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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.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Technician
As a Quality Control Technician, you will be part of the Clinton Laboratories Quality organization supporting laboratory testing activities for oral solid dose medications.
In this role, you’ll assist with sample handling, routine lab testing, and documentation to ensure products meet quality and regulatory standards.
You’ll also help maintain lab equipment, follow standard operating procedures, and contribute to continuous improvement efforts within the lab.
Experience with dissolution or solid oral dose testing is beneficial but not required; training will be provided.
This posting will offer a one-time sign on bonus of $2,500!
Your Responsibilities:
* Prepare, handle, and label samples to support quality control testing activities in accordance with GMP requirements.
* Perform basic laboratory tasks such as weighing, measuring, and recording data following written procedures.
* Maintain and clean laboratory equipment and work areas to ensure readiness and compliance.
* Document test data and observations accurately and promptly in accordance with company procedures.
* Support laboratory investigations and contribute to process and safety improvement initiatives.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma or equivalent required; Associate’s degree in a scientific field preferred.
* Required Experience: Hands-on laboratory or manufacturing experience, ideally within a GMP or quality-focused environment.
* Top 2 skills: Strong attention to detail and comfort working in a laboratory setting following written procedures.
What will give you a competitive edge (preferred qualifications):
* Experience with oral solid dose testing methods such as dissolution or disintegration.
* Proficiency with Microsoft Word, Excel, and laboratory informatics systems.
* Strong written and verbal communication skills.
* Ability to handle multiple priorities while maintaining accuracy and compliance.
* Experience working in a GMP or manufacturing environment.
Additional Informati...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-10-25 09:12:13
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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.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
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!
Historically, the role of IT has been to provide a reliable ecosystem to run the business, drive efficiencies and reduce costs.
These areas remain integral, however, driven by the quickening pace of innovation, IT must evolve, proactively partnering with the business to enable new digital business models that power new types of customer engagement.
At Elanco, we are investing in our Data Engineering capability and are hiring roles that will bring a broad range of skills covering areas such as data ingestion, integration, transformation, and consumption to deliver data products that will transform how we work with data.
As part of the Data Engineering and Platforms team, we are looking for a highly experienced Data Engineer to provide their technical leadership to both internal and partner teams working within our Enterprise Data environment.
This is a broad role which will include coaching and leading junior engineers in their domain, tackling technical challenges and partnering with colleagues in their product team to deliver desired outcomes for Elanco.
To be successful in an engineering role in Elanco requires a highly motivated individual, with an innovative mindset and a willingness to drive tangible outcomes.
The individual must be able to articulate complex technical topics, collaborate with internal and external partners and ensure quality delivery of the required data products.
This role will focus on our R & D function, playing a key role in our implementation of data capabilities to support Elanco’s innovation.
Responsibilities:
Engineering
* Articulate our technical direction and upskill colleagues (both internal and external) in leveraging our Enterprise Data Platforms to deliver data products and ensure value is well understood.
* Provide feedback to our Data Platform Engineering Team to improve their services.
* Drive opportunities from the Data Engineering backlog and provide technical leadership in design and execution of those solutions.
* Drive Elanco’s Data Engineering standards, leveraging standard languages, frameworks and continually reviewing as appropriate ...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-10-25 09:12:06
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PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) process.
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Type: Permanent Location: Memphis, US-TN
Salary / Rate: Not Specified
Posted: 2025-10-25 09:10:18
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Your Job
Phillips Medisize, a Molex company is seeking a Product Development Lead for Medical and Drug Delivery Devices to join our team at our Hudson, WI site.
In this role, you will spearhead the design, development and launch or cutting-edge medical device and drug delivery solutions.
This role offers the opportunity to guide technical direction, oversee system architecture and ensure compliance with industry standards, while working closely with customers and cross-functional teams.
Our Team
At Philips Medisize, we aspire to be the preferred partner of choice for leading global customers, to create innovative products that help people around the world live healthier, more productive lives.
We are an end-to-end provider of innovation, development, and manufacturing solutions to the medical, regulated products, automotive, consumer and defense markets.
Companies count on Phillips Medisize to bring their breakthrough ideas and innovative branded products to market - with confidence.
As a contract design and manufacturing organization (CDMO), we work closely with our customers to deliver proven, highly engineered products.
What You Will Do
* Lead the technical direction and execution of medical device and drug delivery projects from concept through launch.
* Collaborate with customers and cross-functional teams (R&D, Quality, Regulatory, Manufacturing,) to ensure seamless product development and compliance with FDA, ISO 13485, IEC 60601, and related standards.
* Oversee system architecture, design specifications, risk management, and verification/validation plans, while managing and mentoring engineering teams to foster innovation and technical excellence.
* Drive technical decision-making, risk mitigation, and documentation (DHF, DMR, technical files).
Lead root cause analysis and support CAPA for device issues.
* Stay current on emerging technologies and regulatory changes.
* Communicate project status and challenges to internal and external stakeholders.
