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Ardurrra is seeking a Land Use Planner to join our team in Nampa, ID or Meridian, ID!
Job Description:
We are seeking a highly motivated and experienced Land Use Planner to join our team.
In this role, you will be responsible for developing and implementing comprehensive land-use plans and strategies that support our client’s development goals.
You will also be responsible for coordinating the development of multiple projects from start to finish, ensuring that all projects are completed on time, within budget, and to the required quality standards.
The ideal candidate will have a strong understanding of local land use regulations, local planning principles, community engagement, and a passion for creating vibrant and sustainable communities.
Required Qualifications:
* Bachelor’s Degree in Land Use Planning or similar.
* 2+ years of experience in land use planning in the private or public sector.
* A minimum of 2 years of experience in a similar role, with a strong track record of successfully coordinating the development of land development projects.
* Excellent organizational skills, with the ability to manage multiple projects and priorities effectively.
* Strong understanding of local, state, and federal land use regulations and policies.
* Excellent communication, presentation, and interpersonal skills.
* Strong interpersonal and communication skills, with the ability to effectively communicate with a wide range of stakeholders, including engineers, contractors, cities, government agencies, surveyors, attorneys, and various departments within many municipalities.
* Ability to effectively manage multiple projects and meet deadlines.
* Strong problem-solving and decision-making skills, with the ability to identify and manage project risks and issues effectively.
* Ability to work as part of a team, with project managers, engineers, surveyors and other stake holders.
Key Responsibilities:
* Conduct site analyses and research to determine the feasibility of proposed land-use projects
* Prepare and present land use applications and development proposals to clients, government agencies, and community groups.
* Route plats and other necessary project documentation.
* Participate in public meetings and community engagement events to gather feedback and build support for development projects.
* Work to ensure projects meet zoning and other regulatory requirements.
* Collaborate with other departments to ensure projects are completed on time and within budget.
* Stay current on land use planning trends, laws, and regulations.
* Attend professional development opportunities to continue expanding your knowledge and skills.
We offer a competitive compensation and benefits package, as well as opportunities for professional growth and development.
If you are passionate about land use planning and have a track record of success, we encourage you to apply.
...
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Type: Permanent Location: Meridian, US-ID
Salary / Rate: Not Specified
Posted: 2025-03-27 07:08:16
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ERM’s Climate Risk and Opportunity Advisory (CROA) team, within our broader Corporate Sustainability & Climate Change (CS&CC) function, is growing quickly.
We are looking for consultants to support us in helping our clients shape and deliver on their climate strategies and disclosures.
There is a significant opportunity for individuals to progress within the organization, to take increasing responsibility for managing our work within the climate change space and developing market-leading offerings to meet our clients’ needs.
This role will focus on quantifying the financial implications of climate risk, but there are opportunities for the candidate to contribute to all of our team’s work across the climate change space (including relating to the low-carbon energy transition and net zero).
More details of the role, as well as the skills required to fulfil it, are detailed below.
Role Description & Key Responsibilities:
As a member of the Climate Risk and Opportunity Advisory Team, you will:
* Apply quantitative methodologies to climate risk and opportunity assessments, including financial statement analysis, discounted cash flow modelling, cost-benefit analysis, and uncertainty analysis such as Monte Carlo simulations.
* Engage directly with corporate clients, including senior leadership, to provide education on climate-related topics, and present your own analytical work and defend quantitative results.
* Build templated quantitative methodologies for climate risk estimation that can be leveraged on climate projects.
* Incorporate a wide range of data sources into your analyses including corporate financial data, geospatial climate data, academic research and industry-specific reports.
* Support the delivery of client deliverables by working with team members across the business.
* A key aspect of this will be to communicate the findings in a digestible way including developing client curiosity regarding how they start their journey to transitioning to a low carbon economy.
* Support business development and sales-related activities, including helping senior colleagues to draft client proposals and develop new offers.
* Contribute to ERM’s innovation and knowledge-sharing through ad-hoc involvement in thought leadership, internal newsletters, learning sessions, amongst other initiatives
PERSON SPECIFICATION
Well-placed candidates will match some or a significant part of the specification below:
Required:
* Background Academic and professional experience in climate change / sustainability as well as finance/economics. Understands the fundamentals of why climate change is happening, how it will start to affect business models/strategy/company revenue, Capex, Opex and familiar with the concepts of decarbonization & net zero pathways.
* Motivational Fit – Produce high-quality client-ready deliverables, can work independently, team player, demonstrates critical thinking and is comfo...
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Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2025-03-26 07:31:41
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General Summary
Maintains and distributes the sanitation chemicals and tools used in the production facility.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
1.
Mixes, samples, stages, and distributes all chemicals for usage according to company guidelines.
2.
Daily/weekly inventory of all chemicals.
3.
Maintains close relationship with chemical supplier to ensure the appropriate inventory of chemicals, dispensing equipment, parts and supplies.
4.
Assists with producing weekly chemical usage reports.
5.
Maintains the proper labeling of all chemical containers and point-of-use jugs, buckets, foamers, and door foamers according to company guidelines.
6.
Ensures proper storage of chemical containers, cleaning tools and brushes.
7.
Maintains the organization and cleanliness of the sanitation storage areas, chemical rooms, jugs, buckets and tanks.
8.
Maintains operable condition of all chemical dispensing equipment, foamers, door foamers, and pumps.
Troubleshoots any issues and repair leaks/malfunctions.
9.
Follows company safety guidelines and Good Manufacturing Practices.
10.
Regular attendance and punctuality are required due to working with people, items and equipment that are at the facility.
Job Specifications
1.
Sanitation experience is preferred.
2.
English/Spanish bilingual is a plus.
Working Conditions
1.
Refrigerated food manufacturing plant.
2.
The environment may be wet or dry and temperatures may range from 25°F to 110°F.
3.
Frequent exposure to hazardous material and waste.
4.
Repetitive lifting, kneeling, and bending with items in excess of 60 lbs.
is required.
