Gxp validation analyst jobs in United States

The global instrument software validation project covers 200 unique instruments including documenting and validating software installed on lab instrumentation per EMA guidelines. · Gather and document requirements (URS, software configuration) · Write and execute validation test ...

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Shrive Technologies LLC, is seeking the following. Apply via Dice today · 10+ years of software QA/testing experience, with at least 8+ years in regulated environments like life s ...

10+ years of software QA/testing experience, with at least 8+ years in regulated environments like life sciences/ pharma,. · Strong expertise in GxP, CSV. · Experience in functional testing of custom built applications, mobile testing. · In-depth understanding of Software Testing ...

Company Description · GxP Associates is a rapidly expanding talent and workforce solutions company specializing in the pharmaceutical, biotechnology, and medical device industries. By providing engineering, quality, validation, regulatory, and IT professionals, we help organizati ...

Lead coordination between site and global teams to align SOPs and bracketing strategy. Provide regulatory and technical interpretation to ensure compliance with FDA, EMA, and HMRA. · ...

Conduct interviews with Business Stakeholders to gather the business requirements, propose solutions, and finalize the scope Manage action items with business and IT stakeholders Develop User Requirement Specification (URS) and Functional Specification (FS) with required use case ...

This role collaborates with IT members QA leadership Finance/SOX leadership to align plans and activities to achieve successful results for GxP and SOX. · Manage our IT systems SOX related Governance Risk and Compliance SAP-GRC component framework operations to maintain high qual ...

SOKOL GxP Services is seeking an experienced and detail-oriented Validation Engineer to support temperature and environmental mapping activities for GMP-controlled spaces, equipment, and utilities. · ...

SOKOL GxP Services is seeking an experienced and detail-oriented Validation Engineer to support temperature and environmental mapping activities for GMP-controlled spaces, equipment, and utilities. · ...

We are seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Grand Rapids, Michigan. · Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements · Work in ...

We are seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in Indianapolis, IN. · ...

We are seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in Kalamazoo MI. · Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements · Work in ...

A global pharmaceutical manufacturer specialising in · sterile injectables and ophthalmic drug products · is seeking a · Contract Head of Validation · to lead site-wide validation strategy at their North Carolina facility. · The site manufactures high-quality liquid and semi-soli ...

· About Us · Here at Performance Validation, Inc (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for 37 years. We are a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and ...

SOKOL GxP Services is seeking a detail-oriented Validation Engineer to support validation and qualification activities within pharmaceutical and biotechnology environments. · ...

SOKOL GxP Services is seeking a detail-oriented · Validation Engineer to support validation and qualification activities within pharmaceutical and biotechnology environments. · This role is responsible for executing and maintaining validation deliverables to ensure compliance wi ...

Location: Swiftwater, PA · **This role will require full-time presence at our client site in Swiftwater, PA** · **This role is NOT eligible for relocation assistance** · The Zifo Lab Computing Analyst provides technical laboratory services, including multivendor instrument, infor ...

This role will require full-time on-site presence at our client site in Waltham, MA.The Zifo Lab Computing Analyst provides both consulting analytical and technical laboratory services including multivendor instrument information technology as well as in-lab validation compliance ...

The Zifo Lab Computing Analyst provides technical laboratory services including multivendor instrument information technology and validation/compliance services when applicable.Responsibilities: · Provide technical support of customer laboratory environments typically for compute ...

This is a full-time on-site role for a Validation Professional located in Puerto Rico. · Proficiency in cGMP regulatory compliance and industry standards including FDA ISO GAMP 5 GLP GMP and 21 CFR Part 11 · Experience with validation including facilities utilities equipment comp ...