csv

We’re partnering with a major client in Austin, TX to hire a CSV/CSA Engineer with experience in regulated/GxP environments, risk-based validation approaches, validation planning, requirements review, testing, traceability, and compliance with FDA 21 CFR Part 11 and related quality system requirements.Location: Austin, TXRate: $55–$60/hrContract: 12...

**Job Description** - We are seeking a CSV Analyst with Instrument Integration & Validation expertise to support validation and compliance of laboratory, manufacturing, and embedded software systems in regulated environments. - The role focuses on the integration layer, ensuring data moves accurately and completely from instruments through Instrument...

**Job Description** We are seeking a CSV Specialist to support Computer System Validation (CSV) activities for GxP-regulated systems in the pharmaceutical, biotechnology, or medical device industry. The ideal candidate will be responsible for ensuring computerized systems are validated and compliant with regulatory requirements, company procedures, and...

**Job Description** We are seeking an experienced Computer System Validation (CSV) Lead to oversee validation activities for computerized systems used in regulated GxP environments. The ideal candidate will have extensive experience in CSV lifecycle management, FDA and global regulatory compliance, validation documentation, risk assessments, and...

Job Description: We are seeking an experienced CSV Lead to support the validation of computer systems for a newly constructed Sterile Drug Product Clinical Manufacturing Facility. This role will play a key part in supporting the transition from the existing Sterile Drug Product Clinical Manufacturing facility planned for 2028. The selected consultant will...

CSV Engineer (6mo. Contract-to-Hire)Location: Baltimore, MDCompanyJoin a premier global Contract Development and Manufacturing Organization (CDMO) that is rapidly expanding its state-of-the-art sterile manufacturing footprint in Baltimore. This organization is a strategic partner to leading pharmaceutical and biotech companies, specializing in the...

Job Title: IT CSV Engineer                                                              Location: Seattle, WA OR Redmond, WAReports to: Senior Manager/Group Leader, CSVAbout Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we...

Job Summary: The CSV Engineer is responsible for ensuring that GxP computerized systems at the client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role directly supports gene therapy manufacturing operations by leading validation activities for key systems, including Veeva QMS, BMRAM,...

Experience - Validating ERP to AWS Data migration process and Validating Data migration project Experience in the Pharmaceutical, biotechnology, or medical device industry ¿ 5+ years' experience with System Development Lifecyle¿ 5+ years' experience in Computer System Validation (Based on the role selected)¿ Experience in FDA and/or Global regulated...

Roles & Responsibilities: Ex-Pharmaceutical preferred. Experience in the Pharmaceutical, biotechnology, or medical device industry. 2+ years' experience with System Development Lifecyle. 3+ years' experience in Computer System Validation (Based on the role selected). Experience in FDA and/or Global regulated environment with good...

PACIV, a global leader in industrial automation solutions servicing the Life Sciences sector, is seeking a IT / CSV Specialist to provide technical support for laboratory applications, systems, infrastructure, and validation activities within a pharmaceutical manufacturing environment.Position Responsibilities / Essential Functions:Provide IT support for...

Job Summary: We are seeking a CSV Analyst with Instrument Integration & Validation expertise to support validation and compliance of laboratory, manufacturing, and embedded software systems in regulated environments. The role focuses on the integration layer, ensuring data moves accurately and completely from instruments through...

Summary : CSV Validation Engineer is responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment. This role will focus on validating ERP Master Data Governance processes and Data Lake platforms, ensuring compliance with regulatory requirements and data integrity standards. Roles &...

Job Description: We are seeking an experienced Computer System Validation (CSV) Lead to oversee validation activities for computerized systems used in regulated GxP environments. The ideal candidate will have extensive experience in CSV lifecycle management, FDA and global regulatory compliance, validation documentation, risk assessments, and...

Company DescriptionComtech is a woman-owned small business founded in 1998 and headquartered in Reston, VA. We offer IT solutions across the disciplines of program/project management, applications development, infrastructure, Cyber security, and enterprise content/data management services. We have developed our methodologies and processes based on the IT...

Job Description: We are seeking a CSV Analyst with Instrument Integration & Validation expertise to support validation and compliance of laboratory, manufacturing, and embedded software systems in regulated environments. The role focuses on the integration layer, ensuring data moves accurately and completely from instruments through Instrument Manager...

Roles & Responsibilities: Ex-Pharmaceutical preferred. Experience in the Pharmaceutical, biotechnology, or medical device industry. 2+ years' experience with System Development Lifecyle. 3+ years' experience in Computer System Validation (Based on the role selected). Experience in FDA and/or Global regulated environment with good understanding of GxP...

Summary: Our client is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate must have hands-on experience with Veeva platforms and data migration projects in regulated pharma environments. Roles & Responsibilities: Validating...

Job Description: We are seeking an experienced CSV Lead to support the validation of computer systems for a newly constructed Sterile Drug Product Clinical Manufacturing Facility. This role will play a key part in supporting the transition from the existing Sterile Drug Product Clinical Manufacturing facility planned for 2028. The selected...

Job Description: We are seeking a CSV Analyst with Instrument Integration & Validation expertise to support validation and compliance of laboratory, manufacturing, and embedded software systems in regulated environments. The role focuses on the integration layer, ensuring data moves accurately and completely from instruments through Instrument...