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Questline Digital, a division of Harris; is seeking a Sales Account Executive who grows revenue through new business sales as an individual contributor.
The Sales Account Executive identifies prospects, develops qualified leads, forges strong relationships with utility decision-makers, effectively communicates the value of Questline Digital solutions, negotiates terms and closes sales.
Questline Digital offers a unique set of strategic communication solutions that increase customer engagement for our utility clients.
An understanding of digital marketing and the ability to work multi-step, complex sales cycles are essential for this position.
This remote role welcomes candidates anywhere in the US.
Travel is required as needed, approximately 50%. Preference will be given to candidates in the EST and Central Time zones.
Base Salary:
$70,000 to $90,000
OTE:
$100,000 to $140,000+ annually, including uncapped commission.
Top performers may exceed the stated OTE range based on results.
What your impact will be:
* Develop and maintain relationships with key stakeholders at assigned clients and/or prospects that result in new business.
* Master the product portfolio in order to articulate value via presentations and proposals, ensuring that solutions and services are aligned to client needs.
* Attend and present at external customer meetings, industry tradeshows and internal company functions.
* Develop, own and manage a pipeline that results in the achievement of a net-new annual sales quota for an assigned book of business.
What we are looking for:
* 3+ years of relevant sales experience, preferably in a marketing, software and/or the utility market.
* Positive, solutions-oriented approach driven by a passion for expanding relationships with clients, resulting in closed-won opportunities.
* Proficiency in guiding clients to strategic solutions in complex, multi-step sales cycles.
* Ability to travel to industry conferences and client visits.
* Highly motivated self-starter who has the capacity to take ownership of opportunities and help prospects think in a different way.
* CRM experience; Salesforce experience highly preferred.
* Excellent presentation skills and clear, effective writing skills.
* Strong analytical capabilities.
* Proficient in managing the financial aspects of new opportunities.
* Can be positive and respectful in collaborating with internal teams.
* Bachelor's degree or equivalent experience.
* Experience in the energy utility industry preferred, but not required.
What we can offer:
* 3 weeks’ vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Remote work and more!
About Questline Digital:
Questline Digital is a marketing and technology agency that builds e...
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Type: Permanent Location: Tallahassee, US-FL
Salary / Rate: Not Specified
Posted: 2026-06-09 09:06:19
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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.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
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: Quality Control /Environmental Monitoring Technician
Environmental Monitoring / QC Technician Microbiology will report to the QC Supervisor, Microbiology or equivalent.
This position will conduct routine and non-routine environmental monitoring of the manufacturing facilities and associated utilities, as well as microbiology analysis.
Your Responsibilities:
* Conducts Environmental Monitoring: Performs routine and non-routine sampling of manufacturing environments (air and surfaces) and utilities (WFI, USP Water, Pure Steam, Clean Compressed Air).
Maintains gowning qualifications for sterile environments.
* Ensures cGMP Compliance: Upholds cGMP, safety, and environmental standards within the QC lab, generating accurate and compliant data.
Participates in internal assessments and audits.
* Performs Microbiological Testing: Executes routine and non-routine analyses of raw materials, in-process materials, finished goods, and stability samples.
Conducts a variety of microbiology tests, including bioburden, sterility, and microbial identifications.
* Supports Investigations and Deviations: Assists in the investigation of out-of-specification/out-of-trend results, environmental monitoring excursions, and deviations.
Contributes to the preparation of Certificates of Analysis.
* Develops and Maintains QC Methods: Assists in developing, qualifying/validating, and transferring new test methods.
Contributes to the writing and revision of testing methods, specifications, SOPs, and validation protocols/reports.
Maintains lab inventory and performs routine equipment maintenance and cleaning.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma/GED with 5years experience, BA or BS degree in Microbiology, Biological Sciences, Pharmaceutical Sciences, or closely related field, or comparable experience.
* Experience: Technical skills in Environmental Monitoring to include, but not limited to, monitoring of manufacturing environment and utilities.
* Excellent c...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 36.5
Posted: 2026-06-09 08:57:57
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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
Formulations Technical Specialist
Location
Vandalia, OH
Summary
The Formulations Technical Specialist is responsible for supporting projects by developing and maintaining the necessary documentation and tasks required to fulfil project needs.
