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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!
Quality Control (QC) Microbiology Specialist
The Quality Control (QC) Microbiology Specialist is responsible for supporting and leading daily operations within the Quality Control microbiology laboratory at the Elwood, Kansas site.
This role serves as a subject matter expert for microbiological testing methods and ensures the successful execution, validation, and continuous improvement of QC processes.
The Specialist provides leadership and guidance to QC Technicians and peers, oversees lab scheduling and workload delegation, and ensures compliance with quality standards and procedures.
This position plays a key role in investigations, audits, method validation, and cross-functional collaboration with Manufacturing, Validation, and Engineering teams.
Your Responsibilities:
* Review, approve, and report microbiological test data to ensure accuracy and compliance.
* Lead and support QC activities including deviations, investigations, and change controls.
* Author and review technical documentation such as SOPs, validation protocols/reports, specifications, study reports, and logs.
* Coordinate daily lab operations, including scheduling and task delegation across the microbiology team.
* Serve as a subject matter expert for microbiological methods, equipment, and QC processes.
* Collaborate cross-functionally with Manufacturing, Validation, and Engineering teams to support site activities.
* Perform routine release testing as well as method validation, transfer, and development work.
* Train, mentor, and provide guidance to QC Technicians and other team members.
* Ensure compliance with QC policies and identify opportunities to improve or modernize processes.
* Maintain oversight of lab materials, reagents, and equipment qualification and inventory.
* Support audit readiness and participate in internal and external audit activities.
* Drive continuous improvement initiatives within the QC laboratory.
* Provide updates in site and departmental meetings as needed.
* Support manufacturing timelines, including occasional off-hours work when req...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 99300
Posted: 2026-05-06 09:11:20
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Our Business
Adare Pharma Solutions is a global Contract Development and Manufacturing Organization (CDMO) with locations across North America and Italy.
We offer a wide range of manufacturing, packaging, and research and development services.
Our clients range from growing biotech firms advancing groundbreaking clinical trials to established pharmaceutical companies producing high volumes of approved, widely used medicines.
By combining top talent from the life sciences industry with modern research and manufacturing technologies, Adare enables clients to deliver potentially lifesaving medicines in more easily consumable formats - particularly for patients such as infants or the elderly.
This is the meaning behind “Transforming Drug Delivery – Transforming Lives.”
Our Culture
When it comes to being an employee of Adare, although we are located across multiple countries and come from diverse backgrounds, we work together toward a common purpose.
Supported by leadership that is experienced and highly regarded in the industry, we are paving the way for a brighter and better future by attracting top talent from both within and beyond the CDMO space.
In addition to delivering high-quality results for our external clients, we foster a collaborative, client-centric culture internally - one where employees support one another, share knowledge, and encourage each other to bring their best selves to work each day.
Why Come to Adare?
Adare is Private Equity owned and poised for growth.
Employees are provided with internal development opportunities to progress within the organization, enhancing their professional skills and industry knowledge through Adare’s investment in their growth.
We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry, formulations, analytical research and development, finance, supply chain, sales, marketing, project management, human resources, and environmental health and safety.
Our benefits package is highly competitive, offering medical, dental, and vision coverage; a retirement plan with company match, paid time off and company holidays, tuition reimbursement with no waiting period, life insurance, pet insurance, Flexible Spending Accounts (medical and dependent care), and disability coverage.
Position
Formulation Technician
Location
Vandalia, Ohio
Summary
The Formulation Technician I, II, or III will assist the R&D Formulations staff with product development activities from small scale to commercial batch production. The Formulation Technician should be someone with a keen interest in life sciences or drug manufacturing. This is a developmental role where training is provided, offering an opportunity to learn various techniques of drug manufacturing including dispensing, blending, granulation, compression and coating.
Responsibilities
* Assist in running projects associated with product development, product and process optimization batches, a...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2026-05-06 07:58:34
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Your Job
Join Georgia-Pacific's Analytical Services Team at the Neenah Technical Center as an Sr.
Analytical Chemist to deliver actionable chemical and instrumental analysis that supports R&D, operations, and manufacturing.
You'll solve production and analytical challenges, develop and validate methods, and enable data-driven decisions that improve product performance and plant reliability.
The ideal candidate is a practical problem-solver with a generalist mindset-comfortable handling a wide variety of tasks, working across analytical techniques, and shifting priorities as business needs evolve.
Our Team
The Analytical Services Team provides cross-functional laboratory support across the Neenah Technical Center, product development, and manufacturing sites.
We partner with R&D and plant teams to establish testing capabilities, troubleshoot operational issues, and translate analytical results into practical solutions.
What You Will Do
* Translate complex analytical results into clear recommendations that resolve plant issues and improve process performance.
* Characterize and quantify unknown compounds in complex matrices to support troubleshooting and new product work.
* Develop and validate analytical methods that produce reliable data to guide product development and manufacturing decisions.
* Maintain and optimize laboratory instrumentation to ensure consistent uptime and quality of test results.
* Establish and expand testing capabilities for current and future materials in collaboration with product development teams.
* Produce concise technical reports and research summaries that communicate findings to both technical and non-technical stakeholders.
* Apply strong laboratory safety practices and follow established protocols to protect people and data integrity.
Who You Are (Basic Qualifications)
Bachelor's degree in Chemistry.Minimum 5 years' experience in an Analytical Services or similar laboratory environment.Hands-on experience operating and maintaining analytical instrumentation Demonstrated experience with method development, method validation, or routine analytical testing.
What Will Put You Ahead
Advanced degree in Chemistry (MS or PhD).Proven experience developing, validating, and implementing new analytical test methods.Background in analytical, inorganic, polymer, and/or organic chemistry, including prior research experienceExperience troubleshooting instrumentation and performing routine preventive maintenance.Track record of effectively communicating data-driven recommendations to cross-functional teams.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abili...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2026-05-06 07:50:17
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We are currently seeking School Psychologists in the following areas:
Goshen, NY; Wappinger, NY; Sugar Loaf, NY; Ulster County
Liberty POST is currently seeking a motivated and energetic School Psychologist for per diem employment to work with children who are birth-5 years old through Early Intervention and Preschool Special Education programs.
Immediate positions are available.
Liberty POST has offered its clients a range of high-quality and individualized services since 1994.
Backed by Liberty Resources Inc.
and part of a large social services circle, originally POST was a speech-language practice in Syracuse NY and has grown to provide a range of services throughout all of New York State and New Jersey.