5.
Repetitive hand, wrist, and finger activities.
6.
Production demands may require overtime and/or evening or weekend scheduling.
Compensation
$19.40 – $24.25 Hourly/Non-Exempt
Recipe for Success
Reser’s is the leading provider of fresh refrigerated deli salads, side dishes, and prepared foods for the supermarket, club store, and food service industries.
Family owned and operated, Reser’s has been a proud sponsor of good times at racetracks, picnics, B...
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Type: Permanent Location: Pasco, US-WA
Salary / Rate: Not Specified
Posted: 2025-03-26 07:28:43
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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!
$2,500 sign-on bonus eligible!
Why Work at Elwood?
The Elanco Elwood, Kansas facility was acquired from Kindred Biosciences in 2021 which offers a strong pipeline of innovative drugs for companion animals within the monoclonal antibody space.
Working at a monoclonal antibody start-up facility in Elwood, Kansas presents an exciting opportunity to contribute to cutting-edge research: Monoclonal antibodies are an innovative type of biologic drug that can target specific molecules in the body to treat a variety of diseases, including cancer and autoimmune disorders.
Working at a start-up facility that is developing these drugs is an opportunity to be on the forefront of medical research and contribute to developing treatments that can have a significant impact on pets' lives.
Your Role:
An operator is responsible for performing and documenting all tasks and activities associated with biologics manufacturing at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility.
* Execute and monitor critical processes for mAb manufacture such as media and buffer preparation, upstream expression, downstream purification, formulation, fill/finish, and/or secondary packaging.
* Operate in a USDA / FDA / EMA cGMP regulated environment, maintaining strict adherence to all applicable regulations.
* Accurately follow SOP’s and batch production records in operation of production equipment, performance of processing steps, and execution of daily tasks.
* Perform aseptic manipulations and demonstrate knowledge and experience of aseptic techniques.
* Interface with the Quality Control department to submit in-process samples and coordinate environmental monitoring during key process steps.
* Assemble, prepare, and maintain process equipment including, but not limited to biological safety cabinets, incubators, bioreactors, chromatography skids, columns, tangential flow filtration systems, pumps, fill/finish units, labelling/packaging units and ancillary equipment.
* Identify and support the implementation of process improvement ...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 24
Posted: 2025-03-26 07:25:43
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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: Production Operator - API
The Production Operator is responsible for preparing, executing, and cleaning/turnover of production processes in poultry vaccine production.
All tasks are performed in accordance with internal and external guidelines.
Your Responsibilities:
* Egg Handling (egg receipt, traying, disinfection processes, transferring eggs) and egg derived processes & tissue culture (candling, incubation, inoculation, harvest, inactivation)
* Centrifugation, concentration processes, and filling operations (product emulsification, liquid filling processes, lyophilization)
* Process and equipment preparation and process cleaning/disinfection activities including washing, wrapping, and sterilizing of glassware and equipment, loading/unloading autoclaves and disinfecting room surfaces and equipment.
* Ensuring appropriate number of materials (chemicals, consumables, etc.) are available
* Use of electronic systems (e.g.
SAP) to stage materials
What You Need to Succeed (Minimum Qualifications):
* High School Diploma or equivalent
* Ability to perform routine, repetitive tasks with moderate to limited degree of supervision.
* Ability to perform duties according to established SOP's, production records and company safety procedures.
* Complete training on time to maintain a current and up to date learning plan.
What Will Give You the Competitive Edge (Preferred Qualifications):
* Understands and practices proper aseptic technique and biosecurity measures
* Ability to concurrently completes documentation and follows established protocols
Additional Information:
* Shift: Monday-Friday, 7am-3:30pm
* Must maintain procedural conformance during all production hours including and not limited to weekday and weekend operations. This may include notifying supervisors/support staff via phone/email/teams to escalate findings of product non-compliances or equipment failures.
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, r...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: Not Specified
Posted: 2025-03-26 07:25:41
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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!
Grow your career internally at Elanco, our best talent comes from within!
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 env...
....Read more...
Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-26 07:25:37
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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!
Background:
At Elanco, we advance our vision of food and companionship enriching life by developing innovative solutions that protect and enhance animal health.
Since 1954, Elanco has been working to empower veterinarians, food producers, and all those concerned with animal health with the tools needed to help animals live healthy lives.
Job description:
There is an exciting opportunity to join a dynamic process development team responsible for development and scale up of new biopharmaceutical and vaccine products.
The Biopharma technical development team works collaboratively with an inclusive culture to deliver innovation for Elanco.
The Research Scientist is responsible for providing technical and scientific expertise for process development and commercialization activities of new drug substances/products with an emphasis on downstream purification processes.
The individual will be expected to lead downstream process development, scale up, technical transfers, process implementation, and material delivery activities for IVP or CT supply and registration.
Additionally the role will support process validation-related activities.
The role is focused on ensuring that a robust manufacturing process is developed according to quality by design and ‘end in mind’ principles.
The research scientist is expected to be hands on but will provide technical direction, coaching and mentoring to scientists.
The holder of the position is regarded as a technical expert for R&D Elanco globally and will work collaboratively with management and global project groups in line with site, functional and corporate business goals.
Key Responsibilities:
* Provide technical leadership for downstream development (protein purification) from early through late phase large molecule projects, ensuring phase appropriate technical development and collaborating closely with relevant functions.
* Provide technical leadership/expertise for delivery of process development projects based in the laboratories and pilot plant areas.
+ Ensure a sound laboratory/p...
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Type: Permanent Location: Liverpool, GB-LIV
Salary / Rate: 72000
Posted: 2025-03-26 07:25:35
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SBA Communications is a leading independent owner and operator of wireless communications infrastructure, including towers, buildings, rooftops, DAS and small cells.
We offer a competitive benefits and compensation package and are looking for team members who will thrive in our dynamic environment.
* We welcome your interest in SBA.
Let us know a little about you by checking all that apply:
* You are a self-starter.
* You are resourceful and thrive in a fast-paced environment.
