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- Johnson & Johnson Jobs for Entry Level and Internship 25
At Johnson & Johnson, the largest healthcare company in the world, Johnson & Johnson Global Services, the global shared services organization supporting the businesses of Johnson & Johnson, performs select functional work in a consistent manner across regions and sectors using simplified, standardized end-to-end processes and state-of-the-art technology.
Johnson & Johnson J&J Careers Opportunities for Graduate Freshers, Entry Level, Mid Level in various domain such as Technology, Engineering, Healthcare, Operation, Business, Customer services
Calling all big thinkers and world-changers who want to drive their careers forward across more than 250 leading businesses in pharmaceutical, and medical technology.
If you have the talent and desire to touch the world, Johnson & Johnson has the career opportunities to help make it happen.
Johnson & Johnson Jobs for Entry Level and Internship 25
QA Project Engineer MES (Manufacturing Execution Systems) Europe
We are looking for a Quality Assurance Project Engineer who will focus on ensuring the quality of our MES (Manufacturing Execution Systems) projects for the CAR-T hub in Europe. This role involves close collaboration with various teams to support the implementation and optimization of MES solutions. The position will be based in Ghent Belgium.
Job Responsibilities:
Coordinate the quality assurance process within MES projects.
Translation of production processes to MBRs and related master data take into account the strict procedures specific to the pharmaceutical industry
Responsible for QA support of Master batch records (including training and guidance)
Execute tests and quality controls to ensure the efficiency and reliability of systems.
Oversee the implementation process of MES software and applications.
Analyze system errors and propose improvements for enhanced performance.
Collaborate with internal teams to drive continuous process optimization.
Report on project progress and quality to management.
Active participation in project teams, operational teams & system teams
Close collaboration with operations, IT & automation
Support the operational and QA departments by providing coaching and/or training
Qualifications:
A bachelor’s or master’s degree in a technical field (e.g., Engineering, Computer Science, etc.).
Experience with MES systems and quality assurance in production environments is a strong advantage.
Knowledge of software testing and the implementation of technical solutions.
Strong communication skills and a solution-oriented attitude.
Ability to work independently as well as in a team setting.
If you are passionate about quality assurance in the realm of MES projects and seek to make a significant impact in a dynamic environment, we invite you to apply.
For more details to apply, Click here!
Trainee in Quality Control and New Product Introduction, fixed-term 12 months – Switzerland
For our QC department in Schaffhausen, we are looking for an open-minded, goal driven, motivated Specialist QC Services.
Trainee QC NPI (f/m/d), fixed-term 12 months, Location: Schaffhausen
Job Description:
Coordinate and plan the introduction of new products into QC
Review and implementation of test methods for new products.
Create and review GMP documents for new products.
Coordinate and plan the introduction of new technologies and the implementation of software applications (e.g. Empower Master projects).
Review of analytical data.
Coordinate non-conformances, corrective actions (CAPAs) and changes (change control management) related to the introduction of new products.
Support documentation for new product registration.
Qualifications:
You successfully completed your science or technology studies, preferably with a focus on the pharmaceutical, (bio-)chemical or biotechnological fields, or you have several years of experience as a chemical or biological laboratory assistant in quality control, preferably in a GMP-environment.
You have very good project management skills (good communication skills, pro-active).
You have very good organizational and communication skills, a customer-oriented approach and «can do» mentality.
You have very good knowledge of analytical methods.
You have experience in the review of analytical data and GMP documents. Experience in dealing with eLIMS and the Empower laboratory system are beneficial.
You have very good knowledge in the application of Microsoft Office programs.
You are fluent in German and English
For more details to apply, Click here!
Analyst, Procurement Warehousing – Brazil
We are searching for the best talent for a Analyst, Procurement Warehousing to be located at São José dos Campos, Brazil.
Data Analytics & Reporting:
Market & Supplier Analysis:
Procurement Process Support
Supplier & Stakeholder Collaboration:
Performance Monitoring:
Ad-hoc Projects & Reporting:
Required Knowledge:
Strong proficiency in data analysis and reporting, with advanced Excel skills (pivot tables, VLOOKUP, etc.). Familiarity with BI tools (e.g., Power BI, Tableau) is a plus.
Strong analytical thinking and problem-solving skills, with attention to detail.
Ability to collect and synthesize data from various stakeholders.
Excellent communication and interpersonal skills, with the ability to collaborate effectively across regional and global teams.
Ability to work independently, manage time efficiently, and handle multiple priorities in a fast-paced environment.
Ability to own global team responsibility for organization of Microsoft Teams/Sharepoint
Fluent in Portuguese and English (Spanish is a plus).
For more details to apply, Click here!
Automation Engineer, Delta V – United State
Johnson & Johnson is currently seeking an Automation Engineer, Delta V to join our MAKE Asset Management Organization located in US Large Molecule Drug Substance Site located in Wilson, North Carolina.
Job Responsibilities:
Support the automation systems – Delta V.
Support project execution as a project team member and lead complex projects.
Implement or lead execution system code change.
Write and perform validation protocols.
Ensure compliance with global standards.
Support risk assessments.
Support investigations.
Participate in compliance inspections.
Ensure sound technical engineering concepts are applied in all tasks.
Delivery and execution of the Site Delta V strategy.
Utilizes industry experience to identify continuous improvement opportunities of site validation practices.
Qualifications:
Bachelor’s degree in Engineering, IT, Science or related discipline is required.
Required:
A minimum 4 years of experience in a manufacturing environment, biopharmaceutical or pharmaceutical industry, or an equivalent combination of education and experience.
Knowledge of S95 Level 1 systems such as Emerson Delta V, OSI Pi, PLCs, IT Infrastructure & Hardware.
MES (preferably in Werum PAS-X) and DeltaV Batch Control experience.
Knowledge of Industrial Automation Networks and their Communication Protocols.
Understanding of S95 level 4 systems and their capabilities such as ERP, Quality Systems, Data warehouses & CDL.
Understanding of the ISA S95 & S88 standards and how they should be used within the Global Supply Chain.
Understanding of OSI PI Historian and Werum MES
For more details to apply, Click here!
Engineer RD Summer Intern – US
Job Responsibilities:
3D Modeling and Technical Drawings:
Utilize SolidWorks to create and modify 3D models of medical devices.
Prepare detailed engineering drawings to accompany the models.
Ensure that all designs meet technical and industry specifications.
Document Management:
Assist in organizing and maintaining R&D documentation in accordance with FDA regulations.
Support the preparation and revision of documents required for Design History Files.
Ensure all documentation practices align with quality management systems.
Prototyping and Development:
Participate in prototyping efforts, including preparation, testing, and analysis.
Contribute ideas during product development brainstorming sessions.
Assist in evaluating the feasibility of new product concepts.
Qualifications:
Current enrollment in an undergraduate or graduate program in Biomedical Engineering, Mechanical Engineering, or a related field.
Proficiency in SolidWorks or similar CAD software.
Strong organizational skills and attention to detail.
Excellent verbal and written communication skills.
Ability to work collaboratively in a team environment.