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At voco™ Cairo Arabella Plaza, the very first voco in Egypt, we believe in creating a welcoming atmosphere where our guests feel cared for and our colleagues are empowered to deliver memorable experiences.
We are looking for a Receiving cum Stores Clerk who will ensure accurate receiving, storing, and issuing of goods, maintain proper stock levels, and support smooth hotel operations.
A little taste of your day-to-day:
Every day is different at IHG, but you’ll mostly be:
* Receiving deliveries and verifying quantity and quality against purchase orders.
* Recording receipts and updating inventory systems.
* Storing goods in a safe, organized, and hygienic manner.
* Issuing items to departments upon request and updating stock records.
* Conducting regular stock counts and reporting discrepancies.
* Coordinating with Purchasing and Finance for documentation accuracy.
What we need from you:
* Diploma or equivalent qualification.
* 1–2 years’ experience in receiving/stores operations, preferably in hospitality.
* Knowledge of inventory management systems.
* Attention to detail, accuracy, and organizational skills.
What We Offer:
We give our people everything they need to succeed, from a competitive salary that rewards all their hard work to a wide range of benefits designed to help them live their best work life – including a full uniform, impressive room discounts, and some of the best training in the business.
Our mission is to welcome everyone and create inclusive teams where we celebrate differences and encourage colleagues to bring their whole selves to work.
IHG Hotels & Resorts provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
We promote a culture of trust, support, and acceptance.
Always welcoming different backgrounds, experiences, and perspectives.
IHG gives every member of the team the room they need to belong, grow, and make a difference in a collaborative environment.
We know that to work well, we need to feel well – both inside and outside of work – and through our myWellbeing framework, we are committed to supporting wellbeing in your health, lifestyle, and workplace.
So, join us and you’ll become part of our ever-growing global family.
....Read more...
Type: Permanent Location: Cairo, EG-C
Salary / Rate: Not Specified
Posted: 2025-09-26 08:39:35
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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:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
Scientific/Technology
All Job Posting Locations:
Beijing, China, Shanghai, China
Job Description:
* Individual contributor who is a developing subject matter expert in a scientific/technology field.
Supports the operational, medical and scientific components of the organization's drug safety and pharmacovigilance (PV) processes and procedures.
Provides scientific, pharmaceutical, regulatory, and clinical expertise with a strategic focus on the identification, evaluation, reporting, and response to safety risks and signal detections for the organization's products.
Collaborates cross-functionally and cross-regions to actively manage and mitigate risks as clinical products and pharmaceutical drugs move from the discovery and pre-clinical phases to the clinical trial, regulatory approval, and post-marketing phases.
* Develops strategy involving signal identification, evaluation, reporting, escalation, and management activities for assigned products.
* Implements risk-based systems to identify, evaluate, and handle pharmacovigilance requirements.
* Assists with clinical trials and other clinical activities to ensure adverse event reporting processes according to local, regional and global requirements.
* Advises stakeholders on product safety information and organization-implemented updates and changes on pharmacovigilance systems and processes.
* Coaches and trains junior colleagues in techniques, processes, and responsibilities.
* Integrates Johnson & Johnson’s Credo and Leadership Imperatives and departmental/functional strategy into team goals and decision making.
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-09-26 08:38:22
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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:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
West Chester, Pennsylvania, United States of America
Job Description:
2026 J&J Orthopedics Internship – Commercial Operations and Strategy & Innovation
At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world’s most significant healthcare challenges.
Our Corporate, Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines.
We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives.
With a reach of more than a billion people every day, there’s no limit to the impact you can make here.
Are you ready to reimagine healthcare?
Here, your career breakthroughs will change the future of health, in all the best ways.
And you’ll change, too.
You’ll be inspired, and you’ll inspire people across the world to change how they care for themselves and those they love.
Join us!
J&J Orthopedics, a part of the Johnson & Johnson Medical Devices sector, is recruiting for a number of summer 2026 internship positions.
J&J Orthopedics provides the most comprehensive orthopedics product portfolios in the world.
With specialties that include trauma, craniomaxillofacial, joint reconstruction, sports medicine, and spinal surgery, and more, we are designed to advance patient care while delivering clinical and economic value to healthcare systems worldwide.
For more information, visit https://www.jnjmedtech.com/en-US/companies/depuy-synthes.
Our interns play an important role in enhancing our business.
We plan to hire a number of positions across multiple specialties and departments.
Our program will provide you with business problems to solve, coaching, mentoring and networking opportunities.
You will work on projects that improve your leadership and professional skills while learning the orthopedics business.
You will also be a part of the internship cohort, which consists of your peers to learn from, networking opportunities, and developmental sessions.
About our Internships:
* A typical internship is from May/June through mid-August, with opportunity based on business needs and performance for a subsequent 2026 in...
....Read more...
Type: Permanent Location: West Chester, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-26 08:38:18
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
San Diego, California, United States of America, Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Field Clinical Specialist - Shockwave Medical to join our team located in San Diego, California.
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 Field Clinical Specialist is a visible position that will provide case support to physicians within certain territories. Case support will be done on peripheral and coronary interventional procedures in the pre-market and post-market phases of product development with the Shockwave Medical Intravascular Lithotripsy (IVL) ® technology.
