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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Market Access
Job Sub Function:
Health Economics Market Access
Job Category:
Professional
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson Pulmonary Hypertension, is recruiting for a Product Manager, HCP Access Marketing based in Titusville, NJ.
As part of Johnson & Johnson, we are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We collaborate with the world for the health of everyone in it.
Johnson & Johnson PH is a leader in the field of pulmonary arterial hypertension (PAH).
Our portfolio of PAH treatments covers the spectrum of disease, from WHO Functional Class (FC) II through to FC IV, with oral, inhaled and intravenous medications.
This position is a critical part of the Johnson & Johnson PH U.S.
Lifecycle & Therapy Access Marketing team.
This position will be responsible for the development and execution of HCP access resources across the PH portfolio (OPSYNVI®, OPSUMIT®, and UPTRAVI®).
This role will report to the Product Director, Therapy Access & Lifecycle Marketing.
Key Responsibilities:
* Coordinate execution of pull through excellence approach to maximize access investments across the J&J PAH portfolio.
* Lead the development and execution of HCP access messaging and resources for an HCP audience in partnership with the SCG organization.
* Serve as program lead for the PH unbranded Access Speaker Bureau by managing all aspects of execution, including content development, speaker training and program logistics.
* Lead the execution of HCP Access initiatives across the PH portfolio based on business need including the development of non-personal promotion assets.
* Serve as the field sales POA planning lead for the Therapy Access & lifecycle marketing team.
Partner with Sales Learning & Development to create workshops and trainings to elevate access acumen of the field sales organization.
* Cultivate and identify HCP Access insights for the brand, market, and PH landscape in partnership with field-based Therapy Access colleagues, market research, competitive intelligence, and analytics.
* Work productively with external agencies and key internal groups within the organization (SCG, Advocacy, IT, Market R...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:22
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, 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-000701
* Canada - Requisition Number: R-002921
* Belgium, United Kingdom, Switzerland - Requisition Number: R-002952
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 an Associate Director, Global Labeling Product Leader.
This position is a hybrid role and can be located in Raritan, NJ; Titusville, NJ; Horsham, PA.
The Associate Director, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provides advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation.
Ensure high quality and compliant labeling documents.
This role may collaborate with external partners.
* Contribute to and implement the global labeling strategy, including demonstrating an understandi...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:21
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Senior Scientist, Downstream Processing to be in Malvern, PA.
Purpose: This position will lead and perform purification process development for the antibody-based modalities within the API-Large Molecule group in Malvern, PA.
Primary responsibilities will include leading and participating in the design of experiments, executing the planned experiments, and optimizing the process steps to the target process scale.
This will include laboratory and occasional pilot-scale scale chromatography and filtration.
The candidate will lead the design and execution of development studies to identify and determine appropriate conditions and ranges of (critical) process parameters for chromatographic purification and separation and several types of filtration.
The candidate will record and analyze experimental data, verify data integrity and accuracy, interpret analytical characterization results, and report/summarize findings to the project team, and also draft technical documents and perform technology transfer to collaboration partners.
The candidate should have experience with computational modeling/simulations and knowledge of downstream application.
The candidate is expected to work in a team environment as well as contributing individually to meet project timeline and objectives.
You will be responsible for:
* Lead and perform process development for the antibody purification processes.
* Lead, design and execute planned experiments which will include laboratory and occasional pilot-scale chromatography and filtration.
* Lead, design and execute development studies to identify and determine appropriate conditions and ranges of (critical) process parameters for chromatographic purification & separation an...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:18
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
IE004 Barnahely
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
Job Description:
We are searching for the best talent for the Quality Control Analyst role to be in Cork, Ireland.
Purpose:
The QC analyst role is responsible for carrying out tasks and projects related to equipment, lab utilities and testing procedures at Janssen Sciences Ireland (JSI) as required by Good Manufacturing Practice (GMP).
Partners with other departments to ensure that all QC testing activities are completed in an efficient manner.
You will be responsible for:
* Achieves competency in laboratory methods and procedures.
* Trains other QC analysts in laboratory methods and procedures when required.
* Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
* Executes validation, operation, maintenance, calibration and troubleshooting of equipment and its associated software.
* Writes, executes, reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
* Performs routine and non-routine analytical testing activities.
* Review and approval (where appropriate) of laboratory test results.
* Ensures that testing and results approval are completed within agreed turnaround times.
* Writes and reviews laboratory TMs, SOPs, TMDs and WIs as directed by company policy.
* Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
* Is an active member of the QC group and provide assistance with other group activities as required and communicates relevant issues to the QC Specialist, QC Team Leader and Manager.
* Deals with Quality Issues in an accurate and timely manner.
* Maintains and develops knowledge of analytical technology as well as cGMP stan...
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:17
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Clinical Quality
Job Category:
People Leader
All Job Posting Locations:
New Brighton, Minnesota, United States of America, Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring a Senior Manager, Clinical Quality Assurance, to join our team! This is a fully remote role, with flexibility to be based anywhere within a reasonable commute to a major airport.
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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Sr.
Manager, Clinical Quality Assurance will provide GCP and compliance-related oversight and audit of internal and external Clinical Studies in process, support and update procedure compliance with applicable regulations and oversee clinical affairs initial and ongoing vendor audits as needed.