We employ over 500 professionals in a variety of settings and offer a collaborative team approach to provide evaluation, direct therapy, and family education through child-directed play.
We are focused on the importance of a child’s natural learning environment, a family’s unique strengths and needs and the diverse population we serve.
Job Duties and Responsibilities:
* Evaluate, monitor and track child’s progress and adjust treatment plans accordingly.
* Test and evaluate child’s abilities to determine realistic goals.
* Record information on the initial evaluation, treatment, and progress in a timely manner using Electronic Medical Record system.
* Proficient at writing detailed analysis and reports.
* Effectively organize and maintain confidentially of child’s records and other documentations.
* Follow all state laws and regulations as it pertains to Early Intervention, CPSE/CSE special education.
Qualifications, Knowledge and Experience:
* Master's degree in School Psychology required
* Minimum of two years working with children in special education required
* Certification in NYS as a School Psychologist required
* Knowledge and experience administering standardized testing in the following areas: cognitive, achievement, behavioral/social-emotional and adaptive skills.
* Experience using Frontline (formerly IEP Direct) to assist in developing IEPs.
Benefits for this position:
* Health Benefits and Retirement packages available for FT positions
* Accrual of sick time based on NYS Sick time Laws
* Mentoring is offered to all providers
* Access to unlimited CEU courses offered that are accredited through ASHA, AOTA, APTA and CTLE
* Flexible scheduling
* Work with a team of professionals that care about making a difference
* Payment is biweekly with direct deposit
Job Type: Per Diem
Pay Rate:
* Evaluations - Psychological: $180
* Social History: $125
* Observation: $40
* CPSE meetings: $25
Liberty POST is an equal opportunity employer.
We offer equal employment opportunities to all persons without regard to race, color, ethnicity, religion, sex, sexual orientation, national origin,...
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Type: Permanent Location: Goshen, US-NY
Salary / Rate: Not Specified
Posted: 2026-05-06 07:40:07
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Liberty POST is currently seeking a motivated and energetic Early Childhood School Psychologist for per diem employment to work with children who are 3-5 years old through Preschool Special Education programs.
Immediate positions are available throughout Syracuse.
Liberty POST has offered its clients a range of high-quality and individualized services since 1994.
Backed by Liberty Resources Inc.
and part of a large social services circle, originally POST was a speech-language practice in Syracuse NY and has grown to provide a range of services throughout all of New York State and New Jersey.
We employ over 500 professionals in a variety of settings and offer a collaborative team approach to provide evaluation, direct therapy, and family education through child-directed play.
We are focused on the importance of a child’s natural learning environment, a family’s unique strengths and needs and the diverse population we serve.
Job Duties and Responsibilities:
* Effectively communicates and works with related agencies, community members, clients, families and co-workers.
* Establishes and maintains a rapport with clients/family members/caregivers and co-workers.
* Review client information prior to evaluation and complete necessary client forms in collaboration with family, other evaluators and current service providers.
* Complete IEP direct including goals, outcome summary and results.
* Gather outside information regarding child’s performance in a variety of settings.
* Utilize Provider Soft to record notes and evaluation results and submit evaluation write up to team leader.
* Attends and participates in ongoing staff in-services and mandatory quarterly meetings.
* Attend CPSE meetings.
Qualifications, Knowledge and Experience:
* Master’s Degree in School Psychology or Doctor of Psychology
* Evaluation and assessment experience required. Familiarity with a variety of preschool assessment tools.
* Effectively communicates via phone, e-mail, in public, and in large groups.
* Proficient on assessment tools necessary for evaluations.
* Works independently, manages time and prioritizes tasks appropriately.
* Strong organizational skills necessary
* Evidence of independence, initiative and forward thinking related to clinical expertise.
* Open to feedback and commitment to quality of provided services.
* Responds positively to suggestions/directions, maintains a flexible attitude and generates new ideas and process improvements.
* Maintains confidentiality of client records.
Benefits for this position:
* Health Benefits and Retirement packages available for FT positions
* Accrual of sick time based on NYS Sick time Laws
* Mentoring is offered to all providers
* Access to unlimited CEU courses offered that are accredited through ASHA, AOTA, APTA and CTLE
* Flexible scheduling
* Work with a te...
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Type: Permanent Location: Syracuse, US-NY
Salary / Rate: Not Specified
Posted: 2026-05-06 07:38:56
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Sei pronto/a ad entrare a far parte di un’organizzazione in crescita, globale, specializzata nella produzione e sviluppo farmaceutico, che mette le persone al primo posto? Unisciti ad Adare! Noi lavoriamo a stretto contatto con i nostri partner nell’industria farmaceutica durante tutte le fasi di sviluppo e produzione dei farmaci destinati alla commercializzazione, con l‘intento di migliorare le vite dei/delle pazienti e dei farmaci essenziali per le persone di tutto il mondo.
Ogni ruolo all’interno di Adare ti offrirà un’esperienza unica e personalizzata nonché l’opportunità di avere un grande impatto, fondamentale per il successo della nostra azienda. Con l’aiuto di persone come te che si dedicano alla nostra missione, Adare migliora vite migliorando la somministrazione dei farmaci!
Unisciti alla nostra missione, unisciti ad Adare!
La nostra proposta:
* Assicurazione sanitaria
* Piano pensionistico
* Benefit previsti da accordo interno
* Premio di partecipazione
Siamo alla ricerca di un un/una Quality Control Compliance Junior Specialist (tempo determinato 12 mesi) che si unisca al nostro Quality Control Compliance Team di San Giuliano Milanese.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE:
Il/la Quality Control Compliance Junior Specialist risponde alla responsabile del Quality Control Compliance Team e si occupa di assicurare la corretta applicazione delle GMP e l’aderenza alla compliance nel laboratorio Controllo Qualità, supportando il responsabile di reparto nelle attività principali.
COMPITI E RESPONSABILITA’:
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati:
* Organizzazione e gestione dei training del personale del Controllo Qualità, svolgendo, quando necessario, la funzione di docente.
* Redazione, revisione, archiviazione e gestione della documentazione del Controllo Qualità.
* Stesura, revisione, archiviazione e gestione della documentazione tecnica quale: procedure Operative Standard, Procedure Analitiche Standard, metodi di analisi, specifiche, rapporti di validazione, ABR, protocolli e report tecnici.
* Revisione dei dossier nella parte che compete le attività analitiche e del Controllo Qualità.
