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General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
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Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2025-10-22 09:04:21
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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a QC Chemist to join our Quality Control team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required.
Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance.
Responsible for timely analytical data reporting based on project timelines.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Demonstrate a more advanced knowledge of various test methods and instrument analysis techniques and be proficient with all sample types and test methods.
Perform more advanced troubleshooting/maintenance of the instrumentation.
* Responsible for more complex physical and chemical testing of raw material, intermediate, and finished products as described in the documented procedures to support product release and process validation protocols.
* Demonstrate proficient ability to operate the instrument software applications, set up advanced sequences, troubleshoot software and report data while executing the higher complexity test methods that utilize instruments such as UV, FTIR, GC, and HPLC, and IC.
* As required, perform swabbing and analysis of more complex manufacturing equipment with no supervision in accordance with cGMP guidelines.
Provide input on cleaning related issues and investigations.
* Evaluate and maintain assigned calibrations for equipment in the laboratory as required and review the required documentation for compliance.
Review instrument qualification documents to support system change control actions and assist vendors during installation and PM’s.
* Investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines.
* Assist Management with writing and completion of inv...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-10-22 08:30:27
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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 more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Beijing, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% in compliance.
Stra...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-10-22 08:22:43
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POSITION SUMMARY:
This is position that is responsible for the operation and supporting activities surrounding a particular coating process. The primary equipment will be operated through HMIs (Human-Machine Interfaces) and a series of switches, pushbuttons, and other interactive control points. Successful Operators will be capable to produce the required amount of product in a defined period while ensuring all (Environment, Health and Safety (EHS) and Quality requirements are continuously satisfied. The Operator will be required to work as part of a team with Operations Support, Engineering, Maintenance, and Management personnel. Some overtime will be required on occasion to meet production and project schedules. Limited travel may be required in support of training program. Operators will be provided the opportunity to progress within the role as defined below.
DUTIES AND RESPONSIBILITIES:
* Perform complex and multi-level tasks from procedures and work instructions defining the tasks.
* Maintain timely and accurate record keeping using provided tools including digital and handwritten data entry and notes.
* Maintain 100% compliance with personal protective equipment (PPE) requirements while operating equipment and/or performing supporting operations, includes ensuring your personal protective equipment is functioning properly prior to starting a task.
* Effectively identify and communicate non-standard situations including (EHS) and Product Integrity concerns.
* Operate support equipment (pre/post coating) and support Coater Operators
* Maintaining metal coating fixtures for use in coater which including visually verifying condition, removing residual coatings, and removing any contamination that may have affected the fixtures.
* Cross training in other coating process areas as needed to support production requirements. Will be required to complete the training program for each process prior to performed assignments in that area.
QUALIFICATIONS:
* High school diploma or general education degree (GED).
* At least 2 years’ experience working in a production manufacturing environment
* Additional Education, Training, Certifications, or Licenses that are applicable will be considered and may be used to supersede either of the other two requirements.
* Must be able to read, write, and communicate in English.
* Read and interpret documents such as safety rules, operating instructions, and procedure manuals.
* Write routine reports and correspondence either in digital or handwritten formats.
* Good mathematical skills, scientific principles and reasoning ability
* Mechanically inclined individual that thrives in a hands-on, demanding environment with little direct supervision once assignments are handed out.
* May be required to operate of forklift (training provided).
PHYSICAL DEMANDS: Reasonable accommodat...
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Type: Permanent Location: Oldsmar, US-FL
Salary / Rate: Not Specified
Posted: 2025-10-21 08:10:42
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POSITION SUMMARY:
This is position that is responsible for the operation and supporting activities surrounding a particular coating process. The primary equipment will be operated through HMIs (Human-Machine Interfaces) and a series of switches, pushbuttons, and other interactive control points. Successful Operators will be capable to produce the required amount of product in a defined period while ensuring all (Environment, Health and Safety (EHS) and Quality requirements are continuously satisfied. The Operator will be required to work as part of a team with Operations Support, Engineering, Maintenance, and Management personnel. Some overtime will be required on occasion to meet production and project schedules. Limited travel may be required in support of training program. Operators will be provided the opportunity to progress within the role as defined below.
DUTIES AND RESPONSIBILITIES:
* Perform complex and multi-level tasks from procedures and work instructions defining the tasks.
* Maintain timely and accurate record keeping using provided tools including digital and handwritten data entry and notes.
* Maintain 100% compliance with personal protective equipment (PPE) requirements while operating equipment and/or performing supporting operations, includes ensuring your personal protective equipment is functioning properly prior to starting a task.
* Effectively identify and communicate non-standard situations including (EHS) and Product Integrity concerns.
* Operate support equipment (pre/post coating) and support Coater Operators
* Maintaining metal coating fixtures for use in coater which including visually verifying condition, removing residual coatings, and removing any contamination that may have affected the fixtures.
