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Looking for a chance to make a real difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.
Our “People first” approach means we also value our employees, who work relentlessly to help us execute our mission.
Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.
By following these guiding principles, we earn and maintain the confidence of our patients, our partners, and each other.
Together, we’re working to discover and develop innovative cancer treatments that address unmet patient needs and apply the science behind them in novel ways.
As the field of cancer treatment evolves, we evolve with it.
Advanced technology, dedicated investigators, and incomparable facilities: these vast resources empower us to redefine the way the world treats cancer.
It’s our work, our passion, and our legacy.
If the prospect of being part of this sounds exciting, we invite you to join us.
Territory Coverage: PA, Upstate NY, DC, MD, DE
Position Summary:
The Medical Science Liaison (MSL) is a field-facing representative of the Medical Affairs Department with a primary responsibility to engage in the exchange of scientific data, education of health care practitioners on Taiho products and relevant disease states, and facilitation of clinical research.
The MSL integrates clinical/scientific expertise and knowledge to ensure successful implementation of the medical affairs strategic plan within an assigned geographic region.
The MSL brings relevant insights from the field on research developments, treatment landscape and new concepts in medical treatment.
The role of the MSL is non-promotional in nature.
Responsibilities and Duties:
* Product/Therapeutic Area Support to External Stakeholders:
* Act as the primary clinical/scientific resource to HCPs in a specified geography for information pertaining to disease state and Taiho's product(s) and compounds to ensure awareness and understanding.
* Provides high quality scientific information to healthcare professionals (HCPs)
* Serve as a conduit for accurate and updated clinical, scientific and medical information between Key Opinion Leaders (KOLs)/investigators and the company's Medical Affairs and development groups.
* Establish, foster, cultivate and maintain peer relationships with KOLs and HCPs in the therapeutic areas in which Taiho has current and future interests.
* Share knowledge and participate in scientific exchanges and interactions with identified KOLs
* Present clinical and scientific data on Taiho’s products and relevant therapeutic areas as requested.
* Identify and report key scientific, clinical and research insights from KOLs and HCPs to Medical Affairs.
* Respond to unsolicited medical information requests in the field.
* Fulfill Pharmacovigilance responsibilities as defined in the p...
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Type: Permanent Location: Philadelphia, US-PA
Salary / Rate: Not Specified
Posted: 2024-11-22 07:17:15
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We are seeking a Clinic Manager to lead our Pharmacy Disease Management Clinic.
Our clinic helps people with chronic health conditions manage their medications.
Enjoy a work environment with collaborative team model approach as each member of our team works closely together providing advanced patient care.
Kingman Regional Medical Center (KRMC) is located in beautiful northwest Arizona.
Experience the magic of Kingman's stunning Arizona sunsets and thrive in an outdoor enthusiast's dream destination with picturesque mountain ranges, nearby lakes, vibrant parks, and plenty of outdoor activity. Kingman is an incredible community to live, work, thrive, and play!
Position Purpose: The Clinic Manager coordinates the day-to-day staffing and business needs of the clinic(s).
This position troubleshoots and resolves problems as they arise including patient problems or refers patients to appropriate resources.
The Clinic Manager maintains a professional working relationship with billing office, department administration, and others in a team atmosphere and manages the clinic(s) operations fiscal performance to budget.
Shift/Hours: Days / Monday-Friday
Benefits: We offer you an excellent total compensation package, including a competitive salary, comprehensive benefits, and growth opportunities.
We invest in you!
* Relocation Assistance Available
* Exceptional Colleagues
+ Join us and you'll be a part of a culture where we support each other and celebrate what makes each of us a special person as we work together with integrity, compassion, teamwork, respect, and accountability.
+ Our leaders demonstrate their commitment by gathering feedback, supporting, and empowering team members to do their best work through regular leadership rounding.
* Health and Well-Being
+ Medical, Dental, Vision, Employer Paid HSA for HDHP participants, Robust Wellness and Employee Assistance Program, Employer Paid Group Life, Short & Long-Term Disability
+ Generous Paid Leave Accruals
+ 403b Retirement Plan with Employer Contributions
+ Employee Recognition Programs, Employee Discounts, and Employee Referral Bonus Program
+ Employee Identity Theft Protection
+ On-site daycare exclusive to our employees’ children of all ages
* Career Growth and Development
+ Tuition Reimbursement/Scholarships for full-time employees
+ As a not-for-profit organization, our employees who have qualified student loans may be eligible for the Public Service Loan Forgiveness program
* So much more!
Key Responsibilities:
* Exercise judgment to make impactful decisions related to people, costs, and quality of service.
* Maintain a clean, organized clinic environment in collaboration with the Pharmacy Clinical Manager for Ambulatory Care and clinic pharmacists.
* Oversee staffing, provider schedules, and business functions to ensure efficien...
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Type: Permanent Location: Kingman, US-AZ
Salary / Rate: Not Specified
Posted: 2024-11-22 07:15:52
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Ardurra is seeking a Survey RPLS to join team in Houston, TX.
Primary Function
Manages the full life cycle (proposal-initiation-execution/control-closeout) of surveying projects.
This includes managing all activities related to project scope, schedule, cost, cash flow, quality, communications, resources, procurement, and risk elements required to optimize client service, quality, and fiscal responsibility.
The Project Manager’s overall objective is to build and maintain a positive client relationship, and to achieve or exceed the estimated profit margin for the project.
Primary Duties
* Participates in project costing and bid preparation to the extent required
* Reviews assigned project(s) after award to determine work procedures/sequences, develop schedules, budgets, and billing
* Establishes contractor-client liaison network to keep all interested parties informed of project planning, start date, and work progress
* Oversees field crew work and CAD drafting work and sees that responsibilities are assigned, and execution of tasks are begun and completed according to schedule
* Review, sign / seal and delivery of survey product consistent with TX Statutes, client expectations and best surveying procedures and practices
* Maintains a continuing business relationship with major clients as part of ongoing
Education and Experience Requirements
* Professional registration in the state of Texas (PSM / PLS)
* Prior job assignments typically include project engineering responsibilities
#LI-SH1
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers.
We nurture a family-like culture, striving to create a work environment that is enjoyable, challenging and rewarding but also fun.
We are acutely focused on developing our staff, whether through our internal Ardurra Academy or through our industry-leading Leadership program.
We have made a deliberate and focused commitment to nurture a people-centric culture where people are: valued as individuals; supported in their professional and career development with multiple, varied career paths; provided the tools and resources to be successful, engaged, and satisfied in their work; and positive benefits, time-off programs, and flexibility to help maintain a healthy balance between work and home.
