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SRI Healthcare, LLC, a Subsidiary of NOVO Health Services offers a healthcare service that provides a total and unique opportunity for hospitals to source their Sustainable Reusable Sterile Packs as well as other sustainable healthcare linens such as DermaTherapy®, Isolation Gowns, Sterilization Wrap, and cubicle/privacy curtains.
SRI's products and services help Healthcare providers attain their sustainability goals, improve surgeon and staff satisfaction while ensuring continuity of supply.
SRI operates three regional processing facilities located in Raleigh, NC, Chattanooga, TN, and Mason, OH.
Our state-of-the-art, FDA-regulated service centers provide daily processing, assembly, and delivery of reusable products required for surgery.
SRI is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with Sterilized Reusable Surgical Solutions.
Get to know us: SRI Health Care, with headquarters in Atlanta, GA, offers linen management solutions to the healthcare industry.
SRI keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen utilization by department to eliminate excess internal costs.
SRI’s wide range of service programs offer a variety of options to provide a seamless, single source distribution system.
SRI’s regional healthcare linen facilities are HLAC accredited and operate with state-of-the-art processing equipment and processes.
SRI Health Care is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with both Healthcare Laundry Services as well as Sterilized Reusable Surgical Solutions.
Job Summary:
We are currently looking for a Team Lead Soil Sort, at our Chattanooga, TN Healthcare Laundry facility.
We are looking for someone who is confident in decision making, can act quickly, and has excellent communication skills.
If you are ready to make a commitment to measurable performance and continuous improvements, then we want to hear from you!
The successful candidate:
* Know all soil sort operations, including Standard Operating Procedures and Q.A.
functions, and ensure adherence by soil sort personnel to established standards.
* Train all new soil sort employees.
* Make recommendations to facility management on soil sort methods or production standard changes.
* Assist facility management in employee hiring process and evaluations as needed.
* Keep accurate records to comply with written Standard Operating Procedures.
* Facility management in scheduling of any testing, validation, etc.
* Maintain cleanliness
* Ability to read and understand all Standard Operating Procedures.
* Other duties as assigned.
Job Requirements:
* Extremely organized and detail-oriented.
* Able to keep precise records.
* Good interpersonal skills.
* Able to train new...
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Type: Permanent Location: Chattanooga, US-TN
Salary / Rate: Not Specified
Posted: 2025-05-22 09:24:03
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium, Breda, Netherlands
Job Description:
We are looking for a driven Manager Clinical Operations to join our growing Clinical Operations team in Belgium (Beerse) and The Netherlands (Breda).
As a Clinical Research Manager, you will manage a team of Local Trial Managers (Local project managers), Site Managers (Clinical Research Associates) and Clinical Trial Assistants, with a strong focus on staff performance, people development, training/onboarding and resource management.
You are responsible for the successful implementation and execution of phase Ib-IIIb trials from country feasibility through study close-out while keeping clear oversight of timelines, budget, quality & performance indicators and compliance with Standard Operating Procedures (SOPs), Health Care Compliance (HCC) and local regulatory requirements.
We are seeking to hire a strong leader, who is a team player, with quick learning and problem-solving abilities.
You will contribute to the creation of the country strategy in order to optimize ways of working, drive innovation, and strive for continuous improvement and future readiness.
You will be part of a hardworking, enthusiastic, and committed team eager to deliver and helping to improve the lives of millions of patients.
Principal Responsibilities:
* People management: Provide line management to your team including goal setting, performance evaluation and talent development; Build, hire and train a fully effective team; Conduct accompanied site visits; Evaluate and forecast resource needs and manage your team's workload.
* Trial delivery & oversight: Accountable for robust feasibility processes and oversight of site selection.
Responsible for implementation, execution and monitoring of trials in assigned therapeutic area(s).
Empower your team to deliver on your team's quality and performance objectives.
Ensure inspection readiness at all times, adherence to ICH-GCP, local legislation and relevant SOP's.
Support your team in issue resolution and stakeholder management.
Support audits, inspections and timely CAPA resolution.
Build and shape internal and external network in assigned therapeutic area.
* Continuous improvement & organizational change: Lead implementation of innovation and change in the local organization; Cul...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-22 08:49:27
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Enterprise Management
Job Sub Function:
R&D Management
Job Category:
People Leader
All Job Posting Locations:
Galway, Ireland
Job Description:
Johnson & Johnson MedTech Neurovascular are looking for an R&D LCM (Lifecycle Management) Manager / Principal Engineer
Location: Ballybrit, Galway
Johnson & Johnson MedTech Neurovascular
J&J MedTech Neurovascular is a global leader in neurovascular care.
Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship.
J&J MedTech Neurovascular offers a broad portfolio of devices used in the endovascular treatment of hemorrhagic and ischemic stroke.
What is it like to work at J&J MedTech Neurovascular Galway?
* Culturally, we are putting the needs of Our Credo stakeholders first through pursuing the highest standards of quality, compliance, and ethics, ensuring everyday actions contribute to Our Purpose.
* We are continuing to better our understanding of clot science, through our Neuro Thromboembolic Initiative (NTI).
This is a commitment to advance the treatment of stroke through interdisciplinary collaboration and investment in clot and stroke research.
How we understand clots and their behaviour enhances our opportunity to design devices that improve patient outcomes and, overall, advance the treatment of acute ischemic stroke.
* Strong new product pipeline and the fastest growing medical device company within J&J in 2021.
* From a People perspective, we invest in our people, and take great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation.
This is empowered through our employee resource groups (ERGs) focused on further balances of gender, nationality, capability and more, including the additional attracting of qualified diverse candidates for our open roles.