* Cross training in other coating process areas as needed to support production requirements. Will be required to complete the training program for each process prior to performed assignments in that area.
QUALIFICATIONS:
* High school diploma or general education degree (GED).
* At least 2 years’ experience working in a production manufacturing environment
* Additional Education, Training, Certifications, or Licenses that are applicable will be considered and may be used to supersede either of the other two requirements.
* Must be able to read, write, and communicate in English.
* Read and interpret documents such as safety rules, operating instructions, and procedure manuals.
* Write routine reports and correspondence either in digital or handwritten formats.
* Good mathematical skills, scientific principles and reasoning ability
* Mechanically inclined individual that thrives in a hands-on, demanding environment with little direct supervision once assignments are handed out.
* May be required to operate of forklift (training provided).
PHYSICAL DEMANDS: Reasonable accommodat...
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Type: Permanent Location: Oldsmar, US-FL
Salary / Rate: Not Specified
Posted: 2025-10-21 08:10:35
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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 more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson is currently seeking a Lead Local Trial Manager to join our Global Clinical Operations located in Beerse, Belgium.
A Lead, Local Trial Manager is considered as a senior trial management role with at least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience.
This role is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries.
The Lead, Local Trial Manager is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocol(s) from start-up through to database lock and closeout activities as described in GCO procedural documents.
The Lead, Local Trial Manager is responsible for coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements.
The Lead, Local Trial Manager actively leads or contributes to process improvement; training and mentoring of other LTMs and Site Managers (SM).
Compared to Associate, Local Trial Manager and Senior, Local Trial Manager roles, a Lead, Local Trial Manager is often assigned to more complex protocols and can work across Phase 1 – 3 studies in multiple therapeutic areas as needed to drive business needs.
The Lead, Local Trial Manager may also perform the role of Trial Delivery Manager (TDM)/Trial Delivery Leader (TDL) for single country as described in GCO procedural documents.
Principal Responsibilities:
* May be delegated by Functional Manager (FM)/Clinical Research Manager (CRM) to lead country protocol feasibility (if applicable) and site feasibility assessment in conjun...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-20 08:11:17
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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 more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Post Doc – Data Analytics & Computational Sciences
Job Category:
Career Program
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for Postdoctoral Scientist, R&D Data Science and Digital Health, Real-World Evidence (RWE) Oncology
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
The Real-World Evidence (RWE) Oncology team within Johnson and Johnson Innovative Medicines is looking for outstanding postdoctoral scientist whose responsibilities include:
* Analyze observational databases and historical trial data to generate real-world insight to support regulatory agency interactions
* Develop study protocols, statistical analysis plans, and programming specifications.
Deliver high-quality outputs including analysis-ready datasets, tables and figures.
* Perform comprehensive reviews of scientific literature to contextualize findings and support study design and interpretation.
* Communicate research findings effectively through technical reports, presentations, and contributions to peer-reviewed publications
Required qualifications:
* A Ph.D.
degree in epidemiology or biostatistics
* Expert coding skills using R
* Strong expertise in conducting epidemiological research including research questions, designing studies, conducting analyses, and interpreting results
* Hands-on experience with data extraction, cleaning, and analysis, as well as statistical methods to mitigate confounding and selection biases
* Excellent interpersonal, communication and presentation skills
Preferred qualifications:
* Experience with real-world data sources (EHR, insurance claims, registry data)
* Familiarity with clinical trial design and data structure
* Subject matter knowledge in o...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-20 08:11:03
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Manufacturing Scientist/Quality Control Chemist Intern (Summer 2026)
As a Scientist Intern, you will be part of Animal Health Manufacturing (AHM) Lab team to deliver a practical solution to reducing analytical variability, a manufacturing technical project, or implementation of new lab methods.
Interns will have exposure to many career path and diverse subject matter experts as many projects have site-wide impact.
Your Responsibilities:
* Understand the Animal Health Manufacturing process, document using GMP guidelines, and understand the importance of the Quality Unit
* Work within cross-functional teams to implement process or Quality Control lab improvements
* Learn about quality control, fermentation, product recovery, product finishing, or companion animal packaging
* Study design improvement processes
What You Need to Succeed (minimum qualifications):
* Education: Currently enrolled in a Microbiology, Biochemistry, Chemistry, Chemical engineering, or related engineering fields
* Experience with Microsoft Suites
* Demonstrate laboratory/manufacturing experience
* A willingness to learn
What will give you a competitive edge (preferred qualifications):
* Have an interest in animal health manufacturing, problem solving, scientific method, or cross-functional skill development
* Strong communication and interpersonal skills
* Thrive in cross-functional team settings
* Strong organizational and time management skills
* Must be able to work exceptionally well independently and with minimal supervision
Additional Information:
* Travel: 0%
* Location: Elanco Clinton Laboratories – Clinton, IN
Our Internship Program
Our internship program is designed to provide students with experiences! Internships are project based and comprised of business-critical needs.
