Validation Lead
TechDigital Group
Experience with Validation of GEN AI solutions in GxP environment is key. Look for someone who has supported CSV AI projects Job Details: Experience in the Pharmaceutical, biotechnology, or medical device industry 2+ years' experience with System Development Lifecyle 3+ years' experience in Computer System Validation Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. Knowledge of FDA guidance's and industry standards (i.e., GAMP) Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports Experience in QA Methodologies, designing, reviewing and approving User Stories, Test Plans and Reports, System and UAT test scripts, Test procedures, Traceability Matrix, and Design Specs. Strong verbal and written communication skills. Ability to lead a team. Ability to work with remote teams and support several changes/projects simultaneously. Ability to provide Validation guidance, timely reviews, and escalations to TQ management. Ability to work with global project teams during the initial project planning phases Ability to provide guidance on validation strategy and be able to handle the highly fluid state of the project #J-18808-Ljbffr TechDigital Group
- TechDigital Group in the United States is seeking a Validation Specialist with experience validating GEN AI solutions in GxP environments... ...will write and execute documentation for validation deliverables, lead a team including remote members, and collaborate with global...SuggestedRemote work
$110k - $160k
...regulatory requirements. As being a key member, you will also be responsible for development new businesses. Brief Responsibilities Lead and Manage municipal projects from planning through completion. Develop project schedules, budgets, and work plans. Coordinate...SuggestedFull timeContract workFor contractorsWork at office$72.8k - $80.1k
Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated operational...SuggestedWorldwide- ...The Validation Engineer is responsible for executing, maintaining, and continuously improving site validation activities to ensure that equipment, utilities, facilities, processes, and systems remain in a qualified and validated state and comply with current Good Manufacturing...Suggested
$87.1k - $94.6k
...done. We're obsessed with how it will be done.Key ResponsibilitiesCQV Execution & Safety- Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety- Deliver C&Q activities in alignment with project schedules- Track and report...SuggestedFor contractorsWorldwide- ...R3 Technology Inc. seeks Validation Engineer or it Hillsborough NJ office to gather requirements to develop product-level requirements and assist with high level systems view of product design. Conduct multi-disciplined product and process performance testing for both...Work at officeRelocation
- ...Purple Drive Computer System Validation (CSV) Consultant Share Raritan, NJ Overview: Role Descriptions: • Demonstratable... ...support for 21 CFR Part 11 implementation in Pharma industries. • Leading the Tech Writer team for preparing the test cases. • Co-...
- ...Piper Companies is currently looking for an experienced ( CQV) Validation Engineer in Raritan, NJ to work for an innovative and growing pharmaceutical organization. The primary responsibility of this role is to assist with the IQ/OQ/PQ of new instruments/equipment...
$175k - $250k
...hyperscale customersWe are seeking a Principal Optical Engineer to lead the innovation, design, and prototyping of our next-generation... ...of optical systems.Participate in hands-on prototyping and validation activities to ensure strong correlation between design models and...Flexible hours$96.27k - $126.35k
...performed within a team-based environment, on an assigned production shift schedule. Key Responsibilities This individual will lead and supervise multiple units within the CAR-T process operations (i.e. component preparation manufacturing, MFG support operations,...Permanent employmentFull timeTemporary workFor contractorsWork at officeLocal areaWorldwideFlexible hoursShift workDay shiftAfternoon shift- ...personnel maintain proficiency in preventive maintenance, start-up, trouble-shooting, and repair of supported equipment* Generate sales leads; and promotes and develops maintenance/service agreements; estimates and generates bids for contract projects/work* Manages larger...Full timeContract workTemporary workFor contractorsLocal area
$110k - $160k
...requirements. As being a key member, you will also be responsible for development new businesses. \n \n Brief Responsibilities \n \n Lead and Manage municipal projects from planning through completion. \n Develop project schedules, budgets, and work plans. \n...Contract workFor contractorsWork at office- ...instructions, including written, oral, and diagrammatic formats.Possess a valid drivers license.Preferred Qualifications:Demonstrated experience... ...process improvements within a warehouse setting that lead to enhanced operational outcomes and customer satisfaction.Experience...Contract workWork experience placementWork at office
$59.17k - $77.66k
Operations Associate Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative...Temporary workLocal areaWorldwideFlexible hoursShift work- ...Quest Diagnostics Incorporated is seeking a Phlebotomy Supervisor in Bound Brook, NJ to lead daily operations across PSCs and mobile/in-office phlebotomy teams. You will implement SOPs, ensure regulatory compliance, and supervise staff in a fast-paced healthcare environment...Work at office
- ...Description Position Description: Our project managers are technical leads first, with a strong background in CQV strategy, development,... ...800 people worldwide. We provide commissioning, qualification, validation, start-up, project management and other consulting services...Full timeWorldwide
- ...professional to manage stakeholder relationships and coordinate operational services for Global Commercial Data & Analytics supporting a leading biopharmaceutical organization. This is a mid-level, client-facing management position focused on building strong relationships...Full timeWork at office2 days per week
$130k - $165k
Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions... ...accuracy and credibility through strong data governance, validation, continuous improvement, and incorporation of customer and...Temporary workWork at officeRemote workWork visa2 days per week3 days per week- ...and forecast and tracking of study budgets and milestones .Provide periodic updates to the cross-functional team members.The CTM will lead the clinical trial team overseeing all trial activities ensuring timelines are met and budget is managed appropriatelySkills:Strong...Local areaImmediate start
- ...in Oncology is mandatory.• CTOM needs to be able to review and validate patients and data.• Strong interpersonal and communication skills... ...systems), processes and SOPs • Experience in managing and leading international meetings (Clinical Trial Team, expert meeting, etc...Immediate startFlexible hours
- Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets...Work at officeLocal areaImmediate start
$120k - $135k
Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see...Temporary workRemote workWork visa- ...services company established in 1996 that has grown to more than 700 people worldwide. We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission...Worldwide
$26.25 - $42.65 per hour
...possibilities, experience our rewarding culture, and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrow-people with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams...Permanent employmentTemporary workWork experience placementSeasonal workWork at officeLocal areaFlexible hours- ...Chain to deploy CIP programs, improve process outcomes, and sustain operational excellence. The incumbent will also coach teams and lead Lean/Six Sigma initiatives to achieve Right the First Time results. #J-18808-Ljbffr 6062-Janssen Pharmaceuticals, Inc. Legal Entity
- The Director of Operations will lead and optimize the operational backbone of a mid to large staffing and consulting organization. This role is responsible for driving operational consistency, margin performance, scalability, and service excellence across sales, finance...Full time
- Gilder Search Group in Somerville, NJ seeks a licensed Professional Land Surveyor to lead our Survey Department. The role requires directing a team of surveyors and technicians, managing projects and client relationships, and ensuring regulatory compliance. You will apply...
- ...information, or other applicable legally protected characteristic. About the role Generalist is hiring a Robotics Operations Manager to lead and scale the on-site operations that produce high-quality data for our robotic foundation models. You’ll lead robot operators and...Shift work
- Legend Biotech is seeking a Director, QA Operations in Raritan, NJ to lead the Quality Operations team for CAR-T cell therapy manufacturing. You will provide QA oversight, batch record review, and product disposition, ensuring strict adherence to cGMP and regulatory expectations...
- ...up operations, ensuring regulatory compliance, driving continuous improvement, and building high-performing teams. Responsibilities Lead manufacturing operations supporting both clinical and commercial cell therapy. Develop strategic vision for capacity and technology...
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