* Guide system-level integration across technical domains (mechanics, electronics/software, molding/assembly, usability, etc.), and define development strategy with strong engineering and data traceability, especially in customer-driven programs.
Who You Are (Basic Qualifications)
* Bachelor's Degree or higher in Biomedical, Electrical, Mechanical, or Biological Engineering
* 7+ years' experience in medical device design/development, with 3+ years in technical leadership.
* Experience with FDA Class II/III devices, design controls, risk management (ISO 14971), and validation.
* Familiarity with FDA 21 CFR Part 820, ISO 13485, IEC 62304, IEC 60601
* Experience supporting development of regulatory submission documentation packages.
* Experience working with multiple quality management systems.
What Will Put You Ahead
* Experience leading development of Drug Delivery Devices, Wearables or Catheters.
* Worked ac...
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Type: Permanent Location: Hudson, US-WI
Salary / Rate: Not Specified
Posted: 2025-10-25 08:55:26
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Your Job
INVISTA has an immediate need for an R&D Laboratory Technician at our polypropylene plant in Longview, Texas.
Bring your curiosity, ideas, work ethic, and willingness to learn in a fast-paced, collaborative environment.
As an R&D Laboratory Technician, you will contribute as part of a team dedicated to exceeding customer expectations through quality and cutting-edge samples and product solutions.
Our Team
At INVISTA Longview, polypropylene is our specialty and advantage.
Our products are highly competitive due to reliable, flexible polypropylene resin supply with unparalleled application development support.
With more than 40 years of experience and nearly 850 million pounds of capacity, INVISTA is a preferred partner to the customers we serve.
What You Will Do
* Prepare and mix samples (compounding and extrusion) for testing and customer trials
* Maintain accurate records of testing procedures and results
* Collaborate with cross-functional teams while performing hands-on tasks in lab and manufacturing settings
* Support lab housekeeping and equipment maintenance to ensure safety, quality, reliability, and efficiency
* Routinely lift and move materials up to 50 pounds, climb stairs, ladders, and work in varying degrees of temperature
* Operate fork truck, assist loading and unloading materials from trucks, and operate support equipment for extrusion and compounding line.
Who You Are (Basic Qualifications)
* Manufacturing/industrial experience
* High School Diploma or higher
* MS Office experience (Word, Excel, MS Teams, Outlook)
* Must have legal authorization to work permanently in the United States for any employer without requiring a visa transfer or visa sponsorship
What Will Put You Ahead
* Associates degree or higher in Science, Biology, Mathematics, or Chemistry
* Experience in Polymer Laboratory
* Experience operating extrusion and molding equipment
* Experience preparing and/or testing samples
* Technical writing or reporting experience
* Experience with LIMS
* Military experience
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company, INVISTA has a long history of working to make the world around you a better place.
From...
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Type: Permanent Location: Longview, US-TX
Salary / Rate: Not Specified
Posted: 2025-10-25 08:55:14
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Athens, Georgia, United States of America, Atlanta, Georgia, United States, Horsham, Pennsylvania, United States of America, Irvine, California, United States of America, Jacksonville, Florida, United States of America, Miami, Florida, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, Wilson, North Carolina, United States of America
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity.
Quality & Compliance Internship Program Overview
The Quality and Compliance organization within the Enterprise organization for the Med Tech and Innovative Medicine sectors are seeking highly motivated students pursuing Bachelor (Rising Juniors or above), Masters, and PhD who desire a career in the medical device or pharmaceutical industry and are eager to learn technical and leadership skills to start their career journey.
The internship program offers students technical, analytical, and leadership knowledge and skills to build a strong foundation within the Quality and Compliance areas.
The program includes:
* Leading projects within various focus areas using digitalization and data analytics to drive simplicity, innovation, and efficiency
* Gaining an understanding of proactive risk management concepts and identifying potential risks
* Developing foundational knowledge of proactive risk management and learning how to apply risk management basics
* Building or improving your personal brand through skills building workshops and networking mixers.
* Sharpening leadership and presentation skills by presenting learnings and development experience to peers and leadership.
* Empowering community engagement and support within local communities through participation in community activities
The internship program offers hands-on experience in the following dat...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-25 08:31:49
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Product Safety
Job Sub Function:
Product Safety Risk Management MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Lisbon, Portugal
Job Description:
Johnson & Johnson is recruiting for a Medical Review Safety Physician Manager to be located in Lisbon, Portugal.
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
The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall Pharmacovigilance process; this includes single case signal detection activities for selected products as well as operational aspects of individual case medical review.
The Medical Review Safety Physician (MRSP) Manager has responsibility for determining the medical and scientific relevance of adverse event reports within the context of the product’s safety profile as well as other products within the same therapeutic area.
These responsibilities include spontaneous reports, clinical and non-clinical studies, literature reports and other sources of safety data.
Additionally, MRSPs participate in matrix management activities (e.g.