All interns have the opportunity to significantly impact Elanco’s success over the summer and kickstart a career that counts.
* Internship Dates: May 18th – August 7th (12 Weeks)
* Competitive salary: $20-$40/hour (dependent upon major and year in s...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-10-18 08:40:31
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Job Category:
Intern
Job Family:
Student Intern
Job Description:
As a Quality Assurance Intern, you will have the opportunity to work the Summer 2026 with Schreiber Foods at one of our plant locations. This internship will be focused on supporting food safety and quality initiatives, company objectives and plant-specific assignments.
It is designed to prepare successful interns for a possible future career with Schreiber Foods.
This Quality Assurance summer internship is located at our plant in Smithfield, Utah.
Interns relocating more than 50 miles for the internship will receive a lump sum of $1,500.
This position offers a set rate of pay of $20.75 an hour.
What you’ll do:
* Lead small quality improvement projects within the team, working with plants and other areas of Schreiber Foods
* Creating and updating documentation for food safety and quality and lab processes
* Gaining knowledge about our products and applying that knowledge to improve processes and practices
* Inputting and analyzing data
* Completing projects related to testing, quality systems, sanitation, auditing, HACCP, training, SQF, suppliers, and other related topics
* Assisting the quality teams on ongoing projects
* Together with the leadership team, ensures compliance with Food Safety and Food Quality Plans, in addition to customer requirements.
Interprets and communicates customer requirements to plant production and/or support groups.
Establishes and Audits PCPs, CCPs and Standard Operating Procedures to define and monitor processes, to ensure customer requirements are met.
Reviews incidents during which the procedures are not met and determines appropriate corrective action for partners failing to follow standard procedures.
What you will need to succeed:
* Currently pursuing a Bachelor’s or Master’s degree in Food Science, Dairy Science, Microbiology, Bacteriology, Food Microbiology or closely related field.
* Ability to work 40 hours per week during the summer of 2026
* Ability to work at least 10 weeks of the summer, 12 weeks is preferred, with flexible start and end dates
* Effective oral and written communication skills
* Ability to work independently as well as in a team environment
* Ability to take ownership of assignments and complete them
* Desire to grow and take on new challenges and opportunities
* Ability and desire to work within a plant manufacturing setting
* Ability to multi-task
* Possess a strong technical foundation in the sciences; dairy knowledge desired but not required
* Reliable transportation
Internship benefits:
* Opportunity to complete real-world projects, participate in team meetings and contribute your ideas
* Exposure to different areas of the business around the world
* Internship program that includes engaging events and opportunities to build relationships at all levels
* Relocation assistance (...
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Type: Permanent Location: Smithfield, US-UT
Salary / Rate: Not Specified
Posted: 2025-10-18 08:40:10
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Was Dich erwartet:
Als Team Business Finance sind wir flexibel und halten das Business handlungs- und sprachfähig - global wie lokal - intern wie extern.
Der Fokus unserer Arbeit liegt darauf, als Sparringspartner Squads, Teams und Abteilungen der Roche Pharma AG in allen finanziellen und unternehmerischen Entscheidungen unter Einbeziehung vorhandener Informationen als auch zukünftiger, antizipierter Entwicklungen zu beraten und Impulse zu setzen.
Als Praktikant (m/w/d) erhältst Du Einblick in alle Themenbereiche des Controllings und der Vertriebssteuerung.
Dies umfasst unter anderem:
* Unterstützung von Monatsabschluss Aktivitäten
* Mitarbeit in Marktforschungs- und Targetingprojekten im deutschen Pharmamarkt
* Mitarbeit bei der Budgetplanung/-präsentation
* Erarbeitung und Aufbau interner Berichte (z.B.
Sales- und Kostenberichte) sowie Erstellen von Analysen und Auswertungen (z.B.
Sales, Kosten, Headcount, KPI’s)
* Enge Zusammenarbeit mit Kolleginnen und Kollegen in den Fachabteilungen und Mitarbeiter/Übernahme von Projekten
Wer Du bist:
Dein Studiengang ist idealerweise wirtschaftswissenschaftlich ausgerichtet und Du hast Lust darauf, das Erlernte praktisch anzuwenden.
Neben einer hohen Affinität für Zahlen zeichnest Du Dich durch analytische Fähigkeiten, eigenständiges Arbeiten und Engagement aus.
Darüber hinaus bringst Du folgende Qualifikationen mit:
* Hohe Lernbereitschaft und Interesse an neuen Aufgaben
* Sicheres und kommunikationsstarkes Auftreten
* Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift
* Sehr gute MS Office Kenntnisse (Outlook, Excel, Powerpoint); optional Kenntnisse in SAP S/4Hana, SAP/ERP, SAC sowie SAP/BW bzw.
