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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a Analytical Scientist II or Senior to join our Analytical Research and Development team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Analytical Scientist I, II, or Senior is a laboratory-based position and the Scientist will be responsible to support formulation development by performing method development, validation, writing protocols and reports, conducting chemical and physical testing activities for both ANDA and NDA projects.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Develop and evaluate analytical test methods for raw materials and in-process and finished products
* Write protocols and reports
* Conduct and document chemical and physical testing of finished products, raw materials, API, in-process products, stability samples to support new product formulation development for both ANDA and NDA projects
* Conduct and document method verification and method validation as per approved method validation protocols, Company SOPs, FDA Guidance, and ICH Guidelines
* Conduct and document in-process and finished product testing for product release and stability as per the approved test method
* Effectively communicate with cross functional teams like Formulation Development, Quality Control, Quality Assurance, Compliance and Regulatory Affairs
* Attend SOP, Safety and scientific trainings to remain current with cGMP regulations, and safety standards
* Follow relevant Adare SOP’s and FDA/ICH guidance
* Other duties as assigned
REQUIRED SKILLS AND QUALIFICATIONS
* Level II or Senior will depend on education, experience and skillset; a minimum of a Bachelors’ Degree in a Scientific Discipline with 3+ years’ experience is required
* Good understanding of chemical and physical analysis principles, experience in method development
* Fundamental understanding of GMP, ICH and FDA compliance
* Excellent wri...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-08-08 08:17:54
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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:
Business Support
Job Sub Function:
Administration & Secretarial
Job Category:
Business Enablement/Support
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
United Kingdom - Requisition Number: R-023917
Belgium - Requisition Number: R-027219
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson is currently seeking a Lead Administrative Assistant to join our team of Global Clinical Operations organization, Business Operations, Centralized Admin Team, Executive Support CoE to be based in Beerse, Belgium.
Global Clinical Operations plays a vital role in this mission, supporting the journey to bring medicines to patients and make a real difference in their lives.
Join our team and be part of a global organization dedicated to innovation, impactful initiatives, and creating a healthier future.
Are you an organized, proactive, and dependable professional with proven experience supporting executive leadership?
Johnson & Johnson’s GCO is seeking a dedicated Lead Administrative Assistant to provide top-tier support to our Vice President and a key director.
In this dynamic position, you will be the backbone supporting our leadership team by managing complex calendars, coordinating domestic and international travel, preparing key documentation, and facilitating smooth operations across multiple projects and teams.
Your attention to detail, confidentiality, and ability to prioritize will be integral to your success.
Additionally, you will have the opportunity to engage with peers from around the world and contribute to central administrative ac...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-08-08 08:15:53
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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:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Cincinnati, Ohio, United States of America
Job Description:
We are searching for the best talent for an Associate or Area Clinical Consultant to support clients in the Cincinnati, OH area.
About Cardiovascular
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
In this role as an Associate Clinical Consultant, you will be responsible for demonstrating the value and impact of our Impella® product portfolio to physicians and hospital staff.
You will advise Interventional Cardiologists and Surgeons in patient selection, partner on training, and attend implants.
As a key role on the Commercial team, you will acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all their applications.
You will provide comprehensive guidance on the appropriate use of the Impella® devices enabling physicians and staff to deliver positive patient outcomes.
Responsibilities
* Improve patient outcomes through education and medical staff interaction, including clinical demos and ongoing training for new and existing accounts.
* Collect clinically relevant data, complete outcome reviews with customers and communicate activities with other team members and sales counterparts.
* Acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all their applications.
* Attend implants and consult physicians and medical staff on appropriate use and applications Utilizes Integrity Selling to change the standard of care and drive usage of Impella with physicians.
* Ability to set up 1:1 physician meetings/conversations, host physician and...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-08-08 08:15:11
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Quality Control Inspector
Location: Houston, Texas
Overview:
Bray International is seeking a skilled Quality Control Inspector to join our team in a fast-paced industrial manufacturing environment.
If you are passionate about ensuring product quality and have at least four years of experience in quality inspection, we encourage you to apply.
This is an exciting opportunity to contribute to a leading company in the industrial valve and actuator industry.
Key Responsibilities:
* Perform incoming inspections on purchased parts, subassemblies, and finished products to ensure compliance with engineering drawings and customer standards.
* Review Material Test Reports (MTR) and Certificates of Conformance (CofC) against relevant standards.
* Analyze Non-Conformance Reports (NCR) to identify trends and generate Corrective Action Reports (CAR) as needed.