The Field Clinical Specialist will also play a critical role in clinical studies including device training, case support and ensuring timely data collection for clinical programs. Case support may be required to support other territories at certain times.
Essential Job Functions
* Physician and hospital staff training, and procedural case coverage to ensure the safe and effective use of medical devices.
* Effectively meet the needs of internal and external customers with a sense of urgency and drive.
* Present clinical stud...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-26 08:38:07
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, West Chester, Pennsylvania, United States of America
Job Description:
2026 J&J Orthopedics Internship – Marketing
At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world’s most significant healthcare challenges.
Our Corporate, Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines.
We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives.
With a reach of more than a billion people every day, there’s no limit to the impact you can make here.
Are you ready to reimagine healthcare?
Here, your career breakthroughs will change the future of health, in all the best ways.
And you’ll change, too.
You’ll be inspired, and you’ll inspire people across the world to change how they care for themselves and those they love.
Join us!
J&J Orthopedics, a part of the Johnson & Johnson Medical Devices sector, is recruiting for several summer 2026 internship positions.
J&J Orthopedics provides the most comprehensive orthopedics product portfolios in the world.
With specialties that include trauma, craniomaxillofacial, joint reconstruction, sports medicine, spinal surgery, and more, we are designed to advance patient care while delivering clinical and economic value to healthcare systems worldwide.
For more information, visit https://www.jnjmedtech.com/en-US/companies/depuy-synthes.
Our interns play an important role in enhancing our business.
We plan to hire a number of positions across multiple specialties and departments.
Our program will provide you with business problems to solve, coaching, mentoring and networking opportunities.
You will work on projects that improve your leadership and professional skills while learning the orthopedics business.
You will also be a part of the internship cohort, which consists of your peers to learn from, networking opportunities, and developmental sessions.
About our Internships:
* A typical internship is from May/June through mid-August, with opportunity, based on business needs and performance, f...
....Read more...
Type: Permanent Location: West Chester, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-26 08:37:50
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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:
Biological Research
Job Category:
Scientific/Technology
All Job Posting Locations:
Cambridge, Massachusetts, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Principal Scientist, Viral Vectors (Cell and Genetic Medicines Discovery) to be located in Cambridge, MA.
Purpose:
We are seeking a highly motivated and experienced scientist to join our CAR-T cell therapy discovery efforts as a Principal Scientist.
In this role, you will play a key part in advancing our research initiatives by leveraging your expertise in viral vectors and molecular biology. This position presents a unique opportunity to contribute to groundbreaking research in CAR-T cell therapy.
If you are passionate about advancing scientific discovery and possess a collaborative mindset, we invite you to apply!
You will be responsible for:
* Utilize your extensive knowledge in vector engineering, virology, and molecular biology to drive groundbreaking research in our cell therapy platform and pipeline development.
* Design, develop, and implement novel methodologies for vector targeting, packaging, and analytical characterization, including assays for vector quantification, potency, and purity.
* Lead efforts in troubleshooting and refining viral vector quantification techniques such as PCR-based assays, flow cytometry, and vector copy number (VCN) analysis, ensuring robust and reproducible data.
* Drive continuous improvement of vector production platforms, including titers, purity, and scalability, to enhance overall process efficiency.
* Maintain expertise and provide innovative solutions to complex research challenges
* Initiate and foster collaborative projects with internal cross-functional teams, external partners, and academic institutions to accelerate innovation and knowledge sharing.
* Present complex data insights to diverse audiences, including r...
....Read more...
Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2025-09-26 08:37:47
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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:
Non-Standard
Job Sub Function:
Non-Employee
Job Category:
Non-Standard
All Job Posting Locations:
Beijing, China, Shanghai, China
Job Description:
The Epidemiology APAC team is a division of Global Epidemiology Orginization, Johnson & Johnson.
The Epidemiology APAC team exists to be experts in generating, leveraging, and promoting the use of high-quality Real-World Evidence for various stakeholders.
The team shows up every day determined to maximize the utility of Real-World Evidence to achieve regulatory and business priorities.
The team is recruiting an Epidemiology Senior Scientist / Manager in Shanghai/Beijing, China depending on the candidate’s expertise and experience.
The Epidemiology Senior Scientist / Manager will work under the supervision of senior members of the Epidemiology APAC team, the research leader in academia in multiple therapeutic areas in China.
The role will involve participation in various task forces in addressing issues raised by the clinical teams/regulatory agencies by providing epidemiology and statistical support.
The role will be expected to keep up to date with the China real-world data, and communicate with the cross functions or stakeholders in support of the team’s projects.
The primary responsibilities will be:
- to deliver individual programming deliverables (tables, listings, figures and other reports) of projects with low to medium complexity.
- to develop quality control checks for programs or output.
- to develop the statistical analysis plan and maintain programming documentation as appropriate.
- to establish, maintain access, and collaboration with real-world data holders or researchers in China.
- to participate in the development and review of study-specific procedures
- to communicate with internal and external stakeholders to ensure the final high-quality deliverables
Qualifications:
* At least a bachelor’s or master’s degree in Epidemiology, Biostatistics, or Public Health is required.