* Aggiornamento dei documenti analitici in conformità alle principali farmacopee ed ai dossier di riferimento
* Monitoraggio e gestione delle CAPA, dei Change e delle indagini all’interno del laboratorio QC
* Supporta il corretto svolgimento delle investigazioni di laboratorio e della gestione delle deviazioni in conformità alle procedure aziendali e ai requisiti GMP.
Individua-zione delle CAPA e stesura dei report delle investigazioni di laboratorio.
Valutazione dei trend degli eventi, individuazione di eventuali ricorrenze e valutazione delle azioni correttive dedicate.
* Agisc...
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Type: Contract Location: San Giuliano Milanese, IT-25
Salary / Rate: Not Specified
Posted: 2026-05-06 07:36:13
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ERM is hiring Field Biologists to conduct surveys and monitoring for large construction projects in Bishop, CA. Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of a field biologist requires technical skills, as well as strong organizational and communication skills.
This is a full-time (40+ hours/week), limited-term role with a duration of 12 months, with the possibility of extension.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction rare plant and special status species surveys across the client’s project area.
* Work locations are remote and require Biologist to work independently.
* Electronic data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* A bachelor’s degree in Environmental Science, Biology or related discipline preferred.
* Minimum of 2 seasons of experience with waters/wetland monitoring and rare plant identification.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Must have a strong attention to detail in the documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Flexible availability: willingness to work weekends, holidays, and evenings as needed by the project.
* Demonstrated independent and effective problem solving and decision-making skills.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Fluency in English and Spanish a plus.
Pay Transparency:
For the Field Biologist position, we anticipate the annual base pay of $74,825 – $96,901, $35.97/hr – $46.58/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/Flexforce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is l...
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Type: Permanent Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2026-05-06 07:33:44
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ERM is seeking an Environmental, Health and Safety Specialist to work onsite at a key client in Warsaw, IN.
The ideal candidate will bring a wealth of technical capability and deep understanding of regulations, as well as business processes to help our client proactively address their EHS risks and challenges. This is a full-time (40 hours per week) limited-term role, with a duration of 3 months, extendable.
Responsibilities:
* Provide on-site environmental, health and safety support at client facility such as training, review management of change requests, incident investigations, and job hazard assessment reviews.
* Design and implement corporate H&S strategies and programs for safety, compliance auditing, safety management systems, , high-impact training, and general compliance support.
* Support, as needed, environmental, health and safety (EHS) compliance programs, environmental management system, sustainability, environmental compliance programs including multi-media permits, and reports for air quality, hazardous waste, spill prevention, storm water, and wastewater.
* Assist in the development of solutions to technical and regulatory issues and concerns.
* Prepare technical reports and other deliverables.
* Achieve client’s expectations for scope, budget, schedule, and quality.
Requirements:
* BS/MS in environmental, safety, occupational health, engineering, or related science degree preferred.
* Minimum of 3 years relevant EHS experience managing compliance obligations (including industrial wastewater, air registration, haz waste) in a manufacturing setting
* Certification in field; CSP, CIH, PE, or similar registration is desirable but not required.
* Experience with environmental management programs.
* Passionate about EHS performance improvement with substantial experience with practical implementation.
* Solid understanding of the relevant local, state, and federal regulations and how they apply to heavy industry and capital projects.
* Strong written and verbal communication skills and the ability to communicate effectively.
* Local candidates preferred.
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, safety, risk and social i...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2026-05-06 07:32:40
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ERM is hiring an Environmental Health and Safety Associate Manager to support a client’s medical device manufacturing facility in Redmond, WA.
In this critical role, you will be responsible for ensuring safety compliance with applicable regulations and existing company standards and contributing to an environment where employee health and safety are paramount.
This is a full-time (40 hours per week), limited-term role with a duration of 8 months, and the possibility of renewal.
RESPONSIBILITIES:
* Oversee occupational health and safety matters related to facility personnel.
* Develop and maintain a systematic occupational health and safety management program to facilitate identification of occupational health and safety hazards; utilization of physical safeguards and employee personal protective equipment to control such hazards; training of employees in good health and safety management practices; investigation of accidents and occupational injuries and illnesses; and compliance with all applicable health and safety legislation.
* Evaluates deficiencies; establishes and implements written policies and procedures; audits to assess and ensure compliance with policies and procedures; and provides requisite training.
* Manages general compliance matters and projects as necessary, assistance to ensure compliance with relevant policies, and other federal laws relating to health and safety (e.g.
transportation of hazardous materials).
* Oversee environmental matters related to facilities and products.
Develops and maintains a systematic environmental management program to facilitate assessment of environmental impacts of products, facilities and operations; engagement of management and staff in activities related to reducing environmental impacts; and compliance with applicable environmental legislation.
* Serves as a contact regarding products and facility related environmental compliance issues; monitors environmental laws that impact products and operations; evaluates deficiencies in this area; establishes and implements written policies and procedures; audits to assess and ensure compliance with policies and procedures; provides requisite training.
* Strong knowledge of ISO14001 to implement ISO14001 if needed and continue to support and lead sites with ISO14001 currently in place.
* Auditing sites for environmental and safety compliance.
* Includes worker’s safety, industrial safety, fire safety, ergonomics, HazCom, process/work evaluation, accident investigation, safety trainings for employees, and chemical safety.
* Ability to work with management of change/process safety elements including learning the document control system to make annual program changes or institute new programs through document control.
* Develop compliance and other identified training, as necessary.
* Advise the EHS Manager and/or the Site Director and supporting site managerial team on all EHS needs a...
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Type: Permanent Location: Seattle, US-WA
Salary / Rate: Not Specified
Posted: 2026-05-06 07:32:18
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Classification:
Non-Exempt
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The Soil Counter/Sorter handles, counts, sorts and records incoming soiled textiles from the customer.
Identifies damaged or abused textiles.
Prepares and transfers textiles to other departments.
Performs other tasks as needed.
Our full-time employees enjoy:
401K Plan with Company Match
Medical, Dental, Vision, FSA/HSA
Life Insurance, Disability Insurance
Vacation, Sick Time, Holidays
Choice of Global Cash Card or Direct Deposit
Career Advancement
Learning & Development Opportunities
Inclusive and Diverse Team Environment
Essential Functions:
- Open bag of soiled textiles, then sort them by type, size and color.
- Count textiles manually or electronically, and transfer them into sorting systems.