Business Objects
Die Vorteile:
* Flexible Zeiteinteilung
* 2092 € Vergütung im Monat für ein Vollzeitpraktikum > 3 Monate
* Vernetzung mit anderen Studierenden
Deine Bewerbung:
Bitte lade nur den Lebenslauf online hoch.
Denke daran, daß sich dieses Praktikum an Studierende (m/w/d) bei laufender Immatrikulation während des gesamten Zeitraums des Praktikums richtet oder alternativ an Personen in einem maximal einjährigen Gap-Year (zwischen Bachelor und Master Studium), wo es schriftlich nachgewiesen werden kann, auf welcher Universität/Hochschule und genau wann (Monat/Jahr) innerhalb eines Jahres die Studien fortgesetzt werden.
Zeitraum: Ab Januar 2026 für 6 Monate.
Wir freuen uns auf Deine Bewerbung!
Your contact to us! With people.
For...
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Type: Permanent Location: Grenzach, DE-BW
Salary / Rate: Not Specified
Posted: 2025-10-18 08:23:04
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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 more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Electrical Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Yokneam, Haifa District, Israel
Job Description:
Job Description
About Johnson & Johnson MedTech Cardiovascular:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for a LCM Engineer role, to join our team located in Yokneam, Israel.
You will be responsible for:
* Develop hardware solutions to support released HTC systems.
* Write production procedures and define production processes.
* Design, procure parts for, and build production jigs, test benches, and other tools.
* Design new parts/systems to replace existing ones.
* Solve technical issues both individually and collaboratively with the team.
* Provide support on production sites and improve production yield.
* Check hardware to enhance functionality and eliminate unused components.
* Implement process and procedure improvements based on examination of production reports.
* Investigate and support production issues, customer complaints, and RMAs.
* Conduct failure analysis to identify root causes of production issues, customer complaints, and RMAs, and suggest immediate corrective actions.
* Provide feedback and solutions to the production line to enhance testing processes.
* Communicate findings and issues to R&D regarding production-related challenges, customer complaints, and RMAs.
Qualifications and Requirements:
* Bachelor's degree in Electrical Engineering or related field.
* At least 5 years of proven experience in hardware development and manufacturing, including transitioning products from development to production.
* Experience with multidisciplinary products.
* Background in medica...
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Type: Permanent Location: Yokneam, IL-HA
Salary / Rate: Not Specified
Posted: 2025-10-18 08:21:09
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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 more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
Scientific/Technology
All Job Posting Locations:
New Brunswick, New Jersey, United States of America
Job Description:
We are searching for the best talent for Senior Data Scientist: Forecasting, BI to be in New Brunswick, NJ.
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Purpose:
As a Senior Data Scientist in Global Finance Data Science Team: You will be responsible for delivering data science production processes to a high standard, contributing to products that are consumed and scrutinized by senior leadership.
You will work in a global team of Data Scientists, Data Engineers and Machine Learning Engineers to advance data science/AI roadmap for J&J’s Global Finance function.
You will help deliver value-added insights and analytics to our finance and business leaders, reduce manual workload through automation, and enhance user-experience.
Project focus area will also include Predictive Sales Forecasting as part of SAP Analytics Cloud reporting capability, taking it from PoC to Production-grade standards.
This includes aligning finance and business needs, input data validations from different source systems, data reconciliation/validations and work on other ongoing enhancements/ad-hoc requests from leadership etc.
You will help in data science projects across their lifecycle: Design/ proof-of-concept (PoC), development, data pipelines and engineering, deployment, adoption by end-users and ongoing enhancements.
The capabilities developed will include predictive financial forecasting, Gen AI, descriptive analytics, data visualization and decision support.
You will need to ensure that PoC’s are put into production-grade with correct amount of automation, data validations and systems/process integration.
This role will involve understanding the needs of business stakeholders and advocating the merits of data-driven analytics to provide viable solutions.
You will be responsible for:
* Adopting a highly successful ...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-18 08:20:54
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Cayenta and Opportunity Overview:
Cayenta is involved in some of the most challenging and interesting projects in the information technology industry and we're always looking for talented, highly motivated individuals who seek the same.
One of our most important decisions is the next person we invite to join our team.
As a Cayenta employee, you will be consistently challenged to deliver your best, and you will be fairly compensated for your efforts.
Because we provide our customers with the best technologies and services in the industry, you will constantly develop new skills, learn new products, and be involved in activities that are highly valued in the marketplace.
Most of all, any potential employee must be willing and able to represent our core operating principle, which simply states: "We value our customers as partners, therefore their success and satisfaction, as well as our own, depends on delivering excellence in everything we do."
Cayenta is a wholly-owned subsidiary of Harris Computer Systems.
