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Computer System Validation Jobs in Missouri (NOW HIRING)

Evergy

Systems Support Analyst - EEP

Kansas City, MO · On-site

$54.40K - $68K/yr

Kansas City, MO Topeka, KS PAY RANGE: (Minimum - Midpoint) System Support Analyst I: $54,400 - $68 ... Perform solution testing and validation and/or coordinate testing with super users, including ...

Evergy

Systems Support Analyst - EEP

Kansas City, MO · On-site

$54.40K - $68K/yr

Kansas City, MO Topeka, KS PAY RANGE: (Minimum - Midpoint) System Support Analyst I: $54,400 - $68 ... Perform solution testing and validation and/or coordinate testing with super users, including ...

Evergy

Systems Support Analyst - EEP

Kansas City, MO · On-site

$54.40K - $68K/yr

Kansas City, MO Topeka, KS PAY RANGE: (Minimum - Midpoint) System Support Analyst I: $54,400 - $68 ... A bachelor's degree in Business, Finance, Accounting, Computer Science, Information Systems ...

IBD Romania

Contribute to system validation by supporting cable verification and continuity checks during FAT ... Familiarity with cable routing in 3D environments and relevant CAD/PLM tools (e.g., 3DExperience ...

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How much do computer system validation jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for computer system validation in Missouri is $50.95, according to ZipRecruiter salary data. Most workers in this role earn between $39.23 and $60.43 per hour, depending on experience, location, and employer.

What is a Computer System Validation job?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in Computer System Validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.
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Computer System Validation jobs near you
Manager, Molecular & Cellular Biology

Manager, Molecular & Cellular Biology

Catalent, Inc.

Kansas City, MO • On-site

Full-time

Medical, Life, Retirement, PTO

Posted yesterday

Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

46th of 71 rated pharmaceutical

Job description

Manager, Molecular & Cellular Biology
Position Summary
  • Shift: Monday - Friday 8am - 4:30pm
  • 100% on-site

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
The Manager in Molecular and Cellular Biology is primarily responsible for managing various sub-teams comprised of a Group leaders, Scientists and Associate Scientists. Their responsibilities will include serving as technical experts on projects, act as liaison between client and Catalent technical team, coaching and mentoring group leaders, HR activities (e.g., performance reviews, time entry approval, PTO approval, salary adjustments, etc.), supporting client audits/visits, and communicating with cross-functional teams on analytical activities for Biopharma product development under cGMP regulatory guidance for Large Molecules/Biologics product development.
The role:
  • Supervise and manage various method development, method evaluation/feasibility, method transfers, method verifications, qualifications and validations, stability study and adhoc sample testing in Molecular and Cellular Biology.
  • Plan, prioritize, organize, and execute the conduct of analytical work within the Molecular and Cellular Biology Laboratory in accordance with the requirements of the client contract and/or technical agreement.
  • Serve as back up Project Technical Lead and could also serve as Technical Lead on projects pertaining to Molecular and Cellular Biology.
  • Manage and lead computer system validation activities, as required. Ensure various instruments/Equipment in the group are in compliant status.
  • Ensure cGMP practices are implemented and followed by the group and self.
  • Assure the integrity and quality of analytical data produced by ensuring staff are adhering to all relevant in-house and client SOPs and methodologies and following the requirements of GMP.
  • Monitor and manage projects and maintain project timelines and budget.
  • Communicate effectively with clients, auditors, peers, and Directors to facilitate the smooth conduct of project activities.

The candidate:
  • Bachelor's degree: >10 years of relevant experience in department specific techniques with more than 8 years of management experience preferred or based on performance at Catalent, OR
  • Master's degree: >8 years of relevant experience in department specific techniques with more than 6 years of management experience preferred or based on performance at Catalent, OR
  • Doctorate Degree: >6 years of relevant experience in department specific techniques with more than 4 year of management experience preferred or based on performance at Catalent.
  • Applies knowledge of the principles, theories, and concepts applicable to a wide range of work in a discipline (e.g., Biology, Chemistry, Biochemistry) and broad knowledge of principles and concepts in other disciplines.
  • In-depth knowledge in instrumentation, theory, data interpretation and applications in at least one technical area. Can assess new technologies and their impact on Catalent offerings
  • Experienced in most aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones
  • Excellent written and verbal communications skills with internal and external customers, colleagues, and supervisor.
  • Ability to communicate complex technical information to non-technical audiences
  • Able to lead difficult discussions with customers and drive the to an acceptable resolution

Why you should join Catalent:
  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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