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Computer System Validation Csv Pharmaceutical Jobs in Ridott, IL

RR Donnelley

Data Processing Supervisor

Monroe, WI · On-site

Oversee the capture, validation, and preparation of survey results, ensuring data is accurately ... System & Equipment: * Ensure the team effectively utilizes all necessary equipment and software ...

FurstStaffing

Serialization Manager

South Beloit, IL · On-site

$105K/yr

... pharmaceutical supply chain. The ideal candidate will have deep expertise in serialization systems ... Maintain serialization documentation, SOPs, and validation protocols. * Support internal and ...

PCI Pharma Services

Security Specialist

Rockford, IL · On-site

... systems to ensure the safety and security of our premises and assets. Additionally, the Security ... Experience in the pharmaceutical or biotechnology industry is a plus. Essential Duties and ...

PCI Pharma Services

Security Specialist

Rockford, IL · On-site

... systems to ensure the safety and security of our premises and assets. Additionally, the Security ... Experience in the pharmaceutical or biotechnology industry is a plus. Essential Duties and ...

aan

Customer Accounts Advisor

Rockford, IL · On-site

$16.25 - $17/hr

... store computer system and documenting all customer payment appointments. * Direct contact with ... United States at least 21 years old with a valid state Driver's License and compliance with the ...

aan

Customer Accounts Advisor

Rockford, IL

$16.25 - $17/hr

... store computer system and documenting all customer payment appointments. * Direct contact with ... United States at least 21 years old with a valid state Driver's License and compliance with the ...

Mercyhealth

Medical Assistant

Rockford, IL · On-site

$19.79 - $28.69/hr

Makes appropriate changes in computer system and on patient's chart. * Coordinates referrals for ... Maintain a valid driver's license. Have and maintain an acceptable driving record per Mercyhealth ...

TNAA TotalMed Allied

Travel Physical Therapist

Rockford, IL · On-site

$1.9K - $2.3K/wk

Use Medical Center computer systems in performance of daily tasks * Provide timely and accurate ... pharmacists, and other clinicians of all specialties in all 50 states. They offer local and travel ...

Mercyhealth

Medical Assistant

Rockford, IL · On-site

$19.79 - $28.69/hr

Makes appropriate changes in computer system and on patient's chart. * Coordinates referrals for ... Maintain a valid driver's license. Have and maintain an acceptable driving record per Mercyhealth ...

Iff

Production Operator

Beloit, WI · On-site

$16.50 - $19.75/hr

... pharmaceutical, or industrial production environments. * Ability to work independently and make ... Proficiency with Microsoft Office applications and basic computer systems. * Ability to review ...

Green County

Soil and Land Technician

Monroe, WI · On-site

$58K/yr

Must pass background check and will be finger printed to gain access to computer system. Certificates, Licenses, Registrations: Possession of a valid driver's license. For personal vehicle use, proof ...

HTI Technology

Embedded Systems Engineer

South Beloit, IL · On-site

$90 - $120/hr

... system integration, and validation. The ideal candidate has experience with digital and analog ... Maintain professional, technical, and computer knowledge via continuous education * Comply with all ...

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All JobsComputer System Validation Csv Pharmaceutical JobsComputer System Validation Csv Pharmaceutical Jobs in Ridott, IL

Computer System Validation Csv Pharmaceutical information

See Ridott, IL salary details

$10

$51

$81

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

As of Sep 4, 2026, the average hourly pay for computer system validation csv pharmaceutical in Ridott, IL is $51.56, according to ZipRecruiter salary data. Most workers in this role earn between $39.71 and $61.15 per hour, depending on experience, location, and employer.

What is computer system validation (CSV) in the pharmaceutical industry?

Computer System Validation (CSV) in the pharmaceutical industry is a process used to ensure that computerized systems used in drug manufacturing and related processes work as intended and comply with regulatory standards, such as FDA 21 CFR Part 11. CSV involves planning, testing, documenting, and maintaining systems to guarantee the accuracy, reliability, and integrity of data. This is critical for patient safety and product quality, as well as for meeting legal and regulatory requirements. The process typically includes risk assessment, validation planning, protocol execution, and ongoing monitoring of system performance.