This work is accomplished with minimal oversight, requires frequent contact with internal and external customers and is critical to the success of the business.
Essential Job Functions
* Act as a Clinical Quality Lead on clinical trials by supporting project team compliance with national and international regulatory standards and guidance for medical devices
* Develop and manage audit management plans and audit strategy for ongoing clinical trials
* Prioritize audit strategies for GCP programs
* Coordinate, plan and conduct internal system au...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:04
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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: Process Operator – Product Finishing
As a Process Operator for Product Finishing, you will play a key role in the granulating, blending, and bagging of animal health products.
In this role, you'll be responsible for meeting departmental goals, ensuring quality, quantity, and cost targets while maintaining safety, compliance, and industry standards.
This posting will offer a one-time sign on bonus of $2,500!
Your Responsibilities:
* Operate large-scale processing equipment and troubleshoot issues as they arise.
* Drive a fork truck and handle 60-pound bags as part of routine operations.
* Ensure all production operations align with cGMP and ISO 9000 standards.
* Follow proper documentation, verification guidelines, and safety procedures.
* Suggest and implement safety and process improvements to enhance efficiency.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma or equivalent.
* Required Experience: Experience operating industrial processing equipment and working in a manufacturing environment.
* Top 2 skills: Troubleshooting and problem-solving skills
What will give you a competitive edge (preferred qualifications):
* Familiarity with fork truck operation.
* Experience in the animal health or related industry.
* Previous experience with cGMP and ISO 9000 standards.
* Strong initiative and ability to work independently.
Additional Information:
* Location: Clinton, IN Manufacturing Site\
* 12-Hour Rotating Shift (Days/Nights)
This position is a fixed duration employee with a one-year contract, annually renewable for up to 4 years with a potential for a full-time position, based on individual performance and business needs.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: 23
Posted: 2025-03-30 08:08:31
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Georgia-Pacific is actively seeking an Product Compliance Manager-International for our Building Products Gypsum products.
This is an exciting opportunity for an individual who is passionate about product compliance and wants to make a significant impact in a leading company.
As the International Product Compliance Manager, you will be instrumental in building international product compliance administrative programs, managing product testing, and supporting product standard and industry initiatives.
Join us as we transform the compliance capabilities of our building products division!
About the Role:
In this high-level compliance support role, you will focus on ensuring our building products meet the necessary compliance standards in European markets.
By leveraging resources, tools, and a commitment to excellence, you will create value and drive compliance efforts that keep Georgia-Pacific at the forefront of the industry.
Your unique contributions will be key to our success.
This is a remote role with travel to European markets.
Responsibilities:
* Provide expert compliance support, focusing primarily on European market requirements.
* Assess building codes and certification program applicability to our products.
* Determine country-specific requirements and ensure they align with our products.
* Seek, obtain, and maintain necessary certifications.
* Develop and maintain ongoing compliance programs.
* Design and implement test plans for building products in the European market.
* Engage with trade and test standard organizations that influence the European market.
* Collaborate with the broader compliance team to leverage learnings from the North American market
Competencies:
* Strong organizational skills with the ability to maintain certifications.
* Excellent interpersonal and communication skills.
* Capacity to balance multiple priorities effectively.
* Strong decision-making skills and a high degree of self-motivation.
* Keen attention to detail.
(Basic Qualifications):
* Understanding of building and technical standards relevant to the European market.
* Proficiency in Microsoft Office Suite (Teams, Word, PowerPoint, Outlook, Excel).
* Ability to travel approximately 20% to Europe and North America.
What Will Put You Ahead:
* Knowledge of European test standards and certifications, as well as Oceania (AUS/NZ) standards.
* Experience in fire or roof assembly testing.
* Proficiency in English and Spanish, French, or German.
* Familiarity with gypsum products
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abili...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-03-30 08:02:24
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Come grow with us! Georgia-Pacific has an immediate need for a Product Compliance Engineer at the Building Products Decatur Technical Center (DTC) in Decatur, GA.
The Product Compliance Engineer will lead product compliance administrative programs, manage product testing and support product standard and industry initiatives.
The product compliance engineer role will help transform the product compliance capability of building products division! Bring your skills, passion, and willingness to learn and grow in a dynamic team environment!
The Decatur Technical Center primarily focuses on Georgia-Pacific building products Research & Development, Technical Service, and Product Compliance efforts.
As a market leader, Georgia-Pacific has the resources, tools, assets, and commitment for you to be a successful contributor and create value.
At Georgia-Pacific, your unique abilities and contributions will be instrumental to our team & business.
If you aspire to use your skills and passion to create value as a Product Compliance Engineer, we are interested in learning more about you!
The successful Candidate will demonstrate:
* Strong processes development skills
* Strong interpersonal and communication skills
* Ability to balance multiple priorities.
* Strong decision making skills and highly self-motivation
* Strong attention to detail
* Ability and desire to learn and grow
What You Will Do
* Own and manage 3 rd party testing process & program
* Perform product testing needs assessment and establish Scope of Work for all new product testing programs
* Plan resource deployment for testing
* Mange test report document control system
* Support manufacturing facility 3rd party compliance audit program
* Manage renewals and submissions of product evaluations and certifications
Own and manage all existing product evaluation reports and product certifications
* Participate in select standards activities/org (e.g.