* You have a strong work ethic.
* You are passionate and driven to achieve results.
* You are a team player who enjoys working in a collaborative environment.
* You continuously challenge yourself to find innovative ways to improve.
You may be a perfect fit.
At SBA, we operate with the highest sense of integrity and commitment to quality.
We focus on achievement and operate with responsiveness, timeliness and accountability.
Our culture of excellence incorporates working collegially, where every team member can contribute meaningfully and make a difference.
If you are ready to make an impact, join our team!
Your Next Career Opportunity – Business Intelligence Intern
Support the office in general.
Implement administrative policies alone or with other team members, performing the following duties.
What You Will Do – Primary Responsibilities
* Mobile app development.
* Create databases using vendor data.
* Query the SBA database using SQL/Excel to determine carrier frequencies.
* Interpret data of low to medium complexity in order for it to be entered into the research database.
* Assist with miscellaneous administrative duties within the department.
What You’ll Need – Qualifications & Requirements
* H.S.
Diploma/GED plus College Degree seeking student; or recent graduate and ....Read more...
Type: Permanent Location: Boca Raton, US-FL
Salary / Rate: 23
Posted: 2025-03-26 07:18:22
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If you are an expert EHS /Facility Supervisor looking for an opportunity to grow, Emerson, has an exciting opportunity for you! Based in Olive Branch, MS, you will be responsible for leading the Warehouse Facility and powered equipment maintenance, along with Environmental Health & Safety functions to ensure compliance with all applicable environmental, health and safety regulations, policies, & procedures.
If you love working in a fast -paced environment and you have demonstrated mechanical and electrical aptitude, this is the job for you!
Ready to make your mark and embark on an exciting journey with us? We can't wait to hear from you!
In this Role, Your Responsibilities Will Be:
EHS Job Responsibilities:
* Implement, complete, and ensure adherence to Company's Environmental Health and Safety policies and procedures
* Ensure all required company and regulatory reporting requirements are submitted timely
* Develop non-EHS site personnel to support implementation of EHS programs
* Assist in the management of workers compensation
* Collaborate with regulatory agencies (OSHA, EPA, State/Local Regulators)
* Responsible to lead management personnel in the investigations of facility incidents and complaints regarding unsafe working conditions and practices. Help identify an immediate solution, the root cause, and supervise corrective actions to completion.
* Conduct routine safety observations to ensure compliance with regulatory agencies, company environmental, health, and safety policies, procedures and practices.
* Represent management during EHS Meetings along with the other facility personnel.
* Serve as a facilitator for hourly and supervisory employee EHS and New Hire training.
* Serve as an advisory Member of the Safety Committee and adhere to OSHA regulations.
* Performs other EHS duties as required by management.
Facilities Responsibilities:
* Schedule and lead preventative maintenance for all machining, assembly and other equipment located in the Olive Branch facility
* Provide maintenance support for the entire facility including management of utilities, HVAC, fire suppressant systems, etc.
* Plan and lead overall maintenance and special projects.
* Responsible for ensuring facility atmosphere,5S and hygiene compliance.
* Assist in upgrading existing equipment to safer efficient and productive alternatives.
* Establishes and maintains specific preventive maintenance schedules on equipment and facilities.
* Responsible for managing and coordinating outside vendors when onsite.
* Performs other facility duties as assigned.
WHO YOU ARE:
You build and implement plans that allocate resources precisely.
You analyze multiple and diverse sources of information to define problems accurately before moving to solutions.
You marshal resources (people, funding, material, support) to get things done.
FOR THIS ROLE, YOU WILL NEED:
* Bac...
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Type: Permanent Location: Olive Branch, US-MS
Salary / Rate: Not Specified
Posted: 2025-03-26 07:17:40
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Associate Finance Manager - Sam's Club
Job Description
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.
Position Summary:
In this fast paced, highly interactive role, you will contribute to the achievement of net sales, profit and share objectives by partnering with our Customer Development team in the development and execution of effective and efficient customer business plans while providing the team with timely financial analysis and insights to facilitate sound business decisions.
The Associate Finance Manager – Customer Development role provides you an opportunity to influence price and promotional activities with our major strategic customers, in essence, acting as CFO to the Customer Development team.
The position reports directly to the Sr.
Finance Manager – Walmart and is the senior financial advisor to the Director of Sales for the supported team.
Customer Development teams are typically located at remote office sites; therefore, the incumbent is generally the senior finance representative in the field.
Key customers include Customer Development Leaders and Team Members, Logistics Leaders, Headquarter Sales Leaders, Business Service Leaders, and Staff Business Analysis.
You will provide all the financial support for the customer team, supporting the achievement of business results by assisting in effective business and financial planning and by participating in the development and implementation of strategic and tactical operating plans.
A principal activity of this position is to ensure that business and financial planning processes meet business unit and corporate needs, and, through analysis, that plans, and programs are accurately presented and evaluated. It starts with YOU.
In this role, you will:
* Provide the Customer Development team with financial advice and counsel on all pertinent business matters by supplying ongoing, timely, and meaningful financial analysis, both routine and as needed, of business results, trade promotion, and other expenses.
Information provided should include both the impact to K-C and to the Customer.
* Provide external information to the Customer where required in support of joint annual planning, budgeting, and event analysis.
The level of support is dictated by the specific need of the customer.
* Coordinate the Integrated Customer Business Plan process to ensure timelines are met and plans are delivered.
Be the central point of contact for the forecasting of Volume, Sales and Trade Promotion for long range planning.
Identify opportunities for pr...
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Type: Permanent Location: Rogers, US-AR
Salary / Rate: Not Specified
Posted: 2025-03-26 07:17:36
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Logistics Product Owner
Job Description
Kimberly-Clark is seeking a Product Owner to join our Digital Technology Solutions (DTS) department, a role critical to driving our digital transformation initiatives.
As a Product Owner, you are at the heart of maximizing product value, responsible for articulating and prioritizing the product backlog items for a Scrum team.