Ardurra is an Equal Opportunity/ Affirmative Action Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, gender identity or sexual orientation.
NOTICE TO THIRD PARTY AGENCIES:
Ardurra does not accept unsolicited resumes from recruiters or employment agencies.
In the absence of a signed Agency Agreement, Ardurra will not consider or agree to payment of any referral compensation or recruiter fee.
If a resume or candidate is submitted to any hiring manager wit...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2024-11-22 07:06:28
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Ardurra is seeking a Certified Engineer In Training to join our Public Works Group in San Antonio, Texas.
Primary Function
Under general supervision, performs assignments of limited scope which require the application of standard techniques, procedures, and criteria in carrying out a sequence of related design engineering tasks.
Primary Duties
* Participates in the development of project design concepts and criteria
* Organizes project information and records systems
* Designs and prepares working drawings and related project documents
* Makes recommendations on design alternatives and assists in proposal preparation
* Serve as Engineer I for multiple public works projects
* Client management, monitor/manage budgets and schedules
* Coordinate with project design team members, subconsultants, clients, stakeholders, contractors and permit agency representatives regularly
* Manages both internal and external resources required to successfully complete projects including coordination and supervision of design staff
* Cultivates strong relationships with clients
* Provides quality assurance and control for deliverables including proposals
* Attends engineering/industry events and conferences
* Manage time wisely, and effectively prioritize multiple competing tasks
* Highly self-motivated self starter, able to forecast and initiate project management tasks
* Work independently but collaborate as needed
* Ability to take the initiative to resolve conflicts that arise during the project
Education and Experience Requirements
* Bachelor’s Degree in, Civil Engineering from an accredited university or college
* A minimum of 1-2 years of experience in engineering and design with a focus on public works, roadway, drainage and utility design
* Familiarity with local municipalities, CoSA, SAWS and TxDOT design and procedures, regulatory compliance and agency coordination
* State of Texas EIT license
* Strong communication skills both written and verbal
* Strong organizational, analytical, and problem-solving skills
* Knowledge in computer software utilized in the transportation/public works industry, Highway/Roadway Design, Stormwater Design, 3d software, MicroStation/Open Roads, AutoCAD
#LI-SH1
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers.
We nurture a family-like culture, striving to create a work environment that is enjoyable, challenging and rewarding but also fun.
We are acutely focused on developing our staff, whether through our internal Ardurra Academy or through our industry-leading Leadership program.
We have made a deliberate and focused commitment to nurture a people-centric culture where people are: valued as individuals; supported in their professional and career development with multiple, varied career paths; provided th...
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Type: Permanent Location: San Antonio, US-TX
Salary / Rate: Not Specified
Posted: 2024-11-22 07:06:25
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Our Team
Guardian Industries, a subsidiary of Koch Industries, is a global leader in glass manufacturing and coated glass products.
The company is dedicated to innovation, sustainability, and delivering high-quality solutions across various industries, including automotive and building products.
Our Advanced Analytics Capability is at the forefront of leveraging data and AI to drive business growth and operational excellence.
We seek a Senior Data Scientist to join our AI and Data Science team to embark on the journey of developing Large Language Models (LLMs) and Generative AI tools to drive business value and enhance operations and commercial outcomes.
Our highly skilled, enthusiastic data scientists are redefining what's possible for Guardian by utilizing the massive amount of process data to transform operations, research, and development.
We invest in our team by encouraging attendance at industry conferences and ongoing education opportunities, enabling them to stay in the dynamic, ever-changing data science landscape and bring new methods and techniques to their projects.
What You Will Do
* Develop a strong understanding of the operations and business processes and identify possible opportunities that add value.
* Apply machine learning algorithms to perform analysis, create predictive models, visualize data, and drive projects through to delivery toward solving operations problems.
* Interact with business and manufacturing SMEs to identify requirements and propose solutions.
* Have the intellectual curiosity to research and identify new modeling technologies/methodologies/software packages to improve the current modeling processes.
* Continuously scan and test new data sources, tools, and analytical techniques and partner with leading institutions and experts to contribute to our portfolio of next-generation analytics projects.
* Analyze large complex time series datasets to extract useful patterns to deliver business insights and communicate results to key decision-makers.
* Issue reports detailing tool development (including unsuccessful approaches), quality assurance actions performed, results, etc.
* Work with data engineers to improve functionality in data systems (e.g., data reliability, efficiency, usability, and quality) and improve downstream data analysis capabilities.
* Rapidly design, prototype, and test many possible hypotheses .
Further, focus on building minimum viable products toward solving most of the issues instead of "perfecting" the solution unless it is critical to safety.
* Leading and working on multiple projects simultaneously and switching priorities as the business needs require.
* Employ visualization, reporting, and other tools to improve how teams access various datasets.
* Strong data-driven storytelling to present to stockholders.
Who You Are (Basic Qualifications)
* 5+ years of experience in applying ML to solve complex application ...
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Type: Permanent Location: Auburn Hills, US-MI
Salary / Rate: Not Specified
Posted: 2024-11-21 08:40:43
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About Us:
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history.
As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine.
Our purpose is to fuel confidence by helping people look better, feel better, and live better.
We believe you do not have to choose between living life and making a living.
Live your best life with Merz Aesthetics.
A Brief Summary:
The Global Marketing Manager, is responsible for supporting innovation in the development of global marketing strategies, managing the Global Brand for BELOTERO collaborating with internal and external stakeholders to drive growth for the Global Aesthetics Injectables business.
This candidate will be accountable for collecting, organizing, interpreting, and maximizing external marketing efforts including:
* Consumer & HCP Market Research
* Customer Feedback, Market Insights, & Commercial Strategies
* Scientific Publications & Opportunities
* Medical Affairs Inquiries
* Competitive Insights
* IP & Patent Opportunities
* Early-Stage Upstream Developments
Responsibilities
Global Marketing:
*
+ Support pipeline projects by providing customer feedback, market insights, and work cross-functionally to drive product development programs.
The Global Marketing Manager will be responsible for validating product inputs, supporting financial forecasts and business cases, development of launch plans, and collecting research and data to support commercial strategy.
Global Market Research:
*
+ Partner with Market Analytics and external partners to execute market research initiatives around customer needs and product validation.
Provide technical expertise to assist in their execution.
Stay connected with market needs through frequent interaction with regional marketing partners, customers (In-region visits, attendance at industry meetings, review medical journals, etc.).