- Identify damaged or abused textiles and record into sorting systems.
- Meet efficiency and safety standards for the position.
- Follow instructions as directed by supervision.
Additional Functions:
- Work in other production positions as needed.
Qualifications:
- Recognize colors and sizes, count accurately.
- Comprehend and follow direction.
Typical Physical Activity:
- Physical Demands consist of standing, walking, reaching overhead, pushing, pulling, grasping, lifting up to 50 lbs.
and stooping.
- Physical Requirements consist of being able to meet the physical demands for the entire shift.
Typical Environmental Conditions:
- Production areas of a typical industrial laundry facility, which includes variations in temperature, odors, humidity, lint and dust.
Soiled linens come from a variety of customers such as restaurants, hotels, medical facilities and shops.
Travel Requirements:
- none.
Education:
- none.
For a general description of benefits that are being offered for this position, please visit alsco.com/benefits.
Alsco is an Affirmative Action/Equal Employment Opportunity Employer.
Revised: 04/29/2022
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment...
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Type: Permanent Location: Reno, US-NV
Salary / Rate: Not Specified
Posted: 2026-05-05 09:05:14
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Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world's most in demand and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life's essentials - and creates lasting value for its colleagues, customers, and other stakeholders.
Learn more about the company's Customized Polymer, Sustainable Fiber, Durable Metal, and Integrated Solutions at www.greif.com and follow Greif on Instagram and LinkedIn.
OUR VISION:
Being the customer service company in the world.
OUR PURPOSE:
Creating packaging solutions for life’s essentials.
Job Requisition #:
034117 Account Manager (Open)
Job Description:
Ben jij een commercieel talent met een neus voor opportuniteiten en een passie voor klantenrelaties? Werk je graag in een internationale context waar duurzaamheid, innovatie en lange termijn partnerships centraal staan? Dan is deze rol bij Greif Belgium iets voor jou.
Jouw rol?
Als Account Manager draag je de verantwoordelijkheid voor het beheren en uitbouwen van een klantenportefeuille in België en Luxemburg.
De functie combineert relatiebeheer met actieve prospectie en biedt een mooie mix tussen stabiliteit en groei.
Binnen deze rol ligt de focus op het onderhouden en versterken van bestaande klantenrelaties (±70%), terwijl je daarnaast actief nieuwe klanten aantrekt en ontwikkelt (±30%).
De verantwoordelijkheid voor omzet en marges binnen de eigen portefeuille vormt hierbij een belangrijk onderdeel van het takenpakket.
Daarnaast volg je trends en ontwikkelingen op binnen de chemische, smeermiddelen- en voedingsindustrie, zodat je gericht kan inspelen op nieuwe opportuniteiten.
Klanten kunnen bij jou terecht voor advies rond verpakkingsoplossingen, logistiek en de toegevoegde waarde van het Greif productgamma.
Door actief mee te denken, werk je aan nieuwe toepassingen en oplossingen die aansluiten bij hun behoeften.
Het volledige salesproces valt onder jouw verantwoordelijkheid: van het plannen van afspraken en opmaken van offertes tot de opvolging van dossiers.
In nauwe samenwerking met collega’s van productie, logistiek, customer service en Key Account Management zorg je voor een optimale klantenervaring.
Tegelijk stimuleer je cross-selling en benut je de sterktes van de internationale Greif-organisatie.
Wie ben jij?
Een bachelor diploma of gelijkwaardige ervaring vormt de basis voor deze functie, aangevuld met een eerste ervaring in een commerciële rol, bij voorkeur in een B2C-omgeving.
Vlot communiceren in het Nederlands, Frans en Engels is essentieel om succesvol te zijn in deze rol.
Ervaring met CRM- en ERP-systemen is een plus, net als een goede kennis van MS Office, met een sterke focus op Excel.
Dankzij een proactieve houding en een sterk verantwoordelijkheidsgevoel neem je initiatief en wee...
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Type: Permanent Location: Lier, BE-VAN
Salary / Rate: Not Specified
Posted: 2026-05-05 09:05:04
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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: 2026-05-05 09:00:40
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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: EBS Quality Associate
As an EBS Quality Associate, you will be part of the Elanco Business Solutions (EBS) team to deliver independent quality oversight on GxP activities and decisions.
In this role, you will be responsible for advancing the implementation, maintenance, and operations of the Quality Management System, as well as acting as the Regional Quality Master Data Steward.
Your Responsibilities:
* Ensure the Quality Management System complies with local regulations, GxP requirements, and Elanco quality standards.
* Manage EBS operational quality tasks including deviations, change controls, quality documents, Quality Plans, and Quality Agreements.
* Act as Regional Quality Master Data Steward by managing Local Quality Object Requests in SAP S4/HANA and supporting the Affiliate QA organization.
* Drive continuous improvement, risk mitigation, CAPAs, and support audit preparations and observation completion.
* Monitor, trend, interpret, and report on Quality metrics while participating in QA Affiliate activities like document review, recall activities, and inventory management.
What You Need to Succeed (minimum qualifications):
* Bachelor's Degree in Pharmacy, Science, Engineering, or a related field (or equivalent level of experience).
* A minimum of 1 year of experience working in a GxP regulated environment.
* Professional fluency in English (written and verbal) and strong working knowledge of SAP S4/HANA (O2C Module, Quality Module, MMD).
What will give you a competitive edge (preferred qualifications):
* Knowledge of Quality processes including Batch Management, Recall activities, Product Complaint management, and Customer License management.
* Knowledge of Order-to-Cash (O2C) and Supply Chain processes such as Order Management, Return Management, and Inventory management.
* Effective interpersonal skills with experience in cross-functional international cooperation.
* Demonstrated analytical and investigational skills with strong attention to detail.
* Effective organizational, planning, and self-management skills.
Addit...
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Type: Permanent Location: Warszawa, PL-MZ
Salary / Rate: 194000
Posted: 2026-05-05 08:39:17
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper & world-shaper.
Sous la supervision du chef de section, vous êtes responsable de la gestion quotidienne d’une équipe dédiée à l’entretien des équipements.
Vous assurez l’exécution optimale des travaux planifiés et non planifiés (pannes, bris), tout en agissant comme leader et agent de changement.
Vous définissez les objectifs d’entretien, suivez leur atteinte, et intervenez rapidement en cas d’écart.
Vous animez des rencontres d’équipe, collaborez avec les différents services de l’usine et contribuez à améliorer la fiabilité des équipements, dans le respect des normes de santé, sécurité et environnement.