This person will work alongside project teams to drive activities, accelerate timelines, offer ideas to implement future enhancements/work efficiencies, and provide adequate quality oversight and expertise for the creation and review of internal quality documents.
Responsibilities
* Managing Clinical and Registration Batch Preparation and execution. Responsibilities include:
* Initiate and retain stability samp...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2026-06-09 07:49:24
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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
Chemist, Raw Materials
Location
Vandalia, OH
Summary
The Raw Materials Chemist will perform chemical and physical testing on pharmaceutical raw materials (APIs, Excipients and Packaging components).
Responsibilities
* Perform sampling, physical testing, and chemical testing of raw materials as described in the documented procedure or compendia with minimal supervision in accordance with cGMP guidelines.
* Compile samples for send out testing and maintain associated documentation.
* Maintain laboratory equipment and work areas in good working condition.
* Ensure Raw Material documentation is accurate and up to date and revise as needed (...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2026-06-09 07:49:21
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Role Overview
We are seeking a highly motivated Senior Customer Growth Account Manager to drive strategic customer engagement, adoption, retention, and revenue growth across our enterprise customer base.
This role is ideal for someone who combines customer success, account management, and consultative selling skills with the ability to engage technical and executive stakeholders.
You will serve as a trusted advisor to customers while identifying opportunities to expand platform adoption and deliver measurable business value.
The ideal candidate has experience managing complex SaaS accounts, building executive relationships, and driving expansion within technical organizations such as Engineering, QA, DevOps, and Product Development.
Customer Relationship Management
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+ Serve as the primary strategic point of contact for assigned enterprise customers
+ Build trusted relationships with Engineering Leaders, QA Directors, DevOps teams, and executive stakeholders
+ Conduct regular business reviews focused on outcomes, adoption, ROI, and roadmap alignment
Customer Growth & Expansion
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+ Identify and drive upsell, cross-sell, and expansion opportunities within existing accounts
+ Partner closely with Sales and Solutions Architecture to execute account growth strategies
+ Develop account plans that align customer goals with SeaLights capabilities
Adoption & Value Realization
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+ Ensure customers successfully adopt and operationalize the SeaLights platform
+ Drive measurable customer outcomes related to software quality, release confidence, and engineering efficiency
+ Monitor customer health, usage trends, and engagement to proactively mitigate risk
Renewals & Retention
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+ Support renewal strategies and contribute to achieving high Gross Revenue Retention (GRR) and Net Revenue Retention (NRR)
+ Manage escalations and coordinate internal resources to ensure customer satisfaction and success
Cross-Functional Collaboration
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+ Work closely with Customer Success, Solutions Architecture, Product, Support, and Sales teams
+ Advocate for customer needs internally and provide feedback to influence product direction and customer experience improvements
Voice of the Customer
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+ Synthesize customer insights into actionable feedback for internal teams
+ Advocate for customer needs while balancing business priorities
Qualifications
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+ 5 years of progressive Customer Success or Account Management experience with complex enterprise accounts
+ Strong sense of personal accountability and ownership for your assigned account base
+ Passion for helping others and seeing your customers succeed
+ Self-motivated and proactive team player
+ Exceptional communication and organizational skills
+ Projec...
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2026-06-09 07:39:42
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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 #:
034473 SHEQ Manager (Open)
Job Description:
For our manufacturing plant in the heart of Amsterdam we are seeking a Safety, Health, Environment and Quality manager to be responsible for developing, maintaining, and continuously improving the management systems.
In this role you are responsible for ensuring full compliance with legal and Greif standards.
The role drives zero harm, product quality, and process discipline by providing expert guidance, enabling the organisation, and working closely with peer managers to achieve overall plant performance and customer satisfaction in line with the Greif Way.
Key Responsibilities
Safety & Health
* Ensure compliance with safety, health, and environmental regulations and Greif standards
* Develop, maintain, and improve HSE management systems
* Lead risk assessments, audits, and safety inspections
* Drive incident reporting, investigation, and corrective actions
* Promote and embed a strong safety culture across the plant
Quality Management & Compliance
* Maintain and continuously improve the Quality Management System (QMS)
* Conduct audits and ensure closure of non‑conformities
* Drive process control, SOPs, and quality standards
* Lead customer complaint resolution and corrective actions
* Ensure alignment with Greif standards and best practices
SHEQ Governance & Systems Management
* Develop and review SHEQ policies, procedures, and systems
* Ensure alignment with legal requirements and Greif Business System (GBS)
* Monitor performance through KPIs, reporting, and trend analysis
* Advise plant management on risks and improvement actions
* Maintain compliance with certifications and standards (ISO, etc.)
