-
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
Wir sind das Team People Support Solutions Time und treiben mit viel Engagement und Leidenschaft nicht nur die Weiterentwicklung und Optimierung der Arbeitszeit-Prozesse voran, sondern sind auch für die operativen Prozesse rund um das Thema Arbeitszeit Ansprechpartner für alle deutschen Gesellschaften.
Wir denken die Rolle eines klassischen „Arbeitszeitexperten“ weiter und wir möchten Dir als Praktikant (m/w/d) einen Einblick in das „Daily business“ des Time Teams geben.
Deine Aufgaben
* Du betreust die administrativen Themen zur Arbeitszeit
* Du kümmerst Dich um das Case Management und bearbeitest Mitarbeiter-Anfragen
* Du unterstützt bei der Gestaltung von Schulungsmaterial zum Thema Arbeitszeit
* Du unterstützt im Rahmen der Digitalisierung und Automatisierung von Prozessen
* Du gestaltest Kommunikationsmaterial im Rahmen von Projekten und unterstützt Projektteams im Rahmen des Projektmanagement Offices
Dein Profil
* Du bist aktuell in einem wirtschafts-, geistes- oder sozialwissenschaftlichen Studium immatrikuliert oder Du befindest Dich in Deinem Gap-Year
* Du bringst idealerweise erste Kenntnisse im Bereich Human Resources mit und konntest bereits erste Erfahrung in Projektorganisation sammeln
* Mit den gängigen EDV-Systemen (MS-Office) bist Du bestens vertraut, insbesondere im Erstellen von Power Point Präsentationen
* Du hast idealerweise bereits erste Erfahrungen mit KI und Automatisierung von Prozessen
* Du bist engagiert, neugierig und gehst offen auf Menschen zu
* Ein hohes Maß an Flexibilität und Belastbarkeit zeichnet Deine Persönlichkeit aus
* Du kommunizierst fließend und verhandlungssicher auf Deutsch und Englisch
Deine Vorteile
* Flexible Zeiteinteilung
* 2268€ Vergütung im Monat für ein Vollzeitpraktikum >3 Monate
* Vergünstigte Essenspreise (-50 %) in unserer Mitarbeiterkantine
* Fitnesszentrum auf dem Roche-Campus
* Vernetzung mit anderen Studierenden
* Weiterbildungsmöglichkeiten und spannende Gastvorträge
Deine Bewerbung
Bitte lade nur Deinen 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) ...
....Read more...
Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2026-07-18 08:39:48
-
ERM is hiring an EHS Waste and Wastewater Coordinator to work on-site at our client’s two facilities in Lebanon, IN.
The primary function of this role is to support the client’s wastewater management systems by coordinating, conducting and tracking regulatory approvals, confirm sampling has been performed by various internal groups, and that the information and approvals are ready in time for planned discharge events, as required compliance activities.
This person will support facility technicians to ensure compliance with these wastewater aspects of the facility’s compliance program. This is a full-time (40 hours per week) limited-term role with a duration of 12 months, extendable.
RESPONSIBILITIES:
* Coordinate with wastewater technicians for activities related to wastewater sampling, recordkeeping, and reporting (discharge monitoring reports).
These activities include ensuring proper sampling, sample holding, and shipping.
* Assist in obtaining approvals for discharges based on the available samples and quantities planned for discharge.
* Inspect wastewater activities at the facility to ensure regulatory and policy compliance.
* Work with facility personnel to ensure they are prepared with appropriate sampling in time to obtain regulatory discharge approvals; field workforce questions, troubleshoot issues, and help resolve issues.
* Assist EHS Manager with discharge requests and documentation
* Support the plant Health and Safety objectives.
REQUIREMENTS:
* A.S.
or B.S.
degree in related technical field desired but not required.
* 5+ years of directly related wastewater experience in the chemical or pharmaceutical industry is preferred.
* Ability and knowledge in wastewater and NPDES discharge coordination.
* Ability to use a personal computer with proficiency in Microsoft Word, Excel and E-mail
* Self-motivated with the ability and desire to work with others and independently.
* Flexible to evolving business and departmental needs and able to adjust priorities accordingly.
* Strong communication skills, problem solving skills, organization skills, and the ability to learn quickly.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solutions for our clients.
Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safe...
....Read more...
Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2026-07-17 09:50:37
-
Lead the Way in Safety & Industrial Hygiene
Are you an experienced Health & Safety professional ready to make a global impact? ERM is seeking a Managing Technical Consultant, Safety and Industrial Hygiene (Part Time) to join our team and help organizations proactively manage EHS risks.
This is your chance to work with a worldwide sustainability leader, collaborate with experts across 40+ countries, and deliver innovative solutions that truly matter.
Why This Role Matters
Safety and industrial hygiene are at the heart of sustainable business practices.
In this role, you’ll empower clients to protect their people, reduce risk, and achieve compliance—all while shaping strategies that drive long-term success.
