-
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:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
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
We are searching for the best talent for a Director, Global Commercial Strategy, Precision Medicine to be base in Raritan, NJ.
Purpose:
The Director, Global Commercial Strategy, Precision Medicine will have responsibility for supporting the design & execution of J&J’s global commercial Precision Medicine (PM) strategy in close collaboration with key cross-functional stakeholders in the global and regional pharmaceutical organization.
The successful candidate should have diagnostic commercial experience and, preferably, pharma experience, be a strong leader with excellent communication and collaboration skills, possess scientific/technical aptitude and be able to translate the commercial PM strategy into execution for our therapeutic portfolio and pipeline.
Key focus will be to partner with R&D translational biomarker and diagnostic teams across therapeutic areas (TAs) on precision medicine assets in development to help ensure and accelerate their commercial success.
You will be responsible for:
Primary responsibilities for this position will include but not limited to:
* Support the design and implementation of Global Commercial PM strategy for various biomarker-driven assets in collaboration with the Global Brand Teams, Medical Affairs, Market Access, Regulatory, and Research & Development (R&D) teams across various Therapeutic Area’s (TA’s).
* Develop and implement plans for successful launch of PM programs and partnerships, ensuring seamless global access to strategic solutions that support pharmaceutical brand strategies in collaboration with internal global and regional pharmaceutical and PM partners as well as external experts and partners.
* Provide day-to-day oversight of diagnostic partnerships with testing laboratories or test manufacturers, including providing J&J input, coordinating cus...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-29 08:57:07
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Product Submissions and Registration
Job Category:
Professional
All Job Posting Locations:
Beijing, China
Job Description:
* Share the key information with all internal stakeholders in a timely manner.
Professionally interprate and analyze the impacts of new policies and regulations for product full lifecycle.
Represent JNJ to join policy-making discussion, and follow-up the development.
* Familiar with policy/ regulation developing procedure and timely involve in the development.
Timely capture the new regulation or regulation in drafting stage.
Actively contribute to the Medical Device industry associations, especially AdvaMed, Eucomed/COCIR and CAMDI, US & EU Chambers in China; and leading industry discussions on regulations & policies, closely follow-up updates from NMPA.
* Proactively work on China Medical Device regulations and policy, understanding on the relevant overseas regulations (USA, EU, Japan, and IMDRF), provide comprehensive and reasonable regulatory policy proposals, share policies and interpretation with peers and internal/external stakeholders if appropriate.
* Maintain good relationships with internal partners, including global RA, QA, R&D and Manufacture; and connect with medical device healthcare authority, such as NMPA, CMDE, etc.
and industry associations such as AdvaMed, EUCCC, etc.
Facilitate Policy workshops with NMPA and CMDE, follow up the project proposal completion, working on the process and project finalization’s evaluation.
* Lead and delivery internal policy training per needs to improve the registration process.
Participate in the review and revision of SOP and/or working guideline, to improve the process efficiency and effectiveness.
....Read more...
Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-29 08:56:56
-
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:
Project/Program Management Group
Job Sub Function:
R&D Project Management
Job Category:
Professional
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
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
We are searching for the best talent for the role of Director, Global Functions, Data Science Digital Health. We have a strong preference for this hybrid position to be located at one of the following offices; Titusville, NJ; Raritan, NJ; New Brunswick, NJ; Spring House, PA; Horsham, PA; Cambridge, MA; or San Diego, CA.
Remote work options in the US may be considered on a case-by-case basis and if approved by the Company.
At Johnson & Johnson Innovative Medicines R&D, the Data Science & Digital Health (DSDH) function is charged with applying analytic approaches to drug discovery and development across Therapeutic Areas.
We drive and shape internal and external collaborations, working across Janssen’s Therapeutic Areas and R&D functions, including Global Development and other areas.