Global Scientific Strategy:
*
+ Responsible for supporting the development of the scientific publication strategy for responsible products in close partnership with Clinical Affairs, Medical Affairs, Regulatory Affairs and Marketing teams.
Global Launch Strategy:
*
+ Responsible for supporting and executing new product launches in close partnership with regional teams and other key stakeholders.
Global Product Management:
*
+ Contribute to the development of global brand strategies for products, services, programs and other key initiatives, including establishment of value proposition, targeting & segmentation, positioning, global branding, product launch and lifecycle management.
Collaboration:
*
+ Partner closely with regional marketing to gather input on customer needs and ensure strong al...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2024-11-21 08:38:37
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About the Company:
Merz is a family-owned medical device and pharmaceutical company with headquarters in Germany.
Our Global Technical Operations based in WI manufactures, packages, and ships several innovative products so that people all over the world can look better, feel better and live better.
Key Responsibilities:
Microbiological SME / Process Leader:
* Operate as site Microbiological Subject Matter Expert (SME), maintaining high level of expertise in current global regulatory requirements for the manufacture of sterile medical devices, assuring adherence to “state of the art” requirements.
* Own site level Microbiology Testing program, including development, validation and implementation of Test Methods and Equipment.
* Evaluate and implement new microbiology technologies per Quality System Standards, Quality System Regulations, and other company procedures around which the Quality System is developed.
* Proactively Write, revise and review related Standard Operating Procedures (SOPs) and Department related Protocols.
* Establish and Maintain site microbiological and contamination control program(s) including associated employee training.
Microbiological Testing:
* Establish and Maintain Site Programs for:
* a.
Endotoxin and Bioburden testing
* b.
Environmental Monitoring (EM) of the Cleanrooms
* c.
Quality analysis of the water systems
* Coordinate daily operations for a team of microbiologists
Sterilization:
* Responsible for qualifying and maintaining the qualification of quality assurance activities associated with the sterilization of site’s products.
* Maintain risk assessments required for parametric release.
Data Analysis:
* Perform quality review for microbiological testing/EM monitoring data.
* Responsible for the identification and communication of adverse trends in routine microbiological monitoring.
Root Cause Analysis and Corrective Action:
* Lead laboratory root cause analysis investigations and implement corrective and preventive actions, reduce finished product average cycle time, and reduce laboratory related errors through method improvements, and effective training.
Audit Activities:
* Operate as site Microbiological SME in scope of internal and external audits.
* Participate in and/or perform internal and supplier audits as needed.
Operational Support:
* Support site facilities and manufacturing teams to assure compliance to sterilization, product, process, environmental and cleaning requirements to ensure product quality and Quality System requirements are met.
Education:
BS/BA in Microbiology, Biology, or Physical Science.
Required
Masters Degree in Microbiology or equivalent.
Preferred
Experience:
* 8 years Pharmaceutical/ Medical Device Microbiological Quality / Sterility Assurance experience.
Required
* GLP/GMP experience.
Required
Knowledge, Skills and Abilities:
* Strong t...
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Type: Permanent Location: Racine, US-WI
Salary / Rate: Not Specified
Posted: 2024-11-21 08:38:36
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The Global Communications intern would be responsible for supporting Global Communications initiatives related to internal communications, external communications and media relations, corporate branding and marquee events.
Essential Duties and Responsibilities
* Project management on active external and internal communications projects
* Copywriting/drafting content for internal and external use
* Media monitoring and flagging
* Taking notes at internal communications meetings and other cross-functional meetings
* Internal reporting, meeting organization and other admin-related tasks (booking rooms, ordering food, etc)
* Transcribing or synthesizing (for example, audio recordings of Bob speaking)
* Photo and general folder organizing (uploading and creating folders and sorting through photos from events like Town Hall, etc)
* Logistics help for internal events: Town Hall, etc.
* Ownership of one project we define when the candidate enters and will manage during the time of the internship with multiple status/deadlines/presentations for the team
Minimum Qualifications
* Required:
+ Previous internship experience in communications, PR or social media
+ Junior or senior at a full-time college/univserty
+ Available to come to the office twice per week (preferably Tuesday/Thursday)
+ Experience drafting communications materials for internal, external or executive content
+ Industry knowledge
* Preferred:
+ Experience in industry or similar field preferred
Education (Preferred Majors)
* Required:
+ Bachelor’s Degree (Communications, PR, Journalism, Marketing)
+ Rising Junior / Rising Senior
Additional Details
* Hybrid work schedule:
+ 3 Days working from office / 2 Days working from home
* Duration of Internship:
+ Projected dates: January 2025 to May 2025
* Expected hours per week:
+ Up to 20 hours
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.
However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
41 CFR 60-1.35(c)
Communications
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2024-11-21 08:38:35
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Company
Federal Reserve Bank of Kansas City
When you join the Federal Reserve—the nation's central bank—you’ll play a key role, collaborating with leading tech professionals to strengthen and protect our economic, financial and payments systems.
We invest in contemporary and emerging technology each year to support the Federal Reserve and our economy, and we’re building a dynamic and diverse team for our future.
Important Information
* United States citizenship is required for this position.
* The Federal Reserve Bank of Kansas City will not sponsor a new applicant for employment authorization.
* This is a hybrid role and requires working on-site, in Kansas City, MO, a minimum of 50% monthly.
About the Role
* The Treasury Data Transparency & Strategy (DTAS) team is seeking a Cloud DevOps Engineer to support the Fiscal Data Treasury Team. The successful candidate will be a team-oriented DevOps Engineer with experience and eagerness to work on infrastructure, operations, CI, CD, deployment, data management, and information security.
They will maintain operational stability of a platform supporting multiple development teams, app deployments, and databases, to reduce risk to site availability, and security. Daily activities will include executing recurring operations and maintenance tasks such as data snapshotting and archiving, security patching, and infrastructure scaling and monitoring. The desired outcome is to perform DevOps activities to control, automate, and accelerate the Agile SDLC and DataOps to orchestrate the delivery of data among systems.
Key Activities
* Applies the principles of software engineering to the design, implementation, configuration, and optimization of solutions in support of applications, databases, test automation tools, and Commercial Off the Shelf (COTS) products.
* Demonstrates technical skill in at least one programming general purpose language (Python, Terraform, etc.) and domain specific language (SQL, proprietary vendor language, etc.), as needed.
* Performs peer reviews using software engineering principles, patterns, and development guidelines.
* Partners with customers in the development of innovative solutions that achieve business goals.
* Reviews and analyzes business and technical requirements and implements technical solutions to meet those requirements.