Safety Management Team (SMT) and provide pharmacovigilance expertise on individual case reports.
MRSPs support activities such as evaluating safety issues from various sources including Designated Medical Events (DME) and Events of Interest (EVOI), preparation of aggregate safety reports such as PBRERs/PADERs, ad-hoc regulatory reports, Risk Management Plans, and interpretation of surveillance and product quality data.
Responsibilities include, but are not limited to the following:
* Active participation in MRSP activities which include, but are not limited to:
* Analysis and assessment of Critical Cases, including SUSARs
* Detection of single case potential safety signals/ through validation
* Identification and analysis of new safety signals and trends by conducting systematic reviews of aggregate data.
* Review local literature for potential signals assessed by vendors and Local Management Safety (LMS)
* Acti...
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Type: Permanent Location: Lisbon, PT-11
Salary / Rate: Not Specified
Posted: 2025-10-25 08:31:46
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
Latina, Italy
Job Description:
A proposito di Innovative Medicine
La nostra esperienza in Innovative Medicine è ispirata dai pazienti, la cui conoscenza alimenta i nostri progressi scientifici.
I visionari come te lavorano in team che salvano vite sviluppando le cure del domani.
Unisciti a noi nello sviluppo di trattamenti, nella ricerca di cure e nel pionieristico percorso dal laboratorio alla vita, sostenendo i pazienti in ogni fase del percorso.
Per ulteriori informazioni, visitare il sito Web https://www.jnj.com/innovative-medicine
Stiamo cercando il miglior talento ne ruolo di Quality Control Technician basato a Latina.
Scopo:
L’area di Controllo Qualità ha la responsabilità di eseguire le analisi su materie prime, semilavorati e prodotti finiti al fine di assicurare farmaci con adeguati livelli di qualità al paziente, nel rispetto della sicurezza e costi di riferimento.
Per questa posizione si offre contratto a tempo determinato di 12 mesi.
La persona ricercata sarà responsabile delle seguenti attività:
* Eseguire, in accordo al proprio pacchetto training, alle procedure standardizzate ed alle direttive ricevute, tutte le operazioni necessarie per l’esecuzione di analisi chimiche e chimico-fisiche utilizzando apparecchiature e strumentazioni di laboratorio.
* Assicurare l’esecuzione di test analitici definiti dai programmi su materie prime, semilavorati, prodotti finiti, stabilità di monitoraggio, sperimentali, controlli ambientali, cleaning validation, acque di stabilimento, nei tempi richiesti e secondo elevati standard di affidabilità, valutando la conformità e la validità dei risultati.
* Utilizzare in modo autonomo, secondo i programmi standardizzati, attrezzature ed apparecchi complessi; utilizzare unità di elaborazione dati.
* Eseguire correttamente i test di laboratorio attraverso lo studio dei principi elementari di teoria applicata ed alle buone norme di laboratorio (GLP), lo sviluppo dei calcoli numerici necessari nel corso del trattamento dei dati, proponendo idee e suggerimenti frutto delle proprie osservazioni e conclusioni.
* Assicurare la registrazione di tutti i dati relativi a metodologie, osservazioni e conclusioni circa le analisi effettuate utilizzando, quando necessario, anche strumenti informatici.
Garantire...
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Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-10-25 08:31:27
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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:
Pharmaceutical Sales
Job Sub Function:
Sales – Immunology (Commission)
Job Category:
Professional
All Job Posting Locations:
Charleston, South Carolina, United States, Columbia, South Carolina, United States, Greensboro, North Carolina, United States
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Rare Disease Account Manager to be in the territory of Columbia, SC.
Purpose:
The Rare Disease Account Manager will consistently achieve or exceed sales objectives within their Local Healthcare Market (LHM).
The Rare Disease Account Manager will report to a Senior District Sales Manager.
The RAM owns the total market, developing and executing a strategy to identify patient opportunity, drive demand, and remove fulfillment barriers.
To achieve the business goals and meet customer needs, you will also ensure alignment with internal field partners, including Thought Leader Liaisons (TLLs), Area Business Specialists (ABSs), Field Reimbursement Managers (FRMs), Key Account Managers (KAMs) and Medical Science Liaisons (MSLs).
The RAM will be responsible for:
* Drive outstanding territory sales performance and product demand to ensure sales forecasts are met or exceeded within the LHM by building and sustaining strong, trusting relationships with customers and influencing key stakeholders.
* Leverage company approved marketing resources to effectively demonstrate clinical value as a solution to address identified customer and patient needs.
Leverage payer acumen to educate patients on access and affordability options.
* Analyze qualitative and quantitative market data to assess business opportunities and priorities.
* Build an LHM-specific business plan and account plans to drive growth.
* Be the quarterback of the LHM team by setting the local strategy, collaborating with cross-functional LHM field partners, driving alignment, and ensuring priorities are set appropriately.
* Collaborate within LHM to gain formulary status as nec...