* Create Non-Conformance Reports and other departmental reports as assigned.
* Evaluate issues and make initial recommendations for corrective actions to supervisors.
* Investigate failures to determine root causes and propose remedial actions.
Qualifications:
* Minimum of four years’ experience in quality control within the industrial manufacturing sector.
* Experience with Positive Material Identification (PMI) preferred.
* Proficient in computerized record-keeping and standard software applications.
* Strong written and verbal communication skills.
* Skilled in using and calibrating precision measuring equipment (e.g., micrometers, height gauges, calipers, dial indicators, bore gauges).
* Knowledge of ISO 9001:2008/2015 and API standards.
* Ability to analyze and determine the best inspection methods for product conformity.
* Proficient in interpreting engineering drawings and understanding Geometric Dimensioning and Tolerancing (GD&T).
* Experience with Coordinate Measuring Machines (CMM).
* Ability to manage multiple tasks in a fast-paced environment while meeting delivery requirements.
* High School Diploma or equivalent required.
Physical Demands:
* Must have 20/20 vision (correctable) without color blindness.
* Ability to lift up to 20 pounds.
Note: Immigration sponsorship is not offered for this position.
Why Work for Us?
At Bray International, we are a global leader in providing industrial valves, actuators, and related control products.
We are known for our innovative flow control solutions and are looking for individuals who share our commitment to excellence, integrity, and collaboration.
What We Offer:
* Career Growth: We offer numerous opportunities for advancement within the organization.
* Comprehensive Benefits: Enjoy benefits such as:
+ Life, medical, dental, and vision insurance
+ Paid holidays and vacation
+ 401(k) plan with matching contributions
* Healthy Work Environment: We provide a smoke-free, drug-free workplace to ensure a sa...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-08-07 08:44:17
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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 Research Scientist, Non-Clinical Safety & Toxicology
We are seeking an experienced non-clinical toxicology / safety scientist to join the Global Non-Clinical Development team in Global Clinical Development.
As the Senior Research Scientist, Non-Clinical Safety & Toxicology you will be responsible for, or will assist with, human (user & consumer) safety and target animal safety program strategy and execution at all phases of global veterinary pharmaceutical drug/product and feed additive research and development, product safety assessments, and support for marketed products.
This role applies toxicology and immunology expertise to assess safety risks across the full product lifecycle, from early development through commercialization.
Responsibilities include evaluating potential safety concerns related to product design, manufacturing changes, deviations, or consumer complaints that could impact animal safety or end-user health.
The role involves preparing Product Safety Assessments (PSAs) for products in development, production, or on the market, and compiling medical and toxicological data to assess potential health risks for consumers and end users.
Your Responsibilities:
* Independently design, organize, monitor, report, and resolve issues related to outsourced in vitro and in vivo safety/toxicology studies, utilizing external CROs and/or consultants as needed.
These studies may involve typical rodent and non-rodent species.
Target animal safety evaluations may include companion animals (dogs and cats) as well as food-producing animals (e.g., cattle, pigs, chickens).
* Conduct literature reviews and author expert reports, position papers, safety and hazard/risk assessments, and other strategic scientific, technical, or medical evaluations to address safety considerations for veterinary drugs (small molecules and biologics), feed additives, excipients, E&L substances, impurities, or other chemicals.
* Provide internal expert guidance, including expert statements, health-based exposure limits (e.g., PDEs, OELs...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-08-07 08:26:29
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Accounts Receivable Analyst (12 months contract)
Job Description
Accounts Receivable Analyst - (12 months contract) (Global Business Services)
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Role Overview & Primary Accountabilities:
* Responsible in handling daily processing of sales and remittance advice data, and ensure timeliness and accurate processing 3rd Party & Intercompany within the agreed country SLA
* Management of data in strict adherence to internal control procedures are critical to effective credit control and collection of debts.
* Function as the expert on Cash Application processes and related systems.
Collaborate with work streams during process enhancements, acquisitions/divestitures, and major system implementations.
* Ensure that functional issues are appropriately prioritized and resolved.
* The incumbent is required to frequent liaising with internal sales and administrative personnel and customers to identify and resolve customer account issues.
* Engage actively with the business team country supported
* Initiate monthly engagement meeting as pulse check on the service delivery regular basis
* Reporting –KPI –Monthly basis
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 ...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-08-07 08:24:59
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Solution Architect (Blue Yonder) - (Remote)
Job Description
You were made to do this work: designing new technologies, diving into data, optimizing digital experiences, and constantly developing better, faster ways to get results.