* Provides data on-call support, troubleshooting, root cause analysis, incident management, and service request management for supported products and environments.
* Performs other duties as assigned.
Required Qualifications
* Typically requires 3-6+ years of relevant experience.
* Bachelor’s degree specializing in STEM (Science, Technology, Engineering, Mathematics), or a closely related field, from an accredited college or university, or equivalent combination of directly related education and/or experience.
* Experienced to Senior understanding of subject.
H...
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Type: Permanent Location: Kansas City, US-MO
Salary / Rate: Not Specified
Posted: 2024-11-21 08:28:39
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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!
Devenez notre futur(e) Technicien(ne) Contrôle Qualité en charge des équipements de laboratoire
Venez rejoindre une équipe dynamique et riche de sa diversité dans un laboratoire de pointe, modèle de l’excellence opérationnelle ! Vos principales missions seront la réalisation du maintien du statut qualifié des équipements d’analyses du laboratoire.
Dans ce cadre vous :
* Maintenez le statut qualifié des équipements du laboratoire :
* Réalisez des opérations de maintenances préventives et curatives, de métrologie et des qualifications nécessaires selon les plans établis ; (HpLC balances, UV…)
* Vérifiez la conformité des opérations réalisées en termes techniques et BPF;
* Participez aux installations de nouveaux équipements et systèmes :
* Gérez l'interface avec toutes les parties prenantes (achat, informatique, assurance Qualité, fournisseurs, ...);
* Suivez et/ou réalisez les actions induites selon les plannings établis ;
* Mettez à jour les systèmes documentaires.
* Assurez le suivi des relations avec les entreprises extérieures (fournisseurs)
* Négociez des délais, des interventions pour des montants ne nécessitant pas l’intervention du service achat.
* Etablissez les contrats avec les prestataires
* Participerez à l’amélioration continue du laboratoire et à la mise en place des CAPA en étant force de proposition.
Votre profil :
* Votre expérience recouvre au moins 5 ans dans un laboratoire
* Vous disposez à minima d’une formation scientifiques à bac+3 en chimie analytique ;
* Vous maitrisez les outils bureautiques Excel, Word ou autres logiciels
* Votre niveau d’anglais vous permet de lire et comprendre de la documentation de laboratoire technique et des pharmacopées
Les plus qui feront la différence
* Votre rigueur et appétence technique
* Votre esprit d’équipe
* Votre motivation à participer à l’amélioration continue et à relever des challenges collectifs
Nous vous attend...
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Type: Permanent Location: Huningue Cedex, FR-68
Salary / Rate: 38200
Posted: 2024-11-21 07:45:12
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MédiSolution, une division de Harris Computer, est à la recherche d’un développeur BI pour agrandir son équipe de recherche et de développement de nos solutions d’intelligences d’affaires.
Être développeur chez MédiSolution c’est contribuer à la croissance de l’entreprise, à ses développements et à l’amélioration de solutions d’intelligences d’affaires.
Si tu es une personne astucieuse et inventive avec de l’expérience et une bonne connaissance en développement et maintenance de solutions d’intelligences d’affaires, qui sait relever des défis et qui souhaite contribuer à créer de la valeur ajoutée dans nos solutions pour notre clientèle, joins-toi à une équipe compétente où priment la collaboration et l’entraide.
Ce que tu auras à faire :
* Analyser, développer, tester et supporter les applications BI;
* Concevoir du code robuste, fiable et performant;
* Partager ton expérience et tes connaissances avec l’équipe;
* Collaborer et aider les membres de l’équipe;
* Documenter les développements, les correctifs et les solutions;
* Faire évoluer nos plateformes BI selon les meilleures pratiques sur le marché;
* Participer activement aux rencontres Scrum/Agile.
Profil recherché :
* Capacité de gérer de multiples priorités simultanément;
* Minutieux, autonome et rigoureux ;
* Esprit d’analyse et de synthèse développé;
* Respect des objectifs et des échéanciers;
* Approche orientée vers le service client;
* Intérêt développé pour la qualité et l’amélioration continue.
Ce qu’il te faut :
* Parler français;
* Un diplôme d’études collégial ou un baccalauréat en informatique;
* Connaissance des outils Microsoft BI (SSIS, SSAS, SSRS);
* Expérience pertinente dans le développement de systèmes BI en utilisant ETL
* Connaissance de SQL Server et des procédures stockées;
* Connaissance de SQL Server Management Studio;
* Connaissance de SnowFlake;
* Maitriser l’architecture d’entrepôt de données (schéma en étoile/BI);
* Connaissance d’Oracle (un atout);
* Intérêt pour le développement Web (un atout).
Ce que MédiSolution t’offre :
* Des assurances collectives payées par l’employeur;
* Dès la première année, 3 semaines de vacances payées, une 4e semaine après 3 ans et une 5e semaine après 7 années de service dans l’entreprise;
* 5 jours de congés personnels par année;
* Un programme de REER avec participation de l’employeur;
* Un programme de reconnaissance de vie active (prime annuelle);
* Le télétravail et tous les avantages qui en découlent,
* Un horaire flexible;
* Un environnement de travail stimulant et une équipe dynamique et compétente;
* Une possibilité d'évolution de carrière au sein d'une entreprise en forte croissance.
Harris souscrit à un programm...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 90000
Posted: 2024-11-21 07:41:50
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Now offering a $2,000 sign on bonus (external applicants only).
PURPOSE AND SCOPE: performs pre-analytical, analytical, and post-analytical phases of laboratory testing, using manual procedures as well as operating various laboratory equipment and automated analyzer systems.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Reviews and complies with the Code of Business Conduct and both all applicable departmental/company policies & procedures, and all local, state, and federal laws & regulations.
* Works on assignments requiring considerable judgment and initiative.
* Performs routine laboratory protocols; pipetting, measuring, and pouring of samples.
* May perform principal duties and responsibilities of all levels of Laboratory Assistants.
* Responsible for daily/routine instrumental and equipment maintenance and troubleshooting, under general supervision.
* Works with service engineers during extensive troubleshooting, preventative maintenance, or service calls.
* Follows the laboratory’s established policies and procedures whenever test systems are not within the laboratory’s established acceptable levels of performance.
* Under general supervision by Lab Supervisor/Manager, preforms sample preparation, quality controls, instrumental preparation and calibrations, testing, data review of various clinical and environmental tests, and identification of specimens flagged for repeated analysis, as directed within departmental SOPs and applicable state and private regulatory agencies.