ASTM)
* Lead compliance document control projects
Who You Are (Basic Qualifications)
* Bachelor Degree (BS) in engineering (chemical, civil, etc.), environmental studies/policy, chemistry or science field OR building products experience in one or more of the following areas:
* Lab / Product / Quality testing
* Product Stewardship
* Building code interpretation
* Product renewals
* Compliance audits
Experience with Microsoft Office Suite (i.e.
Teams, Word, PowerPoint, Outlook, Excel)
What Will Put You Ahead
* Project Management experience
* Gypsum board manufacturing knowledge, or Gypsum product knowledge, or
Building Code & building product compliance knowledge
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
Th...
....Read more...
Type: Permanent Location: Decatur, US-GA
Salary / Rate: Not Specified
Posted: 2025-03-30 08:02:23
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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: Farm Animal Sales Representative – Cattle (Beef) - Nebraska
Your Responsibilities:
* Generate demand for Elanco products among food animal-focused customers, including veterinary clinics, nutritionists, and key beef and dairy producers.
* Transfer key messages and scientific information about Elanco products to producers and influencers within the designated sales territory.
* Execute business unit consultant strategy effectively.
* Partner with key Channel Partner/Distribution Representatives to ensure successful pull-through of Elanco products.
* Plan and implement sales promotions, meetings, and key customer events; while managing administrative responsibilities such as call notes and territory plans.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree or High School Diploma / GED with equivalent level of experience)
* Experience: 0-2+ years sales experience in beef and/or dairy industry preferably with a feed/nutritional & strategic account background or equivalent selling experience in a competitive selling environment.
* Must be legally authorized to be employed in the US.
Elanco does not anticipate proving sponsorship for employment visa status (e.g., H-1B status) for this position.
* Valid driver’s license and acceptable driving record
* Ability to provide secure and temperature controlled location for product samples may be required.
What will give you a competitive edge (preferred qualifications):
* Demonstrates strong learning agility, a passion for animal agriculture, and a self-starter mentality with a strong work ethic.
* Ability to make decisions in uncertain and ambiguous situations.
* Strategic thinking and experience in Strategic Account Management.
* Strong planning and execution skills with a focus on delivering results.
* Knowledge of food animal production and the animal health industry (economics and drivers).
* Excellent interpersonal and communication skills, with the ability to influenc...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-29 07:35:05
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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: Lab Technician - Quality Control
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 ...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-29 07:35:03
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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!
Position Description:
At Elanco we understand the powerful role healthy animals play in making lives better.
As pets increasingly become important parts of our families, so too does the need to help them live longer, healthier, higher-quality lives.
As the global population grows, so too will the need to meet the demand for safe, affordable food for all.
Elanco has been working to empower our customers—from veterinarians to food producers to all those concerned with animal health—to address these global challenges, and advance a vision of food and companionship enriching life.
We strive to develop and deliver products safe for consumers, animals and the environment through innovation and a shared vision to enrich the life of people worldwide.
Functions, Duties, Tasks:
* Customer Value Selling – ability to execute effective sales calls through focusing on customer needs and wants to drive loyalty, value and sales
* Account Management – ability to partner with key accounts, using strong commercial acumen and customer focus, to build long-term sustainable relationships
* Data analytics – ability to derive key insights from real world data to influence and change current and future working practice of vets and farmers/ Pet owners
* Provide management/technical support – including monitoring (e.g.
diseases, management and tracking) & vet training
* Around 75% field time (with vets, customer visits and some farms), including some overnight stays
* Accountable for the attainment of sales objectives and customer value delivery through the creation, implementation and execution of strategy and tactics.
* Deliver effective working practices, relationships, record keeping and communications within Elanco
* Work closely with the Technical Consultant and wider cross-functional team and in driving solutions to customers
Minimum Qualification (education, experience and/or training, required certifications):
* Veterinary experience in the Pet health sector would be advantageous
* University Bachelor Degree...
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Type: Permanent Location: Kinsale, IE-CO
Salary / Rate: Not Specified
Posted: 2025-03-29 07:35:01
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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: Senior Bioanalytical Scientist
Join Elanco’s RBI Discovery Science team as a Senior Bioanalytical Scientist, where you'll play a key role in developing and validating cutting-edge bioanalytical assays to support the advancement of our biologic's portfolio, including therapeutic proteins and vaccines.
You’ll combine hands-on laboratory expertise with strategic leadership, working across internal teams and managing collaborations with external CROs.
This role offers an exciting opportunity to innovate, lead cross-functional initiatives, and contribute to the development of new bioanalytical technologies, driving products from discovery to clinical development.
We’re looking for expertise in ligand-binding assays (e.g., MSD, ELISA), cell-based assays, immunogenicity assessments, and ideally, assay automation.
A strong background in large molecules like monoclonal antibodies and complex proteins is highly desired.
Success in this role will require a collaborative mindset, leadership skills, and a proven ability to solve problems and communicate effectively in cross-functional environments.
Your Responsibilities:
* Lead the development, validation, and optimization of bioanalytical assays (e.g., MSD, ELISA, cell-based) for therapeutic proteins and vaccines.
* Independently design, execute, troubleshoot, and interpret laboratory studies, contributing directly to data generation and analysis.
* Manage and mentor junior scientists, fostering talent and ensuring excellence in internal and external (CRO) bioanalytical activities.