People Leadership & Capabilities Building
* Lead, coach, and develop SHEQ team members (e.g.
quality inspectors, coordinators)
* Build SHEQ awareness and capability across the plant
* Support managers and supervisors in applying SHEQ standards
* Drive training, engagement, and behavioral change
Continuous Improvement & Risk Reduction
* Lead and support improvement initiatives related to safety, quality, and environm...
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Type: Permanent Location: Amsterdam, NL-NH
Salary / Rate: Not Specified
Posted: 2026-06-06 09:16:31
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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!
Are you a protein purification expert ready to make a significant impact on animal health? Elanco is seeking a Senior Associate Scientist to serve as a technical leader in our Biopharma Technical Development group.
You will drive the discovery and optimization of novel biopharmaceuticals and vaccines by independently managing the entire protein purification and characterization workflow.
This is a key laboratory-based role where you will solve complex scientific challenges and mentor a team of talented scientists.
About the Role
As a Senior Associate Scientist, you will be a high-level technical lead responsible for advancing Elanco’s mission to develop innovative animal health therapies.
You will own the protein purification pipeline for multiple complex biologics, from initial method development through final characterization and data delivery.
In this role, you will partner closely with scientists across our discovery and core research laboratories, providing technical mentorship and leveraging your expertise to influence project direction and success.
Your Responsibilities
* Own the end-to-end protein purification and characterization pipeline for multiple high-priority projects, independently optimizing methods using AKTA, FPLC, and automated HF/TFF systems.
* Serve as the site expert for downstream processing hardware, leading troubleshooting, maintenance, and the strategic selection of chromatography resins and modalities (IEX, SEC, affinity).
* Generate and interpret critical characterization data (SDS-PAGE, endotoxin testing) to provide actionable insights that guide project direction and key decisions.
* Build team capabilities by training and mentoring junior Associate Scientists on advanced laboratory protocols, safety, and technical best practices.
* Drive documentation excellence by authoring and reviewing complex protocols, technical reports, and raw data to ensure the highest standards of quality and compliance.
What You Need to Succeed (Minimum Qualifications):
* Education: BS degree in Biochemistry, Chemistry, Biotechnology, Biology, or...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: 158300
Posted: 2026-06-06 09:10:00
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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: 2026-06-06 09:09:52
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EMS/OHS/QMS Third Party Auditor - Ontario, Canada
Intertek is searching for an EMS/OHS/QMS Third Party Auditor to join our Business Assurance team in our Mississauga, Ontario office.
This is a fantastic opportunity to grow a versatile career in Third Party Auditing!
What you’ll do:
* Represent the audit team and Intertek to clients
* Develop Audit Plans
* Plan and coordinate travel plans for audits as applicable
* Evaluate clients' management systems through documentation review, on-site observation, and interviews
* Identify and document areas of conformance and nonconformance
* Write Comprehensive reports and recommendations based on audit findings
* Evaluate and approve client corrective actions
* Submit time and expense reports on time, for approval
* Train, mentor, and witness (as part of the auditor qualification process) audit teammates if requested.
* Follow Intertek's Compliance Code, Policies and Procedures
·
What it takes to be successful in this role:
Education and advanced course work, training and experience in environmental, safety and quality management required.
* 5+ years of professional experience in industry
* Language requirements, proficiency in spoken and written English.
* Knowledge of principles and practices of manufacturing systems
* Knowledge of EMS/OHS laws and regulations
* Experience in implementation of and/or auditing ISO management systems
* Ability to travel 75% of the time by plane or car
* Valid driver’s license and reliable driving record (required)
* Must have ISO 9001, ISO 14001, or ISO 45001 Lead Auditor Training
* 3rd Party Auditing experience preferred
* This is a remote position; however, applicants must reside in and be able to legally work in Canada.