* Responsible for all aspects of water testing according to ELAP program.
* Approves environmental analysis results; After data review, submits clinical results to MLS or Lab Supervisor for approval.
* Documents daily, weekly, and monthly quality control and maintenance procedures as assigned.
* Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications, and report said documentation to Lab Supervisor for proper record keeping.
* Performs specimen handling for inter-laboratory tests.
* Fully understands policies and procedures prior to performing proficiency testing.
* Provides mentorship and training of Lab Assistants.
* May coordinate and assist in the work activities of Lab Assistants as directed.
* Performs routine monitoring of reagents, chemicals, equipment consumables, and other necessary lab supplies.
* May assist in potential future method development under supervision of Lab Supervisor/Manager.
* Builds stable working relationships internally.
* Complies with all laboratory safety protocols, including, but not limited to, the use of personal protective equipment (PPE), proper laboratory techniques, disposal of biohazard, etc.
* Assists Lab Supervisor with proper records keeping practices, as directed.
* Escalates issues to supervisor/manager for resolution, as deemed necessary....
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Type: Permanent Location: Southaven, US-MS
Salary / Rate: Not Specified
Posted: 2024-11-21 07:41:00
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PURPOSE AND SCOPE:
Supports FMCNA's mission, vision, core values and customer service philosophy.
Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements.
Facilitates the monitoring of the efficiency and efficacy of Call Center offices to ensure the highest quality of customer service to patients and other clients seeking placement.
Assists with the development of policies and procedures for the Call Centers to ensure compliance with all pertinent company, local, state and federal regulations and requirements.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Under the general supervision of the Director of Quality and Training, works to ensure UltraCare for all FMS patients and referral sources through the preparation of Patient Admissions staff with competency-based training and development.
* Creates plans, and executes all formal training within the Patients Admissions Services (PAS) Office including new hire training orientation and ongoing training of personnel as necessary.
* Educates staff regarding the company's expectations for the provision of outstanding customer service to external and internal customers.
* Develops the curricula, directly and in collaboration with appropriate FMCNA Departments, for initial and on-going education relative to a customer service role covering admissions processing of End Stage Renal Disease (ESRD) patients.
* Provides training to ensure the staff members are sensitive to the patient's vulnerable state of mind as well as training regarding Peritoneal Dialysis (PD), and hemodialysis treatments.
* Collaborates with the Education Department to ensure training guidelines and materials are consistent with principles of adult education.
* Serves as the department resource for all Patient Admissions procedures and practices and Continuous Quality Improvement (CQI).
Ensures policies and procedures are current and accurate and makes appropriate revisions based upon business need and operational changes, consistent with company directives.
* Educates PAS team on policies and updates.
Monitors and evaluates, through CQI, the success of policy and procedure implementation.
* Communicates CQI information/outcomes to appropriate Customer Service team members and educates Team Leads on how to implement and monitor an action plan.
* Serves as the department resource for all questions regarding Admissions policies and procedures.
* Maintains resources library for documentation of all Fresenius Admissions policies and procedures.
* Responsible for scheduling clinic visits for new employees.
* Plans and conducts regular training and calibration sessions for current employees to ensure understanding of standard Admissions practices and procedures.
Incorporates remedial education as necessary, based on performance outcomes.
* Conducts needs assessments for PAS department staff, determines methods of trai...
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Type: Permanent Location: Tyler, US-TX
Salary / Rate: Not Specified
Posted: 2024-11-21 07:40:44
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Your Job
At Georgia-Pacific's Innovation Institute in Neenah, WI, we are committed to meeting our customers' needs with solutions that involve great design, consistent quality, and demonstrated customer value.
We are currently seeking a Research Associate with a specific focus on the tissuemaking creping & coating process and related chemical needs.
This role is in Georgia-Pacific's North American Consumer Products Research & Development Tissuemaking Platform.
The Research Associate will create value by evaluating both internally and externally generated creping chemistries and processes that will enable GP to develop new tissue-based consumer products that meet customer needs.
They will also improve and expand the company's process and functional papermaking capabilities, with the same goal in mind.
Serving as the Subject Matter Expert for Creping Chemistry, they will communicate needs to suppliers and evaluate the proposed solutions they develop.
They will also ensure that the production process is ramped up effectively and the end product meets customer standards.
We seek creative and inventive individuals who can work independently and collaboratively as Principled Entrepreneurs™ to conceptualize and profitably translate ideas into successful marketplace options.
This role requires 25% travel.
What You Will Do
* Propose and conduct research projects to address operation's needs, product development projects, or future need states of tissue-based consumer products
* Lead projects and support group goals, identify and proactively address problems by executing experiments that pursue new technology, analyze data with a creative and open-minded approach and communicate results to R&D management, external vendors, and mill operations in a timely and effective way
* Support the organization through developing Intellectual Property strategies that include landscape investigation, invention disclosures and patent applications
* Develop knowledge processes for creping technology that will improve the product or process by fine tuning product formulations or manufacturing processes to ensure end products meet quality and cost goals
* Support scale-up trials and troubleshooting within production facilities
* Manage multiple projects that include both internal development and external collaborations
Who You Are (Basic Qualifications)
* Bachelor's Degree or higher in Paper Science, Chemistry, or Engineering
* Five (5) or more years of industrial work in a papermaking or chemical R&D environment
What Will Put You Ahead
* Experience and knowledge of the tissuemaking process
* Experience and knowledge of Yankee coatings or other process and functional papermaking chemicals
* Experience in product development or industrial work in a papermaking or a chemical R&D environment
* Experience in pilot and production ramp up of new chemicals or new technologies
At Koch companies, we are entrepren...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2024-11-21 07:40:33
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PURPOSE AND SCOPE:
The Sr.
Director, Global Learning & Development, will lead and direct the Frenova Global Learning & Development team and provide organization and oversight to a team of professionals to deliver training and other developmental interventions across the Global organization.
The incumbent will partner and consult with key leaders in various business groups to identify solutions to improve the performance, skills, and knowledge of their employees.
The Sr.
Director, Global Learning & Development, will implement multi-phased learning and development strategies that are aligned with Frenova's goals and support the business objectives and culture while supporting Fresenius’ mission, vision, core values, and customer service philosophy.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Strategy
* Provide a vision and strategic direction for Frenova's global learning delivery, learning operations, and culture functions that is aligned with the business and positively impact their priorities.
* Create and sustain a robust Global Learning Portfolio that brings global learning and business visions to life.
