9 equipment validation opportunities in Fremont updated today
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LonzaComputer Systems Validation (Analytical Equipment), Specialist III Location : On-site, Portsmouth, NH. The Analytical Equipment Validation (AEV) Specialist, Level 3 assesses changing analytical computer systems to ensure compliance with company policies, procedures and industry guidance. Assess risk
LonzaComputer Systems Validation (Analytical Equipment), Specialist III Location : On-site, Portsmouth, NH. The Analytical Equipment Validation (AEV) Specialist, Level 3 assesses changing analytical computer systems to ensure compliance with company policies, procedures and industry guidance. Assess risk
LonzaComputer Systems Validation (Analytical Equipment), Specialist III Location : On-site, Portsmouth, NH. The Analytical Equipment Validation (AEV) Specialist, Level 3 assesses changing analytical computer systems to ensure compliance with company policies, procedures and industry guidance. A ssess ris
A leading engineering services provider is seeking a dedicated Manufacturing Engineer in Santa Clara, CA. This full-time role involves troubleshooting, executing preventative maintenance, and calibrating manufacturing equipment to enhance efficiency. Candidates should have 1-5 years of relevant expe
A global healthcare company in Alameda, California is seeking an Equipment Technician II. The role involves setting up and maintaining manufacturing equipment, performing troubleshooting, and managing spare parts inventory, while adhering to quality systems. Ideal candidates will have at least 3 yea
A leading medical device company in California is seeking a senior Validation Engineer to work in an FDA-regulated environment. This role involves validating mechanical press systems, preparing validation protocols, and collaborating with cross-functional teams. Candidates should have 6-8+ years of
A leading pharmaceutical company is seeking a Validation Engineer to ensure systems remain in control within a GMP environment. The ideal candidate will have experience in Process and Equipment Validation, mastery of IQ/OQ/PQ protocols, and strong technical writing skills. Responsibilities include g
1.0 FTE Full time Night - 08 Hour R2654504 Onsite 107500003 Clin Lab Chem HEMA Coag 300P Allied Health PALO ALTO, 300 Pasteur Dr, California If you're ready to be part of our legacy of hope and innovation, we encourage you to take the first step and explore our current job openings. Your best is wai
If you're ready to be part of our legacy of hope and innovation, we encourage you to take the first step and explore our current job openings. Your best is waiting to be discovered. Day - 08 Hour (United States of America) This role will support the following areas: Coagulation, Special Coagulation,
A consulting firm is seeking a Due Diligence Specialist for a short-term contract focused on industrial manufacturing acquisitions. Role involves on-site equipment audits, asset valuations, and Capex reviews. Ideal candidates have at least 5 years of due diligence experience, strong analytical skill
Job Summary: Seeking a Licensed Professional Engineer (PE) / Chartered Engineer to inspect, evaluate, and certify ~100 used instruments for compliance with import regulations to India. Key Responsibilities: Perform on-site inspection of equipment Assess condition, specifications, and functionality D
Due Diligence Specialist – Equipment Audit and Valuation/Capex Review (Industrial Manufacturing Acquisition) Position Overview We are seeking a highly skilled Due Diligence Specialist for an immediate, short-term contract role on our Value Driven Solutions Due Diligence project. This critical assign
About Veeco You probably don’t realize it, but what we do at Veeco touches the lives of every person, every day. It’s a bold statement, but it’s true. From the smartphones in our pockets that access the world’s collective knowledge, to the cloud-based services where all that information lives, to hi
VeecoAbout VeecoYou probably don’t realize it, but what we do at Veeco touches the lives of every person, every day. It’s a bold statement, but it’s true. From the smartphones in our pockets that access the world’s collective knowledge, to the cloud-based services where all that information lives, to hig
VeecoAbout VeecoYou probably don’t realize it, but what we do at Veeco touches the lives of every person, every day. It’s a bold statement, but it’s true. From the smartphones in our pockets that access the world’s collective knowledge, to the cloud-based services where all that information lives, to hig
EntegeePleasanton, CA 6+ month contract Pay: $40-$50hr Validation Engineers Job Description / Requirements: Bachelor’s degree in Engineering Minimum 2 years of experience within the automotive Engineering industry Experience in automotive and/or heavy-duty vehicle testing/validation Experience working with
United Pharma Technologies IncWe are seeking an experienced Computer System Validation (CSV) Engineer to support validation activities within a regulated pharmaceutical environment. This role will focus on validating Veeva Quality Vault and ensuring compliance with GxP, FDA, and industry standards. Key Responsibilities Support e
Summary : As Qualification Specialist in the Equipment Integration team, you are responsible for caring about the GMP requirements. The team is responsible for transferring existing Lab Equipment from Spark Network to Roche Connect Network (RCN). Including replacing the HW, OS and renewing the appli
$38,000 – $61,000/year
Estimation confidence: Low
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