A minimum of 3 years of experience in the related field is also required.
* Proficiency in SAS programming or other statistical software (such as R, Python) is required.
* Programming and analyzing experience in large real-world databases are highly preferred.
* Ability to work on multiple projects simultaneously is also preferred.
* verbal and written communication skills in China and English (Reading, writing, and sp...
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-09-26 08:37:25
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ERM is hiring a Health & Safety Specialist to support an aerospace client facility in Redmond, WA.
In this critical role, you will be responsible for ensuring safety compliance with applicable regulations and existing company standards and contributing to an environment where employee health and safety is paramount.
This is a third shift, full-time (40 hours), limited-term role with a duration of 12 months and the possibility of renewal.
RESPONSIBILITIES:
* Providing health and safety oversight for an aerospace manufacturing facility.
* Oversee general safety and risk programs in an aerospace manufacturing environment – machine safety, LOTO, electrical safety, PPE, fall protection, confined space, etc...
* Communicating with internal stakeholders.
* Developing, reviewing, and/or updating health and safety documentation such as SOPs, JHAs, and safety plans.
* Conduct inspections and audits.
* Participating in the Emergency Response Team.
* Conduct safety training.
* Participate in incident investigation, root cause analysis, and report writing.
* Participating/leading meetings to support ongoing compliance and safety initiatives.
* Writing and submitting status update reports, and other communications.
REQUIREMENTS:
* Bachelor’s in safety or related discipline preferred.
* 3+ years of health and safety experience in a manufacturing environment, aerospace experience preferred.
* Certification such as ASP/CSP highly preferred.
* Experience with High Hazard Work Activity, Confined Space, LOTO, Machine Guarding, and Fall Protection.
* Familiarity with federal/state health and safety regulations.
* Strong MS Office computer skills.
* Excellent written and verbal communication skills.
For the Health & Safety Specialist position, we anticipate the annual base pay of $80,691 – $97,410, $38.79/hr – $46.83/hr, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/FlexForce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including FlexForce) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible.
See your recruiter for more details.
...
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Type: Permanent Location: Seattle, US-WA
Salary / Rate: Not Specified
Posted: 2025-09-26 08:35:26
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ERM is hiring an on-site Construction Safety Specialist for a key client in Grand Rapids, MI.
The Construction Safety Specialist will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a part-time (20 hours per week), fixed-term position for a duration of 2 months, extendable.
RESPONSIBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in safety-related activities.
* Act as the Owner’s representative while interacting with contractors.
* Provide daily observations of on-site safety practices
* Provide timely, high-quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze Safety performance and initiate action to support or correct trends.
REQUIREMENTS:
* A bachelor’s degree in safety, occupational health, engineering, or a related field is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, preferably with commercial/office building construction or large projects.
CHST certification is a plus.
* Proficient with the management of high-risk activities, including electrical safety, excavation, confined spaces, fall protection, material handling, and rigging
* Experience in communicating and problem-solving as a team with subcontractors is required.
* A background and knowledge working with specific trades such as electricians, ironworkers, pipefitters, etc.
is a plus.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that help...
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Type: Contract Location: Holland, US-MI
Salary / Rate: Not Specified
Posted: 2025-09-26 08:35:24
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Company
Federal Reserve Bank of Dallas
PhD Dissertation Fellow – Federal Reserve Bank of Dallas Research Department
PhD Dissertation Fellow – Federal Reserve Bank of Dallas Research Department
Advertiser: Research department, Federal Reserve Bank of Dallas
Field(s) of specialization: Any field
Position type(s): Other nonacademic
Location of job: 2200 N.
Pearl St., Dallas, TX, 75201, United States
Degree required: Doctorate
Job start date: Negotiable, but with a start date no later than November 1, 2025 and a termination date that should be no later than February 28, 2026 (disclaimer: end date is subject to change).
Job duration: Negotiable, with a minimum of 4 weeks and up to a maximum of 12 weeks
Letters of reference required: 1
Current search status: Position open
Posting end date: October 15, 2025
Call for candidates:
The Research Department of the Federal Reserve Bank of Dallas invites applications for two PhD Dissertation Fellow positions for the summer of 2025.
This program provides an excellent opportunity for PhD students in economics to engage in high-quality research and gain valuable exposure to scholarly work conducted at the Dallas Fed.
Fellows will have the opportunity to collaborate with the Bank’s research economists, visiting scholars, and other dissertation fellows, fostering a rich academic and research environment.
Qualifications/Skills:
* Open to PhD students from all PhD-granting institutions (both domestic and international).
* Applicants must have passed their qualifying exams and reached the dissertation stage of their program.
* Preference will be given to students expecting to complete their PhD in 2026.
* The program will be held in-person in Dallas, lasting from 4 to 12 weeks, during the fall of 2025/spring 2026
* Fellows are expected to deliver a formal presentation at the Dallas Fed’s brownbag seminar series during the last two weeks of their fellowship.
To Apply:.
Submit your application online.
Required documents include:
(1) Curriculum vitae
(2) Paper or writing sample
A letter from your principal academic advisor, commenting on your potential for producing high-quality research, the significance of your dissertation topic, and your progress to date, must also be uploaded to your Econ Job Market submission.
