-
DESCRIPTION
This Environmental Permitting Specialist will lead and coordinate environmental studies and permitting efforts, including wetland delineation, habitat assessments, preparation of Local, State, and Federal permit applications.
Support technical engineering projects in the Great Lakes Region, with a focus on Pennsylvania by leading environmental document preparation and applications such as Erosion and Sediment Control Permits, General Permits, USACE Joint Permit Applications, and Nationwide permits (NPDES).
RESPONSIBILITIES
Coordinate and prepare applications for local, state and federal agencies for a variety of project types, including bridges, highways, dams, public utilities, energy utilities, and other civil/environmental projects, as needed.
This position will leverage experience with agency coordination and agency knowledge/experience to facilitate positive outcomes.
Priorities will include quality control, peer reviews, and coordination among multiple project disciplines.
A knowledge of applicable environmental laws, rules, and regulations to prepare technical reports is required.
Environmental Specialists are an integral part of the team and work closely with planners and engineers through project scoping, design, construction and beyond.
They provide technical guidance to junior environmental staff and assist and/or lead in proposal development, which includes developing environmental scopes, schedules and budgets.
ROLE ACCOUNTABILITIES
* Identify potential permitting requirements and develop permitting strategies to provide guidance to internal and external teams and clients.
* Use strong technical writing and communications skills to support the development of technical reports, work plans, memoranda, and other environmental documents necessary to develop permit applications and supporting materials for various regulatory agencies.
* Support the preparation of permit applications and supporting materials in accordance with specific local, state, and federal regulatory requirements.
* Assist with the coordination of wetlands and waterbodies delineations, flora/fauna surveys, and/or threatened and endangered species field surveys in accordance with applicable regulatory requirements.
* Support task management to assist with the growth of new and existing client relationships through delivery of quality work and data.
* Hybrid work structure allowing remote and office work as needed.
* Coordination of field assessments related to ecological aspects of projects, requiring knowledge of GPS systems and the ability to conduct fieldwork for long hours and in difficult terrain.
* Travel requirements for field assessments.
PROFESSIONAL REQUIREMENTS
* Bachelor’s degree in Environmental Science, Biology, Ecology, or a related field
* 10+ years of related experience
* Relevant regional working knowledge and experience in supporting the preparation of ...
....Read more...
Type: Permanent Location: Moon Township, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-12 08:25:31
-
Global Compliance Specialist
Location: Houston, Texas (Onsite, 5 days a week)
Position Summary:
The Global Compliance Specialist will report directly to the BII Director of Risk and Compliance.
This key role in the Risk Management and Compliance department focuses on ensuring compliance with regulations (both for legal and trade compliance), completing organizational filings and questionnaires, and supporting compliance research and policy writing.
The position is vital for maintaining operational efficiency while adhering to global laws and regulations.
Essential Job Functions and Responsibilities:
Global Compliance:
* Coordinate import and export activities, including audits, record-keeping, and ensuring compliance with U.S.
Customs Regulations, Export Administration Regulations, Foreign Asset Control Regulations, and Anti-boycott Regulations.
* Assign, document, and maintain Harmonized Tariff Codes (HTSUS) and Export Classification Numbers (ECCN) for all products.
* Conduct interviews and compile information for compliance with anti-corruption and other laws and regulations pertinent to the organization’s business activities.
* Develop, implement, and improve internal processes and written work instructions to maintain compliance with regulations.
* Provide training to internal users and gatekeepers on import/export requirements.
* Serve as the primary liaison with Shared Services, customs brokers, and freight forwarders for import/export documentation, licensing, and transaction screenings.
* Stay updated on regulatory changes and update internal policies as needed.
* Coordinate the valuation of imported merchandise, ensuring proper reporting of payments and customs valuation requirements.
* Work with IT to ensure system compatibility with trade compliance requirements.
Patent Administration:
* Maintain a database of patents and trademarks and their respective locations.
* Coordinate communications with intellectual property counsel and advisors.
* Log and track intellectual property registration activity as required.
Compliance Regulations & Research:
* Conduct legal and policy research, interpreting legislation and compliance standards.
* Investigate regulatory requirements, jurisdictional regulations, and government agency guidelines.
* Provide consultation on compliance matters.
* Develop and maintain a global research network.
* Prepare research findings and assist with action planning.
Compliance Policy Writing:
* Develop and draft compliance policies and procedures to support regulatory requirements.
* Assist with the distribution and implementation of compliance policies as directed by the RM&C department.
RM&C Department Support:
* Provide research or project support as assigned by the RM&C Manager.
Position Requirements:
* Highly organized, detail-oriented, and able to manage multiple competing priorities.
...
....Read more...
Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-12 08:16:06
-
Job Category:
Intern
Job Family:
Student Intern
Job Description:
As a Quality Assurance Intern, you will have the opportunity to work the Summer 2026 with Schreiber Foods at one of our plant locations. This internship will be focused on supporting food safety and quality initiatives, company objectives and plant-specific assignments.
It is designed to prepare successful interns for a possible future career with Schreiber Foods.
This Quality Assurance summer internship is located at our plant in Shippensburg, Pennsylvania.
Interns relocating more than 50 miles for the internship will receive a lump sum of $1,500.
This position offers a set rate of pay of $20.75 an hour.
What you’ll do:
* Lead small quality improvement projects within the team, working with plants and other areas of Schreiber Foods
* Creating and updating documentation for food safety and quality and lab processes
* Gaining knowledge about our products and applying that knowledge to improve processes and practices
* Inputting and analyzing data
* Completing projects related to testing, quality systems, sanitation, auditing, HACCP, training, SQF, suppliers, and other related topics
* Assisting the quality teams on ongoing projects
* Together with the leadership team, ensures compliance with Food Safety and Food Quality Plans, in addition to customer requirements.