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Type: Permanent Location: Columbia, US-SC
Salary / Rate: Not Specified
Posted: 2025-10-25 08:31:22
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States
Job Description:
Johnson & Johnson is hiring for a Territory Manager for Shockwave Medical Inc.
located in Cleveland, OH.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
Territory Managers are responsible for cold calling, prospecting, and building relationships that will increase account revenue growth and customer satisfaction within specified product lines and geography. Focus areas will include driving new business with responsibility for achieving sales expectations in an assigned territory while providing exceptional service and support to physicians to meet their patient’s needs. The Territory Manager is responsible for case coverage in catheter labs while working with physicians and key decision makers.
Essential Job Functions
* Develop and implement sales strategies to effectively promote Shockwave products to appropriate hospital personnel and physicians.
* Meet with a variety of physicians and other hospital personnel to determine customers’ needs, goals, product usage, and types of cases handled.
* Educate customers on products and proper clinical usage by delivering presentations and demonstrations.
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-10-25 08:31:21
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Surgeons (Commission)
Job Category:
Business Enablement/Support
All Job Posting Locations:
Gdansk, Pomorskie, Poland, Warsaw, Masovian, Poland
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
CLINICAL ACCOUNT SPECIALIST (Biosense webster)
Location: Gdańsk
Contract: full-time
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
Purpose:
The Clinical Account Specialist will be responsible for: clinical support and promoting BW products among current and potential customers; developing professional education for end-users; effective and strong collaboration with sales team members; developing the business growth on the territory.
You will be responsible for:
* Provide every day in Hospital /EP Lab/ professional clinical & technical support, troubleshooting, and training to Physicians, Electrophysiology Lab Staff, Technicians, Nurses, and administrators staff regarding all aspects of the company’s systems and catheter equipment
* Understand and know clinical environment, competitor products – continuous development of the knowledge
* Serves as a troubleshooting resource during cases.
* Tailors’ product conversations to the audience to ensure proper understanding and optimal utilization.
* Demonstrates products features to meet customers’ unmet needs
* Become fluent in main types of arrhythmias
Qualifications / Requirements:
* University degree level or equivalent experience (Scientific/Business combination would be ideal)
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-10-25 08:31:18
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Pharmacokinetics & Pharmacometrics
Job Category:
Scientific/Technology
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Scientist, Bioanalysis – Target Engagement to be onsite in Spring House, PA.
Purpose:
The Bioanalytical Discovery and Development Sciences (BDDS) organization develops, validates, and conducts bioanalytical sample analysis across the entire J&J Innovative Medicines (JJIM) R&D portfolio from discovery through development.
We are looking for an accomplished and dedicated Scientist to design and perform target engagement assays within BDDS for Johnson & Johnson portfolio projects spanning all modalities and therapeutic areas from nonclinical studies to post-market clinical development.
You will be responsible for:
* Conduct receptor occupancy method qualification and bioanalysis using multi-parameter flow cytometry of samples supporting preclinical and clinical studies to assess target engagement of therapeutics in J&J developmental pipeline.
* Work in a regulated GLP/GCLP environment under limited supervision with a high level of autonomy, encouraging a collaborative and inclusive environment.
* Promote assigned project activities through hands-on data generation, quality control (QC) and data analysis.
* Use advanced computer software packages to collect, analyze, and interpret flow cytometry data.
* Set priorities for experimental work to ensure adequate progress of team projects and objectives. Ensure laboratory efficiency as well as compliance with good laboratory practices and other regulatory guidelines.
* Author assay checklists, work instructions, standard operating procedures (SOPs), and technical reports,
* Mentor more junior colleagues in techniques, processes, and responsibilities.
* Actively participate in internal seminars...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-25 08:31:10
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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:
Wien, Austria
Job Description:
Essential Job Duties and Responsibilities
The role of a Medical Scientific Liaison (MSL) is to be a therapeutic area scientific expert, responsible for proactively or reactively discussing our products, treatment trends incl.
unmet medical needs, scientific insights, studies and projects with Leading Specialists (LS).
The MSL provides fair, balanced, objective, scientific information and education to health care professionals on a peer-to-peer basis and to internal partners, as required by scientific and business needs.
The MSL executes activities described in the country specific MAF plan / MSL activity plan.
Through strategic and key stakeholder engagement, the MSL builds and maintains external relationships with leading specialists and represents the primary MAF contact.
In addition, MSLs captures and logs external medical insights and use these insights to inform the medical affairs - and CVT strategy.
MSLs should be aware of company goals, strategy, and results at country/region level.
The MSL role has a predominantly external/field focus.
A job holder of the role of a MSL will
· demonstrate a long-term commitment for medical affairs and the role of MSL based on track record of success with consistent satisfactory performance on both the achievement of objectives as well as the attitude and behaviours demonstrated
· establish and effectively cultivate a solid long term network of LS within the therapeutic area (as measured by corresponding KPIs) and is genuinely recognized by these leading specialists as a trusted counterpart and a collaborative partner
· be able to quickly obtain insights and identify emerging scientific concepts and its potential future clinical implications
· have an extensive medical and scientific product and disease knowledge within the therapeutic area
· demonstrate strategic capabilities to translate the medical affairs strategy into and impactful region/country specific tactics
· have the ability to identify and act upon new strategic opportunities in the healthcare landscape, lead multiple projects independently and pro-actively create, lead and execute stakeholder plans in collaboration with internal partner...
