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- ...leading technology and consulting firm is seeking an Associate CSV / Systems Support professional. This position is ideal for early... ...in a GMP-regulated environment. The role involves supporting validation documentation, coding and configuration work, and performing testing...SuggestedFull time
$70.49k - $113.52k
...acquire new skills and learn from our experiences to enhance our collective expertise Sr. Validation Engineer Responsibilities: Provide Computer System Validation (CSV) support for site automation systems, including DeltaV DCS, Syncade MES, and the integration of...SuggestedTemporary workWork experience placementLocal areaVerista, Inc.
Boston, MA9 days ago- A biopharmaceutical company is seeking a Validation Engineer II to manage validation activities and technical documentation with minimal supervision. This role includes significant travel to client sites, performing equipment validations and troubleshooting. The ideal...Suggested
$70.49k - $120.79k
...our collective expertise Job Responsibilities: Lead the validation and compliance of multiple systems, including Historian connections... ...~5+ years of experience in Computer System Validation (CSV) with multiple systems, including SAP, Warehouse Execution Systems...SuggestedTemporary workWork experience placementVerista, Inc.
Blue Ash, OH22 days ago- ...leading provider of industrial automation is seeking a Senior Validation Engineer in Columbus, Ohio. This individual will support validation... ...in packaging validation and Computer System Validation (CSV). The ideal candidate will demonstrate strong interpersonal skills...Suggested
$20 - $23 per hour
The Computer System Validation (CSV) Intern will assist the CSV department with day-to-day software application technical support, system administration, system maintenance, and project-based tasks. This internship will provide exposure to various CSV areas, including troubleshooting...SuggestedHourly payInternshipWork at officeRemote work- A management consulting firm in Princeton, NJ, is looking for a Validation Consultant to lead validation activities within GxP-regulated environments. This role requires 6+ years of experience in Computer System Validation, a Bachelor’s or Master’s degree, and strong knowledge...Suggested
- ...oversight for commissioning, qualification, and Computer Systems Validation. The role involves managing QA oversight of various automation... ...degrees and a strong background in quality assurance with experience in CSV and automation support. #J-18808-Ljbffr Planet PharmaSuggested
- A leading CRO in the pharmaceutical sector is seeking a CSV Lead to manage the end-to-end Computer System Validation for GxP systems. This role involves developing and reviewing URS, risk assessments, and ensuring compliance with FDA regulations. The ideal candidate will...Suggested
$123.61k - $162.23k
Role Overview The Sr. QA Validation Specialist, CSV & Equipment role is an exempt level position with responsibilities for providing quality oversight over the validation and qualification activities for equipment, systems, computer systems, and processes within a cell...SuggestedPermanent employmentFull timeContract workTemporary workWork experience placementWork at officeLocal areaFlexible hours- A leading consulting firm is seeking a Senior Validation Engineer (CSV) in Holly Springs, NC. This role focuses on ensuring compliance with validation standards for computer systems. Responsibilities include system design participation, test protocol preparation, and quality...Suggested
- A regulatory compliance firm in New Jersey is seeking a Validation Analyst responsible for planning and executing validation activities to ensure compliance with regulatory standards like FDA and GxP. Key responsibilities include developing validation documentation, performing...Suggested
- A pharmaceutical manufacturer in Bloomingdale, IL, is seeking a Computer System Validation Engineer to execute software validation activities for a new GMP-compliant facility. The role requires strong qualifications in engineering, compliance with cGMP and FDA standards...Suggested
- A leading professional services company in the United States is seeking a Computer Systems Validation Specialist. This role requires expertise in GxP validation documentation and a minimum of 3 years' experience in validation within biotech or pharmaceutical environments...SuggestedFull time
- A clinical research organization is hiring a Sr. Validation Engineer to oversee validation activities in GMP-regulated environments. This position requires 7-11 years of experience in the biotech or pharmaceutical industry, with strong knowledge of cGMP requirements and...Suggested
- An established industry player is seeking a CSV Engineer to support the implementation of manufacturing and laboratory equipment. This hybrid role involves maintaining compliance for qualified systems, developing protocols, and managing projects in a dynamic environment...
$75k - $106k
A professional services company is seeking a Computer Systems Validation Specialist in Rockville, MD. The role involves creating GxP documentation, supporting client engagements, and ensuring validation compliance in FDA-regulated industries. Ideal candidates should have...- A leading services supplier in New Albany, Ohio, is seeking a talented individual for a role that involves compliance and validation within the pharmaceutical, medical device, and biotechnology sectors. Candidates must possess a Bachelor's Degree in Science or Engineering...
- A consulting and technology firm is hiring a Validation Associate Consultant in Princeton, NJ. The role involves managing GxP-compliant validation processes and supporting clients across various projects. Candidates should have a relevant degree and experience in Computer...Remote work
- A leading employee-owned consulting firm based in Greenville, South Carolina is seeking an experienced Computer Systems Validation Specialist. The ideal candidate will have a strong background in authoring GxP validation documentation and a solid understanding of FDA regulations...
- A biopharmaceutical company is seeking a Validation Engineer to support validation activities across equipment and processes. The ideal candidate will have 4-7 years of experience in the biotech field, ensuring compliance with internal quality standards and regulatory...Remote job
$123.61k - $162.23k
A global biotechnology company is seeking a Sr. QA Validation Specialist in Raritan, NJ. This role provides quality oversight for validation activities within a cell therapy manufacturing plant. Candidates should have 7+ years of experience in quality assurance, a Bachelor...- Job Title: Senior Validation Engineer (CSV), Biotechnology - (JP15063) Location: Holly Springs, NC. 27540 Employment Type: Contract Business Unit: Commercial Drug Product Duration: 9+ months (with likely extensions and/or conversion to permanent) Posting Date: 02/23/26...Permanent employmentContract work
- A biotechnology company in Raritan, NJ, is seeking a Sr. QA Validation Specialist to oversee quality validation and qualification for equipment and systems within a sterile GMP environment. The role requires at least 7 years of experience in quality assurance, preferably...
- A leading technology services provider is seeking a Computer Validation Specialist in New Jersey to ensure compliance with regulatory requirements and contribute to validation deliverables for computer systems. You will prepare and approve validation documents, conduct...
- A leading solutions provider in healthcare is seeking a talented individual for a vital role with a background in pharmaceutical and biotechnology industries. Candidates need a Bachelor's Degree in Science or Engineering and at least 5 years of experience in process/laboratory...
- A leading consulting company in Thousand Oaks is seeking a Computer System Validation Lead to oversee the validation for a PAS-X upgrade. The ideal candidate will have over 8 years of experience in regulated life sciences environments, with substantial expertise in GAMP...Full time
- A pharmaceutical technology company in the US seeks a Senior Computer System Validation (CSV) Consultant. The ideal candidate has 7-10+ years of experience in validating high-critical GxP systems, with strong skills in Data Lake platforms and risk-based validation. This...
- A leading biopharmaceutical company in Cleveland, Ohio, seeks a Computer System Validation Engineer to ensure compliance for GxP-regulated computerized systems. This role involves developing validation deliverables and collaborating with cross-functional teams to maintain...
- A clinical research and innovation organization in Missouri seeks a qualified individual to manage Quality oversight in GXP compliant computer systems life cycle. The candidate will contribute to Life Science projects, ensure data integrity, and provide guidance as a Subject...