Job Summary:
Johnson & Johnson MedTech Neurovascular is recruiting for a R&D LCM Manager in Galway Ireland.
The R&D LCM Manager will be responsible for managing design changes and sustaining activities providing technical leadership and judgment to a team of engineers in the life cycle of a portfolio of devices to treat ischaemic and haemorrhage stroke.
The R&D LCM Manager is also responsible for co-ordinating the activities of a multi-disciplinary team to ensure the successful compl...
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Type: Permanent Location: Galway, IE-G
Salary / Rate: Not Specified
Posted: 2025-05-22 08:48:52
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
The Analyst, Global Finance Master Data, is responsible for service delivery of specific Global Finance Master Data process functions serviced by GS Finance-Manila in J&J.
Key Responsibilities:
* Perform day to day operations of Financial Master Data team which includes maintenance of GL Accounts, Profit Center, Cost Center, Internal Order and Exchange Rate in line with Global DTP and defined standards
* Proactively identify, rectify and follow-up errors and causes of errors.
* Ensure timeliness, accuracy and quality of work and service by Finance Master Data team through regular review, checks and approval.
* Resolve complex or critical process issues which go beyond Finance Master Data team member’s capabilities.
* Handle risks through mitigation.
* Ensure that documentations are complete and up-to-date.
* Initiate, monitor and review systems’ accesses of the team.
Identified gaps are to be
* Support auditors and legal authorities with the execution of required activities – ensure staff are available as the need arises.
* Ensure strong internal controls are in place, in order to achieve “adequate” internal and external audit ratings.
* Accurate and timely month-end reporting.
Meet all corporate and regional deadlines
Qualifications:
* Bachelor's Degree in Accountancy or Finance
* Open to fresh graduates
* Experience in Finance Master Data Management or Account to Report is preferred
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-05-22 08:48:06
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Post Doc – Drug Discovery & Pre-Clinical/Clinical Development
Job Category:
Career Program
All Job Posting Locations:
Lisbon, Portugal
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
The GSSRM Pharm.D.
Fellowship is a training program designed to prepare the Fellow to become proficient at safety analyses and ad hoc report writing.
The Fellow, in partnership with the Medical Safety Officer (MSO) and under the mentorship and support from the preceptor, is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.
The Fellow will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a product’s safety strategy, complete safety analyses and evaluations, proactively review safety data/lead safety data review meetings and interpret safety information to make a recommendation, supporting SMT deliverables as required.
The Fellow will gain a high-level understanding of case processing, safety surveillance, and review of medical literature and clinical trial data.
The Fellow will function under the guidance/support from the preceptor, and other team members, be able to link discussions to content, and deliver quality results with guidance from the preceptor and the team.
Key Responsibilities:
* Support safety evaluations, including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)/MSO and other stakeholders as necessary, data retrieval, data analysis, report writing, and report revision.
* With mentorship from the preceptor and/or Safety Analysis Scientist (SAS), ensure high quality safety evaluations and reports with moderate comments from stakeholders and moderate revisions required.
* Provide support to SAS for novel projects, to bring value through completion of task-based activit...
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Type: Permanent Location: Lisbon, PT-11
Salary / Rate: Not Specified
Posted: 2025-05-22 08:47:42
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Specialty Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States, Columbus, Ohio, United States, Detroit, Michigan, United States, Pittsburgh, Pennsylvania, United States of America
Job Description:
This is a field-based role available in multiple states within the US.
While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
We invite candidates from various locations to apply and encourage you to review the following states/cities where this opportunity is available:
Cleveland, OH
Columbus, OH
Pittsburg, PA
Michigan
Johnson & Johnson is recruiting for a District Business Manager to support our J&J Vision business, responsible for key distributor and direct accounts. The district for this position will include Cleveland OH, part of Columbus OH, Pittsburgh PA and Michigan.
This is a field-based position with the ideal candidate residing in Cleveland, OH.
About Johnson & Johnson
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
About Vision
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medte...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-22 08:46:27
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Principal Scientist, Analytical Comparability & Product Characterization – Advanced Therapies to be in Malvern, PA.
Purpose:
The Biotherapeutics Development - Analytical Development (BioTD - AD) group is seeking an upbeat, highly motivated Principal Scientist to focus on analytical comparability and product characterization for advanced therapy modalities. The individual would work with team to develop product comparability study approaches for advanced therapy modalities that will be endorsed by the health authorities. A successful candidate will have experience with the design, execution and optimization of a broad range of characterization assays and will have the opportunity to engage in multi-functional teams.
They will learn from and contribute to industry-leading drug discovery/development programs that has brought numerous quality therapeutics to patients and has made significant contributions to human health.
Primary Responsibilities:
·Design and lead the execution of analytical comparability studies for advanced therapy modalities across various stages of development.
·Lead the execution of the advanced methodologies associated with comparability and deep characterization of cell and gene therapy.
·Author or coordinate appropriate IND/IMPD/BLA/MAA sections & interact with regulatory agencies to address CMC-comparability and product characterization related inquiries.
·Optimally communicate comparability study plans, statistical justifications, and results and scientific data to cross-functional teams, project teams, and health authority as needed.
·Collaborate to develop innovative approaches to challenging solutions for analytical comparability strategy and product characterizati...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-05-22 08:46:24
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Communications & Corporate/External Affairs
Job Sub Function:
External Communications
Job Category:
Professional
All Job Posting Locations:
US017 NJ New Brunswick - 1 J&J Plaza
Job Description:
Johnson & Johnson is recruiting for a Director, Global Finance Communications.
This position is in New Brunswick, New Jersey.
Position Summary
The Director, Global Finance Communications will lead communications strategies that amplify J&J’s narrative regarding its financial positioning, business focus and strategic direction to external, financial and investor community and business media audiences.