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Type: Permanent Location: Wien, AT-9
Salary / Rate: Not Specified
Posted: 2025-10-25 08:30:56
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium, Spring House, Pennsylvania, United States of America, Toledo, Spain
Job Description:
Intelligent Automation refers to the bidirectional coupling between automated lab equipment and Artificial Intelligence (AI).
Through successive iterations, such closed-feedback loop systems facilitate the AI-driven design, execution and analysis of experiments and utilize a wealth of in silico methodologies.
Within the Drug Discovery Data Sciences organization of Johnson & Johnson Innovative Medicine we have an open position for a Senior/Principal Data Scientist that will join the Intelligent Automation efforts for Small Molecule discovery.
To do so, the new member will collaborate within interdisciplinary teams comprising biologists, medicinal chemists, data scientists, computational chemists and IT experts across all therapeutic areas.
Role and responsibilities
· Contribute to the development of intelligent automation platforms, integrating AI/ML suites with wet lab equipment.
· Be part of team of data scientists, aiming on the development and deployment of appropriate AI/ML methods and continuous improvement upon existing solutions.
· Work closely with IT and LabOps to implement solutions in real world conditions.
· Communicate results in audiences with heterogeneous background.
Requirements
· A PhD in a relevant field that reflects expertise with Active Learning & Bayesian optimization.
· Proven experience with Deep Learning architectures and uncertainty quantification frameworks.
· Affinity with multi-parametric optimization methods.
· Knowledge of Small Molecule Drug Discovery (for Principal Scientist).
· Strong knowledge of Python development and affinity with cloud infrastructure.
· Good interpersonal, organizational and communication skills.
· Motivation to be part of a team that celebrates diversity and offers an inclusive working environment where creativity and innovation can thrive.
#JNJDataScience
The anticipated base pay range for this position is :
146.200 USD - 197.800
Additional Description for Pay Transparency:
Subject to the terms of...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-25 08:30:54
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
San Diego, California, United States of America, Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Field Clinical Specialist - Shockwave Medical to join our team located in San Diego, California.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Field Clinical Specialist is a visible position that will provide case support to physicians within certain territories. Case support will be done on peripheral and coronary interventional procedures in the pre-market and post-market phases of product development with the Shockwave Medical Intravascular Lithotripsy (IVL) ® technology.
The Field Clinical Specialist will also play a critical role in clinical studies including device training, case support and ensuring timely data collection for clinical programs. Case support may be required to support other territories at certain times.
Essential Job Functions
* Physician and hospital staff training, and procedural case coverage to ensure the safe and effective use of medical devices.
* Effectively meet the needs of internal and external customers with a sense of urgency and drive.
* Present clinical stud...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-25 08:30:42
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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:
Procurement
Job Sub Function:
Category
Job Category:
Professional
All Job Posting Locations:
Bangalore, Karnataka, India
Job Description:
Job title: Accountant 1, Global Intercompany
Function: Finance
Sub function: Accounting
Work pattern: Hybrid Work
Description
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity.
Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Bangalore, India
Job Description:
“Reimagine the possibilities” at Johnson and Johnson Global Finance! We live this motto every day by crafting exciting business solutions for the world’s largest and most healthcare company.
As a member of our Global Finance team, you will have outstanding access to a network of financial professionals located in over 60 countries.
This new network will help you build on your skills and explore opportunities to grow your career in J&J.
Key Responsibilities:
Be compliant with applicable laws and regulations and follow guidelines in the J&J Credo Maintain Operational Perfection.
* Responsible for implementing accounting and daily operations for Intercompany Accounting process area for sophisticated MRCs.
* Timely closing & execution of financial periods as per closing calendar and in accordance with SLA commitments, fully observing Compliance, Internal Audit & SOX requirements.
* Accountable for completeness, accuracy and validity of the actuals reported within process/entity scope.
* Deep expertise, fully knowledgeable of the Worldwide Procedures and compliance requirements for respective areas.
* Regular focus on Balance Sheet reconciliations to minimize open items.
* On the job training for new team members / BPO partners.
* Support auditors and legal authorities with the execution of required activities.
* Understand, enforce, and implement per worldwide policies and procedures.
Identify compliance risks and recommend s...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2025-10-25 08:30:40
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
As a member of our Global Finance team, you will have exclusive access to a network of financial professionals located in over 60 countries.
This new network will help you build on your current skills and explore opportunities to grow your career in J&J.
At J&J Global Finance, we value ideas for innovation and improvement and are committed to diversity and inclusion.