Physical Requirements:
* Ability to communicate and interact effectively in both verbal and written format.
* Ability to view, read and comprehend a variety of reports and manuals of a technical nature, computer screen, etc.
* Physical dexterity to perform assessment functions which are inherent to the position, such as investigating all areas of client facilities which require bending/stooping, reaching, climbing, etc.
* Mobility to travel by auto and airplane.
* Ability to be on your feet, walking, for typical full shifts of 6 - 8 hours.
* Exposure to various industrial environments.
* The ability to ascend or descend ladders, stairs, scaffolding, ramps, poles and the like, using feet and legs and/or hands and arms.
* The ability to express or exchange ideas by means of the spoken word.
Must be able to convey detailed or important spoken instructions to other workers accurately, loudly, or quickly.
* The ability to perceive the nature of sounds at normal speaking levels with or without correction.
Ability to receive detailed information through oral communication, and to make the discrimination...
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Type: Permanent Location: Mississauga, CA-ON
Salary / Rate: Not Specified
Posted: 2026-06-06 07:52:43
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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!
Siamo alla ricerca di un/una Quality Control Junior Analyst (tempo determinato 12 mesi) che si unisca al nostro QC Team di Pessano con Bornago.
Considerando che il CCNL di riferimento è quello dell’industria chimico-farmaceutica, la nostra proposta prevede:
* RAL a partire da € 29.235,92
* Categoria e posizione organizzativa min.
E1
* Assicurazione sanitaria
* Piano pensionistico
* Premio di partecipazione da accordo interno
* Benefit previsti da accordo interno
* Crescita professionale e opportunità di avanzamento all’interno dell’azienda
* Programma di riconoscimento dei dipendenti.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Quality Control Junior Analyst svolge le attività analitiche e affini all’interno del reparto di Controllo Qualità, in accordo con quanto previsto dalle GMP e dalle Procedure Operative Standard, Procedure Analitiche Standard, metodi di analisi, ed altri regolamenti interni, riportando direttamente al/alla Quality Control Laboratory Supervisor.
COMPITI E RESPONSABILITA’
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati.
* Svolge il proprio lavoro nel rispetto delle procedure aziendali e delle disposizioni di legge in materia di sicurezza sul lavoro e delle Norme di Buona Fabbricazione.
* Tiene in ordine ed aggiornati i propri quaderni di laboratorio e i propri documenti analitici.
* Esegue operazioni di base di laboratorio, quali: preparazione di reattivi e soluzioni, campionamenti di materie prime, prodotti semilavorati e prodotti finiti, ecc.
* Segue scrupolosamente le disposizioni impartite dai superiori.
* Esegue analisi con tecniche analitiche semplici e complesse, seguendo metodi definiti, in autonomia operativa.
* Adempie alle funzioni per la corretta gestione dei reagenti in accordo alle specifiche procedure.
* Lavora in modo efficace nel rispetto delle scadenze.
* Agisce come rappresentante dell'...
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Type: Contract Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2026-06-06 07:37:10
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Classification:
Exempt
Annual base salary: $92K–$135K plus 15% bonus, depending on experience.
About Us:
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 an 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 Safety and Production Specialist is a hybrid role that integrates expertise in safety management and production engineering to foster a safe and efficient working environment, supporting both employee well-being and operational excellence.
The S&P Specialist ensures compliance with safety and quality standards, reduces risks, and enhances operational efficiency.
The position involves designing safety training programs, analyzing workplace incidents, and optimizing production methods to increase productivity and reduce costs.
The S&P Specialist has oversight for Alsco operations in the following states: Alaska, Washington, Oregon, Idaho, Utah, Montana, and Nevada.
This role works closely with facility safety and production teams to help them succeed and deliver high impact results.
Field support execution is the key component of this position, while developing leadership skills and results in continuous improvement, team problem solving, and project management.
Compensation: Competitive Salary; 15% bonus eligibility; full health and welfare benefits
Our full-time employees enjoy:
* 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
Benefits may vary for positions covered by a collective bargaining agreement.
Key Responsibilities:
• Set clear expectations, recognize success, and address performance needs.
• Utilize key performance indicators; lead with a sense of urgency to drive and positively impact safety, quality, cost and speed.
• Partner with Regional Manager and General Managers to develop, coach and train production management teams and build talent pipeline.