Interprets and communicates customer requirements to plant production and/or support groups.
Establishes and Audits PCPs, CCPs and Standard Operating Procedures to define and monitor processes, to ensure customer requirements are met.
Reviews incidents during which the procedures are not met and determines appropriate corrective action for partners failing to follow standard procedures.
What you will need to succeed:
* Currently pursuing a Bachelor’s or Master’s degree in Food Science, Dairy Science, Microbiology, Bacteriology, Food Microbiology or closely related field.
* Ability to work 40 hours per week during the summer of 2026
* Ability to work at least 10 weeks of the summer, 12 weeks is preferred, with flexible start and end dates
* Effective oral and written communication skills
* Ability to work independently as well as in a team environment
* Ability to take ownership of assignments and complete them
* Desire to grow and take on new challenges and opportunities
* Ability and desire to work within a plant manufacturing setting
* Ability to multi-task
* Possess a strong technical foundation in the sciences; dairy knowledge desired but not required
* Reliable transportation
Internship benefits:
* Opportunity to complete real-world projects, participate in team meetings and contribute your ideas
* Exposure to different areas of the business around the world
* Internship program that includes engaging events and opportunities to build relationships at all levels
* Relocation as...
....Read more...
Type: Permanent Location: Shippensburg, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:32:45
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Jacksonville, Florida, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Tampa, Florida, United States of America, Titusville, New Jersey, 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
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-027240
* Toronto, Canada - Requisition Number: R-029840
* United Kingdom - Requisition Number R-029838
* Belgium, Spain - Requisition Number: R-029842
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Manager, Global Clinical Operations Learning and Training.
This position is a hybrid role and can be located in Spring House, NJ; Horsham, PA; Raritan, NJ; Titusville, NJ; San Diego, CA; Jacksonville, Florida; Tampa, Florida.
The Clinical Trial Learning and Training (CTLT) organization develops and implements training strategies and designs for clinical trial training and Global Clinical Operations (GCO) functional role-based global onboarding programs.
This includes determining training needs, developing, and implementing strategic learning initiatives, and leveraging resources to deploy the training plan.
CTLT delivers impactful learning and training programs that address gaps and build capabilities to meet future needs while ensuring compliance with relevant Regulations, Standard...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:42
-
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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, 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
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-027513
* Canada - Requisition Number: R-032876
* United Kingdom - Requisition Number: R-032879
* Belgium, Netherlands - Requisition Number: R-032880
* Switzerland - Requisition Number: R-032883
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Director, Global Regulatory Leader.
This position is a hybrid role and can be located in Titusville, NJ; Raritan, NJ; or Spring House, PA.
The Director, Global Regulatory Leader will be responsible for the development, implementation and maintenance of robust global regulatory strategies for select projects spanning the same target disease areas.
Principal Responsibilities:
* Be a key contributor/leader on the Global Regulatory Team and on multiple cross-functional teams.
* Provide strategic direction to the teams and critical review of key Health Authority submissions such as IND/CTAs, meeting requests, briefing documents, response documents and marketing and supplemental applications.
* Ensure that regulatory strategies are aligned with product portfolio, regional strategies, CMC (Chemistry, Manufacturing, and Controls)-Regulatory Affairs strategy, commercial and market access strategy, and the Target Product Pr...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:37
-
Job Category:
Intern
Job Family:
Student Intern
Job Description:
Schreiber Foods is looking for motivated and talented engineering students to join us as interns for the upcoming Summer 2026 across our manufacturing plants in the U.S. We have opportunities in the following communities: Michigan (Grand Rapids), Missouri (Carthage, Clinton, Monett, Mt.
Vernon), Pennsylvania (Shippensburg), Texas (Stephenville), Utah (Logan, Smithfield), Wisconsin (Green Bay, Richland Center, West Bend).
Relocation Assistance is provided if relocating 50 miles or more for this internship.
This is a paid internship with an hourly rate of pay: $22.00
Our Engineering Internship Program offers an exciting opportunity to gain hands-on experience in a food manufacturing environment. Interns will work closely with skilled engineers, contributing to projects that have a direct impact on our operations and success. We offer internship opportunities in various areas of engineering, allowing you to specialize based on your interests and career aspirations.
Interns will also participate in our company Internship Program which includes Executive Speakers, Social & Networking Events and Career Branding & Professional Development.
What you’ll do:
Manufacturing & Process Engineering:
* Focus on the optimization of manufacturing processes.
* Work on process improvements in efficiency, productivity, process capability, risk, and cost reduction.
* Collaborate with cross-functional teams to design and implement efficient manufacturing workflows.
What you need to succeed:
* Completed Sophomore-level status or higher toward a BS degree in an Engineering or Engineering Technology program (Electrical, Automation, Mechanical, Chemical, Engineering Physics or Manufacturing preferred).
Students must be enrolled as student during the time of the internship (Recent or previous graduates will not be considered).
* Willingness to relocate for Summer of 2026.
* Ability to work a minimum of 10 weeks during the Summer of 2026.
* Ability to work 40 hours/week during the summer.
* Strong analytical and problem-solving skills.
* Excellent communication and teamwork abilities.
* Interest in pursuing a full-time career in the areas listed above.
* Ability to take ownership of assignments and complete them on time and accurately.
* Desire to grow and take on new opportunities.
* Reliable transportation.
Schreiber Foods strives to do good through food every day.
Based in North America, we’re a customer-brand leader in cream cheese, natural cheese, process cheese, beverages and yogurt.