* Own, optimize, and manage Frenova's learning portfolio’s operations, including demand analysis, budgeting, resources, faculty strategy, delivery management, communications, evaluation, deployment technologies, and vendor relationships.
* Create an annual learning plan detailing the curriculum strategy and any associated costs and share with leadership for business planning purposes with key stakeholders.
* Recommend leadership, professional skill, and culture solutions as well as the appropriate delivery mechanisms.
* Execute with strong Project Management Skills, including monitoring work plans and managing against milestones, knowing what to prioritize and why, knowing whom to keep informed and why, and how often and when to escalate.
* Create and sustain a Global Hub Structure ensuring the right resources (facilitators, producers, and other leaders) are located optimally to deliver programs.
This involves having a strategy to inform when the global COE core curricula are managed by COE resources vs local employees and /or vendors and understanding language requirements.
* Partner with senior leaders to assess needs and determine which performance improvement intervention, including training, might close the gap in employee skill and knowledge deficiencies.
* Direct the implementation of large-scale global, organization-wide, learning and development projects to support critical initiatives such as improving business performance, building organizational capability, and improving the work environment while ensuring compliance with all applicable policies, procedures, and regulatory requirements and guidelines.
* Evaluate the effectiveness of learning and development programs by using relevant evaluation data to revise or recommend changes in instructiona...
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Type: Permanent Location: Waltham, US-MA
Salary / Rate: Not Specified
Posted: 2024-11-21 07:40:25
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Safety Leader
Job Description
As a person, you’re a learner – a natural leader – someone who is always taking initiative to make things better and bring others along with you.
You live your life in alignment with the highest values of integrity and quality, always ensuring your responsibilities become a long-term success story.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
In this role, you will be involved in:
* Interpretation and advice of current and new legislation and information to ensure the Mill meets all legislative requirements.
* Liaison with Enforcement Agencies, Insurers and KC Safety Leaders.
* Ensure all the required health and safety responsibilities are being carried out fully.
* Ensure that all appropriate safety matters/issues are correctly reported, managed effectively and communicated.
* Assist in investigation of incidents, injuries and near misses.
* Ensure regular safety audits of the mill take place.
* Lead and assist in the risk assessment of machinery and operational activity.
* Oversee Employer Liability Insurance Claims.
* Provide statistical data and analysis to support asset improvement activities.
* Ensure the Safety forum and other sub groups meet and discuss safety regularly.
* Set standards, drives improvement and ensures regular auditing of the Mill.
* Meet regularly with Mill Leaders and other personnel as appropriate.
* Support Safety Champion’s activities and develops site safety improvement plans.
* Assist in identification of training needs and the provision of training.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with ...
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Type: Permanent Location: Barrow In Furness, GB-CMA
Salary / Rate: Not Specified
Posted: 2024-11-21 07:40:12
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Provides input to integrate the strategic vision of the headquarter organization and relevant stakeholders into the category strategy.
Drives execution of category strategies in the headquarter organization.
Is an active part of the extended team for Logistics.
Provides advanced expert insights on the local/ regional market and industry.
Owns local categories and manages these in line with the overall category strategy.
Presents decision recommendation to the decision board to ensure a transparent and aligned decision making.
PURPOSE AND SCOPE:
Responsible for developing and executing strategies to support Fresenius Medical Care North America's Supply Chain objectives.
Responsible for strategic category management, supplier negotiations, contracts, and ongoing supplier management in assigned materials. Coordinates with Global Strategic Procurement organizations to ensure alignment of procurement strategies where material/service synergies exist.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Strategically manage spend by utilizing a proven sourcing process that engages stakeholders, aligns business objectives, and ensures supply continuity.
* Act as subject matter expert on the supply and demand markets for assigned categories and their impact on the category.
* Gain credibility and secure high levels of internal stakeholder's buy-in to strategic initiatives.
* Analyze global Category or market trends for assigned material/service purchases and communicate opportunities to Executive Management, recommending action plans based on market trends.
* Develop and direct annual cost savings programs that directly affect company financials and growth plans and generate progressive year over year cost reductions.
* Prepare requests for proposals for assigned materials/ services.
* Perform proposal analysis, including price analyses, Should Cost modeling, benchmarking, etc.
* Develop cost targets for negotiations, negotiation strategy, and develop and negotiate supply agreements.
* Lead supplier selection process, qualification of alternative sources, supply base rationalization programs and other relevant strategies to optimize the supply base.
* Active Supplier Relationship Management: Development and measurement of KPI's, supplier audits, business reviews, improvement plans, new opportunities, awards, terminations, etc.
including savings tracking and ongoing communication to management and stakeholders.
* Act as Liaison for resolving supplier/product related issues on assigned materials/services.
* Provides leadership and coaching to all direct reports and partners with human resources on employee matters.
* Works with employees to develop clear and concise development plans to ensure the advancement of future leaders within FMCNA (succession planning).
* Other duties as assigned.
Additional responsibilities may include focus on one or more departments or locations. See...
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Type: Permanent Location: Waltham, US-MA
Salary / Rate: Not Specified
Posted: 2024-11-21 07:40:00
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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!
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 a Technical Services Analyst to join our Technical Services & Validation Team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The essential job function is to provide analytical support for validation and technical services projects including preparation of development, method transfer, and validation documents. Also, to provide procedural training and assisting with planning and execution of Technical Services Projects.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Execute pharmaceutical analytical methods for potency, dissolution, impurities/degradation products, using appropriate laboratory instrumentation e.g.
HPLC, Dissolution Apparatus, GC. Exercise the ability to learn and execute new technologies.
* Execute pharmaceutical analytical methods for physical tests, wet chemistry tests, etc.
* Author procedures, protocols, reports, and ancillary documents in support of projects and regulatory filings.
* Provide training and support to other analysts supporting Validation and/or Technical Transfer projects.
* Provide testing support for validation (process and cleaning), tech transfer feasibility batches, and , as applicable, clinical supplies.
* Take a lead in transferring methods internally (QC) and externally (other Adare sites or customer) during Technical Transfer projects.
* Lead analytical teams, as needed; including coordinating activities designed to achieve project goals in an efficient manner.
* Attend internal and customer project meetings. Supply appropriate input and data prior to and during the meeting.
* Attends work on a regular and predictable basis as set by department management.
* Complete assigned tasks in a safe manner and in a constant state of alertness.
* Uphold Company policies, including the Professional Conduct Policy and Prohibition Against Harassment Policy, and the Business Ethics and Conduct C...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: 85000
Posted: 2024-11-21 07:38:53
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Employer Description:
Legend Brands, an industry leader and long standing, stable company, combines over 185 years of experience in providing equipment, accessories and chemicals for professional cleaning, facility maintenance, portable environmental control, fire remediation and water damage restoration.