Harris Computer Systems has been providing complete Customer Information System (CIS) and Financial Management solutions exclusively to public and municipal utilities for over 27 years.
Our track record speaks for itself. We are an experienced, solid company with proven solutions that are presently in use by over 1,500 customers across North America.
We are the number one provider of powerful Financial and CIS solutions because of our specialized understanding of the electric, water, and gas utility industry and our commitment to customer relationships.
Our implementation team has an exciting opportunity for driven individuals, and we're looking for a BI Business Analyst who is passionate about providing segregated IT transformation for our clients.
It is mission-critical for the BI Business Analyst to evolve into a conduit between BI, and our clients, working cross-functionally to become a product expert and a client process advisor.
The BI Business Analyst role is project-driven and will support clients with the development of BI solutions for a wide array of Cayenta's products.
This remote role welcomes candidates anywhere in Canada and the US.
Up to 25% travel to a mixture of Burnaby, BC, and customer sites across North America is required.
A valid passport/visa is necessary for travel.
What your impact will be:
* Analyze current requirements, design, and implement new and improved business processes
* Improve and implement Business Intelligence infrastructure requirements
* Facilitate communication with clients
* Manage and work on multiple projects with multiple teams and stakeholders
* Create portal statistics to meet client’s requirements
* Provide clients with training on Cayenta's BI solutions
* May perform other tasks as assigned
What we are looking for:
* Problem-solving, critical thinking, and analytical skills.
Must be able to analyze information to make independent decisions q...
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Type: Permanent Location: Burnaby, CA-BC
Salary / Rate: Not Specified
Posted: 2025-10-17 09:10:45
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Laboratory Head (m/f/d) Analytical Development & QC, Small Molecule Technical Development (SMTD)
We are looking for a Laboratory Head Analytical Development & QC, SMTD (m/f/d) to join us as soon as possible at our Monheim am Rhein, Germany location.
This job is a 1-year fixed duration position.
Your Responsibilities:
This role is broadly responsible for leading the analytical development activities for veterinary medicinal products, with concentrated expertise in dissolution development and control strategy.
Your key responsibilities include:
* Represent Analytical Development & QC in international technical development project teams
* Developing and delivering relevant analytical methods, setting specifications, and ensuring compliance with industrial (GxP) and regulatory requirements (VICH/ICH).
* Applying Quality by Design principles for method development, optimization, and validation.
* Conducting analytical tests, stability studies, and preparing analytical registration documentation for worldwide registration.
* Interpreting results, evaluating data, and drawing relevant conclusions, then reporting and presenting scientific/technical results internally and externally.
* Driving the evaluation and implementation of new technologies in dissolution and analytical development.
* Mentoring technical staff and ensuring compliance with internal and external quality standards (e.g., SOPs, GxP, HSE, AW).
What You Bring (preferred qualifications):
Education:
* Completed university degree with a doctorate, preferably in Analytical Chemistry, Pharmacy, Pharmaceutical Sciences, or a related field.
Technical Expertise:
* Profound knowledge in pharmaceutical analytics and techniques.
* Strong expertise in chromatographic (HPLC/UPLC) and spectroscopic (UV/VIS) method development, particularly dissolution with USP Apparatus II (Paddles) and IV (Flow Cell).
* Extensive knowledge of current quality and regulatory requirements for new drug products.
* Demonstrated track record of interactions with regulatory agencies (e.g., FDA/CVM, EMA) on an...
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Type: Permanent Location: Monheim, DE-NW
Salary / Rate: Not Specified
Posted: 2025-10-17 09:10:34
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Company Overview:
Meeco Sullivan - The Marina Company with the addition of Wahoo Docks and Ravens Marine, has over 200 years of experience and a well-earned reputation for the highest quality steel, timber and aluminum dock systems that are time tested and storm proven.
With our four manufacturing facilities in Warwick, New York, McAlester, OK, Dahlonega, GA and Kissimmee, FL we have more production capacity and expertise in galvanized steel, timber, and aluminum than anyone in North America.
Job Posting Title: National Health & Safety Manager
Primary Location: Wahoo Docks, Dahlonega, GA
Reports To: President
Company: Meeco Sullivan
Job Summary
Meeco Sullivan is seeking a proactive and experienced National Health & Safety Manager to lead and support safety initiatives across all divisions.
This role is critical to maintaining a safe and compliant work environment and will report directly to the President.
The successful candidate will oversee health and safety operations across four locations and serve as the company’s expert in safety compliance and training.
Key Responsibilities
* Develop, maintain, and improve behavior-based safety programs.
* Conduct facility audits and implement corrective actions.
* Monitor compliance with OSHA and environmental regulations.
* Deliver safety training to managers, supervisors, and employees.
* Coordinate new hire safety orientation and pre-employment screenings.