Our more than 10,000 employees and presence on five continents enable us to be an essential ingredient in our customers’ success.
With annual sales of more than $7 billion, we partner with the best retailers, restaurants, distributors and food manufacturers around the globe.
We also recognize our responsibility to do good in ...
....Read more...
Type: Contract Location: Green Bay, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-10 08:36:15
-
About the Company
Vantage Group Holdings Ltd.
(Vantage) was established in late 2020 as a re/insurance partner designed for the future.
Driven by relentless curiosity, our team of trusted experts provides a fresh perspective on our clients’ risks.
We add creativity to tech-enabled efficiency and robust analytics to address risks others avoid.
Vantage provides specialty re/insurance through its operating subsidiaries in Bermuda and the U.S.
Vantage has approximately 365 colleagues in both the United States and Bermuda.
We have offices in Chicago, IL, Norwalk, CT, Arlington, VA, Boston, MA, New York, NY, Atlanta, GA and Hamilton, Bermuda.
Additionally, we are a highly geographically diverse workforce with colleagues based in 35 states and counting.
We fully support work flexibility including remote and hybrid work arrangements.
About the role:
The Actuarial Analyst, Pricing Operations & Portfolio Management will play an important role in the Vantage’s Insurance business by supporting the Insurance Pricing and Portfolio Management functions.
These functions, overseen by the Chief Pricing & Portfolio Actuary, are tasked with tracking, analyzing, and reporting key pricing and underwriting metrics.
The Insurance Leadership Team rely on this work as they make decisions for the future of Vantage Insurance.
The successful candidate will work alongside the Head of Pricing Operations & Strategy and the Chief Pricing & Portfolio Actuary to maintain and run models, tools, and processes to ensure the Pricing & Portfolio Management functions are fit for purpose and scalable.
They will take ownership of established pricing operations and portfolio management work.
They should have a keen attention to detail, enjoy solving problems, and proactively contribute to improving pricing operations and portfolio management.
This position will be part of the Insurance Pricing Team and will report to the Head of Pricing Operations & Strategy.
The Pricing Operations & Strategy function has the Pricing Team as their first-line customers.
The other members of the Pricing Team are the business unit pricing actuaries, the Head of Pricing Operations & Strategy, and the Chief Pricing & Portfolio Actuary.
The Pricing Team’s core customers are the Insurance Leadership Team and the underwriting business units.
We prefer this position to be filled by a candidate able to work 2-3 days per week in the West Hartford, Connecticut, office.
However, we are flexible in terms of location, with both remote and in-office options available for the right candidate.
The base salary expectation for this role is between $80,000 and $110,000.
Actual base salary for the selected candidate may be higher commensurate with candidate experience and expectations.
Additionally, Vantage offers its colleagues performance-based bonus potential, strong health & welfare benefits, retirement plans with company match, competitive time off plans, a highly flexible work environment, and much mor...
....Read more...
Type: Permanent Location: West Hartford, US-CT
Salary / Rate: 95000
Posted: 2025-09-10 08:32:57
-
Overview: The Surgical Sales Representative is responsible for the sale and ongoing support of the Company's product(s) in a specified region or major geographical area.
Responsibilities:
* Create demand for Sight Sciences products within both company and industry-compliant guidelines
* Develop effective sales presentations to differentiate product(s) compared to current surgical glaucoma offerings with Ophthalmic surgeons within the assigned territory
* Analyze data and manage territory to create an effective business plan, including regular sales forecasting
* Maintain knowledge of current trends in the industry and competitive products
* Manage territory budget and resource
* Complete administrative paperwork in a timely manner and provide reports to the Manager regarding established average call activity and feedback from physicians
* Attend various sales training workshops, sales meetings, national/regional conferences, and relevant trade shows
* Maintains direct contact with customers before and after the sale:
+ Pre-sale: Responds to customer inquiries to determine appropriate product literature and pricing schedules; influences production and shipping schedules
+ Post-sale: Responds to customer inquiries (RMA, status, delivery, etc.).
Resolves production scheduling and shipping or invoicing problems; determines the validity of warranty claims and schedules repair resources
* Support company goals and objectives, policies, and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic or international requirements
* Maintain a professional and credible image with key physicians, distributors, consultants, vendors, and co-workers
Skills/Qualifications:
* 5+ years of sales experience, with preferably a minimum of 3 years of medical sales experience in ophthalmology, with a proven track record of success
* Successful sales track record in the medical device industry
* Strong relationship-building skills
* Strong sales presentation skills
* Ability to work independently and as well as within a strong team environment
* Bachelor’s Degree or equivalent experience
* Valid driver's license to travel to customer locations
* Required residence in territory geography
#LI-Hybrid
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
....Read more...
Type: Permanent Location: Milwaukee, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-10 08:28:32
-
Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!t
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire an Analytical Sciences Specialist to join our Analytical Sciences team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Analytical Sciences Specialist is responsible for supporting projects by developing and maintaining documentation and tasks required to fulfill project needs as well as auditing.
This Specialist will work alongside Analytical Scientists to drive activities, accelerate timelines, offer ideas to implement future enhancements and efficiencies, and provide adequate quality oversight and expertise for the creation and review of internal quality documents.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
Lab Project Coordination
* Coordinate with the team across multiple projects to ensure that the timelines are met by communicating milestones and other deadlines within the projects.
* Implement procedural changes to existing internal systems to gain efficiencies to get products to clinical trial status earlier by working with Quality Assurance as well as other departments to implement change (i.e., participates in continuous improvement activities within the group).
Data Auditing Support
* Audit laboratory data for correctness, completeness, and compliance with cGMPs and the company’s internal quality standards (i.e., auditing laboratory data for early through late phase CTM and Registration batches).