What are common challenges faced by computer system validation (CSV) professionals in the pharmaceutical industry?

CSV professionals in the pharmaceutical industry often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for audits, and ensuring thorough validation of complex systems within tight project timelines. Collaboration with cross-functional teams, such as IT, quality assurance, and manufacturing, is essential to address technical and compliance issues. Additionally, balancing the need for robust validation with operational efficiency requires strong communication and project management skills.

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

To thrive as a Computer System Validation (CSV) professional in pharmaceuticals, you need a strong background in life sciences or engineering, knowledge of regulatory standards (such as FDA 21 CFR Part 11), and experience with validation protocols. Familiarity with validation lifecycle management tools, quality management systems (QMS), and industry guidelines like GAMP 5 is typically required, along with certifications such as ISPE or PMP being advantageous. Outstanding attention to detail, analytical thinking, and strong communication skills help ensure compliance and effective coordination with cross-functional teams. These competencies are vital for maintaining regulatory compliance, data integrity, and patient safety in pharmaceutical operations.

What is the difference between Computer System Validation Csv Pharmaceutical vs Quality Assurance Specialist?

AspectComputer System Validation Csv PharmaceuticalQuality Assurance Specialist
CertificationsGxP, 21 CFR Part 11, Validation certificationsGxP, ISO, QA certifications
Work EnvironmentPharmaceutical manufacturing, regulated labsQuality departments across industries, including pharma
Employer & IndustryPharmaceutical companies, biotech firmsPharma, biotech, healthcare organizations
Primary FocusEnsuring computer systems meet validation and compliance standardsMaintaining quality standards and process improvements

Computer System Validation Csv Pharmaceutical specialists focus on validating computer systems to ensure compliance with industry regulations, while Quality Assurance Specialists oversee overall quality processes. Both roles require GxP knowledge and are vital in pharmaceutical environments, but their core responsibilities differ in scope and focus.

What cities near Ridott, IL are hiring for Computer System Validation Csv Pharmaceutical jobs?

Cities near Ridott, IL with the most Computer System Validation Csv Pharmaceutical job openings:

Computer System Validation Csv Pharmaceutical jobs near you

Data Processing Supervisor

RR Donnelley

Monroe, WI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired 2 days ago. Applications are no longer accepted.