You want to be part of a performance culture dedicated to building technology for a purpose that matters.
Here, you’ll work in an environment that promotes sustainability, inclusion, wellbeing, and career development while you help us deliver better care for billions of people around the world. It starts with YOU.
In this role, you will:
Be responsible for architecting WMS solutions that meet the needs of some of the most complex business functions in Kimberly Clark.
You will bring deep knowledge of Blue Yonder WMS solution and vast experience on how best it can be leveraged to meet operational needs whilst minimizing technical complexity.
* Involved in leading delivery of most complex client technical projects.
* Support in the definition of business and technical requirements to ensure strategies and solutions are aligned with business needs
* Design high quality end-to-end solutions to meet the business needs both now and in the future by ensuring solutions are fit for purpose, scalable resilient and secure
* Define detailed specifications according to which solutions are defined, managed, and delivered.
* Design and oversee the Design, configuration and build of the WMS solution and its integration with other interconnected systems.
* Ensure design practices, artefacts and processes are in line with leading industry patterns and practices.
* Provide technical governance and assurance for proposed solutions throughout the delivery life cycle.
* Identify and mitigate existing business risk or risks associated with solution design and delivery
* Support and lead in the development of internal architecture best practices and people
* Build expertise of best-in-class solutions / technology
* Works directly with Business resources and Business Analysts to drive technical solutions for business requirements.
* Leads and drives multiple streams within IT and the business teams in coming to a common understanding of processes and technology solutions to support them.
* Mentors and leads a team of software engineers which will be accountable for the WAPITI platform and shares knowledge across the organization.
* Maintains in-depth understanding of technical landscape for their capability area.
* Leads Continuous Improvement (CI) initiatives; consults and shares knowledge across org with full awareness of industry trends.
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 ...
....Read more...
Type: Permanent Location: Roswell, US-GA
Salary / Rate: Not Specified
Posted: 2025-08-07 08:24:36
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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Come join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a Formulation Technician to join our Formulations team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Formulation Technician will assist the R&D Formulations staff with product development activities from small scale to commercial batch production.
The Formulation Technician should be someone with a keen interest in life sciences or drug manufacturing. This is a developmental role where training is provided, offering an opportunity to learn various techniques of drug manufacturing including dispensing, blending, granulation, compression and coating.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Assist in running projects associated with product development, product and process optimization batches, and on completion to ensure robustness of the process and formulation.
* Coordinate and execute cleaning, process validation, and CMS technical / process operations activities with company quality units, operation, R&D and regulatory affairs for commercial or R&D products.
* Ensure sampling and testing are completed as planned.
* Assist in writing reports and preparing master formulary records.
* Follow protocol and batch records in manufacturing development batches and relate observations to CMS Manufacturing Associates and/or R&D Formulation group.
* Perform other duties as assigned.
REQUIRED SKILLS AND QUALIFICATIONS
* High school diploma with 5+ years’ experience in a pharmaceutical environment or equivalent combination of education and experience
* Cross-trained in the manufacturing unit operations such as granulation, blending, compression, coating, and encapsulation.
* Knowledge of manufacturing equipment such as granulators, tableting machines, coaters, and encapsulators.
* Mechanical skills/ability is required.
* Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environmen...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-08-07 08:20:51
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sciAre you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a Senior Formulation Scientist to join our Pharmaceutical Development Team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Senior Formulations Scientist will report to the Associate Director of Formulations, and will be expected to develop pharmaceutical dosage forms with an emphasis on immediate and modified-release solid oral dosage forms. This is a client-facing role providing a career path to advancement within Pharmaceutical Development.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Design and perform formulation development studies on immediate and modified release oral solid dosage forms defined by management/customer and assume the responsibility needed to meet the product specific objectives.
* Develop new products utilizing existing and new technologies available within the industry from pre-formulation to manufacturing stage.
* At times, interact directly with Adare’s clients in project update meetings; provide technical expertise, presentation of data
* Write development and cGMP batch records, stability study protocols, in-process and finished product specifications and product development reports
* Assist both Manufacturing and Quality Assurance departments in scale-up and production trouble-shooting
* Perform technology transfer to customer production sites and train/assist customer personnel in scale-up and production.
* Develop and/or locate new technologies that will be of interest to the Company’s product development objectives.
* Supervise/train formulation scientists and ensure their activities comply with CGMP regulations.
* Conducts and manage development projects with manager’s guidance and ensure the successful scale-up of a new product and/or process.