Vos responsabilités clés comprennent :
* Superviser et mobiliser l’équipe d’entretien pour atteindre les objectifs fixés;
* Assurer la planification et le suivi des travaux d’entretien (préventifs et correctifs);
* Réagir efficacement aux urgences et aux bris d’équipement;
* Contrôler l’exécution des opérations journalières selon les protocoles établis;
* Favoriser une approche client auprès des autres services de l’usine;
* Animer des rencontres d’équipe et promouvoir une culture de fiabilité et d’amélioration continue.
Ce que vous apportez au rôle :
* Diplôme professionnel, collégial ou universitaire (un atout);
* Minimum de 3 ans d’expérience en gestion d’équipe;
* Connaissances en électricité et mécanique (un atout);
* Leadership reconnu et capacité à gérer les priorités;
* Maîtrise du français et des outils informatiques (Excel, Word, PowerPoint);
* Excellentes habiletés de communication et esprit d’équipe.
Ce que nous offrons :
Pour vous soutenir, vous et votre famille, au-delà du travail, Alcoa offre un ensemble d’avantages sociaux exceptionnels à compter du premier jour d’emploi.
En plus des avantages médicaux, nous offrons des programmes structurés de télétravail, des groupes de ressources, des options de plans de retraite et un plan de vacances de premier ordre pour un meilleur équilibre travail-vie personnelle.
*
*Poste 40h semaine du lundi au vendredi
*
*
Alcoa est fier d’être un milieu de travail offrant l'égalité des chances en matière d'emploi et d’être un employeur d’action positive.
Il fait également parti des groupes d'inclusion mondiaux (AWARE, AWN, EAGLE, ABLE).
Seules les personnes sélectionnées dans le processus seront contactées.
#LI-MP1
About the Location
Alcoa's aluminum smelter in Baie-Comeau is the economic engine of Baie-Comeau and the Manicouagan region.
The significant investments made in recent years have allowed the plant to look to the future with optimism.
Working for Alcoa in Baie-Comeau means giving yourself the means to have an excit...
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Type: Permanent Location: Baie-Comeau, CA-QC
Salary / Rate: Not Specified
Posted: 2026-05-05 08:24:28
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OS&H Coordinator
Job Description
Safety Specialist (Manufacturing)
Join the team behind iconic brands like Huggies®, Kleenex®, Cottonelle®, Scott®, Kotex®, Poise®, Depend®, and Kimberly-Clark Professional® [local brands can be input here, be sure to use register sign ®]. At Kimberly-Clark, it’s all here for you—innovation, growth, and the chance to make a real impact.
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
About You
We are seeking a hands-on Safety Specialist to join our manufacturing site in Binh Duong.
This role is site-focused and execution-driven, with a strong emphasis on contractor safety management, shopfloor risk control, and enforcement of safe work practices.
The position supports the implementation of the Occupational Health & Safety Management System in line with ISO 45001 and internal standards, working closely with Operations, Engineering, Maintenance, and contractors on a daily basis.
Key Responsibilities:
Contractor Safety Management – 35%
· Manage contractor OH&S processes including:
o Contractor pre‑qualification and safety assessment.
o Risk assessment and method statement review.
o Permit‑to‑Work (PTW) issuance and monitoring.
o Conduct safety induction and toolbox talks for contractors.
· Perform inspections and observations of contractor activities on site.
· Monitor contractor safety performance and follow up on violations or incidents.
Expected Outcome: All contractor activities are executed safely with controlled risks and with zero serious incidents and full OH&S compliance.
OH&S Management System Implementation – 30%
· Support the implementation, maintenance, and continuous improvement of the KC performance standard system and ISO 45001 Occupational Health & Safety Management System.
· Assist in:
o Hazard Identification and Risk Assessment (HIRA).
o Job Safety Analysis (JSA).
o Incident investigation and root cause analysis.
· Track OH&S actions, KPIs, audit findings, and corrective actions.
· Participate in internal and external OH&S audits and inspections.
· Support OH&S objectives, action plans, and risk‑based planning.
· Promote worker consultation and participation in OH&S activities.
· Serve as the site Performance Standard Owner for relevant Kimberly‑Clark OH&S Performance Standards, including deployment, effectiveness monitoring, gap closu...
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Type: Permanent Location: Bình Duong, VN-57
Salary / Rate: Not Specified
Posted: 2026-05-05 08:21:01
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Position Summary
This position will accomplish tasks towards the development of new products and the continuous improvement of our manufacturing and quality processes. This role is required to maintain a high level of safety and quality while meeting goals. It is not an entry-level position in the R&D group and requires some knowledge of coal and carbon products processing.
Target Responsibilities
* Accept, embrace, and promote the Core Values of CONSOL Innovations: Safety, Sustainability & Continuous Improvement.
* Provide a safe and orderly workspace.
* Ability to follow safety protocols and standards when operating equipment.
* Able to use more complicated equipment such as Parr reactor, mechanical testing device, and particle size analyzer.
* Able to assemble larger pieces of prototype or pilot scale equipment.
* Able to follow technical instructions while working independently or collaboratively.
* Capable of showing initiative in accomplishing tasks.
* Ensure equipment is properly maintained by recognizing concerns and performing high-level maintenance, as necessary.
* Able to diagnose technical problems with equipment and facilitate repair.
* Able to provide keen observations on the results of experiments conducted in the realm of new product development and continuous improvement.
* Able to provide some assistance to R&D Technicians I and II in accomplishing tasks.
* Time is well-managed to accomplish tasks efficiently.
* Safely store and handle potentially hazardous chemicals.
Required Skills and Experience
* At least 5 years of laboratory, manufacturing, or skilled trade experience in coal or carbon products processing.
* Ability to perform fundamental mathematical operations like addition, subtraction, multiplication, and division.
* Experience operating basic hand tools.
* Strong mechanical aptitude with the ability to perform equipment setup and high-level maintenance or repair.
* Must be able to lift 50 pounds without assistance.
* Strong personal commitment to safety.
* Detail oriented with good organizational and interpersonal skills.
* Positive professional attitude.
* Strong written and verbal communication skills.
* Ability to operate well within a team.