The Director will be responsible for partnering directly with Investor Relations, business segments, communications colleagues, media relations and key stakeholders to develop, manage, optimize and executive communications strategies for quarterly earnings, financial reporting, M&A Announcements, and other key financial events.
The Director will serve as the direct partner to the VP, Investor Relations, and Media Relations team, triangulating key messages and communications approaches to critical investor engagements and financial media opportunities for the CFO and other Finance leaders.
Responsibilities
* Lead communications strategies that amplify J&J’s financial positioning, business focus and strategic direction to the external, financial and investor community and business media audiences.
* Partner with Investor Relations and across business segments, communications colleagues, media relations and key stakeholder groups to develop, manage, optimize and executive communications strategies for quarterly earnings, financial reporting, M&A Announcements and other key financial events such as the annual shareholders meeting and investor days.
* Serve as the direct partner to the VP, Investor Relations and Media Relations team, triangulating key messages and optimal communications approaches to critical financial engagements, business and industry media and media opportunities for the CFO and other Finance leaders.
* Develop and maintain relationships with key media, trade, influential stakeholders, and communication partners.
* Lead a matrixed team of indirect resources, peer groups and agency vendors.
Required
* A minimum of bachelor’s degree
* 10+ years of experience in Communications
* People management with a focus on engagement and development
* E...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-22 08:45:50
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At EVRAZ, our strength starts with our people! As a team we collaborate to solve problems, contribute ideas and challenge each other to ensure growth and ultimately success for the business and our employees.
RESPONSIBILITIES:
We are seeking a new crew member that is an enthusiastic team player with a strong desire to learn, high safety consciousness, and good time management skills. Under minimal supervision, this person will cut, mill, and handle steel plate and samples in preparation for laboratory properties testing. Key responsibilities include but are not limited to:
* Cuts test coupons to required dimensions using CNC plasma/oxy-fuel burn table and hand torch
* Prepares steel test samples using CNC and manual lathes, saws, milling machines, and grinders
* Verifies, collects, transports, and checks in samples from other departments to the laboratory
* Inventories samples, including identifying, labeling, organizing, and other material handling concerns
* Performs other duties as they might be assigned
REQUIREMENTS:
* Able to read and follow detailed procedures, roll pages, and quality prints (work documents)
* Maintains accuracy of material identifying labels and descriptors legibly and without transposing figures
* Robust math skills: addition, subtraction, multiplication, division, accurate number identification
* Valid driver license
* High school diploma/GED or equivalent experience
* CNC burn table and hand torch cutting experience preferred
* Experience defining quality sample dimensions using micrometers and precision measuring equipment preferred
* Shop experience, including saws, sanders, cranes and forklift operation preferred
* Machine shop experience, including CNC and manual lathes, mills, grinders, broaches, and laboratory testing preferred
* Must be able to work in an environment subject to fluctuations in heat, humidity, fumes, odors, dust and noise
* Able to regularly lift up to 50 pounds
* Able to stand up to 12 hours per shift
Our total compensation package includes amazing benefits!
* Competitive wages and bonus opportunities
* Family medical, dental, and prescription coverage at minimal employee cost
* Short and long term disability programs
* Competitive retirement plans
* Flexible Spending and Health Savings Accounts
* Employer-provided and Voluntary Life Insurance options
* Paid vacation and recognized statutory holidays
* Apprenticeship and career advancement within the company
* Tuition reimbursement
* Wellness program
All applicants must be eligible to work in the USA.
While we thank all those who apply, only those being actively considered for employment will be contacted.
Equal Opportunity Employer
EVRAZ North America is an Equal Opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, nati...
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Type: Permanent Location: Portland, US-OR
Salary / Rate: Not Specified
Posted: 2025-05-21 08:49:48
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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: SFE & Market Intelligence Analyst
As a Sales Force Excellence & Market Intelligence Analyst, you will be part of the Commercial team to deliver data-driven insights to optimize sales execution.
In this role, you'll be responsible for advancing CRM optimization, performance analytics, and customer segmentation strategies.
Your Responsibilities:
* CRM Management: Maintain, improve, and provide support for CRM systems, ensuring data accuracy and consistency.
* Sales Force Enablement: Train and support sales teams on CRM usage and data-driven decision-making, monitoring key performance indicators.
* Territory Management: Implement and optimize territory strategies, including segmentation, sizing, and route optimization.
* Performance Reporting: Generate reports and dashboards to track and analyze sales execution performance.
* Market Analysis: Collect, analyze, and interpret market, sales, pricing, and competitor data to provide actionable insights.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor's degree in management, finance, technology, or similar field
* Required Experience: A minimum of 2 years of experience in CRM software proficiency (e.g., Salesforce), data management, customer service, Power BI, Microsoft Office Suit.
English is a must
What will give you a competitive edge (preferred qualifications):
* Experience in pharma or animal health
Additional Information:
* Travel: 0% - 10%
* Location: Bogota, Colombia
Don’t meet every single requirement? Studies have shown underrepresented 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 focusing on financial, physical, and mental well-being wh...
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Type: Permanent Location: Bogota, CO-DC
Salary / Rate: Not Specified
Posted: 2025-05-21 08:48:36
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Primary Function
The Global EHS Manager is responsible for developing, implementing, and maintaining innovative EHS programs and systems that foster a robust safety culture, proactive analytics, risk mitigation and ensuring compliance across all AAG facilities worldwide.
This role requires strategic leadership, regulatory expertise, and a proactive approach to health, safety, and environmental stewardship.
Who We Are
At Amsted Automotive, we’re more than just a company—we’re a community of innovators, creators, and dedicated professionals who take pride in our work and each other.