* Write site-specific safety plans and represent the company in client and regulatory meetings.
* Investigate incidents and implement preventive measures.
* Lead monthly safety committee meetings and corporate safety reviews.
* Stay informed on industry trends and regulatory changes.
* Travel to each facility at least twice per year to conduct audits and training.
Qualifications
* High School Diploma required; Bachelor’s degree preferred.
* Experience in manufacturing and construction safety compliance.
* Strong computer skills and ability to present to groups.
* Spanish language skills a plus.
* OSHA 500/501 and industrial hygiene certifications preferred but not required.
* Willingness to travel up to 20% of the time.
Working Conditions
* Combination of office, shop, and outdoor environments.
* Some Exposure to varying weather conditions.
* Travel is required to multiple company locations.
Why you should apply:
If you are looking for a great company to work for with an excellent benefit package to include, paid holidays, PTO, affordable Healthcare plans, Dental, Vision, Life Insurance, STD/LTD and 401(k) with Company Match, then you should Join our Winning Team!
*All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. We are proud to be an equal opportunity workplace and an affirmative action employer.
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Type: Permanent Location: Dahlonega, US-GA
Salary / Rate: Not Specified
Posted: 2025-10-17 08:58:03
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At Stewart, we know that success begins with great people.
As a Stewart employee, you’ll be joining a company that was named a 2024-2025 Best Company to Work For by U.S.
News & World Report, and a 2025 Top Workplace by USA Today.
We are committed to helping you own, develop, and nurture your career.
We invest in your career journey because we understand that as you grow, so does our company.
And our priority is smart growth – by attaining the best people, investing in tools and resources that enable success, and creating a better home for all.
You will be part of an inclusive work environment that reflects the customers we serve.
You’ll be empowered to use your unique experiences, passion and skills to help our company and the communities we serve constantly evolve and improve.
Together, we can achieve our vision of becoming the premier title and real estate services company.
Stewart is a global real estate services company, providing title insurance, settlement, underwriting, and lender services through our family of companies.
To learn more about Stewart, visit stewart.com/about.
More information can be found on stewart.com.
Get title industry information and insights at stewart.com/insights.
Follow Stewart on Facebook @StewartTitleCo, on Instagram @StewartTitleCo and on LinkedIn @StewartTitle
Job Description
Job Summary
Promotes Stewart services and solutions through various outside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share.
Job Responsibilities
* Promotes Stewart services and solutions through various inside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share
* Typically follows existing procedures to perform routine assignments and to solve standard problems
* Analyzes basic information and standard practices to make decisions impacting work performed
* Individual contributor working with direct oversight
* Performs all other duties as assigned by management
Education
* Bachelor’s degree in relevant field preferred
Experience
* Typically requires 0-2 years of related work experience
Equal Employment Opportunity Employer
Stewart is committed to ensuring that its online application process provides an equal employment opportunity to all job seekers, including individuals with disabilities.
If you have a disability and need assistance or an accommodation in the application process, please contact us by email at careers@stewart.com.
Benefits
Stewart offers eligible employees a competitive benefits package that includes, but is not limited to a variety of health and wellness insurance options and programs, paid time off, 401(k) with company match, employee stock purchase program, and employee discounts.
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Type: Permanent Location: Fairfax, US-VA
Salary / Rate: Not Specified
Posted: 2025-10-17 08:57:59
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Essential Duties and Responsibilities:
· Supports implementation and maintenance of ISO based quality system
including internal audits.
· Leads inspection efforts on new products, supporting ramp-up with detailed
inspections and shifting toward process/product auditing as product reaches
production rates.
· Prepares and revises quality plans, inspection checklists, quality instructions and
forms.
· Trains inspectors and production operators in basic measurement and inspection
tasks.
· Creates and implements metrics/charts for tracking key product/process data.
· Establishes receiving inspection requirements; carries out or oversees
inspections.
Maintains material certification and receiving inspection records.
· Works with Purchasing in handling of supplier evaluations and non-
conformances.
· Conducts qualification activities for new tooling and parts.
· Identifies/investigates non-conformances and drives to root cause.
Plays active
role in continuous improvement.
· Conducts and/or coordinates various product tests.
· Write/revise documents required for quality related items.
· Supports Engineering Change Request implementation and configuration
management.
· All other duties and special projects as assigned.
Education/ Skills/ Experience:
· Bachelor’s Degree in Mechanical, Industrial, or Manufacturing-related
Engineering required, ASQ certification is a plus
· Training and experience in field of quality, such as ISO 9001, SPC, Metrology
and Internal Auditing preferred.
· Composites or injection molding experience a plus.
· Minimum 2 years of experience in manufacturing quality.
· Able to understand and interpret complex engineering drawings and
specifications.
· Understands principles of metrology and calibration.
· Capable of performing advanced math and statistical calculations.