You will own the product backlog and ensure that the team builds the right product increments in the most efficient manner.
Your key responsibilities include executing the product vision, managing the backlog, and collaborating closely with multidisciplinary teams to develop innovative solutions that address customer needs and align with business goals.
You will work in an open, collaborative, and approachable manner with the product team (software engineers), inspiring optimal solutions that solve real customer problems and challenging the team to discover the smartest, most efficient solutions.
The ideal candidate should have a strong analytical mindset, excellent communication skills, and the ability to lead through influence.
You are expected to be proactive, enthusiastic about driving technological advancements, and adept at navigating complex challenges in a dynamic environment.
This position offers the opportunity to significantly impact product direction, ensuring operational efficiency and enhanced customer satisfaction.
As a Product Owner at Kimberly-Clark, you will play a crucial role in ensuring that our technology solutions are not only effective but also innovative and aligned with the strategic objectives of the company.
This is an excellent opportunity for a leader looking to make a meaningful impact in a global corporation while shaping the future of our digital operations.
Kimberly-Clark has an amazing opportunity to continue leading the market, and DTS is poised to deliver compelling and robust digital capabilities, products, and solutions to support it.
This role will have substantial influence in this endeavor.
If you are excited to make a difference applying cutting-edge technologies to solve real business challenges and add value to a global, market-leading organization, please come join us!
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 your role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
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 prod...
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Type: Permanent Location: Sao Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-03-26 07:17:28
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SUMMARY
The California Department of Public Health (CDPH) and Heluna Health invites applications for a full-time Research Associate in the CDPH Viral and Rickettsial Diseases Laboratory (VRDL).
In this role, the candidate will work collaboratively and cross-functionally with colleagues to develop molecular methods (PCR) and Next-Generation Sequencing (NGS) workflows that support the surveillance, diagnostics, and research efforts of the California Department of Public Health.
At the VRDL, this work directly supports laboratory testing for SARS-CoV-2, enteroviruses, adenoviruses, and other viral pathogens using molecular methods (PCR) and next-generation sequencing.
The incumbent should be experienced in working with microorganisms (specifically viruses) and using standard laboratory precautions.
Maintaining an organized, neat, and clean work environment, working well in a team environment, and being organized and detail-oriented are essential.
Additional duties include scanning submittal forms, filing patient records, and preparing shipping materials.
The position is in Richmond, CA.
The hourly range for this position is $23.00 to $29.37 per hour depending on experience/qualifications.
Must submit a resume with the application.
This position may be required to work flexible hours and weekends/holidays.
ESSENTIAL FUNCTIONS
* Assist with SOP development for PCR and NGS for viral pathogens.
* Accessioning samples into database (Access and LIMS), tracking specimens in storage, processing samples (nucleic acid extraction), and storing of laboratory specimens for testing and shipping.
* Check in and process samples for testing using pipetting devices.
* Organize and maintain archive repositories for different sample types.
* Autoclave and disinfect laboratory materials containing potentially infectious agents; dispose those materials following autoclaving/decontamination procedures.
* Maintain QA and QC records for the laboratory, when necessary.
* Prepare reagents and media for specimen processing and extraction.
* Perform data entry for patient information, routing samples for testing, and tracking.
* Use of Microsoft Word suite programs such as Microsoft Word, Excel, and Access.
* Other duties as necessary in the laboratory or office when deemed necessary.
* Reports laboratory test results using StarLIMS.
* Ensures adherence to Quality Assurance protocols and standards.
* Maintains laboratory records of specimens, virus stocks, and reagents.
* Performs, interprets, and reports surveillance and reference testing for viruses according to SOPs.
* Performs other related duties as assigned.
JOB QUALIFICATIONS
* Knowledge and experience with laboratory work environments (BSL-2 minimum), sterile technique, and molecular techniques are required.
* Experience with standard precautions for working with potentially infectious clinical specimens, particular...
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-26 07:16:48
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SUMMARY
The California Department of Public Health (CDPH) and Heluna Health invite applications for a full-time Senior Microbiologist in the CDPH Viral and Rickettsial Disease Laboratory (VRDL).
We are a team that works hard, appreciates each other, and strives to build a culture of equity, care, and participation in decisions that affect our work. The candidate will support efforts to enhance surveillance for viral vaccine preventable diseases and rickettsia by assisting with the development and optimization of real-time PCR detection methods and NGS sequencing protocols for measles, mpox, and hepatitis A viruses and Rickettsia.
The Senior Microbiologist will also support other NGS activities at CDPH related to sequence generation and data analysis for phylogenetics, genomic epidemiology, and other characterizations of vaccine preventable viruses and rickettsial pathogens.
The ideal candidate should have a solid laboratory background in molecular microbiology (virology preferred), laboratory experience in metagenomic and targeted sequencing methods, and molecular assay design (e.g., PCR, real-time PCR).
Knowledge of bioinformatics and pathogen genomics is desired.
The incumbent is also expected to stay up to date with scientific literature and contribute to the laboratory academically by assisting with abstracts and manuscripts.
The salary range for this position is $93,603.60 to $110,244.24 annually depending on experience/qualifications.
A cover letter and resume must be submitted with your application.
If hired for this position, applicant will be required to provide proof of full vaccination for COVID-19 prior to the start date or have a valid religious or medical reason qualifying the applicant for an exemption (that may or may not require accommodation).
ESSENTIAL FUNCTIONS
* Design, validate, and implement complex molecular methods for the detection and characterization of diseases of public health importance, including measles, mumps, mpox, and hepatitis A viruses and spotted fever group Rickettsia, with particular emphasis on implementation and use of whole genome sequencing technologies.
* Organize and perform scientific research on viral pathogens and rickettsia using real-time PCR, end-point PCR, and NGS methods in collaboration with other research scientists.
* Work as part of a research team to develop and implement new workflows, molecular assays, and analyses for genomic characterization of pathogens.
* Maintain organized and detailed laboratory records and assist with scientific writing such as SOPs, reports, posters, and manuscripts.