As an employee-owned organization, every team member has a vested interest in our success and shares in our achievements.
This unique ownership culture fosters a collaborative, supportive environment where your ideas and contributions truly matter.
Come join us and be part of a dynamic team that’s transforming the industrial and automotive industries while shaping the future of mobility!
What’s In It for You
We create a supportive environment where employees thrive! With a range of benefits designed to enhance your health, well-being, and financial security, we’re here to support you every step of the way.
Join us and experience the exceptional perks that make Amsted Automotive a great place to work!
Health And Wellness
• Medical Insurance
• Dental and Vision Insurance
• Prescription Drug Benefits
• Wellness Reimbursement
• Telehealth
• Onsite health screenings
• Mental health resources
• Employee Assistance Program that includes counseling and support services for mental health, family support, financial advice, legal guidance, and more
Financial Benefits
• Competitive Salaries
• Employee Stock Ownership Plan
• Annual Bonus Opportunity
• 401k with Company Match
• Health Savings Account with Company Contribution
• Life and Disability Insurance
Work-Life Balance
• Paid Time Off
• Parental Leave
• 14 Annual Company Paid Holidays
Professional Development
• Training Programs
• Education Expense Reimbursement
• Career Advancement Opportunities
Additional Benefits
• Pet Insurance and Discount Program
• Legal Insurance
• Employee Discounts
• Recognition and Rewards
• Community Involvement
• Workplace Giving Matching Gift Program
Duties and Responsibilities
• Develops, in conjunction with plant operations personnel, safety risk assessments to proactively address potential serious injury and fatalities (SIFs).
Creates short-term and long-term safety improvement plans and actions that can be executed by operations.
• Leads the implementation of global safety projects, respective reporting tools, and ensures key stakeholders remain updated.
Establishes and tracks key safety performance indicators to drive continuous improvement.
• Assists in the development and communication of the overall EHS strategy and roadmap with periodic status updates to stakeholders, ensuring alignment across all globa...
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Type: Permanent Location: Saginaw, US-MI
Salary / Rate: Not Specified
Posted: 2025-05-21 08:31:17
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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 birth-5 years old through Early Intervention and 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.
* Willingness to give insight.
* Open to feedback and commitment to quality of provided services.
* Communicates problematic clinical issues with respective supervisor.
* 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
*...
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Type: Permanent Location: Syracuse, US-NY
Salary / Rate: Not Specified
Posted: 2025-05-21 08:29:40
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
People Leader
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
Job Description:
Position Title: Associate Manager Biologics AD (Bioassay)
Department: TDS-AD Cork
Report to: Associate Director/Manager, Bioassay and Advanced Therapy Stability Sciences
Travel: 5%
Global Compensation Framework Band Number: 26
Therapeutics Development & Supply, Analytical Development (TDS-AD) Cork, is a department responsible for the clinical release and stability testing of drug substance and drug product materials and stability management of the large molecule (therapeutic proteins) portfolio.
In addition to clinical release & stability activities, TDS-AD Cork is responsible for analytical support of large molecules through analytical method transfer, evolving method knowledge as part of the product lifecycle and investigations and manufacturing support.
This job description will outline the role of the Associate Manager Biologics AD who will be responsible for people leadership and talent development of a team of scientists that are responsible for the release and stability testing activities with particular emphasis on bioassays, identity and process impurity assays:
Position Summary:
Reporting to the Manager, Bioassay and Advanced Therapy Stability Sciences (TDS-AD) Cork, the person will be focused on the release and stability testing of the large molecule clinical pipeline and be responsible for the resolution of product related issues.
Given the diversifying of the Johnson and Johnson clinical portfolio, this may include a diverse class of molecules/entities including monoclonal antibodies, bis-specific antibodies, antibody drug conjugates and advanced therapeutic medicinal products (ATMP’s).
This individual should demonstrate technical leadership in analytical technologies and stability sciences and will represent the department on cross-functional and external teams and act as a technical expert.
Main duties and responsibilities:
* Manage the laboratory testing of clinical stability and release samples for the Bioassay Technology team.
* Drive and support a proactive safety culture within the Laboratory.
* Ensure laboratory activities are carried out in compliance with cGMP and appropriate regulatory standards.
* Motivate and develop reports in addition to developing and se...
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-05-21 08:27:41
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Pharmacokinetics & Pharmacometrics
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
We are searching for a talented Principal Scientist pharmacokinetic/pharmacodynamic modeling expert in Translation Pharmacokinetic Pharmacodynamic and Investigative Toxicity (TPPIT) group within Preclinical Safety and Translational Sciences (PSTS), to be located in Beerse, Belgium.
The successful candidate will be employed within our PBPK/PD modelling team in TPPIT.
Key responsibilities:
* Represent PSTS/TPPIT as pharmacokinetic/pharmacodynamic modelling expert in cross-functional project teams and external collaborations
* Independently, develop and apply PBPK/PD models to explore the effects of target and pathway modulation, defining candidate drug target profiles and projection of human exposure profiles.
* Predict human dose and regimen, contribute to exposure and pharmacodynamic biomarker-based decision-making for early clinical trials.
* Interpret and communicate modelling results and impact to project teams
* Designs, conducts, interprets and prepares study and regulatory summaries of PBPK and PKPD M&S activities
* Prepare PBPK and/ PKPD M&S-based strategies to support discovery and development programs
* Drive learning through back-translation of clinical exposure and pharmacodynamic data, offering strategic options for future clinical testing.