For More Information:
Enrique Martínez García
Assistant Vice President and Head of the International Group
Email: enrique.martinez-garcia@dal.frb.org
Full Time / Part Time
Full time
Regular / Temporary
Temporary
Job Exempt (Yes / No)
No
Job Category
Internship Family Group
Work Shift
First (United States of America)
The Federal Reserve Banks are committed to equal employment opportunity for employees and job applicants in compliance with applicable law and to an environment where employees are valued for their differences.
Always verify and apply to jobs on Federal Reserve System Careers (https://rb.wd5.myworkdayjobs.com/FRS) or through verified Feder...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-26 08:29:47
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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 / Principal Scientist, Downstream Process Development
The Biopharma Technical Development team located in Indianapolis, IN is seeking a Senior / Principal Research Scientist to provide scientific and technical expertise for the development and launch of new biological drug substances in an innovative and fast-paced organization.
This role is focused on downstream process development with an emphasis on monoclonal antibodies, therapeutic proteins, and other biological modalities.
You will be responsible for leading downstream process development activities at bench and pilot scales, supporting scale-up, technical transfers, process implementation, and clinical material production at both internal and external manufacturing sites.
In addition to technical excellence, this position requires strong organizational management, communication skills, and cross-functional collaboration across departments and geographies.
As a subject matter expert in downstream process development, you will have the potential to lead both projects and people.
Your Responsibilities:
* Provide scientific expertise in downstream process development for early- and late-stage biologic programs (mAbs, therapeutic proteins, and other modalities) using phase-appropriate development strategies.
* Apply Quality by Design (QbD) principles to process development and process characterization.
* Lead and contribute to risk assessments supporting product development stage-gate reviews and robust manufacturing control strategies.
* Develop representative scale-down models from commercial-scale operations and apply prior knowledge to guide development studies.
* Author and review source documents for regulatory submissions; respond to CMC questions from regulatory agencies.
* Partner with R&D, Technical Services/Manufacturing Sciences (TS/MS), supply chain, Quality, Manufacturing, Launch Leaders, external CDMOs, and other stakeholders to ensure successful tech transfers and commercialization.
* Serve as a technical resource to Biopharma Tech...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: 171000
Posted: 2025-09-25 09:20:05
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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: Quality Assurance Intern
As a Quality Intern, you will be part of the Fort Dodge Quality Assurance team to support activities related to the oversight of manufacturing and distribution of commercial products.
There will be several opportunities to gain experience in different areas within Quality, such as Quality Management System, Pharmaceutical Products, and Audits.
Your Responsibilities:
* Defining, measuring, analyzing, and improving identified processes within the quality organization.
* Understand the Manufacturing processes and how Quality supports the process and business.
* Work within cross-functional teams to support inspection readiness activities, investigations, and continuous improvement projects.
* Get real-world experience in the regulated environment.
* Assist with the production and analytical processes the ensure they are carried out with appropriate Sterility Assurance standards.
* Study design improvement process.
What You Need to Succeed (minimum qualifications):
* Education: Currently enrolled in an undergraduate program with a concentration in Science (Biology, Chemistry, Biotechnology, or related field) or Engineering.
* Effective communication and interpersonal skills.
* Strong organizational and time management skills
* A willingness to learn.
* Must be able to work exceptionally well independently and with minimal supervision.
What will give you a competitive edge (preferred qualifications):
* Have an interest in animal health manufacturing, problem solving, scientific method, or cross-functional skill development.
* Thrive in cross-functional team settings.
Additional Information:
* Travel: 0%
* Location: Fort Dodge Manufacturing Plant - Fort Dodge, Iowa
Our Internship Program
Our internship program is designed to provide students with experiences! Internships are project based and comprised of business-critical needs.
All interns have the opportunity to significantly impact Elanco’s success over the summer and kickstart a career t...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: 27
Posted: 2025-09-25 09:19:56
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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: Global Quality Auditor
As a Global Quality Auditor, you will be part of the Elanco Global Quality Compliance and Auditing (EGQCA) organization.
In this role, you’ll be responsible for assuring compliance with company standards and regulatory requirements through internal and external audits of pharmaceutical products and commercial operations.
Your Responsibilities:
* Schedule, prepare, conduct, and report Global Quality audits and assessments of commercial operations.
* Participate in or lead the risk assessment of commercial operations and influence actions within EGQCA and business areas.
* Drive the escalation of compliance issues or significant risks identified during audits or risk assessments.
* Maintain strong interpersonal and communication skills, with an emphasis on verbal and technical writing.
* Lead in the assessment of Top 10 product supply chain audits and conduct Due Diligence audits for new acquisitions.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree (or equivalent work experience) in physical or biological sciences, Engineering, or other technical area.
* Required Experience: A minimum of 5 years of previous auditing experience in aseptic manufacturing platforms.
* Ability to analyze detailed technical scientific information and interpret/apply regulations; excellent interpersonal and communication skills.
What will give you a competitive edge (preferred qualifications):
* Ability to work under pressure on multiple tasks concurrently and meet deadlines.
* Proven ability to think and analyze from a process perspective; project management skills.
* Ability to process information to identify linkages and trends for compliance strategies.
