Kneat jobs in remote

Hybrid in Raritan, New Jersey

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21d ago

GxP Deployment Lead Kneat Gx Location: Lawrenceville, NJ Onsite Experience: 10+ Years Employment Type: W2 / C2C (as applicable) Position Summary: We are seeking an experienced GxP Deployment Lead with hands-on expertise in Kneat Gx to lead the implementation, configuration, validation, and rollout of paperless validation and digital execution processes within a regulated life sciences environment.The ideal candidate will act as a bridge between Business, Quality, IT, and Validation teams, ensu

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Third Party, Contract

60 - 65

CSV Lead

Hybrid in Durham, North Carolina

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16d ago

Role - CSV Lead Location- Durham, NC (Hybrid, must visit site 2-3 days a week) Job Description- Must have worked in CSV in Manufacturing automation systems like DELTA V,PI Historian, PLC, LAB Automation Systems(any one pf the systems or all). Primary: CSV (Computer System Validation) Compliance Secondary: SDLC / CSA / Validation Governance / Quality Compliance. Hands-on experience supporting validation and compliance activities for computerized manufacturing systems in a regulated pharmaceutical

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Contract

Depends on Experience

CSV Analyst

Hybrid in West Point, Pennsylvania

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29d ago

Job Title- CSV Analyst Job Location- WestPoint, PA (Hybrid, 3 days/week need to be on site) Mandatory Skills- CSV ( Manufacturing Systems- DeltaV,Rockwell,MES,PI etc),KNEAT,MEDS Job Description- Hands-on experience supporting validation and compliance activities for computerized manufacture ng systems in a regulated pharmaceutical environment. Provide CSV compliance support for Capital and Strategic Projects to ensure continuity of compliance oversight and project delivery.Develop, review, and a

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Contract

$40 - $50

Process Validation Engineer

Durham, North Carolina

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14d ago

Job Description: Our client is seeking a Process Validation Engineer to support activities within a GMP pharmaceutical manufacturing environment. This individual will be responsible for developing, executing, and documenting process validation studies while partnering closely with Manufacturing, Quality, Engineering, Microbiology, and other cross-functional teams. The role will initially focus on validation planning, protocol generation, and documentation before transitioning into hands-on ex

Full-time

Validation Engineer 2

Bend, Oregon

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14d ago

Job Description: Client is seeking a contractor-level CSV/CQV Specialist to support a high-priority backlog of qualification and validation activities within the CQV department. This role will provide validation support for analytical laboratory instruments, computerized systems, and GMP equipment while partnering closely with both the Instrumentation and CQV teams. The successful candidate will split time supporting Dawn Bosco's CQV priorities and the Instrumentation team's CSV activities. This

Full-time

Validation Engineer I

Waltham, Massachusetts

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Today

ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently. The Role ElevateBio is looking to hire a Validation Engineer I to join the Validation Engineering. The Validation Engineer I will perform qualificati

Full-time

USD 105,000.00 - 145,000.00 per year

CQV Engineer Packaging Validation

Hybrid in Thousand Oaks, California

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20d ago

Job Description - CQV Engineer Packaging Validation Thousand Oaks, California Hybrid Seeking experienced and ambitious engineering professionals looking to advance their careers within the pharmaceutical, biotechnology, and medical device industries. We support some of the leading organizations across the Life Sciences sector, working alongside highly experienced subject matter experts on technically complex and high-impact projects. We are currently seeking a Senior CQV Engineer to support a c

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Contract

$40 - $70

CQV Engineer Packaging Validation

Hybrid in Thousand Oaks, California

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20d ago

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Contract

$40 - $70

CQV Engineers (Multiple Levels)

Minneapolis, Minnesota

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Today

Job Description PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients' success, and you can be a part of our team's achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East

Full-time

Molding Engineer II, Molding & Tooling Engineering

Houston, Texas

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Today

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us? This role is part of Alcon's Engineering function, a team focu

Full-time

Computer System Validation (CSV) Lead - Oracle Fusion

Boston, Massachusetts

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22d ago

No OPT/CPT Job Summary We are seeking an experienced Oracle Fusion Computer System Validation (CSV) Lead to support the implementation, validation, and ongoing lifecycle management of Oracle Fusion applications within a regulated life sciences environment. The ideal candidate will have strong experience validating Oracle Fusion Cloud ERP applications, leading risk-based CSV/CSA activities, and ensuring compliance with 21 CFR Part 11, EU Annex 11, GAMP 5, data integrity, and applicable GxP requi

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Full-time

55 - 60

Equipment Validation Engineer 2

Durham, North Carolina

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Today

Position Overview We are seeking an Equipment Validation Engineer II to support the qualification of manufacturing equipment and utilities in our GMP facility. You will develop and execute risk-based validation strategies, author and run IQ/OQ/PQ protocols, and partner with cross-functional teams to ensure compliant, reliable operations. Company Overview At FUJIFILM Biotechnologies, we're leading the charge in advancing tomorrow's medicines. If you want to be a part of life-impacting projects

Full-time

Commissioning, Qualification, and Validation (CQV) Engineer

Boston, Massachusetts

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Today

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Full-time

Commissioning, Qualification, and Validation (CQV) Engineer

Lancaster, Pennsylvania

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Today

Full-time

Commissioning, Qualification, and Validation (CQV) Engineer

Edison, New Jersey

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Today

Full-time

Commissioning, Qualification, and Validation (CQV) Engineer

Raleigh, North Carolina

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Today

Full-time

CON TSMS SA Scientist

North Carolina

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Today

Sterility Assurance Scientist - Night Shift Charlotte area, NC On-Site role $40 - $80 per hour 12-Month Contract Openings: 2 ABOUT THE ROLE Our client is seeking a Sterility Assurance Scientist for a 12-month contract to support parenteral pharmaceutical manufacturing operations on night shifts in the Charlotte area, NC. This highly hands-on, manufacturing-floor-focused role is responsible for developing and implementing site sterility assurance programs, providing technical guidance in enviro

Contract

$45.00 - $80.00

GxP Systems and Support Administrator

Remote

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Today

Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For mission-critical and regulated industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field-tested processes, and elite expertise developed over 30 years. Our approach is simple because our Purpose inform

Full-time

USD 130,000.00 - 150,000.00 per year

Business Process Analyst

Portsmouth, New Hampshire

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Today

Business Process Analyst Location: Portsmouth, NH. (Additional network location considered: Houston, TX). Relocation assistance is available for eligible candidates and their families. Travel: Will require travel depending on project need for a duration of 2-3 weeks (both domestically and internationally). The Business Process Analyst plays a critical role in the implementation and optimization of the S4/HANA platform, focusing on ?Analyze to Decide? (A2D) related processes. A2D scope covers

Full-time

Principal Automation Engineer - Computer System Validation

Richmond, Virginia

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Today

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but i

Full-time

USD 67,500.00 per year