* Acts as a main contact for team members in discussions relating to the design of their studies and data analysis to support, clinical candidate selection, development and approval of medicines
* Guides junior colleagues through consultation and mentoring in techniques and processes, and provides functional (matrix) supervision
You will be encouraged to have a desire for learning and innovation, and to continue career development through participation in internal and external scientific meetings, and increase visibility for self, J&J IM R&D, and J&J through publications, participation in external organizations, and presentations at major scientific, industry, and regulatory meetings.
Qualifications / Requirements:
Required:
* PhD in a relevant life science subject area, e.g.
pharmaceutical sciences, pharmacometrics, computational biology, chemical/biomedical engineering, or a related field
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-21 08:27:26
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
People Leader
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
Basic purpose of the role
* Leading the EH&S organization for Janssen Biologics (JBV) site in the Netherlands (NL).
This consists in deploying, leading, and implementing EH&S strategies, policies, plans, procedures for JBV.
Key outcome is ensuring the EH&S team has taken all needed EH&S precautions to assure continuous, EH&S reliable & compliant supply chain, research & development activities, and is continuously improving in the field of EHS.
* Familiar with the annual company /division goals and aware of how he/she can influence these through his/her performance.
* Results achieved through effective leadership of the JBV EH&S team and through effective collaboration / influencing key leadership teams on the JBV EHS team as well as with J&J global EH&S.
All their needs/ improvements to be balanced with global/ local context.
The EH&S lead decides how to convert these in a lean, results oriented, compliant EHS approach.
* Responsible for developing and coordinating site EHS&S infrastructure to help GM & Site Management to ensure compliance with legislative and J&J requirements.
* Partner with Site LT to establish and implement site EHS&S strategy and Management Action Plan (MAP) in alignment with the J&J requirements.
* Responsible for site EHS&S department including budget (OPEX &CAPEX)
* Coach and mentor line management to take ownership of EHS&S.
* Ability is to reach outside J&J and represent the JBV EH&S team when meeting with governmental inspectors for the site.
Key Responsibilities
* Shared responsibility with site General Manager for EHS&S performance at the site.
Responsibility to provide advice to Site Manager for EHS&S performance at the site.
* Partner with local Management to develop and implement a site MAP to address EHS&S program deficiencies and ensure EHS&S regulatory compliance.
* Build effective working relationships with staff and key stakeholders including corporate EHS&S function and regulatory authorities.
* Develop EHS&S objectives for the site - auditing, analyzing, documenting, reporting on their implementation / effectiveness to management via dashboards, reports & management re...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-05-21 08:26:31
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ERM is looking to hire an experienced Principal Technical Consultant, Environmental Toxicologist and Ecological Risk Assessor to join our growing Risk Assessment practice. The successful candidate will produce and direct expert ecological risk assessments with a focus on oil and gas exploration locations in Gulf Coast wetland habitats.
Candidates will be considered for offices located in Baton Rouge, LA, New Orleans, LA, Houston, TX, Austin, TX or Dallas, TX, depending on the applicant’s qualifications.
RESPONSIBILITIES:
* Write, manage, and produce ecological risk assessments.
* Design and implement biological field investigations.
* Manage, direct, and train junior environmental staff.
* Research toxicities and physical/chemical properties of oil and gas constituents and develop and implement site specific risk assessment methods.
* Write expert reports, design field investigation plans, write technical papers for clients, conduct large scale ecological risk assessments.
* Work collaboratively with other senior level staff to achieve client goals.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Provide support in ensuring compliance with all federal, state and local regulations.
* Communicate daily with clients, regulatory agents, and subcontractors.
REQUIREMENTS:
* Master’s Degree or Ph.D.
in toxicology, environmental toxicology, chemistry, ecology, or related life science discipline.
* 6-8 years (10+ years preferred) of relevant experience; consulting experience preferred.
* Experience testifying as an expert witness is preferred.
* Strong commitment to safety, including following established Health and Safety protocols.
* Excellent verbal, written, and personal communication skills.
* Strong quantitative skills and experience managing and analyzing large datasets using MS EXCEL.
* 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.
* Ability to succeed in consulting by working efficiently, handling multiple project assignments, maintaining flexibility, and meeting strict deadlines.
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 or...
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Type: Permanent Location: Metairie, US-LA
Salary / Rate: Not Specified
Posted: 2025-05-20 08:57:45
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ERM is looking to hire a motivated, detail-oriented Managing Technical Consultant, Environmental Toxicologist and Risk Assessor to join our growing Risk Assessment practice in Austin, TX. Working under the direction of project managers and partners, the successful candidate will work on interesting ecological risk assessments and projects focused on oil and gas exploration in Gulf Coast wetland habitats.
This position is being offered in our Austin, TX office.
However, candidates may also be considered for offices located in Houston, TX, Baton Rouge, LA, New Orleans, LA, or Dallas, TX, depending on the qualifications of applicants.
This is a great opportunity to work with ERM's technical experts to grow your career providing environmental consulting services.
RESPONSIBILITIES:
* Support ecological risk assessments and site investigations.
* Manage, query, review, and analyze large chemical and biological data sets.
* Conduct literature searches and reviews on toxicological, biological or other risk assessment subject matters.
* Prepare work plans, figures, and technical reports.
* Focus on team project delivery, taking direction primarily from Task Managers and Project Managers.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Support in ensuring compliance with all federal, state and local regulations.
* Assist in communication with clients, regulatory agents, and subcontractors.
REQUIREMENTS:
* Bachelors in toxicology, environmental toxicology, chemistry, public health, ecology, or related life science discipline.
Minimum 3.0 GPA.
Advanced degree (MS or higher) preferred.
* 4 to 5 years of relevant experience; consulting experience preferred.
* Strong commitment to safety, including following established Health and Safety protocols.
* Effective written/verbal communication and organization/analytical skills are required; experience recording/writing detailed technical data and reports a plus.