* Comply with all regulations as specified by OSHA, EPA, FDA, DEA, etc., and as defined in the Corporate Hygiene plan.
* Assist in writing and preparation of ...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-08-07 08:20:39
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program.
The EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Port Edwards and Wautoma, Wisconsin facilities.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits. Manage WPDES permits.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager. Work cooperatively with outside consultants.
* Develop and maintain company environmental, health and safety programs at the facility.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs.
* Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facility.
* Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
* Perform fit-testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks.
* Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations.
* Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corporate EHS department using the RCI reporting program.
* Complete a first report of injury with Workers Compensation Carrier if required for a w...
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Type: Permanent Location: Wautoma, US-WI
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:50
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program..
The EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Fond du Lac, Wisconsin facility.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits. Manage WPDES permits.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager.
* Work cooperatively with outside consultants.
* Develop and maintain company environmental, health and safety programs at the facility.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs.
* Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facility.
Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
* Perform fit-testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks.
* Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations.
* Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corporate EHS department using the RCI reporting program.
* Complete a first report of injury with Workers Compensation Carrier if required for a workplace i...
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Type: Permanent Location: Fond Du Lac, US-WI
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:49
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Sciences function, which enables portfolio decisions through integrative immunosafety, investigative safety and pathology expertise.
We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics.
The Opportunity
The Immunosafety team is seeking an Immunosafety Scientist with a focus on Mechanistic Immunomodulation and Immunosafety project support.
* You provide expert immunological insights for drug candidate risk assessment, designing and interpreting studies to identify and mitigate risks of immunoactivation or immunosuppression.
* You participate in developing and implementing risk mitigation strategies for drug candidates.
* You develop, optimize, and validate immunological assays.
* You apply strong practical experience with in vitro and in vivo immunological models, including New Approach Methodologies (NAMs).
* You evaluate new technologies to enhance research and assay capabilities.
* You act as an immunosafety expert on project teams, contributing to translational strategies that bridge preclinical findings to clinical settings.
Please note this position is temporary for 1 year.
Who you are
* You bring a PhD in Immunology, Toxicology or a related field with > 5 years of experience in drug development.
* You bring expertise in investigative immunosafety.
* You have a strong background in immunological assays and model development and validation (in vitro, in vivo, NAMs).
* You bring experience in providing immunological insights for risk assessment and mitigation.
* You can contribute to translational strat...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:44
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Job Summary
This is an onsite position at Inogen facilities located in Plano, TX or Beverly, MA.
Responsible for the development and execution of regulatory strategy for Inogen products.
The Director of Regulatory Affairs will lead a team and activities resulting in obtaining and maintaining regulatory approval in support of Inogen business objectives and applicable global medical device regulations.
The position plays a critical role in supporting Inogen’s ambitious global growth objectives and will work closely with internal stakeholders such as R&D, Clinical, Commercial, Operations, and Quality, as well as external stakeholders such as FDA, Notified Bodies, etc.
Responsibilities
* Serve as regulatory subject matter expert providing timely, clear, and consistent regulatory guidance for Inogen products throughout their entire lifecycle
* Prepare and obtain approval for product submissions to FDA and other global regulators
* Ensure compliance with all applicable regulatory requirements
* Maintain site registrations, regulatory files, and records
* Provide regulatory support for Inogen cross-functional regulated activities such as design, manufacturing, clinical trials, audits, post-market surveillance, etc.
* Review and approve product design, labeling, manufacturing, and quality assurance changes, as well as marketing advertising and promotional materials to ensure compliance with internal procedures, applicable regulations and guidelines
* Monitor regulatory trends, regulations, and guidance to inform regulatory strategies and ensure ongoing compliance with changing regulatory requirements
* Lead, mentor, and develop a high-performing team of regulatory professionals, fostering a culture of excellence, collaboration, and continuous improvement
* Build and maintain productive relationships with global regulatory authorities and external stakeholders, consultants, regulatory agencies, and industry groups
* Performs other duties as required
Knowledge, Skills, and Abilities
* Demonstrated proficiency and knowledge of current medical device Good Manufacturing Practices, FDA 510(k), EU MDR, FDA Advertising and Promotion guidance, and other global medical device regulations
* Exceptional leadership and team-building skills, with the ability to work highly effectively in cross-functional teams in a dynamic and fast-paced environment
* Analytical mindset, highly organized, detail oriented, and ability to prioritize
* 10 - 15% domestic and international travel required
* Must have exceptional written, verbal, and interpersonal skills with internal and external stakeholders
Qualifications (Education and Experience)
* Bachelor’s degree in engineering, Life Sciences, or technical discipline is required
* Applicable advanced degree preferred
* RAPS Certification (RAC) preferred
* Minimum of 8 years of Regulatory Affairs experience focusing on submi...