• Develop and sustain employee development and training programs to bolster capability.
• Provide concise, action-...
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Type: Permanent Location: Salt Lake City, US-UT
Salary / Rate: Not Specified
Posted: 2026-06-05 08:45:34
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The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Job summary:
The Quality Auditor II reviews GLP studies for completeness, compliance, concurrence, and accuracy.
The auditor provides regulatory and policy and procedural guidance.
The auditor collaborates with lab personnel in design, implementation, and performance of testing with the goal of improving and building quality into the process.
The auditor demonstrates proficient knowledge of quality practices and can perform job functions extending throughout the auditor’s quality audit team.
Additionally, the auditor demonstrates proficiency in independent decision-making in regards to the interpretation of standards and regulations, performance of investigations, and other quality practices.
The auditor has a history of successful process improvement implementation.
Essential job functions:
GLP Studies
Review each GLP study prior to release for testing.
Audit a portion of each GLP study.
Review each GLP study and final report prior to mailing.
Regulatory and Policy & Procedural Guidance
Know and follow GLP, GMP and relevant ISO regulations
Perform quality event investigations and approvals
Trend quality events
Review and approve protocol detail sheets
Review out of range forms
Review discontinued studies
Review and trend amended reports
Review duplicate reports
CAPA: Initiation, investigation, resolution, and verification
Review documents in Master Control (collaboration and approval)
Review logbooks
Process Improvement
Meet regularly with Section Leader, Study Directors and Lab Analysts
Prepare Dashboard and Quarterly Management Review with Section Leader
Audit studies in-process
Assist Regulatory Affairs with internal audits
Review and approve equipment qualifications and test method validations
Perform good housekeeping (GHP) audits
Perform other duties as assigned.
Professional Development
Complete required training on time (includes MasterControl, live company trainings, New Employee Orientation, etc.)
Know and follow company policies and procedures.
Education and experience requirements:
A.A.
/ A.S.
and three years applicable NLI laboratory experience OR B.S...
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Type: Permanent Location: Taylorsville, US-UT
Salary / Rate: Not Specified
Posted: 2026-06-05 08:38:40
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The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Job Summary:
The Quality Auditor I reviews GLP studies for completeness, compliance, concurrence, and accuracy.
The auditor provides regulatory and policy and procedural guidance.
The auditor collaborates with lab personnel in design, implementation, and performance of testing with the goal of improving and building quality into the process.
The auditor demonstrates proficient knowledge of quality practices and can perform job functions extending throughout the auditor’s quality audit team.
Additionally, the auditor demonstrates proficiency in independent decision-making in regards to the interpretation of standards and regulations, performance of investigations, and other quality practices.
The auditor has a history of successful process improvement implementation.
Key Responsibilities:
GLP Studies
* Review each GLP study prior to release for testing.
* Audit a portion of each GLP study.
* Review each GLP study and final report prior to mailing.
Regulatory and Policy & Procedural Guidance
* Know and follow GLP, GMP and relevant ISO regulations
* Perform quality event investigations and approvals
* Trend quality events
* Review and approve protocol detail sheets
* Review out of range forms
* Review discontinued studies
* Review and trend amended reports
* Review duplicate reports
* CAPA: Initiation, investigation, resolution, and verification
* Review documents in Master Control (collaboration and approval)
* Review logbooks
Process Improvement
* Meet regularly with Section Leader, Study Directors and Lab Analysts
* Prepare Dashboard and Quarterly Management Review with Section Leader
* Audit studies in-process
* Assist Regulatory Affairs with internal audits
* Review and approve equipment qualifications and test method validations
* Perform good housekeeping (GHP) audits
* Perform other duties as assigned.
Professional Development
* Complete required training on time (includes MasterControl, live company trainings, New Employee Orientation, etc.)
* Know and follow company pol...
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Type: Permanent Location: Taylorsville, US-UT
Salary / Rate: Not Specified
Posted: 2026-06-05 08:38:39
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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: 2026-06-05 08:17:47
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Position Summary:
The Environmental, Health & Safety (EHS) Specialist is responsible for supporting the effective EHS management system that will ensure ongoing compliance towards TPI Composite’s EHS standards and regulatory compliance, while improving site safety culture.