* Strong quantitative skills and experience managing and analyzing large datasets using MS EXCEL.
* Ability to work independently and as part of a team.
* 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.
* Ability to succeed in a consulting pace, handling multiple project assignments, and maintaining flexibility, while meeting strict deadlines.
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 esse...
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-05-20 08:57:44
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Classification:
Non-Exempt
Job Summary:
As a Sales Consultant, you’ll be the driving force behind the top-line growth of the branch you report into.
In this position, you will report to a Regional Sales Manager that will train you, coach you and assist you in closing new business.
After your 13-week training period, you will be ready to identify and secure new customers, build relationships, and deliver customized solutions for all types of businesses in food & beverage, industrial and healthcare industries that use linen, uniforms, and facility services like first aid and restroom supplies. With the support of a dedicated team, you’ll develop your skills, meet your financial goals, and help your branch achieve its growth goals.
About Us:
At Alsco Uniforms, we don’t just sell uniforms and linen laundry services – we offer solutions to help businesses maintain a safe and clean environment for their employees and customers.
Since 1889, Alsco Uniforms has been a family-owned company that is headquartered in Salt Lake City, Utah.
Today, the company operates over 80 laundry facilities throughout North America and proudly serves more than 125,000 customers in all industries.
What makes Alsco Uniforms special? It’s our people.
Our team members are the driving force behind our success, fueling decades of strong financial performance, innovation, and unmatched service.
We’re looking for ambitious sales professionals who are ready to grow their careers with us.
If you’re seeking competitive pay, excellent benefits, and a company that invests in your success, Alsco Uniforms is where you belong.
Your sales mission is simple: Showcase to prospects why It Pays to Keep Clean with Alsco Uniforms.
This is done by offering tailored solutions that keep businesses safe, spotless, and ready to thrive, ensuring a healthier and more professional environment for their employees and customers.
Join our team and take the next step toward a fulfilling and dynamic career path!
Why Choose Alsco Uniforms?
* The solutions we offer are essential laundry services to all types of businesses.
Any business is a prospect of ours, and we give our Sales Consultants territories with plenty of prospects.
* We operate over 80 laundry facilities across North America and have a global presence in more than 13 countries.
Despite our worldwide reach, our culture remains people-focused, prioritizing stability while offering a career with strong growth potential and clear paths for advancement.
* Professional training along with ramp-up quotas to ensure you are successful from day one.
* The corporate marketing team and local service team that is dedicated and compensated to provide high quality leads to you.
* Opportunities for professional growth and leadership development.
* An inclusive and diverse team environment that values your unique contributions.
Our full-time employees enjoy:
* 401K Plan with Company Match
* Medical...
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Type: Permanent Location: New Castle, US-DE
Salary / Rate: Not Specified
Posted: 2025-05-20 08:57:35
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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!
Scope:
The account person is responsible for developing business relationships with targeted poultry farm, swine farm and vaccine product distributions, veterinarians that are involved in vaccine business.
Responsibilities:
* Develop annual business plans for targeted key account incorporation execution plans by species and products.
* Accountable for achieving annual sales quotas within allocated expenses.
* Incorporate the Concepts of Customer Selling Skill (CVS) and Strategic Account Management (SAM).
* Apply territory management to optimize time and selling efforts.
* Submit monthly forecast by customer
* Work to satisfy customers’ needs – for example recommending solutions to the problems regarding diseases, managements, food safety, etc.
* Convey solutions/recommendations to customer’s management from the farm, technical, procurement, manufacturing, sales and distribution to the top of a complex organization.
* Propose ideas to build up high quality tailored-made technical service to each KA feed millers including training/consultancy, technical materials and lab analysis support
* AE/PC – Report adverse events and product complaints as per global and local regulatory requirements.
* Adhere to company policies and procedures when interacting and promoting products to customers, to protect the Elanco brand and business.
* Adhere to safe working practices and take reasonable care of self and others.
* Comply with other policies sated in Elanco Code of Conduct as well as Elanco SOPs.
Ensuring myself and my subordinates (if any) comply with the company rules and regulations including Ethics and Compliance and external laws and regulations.
Minimum Qualification (education, experience and/or training, required certifications):
Education/Experience
Graduate of any four year course preferably business or science course. Degree in Veterinary Medicine, Animal Science or any related course is an advantage
Skills and Knowledge:
With at least three years sales experience with proven...
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Type: Permanent Location: Ho Chi Minh City, VN-SG
Salary / Rate: Not Specified
Posted: 2025-05-20 08:51:16
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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: Sr.
Analytical Scientist, Biologics
As an Sr.
Analytical Scientist, Biologics you will be part of Elanco’s R&D team, driving the development of chromatographic, electrophoretic, and LC/MS analytical methods for biopharmaceutical products.
In this role, you’ll be responsible for advancing analytical techniques for therapeutic proteins and vaccines, supporting bioprocesses, and leading method development, validation, and transfer efforts across global sites.
If you are passionate about advancing analytical methodologies and playing a key role in biopharmaceutical development, we invite you to apply and join our innovative team!
Your Responsibilities:
* Develop and optimize chromatographic, electrophoretic, and LC/MS analytical methods for vaccine and therapeutic protein products.
* Innovate and implement analytical solutions for diverse drug formulations and bioprocess support.
* Lead method validation, verification, and transfer activities across global sites and CROs.
* Train and mentor associates and scientists globally to ensure consistency in analytical practices.
* Author technical reports, review scientific documents, and maintain laboratory safety standards.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree with 12+ years or Master’s Degree with 10+ years of experience in Analytical Chemistry, Biochemistry, Biophysics, or a related scientific field.