* Ability to work independently and collaboratively within a global team environment.
* Ability to influence and manage change/conflict, and be pragmatic in decision making.
Additional Information:
* Travel: Up to 50% (domestic and international, trip duration 1-2 weeks), somet...
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Type: Permanent Location: Warszawa, PL-MZ
Salary / Rate: 380000
Posted: 2025-09-25 09:19:49
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Please note that this job posting is for an evergreen position and does not represent an active or current vacancy within our organization.
We continuously accept applications for this role to build a talent pool for future opportunities.
While there may not be an immediate opening, we encourage qualified candidates to submit their resumes for consideration when a suitable position becomes available.
Chronic Care Manager
Location: Remote
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 Nurse Chronic Care Coordinator, Remote 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).
Harris CCM is seeking Nurses to work part-time from their home office while complying with HIPAA privacy laws.
You will set your own hours and will not be held to a daily work hour schedule.
You will be contracted to work a minimum of 20hrs/wk.
Harris CCM 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.
Care Coordinators will be expected to complete encounters on 90 percent of the patients they are assigned.
Harris CCM utilizes a productivity-based pay structure and pays $10.00 per completed patient encounter up to 99 encounters/month, $10.25/encounter from 100-149 encounters/month, $12/encounter from 150-199 encounters/month, $14/encounter from 200-249 encounters/month, and $16/encounter for >250 encounters/month.
Payment tier increases require 3 months consistency to achieve.
A patient encounter will take a minimum of 20 minutes (time is cumulative).
What your impact will be:
* The role of the Care Coordinator is to abide by the plan of care and orders of the practice.
* Ability to provide prevention and intervention for multiple disease conditions through motivational coaching.
* Develops a positive interaction with patients on behalf of our practices.
* Improve revenue by creating billable CCM episodes, increasing visits for management of chronic conditions.
* Develops detailed care plans for both the doctors a...
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Type: Contract Location: Springfield, US-IL
Salary / Rate: Not Specified
Posted: 2025-09-25 09:16:55
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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 Nurse Chronic Care Coordinator, Remote 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 while complying with HIPAA privacy laws.
You will set your own hours and will not be held to a daily work hour schedule.
You will be contracted to work a minimum of 20hrs/wk.
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.
Care Coordinators will be expected to complete encounters on 90 percent of the patients they are assigned.
Esrun Health utilizes a productivity-based pay structure and pays $10.00 per completed patient encounter up to 99 encounters/month, $10.25/encounter from 100-149 encounters/month, $12/encounter from 150-199 encounters/month, $14/encounter from 200-249 encounters/month, and $16/encounter for >250 encounters/month.
Payment tier increases require 2 months consistency to achieve.
A patient encounter will take a minimum of 20 minutes (time is cumulative including chart review, call times/attempts/texts, care plan development, care coordination, and documentation time).
What your impact will be:
* The role of the Care Coordinator is to abide by the plan of care and orders of the practice.
* Ability to provide prevention and intervention for multiple disease conditions through motivational coaching.
* Develops a positive interaction with patients on behalf of our practices.
* Improve revenue by creating billable CCM episodes, increasing visits for management of chronic conditions.
* Develops detailed care plans for both the doctors and patients.
The care plans exist for prevention and intervention purposes.
* Understand health care goals associated with chronic disease management provided by the practice.
* Attend regularly scheduled meetings (i.e., Bi-Monthly Staff Meetings, monthly one on one's, etc.).
These “mandatory” meetings will ...
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Type: Contract Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-25 09:16:52
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Job Category:
Intern
Job Family:
Student Intern
Job Description:
As a Quality Assurance Intern, you will have the opportunity to work the Summer 2026 with Schreiber Foods at one of our plant locations. This internship will be focused on supporting food safety and quality initiatives, company objectives and plant-specific assignments.
It is designed to prepare successful interns for a possible future career with Schreiber Foods.
This Quality Assurance summer internship is located at our plant in Carthage, Missouri.
Interns relocating more than 50 miles for the internship will receive a lump sum of $1,500.
This position offers a set rate of pay of $20.75 an hour.
What you’ll do:
* Lead small quality improvement projects within the team, working with plants and other areas of Schreiber Foods
* Creating and updating documentation for food safety and quality and lab processes
* Gaining knowledge about our products and applying that knowledge to improve processes and practices
* Inputting and analyzing data
* Completing projects related to testing, quality systems, sanitation, auditing, HACCP, training, SQF, suppliers, and other related topics
* Assisting the quality teams on ongoing projects
* Together with the leadership team, ensures compliance with Food Safety and Food Quality Plans, in addition to customer requirements.
Interprets and communicates customer requirements to plant production and/or support groups.
Establishes and Audits PCPs, CCPs and Standard Operating Procedures to define and monitor processes, to ensure customer requirements are met.
Reviews incidents during which the procedures are not met and determines appropriate corrective action for partners failing to follow standard procedures.
What you will need to succeed:
* Currently pursuing a Bachelor’s or Master’s degree in Food Science, Dairy Science, Microbiology, Bacteriology, Food Microbiology or closely related field.