Together we will reimagine business processes to become more effective, more efficient, and improve customer experience.
We are proud to be an equal opportunity employer.
This role will be part of the Global Services Finance team in the Account to Report.
The Global Services Finance organization provides best-in-class, cost-effective financial services, and compliance—in a J&J way—to our Operating Companies around the world.
* Contributes with the establishment and implementation of cost-effective, results-based, and profesionally-managed programs and innovative initiatives for the accounting area, under direct supervision.
* Assists with less complex components of projects, programs, or processes for the accounting area in compliance with GAAP (Generally Accepted Accounting Principles) and applicable governance policies
* Performs simple trend analysis to support continuous improvement efforts for the organization's accounting strategy.
* Participates in the completion of internal and external audit, and ad hoc requests.
* Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
Key Responsibilities:
* Responsible for implementing accounting and daily operations for Intercompany Accounting process area for sophisticated MRCs.
* Timely closing & execution of financial periods as per closing calendar and in accordance with SLA commitments, fully observing Compliance, Internal Audit & SOX requirements.
* Accountable for completeness, accuracy and validity of the actuals reported within process/entity scope.
* Deep expertise, fully knowledgeable of the Worldwide Procedures and compliance requirements for respective areas.
* Regular focus on Balance Sheet reconciliations to minimize open items.
* On the job training for new team members
* Support au...
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-10-25 08:30:38
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
People Leader
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Are you ready to make a difference?
At Johnson & Johnson, we are committed to addressing and solving some of the most meaningful unmet medical needs through creating an environment where our employees feel valued and can reach their potential.
This commitment is embedded in our Credo!
Role Overview:
The Manager, Analytical Monitoring Leader is a strategic and operational leader responsible for driving analytical monitoring activities across clinical development and innovation programs.
This role requires deep expertise in Site Monitoring, Central Monitoring, Data Management, and Analytical Risk-Based Monitoring (ARBM), along with strong leadership, stakeholder engagement, and people management capabilities!
You will lead the planning, execution, and delivery of analytical monitoring strategies, ensuring compliance, quality, and efficiency.
You’ll also play a key role in shaping the function’s growth, innovation, and capability development, while fostering a diverse and inclusive team culture.
Key Responsibilities:
Strategic & Operational Leadership
* Lead analytical monitoring strategy and execution across assigned programs.
* Ensure timely delivery of monitoring activities aligned with regulatory and quality standards.
* Drive continuous improvement in processes, tools, and methodologies.
Stakeholder Engagement
* Represent Analytical Monitoring in cross-functional forums (GCO, IDAR, GD, JJIM).
Influence strategic decisions and collaborate with internal and external stakeholders.
* Serve as primary point of contact for regional/TA/program-level monitoring activities.
Risk & Issue Management
* Proactively identify, assess, and mitigate risks impacting delivery.
* Manage escalations and ensure resolution through appropriate channels and maintain inspection readiness and support audits and CAPA processes.
People & Team Leadership
* Lead, mentor, and develop a team of Analytical Monitors while overseeing recruitment, onboarding, performance management, and career development.
* Promote a culture of inclusion, innovation, and accountability.
Process & Compliance
* Ensure adherence to SOPs, policies, and regulatory guidelines (e.g., ICH-...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-10-25 08:30:33
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
People Leader
All Job Posting Locations:
Mexico City, Mexico
Job Description:
REGULATORY COMPLIANCE
▪ Ensure implementation and compliance with global, regional and local procedural documents applicable to Pharmacovigilance.
Accountable internally for ensuring that the LOC meets procedure defined timelines for management of safety information and any local regulatory agency defined timeline for submission of individual reports.
▪ Oversight responsibilities of case processing operational activities delegated to the Center of Excellence Case Processing hub for Latin America or external vendor as appropriate.
Case processing activities include but not limited to Inbound reporting, outbound reporting, translation of AEs/Special Reporting Situations/PQCs, literature search, due diligence.
▪ Accountable for compliance monitoring for submissions to Competent Authorities (HAs).
Reconcile compliance data provided and take appropriate corrective actions as defined by company policies and procedures.
▪ Ensure awareness of changes in regulations which may have an impact on PV activities and responsibilities.
Inform the appropriate global and regional groups (i.e.
QPPV office and regional heads) of any changes to local laws and regulations regarding Pharmacovigilance
▪ Oversight of timely elaboration and submission of all documents required by local PV legislation.
PV SYSTEMS COMPLIANCE
▪ Oversight of timely and appropriate communication & follow up of the activities related with Global Clinical Operations (GCO & GCO MAO) to comply with PV local regulations regarding clinical trials conducted in the territory as applicable, including those carried out by third parties, as per the contracts & agreements.
▪ Oversight of timely and appropriate Development of Local Implementation Memos (LIM) for Regional / PV Standard Operating Procedures/Working Practices and verify adherence.
▪ Managing and scheduling of the preparation of necessary outlines, status reports, graphs, charts, tables, and slides for periodic reviews for the Pharmacovigilance specialists.