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Type: Permanent Location: Plano, US-TX
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:39
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Sciences function, which enables portfolio decisions through integrative immunosafety, investigative safety and pathology expertise.
We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics.
The Opportunity
The Immunosafety team is seeking an experienced Immunologist focused on Translational Immunosafety, Safety Biomarkers, and Immunosafety project support.
This role is crucial for expanding our presence in Translational Immunosafety & Safety Biomarkers to meet the evolving demands of our portfolio.
* You develop strategies to bridge preclinical findings to clinical settings, informing clinical trial design, patient selection, and monitoring.
* You provide comprehensive Immunosafety project support across the drug development value chain.
* You identify and characterize new safety biomarkers for immune-related adverse events (e.g., immunotoxicity, cytokine release syndrome (CRS), autoimmunity).
* You provide immunological insights for integrated risk assessment of drug candidates and contribute to risk mitigation strategies.
* You develop, optimize, and validate immunological assays, applying expertise in in vitro and in vivo immunological models, including New Approach Methodologies (NAMs), and other new technologies.
Who you are
* You bring a PhD in Immunology, Toxicology or a related field with > 5 years of experience in drug development.
* You have expertise in translational immunosafety, including safety biomarker discovery and development.
* You bring expertise in tissue-specific immunology and application in a mechanisti...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:31
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Sciences function, which enables portfolio decisions through integrative immunosafety, investigative safety and pathology expertise.
We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics.
The Opportunity
The Immunosafety team is seeking an experienced Immunologist to provide expert immunology support across a diverse portfolio of drug development projects.
This role is critical for maintaining robust portfolio support and introducing new perspectives on addressing immunosafety questions within a drug development setting.
* You serve as a drug safety immunology subject matter expert, staying current with advancements in the field and integrating relevant insights into drug development strategies.
* You provide comprehensive Immunosafety project support and guidance for human risk assessment across the drug development chain.
* You evaluate potential immunotoxicity, design and oversee studies, and interpret data to assess risks in the preclinical space.
* You stay updated on regulatory requirements pertaining to immunotoxicity and integrate them into study designs and interpretations.
* You develop, optimize, and validate immunological assays, demonstrating expertise in both in vitro and in vivo models, including New Approach Methodologies (NAMs).
* You mentor junior scientists within the team, fostering their scientific growth and development.
* You lead cross-functional teams, collaborating effectively with colleagues across various departments.
* You represent the organization at scientific forums, conferences, and external me...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:29
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
pRED's Pharmaceutical Sciences (PS) group enables discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
PS supports discovery and development across the whole value chain from target assessment to on-market and beyond.
This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Science function, which enables portfolio decisions through proactive and integrative pathology expertise.
We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics.
The Opportunity
We are offering an outstanding opportunity for a veterinary clinical pathologist to work with multidisciplinary teams in preclinical drug discovery and development with a focus on mechanistic, translational and regulatory aspects.
Your impact:
* You collaborate within an interdisciplinary team of pathologists, scientists and laboratory experts to ensure high-impact clinical pathology assessments are appropriately reported and integrated into investigative and regulatory pathology
* You provide scientific guidance for laboratory activities and participate in the generation of high-quality clinical pathology readouts
* You participate in the establishment and development of emerging safety biomarkers
* You nurture trustful relationships and effective collaboration with internal and external partners to characterize clinical pathology findings and identify potential safety risks
This position is a temporary contract for 2 years.
Who you are
* You are bo...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:25
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche’s Pharmaceutical Research and Early Development organization (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
This position is located in TSAC, a department within the Pharmaceutical Sciences function. We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products during the discovery and development phases at Roche.
The Opportunity
We are offering an outstanding opportunity for a Senior Toxicologist to serve as the single point of contact for impurities assessments at Roche Basel.
The position is placed in the Translational Safety Assessment chapter (TSAC) within Pharmaceutical Sciences at pRED Basel.
This is a critical role within our team, requiring a strong scientific background and excellent communication skills to collaborate across various departments.
You will play a key role in supporting the safety assessment of impurities and extractables/leachables throughout the value chain from late discovery to clinical development, as well as for established medicines, with compliance to the most current regulatory guidelines.
Utilizing your expertise, you will collaborate with cross-functional teams to ensure the delivery of high-quality and compliant safety evaluations.