The EHS Specialist will actively collaborate and participate as a valued member of the site team to provide EHS guidance, technical support and coordinate activities and processes across the site.
The position includes a balance of environmental and safety experience/responsibilities.
Essential Duties and Responsibilities:
• Coordinates and implements EHS programs designed to provide and maintain a sustainable work environment.
• Establishes best practices and develops and implements training programs to maintain compliance with applicable local, state, and federal EHS regulations, as well as internal policies and procedures.
• Works with EHS Manager to oversee the development and advancement of the EHS management system, self-audit compliance program and internal inspections.
• Evaluates and implements productivity improvements within the EHS discipline using TIPS and Lean tools.
• Leads cross-functional efforts to continuously improve plant improvement processes.
• Attends team meetings in support of the site’s compliance efforts.
• Provides interpretation of existing and upcoming EHS issues/legislation affecting the plant.
• Provides expert guidance to EHS and site leaders on environmental matters and compliance system design and implementation.
• Proposes innovative strategies and programs for existing, emerging and new environmental concerns.
• Serves as EHS focal point for designated plant product line(s).
• Investigates incidents and compliance issues to determine and eliminate root causes.
• Develops cost effective programs/procedures to minimize plant’s impact on the environment due to discharges, emissions, and releases.
• Prepares and/or reviews routine reports for submission to agencies, trade associations, and company.
• Supports site emergency response processes.
Education/ Skills/ Experience:
• Bachelor’s degree (B.S.) or equivalent from four-year college or technical school and one to four years’ related experience and/or training in EHS with experience in regulatory structure in a manufacturing; or equivalent combination of education and experience.
• Proven track record of results; providing functional coaching in a manufacturing environment.
• Effective communicator with demonstrated ability to communicate effectively at all levels of the organization.
Able to interact comfortably with business and operations leaders to establish credibility and influence where necessary.
• Strong computer and data management skills desired.
Experience with web-based applications, ...
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Type: Permanent Location: Newton, US-IA
Salary / Rate: Not Specified
Posted: 2026-06-05 07:53:19
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Who we are
Tricentis is a global leader in continuous testing and quality engineering.
The Tricentis AI-based, continuous testing portfolio of products provides a new and fundamentally different way to perform software testing.
An approach that’s totally automated, codeless, and intelligently driven by AI.
It addresses both agile development and complex enterprise apps, enabling enterprises to accelerate their digital transformation by dramatically increasing software release speed, reducing costs, and improving software quality.
Widely credited for reinventing software testing for DevOps, cloud, and enterprise applications, Tricentis has been recognized as a leader by all major industry analysts, including Forrester, Gartner, and IDC.
We empower innovators to push the boundaries of software testing, fostering a global community of continuous learners who pioneer AI-powered, highly performant, highly secure end-to-end testing tools that accelerate our customers’ time to market including the largest brands in the world.
About the role
As a Tricentis Commercial Customer Growth Account Manager, you will be the main point of contact for customers after the sale, ensuring they get value from their purchase and maximize the value of their Tricentis investment.
Your role will involve managing customer relationships to foster ongoing engagement, accelerate time to value, promote continuous usage, and resolve issues promptly.
A key focus will be driving renewals and expanding accounts by navigating enterprise organizations and working closely with Champions and account teams to secure timely renewals.
Key Responsibilities
* Be primary post-sale point of contact for all Customer Accounts tied to your role by engaging proactively with various customer teams on a regular basis
* Establish an action-oriented and rigorous approach to regularly engage with customers, ensuring consistent communication and driving results.
Maintain visibility to your communications by accurately reporting customer interactions and updating systems and tools with critical insights and key findings
* Collaborate with customers to deeply understand their unique business goals and objectives, aligning product capabilities to their strategic priorities
* Develop and maintain a shared success plan with each customer, outlining key milestones and measurable outcomes that demonstrate progress toward their goals
* Proactively guide customers in achieving their objectives by leveraging product features, providing recommendations, and connecting them with additional resources or services
* Lead discovery sessions to identify additional use cases or unmet needs where the company’s solutions can add value, expanding the footprint within the customer’s organization
* Build relationships with stakeholders beyond the primary point of contact, proactively engaging with executives, influencers, and end-users to uncover ne...
