform validation planning, system testing, and troubleshooting to verify ...

POWERX

P&C Senior Test Engineer

Kalamazoo, MI · On-site

Treat every testing scope as a system validation exercise, not an isolated component check ... Senior-level independence. * Reinforce safe work practices, HP tool use, and verification culture ...

POWERX

P&C Senior Test Engineer

Kalamazoo, MI · On-site

Treat every testing scope as a system validation exercise, not an isolated component check ... Senior-level independence. * Reinforce safe work practices, HP tool use, and verification culture ...

Perrigo Company plc

Vision Engineer

Allegan, MI · On-site

Experience with computer system validation and change management in an FDA regulated environment. * Experience and familiarity with current Good Manufacturing Practices (cGMP). * Excellent problem ...

Perrigo

Vision Engineer

Allegan, MI · On-site

Experience with computer system validation and change management in an FDA regulated environment. * Experience and familiarity with current Good Manufacturing Practices (cGMP). * Excellent problem ...

Perrigo Company plc

Vision Engineer

Allegan, MI · On-site

Experience with computer system validation and change management in an FDA regulated environment. * Experience and familiarity with current Good Manufacturing Practices (cGMP). * Excellent problem ...

ACTIA Corporation

Senior Software Engineer

Elkhart, IN · On-site

$116K - $153K/yr

... systems, validation, and manufacturing teams to integrate and validate software solutions. · ... Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Electronics ...

Harris

Senior Software Engineer

Three Rivers, MI · Remote

$120/hr

As a Senior Software Engineer, this professional will lead the design and development of entire computer systems and application software. They will leverage their expertise to create scalable and ...

Harris

Senior Software Engineer

Three Rivers, MI · Remote

$120/hr

As a Senior Software Engineer, this professional will lead the design and development of entire computer systems and application software. They will leverage their expertise to create scalable and ...

Safari Circuits, LLC.

Senior Electrical Engineer

Otsego, MI · On-site

$87K - $114K/yr

In this role, you will design, build, validate, and document high-performance testing systems while ... Experience with one or more PCB CAD layout packages (Altium preferred) * Experience in writing ...

Dometic

Senior Materials Planner

Elkhart, IN · On-site

As the Senior Materials Planner, you will play critical execution role within Dometic's Elkhart ... Review, analyze, and action material purchase proposals generated by the ERP system - validating ...

next page

Showing results 1-20

All JobsComputer System Validation Csv JobsSenior Computer System Validation Csv JobsSenior Computer System Validation Csv Jobs in Decatur, MI

Senior Computer System Validation Csv information

See Decatur, MI salary details

$32

$59

$91

How much do senior computer system validation csv jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for senior computer system validation csv in Decatur, MI is $59.77, according to ZipRecruiter salary data. Most workers in this role earn between $47.69 and $67.88 per hour, depending on experience, location, and employer.

What is a senior computer system validation (CSV) specialist?

A Senior Computer System Validation (CSV) specialist is an experienced professional responsible for ensuring that computer systems used in regulated industries—such as pharmaceuticals, biotechnology, or medical devices—meet compliance standards. This involves planning, executing, and documenting validation activities to demonstrate that systems consistently perform according to predefined specifications and regulatory requirements. Senior CSV specialists often lead validation projects, manage teams, and interact with regulatory auditors, making sure that systems are reliable, secure, and compliant with guidelines like FDA 21 CFR Part 11 and GxP. Their expertise helps organizations avoid compliance issues, data integrity problems, and costly system failures.

What are the key skills and qualifications needed to thrive as a senior computer system validation (CSV) professional?

To excel as a Senior Computer System Validation (CSV) professional, you need deep knowledge of regulatory compliance (such as FDA 21 CFR Part 11), validation lifecycle methodologies, and a background in computer science, engineering, or life sciences. Familiarity with validation management tools, risk assessment software, and quality management systems (QMS) is typically required, along with certifications like GAMP or Six Sigma being highly valued. Outstanding analytical skills, attention to detail, and strong communication abilities set high performers apart in this role. These competencies ensure validated systems meet regulatory requirements, maintain data integrity, and support quality operations in regulated industries.

What are some common challenges senior computer system validation (CSV) professionals face when working on large-scale projects?

Senior CSV professionals often encounter challenges such as coordinating validation activities across multiple departments, managing evolving regulatory requirements, and ensuring thorough documentation throughout the project lifecycle. They also need to balance project timelines with the need for comprehensive testing and risk assessments. Effective communication and collaboration with IT, QA, and business stakeholders are essential to address issues proactively and ensure compliance in complex, regulated environments.

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

AspectSenior Computer System Validation CsvComputer System Validation Specialist
CertificationsGxP, 21 CFR Part 11, CSV certificationsGxP, 21 CFR Part 11, CSV certifications
Work EnvironmentRegulated industries like pharma, biotech, medical devicesRegulated industries like pharma, biotech, medical devices
ResponsibilitiesLeading validation projects, ensuring compliance, mentoringExecuting 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.

What are the most commonly searched types of Computer System Validation Csv jobs in Decatur, MI?

The most popular types of Computer System Validation Csv jobs in Decatur, MI are:

What job categories do people searching Senior Computer System Validation Csv jobs in Decatur, MI look for?

The top searched job categories for Senior Computer System Validation Csv jobs in Decatur, MI are:

Senior Computer System Validation Csv jobs near you

Scientist II or III - Metrology Specialist - FSP

Parexel

Three Rivers, MI

Full-time

Retirement, PTO

Re-posted 23 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

31st of 74 rated research

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

We are looking tofill aScientistIIorIII- Metrology Specialistposition working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clientslocatedinRahway,NJ.This position offers full benefits, sick time, 401K, paid holidays, and paid time off.This position does not offer any sponsorship.

Metrologyspecialistisresponsible for the oversight of regulated and non-regulated laboratory equipment.This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement

Qualifications-B.S./M.S.in Chemistry, Biochemistry, Engineering, or a related discipline

  • Scientist2- B.S. with1-2years of relevant experienceor M.S. with0-1years of relevant experience

  • Scientist 3- B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience

Required Skills and Experience

  • Experience working within a regulated (GMP) laboratory

  • Experiencemaintaining, operating, and troubleshooting laboratory equipment including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet-Visible spectroscopy (UV-Vis), dissolution systems, and other specialized computerized systems.

  • Familiarity with standalone computer systemGMPvalidation requirements

  • Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks

  • Capable of working independently under moderate supervision

  • Strong verbal and written communication skills

  • Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators

  • Familiarity with authoring relevant instrument standard operating procedures (SOPs)

Responsibilities

  • Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation

  • Coordinate service activities across a variety of vendors and service engineers while building andmaintainingstrong working relationships

  • Gain a working knowledge of laboratory equipment tofacilitatewith troubleshooting and/or perform maintenance or calibration activities

  • Participate in computer system validation activities associated with new or upgraded equipment or software packages

  • Support the purchase, installation, and equipment qualification of new laboratory equipment

  • Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support

  • Originate and progress Notice of Event (NOE) and Change Management (CM) records

  • Perform and document investigations andassistin developing/implementing CAPA plans

  • Represent the laboratory on all aspects of laboratory equipment during audits

  • Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures

About Parexel

Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.

For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.

Come join us!

#LI-DK1

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

What Parexel employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

PAREXEL logo

About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

View All PAREXEL Jobs

Apply