* As part of the stability program, audit laboratory stability data and coordinate with the Stability Department to manage the stability testing schedule.
* Follow-up with Quality Assurance and Analytical Sciences staff to facilitate any corrections to data as required.
Lab Compliance Support
* Contribute to the creation and/or review of Quality and Regulatory documents, as needed.
* Managing the action items assigned to the group in various compliance documents (e.g., Change Controls, CAPAs, and Investigations). These ac...
....Read more...
Type: Permanent Location: Vandalia, US-OH
Salary / Rate: 76500
Posted: 2025-09-10 08:25:22
-
? À propos de CTI Santé
CTI Santé est une entreprise innovante spécialisée dans le développement et la mise en œuvre de solutions technologiques au service des professionnels de santé.
Basée à Hossegor, elle accompagne ses clients sur tout le territoire avec une approche humaine, sécurisée et performante de la donnée médicale.
La société a rejoint le Groupe HARRIS Computer en avril 2025, renforçant ainsi son positionnement et son rayonnement à l’échelle internationale.
? Vos missions
Rattaché(e) au directeur du développement, vous interviendrez sur trois grands axes :
? 1.
Gestion du parc matériel interne
* Suivi des postes en collaboration avec l'équipe Harris (ordinateurs, téléphones, accessoires)
* Accompagnement des utilisateurs internes
?️ 2.
Infrastructure et sécurité interne
* Supervision et maintenance des serveurs physiques et virtuels
* Gestion des comptes et authentification centralisée (Keycloak)
* Mise à jour des outils internes (Docker, Debian, Windows)
* Suivi des sauvegardes, journaux et sécurité
? 3.
Environnements clients
* Installation, maintenance et suppression de la solution CTI
* Communication avec les équipes techniques clients
* Mise en place des connexions aux sources de données clients
* Gestion des accès distants, licences, certificats de sécurité
?️ Environnement technique
* Jira, Jenkins, Docker, ElasticSearch (Kibana, Fleet)
* Infomaniak (DNS, e-mails, newsletters)
* Windows / Windows Server (clients), Debian / Windows (interne)
* Bitwarden, Keycloak, RabbitMQ
? Profil recherché
* Formation Bac+2/+3 en informatique ou équivalent
* Expérience d'1 à 3 ans souhaitée en gestion d’infrastructure et support technique
* Autonomie, rigueur et bonne communication
* Sensibilité à la sécurité
? Avantages proposés
* Mutuelle prise en charge à 100%
* Tickets restaurant
* Un cadeau offert pour votre anniversaire ?
* Prime vacances
* Télétravail partiel sur conditions
✅ Pourquoi rejoindre CTI Santé ?
* Une entreprise à taille humaine et en pleine croissance
* Une ambiance de travail conviviale à deux pas de l’océan
* Des valeurs fortes : engagement, innovation, proximité
....Read more...
Type: Permanent Location: Paris, FR-75
Salary / Rate: 30000
Posted: 2025-09-09 08:26:56
-
What will your job look like?
The Manager, Safety and Training is responsible for implementing safety and training programs as defined by the Leadership of Safety Administration and will ensure compliance with State and Federal regulations, as well as corporate, client guidelines and policies.
This position is contingent on the award of contract.
Location: Concord, NC
What you’ll do:
* Manage a consistent safety culture that incorporates various departments, such as operations, safety and maintenance
* Oversee Corporate Safety Incentives and programs effectively and consistently, including assignment of Safety Points
* Implement and support the company and client’s safety management system (SMS) safety plan and initiatives Manage and monitor the FTA’s drug and alcohol DAMIS reporting requirements
* Monitor and support all location insurance claims activities to ensure effective communication with claimants, to help control claims costs and support claims closure
* Lead and support the local safety committee and SMS Ambassador group
* Oversees the locations worker compensation program to ensure compliance and effectively reduce/eliminate claims
* Deliver proper classroom, behind the wheel and mobility management training in accordance with contractual and company requirements
* Promote employee self-responsibility to achieve all safety goals and training requirements
* Ensures all new hires meet minimum qualifications for each division including, background and DMV checks
* Ensure all safety manuals, programs and policies and practices are current and meet the needs of the operating divisions; updating as appropriate
* Successfully complete all related audits including those conducted by the Company, the Client, internal staff members, and state and federal regulatory agencies
* Review, determine and respond to all vehicular, passenger and employee accidents/incidents, indicating the cause and preventability, identifying potential trends to be addressed in future training efforts
* Provide functional expertise in safety regarding hiring of safety department employees
* Collaborate with local Leadership to deliver comprehensive safety meetings and plans
* Act as the location drug program manager, ensuring compliance of FTA/DOT regulations
What you’ll need:
Experience, Education & Certifications:
* High School Diploma or G.E.D.
* Bachelor’s Degree (or equivalent combination of education and experience) in a related field
* Minimum 5 years of transit/paratransit safety management experience
* Previous management experience in a union environment
* Thorough knowledge of all applicable safety rules, regulations – ADA, FTA and DOT to include all corporate programs
* Must possess a valid driver’s license
* Must be able to pass a pre-employment drug test and DOT physical and maintain physical throughout employment
Skill...
....Read more...
Type: Permanent Location: Charlotte, US-NC
Salary / Rate: Not Specified
Posted: 2025-09-09 08:23:12
-
Your Job
Are you passionate about driving efficiency, quality, and innovation in manufacturing? We're looking for a Process Improvement Specialist who will play a critical role in enhancing operations, supporting R&D initiatives, and ensuring product quality excellence.