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Type: Permanent Location: Triadelphia, US-WV
Salary / Rate: Not Specified
Posted: 2026-05-05 07:58:01
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Under the direction and supervision of the Lucas County Child Support Agency Case Financial Supervisor or designee, the assistant is responsible for but not limited to providing supportive leadership and work direction of assigned team and/or area of responsibility to ensure consistency, standardization and development of best practices as they relate to division services.
Responsible for the interpretation and clarification of work procedures.
ESSENTIAL FUNCTIONS
In coordination with the unit supervisor responsible for managing work assignments and daily phone coverage.
Ensures the unit has adequate supplies to perform their job duties.
Assists the Supervisor with assigning tasks and setting unit priorities to ensure timely and accurate completion.
Delegates and follows up on the completion of the following: Financial Institution Data Matches, Reduction of Permanently Assigned Arrears (ROPAA), Incorrect Caseload report, Case Closure report, Default with no Ordered Payment on Arrearage (OPA), No default with OPA.
Updates ROPAA database quarterly, monitors and keeps track of current ROPAA accounts and adds additional cases when necessary.
Assists with audits and distributions.
Monitors the Lucas financial mailbox to facilitate communication with the state Payment Analysis and Account Reconciliation (PAAR) team, Ohio Child Support (OCS), and Smart Applications, as required by state and federal guidelines.
Processes child support payments with accuracy using check scanning equipment and payment posting software.
Processes financial corrections as identified when necessary or at the direction of PAAR, OCS, or the Support Enforcement Tracking System (SETS) Help Desk.
Manages misallocated payments and voids by reissuing and reposting payments as needed or requested.
Monitors the shared email account for releases and processes payment.
Performs the duties of Transfer Coordinator by managing cases transferred to or from our county to another county or the state according to the established workflow.
Performs the duties of the SETS Third Party Coordinator by maintaining the integrity of the directory for employers, courts, agencies, labs, prisons, insurance companies and others in connection with the OCS Third Party Team.
Provides oversight of records retention in either digital or paper format in accordance with local, state, and federal guidelines.
Resolves complex and/or unusual situations independently; identifies and escalates high-level issues to the supervisor when necessary.
Assists the unit supervisor with projects as needed.
Provides coverage for the Case Financial Supervisor in their absence.
Acts as a back-up for bank monitoring/reconciliation.
Processes genetic testing payments (includes building shell case, sub order, routing payments to Child Support Payment Central for proper posting, closing out case after payment processes).
Offers input into the development of policies and procedures as required to accomplish the...
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Type: Permanent Location: Toledo, US-OH
Salary / Rate: Not Specified
Posted: 2026-05-05 07:49:11
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
Roche Personalized Healthcare Solutions (PHCS) is seeking a full-time Pathology Scientist (m/f/d) to join the Pathology team of the US-accredited Companion Diagnostics (CDx) laboratory located in Penzberg.
If you have experience in Immunohistochemistry (IHC), in situ hybridization (ISH), or quantitative image analysis using artificial intelligence or machine learning, we want to hear from you!
At Roche PHCS, we value collaboration, innovation, and the drive to make significant contributions to healthcare.
As part of our team, you'll work in a multidisciplinary environment, engaging with experts in bioinformatics, oncology, digital pathology, and biomarker development.
The Opportunity
Join a global team of over 20 pathologists located in both Germany and the United States who work together to drive innovation and bring new products to market.
In this challenging role you will
* Provide medical oversight for pathology and slide reading for early phase clinical trials, assay development, CE-IVD and Pharma clients.
Ensure quality and continuous improvement initiatives in collaboration with internal and external stakeholders.
* Support R&D activities for primary antibodies, detection systems, probes, special stains, and digital pathology, contributing to new product development and process improvements.
* Serve as the medical representative on project teams, addressing all pathology-related aspects and queries, and making strategic contributions through medical knowledge.
* Participate in Pharma client meetings to support biomarker hypothesis testing strategies, and drive activities for publication and/or patent potential.
* Coordinate the work of contracted pathologists, including training, assigning work and advising on day-to-day activities, as needed.
* Contribute to internal pathology education programs, perform training and scoring of slides, read clinical trial patient samples for the CDx laboratory (Penzberg), and stay up-to-date on pathology, oncology, and molecular biology literature.
* Serve as Principal Investigator with medical accountability across multiple European clinical trials within global CDx development programs, acting as the primary medical...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-05-05 07:41:56
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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
Deine Abteilung
Eingebettet in eine globale Organisation verbindet das Center for Cross-Functional Development (CXD) regionale Fachexpertise in Zellkultur und Aufreinigung mit globalen Kompetenzen – von der Prozessvalidierung bis zur Bioprozesstechnologie.
Dank unserer flexiblen, multifunktionalen Laborausstattung unterstützen wir unterschiedlichste Projekte und fungieren als Motor für Innovation.
Deine Aufgaben
* Du unterstützt bei der Durchführung von enzymatischen Assays und der Entwicklung biochemischer Reaktionen, die unter Einhaltung der gültigen Arbeitssicherheits- und Sicherheitsvorgaben durchgeführt werden.
* Nach einer Einweisung führst Du Experimente zur Optimierung enzymatischer Reaktionen und zur Charakterisierung von Biomolekülen durch.
Deine Arbeit erfolgt unter der Anleitung und Überwachung einer qualifizierten Fachkraft.
* Du dokumentierst Deine Ergebnisse und Arbeiten.
* Du beachtest die internen und externen Vorgaben hinsichtlich Arbeitssicherheit und Umweltschutz.
Dein Profil
* Du bist aktuell in einem Masterstudium in Biochemie oder einer verwandten Fachrichtung immatrikuliert oder befindest Dich in einem Gap-Year (mit Immatrikulationsbescheinigung).
* Idealerweise bringst Du theoretische Kenntnisse in Enzymologie, Biochemie und Biokatalyse sowie praktische Kenntnisse in biochemischen Methoden und im Umgang mit Proteinen mit.
* Kenntnisse in der Flüssigkeitschromatographie (LC) und Massenspektrometrie (MS) sind von Vorteil.
* Du arbeitest gern in einem Laborumfeld.
* Du verfügst über sehr gute Englischkenntnisse und hast keine Scheu davor, mit internationalen Kollegen zu kommunizieren.