* Adhere and contribute to Quality Assurance protocols and standards.
* Follow safety and quality control procedures in the handling of hazardous biological and chemical materials.
* Participate in training of other technical staff and scientists.
* Perform other related duties as assigned.
JOB QUALIFICATIONS
* Proficiency in molecular bio...
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: 96603.6
Posted: 2025-03-26 07:16:48
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SUMMARY
Heluna Health and the California Department of Public Health’s (CDPH) Drinking Water and Radiation Laboratory Branch (DWRLB) seeks a Microbiologist (Wastewater Surveillance) to begin work immediately to support the CDPH wastewater surveillance (WWS) laboratory.
The CDPH DWRL WWS laboratory tests wastewater, or sewage, for fragments of the SARS-CoV-2 virus and other infectious diseases.
Results are used to supplement existing public health surveillance and monitor infectious disease trends and outbreaks.
The CDPH WWS program is a part of the Centers for Disease Control and Prevention (CDC) National Wastewater Surveillance System (NWSS) and is recognized as a national Center of Excellence (CoE).
This position is funded under the U.S.
Centers for Disease Control and Prevention (CDC) Epidemiology and Laboratory Capacity (ELC) cooperative agreement.
The Microbiologist will perform laboratory testing using PCR-based molecular platforms (e.g., digital droplet PCR) to detect and identify the SARS-CoV-2 virus and related variants in wastewater, as well as other pathogens of public health importance (e.g., influenza, respiratory syncytial virus, Mpox), as a public health surveillance tool for routine and outbreak monitoring.
The project involves routine environmental sample (wastewater) handling, concentration, and analysis, as well as evaluation of new methods and applications, for instance, different wastewater matrices (e.g., influent, solids) to enhance detection sensitivities.
Under supervision of the DWRL Microbiology Unit Supervisor, the Microbiologist will support data formatting, quality assurance/control, and reporting to other CDPH programs and the CDC.
The Microbiologist will work with the WWS laboratory team and laboratory tech/coordinator to maintain inventories and equipment.
Collaboration with other programs, including the CDPH wastewater surveillance epidemiology team and the CDC, are expected.
The Microbiologist will work to implement laboratory operational improvements as necessary, and contribute to documentation of processes (e.g., standard operating procedures) as necessary.
Applicant should possess approximately two years of relevant laboratory experience and possess a bachelor’s degree in biological science, molecular biology, or biochemistry.
A certified Public Health Microbiologist or having specific relevant microbiological and/or environmental laboratory training can substitute for some work experience.
The incumbent must be experienced in working with microorganisms and molecular techniques, exercise standard precautions, and be experienced with applied PCR-based methods.
Maintaining an organized, neat, and clean work environment, working well in a team environment, and being detail-oriented are essential.
The hourly range for this position is $32.30 to $37.70 per hour per hour depending on experience/qualifications.
If hired for this position, applicant will be required to provide proof of full vaccinatio...
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: 32.3
Posted: 2025-03-26 07:16:47
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SUMMARY
The San Francisco Department of Public Health (SFDPH) Population Health Division (PHD) Applied Research, Community Health Epidemiology, and Surveillance (ARCHES) Branch is seeking an Epidemiologist/Data Manager to support the Combating Antimicrobial Resistant Gonorrhea and Other Sexually Transmitted Infections (STIs) (CARGOS) project, a California Bay Area collaborative effort with the California Department of Public Health (CDPH).
The CARGOS Epidemiologist/Data Manager will primarily serve as the lead analyst and data manager for a multi-site CDC initiative on rapidly detecting and responding to antimicrobial resistant gonorrhea (ARGC), as well as support other STI surveillance and evaluation activities.
The salary range for this position is $78,144.00 to $97,116.00 annually depending on experience/ qualifications.
ESSENTIAL FUNCTIONS
Under the general supervision of the Director of the SFDPH ARCHES STI Epidemiology, Surveillance, and Program Evaluation Section, the CARGOS Epidemiologist/Data Manager will perform the following essential job functions:
* Apply strong database management and analytical skills and knowledge using statistical and database management software (e.g., SAS and SQL) to evaluate and enhance quality of all CARGOS clinical, laboratory, and investigation data;
* Prepare regular data submissions passing all quality assurance checks to CDC, following project’s data schedule and requirements, and ensure complete and accurate data-sharing with CDPH and project sites as needed;
* Conduct epidemiologic and other analyses using clinical, laboratory, and investigation data to describe patients with and without ARGC and trends in changing levels of ARGC, including among racial/ethnic and sexual and gender minorities;
* Evaluate data using descriptive and multivariate statistics as part of verifying, analyzing, interpreting, and summarizing data for reports, as well as for dissemination of findings to appropriate stakeholders;
* Lead program evaluation and quality improvement of CARGOS activities at the SF Public Health Laboratory and SF City Clinic, and collaborate with CDPH to conduct similar activities with participating CARGOS community clinics (e.g., increased culture isolation, high culture positivity with fewer specimens collected, equitable culture collection by race/ethnicity and gender identity);
* Develop multi-year and multi-site analyses using local and statewide CARGOS Project data, to inform epidemiology of and trends in ARGC, as well as opportunities for identification and rapid response;
* Serve as primary SF data liaison to all project partners including: CDC, CDPH Sexually Transmitted Diseases (STD) Control Branch, SF Public Health Laboratory, participating local health jurisdictions, and participating STI and non-STI community clinics;
* Respond to ad-hoc data requests by CDC, CDPH, or other SFDPH partners including external researchers and the public;
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Type: Permanent Location: San Francisco, US-CA
Salary / Rate: 78144
Posted: 2025-03-26 07:16:46
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SUMMARY
The Epidemiology and Laboratory Capacity (ELC) Program addresses emerging infectious disease threats and is one of the Center for Disease Control and Prevention’s (CDC) key nationwide cooperative agreements for supporting state epidemiology, laboratory and health information systems capacity to address infectious diseases.