* Ability to work 40 hours per week during the summer of 2026
* Ability to work at least 10 weeks of the summer, 12 weeks is preferred, with flexible start and end dates
* Effective oral and written communication skills
* Ability to work independently as well as in a team environment
* Ability to take ownership of assignments and complete them
* Desire to grow and take on new challenges and opportunities
* Ability and desire to work within a plant manufacturing setting
* Ability to multi-task
* Possess a strong technical foundation in the sciences; dairy knowledge desired but not required
* Reliable transportation
Internship benefits:
* Opportunity to complete real-world projects, participate in team meetings and contribute your ideas
* Exposure to different areas of the business around the world
* Internship program that includes engaging events and opportunities to build relationships at all levels
* Relocation assistanc...
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Type: Permanent Location: Carthage, US-MO
Salary / Rate: Not Specified
Posted: 2025-09-25 09:16:42
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At Stewart, we know that success begins with great people.
As a Stewart employee, you’ll be joining a company that was named a 2024-2025 Best Company to Work For by U.S.
News & World Report, and a 2025 Top Workplace by USA Today.
We are committed to helping you own, develop, and nurture your career.
We invest in your career journey because we understand that as you grow, so does our company.
And our priority is smart growth – by attaining the best people, investing in tools and resources that enable success, and creating a better home for all.
You will be part of an inclusive work environment that reflects the customers we serve.
You’ll be empowered to use your unique experiences, passion and skills to help our company and the communities we serve constantly evolve and improve.
Together, we can achieve our vision of becoming the premier title and real estate services company.
Stewart is a global real estate services company, providing title insurance, settlement, underwriting, and lender services through our family of companies.
To learn more about Stewart, visit stewart.com/about.
More information can be found on stewart.com.
Get title industry information and insights at stewart.com/insights.
Follow Stewart on Facebook @StewartTitleCo, on Instagram @StewartTitleCo and on LinkedIn @StewartTitle
Job Description
Job Summary
The Quality Review Specialist is responsible for various job tasks including reviewing signed loan and title company documents to ensure accuracy and the resolution of various post-closing issues prior to disbursement.
The ability to work quickly, with accuracy, and professionalism is paramount since the reviews and issue resolution occur during the rescission period between closing and loan disbursement
Job Responsibilities
* Monitor a pipeline of loans to ensure critical documents are received and reviewed timely for disbursement
* Appropriately prioritize a pipeline of loans to support Service Level Agreement targets
* Drive resolution for the customer, agency and client by engaging appropriate parties to include Fulfillment partners, borrowers, notaries, underwriting and other parties
* Complete a Compliance Review to confirm all funds are collected, all appropriate documents are checked for accuracy, signatures are collected, and acknowledgements and legal descriptions are correct in the critical document set to determine if resolution is required prior to disbursement
* Responsible for owning resolution on defects identified during the Compliance Review of critical documents
* Responsible for research and clean-up of data in company production systems
* The priority of data clean-up is directed by upper management and the audit committee in an effort to reduce non-compliance with company standards
* Performs a wide range of support functions to assist in departmental processes
* Follows clearly defined procedures to complete daily tasks and responsibilities
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-25 08:46:45
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The Mission, Concepts and Capabilities (MCC) division of Applied Research Associates, Inc.
(ARA) is searching for a talented Atmospheric Scientist.
The successful candidate will provide general knowledge and subject matter expertise in all facets of atmospheric science and meteorology, with a particular focus on how different types of weather impact transport and dispersion of chemical, biological, radiological, and nuclear (CBRN) hazards/phenomena.
Hazard prediction modeling of incidents across the CBRNE realm is required, and it is expected that the candidate will develop a basic understanding/modeling capability across all the scientific areas that DTRA supports.
Some natural hazard modeling and decision support will also be required.
The successful candidate must demonstrate a willingness to learn from and interact with individuals across a wide variety of subject matter backgrounds.
Below are additional expectations of this position:
* Analyze and interpret meteorological data gathered by surface and upper-air stations, satellites, and radar to prepare reports and forecasts for the public and other users.
* Prepare scientific reports, provide technical support, and assist with the development of chemical, biological, radiological, nuclear, and high-yield explosive (CBRNE) effects models.
* Assist in developing, integrating, testing, verifying, validating, and applying CBRNE software based on the results of experiments, and predict phenomena based on their theoretical and computational methods.
* Demonstrate an understanding of the concepts involved with atmospheric transport/dispersion models and/or air quality studies.
* Collaborate routinely with other subject matter experts to provide the best products possible to customers.
* Provide meteorological support to customers on a 24/7/365 basis.
Shift work is required, and extended hours may be required due to operational requirements.
Some holiday and weekend work will be expected.
* Demonstrate a solid, operational understanding of Numerical Weather Prediction.
Basic and applied meteorological research will also be expected.
*
REQUIRED QUALIFICATION:
* M.S.
in Atmospheric Science, Meteorology or related field
* 0-2 years of hands on experience
* Eligibility to obtain and maintain a US DoD TS/SCI security clearance
* Willingness to become trained to provide modeling across the CBRNE spectrum
* Must be a US Citizen
DESIRED QUALIFICATION:
* Top Secret Clearance
* Ph.D.
in Atmospheric Science or related field
* Applicants with strong, balanced backgrounds in both operational and research atmospheric science, particularly atmospheric boundary layer and turbulence, atmospheric transport and dispersion, space weather, and/or numerical weather prediction.