Deine Vorteile
* Flexible Zeiteinteilung
* 2268 € Vergütung im Monat für ein Vollzeitpraktikum
* Vergünstigte Essenspreise (-50 %) in unserer Mitarbeiterkantine
* Fitnesszentrum auf dem Roche-Campus
* Vernetzung mit anderen Studierenden
* Weiterbildungsmöglichkeiten und spannende Gastvorträge
* Möglichkeit der Unterbringung im Roche Boardinghaus
* Gut organisierte Verkehrsanbindung nach München mit unserem Roche-Shuttle
Deine Bewerbung
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/Ho...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-05-05 07:41:08
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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
Unsere Mission
Die Organisation Manufacturing Science and Technology (MSAT) übernimmt die Verantwortung für Design Transfers, Product Care und große Investitionsprojekte für die Diagnostics Manufacturing Einheit.
Dabei arbeitest du in einem hochmotivierten Team mit 5 Kolleg
*innen in der Abteilung Multiprojektmanagement.
Das Team begleitet die Produktneueinführungen in engem Austausch mit vielen Schnittstellen, sowohl standortgebunden als auch global.
Die Vielfalt der Projekte und damit verbundenen zahlreichen Gruppierungen bietet eine anspruchsvolle und sehr abwechslungsreiche Tätigkeit.
Als Praktikant im Launch Management unterstützt du bei der Erstellung für DOZ Logistikkonzepte, planst du Produktionen im Projektumfeld und trackst den Fortschritt der Master Data und damit stellst sicher, dass alle am Projekt beteiligten Schnittstellen entsprechend der Kernkompetenzen von Roche motiviert und zielorientiert zusammenarbeiten.
Außerdem sorgst du für einen reibungslosen Projektablauf im Bezug auf den logistischen Part, trägst zu den Meilensteinen bei und verbessert kontinuierlich die Durchführung des Prozesses.
Du fühlst dich zudem in der Projektmatrix zu Hause und trägst mit deinem Beitrag zum Erfolg bei.
Dein Team
Du arbeitest in einem neuen Team mit weiteren 5 Kolleg
*innen in der Abteilung Multiprojektmanagement.
Das Team koordiniert das logistische Set up in vor allem Neueinführungsprojekten, unterstützt aber auch in anderen Projekte.
Dabei arbeiten wir gemeinsam mit Engagement und Spaß an unterschiedlichsten Projekten innerhalb der Diagnostik-Welt von Roche.
Deine Aufgaben
* Du begleitest und unterstützt teilweise bereichsübergreifende/internationale und crossfunktionale Projekte in der Matrix
* Du übernimmst eine Rolle in der Planung der Projektproduktionen
* Du unterstützt bei der Erstellung von fundierten Logistikkonzepten und Materialflussplänen
* Du trackst den Materialnummern Setup Prozess in SAP, begleitest & treibst den lokalen Anlageprozess
* Du zeigst eine selbstständige, zuverlässige und flexible Arbeitsweise und hast einen klaren Blick für das Wesentliche
* Du bist ein wahrer Teamplayer und verfügst über Überzeugungskraft, behältst auch in Belastungssituationen den Überblick und vergisst dabei den Spaß an der Arbeit nicht
Wer du bist
* Du hast eine erfolgreich abgeschlossene kaufmännische Ausbildung/Studium (Bachelorabschluss) oder vergleichbares
* Du verfügst...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-05-05 07:41:06
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Specific Responsibilities
1.
Provide Scientific Support to Food & Nutrition Group
* Area of focus is to provide scientific support to the Food & Nutrition group related to safety assessment and health claims substantiation of food ingredients, additives and supplements
* Assist with reviewing results of literature searches
* Assist with tabular summaries of scientific information
* Extract and tabulate information from scientific publications
* Review data for completeness, relevance, etc.
* Present accurate summaries of literature/data to manager for review
* Address comments and make revisions, as required
* Assist with dossier preparation
2.
Co-ordination of Contract work requests
* log in work requests from customers
* communicate data requirements to customer in clear and straightforward terms
* ensure all scientific data required to complete request is obtained
* assist scientific staff with identifying scientific data
* assist with preparation of reports
* revise reports based on senior toxicologist’s review
* co-ordinate efforts of customer, administrative staff, scientific staff, senior toxicologists
* provide customers with finalized reports
* assist with updating databases and invoicing requested work
C.
Assist scientific staff with special requests: e.g., editing documents, researching information on various topics, document preparation, organization and collation of government dossiers.
Other duties related to the above, as assigned
* Carrying out all responsibilities in a supportive manner with total adherence to the Company’s Health, Safety and Environmental Policies and Procedures, Quality Management System, Compliance and Ethics Policies, Vision, Mission and Strategy, and exercises good judgment, common sense, and diplomacy.
Education and Experience Requirements
* diploma from an accredited College in a researcher or sciences-based area of study (0-1 years’ experience)
* strong writing skills and communications skills
* Exceptional attention to detail
* highly organized and ability to manage short deadlines for contract work
* personable and courteous to facilitate client interactions
* familiarity with software packages
* ability to prioritize and manage time effectively and work on multiple projects at once
* team player
This position outline is a general guideline and does not represent all encompassing details.
The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties.
Salary & Benefits Information
The hourly rate for this position is $22.00 per hour.
Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons.
Intertek’s Commitment
Intertek is a world leader in the Quality Assurance market, w...
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Type: Permanent Location: Mississauga, CA-ON
Salary / Rate: Not Specified
Posted: 2026-05-05 07:40:48
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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
Diagnostics Operation Penzberg ist das Herzstück der weltweiten Produktion diagnostischer Einsatzstoffe innerhalb des Roche-Konzerns.
Als Weltmarktführer im Bereich der In-Vitro-Diagnostik verbinden wir höchste GMP-Qualitätsstandards mit technologischem Fortschritt.
Hier arbeitest du an der Schnittstelle zwischen klassischer Qualitätskontrolle und der digitalen Transformation der Gesundheitsbranche.
Als Praktikant:in (m/w/d) geben wir dir nicht nur Einblick in das „Daily Business“ der Qualitätskontrolle, sondern lassen dich aktiv an der Schnittstelle zwischen klassischer Laborarbeit und moderner IT-Infrastruktur mitwirken.
Du lernst hautnah, was es bedeutet, in einem hochregulierten GMP-Umfeld beim weltweit größten Hersteller von In-Vitro-Diagnostik-Produkten zu arbeiten.
Deine Aufgaben
In diesem Praktikum bist du der Treiber unserer nächsten digitalen Evolutionsstufe.
Wir arbeiten bereits digital – mit der Implementierung und Optimierung eines Labor-Informations-Management-Systems (LIMS) heben wir unsere Prozesse nun auf das nächste Level an Vernetzung und Effizienz.