* Oversee CRO activities, including assay transfer, study monitoring, data review, and issue resolution, ensuring timelines and data quality.
* Drive innovation by developing creative solutions for bioanalytical challenges and implementing new technologies and platforms.
* Collaborate across teams (Discovery, PK, Pharmacology, Toxicology, Clinical) to align on assay design, development, and implementation.
* Design and execute assays for PK/TK studies, immunogenicity assessments (incl...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 171000
Posted: 2025-03-29 07:34:45
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At SmartWorks, a division of Harris, we are passionate about driving innovation in the utility industry.
We are seeking talented software developers, designers, and architects who are eager to contribute to cutting-edge products and solutions.
As a valued member of our team, you will have the opportunity to work on enhancing our existing products with a keen focus on customer requirements and quality.
What sets SmartWorks apart is our commitment to a people-first culture.
We believe in fostering a supportive and community-like environment where every team member feels valued and empowered.
Our remote workforce spans across the US and Canada, with our main office located in Ottawa, Ontario.
This flexibility allows you to work from the comfort of your home while still being connected to a dynamic team.
We highly value clear and concise communication, and we strive to build a positive and enjoyable workplace.
At SmartWorks, continuous learning and professional growth are not just encouraged but ingrained in our culture.
You will have access to a wealth of resources and opportunities to expand your skills and advance your career.
Why SmartWorks?
* People-First Culture: We prioritize the well-being and development of our team members, creating a supportive and inclusive environment
* Community Vibe: Join a team that values collaboration, mutual respect, and a strong sense of community
* Continuous Learning: Benefit from ongoing professional development opportunities to enhance your skills and career growth
* Innovative Projects: Work on exciting and innovative products that make a real impact in the utility industry
* Remote Flexibility: Enjoy the freedom to work remotely from anywhere in the US or Canada, with occasional travel within North America
If you are a qualified professional looking to be part of a dynamic and forward-thinking team, we invite you to join us at SmartWorks.
Together, we can build the future of utility solutions.
Apply now and become a part of our thriving community where innovation meets support, and your potential is our priority.
This position is open to qualified individuals living anywhere in the US or Canada who are willing to work remotely from home and travel within North America on occasion.
A valid passport is needed for travel between Canada and the US.
Reporting to the Development Team Lead, the Software Engineer will:
* Implement product designs by programming in a variety of languages and using a variety of technologies
* Work with Development Team Lead to define appropriate estimates and communicate development progress
* Assist with software maintenance tasks assigned to the team – bug fixes, customer-driven feature development, etc.
* Collaborate with the R&D team on development methodology, processes, and associated tools
* Assist Support and Professional Services groups with design reviews and escalated issues
* Learn, practice and promote bes...
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Type: Permanent Location: Victoria, CA-BC
Salary / Rate: 95000
Posted: 2025-03-29 07:27:18
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CIS Implementation Consultant
Systems & Software - Remote
Systems and Software is seeking an Implementation Consultant to join our Professional Services team! The ideal candidate is an enthusiastic, team-oriented professional that provides outstanding customer service, has excellent deductive abilities, and thrives on delivering project milestones in a fast-paced environment.
Utilizing industry best practices, methodologies, and process controls, the Implementation Consultant will be responsible for working with a project team to deliver enQuesta CIS solutions and associated value-added services to both new and existing customers. This includes performing business process requirements analysis and documentation as well as system configuration, testing, implementation, training, and support.
The Implementation Consultant is customer-facing and plays a key role in effectively translating customer requirements into solution deliverables.
This remote role welcomes candidates anywhere in Canada and the US in the EST timezone.
This role requires up to 25% travel in North America.
A valid passport is needed for the travel.
What will be your impact?
* Define and understand client business requirements; interpret and apply the information within the scope of the project
* Configure the software using workflow and business rules to allow clients to conduct their business processes
* Work with data conversion specialist to achieve a smooth transition of legacy data
* Train the end-users in how to use the software in both remote and classroom-led sessions
* Be adept on the functionality and capabilities of the software, making enhancement requests to our product development team when appropriate
* Work with cross-functional team members including Project Managers, Data Conversion Specialists, Quality Assurance, Technical Support Analysts, and other Implementation Specialists
* Provide CIS subject matter expertise and consulting services for one or more projects teams assigned to new customer implementations, upgrades, and quotes
* Participate in discovery sessions with clients to establish “As-Is” and “To-Be” processes and produce documentation as required
* Assist data conversion resources with data mapping and validation
* Draft and execute software testing based on best practices and customer requirements
* Document training materials and effectively train the end-users
* Serve as a customer advocate and facilitate communication with other internal departments
* Provide support during customer testing, production implementation and beyond
What are we looking for?
* Bachelor's Degree in Business, Accounting, Information Systems, related field or equivalent work experience
* 5+ years of CIS, Utility Industry, S&S enQuesta, JIRA, Confluence, and Clarizen is a plus.
* Experience with electric rate c...
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Type: Permanent Location: Montpelier, US-VT
Salary / Rate: 100000
Posted: 2025-03-29 07:27:13
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Are you ready to dive into the world of creative problem-solving? Are you up for exciting challenges and eager to expand your knowledge? If so, we have an incredible opportunity for you!