Your expertise will help organizations navigate complex technical and regulatory challenges, ensuring safer workplaces and stronger cultures.
What Your Impact Is
* Design and implement Safety Management Systems and risk assessments for effective risk control and compliance.
* Lead incident investigations, root cause analyses, and corrective action planning.
* Drive life safety programs—from hazardous energy control to fire safety.
* Champion industrial hygiene programs, including qualitative and quantitative exposure assessments.
* Develop innovative solutions for complex EHS issues and regulatory concerns.
* Expand ERM’s Safety Services business through client relationships, proposals, and strategic growth.
* Deliver corporate H&S strategies in areas like behavior-based safety, safety culture, process safety, and compliance auditing.
What You'll Bring
Required
* BS/MS degree preferred.
Or equivalent experience.
* Certification in field: CIH required; CSP, CHMM, PE desirable.
* 4+ years (10+ years preferred) experience in safety, risk management, and EHS compliance programs.
* Proven expertise in life safety programs and industrial hygiene.
* Ability to work independently and collaboratively, adapt to ambiguity, and think creatively.
* Strong written and verbal communication skills.
* Willingness to travel up to 80%, including international assignments (valid passport required).
* This position is not eligible for immigration sponsorship.
Preferred
* Consulting experience.
* Passion for EHS performance improvement and delivering world-class program solutions.
Key Responsibilities
* Develop and implement Safety Management Systems and risk assessments.
* Conduct incident investigations, corrective actions, and verification of controls.
* Support life safety programs (hazardous energy, fall protection, electrical safety, etc.).
* Lead industrial hygiene assessments and exposure risk evaluations.
* Create solutions for complex technical and regulatory challenges.
* Build and expand client relationships, generate repeat business, and contribute to ERM’s growth.
* Design and direct corporate ...
....Read more...
Type: Contract Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2026-07-17 09:50:36
-
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: Pharmacovigilance Services Associate with German
The role of the Pharmacovigilance Services Associate is to be the first-line customer contact for all customer enquiries by phone and e-mail.
Examples of such enquiries include product technical enquiries, possible adverse events, or product complaints.
Associates will submit and follow up suspected adverse events and product complaints in accordance with Elanco global and local guidelines.
Also, the Pharmacovigilance Services Associate will support Sales and Marketing activities, as well as providing administrative support for ad hoc projects during the periods of the year when the workload related to adverse events and product complaints allows (outside of parasitic season).
Your Responsibilities:
Technical Enquiries, Adverse Event and Product Complaint Reporting
* Receive inbound e-mails, calls (if necessary) report forms from current and potential customers (e.g.
veterinarians, pharmacists, animal owners etc.) and Elanco personnel.
* Examples of such enquiries include technical enquiries, adverse events, product complaints, product return/refund, or compensation.
* Place outbound follow-up emails and calls when required to acquire additional information.
* Answer questions and provide information based on relevant product documentation, training materials and Quality Documents, FAQ databases, SPCs (Summary of Product Characteristics), package leaflets and material provided.
* Assist customers with any issues regarding Elanco products and document any adverse event or product complaint reported in the Elanco PV system in accordance with policies and regulations.
* Ensure the timely reporting of high quality, accurate, complete adverse event and product complaint reports, obtaining additional information as required.
* Meet Quality Assurance Requirements and other key performance metrics.
Affiliate Sales Support
* Working closely with the DACH Sales & Marketing Managers to ensure timely, effective, and optimized execution across multiple touchpoints of Sales and Marketing activities in the DACH.
*...
....Read more...
Type: Permanent Location: Warszawa, PL-MZ
Salary / Rate: 121000
Posted: 2026-07-17 09:24:35
-
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!
$2,500 Sign-On Bonus! Apply Today!
Relocation Assistance Available
Your Role: Sr.
Downstream Bioprocess Specialist (Night Shift)
The Sr.
Downstream Bioprocess Specialist (Night Shift) is a technical process leader on the Downstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of the Clarification, Chromatography, and Tangential Flow Filtration operations.
Your Responsibilities:
* Executes the operation with team serving as process leader, coach, trainer, and responsible party
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Operations representative for cross-functional process support team, engaging in process
* Real-time problem solving, process intervention, and technical experiment delivery
* Ensures process documentation is prepared and completed with accuracy and concurrence
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: A minimum of 3 years of experience in Liquid Protein A Chromatography at manufacturing scale
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Proficiency with SAP
* GMP manufacturing
* Tangential Flow Filtration
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
* Qualified candidates must be legally authorized to be employed in the United States.
Elanco does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: 37.55
Posted: 2026-07-17 09:21:42
-
Applications due by July 24th, 2026
Goodwill of Colorado
Job Description
Pay Rate: $25.00/hour
Work Schedule: 2nd Shift, Mon- Fri 3:30 pm to midnight
Duties include but are not limited to:
* Maintaining Quality Control Processes.