* Experience: Extensive hands-on experience developing HPLC/UPLC-based, electrophoretic, and LC/MS analytical methods for large molecule characterization.
* Top 2 skills: Strong expertise in analytical method development and validation, with excellent problem-solving and communication skills.
What will give you a competitive edge (preferred qualifications):
* Expertise in recombinant proteins, monoclonal antibodies, oligonucleotides, and peptides.
* Experience with method validation, transfer, and qualification under GMP conditions.
* Strong statistical knowledge and proficiency with statistica...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 123500
Posted: 2025-05-20 08:51:07
-
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 Master Data Consultant
As a Quality Master Data Consultant, you will be part of our Global Master Data team, ensuring best-in-class data governance, process standardization, and optimization of SAP master data.
In this role, you’ll lead a team of analysts, execute master data maintenance, resolve quality management (QM) and vendor master data issues, and drive continuous improvement efforts.
Your focus will be on enhancing data integrity, system capabilities, and business efficiencies.
Your Responsibilities:
* Lead the execution and governance of master data maintenance within SAP and related systems.
* Manage and resolve QM object data issues while ensuring compliance with Standard Operating Procedures (SOPs).
* Assess the impact of data changes and ensure consistency across global business units.
* Identify and lead process improvement initiatives, including troubleshooting SAP execution issues and implementing solutions.
* Support global Quality Master Data Management initiatives, participating in power user forums and knowledge-sharing efforts.
* Drive standardization of data-related processes to enhance organizational efficiency and value.
* Support system releases, scope changes, and process enhancements in SAP.
* Provide transparent reporting and recommendations to leadership to improve data accuracy and compliance.
* Promote SAP as the single source of truth for master data while ensuring proper training and adoption across teams.'
What You Need to Succeed (Minimum Qualifications):
* Education: Bachelor’s degree in a scientific field (quality assurance, computer systems) or equivalent experience.
* Experience: 8+ years of experience as a compliance expert in and ERP within a related industry, specializing in quality and data management.
* Strong knowledge of ERP software, preferably SAP.
* Proven ability to analyze, anticipate, and resolve complex technical and business-related issues.
What Will Give You a Competitive Edge (Preferred Qualifications):
...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 135000
Posted: 2025-05-20 08:51:05
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Your Job
Georgia-Pacific, LLC (GP) is now hiring a R&D Process Engineer for its Tolleson, Arizona Mailers facility.
The R&D Process Engineer supports manufacturing on site including equipment installation, training, acceptance testing, performance testing, and process and equipment upgrades.
The R&D Process Engineer must be able to present data in a concise way to both technical and non-technical audiences.
We believe in the challenge process and this person must be open to the ideas and recommendations of others to create the best outcome for both the site, R&D and i2.
Typical work schedule would be weekdays from 8am-5pm.
Our Team
The GP Tolleson facility employs about 115 people and serves converting customers throughout the Southwest with sustainable packaging products.
This position provides opportunities for promotion within GP Tolleson, as well as many other Georgia-Pacific and Koch facilities across the country.
Come join our team!
You know us already! Georgia-Pacific is one of the nation's leading corrugated sheet and box manufacturers.
Check out these videos/links to learn more about the Corrugated Business at Georgia-Pacific:
www.gppackaging.com
What You Will Do
* Actively engage with Operations, Maintenance, and R&D to identify opportunities for evolutionary changes to the process and equipment
* Update process control and troubleshooting procedures and train plant personnel on current and updated process procedures
* Identify and lead process improvement projects to improve OEE (Overall Equipment Effectiveness)
* Translate learnings and technology upgrades from other sites and work with EHS and site operations to deploy on site
* Support new customer and product trials and production campaigns
* Employ process control best practices and strategies to centerline the process
Who You Are (Basic Qualifications)
* Bachelor's degree in engineering or science
* Previous experience using Microsoft Office programs and other software programs to present data (Word, Excel, Outlook, Teams, Power Bi, etc.)
* Previous experience in a manufacturing facility
* Previous experience moderating meetings and training sessions
* Must be willing and able to travel up to 25%
* Must have legal authorization to work permanently in the United States for any employer without requiring a visa transfer or visa sponsorship
What Will Put You Ahead
* Bachelor's degree or higher in Mechanical, Chemical or Electrical Engineering
* 2+ years of hands-on experience in a manufacturing facility interfacing with quality, operations leadership, maintenance and hourly employees
* Previous experience within a corrugated and/or converting manufacturing facility
* Previous experience developing and executing experiments and monitoring process data
* Previous experience leading process improvement initiatives
* Previous experience in data analysis and/or statistical software (JM...
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Type: Permanent Location: TOLLESON, US-AZ
Salary / Rate: Not Specified
Posted: 2025-05-20 08:46:29
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We are seeking to hire a QC Chemist to join our Quality Control team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required.
Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance.
Responsible for timely analytical data reporting based on project timelines.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
• Demonstrate a more advanced knowledge of various test methods and instrument analysis techniques and be proficient with all sample types and test methods.
Perform more advanced troubleshooting/maintenance of the instrumentation.
• Responsible for more complex physical and chemical testing of raw material, intermediate, and finished products as described in the documented procedures to support product release and process validation protocols.
• Demonstrate proficient ability to operate the instrument software applications, set up advanced sequences, troubleshoot software and report data while executing the higher complexity test methods that utilize instruments such as UV, FTIR, GC, and HPLC, and IC.
• As required, perform swabbing and analysis of more complex manufacturing equipment with no supervision in accordance with cGMP guidelines.
Provide input on cleaning related issues and investigations.
• Evaluate and maintain assigned calibrations for equipment in the laboratory as required and review the required documentation for compliance.
Review instrument qualification documents to support system change control actions and assist vendors during installation and PM’s.
• Investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines.
• Assist Management with writing and completion of investigation sections and product impact as required.
Train others as required as it pertains to LIR/OOS procedures.
• Perform method validation and method transfer activities as required.
• Train other Chemists, Lab Assistants, and temporary personnel.
• Assist with customer and regulatory audits as required for Data Integrity and/or instrument file review.
• Author, revise and update laboratory test methods and Standard Operating Procedures.
• Accurately maintain notebooks and files compliant with current GMPs and internal Standard Operating Procedures.
Peer review and/or audit others work as required for verification of GMP compliance.
• Auditing of laboratory testing data as required.
• Demonstrate consistent ability to perform testing with limited investigations and repeat analyses.
Ability to accurately report test data in various formats along with advising less experienced Chemists.
• Perform cost savings and process improvement ...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-20 08:43:54
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Job Description
Provides support for funded research projects.
Education: Bachelors Degree.
Department
CS-Methods and Applications for Probing Deep Neural Network
General Submission Guidelines:
Please submit an online application to be considered a candidate for any job at Stevens.
Please attach a cover letter and resume with each application.
Other requirements for consideration may depend on the job.
Still Have Questions?
If you have any questions regarding your application, please contact Jobs@Stevens.edu.
EEO Statement:
Stevens Institute of Technology is an Equal Opportunity Employer.
Accordingly, Stevens adheres to an employment policy that prohibits discriminatory practices or harassment against candidates or employees based on legally impermissible factor(s) including, but not necessarily limited to, race, color, religion, creed, sex, national origin, nationality, citizenship status, age, ancestry, marital or domestic partnership or civil union status, familial status, affectional or sexual orientation, gender identity or expression, atypical cellular or blood trait, genetic information, pregnancy or pregnancy-related medical conditions, disability, or any protected military or veteran status.
Stevens is building a diverse faculty, staff, and student body and strongly encourages applications from people of all backgrounds.
Stevens is a federal contractor under the Vietnam Era Veterans' Readjustment Assistance Act (VEVRAA) and the Rehabilitation Act of 1973, as well as other federal statutes.
NSF ADVANCE Institution Stevens values diversity and seeks candidates who will contribute to a welcoming and inclusive environment for students, faculty, and staff of all backgrounds.
We are an NSF ADVANCE institution committed to equitable practices and policies and strongly encourage applications from women, racial and ethnic minority candidates, veterans, and individuals with disabilities.
Jeanne Clery Disclosure:
In accordance with the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act (Clery Act), the Department of Public Safety is required to publish an annual security report which includes statistics mandated by the Clery Act.
Click here for a copy of this report.
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Type: Contract Location: Hoboken, US-NJ
Salary / Rate: 15.49
Posted: 2025-05-20 08:40:23
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Per il potenziamento del Laboratorio Analisi Centrale, che opera al servizio ed in sinergia con i dipartimenti formulativi della sede R&S di Milano ricerchiamo un/una:
R&D Analysis Technician
Principali attività:
* preparare soluzioni reagenti e campioni per le analisi di laboratorio
* lettura schede tecniche e schede di sicurezza dei reagenti di laboratorio
* calibrazione e utilizzo di strumentazione analitica (titolatore, spettroscopie FT-IR, UV-VIS, TOC, analisi chimico-fisiche)
* eseguire analisi in base a norme e procedure interne prestabilite
* registrare nel software di gestione i dati relativi alle analisi
* housekeeping dell’ambito del laboratorio dopo il suo utilizzo
Requisiti richiesti:
* Diploma tecnico a indirizzo chimico/biologico o similari
* Gradita eventuale breve esperienza nel ruolo in settori affini
* Buona conoscenza della lingua inglese
* Approccio metodico e preciso, senso di responsabilità, proattività
* Buone capacità relazionali e team working con diversi interlocutori e livelli
* Curiosità e capacità analitica per portare avanti progetti in autonomia
* Buona conoscenza del pacchetto Office
Ulteriori informazioni:
* Sede di lavoro: Milano
* Contratto da valutare in base alla seniority del candidato
Filosofia aziendale:
* Innovazione e specializzazione
* Internazionalizzazione
* Sostenibilità sociale e ambientale
* Persone al centro
* Pari opportunità e inclusione
Benefits:
* Formazione continua e sviluppo
* Welfare aziendale
* Fondi CCNL (Assicurazione sanitaria e pensionistica)
* Convenzioni aziendali
Chi siamo:
Mapei, fondata nel 1937 a Milano, è una realtà leader nello sviluppo, nella produzione e distribuzione di prodotti chimici e soluzioni per l'edilizia, con oltre 24 Linee di Business in grado di rispondere a qualsiasi necessità nel mondo delle costruzioni.
Attualmente il Gruppo coinvolge oltre 12.000 persone nel mondo ed è composto da 102 Consociate con 81 stabilimenti produttivi nei 5 continenti e 32 centri di ricerca.
Lavorare in Mapei significa far parte di una squadra vincente con grande senso di appartenenza e valori.
Cerchiamo persone con una forte motivazione, flessibilità e passione orientate a sviluppare le proprie competenze ed essere sempre un passo avanti.
MAPEI, il cantiere più importante per il tuo Talento!
L’azienda garantisce il trattamento dei dati ai sensi del Regolamento Europeo n.
2016/679, rinviando all’informativa privacy disponibile proseguendo con la presente candidatura.
La ricerca è rivolta a candidati di entrambi i sessi.
(L.
903/77).
Esplora le Opportunità di carriera sul sito www.mapei.com
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Type: Contract Location: Milano, IT-MI
Salary / Rate: Not Specified
Posted: 2025-05-20 08:31:38
