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Csv Manager Jobs Near Me

Pinnaql

Validation Engineer

New Albany, OH · On-site

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... FAT, SAT, CSV, equipment integration, and startup. * Drive process design for new equipment and ...

SysMind, LLC

Sr. EDI Developer.

Westerville, OH · On-site

Good experience with various file formats like ANSI X12, EDIFACT, XML, cXML, CSV,JSON, Flat files. * Proficiency in DB2+SQL, XML, XSLT, Web services, APIs, FTP/SFTP. * Manages all aspects of ...

ATS Automation

Automation Engineer

Lewis Center, OH

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT ... Collaborate with users, peers, and management to ensure appropriate standardization and alignment.

ATS Automation

Senior Automation Engineer

Lewis Center, OH

$98K - $129K/yr

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT ... Strong project management and communication skills * Strong knowledge of cGMP and validation ...

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How much do csv manager jobs pay per year?

As of Aug 30, 2026, the average yearly pay for csv manager in the United States is $104,575.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,000.00 and $116,500.00 per year, depending on experience, location, and employer.

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A map of the United States highlighting the number of Csv Manager job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Csv Manager job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Business Systems Analyst II

American Regent, Inc.

New Albany, OH • On-site

Full-time

Re-posted 14 days ago

American Regent rating

7.2

Company rating: 7.2 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

72nd of 86 rated pharmaceutical

Job description

Nature and Scope
The Business Systems Analyst II (BSA-II) serves as a liaison between business stakeholders and information technology, translating business needs into system requirements and ensuring technology solutions support operational, regulatory, and quality objectives. This role supports the implementation, validation, and lifecycle management of GxP-regulated computerized systems within a regulated pharmaceutical environment. The BSA-II will ensure adherence to industry standards and regulations pertaining to CSV, data integrity as well as all internal quality system requirements. The BSA-II independently executes moderately complex assignments within established system governance and validation frameworks.
The BSA-II will report directly to the CSV Manager and work closely with members of the CSV team, IT, QA, Business and System Owners.
Essential Duties and Responsibilities
Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time.
  • Obtain, analyze, document, and validate business, functional, and system requirements for new and existing applications supporting GxP business processes.
  • Translate business and regulatory requirements into system-based solutions in collaboration with IT, Quality, system owners, the business and vendors.
  • Assess the impact of system changes on validated state, business processes, and data integrity.
  • Support CSV activities across the system lifecycle, including implementation, configuration changes, upgrades, and retirement.
  • Author, review, approve and maintain CSV deliverables including User Requirements Specifications (URS), Risk assessments (e.g., system impact, data integrity, patient safety), Functional Specification (FS), Configuration Specifications (CS), Security Specifications (SS), Design Specifications (DS), Qualification Protocols (IQ/OQ/PQ), Traceability matrices, Validation plans and summary documentation (as applicable).
  • Ensure system requirements are testable, traceable, and inspection-ready.
  • Ensure system changes are appropriately assessed for risk and documented according to change management procedures.
  • Identify and communicate data integrity, compliance, or validation risks associated with system changes.
  • Contribute to audit and inspection readiness activities by ensuring documentation is complete, current, and accurate.
  • Support responses to audit/inspection requests and observations related to computerized systems, when applicable.
  • Support system implementations including validation execution and support testing activities (e.g., IQ/OQ/PQ/UAT, protocol review, defect assessment), enhancements, periodic reviews, and retirement activities.
  • Participate in development and maintenance of SOPs, work instructions, and validated system documentation.
  • Partner with Quality, Manufacturing, Supply Chain, Regulatory, IT, and other stakeholders to align system functionality with regulated business needs and to support continuous improvement while maintaining compliance.
  • Facilitate workshops, risk discussions, and validation reviews to obtain requirements.
  • Communicate effectively with both technical and non-technical stakeholders using clear, structured communication and documentation.
  • Consistently perform all duties in accordance with American Regent and Daiichi Sankyo Business Principles, corporate directives, SOPs, policies, and government and industry regulatory guidelines.
  • Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.
  • Bachelor's degree in Information Systems, Engineering, Business, Computer Science, or STEM related discipline (or equivalent experience).
  • 3-6 years of experience as a Business Systems Analyst, Business Analyst, Computer System Validation or similar role.
  • Hands-on experience supporting administrative activities for validated or GxP-regulated computerized systems.
  • Experience working within SDLC and CSV frameworks in a pharmaceutical, biotech, or other regulated environment.
  • Strong requirements elicitation and documentation skills in regulated environments.
  • Working knowledge of CSV concepts, including requirements, risk management, and traceability.
  • Strong understanding of FDA, EU, GAMP, ICH and data integrity expectations for computerized systems.
  • Ability to apply risk-based thinking to validation and system changes.
  • Strong analytical, organizational, and problem-solving skills.
  • Clear written and verbal communication suitable for audits and inspections.
  • Ability to manage multiple priorities while maintaining compliance rigor.
  • Experience with FDA Computer Software Assurance (CSA) and Computer Software Validation (CSV) principles.
  • Experience supporting validated COTS platforms (e.g., LIMS, QMS, ERP, TrackWise, Veeva, SAP, MES, Empower, OpenLab, Chromeleon).
  • Experience with change control, periodic reviews, and system retirement activities.
  • Experience using validation lifecycle management tools (e.g., Res_Q, ValGenesis, KNEAT).

Physical Environment and Requirements
  • Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE is essential for the health and safety of employees.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.
Applicants have rights under Federal Employment Laws.
  • FMLA poster: https://www.dol.gov/whd/regs/compliance/posters/fmlaen.pdf
  • Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov)
  • Employee Polygraph Protection Act: https://www.dol.gov/whd/regs/compliance/posters/eppac.pdf

Alert: We're aware of individuals impersonating our staff to target job seekers. Please note:
• All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.
• Our recruiting process includes multiple in person and/or video interviews and assessments.
• If you are unsure about the legitimacy of a message, contact John Rossini at jrossini@americanregent.com before responding.
• We never request payment, bank information, or personal financial details during our offer process.
Your security is important to us, and we encourage you to stay vigilant when job searching.
American Regent Inc. endeavors to make https://careers.americanregent.com/ accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email hrtalentacquisition@americanregent.com.

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