Senior Validation Lifecycle Lead - GMP & Compliance
Veg Group
Veg Group is seeking a Validation Lifecycle & Periodic Review Program Manager to lead and manage validation lifecycle and periodic review programs for various clients in regulated industries. This role plays a critical part in ensuring compliance with GMP and quality standards. The ideal candidate will possess a Bachelor's degree and have extensive experience in pharmaceutical and biotechnology environments. Key responsibilities include client interface, execution plan management, and technical leadership to project teams. #J-18808-Ljbffr Veg Group
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$60 - $65 per hour
Crystal Equation Corporation in Thousand Oaks is seeking a Senior Validation Engineer to lead the commissioning and qualification activities for new or modified GMP analytical and process equipment. The ideal candidate will possess demonstrable experience within a pharmaceutical...Hourly pay- Radiant Systems Inc is seeking a LabWare LIMS Validation Specialist for an onsite role in Thousand Oaks, California. This position involves configuring LabWare LIMS and ensuring compliance with GMP standards. The ideal candidate will have proven experience in implementing...
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$46 - $51 per hour
Crystal Equation Corporation is seeking a Validation Engineer to plan and conduct GMP equipment reviews, ensuring compliance and suitability for use. Collaborating with Engineering and Quality teams, the role includes generating reports and assessing equipment performance...Remote jobHourly pay$116k - $182.27k
Initial Therapeutics, Inc. is looking for a Validation Engineer in Thousand Oaks, CA. This role is critical for overseeing validation activities, ensuring compliance with regulations, and implementing improvements. The ideal candidate has at least 10 years of validation...Senior- Takeda Pharmaceuticals International GmbH is seeking a Validation Engineer in Thousand Oaks, CA. The role involves leading validation activities, managing project timelines, and ensuring compliance with regulations. The ideal candidate will have more than 10 years of experience...Senior
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- Veg Group seeks a Validation Lifecycle & Periodic Review Specialist in California to maintain validated systems throughout... ...involves supporting validation activities for GMP equipment and systems, ensuring compliance and suitability. The ideal candidate has a bachelor...
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- ...AutomationEngineer Senior, DeltaV/Rockwell PLCs/GMP - (JP15196) Location... ...direct client, a leading global biopharmaceutical... ..., installation and lifecycle management of... ...DeviceNet technologies • Compliance and regulatory... ..., engineering and validation documentation and project...SeniorContract workWork experience placementWork at officeMonday to FridayShift work
- ...timely delivery of cell therapy products while maintaining compliance with GMP standards. The ideal candidate will have a strong background... ...Engineering is required along with extensive experience at the senior leadership level. #J-18808-Ljbffr FUJIFILM Holdings America...Senior
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$44 - $48.5 per hour
3key Consulting, Inc. is seeking a Senior Device Engineer specializing in electromechanical combination products in Thousand Oaks, CA... ...and testing for medical devices. This contract position involves lifecycle management, complaint investigations, and cross-functional...SeniorContract work- Job Title Senior Automation Engineer - DeltaV... ...PLC & SCADA (GMP Biopharma Capital... ...engagement with a leading global biopharmaceutical... ...PLC Experience, Compliance with regulatory requirements... ..., product lifecycle management, and... ...engineering, commissioning, validation, and project...SeniorPermanent employmentContract work
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- ...drug product manufacturing operations at our Thousand Oaks facility. This role requires managing operational schedules ensuring compliance with GMP and supporting new product introductions. The ideal candidate will possess a strong background in drug product manufacturing,...SeniorFlexible hours
- A leading consulting firm is seeking a Sr Engineer for a consulting engagement in biotechnology. This remote role focuses on lifecycle analysis, data management, and compliance with environmental standards. The ideal candidate will have a strong background in lifecycle...SeniorRemote job
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- US Tech Solutions is seeking a Senior Associate, Quality Assurance to provide onsite QA support at their Thousand Oaks location. The role... ...ideal candidate will have QA or manufacturing experience in a GMP environment, strong critical thinking skills, and a relevant degree...SeniorRotating shiftDay shiftAfternoon shift
- ...transforming your career. Senior Specialist, Quality... ..., quality is more than compliance; it is a strategic capability... ...across the product lifecycle. We are seeking a... ...multiple GxP domains (GMP, GCP, GLP, GVP, GDP, etc... ...ISO 14971. Experience leading and/or executing governance...SeniorRemote workFlexible hoursShift work
- We are seeking a Senior Validation Lead with strong experience supporting GMP qualification and validation programs across... ...leading end‑to‑end validation lifecycle activities, authoring and reviewing... ...functional teams, and ensuring compliance with FDA, cGMP, GAMP 5, 21 CFR...Senior
$23 - $24 per hour
...seeking a responsible individual to train attorneys and manage legal documentation for asset recovery. The role involves ensuring compliance, auditing files, and maintaining communication with attorneys. Compensation ranges from $23 to $24 per hour, alongside benefits...SeniorHourly pay
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