The ELC Laboratory-Epidemiology (Lab-Epi) Coordinator will be housed under California Department of Public Health (CDPH)’s Center for Laboratory Science (CLS).
This individual will work closely with ELC Program Manager and support communication between CLS laboratory staff and Center for Infectious Diseases (CID) epidemiologists as well as clinical lab partners.
This individual will address cross cutting needs of both labs and epidemiologists.
They will assess laboratory gaps and coordinate lab-epi stakeholder meetings.
Under the direction of the CLS Deputy Director, the ELC Lab-Epi Coordinator will develop and implement processes, collaborate with key partners to evaluate program activities, and manage day-to-day program operations.
The ELC Lab-Epi Coordinator will assist with the coordination of federal grant deliverables including progress reports, and monitoring program budgets.
If hired for this position, applicant will be required to provide proof of full vaccination for COVID-19 prior to the start date; or have a valid religious or medical reason qualifying the applicant for an exemption (that may or may not require accommodation).
Salary range: $70,000 to $85,000 annually depending on experience/qualifications.
ESSENTIAL FUNCTIONS
* Coordinate ELC-project conference calls and meetings, track progress, and provide administrative and fiscal updates.
* Analyze project operations and implement strategies to improve effectiveness and efficiency.
* Develop project budgets, in collaboration with CDPH CLS and CID project staff, and Heluna Health.
* Review budgets with ELC CLS Principal Investigators to forecast progress and potential challenges, in collaboration with the ELC Program Manager.
* Assist in monitoring and tracking of performance measures.
* Write and compile fiscal or programmatic reports for submission to CDC, meeting critical deadlines.
* Oversee and review the development of duty statements, hiring, onboarding, and performance evaluations of project staff, ensuring consistency with ELC Enhancing Detection project mandates and objectives.
* Maintain excellent working relationship with CDPH CLS and CID, Heluna Health, and other partners.
* Conducts other duties as requested or assigned.
JOB QUALIFICATIONS
Education/Experience
* Bachelor’s degree, required.
* Graduate degree in Public Health or related field, preferred.
* A minimum of two years’ experience in program and federal grant management, required.
* Experience working collaboratively with diverse groups with multiple activities, timelines, and de...
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: 70000
Posted: 2025-03-26 07:16:43
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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:
Schaffhausen, Switzerland
Job Description:
Johnson & Johnson Innovative Medicine ist durch seine Tochtergesellschaften der weltweit umfassendste Hersteller von Gesundheitsprodukten sowie Anbieter verwandter Dienstleistungen für die Märkte der Verbraucher-, Pharma- und Medizintechnik sowie Diagnostik.
Wir streben an, wissenschaftlich fundierte, hochwertige Produkte und Dienstleistungen bereitzustellen, um Krankheiten zu heilen, zu heilen und die Lebensqualität zu verbessern.
Weitere Informationen finden Sie unter https://www.jnj.com.
Johnson & Johnson Innovative Medicine, Schweiz, ist eine erfolgreiche internationale Entwicklungs- und Produktionsstätte im Pharmasektor.
An unserem Standort in Schaffhausen arbeiten etwa 130 Personen für die globale Forschungs- und Entwicklungsorganisation von Johnson & Johnson Innovative Medicine, die innovative Behandlungen entwickelt, die die Gesundheit und den Lebensstil von Menschen weltweit verbessern.
Weitere Informationen finden Sie unter https://www.jnj.com/innovative-medicine.
Die analytische Entwicklungsorganisation für biologische Moleküle (z.B.
Antikörper) in Schaffhausen bietet hochspezialisierten und einzigartigen Support in den Bereichen kommerzielle Produkte, Füll- und Finish-Analytik in der Pilotanlage sowie Charakterisierung von Autoinjektoren.
In dieser Organisation bieten wir eine herausragende Gelegenheit für einen
* Wissenschaftliche(r) Mitarbeiter(in) (Scientist; 100%)
In dieser Position sind Sie verantwortlich für die Unterstützung der weiteren Entwicklung des Kompetenzzentrums (CoE) im Bereich Materialidentifikation und -charakterisierung.
Ihr Engagement und Ihr Kundenfokus sind entscheidend, um qualitativ hochwertige, technisch fundierte und zeitnahe Untersuchungen in einem dynamischen F&E- und Handelsumfeld sicherzustellen.
Nach einer gründlichen Einarbeitung sind Sie verantwortlich für die Durchführung von Materialdefekt- und Partikeluntersuchungen unter Verwendung hochspezialisierter und modernster Technologien.
Sie sind auch verantwortlich für die Durchführung und Berichterstattung der entsprechenden Analysen in einem GMP-regulierten Umfeld, indem Sie den Prozess und die Dringlichkeit der Unterstützung analytischer Untersuchungen im CoE für Material- und Partikelid...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:47
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium, Spring House, Pennsylvania, United States of America, Toledo, Spain
Job Description:
AI/ML Senior Scientist in Drug Discovery Data Sciences
Next Generation Automation refers to the bidirectional coupling between automated lab equipment and Artificial Intelligence (AI). Through successive iterations, such closed-feedback loop systems facilitate the AI-driven design, execution and analysis of experiments and utilize a wealth of in silico methodologies including active learning, multi-parametric dynamic optimization, model predictive control, Model-based Design of Experiments, and others.
Within the Drug Discovery Data Sciences organization of Johnson & Johnson Innovative Medicine we have an open position for a senior scientist that will play a pivotal role in our strategic effort to transition automation into the next generation.
To do so, the new member will collaborate within interdisciplinary teams comprising biologists, medicinal chemists, data scientists, computational chemists and IT experts across all therapeutic areas.
They are expected to utilize their expertise and know-how to bridge the gap and close the loop between existing automation and in silico solutions and develop new modeling suites according to the needs of each project.
Role and responsibilities
* Co-develop system engineering plans for closed loop automation projects from PoC to production.
* Develop and productionize the in silico suites by using AI/ML and other appropriate modelling methodologies.