In this role, you'll be at the center of continuous improvement, troubleshooting production challenges, implementing cost-saving solutions, maintaining product compliance, and training plant personnel on best practices.
Partnering closely with R&D, Quality, and Operations, you'll help bring new products to market, optimize processes, and deliver lasting value for both our team and customers.
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!
What You Will Do
* Serve as the onsite Process Improvement Specialist to enhance operational efficiency
* Support R&D initiatives through technology implementation, raw material qualifications, and production line enhancements
* Troubleshoot issues and develop Design of Experiments (DOE) to identify and resolve recurring manufacturing challenges
* Identify and implement cost-saving opportunities after validation
* Assist with new product development and ensure compliance through the New Substance Request (NSR) process.
* Facilitate the Change Request process by receiving requests, uploading them to the PLEX change module, monitoring approvals, and collaborating with requesters to update SOPs on SharePoint
* Update customer specifications and establish product attribute limits
* Assist the Product Quality Supervisor by:
* Maintaining accurate BOMs and Specifications in PLEX and keeping SOPs and OPLs updated in SharePoint.
* Training new plant personnel on current Product Quality procedures and updating all personnel on revised procedures.
* Collaborating with the Quality Manager to maintain training logs.
* Providing timely recommendations (Release/Scrap/Rework) for products on "Hold" using a risk management approach and entering resolutions into Plex.
* Managing lab equipment calibration and ensuring the R&D lab adheres to 6S standards.
* Supporting customer complaint resolution through collaborative root cause analysis and documenting in Plex.
* Evaluating and testing incoming raw materials for specification adherence, documenting results, and facilitating early invoice payments for contractual price discounts.
Maintain regular structured and informal communication with Product Quality Specialists, the R&D team, Quality Manager, and Operations team
Who You Are (Basic Qualifications)
* Bachelor's degree in Science of Engineering OR 4 years of work experience in a quality or process imp...
....Read more...
Type: Permanent Location: TOLLESON, US-AZ
Salary / Rate: Not Specified
Posted: 2025-09-08 08:17:01
-
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:
Finance LDP
Job Category:
Career Program
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
The Finance MBA Leadership Development Program (LDP) Internship is a full-time 10-week program where MBA students are responsible for leading project(s) that support strategic business initiatives within the Finance function. Internship assignments may include Financial Planning & Analysis, Commercial Finance, Supply Chain Finance, Research & Development Finance or Corporate Services.
Intern assignments will be within the J&J operating companies, supporting either Medical Technology, Innovative Medicine, or Corporate Services Sectors. The MBA Internship positions are typically located in or near New Brunswick, Raritan, Titusville, NJ or Horsham, Spring House, PA.
Successful candidates will possess the ability to work independently, and have strong problem solving, organizational, communication and analytical skills.
Interns will participate in organized activities, including live trainings to build J&J business acumen, networking with peers and senior leaders, opportunities to experience company culture and build understanding of career opportunities within J&J.
The Finance MBA LDP Intern program is one of the primary sources of talent for the full-time Finance MBA Leadership Development Program (MBA LDP). The Finance MBA Leadership Development Program (MBA LDP) is a four-year program designed to successfully develop a pipeline of future leaders for Johnson & Johnson through a combination of diverse rotational assignments, targeted training, and continuous coaching and development.
The anticipated base pay for this position is $51/hour, but will be based on candidate’s program year, discipline, degree and/or experience.
This position is overtime eligible.
Co-Ops/Interns may be eligible to participate in Company employee benefit programs such as medical insurance, sick time, and holiday pay in accordance with the terms of the applicable plans.
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
Ineligibility for severance.
#JNJFinance
...
....Read more...
Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-08 08:06:30
-
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:
Nonclinical Safety
Job Category:
Scientific/Technology
All Job Posting Locations:
Spring House, 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
Johnson & Johnson Innovative Medicine R&D is recruiting for a Distinguished Scientist, Nonclinical Safety Leader within Preclinical Sciences and Translational Safety (PSTS). This position is a hybrid role and will be located in Spring House, PA.
As a Distinguished Scientist, Nonclinical Safety (NCS) Leader, you will collaborate with innovative and diverse scientists to support projects in our large and varied portfolio that spans multiple therapeutic areas and includes innovative modalities. In this vital role you will provide toxicology leadership for all aspects of discovery and development projects, with flexibility to specialize or work across stages of development, therapy areas, and modalities. You will also collaborate with discovery scientists to identify and nominate candidate molecules, and with development teams to bring these molecules to humans and ultimately through global registration.
Principal Responsibilities:
* Lead PSTS project teams of nonclinical safety and Pharmacokinetic (PK) scientists, ensuring efficient information transfer within the team.
* Serve as the NCS representative for global project teams, providing toxicology expertise and interfacing with senior management.
* Create target risk assessments and develop plans to screen for and mitigate potential risks; analyze toxicology and safety pharmacology studies, contextualizing results for human safety and preparing nonclinical safety assessments.
* Contribute to issue-resolution teams by generating hypotheses and investigative strategies.
* Accountable for global regulatory nonclinical documents and health authority responses to support clinical trials and compound registrations.
* Participate in medical safety teams, signal detectio...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-08 08:05:24
-
Quality Control Inspector
Location: Houston, Texas
Overview:
Bray International is seeking a skilled Quality Control Inspector to join our team in a fast-paced industrial manufacturing environment.
If you are passionate about ensuring product quality and have at least four years of experience in quality inspection, we encourage you to apply.
This is an exciting opportunity to contribute to a leading company in the industrial valve and actuator industry.
Key Responsibilities:
* Perform incoming inspections on purchased parts, subassemblies, and finished products to ensure compliance with engineering drawings and customer standards.