Als Content Creator überarbeitest du die bisherigen Dokumente und hilfst uns beim Erstellen neuer Stammdaten.
* Methoden-Check & Optimierung: Du hinterfragst Methodentexte kritisch, prüfst sie auf Aktualität und Logik und hilfst dabei, diese für die digitale Nutzung aufzubereiten
* Recherche & Dokumentation: Du führst eigenständige Recherchearbeiten durch und unterstützt bei der Erstellung technischer Dokumente
* Projektarbeit: Du übernimmst die Verantwortung für kleinere, eigenständige Projekte im Bereich der QC
Dein Profil
* Hintergrund: Du studierst Naturwissenschaften (Chemie, Biologie, Pharmazie), Bioinformatik, Medizintechnik oder einen vergleichbaren Studiengang
* Mindset: Du bist motiviert, neugierig und hast eine schnelle Auffassungsgabe.
Du liebst es, Dingen auf den Grund zu gehen und Texte kritisch zu hinterfragen
* IT-Affinität: Du bist sicher im Umgang mit MS Office und hast ein ausgeprägtes Interesse an digitalen Systemen (LIMS)
* Sprache: Du beherrschst die deutsche Sprache fließend in Wort und Schrift
* Arbeitsweise: Du arbeitest gewissenhaft, strukturiert und hast Freude an der Dokumentation
Deine Vorteile
* Flexible Zeiteinteilung für eine gute Work-Life-Balance
* 2268 € Vergütung im Monat für ein Vollzeitpraktikum
* Vernetzung mit anderen Studierenden (online/offline)
* Ermäßigte Preise (...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-05-05 07:38:48
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Ton rôle, en bref :
En tant que Team Lead R&D, ton rôle principal sera de coordonner la maintenance continue de nos produits, d’accompagner ton équipe dans la gestion des correctifs et des améliorations, et d’assurer la performance et la fiabilité des systèmes.
Tu devras démontrer des compétences supérieures en gestion d’équipe, en planification et en suivi de projets, tout en contribuant à améliorer constamment les processus de développement dans un environnement agile.
Possédant un niveau d’engagement élevé démontré par l’action, tu devras également faire preuve d’une forte autonomie et d’une capacité à mobiliser et inspirer ton équipe.
Tu feras partie d’une équipe de développement solide et en pleine évolution technologique, et tu collaboreras étroitement avec des chefs produit, des architectes, des analystes et des développeurs expérimentés pour atteindre nos objectifs stratégiques.
Ton profil :
* Tu as d’excellentes capacités de leadership et sais mobiliser une équipe autour d’objectifs ambitieux?
* Tu es motivé par le besoin de donner du sens à ce que tu fais et à ce que ton équipe réalise?
* Tu aimes améliorer constamment les processus de développement en mode Agile et inspirer les bonnes pratiques?
* Tu apprécies le télétravail pour maintenir un équilibre travail-famille, tout en gardant une forte cohésion d’équipe?
Les avantages offerts :
* D’excellents avantages sociaux (dentaire, optométrie, médical, programme vie active de 325$ annuellement, programme REER, programme d’aide aux employés, programme d’achat d’actions)
* Du télétravail presque 100% de ton temps
* Des collègues en or, de bonnes relations, de l’entraide et de l’esprit d’équipe
* De la reconnaissance sous toutes ses formes
* Des possibilités d’évolution et d’avancement
* Des options pour mieux concilier vie personnelle et travail (complément maternité pour les 6 premières semaines, congés personnels, journée de bénévolat)
* Et surtout, des fous rires au quotidien!
Tes responsabilités, plus en détails :
* Encadrer et motiver une équipe multidisciplinaire
* Planifier et suivre les projets R&D via un roadmap, des jalons et des livrables
* Garantir la qualité du code et des solutions au travers les revues, les normes et les tests
* Collaborer avec les équipes produits, QA et opérations afin d’assurer l’intégration
* Assurer la veille technologique et proposer des améliorations continues
* Gérer les priorités et résoudre les obstacles techniques avec l’équipe
Ton expertise et tes compétences :
* Diplôme en informatique, génie logiciel ou domaine connexe
* Expérience 4-6 ans en développement logiciel ou en gestion de projets de développement
* Connaissance des pratiques Agile/Scrum, CI/CD, et outils de gestion tel Azure DevOps
* Capacité ?...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 85000
Posted: 2026-05-04 07:30:18
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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!
Job Description
Position Description
The Senior Scientist – Clinical Development, Animal Health is responsible for leading and executing target animal safety and effectiveness studies within animal health.
This role is focused on hands-on study ownership, working with external partners and investigators to deliver high-quality data that supports regulatory and development decisions.
Key Responsibilities
* Lead end-to-end execution of target animal safety and effectiveness studies
* Develop and own study protocols, ensuring successful delivery through contract research organizations (CROs) and Elanco study sites
* Oversee external partners and investigators, ensuring timelines, quality, and compliance are met
* Monitor study progress, troubleshoot issues, and ensure data integrity throughout execution
* Analyze and interpret study data to support regulatory and development outcomes
Minimum Qualifications
* PhD or DVM required
* 5+ years of direct experience in animal health study execution (TAS and/or effectiveness required)
* Proven experience leading studies, not supporting, within clinical settings
* Hands-on experience managing CROs, investigators, or external study partners
* Working knowledge of FDA-CVM requirements and GLP/GCP for animal studies
Preferred Qualifications
* Experience across different livestock species
* Background specifically in target animal safety and field-based effectiveness studies
* Experience supporting regulatory submissions or study reports for regulatory review
* Ability to manage multiple studies with minimal oversight
* Strong communication skills with experience working cross-functionally
What You Will Gain
* Full ownership of study execution in a focused animal health environment
* Direct impact on safety and effective decisions tied to product development
* High visibility across R&D, regulatory, and external partners
* Opportunity to work on multi-species programs with real-world application
* A role built for execution, not bench or discovery work
Don’...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: 157800
Posted: 2026-05-04 07:29:10
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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!
$2,500 Sign-On Bonus! Apply Today!
Relocation Assistance Available
Your Role: Sr.
Downstream Bioprocess Specialist (Day Shift)
The Sr.
Downstream Bioprocess Specialist (Day 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
* Must be authorized to work in the US.
This position does not offer sponsorship.
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.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 40
Posted: 2026-05-04 07:28:47