Your main responsibilities will be:
* You are the single point of contact for impurity and E&L risk assessments in drug substances and drug products
* You conduct comprehensive risk assessments of genotoxic impurities in line with ICH M7 and related guidance
* You perform toxicological evaluations of E&L profiles associated with container closure systems, devices, and manufacturing components
* You provide guidance on thresholds of toxicological concern (TTC), supporting product compatibility and safety dossiers
* You design and interpret in silico (Q)SAR analyses and, where appropriate, prop...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:24
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
pRED's Pharmaceutical Sciences (PS) group enables discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
PS supports discovery and development across the whole value chain from target assessment to on-market and beyond.
The position is within the Translational Safety Assessment Chapter in Pharmaceutical Sciences.
We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products through all the discovery and development phases at Roche.
The Opportunity
We are offering an outstanding opportunity for a Project Toxicologist to work with multidisciplinary teams in preclinical drug discovery and development with a focus on mechanistic, translational and regulatory aspects.
Your main responsibilities in this position are:
* The development and execution of an integrated and scientifically sound nonclinical safety strategy from target assessment through clinical trial conduct to registration
* Representing Pharmaceutical Sciences in Global project teams and acting as a key contributor to the selection and timely development of potential new medicines through close interactions with discovery therapeutic areas, and affiliated non-clinical, clinical development and regulatory functions
* Steering non-clinical safety evaluations for potential in-licensing opportunities as well as representing non-clinical safety on collaborations with external partners
* Generating concise safety assessments for internal decision-making, as well as regulatory submission documentation to faci...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:23
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
pRED's Pharmaceutical Sciences (PS) group enables discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
PS supports discovery and development across the whole value chain from target assessment to on-market and beyond.
In the Translational PKPD and Clinical Pharmacology chapter, our purpose is to select the right drug to deliver the right dose and dosing schedule to patients to provide a meaningful benefit through strong collaboration, strategic thinking and regulatory and scientific excellence.
The Opportunity
As Neuroscience (NRD) Clinical Pharmacology subchapter leader for the clinical pharmacologists, you oversee the therapeutic area from end to end with a strategic and systems view, and ensure the functional excellence of the deliverables as well as the people leadership. Interacting with key stakeholders is part of your core competencies, as are excellent communication skills. This leadership role is embedded in the Translational PKPD and Clinical Pharmacology chapter, where key contributions to programs are provided from pre-target assessment to established products.
Key areas of impact within this role include:
People leadership
* Line management responsibilities in line with P&C practices to promote development, performance, balanced resourcing and well-being of the colleagues.
* Build a strategy for workforce planning and implement it
* Demonstrate agile leadership skills and exemplary Roche operating practices.
* Embrace agile ways of working and catalyze individual contributor contributions.
...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:21
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ERM is seeking an experienced ISO Management Systems Consultant to support a key client in San Jose, CA.
This role is focused on the sustainment and enhancement of operations with respect to EHS compliance aligned with an existing certified management systems ((R2, ISO 9001, ISO14001,ISO 45001).
The position will play a key role in advancing operational excellence, risk reduction, and environmental compliance at an e-waste recycling facility.
This is a full-time (40 hrs./week), limited-term role for 12 months, renewable.
RESPONSIBILITIES:
* Maintain a strong on-the-ground presence at the facility in support of day-to-day operations.
* This candidate is expected to follow the existing management system processes and procedures, as well as identify potential risks, and drive action and closure of corrective actions stemming from root cause assessments of issues.
* Demonstrate deep expertise in operational workflows and regulatory compliance in industrial operations.
* Exhibit a high level of self-direction and initiative, with minimal need for supervision.
* Proactively identify issues or potential risks and coordinate with the appropriate teams to ensure timely resolution.
* Gain a thorough understanding of the site’s management systems and provide support across departments as needed.
* Ensure ongoing compliance with all relevant EHS regulations, with specific knowledge of California and San Jose requirements (e.g., air permitting, universal waste, lockout/tagout, confined space entry, dust control, waste labeling and containerization, stormwater management, and such).
* Detailed knowledge of health and safety regulations issued by CalOSHA and other governmental agencies.
* May need to move light equipment or supplies from one place to another and climb stairs.
REQUIREMENTS:
* Minimum of 7 years of professional experience in EHS regulatory compliance and working with ISO 9001, ISO 14001, and/or ISO 45001 systems in an industrial, logistics, recycling, or manufacturing setting.
* Preferred Bachelor’s degree in science or engineering discipline.