* Review Material Test Reports (MTR) and Certificates of Conformance (CofC) against relevant standards.
* Analyze Non-Conformance Reports (NCR) to identify trends and generate Corrective Action Reports (CAR) as needed.
* Create Non-Conformance Reports and other departmental reports as assigned.
* Evaluate issues and make initial recommendations for corrective actions to supervisors.
* Investigate failures to determine root causes and propose remedial actions.
Qualifications:
* Minimum of four years’ experience in quality control within the industrial manufacturing sector.
* Experience with Positive Material Identification (PMI) preferred.
* Proficient in computerized record-keeping and standard software applications.
* Strong written and verbal communication skills.
* Skilled in using and calibrating precision measuring equipment (e.g., micrometers, height gauges, calipers, dial indicators, bore gauges).
* Knowledge of ISO 9001:2008/2015 and API standards.
* Ability to analyze and determine the best inspection methods for product conformity.
* Proficient in interpreting engineering drawings and understanding Geometric Dimensioning and Tolerancing (GD&T).
* Experience with Coordinate Measuring Machines (CMM).
* Ability to manage multiple tasks in a fast-paced environment while meeting delivery requirements.
* High School Diploma or equivalent required.
Physical Demands:
* Must have 20/20 vision (correctable) without color blindness.
* Ability to lift up to 20 pounds.
Note: Immigration sponsorship is not offered for this position.
Why Work for Us?
At Bray International, we are a global leader in providing industrial valves, actuators, and related control products.
We are known for our innovative flow control solutions and are looking for individuals who share our commitment to excellence, integrity, and collaboration.
What We Offer:
* Career Growth: We offer numerous opportunities for advancement within the organization.
* Comprehensive Benefits: Enjoy benefits such as:
+ Life, medical, dental, and vision insurance
+ Paid holidays and vacation
+ 401(k) plan with matching contributions
* Healthy Work Environment: We provide a smoke-free, drug-free workplace to ensure a sa...
....Read more...
Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-07 08:13:52
-
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: Senior Research Scientist, Non-Clinical Safety & Toxicology
We are seeking an experienced non-clinical toxicology / safety scientist to join the Global Non-Clinical Development team in Global Clinical Development.
As the Senior Research Scientist, Non-Clinical Safety & Toxicology you will be responsible for, or will assist with, human (user & consumer) safety and target animal safety program strategy and execution at all phases of global veterinary pharmaceutical drug/product and feed additive research and development, product safety assessments, and support for marketed products.
This role applies toxicology and immunology expertise to assess safety risks across the full product lifecycle, from early development through commercialization.
Responsibilities include evaluating potential safety concerns related to product design, manufacturing changes, deviations, or consumer complaints that could impact animal safety or end-user health.
The role involves preparing Product Safety Assessments (PSAs) for products in development, production, or on the market, and compiling medical and toxicological data to assess potential health risks for consumers and end users.
Your Responsibilities:
* Independently design, organize, monitor, report, and resolve issues related to outsourced in vitro and in vivo safety/toxicology studies, utilizing external CROs and/or consultants as needed.
These studies may involve typical rodent and non-rodent species.
Target animal safety evaluations may include companion animals (dogs and cats) as well as food-producing animals (e.g., cattle, pigs, chickens).
* Conduct literature reviews and author expert reports, position papers, safety and hazard/risk assessments, and other strategic scientific, technical, or medical evaluations to address safety considerations for veterinary drugs (small molecules and biologics), feed additives, excipients, E&L substances, impurities, or other chemicals.
* Provide internal expert guidance, including expert statements, health-based exposure limits (e.g., PDEs, OELs...
....Read more...
Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-09-07 08:10:19
-
At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program..
The EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Adell, Wisconsin facility and after 60 days of training, would support the New Holstein, WI and Boscobel, WI facilities.
Position would be based out of Adell.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits
* Maintain required wastewater discharge permits, renewals, and related documentation.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager. Work cooperatively with outside consultants.
* Develop and maintain company environmental, health and safety programs at the facility.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs. Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facility.
Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
Perform fit-testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks. Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations. Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corp...
....Read more...
Type: Permanent Location: Norfolk, US-NE
Salary / Rate: Not Specified
Posted: 2025-09-07 08:05:06
-
Applied Research Associates, Inc.
(ARA) is seeking a Staff Scientific Data Analyst to join the Health Effects, Analytics, Risk, and Technology (HEART) located in Raleigh, NC.
The candidate will support physiological modeling for exposure risk assessment in support of the National Institutes of Health (NIH) Division of Program Coordination, Planning, and Strategic Initiatives (DPCPSI).
The successful candidate will be on a new team supporting the NIH DPCPSI Office of Research Innovation, Validation and Application (ORIVA).
Working at ARA, there will be opportunities to work with a multi-disciplinary team focused on toxicology, physiological modeling, and risk assessment.
Responsibilities include but are not limited to:
* Data development, analysis and evaluation, including cleaning and analyzing data and utilizing methods (e.g., knowledge graphs to explore chemical-biological effect relationships).
* Routinely review, evaluate, curate, and integrate data from relevant databases (e.g,NCATS N3C, NCI CRDC, ToxRefDB, ToxCast, ExpoCast, DSSTox, CEBS, IUCLID, MassIVE and others).
* Ensure data integrity including preparing program guidelines, performing necessary data checks and managing datasets and data documentation.
* Ensure customer satisfaction by providing high quality deliverables and anticipating needs.
Position Requirements:
* Masters in bioinformatics, mathematics, statistics, computational linguistics, computer science, data science, or other relevant field with 4 years or PhD with 0 years.