RR Donnelley rating

6.4

Company rating: 6.4 out of 10

Based on 134 frontline employees who took The Breakroom Quiz

36th of 52 rated marketing agency

Job description

Company Description
RR Donnelley is looking for a client-focused Data Processing Supervisor with experience growing business to join the team at the Monroe, WI location! This position will act as a business partner to the sales team to scope for new opportunities in the market.
RRD is a leading global provider of marketing, packaging, print, and supply chain solutions that elevate engagement across the complete customer journey. The company offers the industry's most trusted portfolio of creative execution and world-wide business process consulting, with services designed to lower environmental impact. With 22,000 clients, including 93% of the Fortune 100, and 32,000 employees across 28 countries, RRD brings the expertise, execution, and scale designed to transform customer touchpoints into meaningful moments of impact.
Job Description
Job Summary:
The Data Processing Supervisor is responsible for overseeing daily operations related to complex
document handling and data conversion, including leading a team dedicated to receiving, sorting, and
converting physical returned mail and survey results into accurate, actionable electronic data files for the end-customers. The supervisor is also tasked with ensuring operational efficiency, data quality, security, and strict adherence to service level agreements (SLAs). Beyond internal operations, this role partners closely with sales teams and external clients to scope new growth opportunities, build pricing models, and actively contribute to business growth.
Responsibilities:
  • Operations & Processing:
    • Manage the end-to-end process for handling both returned mail and physical survey results; from physical receipt, sorting, and scanning, to data entry and conversion into required electronic formats for the end-customers.
    • Oversee the capture, validation, and preparation of survey results, ensuring data is accurately converted and formatted into final electronic data files (e.g., CSV, delimited files) ready for end-customer delivery.
    • Ensure the physical security of all sensitive documents and the electronic security and privacy of converted customer data.
    • Oversee the quality assurance process to guarantee the accuracy and integrity of all data converted from physical documents.
    • Identify bottlenecks and inefficiencies in document handling and data conversion workflows and implement solutions to optimize processes.
  • Compliance & Reporting:
    • Maintain strict compliance with all customer SLAs, regulatory requirements, and internal security protocols.
    • Generate regular reports on team performance, productivity, mail/document volume, error rates, and progress toward operational goals.
    • Serve as the primary escalation point for complex processing issues or discrepancies.
    • Calculate and prepare new customer pricing proposals; perform pricing audits to ensure alignment with targets and overhead expenses; prepare invoicing documentation based on processed volumes and established contract rates.
  • System & Equipment:
    • Ensure the team effectively utilizes all necessary equipment and software systems required for data conversion and workflow management.
    • Collaborate with IT or technical support teams on system maintenance, troubleshooting, and upgrades.
  • Team Leadership & Management:
    • Supervise a team of associates, including scheduling, performance management, training, and professional development.
    • Monitor team workload and workflow to ensure timely processing and achievement of productivity and quality targets.
  • Client & Sales Collaboration:
    • Partner directly with the sales team and external clients to understand project scopes, calculate pricing proposals, and conduct pricing audits to maximize profitability.
    • Actively support client onboarding and ongoing relationships to identify operational opportunities to expand and grow existing business accounts.
    • Serve as a highly responsive point of contact for clients and internal partners including host alignment meetings, address inquires, and provide proactive problem-solving to ensure exceptional customer service and contribute to customer relationship retention.

Qualifications
  • Minimum of a High School Diploma or GED is required. Bachelor's degree preferred in Business Administration, Operations Management, or related field.
  • Minimum of 3 years of experience in data processing, document management, mailroom operations, or a production environment.
  • Minimum of 1 year of experience in a supervisory or team lead role.
  • Demonstrated knowledge of security and compliance best practices related to handling sensitive customer data.
  • Strong organizational and problem-solving skills with a keen attention to detail.
  • Experience working with production workflow or data management system.
  • Experience with lean manufacturing or process improvement methodologies.
  • Familiarity with high-volume mail sorting and scanning technology.
  • Understanding of data conversion techniques and quality control measures for electronic data
    entry.

Physical Demands
  • Sitting - Frequent
  • Standing - Occasional
  • Walking - Occasional
  • Twisting - Occasional
  • Bending - Occasional
  • Ability to Push/Pull <5-10lbs - Occasional
  • Ability to Push/Pull 10-15lbs - Occasional
  • Ability to Push/Pull 15-20lbs - N/A
  • Ability to Push/Pull 20-25lbs - N/A
  • Ability to Push/Pull >25lbs - N/A

The physical demands described here are representative of those that must be met by employees to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Travel Requirement <10%, Possible travel to RR Donnelley corporate or other facilities.
Additional Information
The pay range for this role at the noted location is $57,300 to $87,100 annually. The actual rate of pay offered may vary based upon, but not limited to: education, skills, experience, proficiency, performance, shift, and location. In addition to base salary, depending on the role, overtime, shift differential, call-in, and stand-by pay. RRD offers benefits including medical, dental, and vision coverage, paid time off, disability insurance, 401(k) with match, life insurance and other voluntary supplemental insurance coverages, plus tuition assistance, paternity leave, adoption assistance, and employer/partner discounts.
All your information will be kept confidential according to EEO guidelines.
All employment offers are contingent upon the successful completion of both a pre-employment background and drug screen.
RRD is an Equal Opportunity Employer, including disability/veterans

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