A vibrant division of Harris; Advanced Utility Systems' Client Services is on the lookout for a dynamic Technical Consultant who can deliver top-notch customer care.
As part of this role, you'll become a subject matter expert in our products through client training, troubleshooting issues, and addressing client requests.
But that's not all! You'll also get to flex your skills by effectively integrating functionalities in our CIS Infinity system and taking charge of multiple projects independently.
What's even better? You won't be alone in this journey.
You'll be collaborating closely with an amazing team to implement new enhancements and seamlessly integrate our web solutions with CIS Infinity.
If you're ready to take on this thrilling challenge and be part of an innovative team, we can't wait to hear from you! Let's embark on this exciting adventure together.
Apply now!
This remote role welcomes candidates anywhere in Canada and the US.
This role will be working in the EST timezone.
What your impact will be:
* Assess and translate client’s requests into what the client truly needs
* Find and implement creative and optimal solutions to accommodate the requirements within our applications
* Analyze and troubleshoot product stability inquiries or issues of both product and technical nature by phone or electronically through the ticketing system
* Liaise with 3rd party vendors, end-users, and our client’s IT
* Document configuration, enhancement, and testing notes for various projects through the ticketing system
* Work closely with other team members as part of a cohesive group on various projects
* Provide client training or assistance remotely or occasionally onsite
* Maximize and maintain current knowledge and awareness of applications and related technologies
What we are looking for:
* 2-5+ years of experience in customer support/business analyst
* Ability to review and analyze the following programming languages: VFP, C#, ASP.NET, and Powershell
* Ability to create and modify complex SQL scripts
* Ability to interpret requirements, and recommend solutions that best address clients' needs
* Ability to travel up to 25% in North America
* College Diploma in Computer Science or equivalent industry experience
* Excellent analytical, research and problem-solving skills
* Exceptional verbal and written communication skills
* Exceptional attention to detail and the ability to grasp concepts quickly
What would make you stand out:
* Experience with Remote Desktop Services/RemoteApp
* Experience with multiple remote access tools & techniques such as webex, remote desktop, VPN
* Oral or written communication in French
* Customer Service Training or Certif...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: 90000
Posted: 2025-03-29 07:27:10
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Chronic Care Coordinator
Location: MICHIGAN - 100% REMOTE (NOT A COMPACT STATE)
Join our mission to help transform healthcare delivery from reactive, episodic care to proactively managed patient care that prevents live-changing problems before they happen for patients with two or more chronic conditions.
We believe every patient with chronic disease deserves consistent check-ins, follow-up, and support.
The position of the Remote Chronic Care Coordinator will perform telephonic encounters with patients on behalf of our partners each month and develops detailed care plans within our care plan templates in the electronic health record.
This begins as an Independent 1099 Contractor position but offers the potential to reach full-time W2 employment (with employee benefits).
Esrun Health is seeking nurses to work part-time from their home office as independent contractors while complying with HIPAA privacy laws.
You will set your own hours and will not be held to a daily work hour schedule.
Esrun Health wants its team members to have the flexibility to balance their work-life with their home life.
Part-time team members will typically need to dedicate an average of 20-30 hours per week to care for their assigned patients.
This unique business model allows you to choose what days and what hours of the day you dedicate to care for your patients.
The Care Coordinator will be assigned a patient panel based on skill and efficiency level and is expected to carry a patient panel of a minimum of 100 patients per calendar month within the first three months of assignment.
Care Coordinators will be expected to complete encounters on 90 percent of the patients they are assigned each month unless patients are unable to participate due to current health conditions.
Compensation Structure
Esrun Health utilizes a productivity-based pay structure:
$10.00 per completed patient encounter up to 99 encounters/month.
$10.25 100-149 encounters/month
$12.00 150-199 encounters/month,
$14.00 200-249 encounters/month
$16.00 >250 encounters/month.
Payment tier increases require 3 months consistency to achieve.
There is a $1/encounter incentive compensation for bilingual nurses equal to $3/hr.
A patient encounter will take a minimum of 20 minutes (time is cumulative to include chart review time, time spent during call attempts and the non-face-to-face encounter, time for care coordination, and time spent for documentation/billing time).
Wha...
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Type: Contract Location: Lansing, US-MI
Salary / Rate: Not Specified
Posted: 2025-03-29 07:27:00
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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. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) process.
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Type: Permanent Location: Lenexa, US-KS
Salary / Rate: Not Specified
Posted: 2025-03-29 07:25:50
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PURPOSE AND SCOPE:
An important role in shaping the future of Fresenius Medical Care, the Manager, Corporate Strategy will work closely with the executive team and business leaders in the development of strategy for the organization, enabling company growth in core and adjacent markets.
Leads initiatives to analyze complex business problems and issues using data from internal and external sources. Develops senior relationships across the company and partners with business leaders and functions to develop best in class strategies and analysis of business-critical issues. Part of a dynamic, high performing team with both opportunities to develop others and further develop this leader’s own career.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Identifies, analyzes, and prioritizes actionable growth opportunities or new services supporting existing businesses
* Develops strategic and business plans for various product and service lines and facilitating integration of these plans into strategic planning process
* Leads cross functional team in problem solving of complex and high-impact issues and implementing high-impact opportunities
* Empowers the Field to develop and implement market-level strategies through developing frameworks/processes/tools - and driving their adaption in the Field.