▪ Monitor data generating activities to ensure any solicitation for information includes an appropriate review and reporting process for reporting potential AEs (e.g.
patient support programs, market research studies, marketing activities, internet sites, surveys, etc.), as applic...
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Type: Permanent Location: Mexico City, MX-CMX
Salary / Rate: Not Specified
Posted: 2025-10-25 08:30:31
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Primary Care Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Shijiazhuang, Hebei, China
Job Description:
工作职责：
* 利用专业的电生理知识和技能，为术者提供手术支持，确保手术安全顺利进行；
* 熟悉客户手术习惯，与术者高效沟通，不断精进专业技能，在区域独立完成从简单到复杂的心律失常手术支持
* 紧跟行业和公司发展趋势，主动学习和掌握行业内新理念、新技术，新产品的优势和使用，能够制定针对性、可拆解的推广沟通方案
* 熟练使用新产品、数字化等新工具以及新技术，协助专业教育团队提升术者理念，技能和信心
* 有效传递新产品、新技术的价值，不断提升客户对于新技术的接受度，以安全高效的方式开展手术，服务病患
* 承担团队内教学带教工作，与团队共同进步，通过理论授课、模拟器练习、术中导管室带教、病历复盘等，有效提升新同事/初阶同事的知识和手术支持能力
* 严格遵守公司的合规政策，完成上级交予的其他任务
* 接受一定程度出差
能力要求：
* 具有自驱力，不断精进专业水平，积极学习业内不断发布涌现的新产品、新技术知识，并进行应用；
* 乐于沟通协作，与团队共同进步，共同承担团队目标，互相协助
* 有坚韧不拔的精神，遇到困难不轻易放弃，
* 有创新思维，积极探索方案并解决问题
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Type: Permanent Location: Shijiazhuang, CN-13
Salary / Rate: Not Specified
Posted: 2025-10-25 08:30:15
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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
Shape the future with us – as a Manager Technical Study Coordination (m/f/d)
In the Research & Development department, as a Manager Technical Study Coordination (f/m/d), you will support our organization with your broad expertise at the interface between the development and clinical testing of medical devices.
Your ability to think abstractly and your profound understanding of the development and approval processes enable you to plan and manage technical documentation adapted to different development stages.
Your Tasks
As part of our team, your responsibilities will include the following:
* You contribute to developing a project-specific strategy for the planning, execution, and objectives of studies.
* You oversee and support the creation of high-quality, fit-for-purpose documentation that accompanies development and is relevant for submissions.
* You identify (study) approval-relevant questions and mediate between various stakeholders.
* You shape the practical and pragmatic application of relevant regulations and standards in the area of technical documentation necessary for study approvals.
* You coordinate the collaboration of cross-functional teams on these topics.
* You either define requirements in specification documents yourself or support others in doing so.
* You look for potential for improvement in established processes and try to implement it on a case-by-case basis.
What you bring to the table
* You have successfully completed your Bachelor's or Master's degree in a scientific or technical field, ideally with a relevant specialization (medical device technology).
* Your several years of professional experience enable you to work independently in an international environment.
* You have experience in the interpretation and practical implementation of regulations and standards relevant to medical device development, preferably the MDR/IVDR.
* You have expertise in the development and approval of medical devices across several functional areas (documentation, risk management, quality engineering, regulatory affairs, etc.).
* You have successfully supported development-accompanying studies from the development side.
* You enjoy direct and indirect exchange with partners relevant to clinical studies, such as regulatory authorities, notified bodies, and ethics committees.
* You successfully moderate cross-functional teams and achieve consensual decisions even on complex issues with far-re...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-10-25 08:29:59
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ERM is seeking a self-starting Consultant, Environmental Permitting Specialist, FERC Generalist to join our consulting firm. This role can be based anywhere in the United States.
As part of our team, you will provide high-quality analytical support to ERM clients while working closely with other team members.
Assignments will be a mix of field and desktop work focused on but not limited to, impact assessment and permitting for new energy projects (e.g., natural gas pipelines, Liquified Natural Gas terminals, renewables, transmission lines, etc.).
This is an excellent opportunity for a professional looking to advance their career with a global sustainability leader.
RESPONSIBILITIES:
* Prepare permit applications where required by federal, state or local environmental regulatory authorities for energy/industrial facility development, expansion, maintenance, or decommissioning.
* Evaluate regulatory requirements.
* Maintain records and survey reports.
* Assist with the preparation of technical project documents, including, but not limited to: writing, word processing, building tables and spreadsheets, tabulating and manipulating data, producing hard copy documents, completing air and erosion control engineering calculations commensurate with the candidate’s background.
* Assist with the development of project plans and schedules; and assist with the development of project management reporting, such as monthly progress reports.
* Communicate with clients, including requesting project information, answering regulatory questions, and providing recommendations.
REQUIREMENTS:
* Bachelor’s degree in a natural science or engineering field of study; or equivalent experience.