Job Summary
The EHS Manager is responsible for providing leadership for the EHS staff to implement EHS standards & procedures, provide expert technical assistance on EHS issues and will partner with functional leadership on compliance, project management, environmental compliance, reporting matters and related EHS management issues for all Legend Brands facilities.
Please apply directly on our careers page - https://hcwx.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2
Examples of Essential Duties
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Reasonable accommodations may be made to enable qualified individuals with a disability to perform the essential duties.
The below list is intended to be illustrative of the responsibilities of this position and is not all encompassing.
This job description does not constitute an employment agreement and may change these duties at any time.
* Safety audit process, reporting, and develop action items to drive improved safety culture.
* Completes required air permit reports.
* Completes wastewater reports
* Maintains EHS records.
* Coordinates with Production Manager and facility managers on preventive safety and environmental related issues.
* Ensures compliance with all safety standards and compliance for the States and local jurisdictions where we have operations.
* Assists in gathering data for environmental reports.
* Oversees Inspection of facilities to identify safety, health, and environmental risks.
* Proactive in addressing preventative issues.
* Develops and implements inspection policies and procedures, and schedules routine inspections.
* Develops health, safety, and environmental procedures for all areas of the company.
* Investigates any safety incidents, provide root cause analysis, and set plans to address improvement opportunities.
* Works with various contractors/vendors as needed.
* Prepares and schedules training to cover emergency procedures, workplace safety, and other relevant topics.
Monitors compliance with safety procedures.
* Drafts inspection reports to document inspection findings.
* Maintains records of discharge of, or employee exposure to, hazardous waste and/or pollutants, as required.
* Completes all required OSHA forms and postings.
* Performs other related duties as assigned.
Minimum Qualifications
The requirements listed below are representative of the education, experience, certification and/or licensure required.
An equivalent combination of education and experience to perfo...
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Type: Permanent Location: Burlington, US-WA
Salary / Rate: Not Specified
Posted: 2024-11-21 07:38:22
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ERM is a global consulting firm, in the business of sustainability since 1971.
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 opportunities for future generations.
Recognizing that environmental, health, safety, and social performance have become business-critical issues for many enterprises, ERM, as the world’s leading provider of environmental, health, and safety (EHS); risk; and environmental, social, and governance (ESG) consulting services, is helping companies deliver sustainable, safe, and compliant performance throughout all aspects of their operations.
Our Sustainable Operations team provides highly innovative services across the full breadth of EHS advisory areas such as sustainability auditing, information solutions, safety programs, compliance and management systems, training, and corporate reporting.
As part of the continued growth and innovation of our Sustainable Operations team, ERM has an opportunity for an experienced leader to join our global consulting firm as a Technical Director to provide technical leadership and mentoring. We will consider strong candidates based in Indianapolis, Indiana.
The Role
As a Technical Consulting Director, EHS Compliance and Management Systems, you will develop compliance, assurance, and management systems for our clients in a wide range of industries.
In this role, you will engage with large, exciting, and innovative clients to develop world-class EHS solutions.
You will have access to EHS leaders at these companies that will value your expertise and ERM’s outstanding global team of experts.
You will have the opportunity to implement novel and far-reaching solutions at the nexus of compliance and sustainability.
A highly organized technical leader who is a strong communicator and influencer will flourish in this role.
A candidate with strong Operational Risk & EHS Management solutions experience will engage and support the shaping a growth of EHS solutions.
In this position, you will provide intelligent and sustainable solutions that foster strategic operational processes, reduce risks, maintain compliance, increase safety, and deliver efficiencies for clients operationalizing their sustainability and ESG goals.
We seek individuals to help us drive the continued growth of ERM’s business through performing great work and achieving repeat business to EHS leaders where relationships are important and by delivering world-class services and mentoring our next generation of technical leaders, and further advancing our reputation for EHS sustainability solutions.
Key Responsibilities:
* Primary focus on EHS Industry relationships and world class delivery of services that are of value to our clients.
+ Developing and deploying EHS compliance solutions and management systems.
+ Delivering Air, water, and solid...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2024-11-21 07:27:25
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ERM is a global consulting firm, in the business of sustainability since 1971.
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 opportunities for future generations.
Recognizing that environmental, health, safety, and social performance have become business-critical issues for many enterprises, ERM, as the world’s leading provider of environmental, health, and safety (EHS); risk; and environmental, social, and governance (ESG) consulting services, is helping companies deliver sustainable, safe, and compliant performance throughout all aspects of their operations.
Our Sustainable Operations team provides highly innovative services across the full breadth of EHS advisory areas such as sustainability auditing, information solutions, safety programs, compliance and management systems, training, and corporate reporting.
As part of the continued growth and innovation of our Sustainable Operations team, ERM has an opportunity for an experienced leader to join our global consulting firm as a Technical Director to provide technical leadership and mentoring. We will consider strong candidates based in Indianapolis, Indiana.
The Role
As a Technical Consulting Director, EHS Compliance and Management Systems you will develop compliance, risk, assurance, and management systems for our clients in a wide range of industries.
In this role, you will engage with large, exciting, and innovative clients to develop world-class EHS solutions.
You will have access to EHS leaders at these companies that will value your expertise and ERM’s outstanding global team of experts.
You will have the opportunity to implement novel and far-reaching solutions at the nexus of compliance and sustainability.
A highly organized technical leader who is a strong communicator and influencer will flourish in this role.
A candidate with strong Operational Risk & EHS Management solutions experience will engage and support the shaping a growth of EHS solutions.
In this position, you will provide intelligent and sustainable solutions that foster strategic operational processes, reduce risks, maintain compliance, increase safety, and deliver efficiencies for clients operationalizing their sustainability and ESG goals.
We seek individuals to help us drive the continued growth of ERM’s business through performing great work and achieving repeat business to EHS leaders where relationships are important and by delivering world-class services and mentoring our next generation of technical leaders and further advancing our reputation for EHS sustainability solutions.
Key Responsibilities:
* Primary focus on EHS Industry relationships and world class delivery of services that are of value to our clients.
+ Developing and deploying EHS compliance solutions and management systems
+ Delivering Air, water, and so...
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Type: Contract Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2024-11-21 07:27:24
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Who We Are:
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history.
As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine.
Our purpose is to fuel confidence by helping people look better, feel better, and live better.
We believe you do not have to choose between living life and making a living.
