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- Responsible for validation strategy and planning, executing and qualification of computer systems and/or infrastructure components in accordance with applicable policies procedures and regulatory requirements Define validation Strategy for computerized systems and platforms...SuggestedRemote workFlexible hours
- ...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
- 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
- Job Title: Validation Engineer, CSV Biopharma (JP13826) Location: New Albany, OH. 43054 Business Unit: Ops Digital Technology Innovation Employment Type: Contract Duration: 6+ months with likely extension Rate : $35-40/Hr on W2 with benefits Posting Date: 3/18/2025 Target...SuggestedContract workLocal area
- ...integration of Thermo Fisher SampleManager LIMS in Pennington, NJ. Candidates should have substantial experience in GMP environments, CSV processes, and integrating LIMS with laboratory systems. A minimum of a Bachelor's Degree in a STEM field is required. This role...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 medical technology company located in Fort Worth, Texas, is seeking a Laboratory Validation Specialist to ensure compliance with regulatory standards in quality control laboratories. The successful candidate will lead qualification activities for laboratory instruments...Suggested
$95k - $110k
...it’sabout more than just a job—it’s about your career and yourfuture. Your Role We are seeking an experienced Computer System Validation (CSV) Engineer to support Manufacturing Execution Systems (MES) within a GMP-regulated biopharmaceutical manufacturing environment....SuggestedTemporary workInternshipLocal area$80.9k - $127.05k
...Available) Perform and document risk assessments to determine validation scope and testing depth Ensure appropriate controls for audit trails... ...Strong background in Computerized System Validations (CSV) preferred Experience working in a regulated industry preferred...SuggestedTemporary workWork experience placementLocal areaImmediate startFlexible hours- A leading pharmaceutical company is seeking a Lead for Computer System Validation in College Park, Maryland. The role involves overseeing GxP-compliant computerized systems across internal manufacturing sites. Candidates should have significant experience in validation...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 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 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
- ...Senior Project Specialist to support technology projects in Quality and Regulatory Affairs. This role involves project execution, validation documentation, and user training. The ideal candidate should have a Bachelor's degree and over 5 years of relevant experience in...SuggestedWork at officeRemote work
$80.9k - $127.05k
A healthcare solutions provider in Indianapolis seeks a Validation Engineer to manage regulatory compliance, support audits, and lead validation... ...preferably with expertise in Computerized System Validations (CSV). This full-time role offers a competitive salary range of $80,...SuggestedFull time- A leading technology consulting firm in Indianapolis seeks a Software Tester/Validation Engineer with strong GxP validation experience. You will design and execute test plans while collaborating with cross-functional teams including Quality and IT. The ideal candidate...
- Senior Computer System Validation (CSV) Consultant San Diego, United States | Posted on 03/12/2026 Job Duration: Long Term Contract (Possibility Of Extension) Pay Rate: $70/hr - $78/hr on W2 DOE Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K We are...Long term contract
- A leading technology solutions provider located in Dallas, TX, is searching for a Computer System Validation Specialist. In this role, you will manage the validation of laboratory systems to ensure compliance with regulatory standards. Your responsibilities include leading...
- A leading life sciences company is looking for a Sr. Associate, Quality Assurance Validation in Elwood, Indiana. This role includes providing quality oversight for capital projects, reviewing validation documentation, and ensuring compliance with cGMP standards. Applicants...Full timeRelocation
- 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...
- 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...
- 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...
- ...Therefore, we make quality and reliability our number one priority. Get to know us and join our teamas Senior Computer Systems Validation (CSV) Specialist Senior Computer Systems Validation (CSV) Specialist Location: Charlton, MA or Goleta (Santa Barbara), CA Join a global...Flexible hours
- 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
- 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 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...Full time
- A leading technology consulting firm in Indianapolis is seeking a Software Tester/Validation Engineer. The candidate will design test strategies for applications, ensure compliance with GxP regulations, and collaborate with various teams. Required qualifications include...
- 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...
- 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 biotechnology firm based in Raritan, NJ, is seeking a Sr. QA Validation Specialist to provide quality oversight for validation and qualification activities in cell therapy manufacturing. Candidates should have at least 7 years of experience in related fields and a Bachelor...