* Actively participate in evaluation of third-party solutions.
* Work closely with IT, engineering and Lab-tech to implement solutions.
* Communicate results in audiences with heterogeneous background.
Requirements
* A PhD with an AI/ML publication track record.
* Previous experience with Process or Lab Automation.
* Familiarity with Model Predictive Control and DOEs or similar mathematical capabilities.
* Knowledge of Python development and affinity with AWS (or similar cloud environments).
* Strong interpersonal, organizational and communication skills.
* Motivation to be part of a team that celebrates diversity and off...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:46
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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:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Lexington, Kentucky, United States, Morgantown, West Virginia, United States, Nashville, Tennessee, United States
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Senior Medical Science Liaison, Lung Oncology, to cover the Tennessee, Kentucky, and West Virginia territory.
About Oncology
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.
Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
The Senior Medical Science Liaison (MSL) is considered the field- based scientific and clinical expert on current and future Janssen products. The Senior MSL is responsible for providing fair balanced, objective, scientific information, and education to health care professionals and to internal partners as required by scientific and business needs.
The Senior MSL is also responsible for staying abreast of current scientific and treatment landscape trends in the relevant therapeutic areas and providing research support for company as well as investigator-initiated studies.
The Senior Medical Science Liaison will:
• Develop and maintain a strategic and comprehensive territory plan and will build strong relationships with various community and academic opinion leaders/ KOLs in the territory.
• Engage in high-level scientific and research discussions with KOLs and OLs to serve as a resource for them and to understand their perspectives on the current treatment landscape in the relevant disease area.
• Identify provider educational needs and address those with tailored responses.
• Deliver relevant scientific data tailored to HCP needs through clear and effective dialog/ presentation.
• Consistently execute upon the current Medical Affairs strategy and MSL priorities
• Respon...
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Type: Permanent Location: Nashville, US-TN
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:36
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Business Intelligence
Job Category:
Professional
All Job Posting Locations:
Norderstedt, Schleswig-Holstein, Germany
Job Description:
About Cardiovascular
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are looking for an innovative, proactive Senior Business Intelligence Analyst (w/m/d) to develop and maintain advanced Power BI solutions within the Shockwave Medical business unit, now part of Johnson & Johnson MedTech.
This role directly supports global stakeholders across various departments, ensuring data-driven insights and optimized performance.
Responsibilities
* Data Modeling: Build, optimize, and maintain Power BI semantic models to support advanced analytics and reporting.
* Report Development: Develop both standard and paginated reports, managing distribution through the Power BI service platform.
* Data Integration & Quality: Collaborate with cross-functional teams to ensure seamless data integration and uphold data quality standards (SQL proficiency is essential; Snowflake experience is a plus).
* Global Support & Training: Provide BI services worldwide, adapting solutions for localized requirements and training end-users on best practices.
* Performance & Continuous Improvement: Monitor and enhance reporting performance, staying abreast of new Power BI features and driving ongoing improvements.
* Documentation: Create comprehensive documentation for data models and reports to ensure ease of use and maintenance.
* Technical Consultation: Act as the go-to technical expert on Power BI within the Business Intelligence & Analytics department, providing guidance and best practices.
Qualifications
* Minimum 5 years of proven experience with Power BI (semantic modeling, DAX, M language...
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Type: Permanent Location: Norderstedt, DE-SH
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:29
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
AP/AR
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
We are seeking a meticulous and analytical Reporting Analyst to join our Reporting Team.
The ideal candidate will possess strong analytical skills and be dedicated to producing high-quality reports that drive decision-making across the organization.
Job responsibility
* Data Collection & Analysis.
Capture and compile data from various sources, including databases and spreadsheets.
* Report Generation.
Ensure accuracy and timeliness of report delivery.
* Stakeholder Collaboration: Work closely with internal partners to understand reporting needs and provide relevant insights.
Support decision making processes with clear data story telling.
* Quality Assurance.
Conduct data validation checks and ensure data quality and consistency in reporting.
Continuously improve reporting processes for efficiency and effectiveness.
* Other ad-hoc tasks assigned by Manager
Professional Qualification
* Bachelor degree or equivalent experience in Accounting, Finance, Economics or related business course
* 1-3 working experience in AR, preferrably from MNCs
* Experience in shared services center of a multinational corporation, banking industry or those supporting credit agencies are desirable
* Superb interpersonal skills, with the ability to collaborate with a variety of stakeholders.
* Good command of English, both oral and written
* Knowledge of ERP systems (e.g.
SAP), Tableau, UiPath or other financial modelling is a plus
* Technology proficiency in Microsoft Office and ERP (SAP is helpful)
* Teamwork spirit and can work under pressure
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:26
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Animal Medicine
Job Category:
Scientific/Technology
All Job Posting Locations:
Cincinnati, Ohio, United States of America
Job Description:
We are searching for the best talent for a Research Associate to be located in Cincinnati, OH
Purpose: Johnson & Johnson’s long-term vision is to use digital technology as part of a holistic approach to surgery across the episode of care to enhance surgical efficiency, promote better clinical outcomes and increase patient satisfaction.
This position will serve in support of the development and execution of preclinical evidence strategies necessary to competitively position a product for domestic and international regulatory and clinical acceptance.
You will be responsible for:
* Assist in research and testing which support development of products or procedures, collect and manage data, provide technical surgical assistance during animate and inanimate labs, and coordinate appropriate project/study logistics while ensuring data integrity and regulatory compliance.
Responsible for conducting research in assigned areas under direct supervision using established methodology.
* Provides documentation to help scientific staff with the preparation of technical reports, manuscripts, and other documents that record data or results.
Assists with writing and updating protocols, test methods and standard operating procedures.
* Coordinate study logistics, contribute to the collection and management of data, support study execution and study completion
* Ensure the highest standards of biomedical research & development are upheld & carried out by meeting the standards of USDA (United States Department of Agriculture), AAALAC (Association for Assessment & Accreditation of Laboratory Animal Care), J&J Animal Use Policies, GLP (Good Laboratory Practice) guidelines, and Good Documentation Practices.