Live your best life with Merz Aesthetics.
A Brief Summary:
The Publications Manager, reporting to the Senior Director of Global Publications, will plan, develop, and execute various publication projects (including global congress planning), ensuring timely delivery and high-quality output.
The role includes oversight of publication management platforms and regularly updating the publications repository with Merz-sponsored literature.
The ideal candidate has strong organizational, communication, and project management skills.
Duties and Responsibilities
* Project Planning:
+ Support the Global Medical Affairs Publications team in planning and scheduling publication projects that align with the department’s global objectives.
+ Coordinate with Publications team members, writers, editors, designers, and cross-functional stakeholders to ensure content is produced and delivered according to the project timeline.
+ Monitor the progress of each publication project to ensure adherence to deadlines and quality standards.
* Management of scientific materials for congress presentations:
+ Oversee and manage year-long congress planning activities, focusing on the publication of key materials.
This includes monitoring deadlines, coordinating with authors and contributors, and managing the logistics and schedules for congress publications.
+ Collaborate closely with internal and external stakeholders to ensure that global congress materials (e.g., abstract, poster) are developed, submitted, and approved compliantly to meet congress timelines.
* Management of publications platforms:
+ Manage publication management platforms and procedures for scientific content development, review and approval processes, and timelines in accordance with internal processes.
+ Update the publications repository platform with published Merz Ax-sponsored studies.
* Further tasks:
+ Maintain detailed records of all publication projects, including timelines, budgets, and communications.
+ Prepare reports on project status and outcomes for management.
+ Assist with preparing presentations, reports, contracts, and other materials.
Job Related Qualifications / Skills
* Professional Experience:
+ Minimum of 2 years of experience in publication planning, project management, or a similar role in the pharmaceutical, biotech, or healthcare industry
* Knowledg...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2024-11-20 07:39:45
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Fundamental Mission:
The Environmental Technician will assist with management of Environmental programs and initiatives for the Vallourec Star Houston sites, assist/support in the oversight of site environmental compliance, and programs and initiatives, assist with internal data collection, entry and reporting related monthly indicators, and CMR field inventories, inventory review and database updates related to the inventories.
This position will report directly to the EHS Manager, South.
Essential Duties and Responsibilities include the following:
* Assist with management of site environmental issues related to topics including: storm water, air, waste, wastewater, emergency plans, energy management, etc.
* Assist EHS personnel with site recordkeeping, as needed
* Assist with collection, review and reporting of environmental and safety indicators, as required, to support company objectives
* Participate in internal and external audits and program evaluations
* Direct department sub-contractor support as needed
Competency:
To perform the job successfully, an individual should demonstrate the following competencies:
* Outstanding communication skills
* Highly organized and able to successfully manage multiple projects
* Capable of working independently in a self directed environment
Education & Experience:
* Experience with data management
* Minimum of 1 years of experience in an environmental position
Skills and Knowledge:
* Outstanding communication skills
* Highly organized and able to successfully manage multiple projects
* Capable of working independently in a self - directed environment
Quality
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2024-11-20 07:34:50
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Technician
As a Quality Control Technician, you will play a crucial role in ensuring the accuracy and integrity of laboratory testing within our Quality Control and Environmental Control Laboratories.
In this position, you will be responsible for executing precise testing, participating in laboratory investigations, and maintaining equipment in compliance with GMP and safety guidelines.
This position will offer a one-time sign on bonus of $2,500!
Your Responsibilities:
* Perform timely and accurate testing of laboratory samples according to approved methods.
* Adhere to safety protocols and serve as a role model for safety practices on your shift.
* Conduct data entry and verification reviews with high attention to detail.
* Troubleshoot equipment and methodologies as needed.
* Engage in continuous improvement activities and self-inspections.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma or equivalent.
* Required Experience: Experience in a laboratory environment with a focus on quality control.
* Top 2 skills: Strong attention to detail and ability to work in a highly regulated environment.
What will give you a competitive edge (preferred qualifications):
* Familiarity with GMP and safety guidelines.
* Experience with laboratory investigations and equipment maintenance.
* Ability to work flexible shifts, including 12-hour and 8-hour schedules.
* Previous involvement in safety and ergonomic initiatives.
* Strong problem-solving skills related to laboratory operations.
Additional Information:
* Location: Clinton, IN Manufacturing Site
* Required to work in a laboratory environment (wearing safety glasses and laboratory clothing/PPE required). Some exposure to allergens is possible in the laboratory environment.
* Shifts may vary to include: 12-hour rotating (5:45-6:00), 12-hour day (5:45-6:00), 12-hour night (5:45 – 6:00), and/or 8-hour shifts.
* Unscheduled overtime may be required.
This positi...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2024-11-20 07:24:10
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
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: Occupational Health Nurse
As the Occupational Health Nurse at the Clinton Labs manufacturing site, you will lead the Occupational Health Services (OHS) clinic, ensuring the effective delivery of health and safety programs for employees.
In this role, you’ll be responsible for managing medical treatment for work-related injuries, conducting health assessments, and supporting wellness initiatives.
Your Responsibilities:
* Oversee medical surveillance and testing for compliance with occupational health standards.
* Triage and treat work-related injuries according to established medical guidelines.
* Provide emergency medical treatment and collaborate with the Emergency Response Team.
* Support return-to-work assessments and ensure safe transitions for employees post-medical leave.
* Implement and support employee wellness programs, including voluntary screenings and special projects.
What You Need to Succeed (minimum qualifications):
* Education: Registered Nurse (RN) license in Indiana or U.S.
compact RN licensure.
* Required Experience: Minimum 3 years of clinical experience in an acute healthcare setting and 1 year of occupational health experience.
* Top 2 skills: Proficiency in Microsoft Office (Excel, Teams, Word, Outlook) and strong organizational and communication skills.
What will give you a competitive edge (preferred qualifications):
* Certified Occupational Health Nurse (COHN or COHN-S).
* Certified Case Manager (CCM, COHN/CM, or COHN-S/CM).
* Experience with workers' compensation and workplace accommodations (ADA).
* Experience in a manufacturing or biotech/pharma environment.
* Experience with Family Medical Leave (FMLA) processes.
Additional Information:
* Location: Clinton, IN Manufacturing Site
* Travel: Occasional travel to other Elanco facilities in Indiana (Greenfield, Terre Haute, Indianapolis).
* Physical Requirements: Must be able to lift/carry up to 20 lbs frequently and up to 50 lbs infrequently; position may be required to enter manufa...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2024-11-20 07:24:09