* Expertise in NAMs or a related scientific field.
* U.S.
Citizenship Required.
* Capable of fundamental programming for data analysis, survey data analysis, and data management.
* Providing quality assurance on deliverables and timely delivery.
* Excellent verbal and written communications skills.
COMPANY INFORMATION:
Applied Research Associates, Inc.
is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems in the physical sciences.
The company, founded in Albuquerque, NM, in 1979, currently employs over 2,353 professionals and continues to grow.
ARA offices throughout the United States and Canada provide a broad range of technical expertise in defense technologies, civil technologies, computer software and simulation, systems analysis, environmental technologies, and testing and measurement.
The corporation also provides sophisticated technical products for environmental site characterization, pavement analysis, and robotics.
At ARA, employees are our greatest assets.
The corporation realizes that employee ownership spawns greater creativity and initiative along with higher performance and customer satisfaction levels.
ARA gives employees the tools, training, and opportunities to take more active roles as owners.
The culture is challenging and innovation and experimentation are the norm.
Emplo...
....Read more...
Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-09-06 08:20:48
-
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:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson is currently seeking a Quality Control – Micro analyst in an Early-Late shift or Weekend shift to join our CAR-T Hub located in Beerse.
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/.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, Janssen has built two CAR-T manufacturing centers in the Ghent area (Belgium).
The QC laboratories will be operated from the existing Janssen Beerse site.
The QC Micro analyst, CAR-T Europe is responsible for preparing and conducting testing of the different samples taken during the production process.
You are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
You will be responsible for:
* Perform analytical testing in compliance with all applicable specifications, procedures, GMP regulations.
* Maintain a safe work environment in compliance with all applicable environmental, health, and safety regulations.
* Perform peer review of laboratory data.
* Author and update SOPs, WIs and Protocols to support daily operations of the lab using the Document Management System.
* Support laboratory related investigation records and CAPAs.
* Assist in the execution of internal audits.
* Provide input to functional laboratory meetings.
* Provide input and take actions as a QC representative at cross-laboratory meetings.
* You will work in an Early-Late or weekend shift regime.
Qualification and requirements:
* A minimum...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-06 08:19:30
-
General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
....Read more...
Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2025-09-05 08:51:40
-
General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
....Read more...
Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2025-09-05 08:51:38
-
Juris Concept est à la recherche d'un gestionnaire de compte.
Cette opportunité excitante vous permettra d'établir des liens avec une clientèle de bureaux d'avocats, apprendre de nouveaux domaines d'affaires et offrir des produits à la fine pointe de la technologie.
En tant que Gestionnaire de compte, vous ferez partie d'une entreprise solide et reconnue.
Le titulaire identifiera les besoins du client, démontrera les avantages du logiciel et présentera le portefeuille de solutions informatiques Juris Concept aux bureaux d'avocats et entreprises gouvernementales, augmentant ainsi la clientèle sur leur territoire et améliorant les relations avec les clients existants.
Le candidat idéal est un curieux, entreprenant et désireux de trouver la meilleure solution pour répondre aux besoins de nos clients.
Ce que nous recherchons
Nous recherchons un professionnel polyvalent et bilingue qui aime à la fois le côté humain et le côté bâtiment des ventes.
Nous recherchons également quelqu'un qui a :
* Une feuille de route éprouvée en matière d'atteinte et de dépassement de quotas.
* Expérience dans la vente de solutions logicielles SaaS ou B2B.
* Curiosité, dynamisme et aisance démontrés de travailler dans des environnements moins structurés.
* Capacité à créer et à gérer un pipeline de ventes avec discipline et responsabilité.
* Familiarité avec Office 365 et les outils CRM comme HubSpot.
Les responsabilités du poste:
* Participer à l'élaboration et l'exécution du plan de vente et de marketing du territoire ;
* Commercialiser et vendre de manière proactive la suite de solutions et de services Juris Concept;
* Présenter des démonstrations logicielles;
* Coordonner les négociations contractuelles;
* Planifier et exécuter des activités et des événements de prospection ciblés pour générer des prospects;
* Assurer la qualité et la rapidité des réponses aux appels d'offres;
* Enregistrer les informations et les progrès des clients dans le CRM des ventes;
* Maintenir un pipeline de ventes pour s'assurer que les objectifs de ventes soient atteints de manière cohérente et durable;
* Participer activement aux conférences nationales et régionales ainsi qu'aux réunions des groupes d'utilisateurs;
* Mener des affaires avec un niveau d'éthique exceptionnel;
* Établir des relations avec les pairs et les clients;
* Suivi avec le client après la vente pour assurer la satisfaction du client.
Points bonus si:
* Expérience dans la vente à des cabinets de services professionnels (juridiques, financiers, etc.).
* Être à l'aise avec les outils d'administration CRM ou d'aide à la vente.
* Une bonne maîtrise du français et de l’anglais est requise car le titulaire du poste aura à communiquer fréquemment dans les deux langues, tant oralement que par écrit.
Nous avons des collègues, des clients et des par...
....Read more...
Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-09-05 08:39:18
-
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: R&D and Regulatory Intern
As an R&D and Regulatory Intern, you will be executing a project that impacts Elanco’s regulatory, clinical development, or innovation processes.
In this role you will directly enable Elanco to deliver products to our customers in ways such as identifying regulatory pathways to approval, improving internal data management systems, evaluating the competitive landscape, or assessing clinical efficacy models.
