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Validation Manager To manage all validation activities at the plant. This includes but is not limited to facility, equipment, cleaning, computer and process validation. This position will lead the site to ensure compliance to all applicable regulations and requirements. Ensures implementation of compliant validation master plan for the site and ensures all activities within the master plan are planned and executed. Writes, reviews and executes any required validation protocols to ensure....


RETAINED SEARCH ASSIGNMENT Quality Assurance Validation, ManagerVMP – Validation to include: Facility, Utilities, Equipment, Computer, etc.QA Validation MgrMUST have Bio Pharma experienceManage Validation, Write Protocols,Manage EquipmentProject Manager for all Validation ProjectsResponsible that Validations are prepared and executedDesign Validation studies; USA & EUExecute CAPA action plan9CFRDegree BS a Science or relatedPrefer 2+ yrs supervision & experience designing and....


RETAINED SEARCH ASSIGNMENT Quality Assurance Validation, ManagerVMP – Validation to include: Facility, Utilities, Equipment, Computer, etc.QA Validation MgrMUST have Bio Pharma experienceManage Validation, Write Protocols,Manage EquipmentProject Manager for all Validation ProjectsResponsible that Validations are prepared and executedDesign Validation studies; USA & EUExecute CAPA action plan9CFRDegree BS a Science or relatedPrefer 2+ yrs supervision & experience designing and....


Minimum Requirements: B.S. or M.S. degree in Organic Chemistry10+ years of experience with lubricant additives used in greases and machining oils.Must have experience developing, formulating and testing lubricant additives and specialty lubricants.Plus would be supervision experience.Job Description: Our client is a family oriented, specialty chemical producer with multiple product lines. This person will be working with the lube oil additives division. These lube oils are used for....

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Our client needs a doctor with experience in oncology clinical drug development to serve as a medical monitor. Work is estimated to take 10 hours per week to start.RequirementsMedical Doctorate (MD) or equivalent5 years clinical drug development experience in oncologyPhase 1 and phase 2 studiesResponsibilities1. Available to clinical investigator sites as a go-to person in the US for checking eligibility2. Be responsible for interacting with sites on safety management of the study. This will....


Lead the development and execution of all engineering and construction projects associated with midstream natural gas production, compression, and transmission for energy clients throughout the Marcellus and Utica Shale plays. As the principal Mechanical Lead and Subject Matter Expert (SME) for all midstream and upstream operations, you will support new business development in securing EPC work with a variety energy companies throughout the western PA, eastern OH, and WV. The Mechanical Lead....


Lead the development and execution of all engineering and construction projects associated with midstream natural gas production, compression, and transmission for energy clients throughout the Marcellus and Utica Shale plays. As the principal Mechanical Lead and Subject Matter Expert (SME) for all midstream and upstream operations, you will support new business development in securing EPC work with a variety energy companies throughout the western PA, eastern OH, and WV. The Mechanical Lead....


Reporting to the Executive Director of Early Development this physician will serve inside the medical sciences group as a leader in Hematology/Oncology early development. This Oncologist will lead early phase clinical development of oncology compounds from first-in-man studies through proof of concept. They will define, design, and execute early phase clinical and translational projects as the initial strategy for drug development. This physician should be trained in Oncology and have....

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