* Develops strategy in partnership with the Executive team, articulates strategy in clear and concise manner, including near term tactical components to accelerate growth and profitability of the existing business longer term transformational strategy to pursue new opportunities and address changes in healthcare market
* Conducts strategic analyses of market and internal data to identify trends and model financial impact
* Leads nimble cross-functional teams to explore, evaluate, analyze ideas as well as implement high-impact opportunities through meaningful and practical assistance with their incubation
* Raises the level of strategy skills across the organization by advising leaders and sharing appropriate best practices, tools and frameworks
* Manages external consultants in exploring and developing opportunities for value-based care in a broader healthcare market
* Performs other related duties as assigned.
SUPERVISION:
Typically supervises exempt staff.
EDUCATION AND REQUIRED CREDENTIALS:
Bachelor's Degree; Advanced Degree (MBA) desirable or an equivalent combination of education and experience
EXPERIENCE AND SKILLS:
* 5-7 years of experience with a multi-divisional Healthcare company or strategy consulting, or an MBA with 2-3 years of experience.
* Demonstrated ability to manage one or more departments.
* Healthcare industry experience.
* Strong inductive thinking ability - the ability to connect the dots and to identify and recognize growth opportunities that are beyond the surface.
* Structured deductive thinking- the ability to frame an ambiguous p...
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Type: Permanent Location: Waltham, US-MA
Salary / Rate: Not Specified
Posted: 2025-03-29 07:25:28
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Supply Chain Accounting Analyst II - 12 Months Contract (Global Business Services)
Job Description
Supply Chain Accounting Analyst II (12 Months Contract) - Global Business Services
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Role Overview & Primary Accountabilities:
* Prepare analysis, reporting of actual, budgets and forecasts of the manufacturing operations in accordance with US GAAP and accepted inventory valuation methodologies
* Provide a source of financial and product costing expertise, business knowledge and problem solving capabilities to ensure sound reporting and analysis which accurately reflect the performance and integrity of the manufacturing operations, product costs and transfer pricing.
* Maintain assigned systems, processes, or process components (including valuation of raw materials and finishing supplies) in good working order
* Implement and conform to applicable cost accounting policies, internal control procedures and generally accepted accounting principles.
* Work collaboratively with internal customers to achieve business objectives and efficiently provide the essential administrative support services to the organization.
* Identify and make recommendations that optimize business processes and improve financial and internal controls and other business practices in alignment with LEAN and culture of continuous improvement.
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 151 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 joi...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-03-29 07:23:29
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ABOUT THE ROLE
Amsted Automotive, Sterling Heights, is seeking Quality Auditors who will be responsible for all phases of inspection and quality audits. The Quality Auditor ensures conformance to blueprint as appropriate, customer specific and internal procedure requirements for all products, and processes.
This is a day shift direct-hire opportunity, 7:00 am - 3:00 pm, with overtime and weekends as needed.
WHAT YOU’LL DO
* Perform receiving, in process and final audit inspection as directed
* Record attribute and variable data on in process inspection record according to parts-specific dynamic control plans
* Verify that procedures are being followed and inspections performed by operators
* Responsible for supporting the team efforts of set up and operation of stamping presses as related to inspection tools, etc.
* Perform final audit inspection which requires tagging parts and dunnage properly for storage in work in process areas or for shipment to the customer
* Responsible for notifying press and/or production if non-conforming material is detected, suspect material is to be identified and isolated.
Assist in identification of “Clean Point”.
* Communicate findings, regarding trends or nonconforming parts or processes to appropriate personnel and participate in corrective action process
* Perform First piece and in-process inspections and log in process inspection record, as applicable, including contamination testing, as applicable
* Perform Last Off inspections, including provide part data to assist in tooling repairs on last off report
* Generate reports of nonconforming material or product(s)
* Identify nonconforming material and quarantine
* Assist in root cause analysis and problem-solving tasks as assigned
* Assist in Gage R&R’s and Part Capability Studies as assigned
* Identify trends using basic statistical process control techniques
* Other duties as assigned
* Communicates to next shift personnel
WHAT YOU’LL NEED TO SUCCEED
* All inspection work requires proficient use of measuring equipment (scales, micrometers, calipers) and checking fixtures, and metrology tools (surface testers, CMM’s, )
* Must be computer literate and have working knowledge of other workplace machinery such as a SAP hand held scanners calculators and printers
* Must be able to read blueprints as appropriate
* Possess working knowledge of IATF16949, ISO 14001, and Q1 Compliance Criteria
WHAT’S IN IT FOR YOU
* Employee Stock Ownership Plan
* Incentive Bonus
* Medical, Vision, Dental
* Prescription Drug Plan
* 401K
* Paid Vacation & Holidays
* Short-Term Disability
* Tuition Reimbursement
* Health and Wellness Reimbursement
* Employee Recognition
* Discount Programs
WHAT ELSE YOU’LL NEED TO KNOW
* Excellent communication skills, both verbal and written for interaction with...
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Type: Permanent Location: Sterling Heights, US-MI
Salary / Rate: Not Specified
Posted: 2025-03-29 07:17:24
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Looking for a chance to make a meaningful 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 highly value our employees, who work relentlessly to help 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 patients, the global healthcare community, collaborators and partners, and each other.
Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.
It’s our work, our passion, and our legacy.
We invite you to join us.
Hybrid
Employee Value Proposition:
At Taiho Oncology, the compassion we practice for our patients extends to our team, empowering and motivating them to do their best work for those who need it most.
This is an exciting opportunity to work in a diverse, talented, and committed group of people to advance the treatment for oncology patients and experience multiple facets of regulatory affairs in a dynamic, collaborative, and global cross-functional environment.
Position Summary:
* The incumbent is responsible for supporting Regulatory Affairs activities (nonclinical, clinical and safety) for assigned investigational development products from nonclinical candidate designation through product approval, including regulatory submissions.
This individual is responsible for maintaining an in-depth awareness of relevant federal and international regulations and policies to optimize regulatory input to assigned projects and teams.
Performance Objectives:
* Work with Regulatory strategists to implement process and ensure on-time Regulatory routine submissions for assigned programs
* Support Regulatory strategists in coordination of Regulatory Submission teamwork and meetings (e.g., help to maintain resource plans, initiate intranet document workflows for review and approval, help to maintain submission timelines, and initiate document inventories in collaboration with the RA lead and Regulatory Operations Publisher)
* Collect Regulatory information to support QP product specification files
* Coordinate archival of submission information and Regulatory Health Authority
* acknowledgement
* Train on CREDO to maintain and update published documentation in that repository for
* assigned projects
* Provide regulatory project management to support submissions
* Independently prepare routine regulatory submissions
* Review relevant documents from a regulatory perspective
* Other tasks and...
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Type: Permanent Location: Pleasanton, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-29 07:16:42
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INVISTA is looking for a Document Control Specialist.
The successful individual will manage company intellectual property and project documentation efficiently while practicing careful communication.
You will serve as the key resource for specialized knowledge in the use and optimization of document management systems across the organization.
Your expertise will be critical in ensuring that these systems meet organizational needs and provide value to all users, facilitating efficient document handling and compliance with company standards.
Our Team
This role is based on the north side of Houston, in the Greenspoint area.
This position offers a flexible hybrid schedule, allowing for a blend of remote and on-site work to support work-life balance and productivity.
This person should be prepared to work on-site as needed to collaborate effectively with team members and engage with projects that require in-person attention.
What You Will Do
* Requirements Gathering: Collaborate with various departments to gather and analyze document management needs.
Ensure that system requirements are well-defined, understood, and communicated efficiently across the organization.
* Technical Guidance: Provide support and guidance to IT and other technical teams, ensuring a clear understanding of document management requirements and facilitating system integration.
* Functional Specifications: Translate organizational needs into functional specifications, ensuring alignment with corporate objectives and compliance standards.
* Problem Solving: Proactively identify and resolve issues related to document management systems, proposing effective solutions and escalating as necessary.
* Quality Assurance: Oversee and participate in testing and validation processes to ensure that document management systems meet required standards and fulfill user needs.
Identify and implement improvements as needed.
* Training and Mentorship: Act as a mentor to colleagues, providing training and guidance to enhance document management skills and improve overall performance.
Develop, implement and distribute procedures to streamline document management.
* Tool Ownership: Take ownership of document management tools by driving continuous improvement and maximizing their value to the organization.
* Organizational Change Management: Support the organization in adopting changes related to document management strategies and tools.
Who You Are (Basic Qualifications)
* Experience in managing document management processes and analyzing user requirements
* Proven experience in advocating for document management systems that improve operational efficiency
* Demonstrated ability to convey complex information clearly and concisely to both technical and non-technical audiences, with a keen attention to detail
* Experience in analyzing and resolving document management issues, with the ability to identify patterns and propose solutions...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-03-29 07:16:24
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Roche in 50 Worten
Eine gesündere Zukunft.
Das treibt uns an, innovativ zu sein. Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die benötigt wird.
Wir schaffen eine Welt, in der wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Das macht uns zu Roche.
Was macht unseren Bereich aus:
Der Bereich Diagnostics Operations Penzberg ist weltweit der wichtigste Roche Diagnostics Produzent von qualitativ hochwertigen Einsatzstoffen bis hin zu speziellen Kits.
In der Qualitätskontrolle für diesen Bereich unterstützt Du bei der Analytik und Freigabe von Reagenzien und Kits, welche im Anschluss vielfältige Verwendung in der Diagnostik und Pharma finden.
Dabei arbeitest Du mit einer Vielzahl von molekularbiologischen und immunologischen Methoden zur Sicherstellung der Produktqualität.
Das Team:
Im modernen Labor der Gruppe DOZQSI erwarten Dich 12 KollegenInnen, welche im engen Austausch untereinander und weiteren Qualitätskontrolle-Gruppen arbeiten.
Zur Seite stehen Dir Laborassistenten, die als „rechte Hand“ des Gruppenleiters den Laborbetrieb planen und Fragen rund um die Analytik beantworten können.
Über die Gruppen hinaus sind wir mit den Schnittstellen Musterziehung, Planung und Produktion eng vernetzt.
Es erwartet Dich ein Arbeitsumfeld, das es Dir leichtmachen wird, Fuß zu fassen.
Wir haben eine gute Mischung aus langjährig erfahrenen und jungen Mitarbeitern.
Die gute und vertrauensvolle Zusammenarbeit im Team ist ein wichtiger Baustein unseres Erfolges.