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Type: Permanent Location: Bonifacio Global City, PH-00
Salary / Rate: Not Specified
Posted: 2026-06-05 07:41:24
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ERM has an immediate hiring need for multiple Field Biologists to conduct plant and wildlife surveys in New Mexico and Arizona. Successful candidates must be flexible and responsive to a 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 (50+ hours a week) limited-term role, with a duration of 2 months and the possibility of extension.
RESPONSIBILITIES:
* Field biologist position to conduct plant and wildlife surveys across the Arizona and New Mexico territory.
* Work locations are often remote and requires bio to work independently or with teams.
Other special status species surveys and monitoring may be required, based on available skills.
* Plant and wildlife surveys following strict protocols and providing quality data for reports to multiple different agencies and the client.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s safety program.
REQUIREMENTS:
* Minimum of 2 seasons of Field Biologist survey experience required.
* Bachelor’s degree in environmental science or related field preferred.
* Burrowing owl, Desert Tortoise, and native plant experience preferred.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in 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.
* Demonstrated independent and effective problem-solving and decision-making skills.
* Possess a valid driver’s license.
* Fluency in English and Spanish a plus.
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, healt...
....Read more...
Type: Permanent Location: Scottsdale, US-AZ
Salary / Rate: Not Specified
Posted: 2026-06-05 07:29:44
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ERM is hiring Archaeological Field Technicians to support future needs of survey efforts for projects located across Arizona.
Archaeological Field technicians will assist with or conduct archaeological field surveys or monitoring.
This is a full-time (40+ hours per week), limited-term role with possible extension.
RESPONSIBILITIES:
* Conduct intensive pedestrian surveys consisting of visually inspecting the ground surface for presence of artifacts;
* Monitoring alongside construction crews to avoid impacts to resources;
* Properly identifying artifacts and recording their provenience;
* Delineating site boundaries;
* Maintaining field notes;
* Assist with background research, tabulating results and drafting portions of technical reports as needed;
* Compliance with corporate and client Health and Safety Requirements;
* Work as part of a team to collaborate with others to meet project expectations such as communication, scheduling, and budgeting; and
* Performing other duties as assigned or required.
REQUIRED:
* B.A.
in Anthropology or closely related field is preferred;
* 1 year of related experience with Southwest perfered;
* Ability to travel extensively throughout Arizona;
* Archaeological field school or prior archaeological field survey experience;
* Ability to work outdoors in variable weather conditions and on varied terrain;
* Ability to work weekends and over 40 hours per week when needed;
* Working knowledge of archaeological survey and monitoring protocols;
* Ability to work in the field for extended periods of time;
* Ability to work independently and as a part of a crew;
* Must meet criteria identified in Job Demands & Conditions Analysis for Office and Field Positions;
* Master’s in Anthropology 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 issues.
We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strategic and technical solutions that advance objectives on the ground or at the executive level.
Please submit your resume and brief cover letter.
Based on review of these re...
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Type: Permanent Location: Scottsdale, US-AZ
Salary / Rate: Not Specified
Posted: 2026-06-05 07:29:42
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ERM has an immediate hiring need for multiple Field Biologists to conduct plant and wildlife surveys in New Mexico and Arizona. Successful candidates must be flexible and responsive to a 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 (50+ hours a week) limited-term role, with a duration of 2 months and the possibility of extension.
RESPONSIBILITIES:
* Field biologist position to conduct plant and wildlife surveys across the Arizona and New Mexico territory.
* Work locations are often remote and requires bio to work independently or with teams.
Other special status species surveys and monitoring may be required, based on available skills.
* Plant and wildlife surveys following strict protocols and providing quality data for reports to multiple different agencies and the client.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s safety program.
REQUIREMENTS:
* Minimum of 2 seasons of Field Biologist survey experience required.
* Bachelor’s degree in environmental science or related field preferred.
* Burrowing owl, Desert Tortoise, and native plant experience preferred.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Demonstrated independent and effective problem solving and decision-making skills.
* Possess a valid driver’s license.
* Fluency in English and Spanish a plus.
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 environ...
....Read more...
Type: Permanent Location: Scottsdale, US-AZ
Salary / Rate: Not Specified
Posted: 2026-06-05 07:28:03