* Analyzing the Results
* Giving Feedback and Guidance to the Production and Engineering Team
* Perform Safety Assessments, Develop EHS Programs, and Ensure Guidelines are Met
He or she will exhibit strong organizational skills, drive to create and follow processes and is very disciplined.
A strong quality control background is important.
Core Responsibilities:
* Implement methods to inspect, test and evaluate the reliability of manufacturing processes, products and production equipment.
* Develop and support comprehensive EHS programs and initiatives that comply with regulatory requirements to help promote employee participation and accountability, as well as conduct training in compliance with regulatory requirements and company policies.
* Assist with the development of finished product and component receiving inspection procedures and requirements.
* Inspect, test and/or measure materials, components, assemblies, etc.
and compare these items to applicable requirements (drawings or approved process documentation).
* Maintain quality control records (inspection records) in an accurate, well-organized and timely manner for easy retrieval and audit.
* Participate in the review of design, manufacturing, purchasing and test documentation to ensure conformance to quality control standards.
This can include review of drawings, spec sheets, production procedures, testing and inspection standards, supplier inspections and customer contract specifications.
* Make recommendations regarding facilities, equipment personnel, procedures and systems to carry out quality control functions, as well as identify/implement improvement for the facility’s loss-prevention, emergency management, high-risk, and life safety programs.
* Work with engineering and manufacturing to develop and implement quality control tests, inspect products at various stages and write reports documenting issues.
* Manage first article, local supplier source inspections, final product inspection, and performing safety assessments for new product introductions.
* Prepare and review quality metrics.
Report serious or repeated failures or unreliability in quality of products.
Recommends corrective actions or plans/programs for overall defect reductions in products.
* Maintain test equipment and cleanliness of the Quality Assurance Lab that include responsibility for in-house calibration program.
* Investigate root cause and corrective actions.
* Assist with auditing, writing, revising and verifying quality standards and developing forms and instructions for recording, evaluating and reporting quality data, as well as participate in audits related to Envi...
....Read more...
Type: Permanent Location: Colorado Springs, US-CO
Salary / Rate: Not Specified
Posted: 2026-07-17 08:38:50
-
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
Als Teil von Roche Diagnostics Near Patient Care (NPC), ist unsere Abteilung an einer Vielzahl von Projekten beteiligt, die von der Entwicklung von Blutzuckermessungen bis zur Entwicklung von Kardiologie- und Gerinnungsassays reichen.
Das NPC Analytics Subchapter ist in Mannheim lokalisiert und unterstützt verschiedene Produkte in frühen Entwicklungsstadien, bis hin zu Produkten, die bereits am Markt eingeführt sind.
Im Rahmen dieses Vorpraktikums (2 Monate) anschließender Masterarbeit (6 Monate) knüpfst Du direkt an ein erfolgreiches Vorgängerprojekt an.
Deine Aufgabe ist die Weiterentwicklung einer Methode zur photometrischen Messung des Ethanolgehaltes in einer unserer Tauchlösungen, basierend auf einem bereits identifizierten Zwei-Farbstoff-Gemisch.
Dabei verbindest Du klassische nasschemische Analytik und Gaschromatographie mit neuen bildgestützten Detektionsmethoden.
Deine Hauptaufgaben
* Methodenentwicklung & Optimierung: Weiterentwicklung und Etablierung des bestehenden Farbstoff-Mixes zu einem praxistauglichen photometrischen Kalibrierkonzept
* Erforschung der Fluoreszenz-Option: Untersuchung der Fluoreszenzeigenschaften von Nilrot und optionale Integration dieser Parameter in den Assay zur Erhöhung der Messgenauigkeit
* Instrumentelle Analytik (GC & Viskosität): Optimierung und optionale Validierung einer bereits etablierten Gaschromatographie-Methode (GC) zur Ethanolbestimmung sowie Verknüpfung der Ergebnisse mit der bestehenden Viskositäts-Methode
* Bildgestützte Detktion: Erprobung innovativer Ansätze zur Auswertung – insbesondere die Evaluation eines kalibrierten Smartphones als Detektor anstelle eines klassischen Photometers sowie die Prüfung weiterer bildgestützter Messtechnik (z.
B.
Thermografie)
* Dokumentation & Evaluation: Präzise Dokumentation aller Testverfahren und kontinuierliche Analyse der Messergebnisse im Hinblick auf GxP- Anforderungen
Dein Profil
Bei der Auswahl neuer Mitarbeiter legen wir Wert auf Kandidaten, die von unserer Mission inspiriert sind und die gut in die kollaborative Einstellung unserer Unternehmenskultur passen.
Weil uns bewusst ist, dass unsere Mitarbeiter maßgeblich am Erfolg neuer diagnostischer Lösungen für unsere Patienten beteiligt sind, ist es unsere Aufgabe einen great place to work zu bieten und zu wahren und Programme, Services und Benefits anzubieten, die es erlauben, das Beste in die Arbeit, sowie in das Privatleben einzubringen.
Damit überzeugst Du uns: :
...
....Read more...
Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2026-07-17 08:37:08