The Global Functions, Data Science & Digital Health (GF, DSDH) group within the R&D Data Science organization has the accountability for full scale impact across the Development pipeline via AI/ML-driven site recommendation trial design optimization, real-world evidence (RWE) generation, digital endpoints, decentralized trials, and external policy, with the key pillars being:
* Manage the development of solutions for the purpose of driving Trial Acceleration & Optimization using data science, including but not limited to:
* Enrollment modeling, feasibility analytics, country footprint expansion, advanced AI/ML modeling for predictive site recommendations
* Leverage real-world data for pat...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-29 08:55:45
-
ERM is hiring Field Biologists to conduct surveys and monitoring for special status species for large construction projects in Fresno/Tulare, California.
Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of a field biologist requires technical skills, as well as strong organizational and communication skills.
This is a full-time (40+ hours/week), limited-term role with a duration of one year, and the possibility of renewal.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction special status species surveys across the client’s project area.
* Work locations are often remote and require biologists to work independently.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* At least 2+ years of Biology + Other Special Status Species Experience required.
Expertise should include more than one of the following species: Fisher.
* Must have experience with delineation, installation, or maintenance of wildlife exclusion fence, environmentally sensitive areas, no work buffers, or wildlife exclusion zones.
* Familiarity with nesting bird survey protocols and/or general bird identification skills is required.
* Experience with San Joaquin Kit Fox (SJKF), California Tiger Salamander (CTS), Swainson's hawk (SWHA) a plus.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in the documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Flexible availability: willingness to work weekends, holidays, and evenings as needed by the project.
* Demonstrated independent and effective problem-solving and decision-making skills.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Fluency in English and Spanish is highly preferred.
Pay Transparency:
For the Field Biologist position, we anticipate the annual base pay of $74,825 – $96,901, $35.97/hr – $46.58/hr USD, limited-term, non-exempt limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant ...
....Read more...
Type: Permanent Location: Carpinteria, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:55:08
-
ERM is hiring Field Biologists to conduct surveys and monitoring for special status species for large construction projects in San Jacinto, California.
Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of field biologist requires technical skills, as well as strong organizational and communication skills.
This is a full-time (40+ hours/week), limited-term role with a duration of one year, and the possibility of renewal.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction special status species surveys across the client’s project area.
* Work locations are often remote and require Biologist to work independently.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* At least 2+ years of Biology + Other Special Status Species Experience required.
Expertise should include more than one of the following species: Kangaroo Rats.
* Minimum experience requirements for these species are as follows:
+ Kangaroo Rats – Resume demonstrates ability to differentiate Kangaroo Rats from other Dipodomys species (e.g., coursework/training/experience).
* Must have experience with delineation, installation, or maintenance of wildlife exclusion fence, environmentally sensitive areas, no work buffers, or wildlife exclusion zones.
* Familiarity with nesting bird survey protocols and/or general bird identification skills is required.
* Experience with San Joaquin Kit Fox (SJKF), California Tiger Salamander (CTS), Swainson's hawk (SWHA) a plus.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in the documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Flexible availability: willingness to work weekends, holidays, and evenings as needed by the project.
* Demonstrated independent and effective problem-solving and decision-making skills.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Fluency in English and Spanish is highly preferred.
Pay Transparency:
For the Field Biologist position, we anticipate the annual bas...
....Read more...
Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:55:07
-
ERM is looking for a motivated, detail-oriented Managing Consultant, Hydrogeologist to join our growing team in Boston, Massachusetts.
Working under the direction of project managers and partners, the successful candidate will work on interesting site investigation and remediation projects in the northeast region and throughout the United States.
You may also have the opportunity to work on international site investigation and remediation projects. This is a great opportunity to work with ERM's technical experts to implement the latest site investigation and remediation technologies.
RESPONSIBILITIES:
* Plan and oversee field data collection, including sampling, drilling, well installation, aquifer hydraulic conductivity testing, remedial pilot tests, and remedial system operation and maintenance.