· Familiarity with Statistical Process Control (SPC).
· Lean Manufacturing experience.
· Project Management: ability to organize and manage multiple projects.
· Computer proficiency including MS Office and Minitab.
· Excellent interpersonal and communication skills.
Training Requirements:
· ISO Lead Audito
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Type: Permanent Location: Newton, US-IA
Salary / Rate: Not Specified
Posted: 2025-10-17 08:49:50
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Was Dich erwartet
Die Pandemie hat gezeigt, wie wichtig die Labordiagnostik für unser Gesundheitswesen und für jeden oder jede Einzelne von uns ist.
Die Zuverlässigkeit unserer Systeme ist die Voraussetzung für viele Diagnosen und Entscheidungen.
Schätzungsweise werden ca.
70% der klinischen Entscheidungen durch In-vitro-Diagnostische Tests beeinflusst.
Für unser Praktikantenprogramm suchen wir motivierte und wissbegierige Studierende, die unser Service Team unterstützen und sich auch in Zukunft eine Karriere bei Roche vorstellen können.
Werde Teil unserer Serviceorganisation, in der wir mit viel Energie und Leidenschaft die Labordiagnostik in Deutschland nach vorne bringen und das Gesundheitswesen aktiv mitgestalten.
Bringe tagtäglich Deine Ideen und Dein Wissen ein, um komplexe Fragestellungen gemeinsam mit Kolleg:innen zu lösen.
Als Praktikant:in (m/w/d) wirst Du unsere Mitarbeitenden bei der Planung und Installation unserer Laborsysteme cobas® pro und cobas® pure sowie bei Wartungen und Modifikationen unterstützen.
Außerdem wirst Du in die IT Vernetzung unserer Systeme Einblicke erhalten.
Viel Eigeninitiative, Kundenorientierung und technisches Geschick ist bei unseren Kundenbesuchen in den verschiedenen Krankenhaus- oder Privatlaboren gefragt.
Zu Beginn erhältst Du eine Ausbildung auf unseren Immunologie cobas® Systemen und wirst außerdem von einem Mentor/einer Mentorin im Außendienst begleitet.
Du wirst im Raum Bayern eingesetzt und kannst innerhalb des Gebiets Deinen Wohnort frei wählen.
Idealerweise wohnst Du im Raum München, Augsburg, Landshut oder Nürnberg.
Folgende Schwerpunkte erwarten Dich bei Deinem Praktikum im Service Außendienst
* Du erhältst im März (09.03.
bis 13.03.2026) ein Wartungstraining an zwei Immunologie Modulen (cobas® e402 und cobas® e801)
* Dein technisches Geschick stellst Du bei Geräteinstallationen und bei Wartungen unter Beweis
* Du erhältst Einblicke in die Analyse und Behebung von komplexen technischen und applikativen Fragestellungen und unterstützt unsere Mitarbeitenden bei der Problemanalyse
* Du erhältst Einblicke insbesondere in unsere klinische Chemie und Immunologie, Hospitationen in anderen Bereichen sind ebenfalls möglich
* IT Netzwerke und IT Sicherheit wecken Dein Interesse und Du kannst bei Firewall Installationen viel von unseren Mitarbeitenden lernen
* Du bringst Deine organisatorischen Fähigkeiten mit ein und übernimmst eigenständig definierte ...
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Type: Permanent Location: Bavaria, DE-BY
Salary / Rate: Not Specified
Posted: 2025-10-17 08:47:24
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Was Dich erwartet:
Die Pandemie hat gezeigt, wie wichtig die Labordiagnostik für unser Gesundheitswesen und für jeden oder jede Einzelne von uns ist.
Die Zuverlässigkeit unserer Systeme ist die Voraussetzung für viele Diagnosen und Entscheidungen.
Schätzungsweise werden ca.
70% der klinischen Entscheidungen durch In-vitro-Diagnostische Tests beeinflusst.
Für unser Praktikantenprogramm suchen wir motivierte und wissbegierige Studierende, die unser Service Team unterstützen und sich auch in Zukunft eine Karriere bei Roche vorstellen können.
Werde Teil unserer Serviceorganisation, in der wir mit viel Energie und Leidenschaft die Labordiagnostik in Deutschland nach vorne bringen und das Gesundheitswesen aktiv mitgestalten.
Bringe tagtäglich Deine Ideen und Dein Wissen ein, um komplexe Fragestellungen gemeinsam mit Kolleg:innen zu lösen.
Als Praktikant:in (m/w/d) wirst Du unsere Mitarbeitenden bei der Planung und Installation unserer Laborsysteme cobas® pro und cobas® pure sowie bei Wartungen und Modifikationen unterstützen.
Außerdem wirst Du in die IT Vernetzung unserer Systeme Einblicke erhalten.