COMPANY INFORMATION:
Applied Research Associates, Inc.
is an employee-owned international research and engineering company recognized for providing technica...
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Type: Permanent Location: Fort Belvoir, US-VA
Salary / Rate: Not Specified
Posted: 2025-09-25 08:30:15
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Your Job
INVISTA has an immediate need for an R&D Laboratory Technician at our polypropylene plant in Longview, Texas.
Bring your curiosity, ideas, work ethic, and willingness to learn in a fast-paced, collaborative environment.
As an R&D Laboratory Technician, you will contribute as part of a team dedicated to exceeding customer expectations through quality and cutting-edge samples and product solutions.
Our Team
At INVISTA Longview, polypropylene is our specialty and advantage.
Our products are highly competitive due to reliable, flexible polypropylene resin supply with unparalleled application development support.
With more than 40 years of experience and nearly 850 million pounds of capacity, INVISTA is a preferred partner to the customers we serve.
What You Will Do
* Prepare and mix samples (compounding and extrusion) for testing and customer trials
* Maintain accurate records of testing procedures and results
* Collaborate with cross-functional teams while performing hands-on tasks in lab and manufacturing settings
* Support lab housekeeping and equipment maintenance to ensure safety, quality, reliability, and efficiency
* Routinely lift and move materials up to 50 pounds, climb stairs, ladders, and work in varying degrees of temperature
* Operate fork truck, assist loading and unloading materials from trucks, and operate support equipment for extrusion and compounding line.
Who You Are (Basic Qualifications)
* Manufacturing/industrial experience
* High School Diploma or higher
* MS Office experience (Word, Excel, MS Teams, Outlook)
* Must have legal authorization to work permanently in the United States for any employer without requiring a visa transfer or visa sponsorship
What Will Put You Ahead
* Associates degree or higher in Science, Biology, Mathematics, or Chemistry
* Experience in Polymer Laboratory
* Experience operating extrusion and molding equipment
* Experience preparing and/or testing samples
* Technical writing or reporting experience
* Experience with LIMS
* Military experience
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, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company, INVISTA has a long history of working to make the world around you a better place.
From...
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Type: Permanent Location: Longview, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-25 08:26:55
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Athens, Georgia, United States of America, Atlanta, Georgia, United States, Horsham, Pennsylvania, United States of America, Irvine, California, United States of America, Jacksonville, Florida, United States of America, Miami, Florida, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, Wilson, North Carolina, United States of America
Job Description:
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.
Quality & Compliance Internship Program Overview
The Quality and Compliance organization within the Enterprise organization for the Med Tech and Innovative Medicine sectors are seeking highly motivated students pursuing Bachelor (Rising Juniors or above), Masters, and PhD who desire a career in the medical device or pharmaceutical industry and are eager to learn technical and leadership skills to start their career journey.
The internship program offers students technical, analytical, and leadership knowledge and skills to build a strong foundation within the Quality and Compliance areas.
The program includes:
* Leading projects within various focus areas using digitalization and data analytics to drive simplicity, innovation, and efficiency
* Gaining an understanding of proactive risk management concepts and identifying potential risks
* Developing foundational knowledge of proactive risk management and learning how to apply risk management basics
* Building or improving your personal brand through skills building workshops and networking mixers.
* Sharpening leadership and presentation skills by presenting learnings and development experience to peers and leadership.
* Empowering community engagement and support within local communities through participation in community activities
The internship program offers hands-on experience in the following dat...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-25 08:25:18
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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:
Sales Enablement
Job Sub Function:
Sales Training
Job Category:
Professional
All Job Posting Locations:
Bangkok, Bangkok, Thailand, Jakarta, Indonesia, Kuala Lumpur, Kuala Lumpur, Malaysia, Singapore, Singapore
Job Description:
Position Overview:
The role will lead the development and execution of education strategies across Southeast Asia, including shape the learning experience for both internal teams and external healthcare professionals in the rapidly evolving field of robotic and digital-assisted surgery.
The current scope includes on the VELYS™ Robotic-Assisted Solution and the broader complementary orthopaedic portfolio.
Secondly, as the clinical lead, this individual will support VELYS funnel development in presenting clinical and technical advantages of VELYS during product demos and clinical evaluation.
He or she will also provide hypercare support during critical evaluation period as well as starting up first few cases.
Where necessary, this lead will also help to address technical questions around VELYS and to escalate clinicians concerns to the global R&D team.
Strategically, this role will support the development of product business plans, ensuring product-market relevance that marketing plans are grounded in sound clinical imperatives.
Key Responsibilities:
1.
Professional & Commercial Education Development
* Design and implement VELYS Professional Education programs to support surgical excellence and improved clinical outcomes in knee and hip arthroplasty.
* Create Commercial Education Programs tailored to sales and marketing teams to enhance technical knowledge and value-based selling capabilities.
* Collaborate with regional and global stakeholders to ensure alignment with APAC education standards and compliance requirements.
2.
Market & Content Strategy
* Assess market dynamics, customer insights, and training gaps across SEA to inform educational priorities.