* Compile and evaluate site investigation and remedial system monitoring data.
* Synthesize site characterization and remediation information to develop and refine conceptual site models.
* Utilize conceptual site models to communicate findings, identify data gaps, and focus additional data collection efforts.
* Review investigation and remediation data developed by other consultancies and develop recommendations for additional investigation and remediation activities.
* Work closely with geographic information system experts to develop visually compelling and informative graphics.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Communicate with subcontractors, regulatory agents, tenants, and clients during field activities.
REQUIREMENTS:
* Master's degree in hydrogeology, geology, environmental engineering or related degree.
* Minimum 5 years of experience.
* Strong written/verbal communication and organization/analytical skills; experience writing detailed technical reports.
* Willingness/interest in travel for field assignments.
* Environmental field work experience and 40-hour OSHA HAZWOPER certification a plus.
* Strong commitment to safety, including following established Health and Safety protocols.
* Valid driver’s license and a good driving record.
* Ability to work independently and as part of a team.
* Detail-oriented with mechanical aptitude and hands-on trouble-shooting/problem-solving skills.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
For the Managing Consultant, Hydrogeologist position, we anticipate the annual base pay of $83,318 – $98,209 USD. 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...
....Read more...
Type: Permanent Location: Boston, US-MA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:54:43
-
Accounting Analyst II - RTR Operations (Korean Speaker) - (Global Business Services)
Job Description
Accounting Analyst II - RTR Operations (Korean Speaker) - (Global Business Services)
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Role Overview & Primary Accountabilities:
* Maintain assigned SAP systems by ensuring that all relevant RTR Finance master data changes for SAP security, system tables, chart of accounts, internal orders, cost centers and profit centers are appropriate, authorized and documented.
* Ensure Finance security roles are in compliance with global segregation of duties matrix.
* Provide a source of system expertise, business knowledge and problem solving capabilities to ensure sound analysis, recommendations and action programs in the maintenance and development of RTR module
* Perform period end closing for CO-PA (customer and product profitability analysis) for management reporting purposes.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact.
We’re founded on 151 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and the business.
In one of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.
To succeed in this role, you will need the following qualifications:
...
....Read more...
Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-05-28 08:30:58
-
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
Promotes Stewart services and solutions through various outside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share.
Job Responsibilities
* Promotes Stewart services and solutions through various inside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share
* Typically follows existing procedures to perform routine assignments and to solve standard problems
* Analyzes basic information and standard practices to make decisions impacting work performed
* Individual contributor working with direct oversight
* Performs all other duties as assigned by management
Education
* Bachelor’s degree in relevant field preferred
Experience
* Typically requires 0-2 years of related work experience
Equal Employment Opportunity Employer
Stewart is committed to ensuring that its online application process provides an equal employment opportunity to all job seekers, including individuals with disabilities.
If you have a disability and need assistance or an accommodation in the application process, please contact us by email at careers@stewart.com.
Benefits
Stewart offers eligible employees a competitive benefits package that includes, but is not limited to a variety of health and wellness insurance options and programs, paid time off, 401(k) with company match, employee stock purchase program, and employee discounts.
....Read more...
Type: Permanent Location: Bloomington, US-MN
Salary / Rate: Not Specified
Posted: 2025-05-28 08:28:41
-
Title: Intelligence Analyst IV
Location: Washington D.C., Merrifield, VA
Security Clearance: Secret
Schedule: Due to the nature of law enforcement work and operation, position may require occasional support outside of core working hours, as well as intermittent weekend support, mission dependent.
*
*
*CONTINGENT UPON AWARD
*
*
*
About KACE:
When you make the decision to join KACE, you are choosing to work alongside talented professionals that have one thing in common; the passion to make a difference! KACE employees bring their diverse talents and experiences to work on critical projects that help shape the nation’s safety, security, and quality of life.
The desire to have a career that is purposeful and forward thinking is woven into every KACE employee…it’s The KACE Way.