* Strong working knowledge of San Jose-area regulatory requirements is essential—experience in warehouse or logistics environments is a plus.
* Demonstrated ability to work independently with minimal oversight in a fast-paced, operational environment.
* Strong communications skills, both written and spoken.
* Ability to pivot as needed, based on client needs.
* Ability to pick up technology quickly, such as programs/software.
* Excellent communication with cross-functional teams.
* Expected to perform well in a collaborative environment.
Pay Transparency:
For the ISO Management Systems Consultant position, we anticipate the annual base pay of $72,608 - $94,867, $34.90/hr – $45.60/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors inc...
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Type: Permanent Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2025-08-07 08:15:11
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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:
Suzhou, Jiangsu, China
Job Description:
Contributes to assigned team at J&J.
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-08-07 08:14:00
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Freiburg, Baden Württemberg, Germany, Karlsruhe, Baden-Wurttemberg, Germany, Neuss, North Rhine-Westphalia, Germany, Stuttgart, Baden Württemberg, Germany
Job Description:
Zur Unterstützung unseres Teams suchen wir eine/n
Medical Science Liaison MSL (m/w/d) Lung Cancer
für Region Deutschland Baden-Württemberg (Heidelberg, Mannheim, Karlsruhe, Stuttgart, Heilbronn, Freiburg, Ulm)
in Vollzeit oder Teilzeit (80%) in einem flexiblen Arbeitszeitmodell
Aufgaben
* Agiert als wissenschaftlicher Experte, implementiert die Medical Affairs Produkt Pläne in dem zugewiesenen medizinisch wissenschaftlichen Bereich in seiner Region.
* Proaktiver und reaktiver (HCP-Anfragen) wissenschaftlicher Austausch medizinisch wissenschaftlicher Informationen mit externen Experten aus Medizin und Forschung.
Kommuniziert hierfür u.a.
in-Label Produktdaten, diskutiert das klinische Studienprogramm und wissenschaftliche Informationen zu Produkten und Indikationen in Entwicklung.
* Der Hauptverantwortliche für das jeweilige regionale Leitungsteam (LT) kommuniziert den zentral verabschiedeten Medical Plan in sein Team.
Er koordiniert die indikationsspezifische Themenabfrage im LT, bei den Med Advisor Kollegen und anderen medizinischen Funktionen und erhält von den MAF-Kollegen Antworten auf die zuvor gestellten Fragen und Kerninformationen der Indikation.
Indikationsspezifische regionale Treffen mehrerer LT sollten bei Bedarf organisiert werden.
* Erlangt wertvolle strategische Kenntnisse über die Therapiepfade, wissenschaftliche Aktivitäten und Entwicklungen in den Kernindikationen und liefert einen Beitrag zur Identifikation der offenen Kernfragen, Data Gaps und Medical Needs als Basis der Entwicklung von Patient Outcome Lösungen.
* Proaktive Unterstützung der Erarbeitung und Implementierung einer medizinischen Strategie.
* Unterstützt in Kooperation mit Global Clinical Operations (GCO) die Identifikation potentieller Studienzentren und die Bildung und Unterhaltung starker, tragfähiger Partnerschaften mit diesen.
Unterstützung bei der Aufsetzung, Planung und Umsetzungen von Arzneimittelstudien (interventionelle und nicht-interventionelle) u.a.
bei der Auswahl von Studienzentren und Studienärzten, Vorbereitung und Teilnahme an Investigator Meetings, P...
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Type: Permanent Location: Neuss, DE-NW
Salary / Rate: Not Specified
Posted: 2025-08-07 08:13:58
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At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯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.â¯Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Hangzhou, Zhejiang, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
â¢Â      Actively identify, develop, and engage key KOLs at regional level.
â¢Â      Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
â¢Â      Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
â¢Â      Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
â¢Â      Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
â¢Â      To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
â¢Â      To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
â¢Â      To organize and moderate advisory boards in cooperation with TA groups.
â¢Â      To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
â¢Â      To collect insights from external customers and feedback timely to shape Brand/medical strategy    Â
Scientific Communication Effectiveness with external/internal customers
â¢Â      To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
â¢Â      To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
â¢Â      Support medical affairs program and activities at local and regional level.
â¢Â      Ensure program implementation 100% in compliance.    Â...
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Type: Permanent Location: Hangzhou, CN-33
Salary / Rate: Not Specified
Posted: 2025-08-07 08:13:48
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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
031468 Quality Control Technician (Open)
Job Description:
Key Responsibilities
* Able to understand and teach others how to read Work Orders, RGA, RED TAG and related documents.