Your Responsibilities:
* Managing regular check-ins and reporting/presenting work to your direct supervisor
* Managing data in accordance with project deliverables
* Providing recommendations on process improvements or competitive landscape
* Working within cross-functional teams to implement project outcomes
* Some roles may include hands-on animal experience
What You Need to Succeed (minimum qualifications):
* Education: Currently enrolled in a field such as animal science, veterinary medicine (pre-vet or DVM), chemistry, biology, biochemistry, chemical engineering, pharmaceutical science, molecular biology or other related fields
* Degree: This role is open to students pursuing a Bachelors, Masters, PhD, or professional degree (e.g., DVM, MBA, PharmD, etc.)
* Microsoft PowerPoint and Excel experience
* Highly self-motivated, demonstrated learning agility, and critical thinking
What will give you a competitive edge (preferred qualifications):
* Experience working with statistical software or data management tools, proficient in Microsoft Excel
* Innovation and ideation mindset
* Hands-on experience with companion or farm animals and/or veterinary clinics
* Ability to work exceptionally well independently and with minimal supervision
* Have an interest in wanting to make a difference for pets, sustainability, veterinary medicine, or data-driven approaches
* Strong communication, interpersonal skills, speaking, and presentation skills
* Ability to make ...
....Read more...
Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-09-05 08:39:00
-
At CF&I Steel, L.P., 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.
Job Description and Responsibilities
As a Quality Systems Coordinator, you will maintain the Quality Assurance System including, but not limited to, recording and updating daily quality assurance and ISO 9001-2015, maintaining claim log, customer database, test report database, scheduling and training records, and job manuals, including all administrative functions.
Additional responsibilities include:
* Internal and external process and product audits
* Maintaining the SOPs which includes contacting/training the workforce when changes are made
* Management of the calibration system, issuing and recording process deviations
* Initiating, following and distributing Trials and their results
* Reporting daily and monthly Quality Index information
* Helping to communicate information associated with product quality and improvements to the workforce
* Helping with the daily management and maintenance of the quality system which can include assignments that may require off-hour or weekend work
* Maintaining scrap recipes, evaluating performance changes, reason, and auditing of charges
Requirements
* Bachelors of Science Degree or equivalent experience; Metallurgy/Materials Engineering, Chemical Engineering or Mechanical Engineering preferred
* Proficient in Microsoft Office - Word and Excel
* Proven written and verbal communication skills, including Quality Manual and Second-Tier Procedure Writing skills
* Excellent planning, time management, and organizational skills
* Strong problem-solving and proven decision-making skills
* Understanding of Steel mill processes: Rail, Rod & Bar, Seamless, Steel-making
* Initiative to identify areas, propose and initiate solutions
* Experience in the management of 6S projects
* Two years of Quality Assurance experience, preferred
* Familiar with Quality Management systems, preferred
* Certified Quality Auditor, preferred
* Experience in ISO 9001/Quality Systems, preferred
#TAS
COMPENSATION
* $80,000 – $87,000
Open & Closing Dates: 09/4/2025 – 10/30/2025
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 thos...
....Read more...
Type: Permanent Location: Pueblo, US-CO
Salary / Rate: Not Specified
Posted: 2025-09-05 08:38:57
-
Face à la Méditerranée, sur la légendaire Croisette, le Carlton Beach Club incarne l’élégance balnéaire été comme hiver, dans un esprit résolument chic et décontracté,
Nous recherchons notre Directeur/Directrice du Carlton Beach Club, un(e) chef d’orchestre passionné(e) et visionnaire, capable de faire rayonner cette adresse mythique auprès d’une clientèle locale et internationale.
Les principaux objectifs du poste :
Sous l’autorité de notre Directeur de la Restauration, vous déployiez les orientations définies et dirigez le fonctionnement des différents points de vente du Carlton Beach Club : le Restaurant de la Plage, le Beach Bar, notre Page Balnéaire ainsi que la Cuisine de la plage, en veillant à l’exécution d’un service de haute qualité et au maintien de standards d’un niveau irréprochable.
Vos missions seront les suivantes :
* Créer l’expérience – Transformer chaque visite en moment d’exception, en incarnant l’hospitalité du Carlton Cannes.
* Inspirer et guider – Fédérer, former et élever votre équipe pour atteindre l’excellence au quotidien.
* Piloter et innover – Développer les performances économiques tout en proposant de nouvelles expériences.
* Sublimer l’offre – Collaborer avec nos chefs et mixologues pour offrir une gastronomie raffinée et créative.
* Rayonner – Faire du Carlton Beach Club un incontournable de la Croisette, pour les Cannois comme pour les voyageurs du monde entier.
Ce que nous attendons de vous :
Pour remplir ce rôle avec succès, vous devez posséder les qualifications, l'attitude, les comportements, les compétences et les valeurs suivantes :
* Leader inspirant, avec une solide expérience (5 à 7 ans minimum) dans la direction d’un établissement haut de gamme (plage privée, restaurant, hôtel 5
*).
* Passionné(e) par l’art de recevoir, attentif(ve) au moindre détail.
* Capacité à performer dans un environnement saisonnier, exigeant et stimulant.
* Français et anglais courants (toute langue additionnelle est un atout).
* Créatif(ve), ambitieux(se) et déterminé(e) à faire rayonner un lieu iconique.
Ce que nous offrons :
* Poste à pourvoir en CDI – date de prise de poste à définir.
* Un package attractif (salaire attractif sur 13 mois + primes).
* L’opportunité d’écrire un nouveau chapitre de l’histoire du Carlton Cannes.
* Un cadre de travail exceptionnel, entre ciel et mer.
* La possibilité de créer, d’innover et de laisser votre empreinte sur une adresse légendaire.
....Read more...
Type: Permanent Location: CANNES, FR-PAC
Salary / Rate: Not Specified
Posted: 2025-09-05 08:34:48