KACE employees are; purpose driven, forward focused, open-minded, trustworthy, and invested.
The KACE Way is our commitment to our employees, to our customers, and to our communities.
Join KACE and make a difference!
Job Summary:
Serves as a technical authority in one or more intelligence disciplines.
Is responsible for planning, coordinating, and synthesizing research from other Intelligence Analysts to prepare and disseminate all-source intelligence products and responses.
Determines research methodology and work approach and revises as appropriate.
Evaluates incoming intelligence and determines pertinent data that should be directed to the attention of the Senior Intelligence Officer.
Assesses progress of research efforts and redirects efforts.
Evaluates correctness and accuracy of researched material.
Essential Functions and Responsibilities:
* Briefs intelligence assessments and positions to principals and subordinates.
* Ensure team products fulfill National-level intelligence requirements.
* Provides technical guidance to staff principals and subordinates.
* Conducts complex research and analysis of intelligence, counterintelligence, counternarcotic, organized crime operations, capabilities, and trends supporting all source intelligence and threat production.
* Leads the preparation, coordination, and implementation of intelligence production and analysis activities in support of OCDETF operations.
* Develops intelligence estimates and projections.
Presents, advocates, and defends OCDETF positions effectively within the intelligence, planning, and operational communities.
* Coordinates, develops, drafts, writes, produces, revises, and ensures completeness of intelligence plans, annexes and associated appendices that require management input.
* Formulates and prepares the intelligence plans and security portions of exercises.
* Plans and coordinates intelligence support of joint and combined exercises.
Serves as intelligence representative, liaison, site survey officer, and focal point staff officer for exercises and real-world crisis operations.
* Maintains close liaison with counterparts in other intell...
....Read more...
Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2025-05-28 08:28:01
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Post Doc – Drug Discovery & Pre-Clinical/Clinical Development
Job Category:
Career Program
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
We are seeking a highly skilled and motivated postdoctoral scientist, with a fixed term of 2 years, o join the team of Global Safety Pharmacology located in Beerse, Belgium.
The postdoctoral scientist will focus on de-risking drug-induced peripheral neuropathies (DIPNs) to support our drug discovery and development programs.
The successful candidate will apply their expertise in neuroscience to establish translatable human in vitro models of peripheral neuropathies with robust read-outs for functional and molecular biomarkers of DIPNs and perform intricate data analyses.
Responsibilities include experiments such as 2D co-culture of hiPSC-derived sensorimotor neurons and Schwann cells, multi-electrode array recordings, and various gene and protein expression analyses.
Collaboration with cross-functional teams and a commitment to ethical research practices aligned with the 3Rs principles will be essential.
Proficiency in English and strong communication skills will facilitate effective collaboration and dissemination of findings through scientific writing and presentations.
Major Duties & Responsibilities
* Establishing in vitro platforms of drug-induced peripheral neuropathies (DIPNs) using co-culture models of hiPSC-derived peripheral neurons and human Schwann cells
* Identification, testing and validation of human-relevant biomarkers for DIPNs in the in-vitro platforms
* Define strategies whilst collaborating with cross-functional teams and establish in-vitro screening tools to assess DIPN liabilities
* Data analysis and reporting
* Development, training, conferences and writing scientific papers for publication in relevant journals
Required Knowledge, Skills, and Abilities:
* PhD in Neuroscience, Physiology, Cell Biology, or a relevant field focused on CNS and PNS safety pharmacology/toxicity
* In-depth knowledge and experience in the mechanisms of peripheral neuropathies (up to the molecular level), electrophysiology, and hiPSCs, with a proven track record
* Hands-on experience in the experimental techniques mentioned below
* hiPSC-derived sensory or motor neurons co-cultured with human Schwann cells (or other human glial cells) on microfluidic platform...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-28 08:22:28
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
ES024 Janssen Madrid Oficinas
Job Description:
Position Summary:
Manager Clinical Operations is accountable for the operational management and successful country execution of all phases of clinical trials within assigned therapeutic area(s) or specific role(s), including resource allocation, adherence to timelines and budget, compliance with relevant Standard Operating Procedures (SOPs), policies, Health Care Compliance (HCC) and local regulatory requirements.
