good manufacturing practice Jobs

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Validation EngineerJob Title - Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Fall River, Massachusetts, USA

Full-time

Job Description: The Validation Engineer is responsible for developing DQ/IQ/OQ/PQ protocols and coordinating and performing equipment qualifications, ensuring that automated process equipment that mass produce medical device consumables and other products, are designed, developed or changed in compliance with specifications, requirements, safety and Company and regulatory guidelines. The Validation Engineer will work closely with Senior validation staff, maintenance, operations, and R&D teams t

Staff Reliability EngineerJob Title - Staff Reliability Engineer

Johnson & JohnsonCompany Name - Johnson & Johnson

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Athens, Georgia, USA

Full-time

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

EngineerJob Title - Engineer

ACL DigitalCompany Name - ACL Digital

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Holly Springs, North Carolina, USA

Full-time

Onsite: Client North Carolina (Holly Springs) - Relo candidates can be considered Duration: 3-year contract Openings: 3 Standard business hours (~8 to 5) with flexibility for: Evening or weekend work, Occasional holiday support, Up to ~50 hours/week, assuming occasional OT Department: ANC Engineering Ideal candidate is a commercially experienced Process Engineer with a BS in Chemical, Mechanical, or Biomedical Engineering, who has supported large-scale drug substance operations in biotech or

Validation EngineerJob Title - Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Thousand Oaks, California, USA

Full-time

Responsibilities: Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines. Author/evaluate qualification/validation protocols including DQ, IQ, OQ, FT, PQ protocols and final reports for new or modified GMP utilities, facilities, and process equipment. Execute DQ, IQ, OQ, FT, PQ protocols, which involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP utilities, facilities, and process equi

Validation Engineer IIIJob Title - Validation Engineer III

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Plainsboro Township, New Jersey, USA

Full-time

Job Description: Qualified candidates must be experienced in one or more of the following areas of validation: Equipment Qualification Process Qualification The candidate must utilize problem solving techniques to resolve issues and conflict in order to meet the high level goals set forth by the organization. The candidate must be well organized and technically sound in understanding scientific rationale and justifying criterion from a quantitative standpoint. The candidate must be familiar with

Computer System Validation EngineerJob Title - Computer System Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Libertyville, Illinois, USA

Full-time

Responsibilities: The Manufacturing IT Systems Quality & Compliance Specialist- Cell Therapy Manufacturing Systems supports the successful operation of manufacturing and business functions at Libertyville site through interaction with internal team members, peer and higher-level customers as well as external service providers. The individual is responsible for the development of and adherence to system governance procedures. The individual supports multiple IT projects/systems and ongoing work a

Validation Engineer SeniorJob Title - Validation Engineer Senior

ACL DigitalCompany Name - ACL Digital

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Thousand Oaks, California, USA

Full-time

Responsibilities: Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines. Work with project teams to develop the commissioning and qualification strategy and document in qualification plans. Author/evaluate qualification/validation protocols including DQ, IQ, OQ, FT, PQ protocols and final reports for new or modified GMP utilities, facilities, and process equipment. Execute DQ, IQ, OQ, FT, PQ protocols, which involve protocol discrepancie

Validation EngineerJob Title - Validation Engineer

ACL DigitalCompany Name - ACL Digital

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Thousand Oaks, California, USA

Full-time

Senior Validation EngineerJob Title - Senior Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Vacaville, California, USA

Full-time

Responsibilities: Supervisor Principal Validation Engineer. Responsible for defining qualification / validation strategies and coordinating testing activities required to complete assigned projects in support of continued cGMP operations at the Polaris Vacaville commercial manufacturing facility. This consists of initial qualification, requalification, periodic review and Validation activities associated with capital/expense projects. Performance of such validation activities includes equipment

Systems Administrator / Technical Lead - Process Control SystemsJob Title - Systems Administrator / Technical Lead - Process Control Systems

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Foster City, California, USA