* 2+ years of applicable work and/or internship experience.
* Experience with the Federal Energy Regulatory Commission (FERC) is a plus
* Up to 40% travel.
* Strong working knowledge of MS Office Suite software.
* Experience conducting desktop and online studies or research on a wide variety of natural resource or resource planning topics, Geographic Information System, map interpretation (National Wetland Inventory, U.S.
Geological Survey, aerial photography).
* Ability to work effectively in the field during cold and hot weather conditions.
* Ability to navigate in the field using Global Position System, maps and aerial photographs.
* Demonstrated ability to prepare concise and accurate technical documents and reports.
* Excellent interpersonal communication skills, which includes being comfortable and effective at communicating technical knowledge and concepts to other staff, clients, regulatory agencies, and project stakeholders.
* Strong commitment to safety, including following established Health & Safety protocols.
* Ability to multi-task, maintains flexibility, and works independently with minimal supervision.
* Driver's License Required: This position requires a valid ...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-10-25 08:28:41
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ERM is hiring a Construction Safety Specialist onsite at a key technology clients Data Center construction project in Burlington, Texas.
In this critical role, you will be responsible for establishing, implementing, managing, and continuously improving the safety programs.
The Construction Safety Specialist will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a full-time (40 hours a week), limited-term role for a duration of 12 months, extendable.
RESPONSIBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Provide timely, high quality safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans.
* Prepare and submit local, state, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze safety performance and initiate action to support or correct trends.
* Coordinate local business continuity, emergency response, and crisis management plans.
Develop and test the plans.
REQUIREMENTS:
* A bachelor’s degree in safety, occupational health, engineering, or a related field is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, 2 years of data center construction project experience preferred.
CHST/CSP certification is a plus.
* Proficient with the management of high-risk activities, including electrical safety, excavation, fall protection, material handling, and crane operations.
* Experience in communicating and problem-solving as a team with subcontractors is required.
* A background and knowledge working with specific trades such as electricians, ironworkers, pipefitters, etc.
is a plus.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for f...
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-10-25 08:28:17
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ERM is hiring a Health & Safety Specialist to support an aerospace client facility in Redmond, WA.
In this critical role, you will be responsible for ensuring safety compliance with applicable regulations and existing company standards and contributing to an environment where employee health and safety is paramount.
This is a third shift, full-time (40 hours), limited-term role with a duration of 12 months and the possibility of renewal.
RESPONSIBILITIES:
* Providing health and safety oversight for an aerospace manufacturing facility.
* Oversee general safety and risk programs in an aerospace manufacturing environment – machine safety, LOTO, electrical safety, PPE, fall protection, confined space, etc...
* Communicating with internal stakeholders.
* Developing, reviewing, and/or updating health and safety documentation such as SOPs, JHAs, and safety plans.
* Conduct inspections and audits.
* Participating in the Emergency Response Team.
* Conduct safety training.
* Participate in incident investigation, root cause analysis, and report writing.
* Participating/leading meetings to support ongoing compliance and safety initiatives.
* Writing and submitting status update reports, and other communications.
REQUIREMENTS:
* Bachelor’s in safety or related discipline preferred.
* 3+ years of health and safety experience in a manufacturing environment, aerospace experience preferred.
* Certification such as ASP/CSP highly preferred.
* Experience with High Hazard Work Activity, Confined Space, LOTO, Machine Guarding, and Fall Protection.
* Familiarity with federal/state health and safety regulations.
* Strong MS Office computer skills.
* Excellent written and verbal communication skills.
For the Health & Safety Specialist position, we anticipate the annual base pay of $80,691 – $97,410, $38.79/hr – $46.83/hr, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/FlexForce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including FlexForce) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible.
See your recruiter for more details.
...
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Type: Permanent Location: Seattle, US-WA
Salary / Rate: Not Specified
Posted: 2025-10-25 08:28:12
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ERM is hiring an on-site Construction Safety Specialist for a key client in Grand Rapids, MI.
The Construction Safety Specialist will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a part-time (20 hours per week), fixed-term position for a duration of 2 months, extendable.
RESPONSIBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in safety-related activities.
* Act as the Owner’s representative while interacting with contractors.
* Provide daily observations of on-site safety practices
* Provide timely, high-quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze Safety performance and initiate action to support or correct trends.
REQUIREMENTS:
* A bachelor’s degree in safety, occupational health, engineering, or a related field is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, preferably with commercial/office building construction or large projects.
CHST certification is a plus.
* Proficient with the management of high-risk activities, including electrical safety, excavation, confined spaces, fall protection, material handling, and rigging
* Experience in communicating and problem-solving as a team with subcontractors is required.
* A background and knowledge working with specific trades such as electricians, ironworkers, pipefitters, etc.
is a plus.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that help...
....Read more...
Type: Contract Location: Holland, US-MI
Salary / Rate: Not Specified
Posted: 2025-10-25 08:28:12