* Translate clinical and commercial needs into engaging, data-driven educational content and tools that address surgeon concerns and support decision-making.
* Monitor clinical trends, competitive landscape, and surgeon feedback to proactively evolve the education strategy.
3.
Clinical Insight & Portfolio Strategy
* Act as a clinical subject matter expert for VELYS Knee and Hip solutions—helping address key clinical concerns and guiding internal teams on evidence-based posi...
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Type: Permanent Location: Singapore, SG-01
Salary / Rate: Not Specified
Posted: 2025-09-25 08:25:13
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
Contributes with the establishment and implementation of cost-effective, results-based, and professionally-managed programs and innovative initiatives for the accounting area, under direct supervision.
Assists with less complex components of projects, programs, or processes for the accounting area in compliance with GAAP (Generally Accepted Accounting Principles) and applicable governance policies.
Performs simple trend analysis to support continuous improvement efforts for the organization's accounting strategy.
Participates in the completion of internal and external audit, and ad hoc requests.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
This job does not require any experience.
This job is overtime eligible.
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-09-25 08:25:01
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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:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
* Establish and maintain appropriate documentation as required for Quality Assurance activities and the Quality Documentation Systems.
* Maintain and improve incoming, in-process quality control, finish good release procedure, provide technical support of process validations and risk management control.
* Responsible for inspection instrument qualification and test method validation.
* Provide Quality support in product transfers project, in terms of cooperate with local and global team to deliver Quality talks.
* Perform investigation of NC, CAPA, complaint, observation investigation as needed;
* Review NCR and disposition of nonconforming products.
* Assist in training of production and inspectors on quality knowledge.
* Participate in process/quality improvement projects.
* Develop and implement appropriate process monitoring and control methods to maintain consistency with process/product risk
* Support COGs initiatives.
* Responsible for following and administering safety.
* Compliance with safety policies and procedures.
* Follow J &J and Ethicon Records Management Policies for Convenience information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and the third-party vendor if applicable.
* Provide as needed, subject matter expert feedback on manufacturing process changes.
* Responsible for communicating business related issues or opportunities to next management level.
* Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
* Performs other duties assigned as needed.
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-09-25 08:24:57
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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:
Irvine, California, United States of America
Job Description:
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.
About the Role
The Lead Clinical Data Scientist will serve as a key technical expert within our organization, driving machine learning and AI-driven data science initiatives to support clinical studies, publications, and regulatory submissions.
This role will focus on leveraging advanced Machine Learning techniques to enable personalized treatment strategies, enhancing patient outcomes through innovative data science methods.
They will play a vital role in shaping standards, processes, and technical strategies related to machine learning within the broader Clinical Data Science team.
The Lead will ensure that all analyses are conducted with the highest level of scientific integrity, strictly adhering to regulatory requirements for both pre- and post-market clinical trials.
This position offers an exciting opportunity to influence the future of healthcare by integrating cutting-edge AI and machine learning solutions in a fast-paced, collaborative environment.
This is a hybrid role based in Irvine, CA
Key Responsibilities:
* Conceive, develop, and implement AI/machine learning and advanced analytics approaches to develop novel solutions to high-priority scientific problems, focusing on the application of AI to clinical trials
* Design and execute analysis plans independently for various phases of clinical studies, assuming a leadership role in creating the data science strategy.
* Review clinical study protocols and Case Report Forms (CRFs) for proposed studies with respect to data science and statistical methodology needs.
* Interact with Biostatistics, Data Management/Engineering, Regulatory, and Clinical staff to define and clarify project requirements.
* Produce data science reports that may be incorporated into internal clinic...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-25 08:23:50
-
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:
Biostatistics
Job Category:
People Leader
All Job Posting Locations:
Irvine, California, United States of America
Job Description:
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.
About the job
The Associate Director of Clinical Data Science - Biostatistics will lead a team of statisticians within Johnson & Johnson MedTech's Electrophysiology business, supporting comprehensive evidence generation and the dissemination of scientific findings from clinical trials and post-market studies.
This leader and their team will generate robust clinical evidence for the company’s devices, with a vital impact on patient lives.
In collaboration with the Clinical Science & External Research (CSER) team, they will contribute to statistical design, analysis, and the development of scientific presentations and publications.
This individual will be responsible for formulating and executing the statistical strategy in compliance with relevant regulations for post-market clinical trials across Johnson & Johnson MedTech Electrophysiology.
They will ensure that all statistical analyses uphold the highest standards of scientific integrity while adhering to timelines and budgets.
This role is based in Irvine, CA and will work on a hybrid schedule.
Key Responsibilities:
* Provide leadership and strategic direction for the Biostatistics team supporting evidence generation from clinical trials and post-market studies in Johnson & Johnson MedTech’s Electrophysiology business, ensuring high-quality statistical support for scientific outcomes with a crucial impact on patient lives.
* Lead the development and execution of statistical strategies for collaborative clinical studies, including study design, data analysis, and reporting, to ensure the generation of high-quality evidence and successful outcomes.
* Collaborate closely with the Clinical Science & External Research (CSER) team to contribute to the design, analysis, and interpretation of data s...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-25 08:23:49