Viel Eigeninitiative, Kundenorientierung und technisches Geschick ist bei unseren Kundenbesuchen in den verschiedenen Krankenhaus- oder Privatlaboren gefragt.
Zu Beginn erhältst Du eine Ausbildung auf unseren Immunologie cobas® Systemen und wirst außerdem von einem Mentor/einer Mentorin im Außendienst begleitet.
Du wirst überwiegend in den Bundesländern Saarland, in Rheinland-Pfalz und Hessen eingesetzt und kannst innerhalb des Gebiets Deinen Wohnort frei wählen.
Idealerweise wohnst Du im Raum Frankfurt, Darmstadt, Mainz, Wiesbaden, Kaiserslautern, Koblenz, Marburg, Gießen.
Folgende Schwerpunkte erwarten Dich bei Deinem Praktikum im Service Außendienst:
* Du erhältst im März (09.03.
bis 13.03.2026) ein Wartungstraining an zwei Immunologie Modulen (cobas® e402 und cobas® e801)
* Dein technisches Geschick stellst Du bei Geräteinstallationen und bei Wartungen unter Beweis
* Du erhältst Einblicke in die Analyse und Behebung von komplexen technischen und applikativen Fragestellungen und unterstützt unsere Mitarbeitenden bei der Problemanalyse
* Du erhältst Einblicke insbesondere in unsere klinische Chemie und Immunologie, Hospitationen in anderen Bereichen sind ebenfalls möglich
* IT Netzwerke und IT Sicherheit wecken Dein Interesse und Du kannst bei Firewall Installationen viel von unseren Mitarbeitenden lernen
...
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Type: Permanent Location: Hesse, DE-HE
Salary / Rate: Not Specified
Posted: 2025-10-17 08:47:20
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Was Dich erwartet:
Die Pandemie hat gezeigt, wie wichtig die Labordiagnostik für unser Gesundheitswesen und für jeden oder jede Einzelne von uns ist.
Die Zuverlässigkeit unserer Systeme ist die Voraussetzung für viele Diagnosen und Entscheidungen.
Schätzungsweise werden ca.
70% der klinischen Entscheidungen durch In-vitro-Diagnostische Tests beeinflusst.
Für unser Praktikantenprogramm suchen wir motivierte und wissbegierige Studierende, die unser Service Team unterstützen und sich auch in Zukunft eine Karriere bei Roche vorstellen können.
Werde Teil unserer Serviceorganisation, in der wir mit viel Energie und Leidenschaft die Labordiagnostik in Deutschland nach vorne bringen und das Gesundheitswesen aktiv mitgestalten.
Bringe tagtäglich Deine Ideen und Dein Wissen ein, um komplexe Fragestellungen gemeinsam mit Kolleg:innen zu lösen.
Als Praktikant:in (m/w/d) wirst Du unsere Mitarbeitenden bei der Planung und Installation unserer Laborsysteme cobas® pro und cobas® pure sowie bei Wartungen und Modifikationen unterstützen.
Außerdem wirst Du in die IT Vernetzung unserer Systeme Einblicke erhalten.
Viel Eigeninitiative, Kundenorientierung und technisches Geschick ist bei unseren Kundenbesuchen in den verschiedenen Krankenhaus- oder Privatlaboren gefragt.
Zu Beginn erhältst Du eine Ausbildung auf unseren Immunologie cobas® Systemen und wirst außerdem von einem Mentor/einer Mentorin im Außendienst begleitet.
Du wirst im Raum Baden-Württemberg eingesetzt und kannst innerhalb des Gebiets Deinen Wohnort frei wählen.
Idealerweise wohnst Du im Raum Pforzheim, Ludwigsburg, Stuttgart, Offenburg, Tuttlingen, oder Mannheim.
Folgende Schwerpunkte erwarten Dich bei Deinem Praktikum im Service Außendienst:
* Du erhältst im März (09.03.
bis 13.03.2026) ein Wartungstraining an zwei Immunologie Modulen (cobas® e402 und cobas® e801)
* Dein technisches Geschick stellst Du bei Geräteinstallationen und bei Wartungen unter Beweis
* Du erhältst Einblicke in die Analyse und Behebung von komplexen technischen und applikativen Fragestellungen und unterstützt unsere Mitarbeitenden bei der Problemanalyse
* Du erhältst Einblicke insbesondere in unsere klinische Chemie und Immunologie, Hospitationen in anderen Bereichen sind ebenfalls möglich
* IT Netzwerke und IT Sicherheit wecken Dein Interesse und Du kannst bei Firewall Installationen viel von unseren Mitarbeitenden lernen
* Du bringst Deine organisatorischen Fähigkeiten mi...
....Read more...
Type: Permanent Location: Baden-Wurttemberg, DE-BW
Salary / Rate: Not Specified
Posted: 2025-10-17 08:47:04