The Manager Clinical Operations supports Country Head in shaping and managing local organizational structure to ensure its optimal efficiency and demonstrates effective issue management.
This individual is responsible for line management of Local Trial Managers (LTM), Site Managers (SM), Clinical Trial Assistants (CTA) and/or other GCO staff, as required.
Oversees staff performance, development, training, project assignments, workload distribution and supports issue resolution with direct reports.
Ensures alignment of local goals with organizational objectives.
Drives innovative solutions and process improvements for the assigned therapeutic area(s), country, and GCO/Global Development (GD) overall.
Principal Responsibilities:
1.
Provide line management to direct reports including setting goals and objectives, performance evaluation and talent development.
2.
Evaluate and forecast resource needs for assigned portfolio and/or other specific area of responsibility, as required and agreed with local GCO management accordingly.
3.
Responsible for deployment of the One Delivery Model through collaboration and oversight of vendors.
4.
Accountable for the acquisition of new talents and development of human resources.
5.
Guide direct reports in issue resolution and communication with involved stakeholders.
6.
Lead organizational changes and effectively communicate on priority shifts as required.
7.
Review and approve expenses in compliance with the company policies.
8.
Demonstrate leadership behaviors in alignment with J&J Leadership Imperatives.
9.
Foster an environment that encourages sharing of ideas, information and best practices (internal and external to the organization).
10.
Provide coaching and mentorship as needed, including conduct of accompanied site visits as appropriate.
11.
Define, execute or support of long ...
....Read more...
Type: Permanent Location: Madrid, ES-M
Salary / Rate: Not Specified
Posted: 2025-05-28 08:22:20
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Market Access
Job Sub Function:
Health Economics Market Access
Job Category:
People Leader
All Job Posting Locations:
Beijing, China, Shanghai, China
Job Description:
Key Responsibilities:
Lead product value proposition and access.
Working closely with Sales/Marketing/Strategical Key Account/Government Affairs team to identify key business challenges then to provide appropriate HEMA solution to help addressing access related challenges.
Lead and coordinate HEMA project development, design, planning and delivery of HEMA projects to agreed timelines, quality and budget, using appropriate data, analytical expertise, and rigorous methodology.
Support products HEMA assessment and actively involved in evidence generation discussion then prepare HEMA evidence to support launch.
Lead and Influence cross functional internal stakeholders and multi-disciplinary matrix functions to incubate collaboration in (but no limit to) internal education, strategic project, etc.
Proactively identify, initiate and manage collaborations with external stakeholders and execute environment shaping program.
Provide technical review support for team members’ study protocol and appropriate consultant in related field.
....Read more...
Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-27 08:07:54
-
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:
Shanghai, China
Job Description:
工作内容（Job Description）：
* 协助真实世界研究
* 数据整理与分析
* 撰写流行病学研究报告
职位要求（Job Requirement）：
* 对真实世界数据研究有浓厚兴趣
* 有相关医学科研背景
* 流行病学或统计学本科在读及以上
....Read more...
Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-05-27 08:07:48
-
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.
Shift: This role currently operates on an 8-hour shift schedule.
Starting in July 2025, the position will transition to a 12-hour shift schedule.
Further details about the specific 12-hour shift schedule (days of the week, start/end times) will be discussed during the interview process.
Please note that weekend work will have a 4% premium and work outside of your shift hours will have 10% premium.
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 en...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: 24
Posted: 2025-05-26 08:00:28
-
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:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
Warsaw, Masovian, Poland
Job Description:
For J&J Innovative Medicine we are looking for a Commercial Quality Specialist (CQS) reporting to Quality Head Poland and to be hired with a fixed-term contract (until April 2026).