* Inspect incoming, in-process, and finished goods for compliance with established quality specifications.
* Work with manufacturing and shipping/receiving personnel to complete required production line QC testing and documentation in a timely manner.
* Analyze data to specifications and designate as accept/reject. Initiate documentation for nonconforming materials as required.
* Assist Quality Analyst in development of new and revised quality specifications, methods, and standard operating procedures.
* Actively engage in sample testing with line crews and help develop their knowledge of the Quality Process.
* Assist with testing product returns and performing investigation of product complaints.
* Verify in-process quality checks, downtime recorded, and file paperwork as required.
* Take the lead on all quality-related issues. Act as the back-up point of contact to the Quality Analyst with customers and regulatory agencies on all quality related issues and audits.
* Assures compliance with the Greif Quality Management System.
* Actively engage in problem solving activities on matters pertaining to product quality concerns, corrective actions, supplier corrective actions and customer concerns.
* Visually inspects product.
* Cut samples to specified length using various saws.
* Capable of performing other duties assigned by management as required.
Education and Experience
* Typically possesses a high school diploma (or equivalent) and 2 years of relevant manufacturing experience.
Knowledge and Skills
* May lift as much as 35 pounds
* Able to communicate effectively with colleagues and management
* Able to stoop, bend, and move throughout plant for up to 8 hours per day
* Adheres to all safety policies and procedures. Participates in plant-wide safety, housekeeping, and continuous improvement processes.
* Possess above average computer skills, including prior experience with quality databases, Google Docs, and MS Excel, Outlook, and Word.
* Demonstrate proficiency using dial and electronic calipers, micrometers, and tape measures.
* Must possess the skills and abilities to train colleagues in using all calibration instrumentation on the production floor.
* Must be self-motivated and capable of working with minimum supervision.
Compensation Range:
The pay range for this position is $19.23 - $28.85.
Typically, a competitive wage for new hires will fall between $18.85 to $23.56.
Offers for this position may vary based on market data and other factors such as job-related knowledge, skills, ...
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Type: Permanent Location: Austell, US-GA
Salary / Rate: 22.98
Posted: 2025-08-06 08:55:33
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Global Human Resources Director
Location: Houston, TX (3-4 days weekly onsite when not traveling)
Reports To: Chief Financial Officer (CFO)
Travel Requirement: Up to 50% international
About Bray International
Bray International is a leading provider of industrial valves, actuators, and related control products, offering innovative flow control solutions worldwide.
As a privately-owned business with over 35 years of engineered excellence, Bray is known for its commitment to excellence, integrity, and collaboration.
Join our team to become part of a dynamic, forward-thinking organization shaping the future of flow control solutions.
About the Role
Bray International, a global leader in flow control solutions, is seeking a hands-on, detail-oriented Global HR Director to lead human resource initiatives across our 40-country footprint.
Reporting directly to the CFO, the successful candidate will have oversight of both solid-line and dotted-line HR teams globally, driving operational efficiency, compliance, and people-centric growth.
This role is heavily focused on tactical execution and project management, ideal for a professional who thrives on implementing process-driven systems, managing international compliance, managing specific employee matters, and collaborating cross-functionally with global finance and operations teams.
Key Responsibilities
* Global Oversight: Manage international HR teams (solid and dotted-line) across 40 countries, ensuring consistency, compliance, and alignment with business goals.
* Tactical Execution: Drive the implementation of process-driven HR projects and initiatives with measurable outcomes, from policy rollouts to process standardization.
* Compliance & Employment Law: Ensure adherence to global labor laws, including GDPR and local country employment regulations; guide U.S.
HR on federal/state compliance matters.
* HR Systems & Payroll: Lead the development of a global HR database and oversee country-specific payroll systems.
* Workforce Strategy: Support global recruitment, visa and immigration processes, and act as an advisor to regional managers on workforce management.
* Employee Engagement & Culture: Lead global engagement, recognition, and retention initiatives tailored to culturally diverse teams.
* Project Leadership: Take active ownership of open HR projects, driving them to completion and ensuring measurable business outcomes.
* Performance & People Management: Coach, mentor, and support HR team members in delivering business-aligned services.
Qualifications
Required:
* Bachelor’s degree in Human Resources, Business Administration, or related field
* 10+ years of progressive HR leadership experience in a global manufacturing, industrial, or engineering environment
* Demonstrated success managing HR operations and compliance across multiple countries
* Strong project management skills and attention to detail
* Profici...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-08-06 08:55:24