Full-time

Job Summary: We are looking for an experienced professional who will be responsible for administration of Rockwell FactoryTalk-based process control systems and Inductive Automation's Ignition-based process control and environmental monitoring systems. The candidate should have hands-on experience deploying, configuring, and troubleshooting these systems in a Good Manufacturing Practice (GMP) environment, with a good understanding of FDA regulations. This role focuses on deploying system updates

Global MES System Engineer - API New FacilitiesJob Title - Global MES System Engineer - API New Facilities

Eli Lilly and CompanyCompany Name - Eli Lilly and Company

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Lebanon, Indiana, USA

Full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

CQV EngineerJob Title - CQV Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Rocky Mount, North Carolina, USA

Full-time

Responsibilities: Lead CQV activities for new and modified filling lines, including isolator systems. Develop and execute IQ, OQ, and PQ protocols for filling equipment such as vial washers, dehydrogenation tunnels, filling machines, and capping systems. Perform risk assessments (e.g., FMEA) for filling line modifications and qualifications. Troubleshoot and resolve technical issues during qualification activities Clean Utility System. Manage CQV processes for clean utility systems, including pu

Technician III, Engineering - Process (Weekend AM)Job Title - Technician III, Engineering - Process (Weekend AM)

Novo Nordisk IncCompany Name - Novo Nordisk Inc

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Bloomington, Indiana, USA

Full-time

About the Department At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana site is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product f

Automation Engineer - Peptides Nano FiltrationJob Title - Automation Engineer - Peptides Nano Filtration

Eli Lilly and CompanyCompany Name - Eli Lilly and Company

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Lebanon, Indiana, USA

Full-time

MES System EngineerJob Title - MES System Engineer

Eli Lilly and CompanyCompany Name - Eli Lilly and Company

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Pleasant Prairie, Wisconsin, USA

Full-time

PROCESS DEVELOPMENT ENGINEER IIIJob Title - PROCESS DEVELOPMENT ENGINEER III

Becton Dickinson & CompanyCompany Name - Becton Dickinson & Company

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Tempe, Arizona, USA

Full-time

Job Description Summary This position actively participates as a key cross-functional team member on new product development projects with a focus on design for manufacturability and the design, development, implementation and validation of manufacturing processes, test methods and equipment. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the

IDAP MES System Engineer Tech@LillyJob Title - IDAP MES System Engineer Tech@Lilly

Eli Lilly and CompanyCompany Name - Eli Lilly and Company

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Indianapolis, Indiana, USA

Full-time

Supply Chain Business Analyst- SAP ERPJob Title - Supply Chain Business Analyst- SAP ERP

TSR Consulting Services, Inc.Company Name - TSR Consulting Services, Inc.

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Summit, New Jersey, USA

Contract

Our client, a leading pharmaceutical company, is hiring a Supply Chain Business Analyst, on a contract basis. Job ID: 82493 Work Location: Summit, NJ - 50% on site (flexible to come more than 50% if needed) Job Title: Supply Chain Business Analyst- SAP ERP Summary: The Cell Therapy External Manufacturing ERP Systems business analyst is part of the Cell Therapy Vector & External Manufacturing Operations (VEXMO) organization and will support the ERP business process for the external network. This

LIMS Master Data SpecialistJob Title - LIMS Master Data Specialist

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Summit, New Jersey, USA

Full-time

Position Summary: Responsible for the creation and execution of computer system validation document as well as providing operational support and guidance related to system use and improvement. Responsibilities: Create and execute computer system validation documents (i.e., UAT, URS, OQ, PQ, etc.) as applicable and guide QC end users on the development of system enhancements with user requirements and business drivers. Provide electronic systems operational support and troubleshooting to end use

Test Fixture Engineer IIJob Title - Test Fixture Engineer II

Boston Scientific CorporationCompany Name - Boston Scientific Corporation

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Irvine, California, USA

Full-time

Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your