* Partner with preclinical peers to identify and prioritize critical equipment and model capabilities needed in the animal test facilities.
Education:
* Bachelor's degree with minimum of (2) years of experience in a preclinical operational role in a pharmaceutical, medical device, or contract lab setting (or related industry) is required.
Required Skills & Experience:
* Demonstrated knowledge of preclinical practices and procedures
* Experience working with large animal...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:21
-
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:
Ringaskiddy, Cork, Ireland
Job Description:
J&J IM is recruiting for a QC Scientist within the Quality department and to be based in Cork (Ireland).
POSITION SUMMARY:
This position is responsible for carrying out tasks and projects related QC Microbiological
activities at Janssen Sciences Ireland UC (JSI) as required by Good Manufacturing
Practice (GMP).
Partners with other departments to ensure that all QC Microbiology
testing activities are completed in an efficient manner.
GENERAL SCOPE OF RESPONSIBILITIES:
• Achieves proficiency in JSI microbiology laboratory methods and procedures.
• Supports investigational microbiological testing activities during complex
investigations while managing the communication flow of QC data within QC to
Operations.
• Ensures that testing and results approval are completed within agreed
turnaround times.
• Performs Microbiological testing activities in relation to method validation and
technical transfer activities.
• Executes validation, operation, maintenance, calibration and troubleshooting of
equipment and its associated software.
• Executes and reviews IQ/OQ and PQ protocols so as to ensure that all relevant
equipment is qualified for cGMP use.
• Writes and reviews laboratory TMs, SOPs and WIs as directed by company
policy.
• Ensures QC activities are carried out in compliance with product licence
commitments, cGMP and company quality standards.
• QC Micro data collating, trending analysis and reporting.
• Change management SME for QC Microbiology.
• Is an active member of the QC Technical Team supporting and providing
guidance to the QC microbiology group and provide assistance with other group
activities as required and communicates relevant issues to the QC Team Leader
and Manager.
• Anticipates and plans for future requirements in the area.
• Deals with non-conformances/ deviations in an accurate and timely manner.
• Deputizes for the QC Technical Team Leader as appropriate.
• Maintains and develops knowledge of analytical technology as well as cGMP
standards.
• Identify and implement new technologies in addition to supporting the validation
and filing requirements for the identified new technologies.
• Ownership of the Microbial Control strategy.
KEY COMPETENCIES REQUIRED:
• Collabor...
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:19
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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:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
People Leader
All Job Posting Locations:
US010 PA Horsham - 800/850 Ridgeview Dr
Job Description:
The Head Field Based Medical Psoriatic Disease, is responsible for establishing the vision and strategy for the MSL team, including accountability for execution and attainment of medical objectives in compliant alignment with the business strategy.
They will be responsible for ensuring that the MSL team receives a high-level of direction, training, coaching, and development via oversight of the regional Field Directors and in collaboration with the HQ TA team and MSL training and analytics team.
The individual will be accountable for team delivery of high-quality communications regarding the science and clinical applications of our products and/or the disease state to external stakeholders on a regional and national level, acquiring important insights about current practice, treatment landscape, and emerging scientific and clinical data following compliance policies.
The ideal candidate will have a record of strong leadership combined with outstanding business acumen and clinical expertise as this individual is expected to build strong cross-functional relationships with internal colleagues as well as external relationships with HCPs.
Core Responsibilities:
* Maintains a high level of therapeutic area medical and scientific expertise and business acumen to support brand strategy and to coach/develop team
* Translates medical strategic priorities into clear field medical goals, objectives, and initiatives with performance metrics to demonstrate the value proposition of the Field Medical team
* Works with Field Directors to develop the external KOL and HCP engagement strategy to maximize field territory plans
* Cross-functional collaboration within Medical Affairs, US Commercial, Clinical Development, Business Development, and other functions for synergistic opportunities
* Management and development of all team members including hiring, training, mentoring, coaching, performance management, and career development
* Routine oversight of team metrics/requirements to ensure appropriate coaching/intervention for Field Directors and MSLs as needed
* Participates in ride-alongs with MSLs and Field Directors within territories as well as observation at Advisory Boards, congresses, etc.
for coa...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:04
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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 Engineering
Job Sub Function:
Manufacturing Engineering
Job Category:
People Leader
All Job Posting Locations:
Zug, Switzerland
Job Description:
Job Description
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson Services is recruiting for a Global Lead of Maintenance & Reliability, based in a J&J manufacturing site in Athens GA, Gurabo PR, Cork IR, Leiden NL, Beerse/Geel BE, Schaffhausen CH, or Latina IT. This position is required to be on site 3 days per week.
The Global Lead of Maintenance & Reliability owns the global maintenance strategy that aligns with the company’s overarching objectives, including those related to manufacturing, operational excellence, and asset reliability.
This leadership position is responsible for driving innovation in maintenance practices, enhancing reliability engineering, and advancing maintenance capabilities through predictive and preventive approaches, aligned with the company’s strategic objectives.
The successful candidate will ensure that maintenance functions align with overall business objectives and regulatory compliance while continuously improving operational efficiency and asset reliability.
Key Responsibilities:
* Develop and implement a comprehensive global maintenance strategy that focuses on long-term asset reliability, cost efficiency, and operational excellence, and is aligned with IMSC and MTO Strategy as well as Site Strategies.
* Lead and oversee the implementation of the Assets Management Framework and maturity roadmaps.
Standardize maintenance practices and tools across all global sites to ensure consistency and compliance with industry regulations.
* Lead efforts to improve equipment reliability, availability, and performance by developing and implementing reliability-centered maintenance (RCM) and total productive maintenance (TPM) programs.
* Spearhead the transformation of maintenance practices from reactive to predictive and preventive maintenance through advanced technologies (e.g., IoT, AI-based pr...
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-03-26 07:06:00