Essential Duties and Responsibilities
* Perform tasks according to quality system standards and procedures for distribution, storage, and transportation of medicinal products (GDP).
* Participate in Quality Management System processes, including Change Control, Corrective and Preventive Actions (CAPA), deviations, complaints, and documentation management.
* Oversee GxP documentation, including updates, distribution, archiving, and compliance analysis.
* Participate in internal audits.
* Investigate quality problems, conducting risk and root cause analyses.
* Participate in supplier qualification processes.
* Conduct staff training on the Quality Management System and GxP requirements.
* Engage in quality development projects and review quality procedures/instructions.
* Collaborate with internal and external partners.
* In the absence of Responsible Person for Controlled Substances:
- Manage end-to-end import licenses and quality oversight for controlled substances.
- Ensure documentation related to controlled substances distribution is implemented and updated.
Activities Requiring Physical Presence at Distribution Center
* Act in the absence of the Responsible Person or Responsible Person for Controlled Substances as per delegated duties.
* Finalize product releases for distribution based on inbound documentation.
* Handle complaints & returns in collaboration with Customer Service.
* Collaborate with Logistics Operator on daily basis.
Requirements
* Education: Must be a pharmacist.
* Experience: Minimum of 2 years of experience working in a pharmacy or pharmaceutical wholesale.
* Language Skills: English (good knwoledge), fluent in Polish.
....Read more...
Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-05-26 07:56:36
-
WK Dickson (an Ardurra company) is seeking an Environmental Scientist/Wetland Scientist to join our team in our Charlotte, NC office!
We are a trusted leader in providing reliable and innovative water resource solutions across the Southeast.
We offer tailored and cost-effective approaches to improve watershed functions, protect public safety, and enhance quality of life.
As advisors to municipal clients, we guide communities in developing sustainable stormwater programs focusing on nature-based solutions.
Our expertise includes watershed planning, ecosystem restoration, regulatory permitting, water quality and quantity control, and capital design projects.
Primary Function:
We are seeking a motivated and knowledgeable Wetland Scientist to play a key role in the planning, execution, and management of wetland and natural resource projects throughout the Southeast.
This is an exciting opportunity to work on diverse watershed projects in a collaborative and supportive work environment.
Primary Duties:
* Conduct wetland and stream delineations per USACE Manual and applicable Regional Supplements
* Prepare technical documents: delineation reports, jurisdictional determination packages, mitigation plans, and environmental permits
* Manage the environmental permitting process (404/401, NPDES, etc.) at the federal, state, and local levels to support various practice areas firmwide
* Conduct site evaluations and assist in environmental impact assessments.
* Collaborate with senior engineers and multidisciplinary teams to develop innovative watershed planning and nature-based stormwater
* Lead fieldwork efforts, data collection, and ecological assessments with a strong emphasis on collaboration and safety
* Coordinate directly with clients, regulatory agencies, and multidisciplinary project teams
* Mentor junior staff and contribute to the professional growth of our team
Education and Experience Requirements:
* Bachelor’s or Master’s degree in Environmental Science, Biology, Ecology, or a related field
* Approximately 7+ years of experience in wetland science and delineations
* Proficiency in ArcGIS, GPS data collection, and technical writing
* Understanding of the Clean Water Act, USACE protocols, and Section 404/401 permitting
* PWS (Professional Wetland Scientist) is preferred but not required
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers.
We nurture a family-like culture, striving to create a work environment that is enjoyable, challenging and rewarding but also fun.
We are acutely focused on developing our staff, whether through our internal Ardurra Academy or through our industry-leading Leadership program.
We have made a deliberate and focused commitment to nurture a people-centric culture where people are: valued as individuals; supported in their professional and car...
....Read more...
Type: Permanent Location: Charlotte, US-NC
Salary / Rate: Not Specified
Posted: 2025-05-26 07:55:36