Deine Aufgaben:
* Du führst Analytik von Einsatzstoffen und Kits im Bereich der Immunologie (ELISA etc.),
* Molekularbiologie (MagNA Pure, Cobas, MGPs etc.) und Zellkultur durch
* Du wertest Analytik-Ergebnisse selbstständig aus und dokumentierst diese gemäß DIN ISO /
* GMP bzw.
geltenden Arbeitsanweisungen
* Du erkennst, dokumentierst und meldest Abweichungen
* Du pflegst Deinen Laborarbeitsplatz und übernimmst die Verantwortung für Equipment und
* Material
* Anfallende Zusatzaufgaben sowie Spezialanalysen erledigst Du nach Einweisung durch Deinen
* Vorgesetzten selbstständig
Die Bereitschaft zum Einsatz in einem biologischen Sonderlabor und dort der Umgang mit infektiösem Material ist für die Position erwünscht.
Dein Profil:
Für diese Position bringst Du folgende Voraussetzungen mit:
* Deine Ausbildung zum Laborant Chemi...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-03-29 07:10:47
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As a Customer Growth Solution Architect, you will work closely with customers to design, implement, and adapt a strategic roadmap that aligns with their evolving business quality engineering transformation objectives.
Key Responsibilities:
Customer Strategy:
* Strategy Development: Craft outcome-based value roadmaps to drive adoption and ensure technical alignment with customer business goals.
* Technical Reviews and Adaptive Roadmap Refinement: Establish strategic checkpoints to review the product’s impact on the customer business and realign as necessary with evolving customer needs.
Develop and implement actionable plans for product value assurance.
Customer Retention and Growth:
* Value Realization and Growth: Capture and communicate success stories, highlighting the impact on customer business backed by business metrics and outcomes.
Assist the account team in identifying opportunities to enhance value gains by adopting the Tricentis product portfolio corresponding to evolving customer use cases.
* Renewal: Proactively mitigate retention risk by monitoring customer health scores and identifying signs of churn.
Implement and execute preemptive action plans to address potential issues using value strategy and roadmaps.
* Cross-functional collaboration: Work closely with product strategy and account teams to review customer feedback and identify opportunities for product enhancements to ensure our solutions remain aligned with customer needs and market trends.
Technical Solution Architecture:
* Solution Design & Framework Development: Work closely with product specialists and customers to develop adaptable, high-value quality frameworks tailored to customer goals, utilizing advanced Tricentis tools and expertise in testing methodologies.
* Value Metrics & KPI Alignment: Define quantifiable KPIs to monitor and demonstrate Tricentis portfolio impact on client quality goals, ensuring continuous alignment with business objectives.
* Customer Enablement: Collaborate with Tricentis Professional Services to offer tailored advanced enablement and define standards and best practices that ensure high value and efficient adoption of Tricentis products.
Provide insights and recommendations for new features and functionalities that could enhance customer workflows, increasing product impact and satisfaction.
Competencies:
* Bachelor’s degree in computer science, Information Technology, or a related field.
A master’s degree in the listed field would be nice to have.
* 5+ years of experience in architecting and implementing quality frameworks using Tricentis products portfolio and advanced testing methodologies.
* 3+ years of experience consulting on quality engineering roadmaps and delivering measurable outcomes.
* Strong leadership, customer relationship management, and decision-making skills with, a proactive solutions-oriented approach.
* Strong analytical skills with experie...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-03-29 07:09:23
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Planning
Job Sub Function:
Inventory Management
Job Category:
People Leader
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
Job Description:
Johnson & Johnson is currently recruiting for a Senior Manager, Global Inventory Management.
This position is primarily located in West Chester, PA with consideration for other J&J Medtech locations within the US, Ireland, and Switzerland.
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 - R-005629
Switzerland - R-006579
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
The manager will be accountable for delivering inventory targets and optimization programs for DPS (globally); covering Joints Reconstruction, TECA (Trauma-Extremities-Craniomaxillofacial-Animal), Spine, Sports & Shoulders and Power Tools/ Robotics.
This program covers primary and secondary Hubs Entitlement, including some Regional/Market DCs (via MEIO), Lead Time improvement, Cycle Inventory optimization, among others.
Responsibilities:
* People: Leads and develops a team of planning analysts, who drive Inventory Management for all DePuy Synthes Platforms: Joints and TECA (Trauma / Extremities / Craniomaxillofacial / Animal), assessing and implementing improvement plans.
* Process: Drives adherence to Plan Transformation Blueprints
* Lead: Serves as planning primary point of contact for Global Inventory; collaborates with DPS Regional SC Planning teams, Finance and Commercial Business Partners to deliver targets and contingency plans.
* S&OP/IBP: Accountable for Global operational inventory monthly reporting process and budget cycles (BP, JU, NU and revisions).
* Parameter optimization: Drives detailed understanding of key inventory parameters, such as MOQ, EOQ, lead times, master data and supply variability trends.
* Multi-Echelon Inventory Optimization (MEIO): Drives maturity of MEIO process / tool and challenges inventory policies.
* LRFP: Coordinates annual Long Term / Strategic inventory planning activities
* Team leader: Engagement with S&OP, Demand Planning, New Produc...
....Read more...
Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-03-29 07:08:24
