-
$56,925 - 65,463.75 /Yr.
Schedule: Monday - Friday; 8:00 am - 4:30 pm
Location: Rogers Park
The Care Coordinator will work directly with contracted MCOs to locate, engage, assess, and connect members to essential healthcare and supportive services.
This includes assisting clients with Medicaid and SNAP applications, SOAR/SSA applications, nursing home referrals through Maximus, homemaker services, and other care coordination needs.
As the first point of contact for many clients, the Care Coordinator will collaborate closely with teams through out the agency to provide responsive, in-person support and follow-through on client referrals.
This position plays a key role in monitoring and reporting metrics and outcomes, while ensuring care coordination standards are upheld across departments and programs within the organization.
The Care Coordinator will deliver and support services that are client-centered, strengths-based, trauma-informed, and guided by a harm reduction approach—particularly for individuals with severe mental illness and co-occurring substance use disorders.
Responsibilities
* Liaison between Trilogy and MCOs to locate members disconnected with MCOs and treatment.
Engage, assess, and connect them to necessary health care (e.g.
review of claims if available)
* Prioritize clients in potential need of community-based care coordination with MCOs
* Conduct health assessments related to member’s personal, medical, emotional, social, and environmental situation and make referrals to appropriate levels of care.
* Contact identified members to provide education on programs that will address their healthcare needs and linking them to needed community services.
Engage members in discussion of adherence to personal health plans.
* Organize and direct care coordination efforts across departments and programs
* Assist clients with homemaker referrals, DON scores, Medicaid redeterminations, Medicaid and SNAP applications, SSA/SOAR applications, and make referrals for nursing home placement.
* Successfully complete SOAR Certification and provide SOAR support in SSA applications for disability across the agency.
* Connect clients to resources in the community related to their social determinants of health needs and support with entitlement applications and navigation as needed.
* Develop and maintain positive working relationships with partner organizations in Trilogy’s Prime, MCO’s, IHPA, and IHH
* Meet deliverables based on MCO care coordination contracts and complete required reporting.
* Attend inter-department team meetings as needed to gather information for care coordination purposes and ensure high quality service for clients
* Develop, implement, and track HEDIS measures across the organization.
* Maintain prior authorization, documentation, and ensure charting is in compliance with MCOs, Medicaid, state specific accreditation, and organization standards.
...
....Read more...
Type: Permanent Location: Chicago, US-IL
Salary / Rate: Not Specified
Posted: 2025-11-27 07:27:14
-
Werde Paketverteilkraft für Pakete in Darmstadt
Was wir bieten
* 15,63 € Tarif-Stundenlohn (16,24 € inkl.
50% Weihnachtsgeld)
* Du kannst bei uns sofort starten
* Ein krisensicherer Arbeitsplatz, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Ausführliche Einweisung (bezahlt) – wir machen dich fit für deine Tätigkeit
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Standortleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote wie z.B.
arbeitgeberfinanzierte betriebliche Altersvorsorge, Fahrradleasing, Rabatte bei Mobilfunkanbietern, etc.
Deine Aufgaben als Paketverteilkraft bei uns
* Ausladen von Roll-Containern oder lose verladenen Paketen
* Heben von Lasten bis maximal 31,5 kg (im Durchschnitt unter 10 kg)
* Sortieren von Paketen für die Zustellung
* platzsparendes Stapeln der Pakete zur optimalen Auslastung der Transportkapazität
* Beachtung von Vorschriften zur Ladungssicherung
Was du als Paketverteilkraft bietest
* Du kannst anpacken und bist körperlich fit
* Du hast vormittags im Zeitraum von 06:00-10:00 Uhr Zeit? Dienstag bis Samstag, 16 Stunden die Woche.
* Du arbeitest zuverlässig, hängst dich rein und bist flexibel
* Du arbeitest gern im Team
* Du kannst dich auf Deutsch unterhalten
* Du bist mindestens 18 Jahre alt
Werde Paketverteilskraft bei Deutsche Post DHL
Wir freuen uns auf deine Bewerbung, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#jobsnlwiesbaden
....Read more...
Type: Contract Location: Darmstadt, DE-HE
Salary / Rate: Not Specified
Posted: 2025-11-27 07:27:06
-
Werde Paketverteilkraft für Pakete in Büttelborn / Groß-Gerau
Was wir bieten
* 15,63 € Tarif-Stundenlohn (16,24 € inkl.
50% Weihnachtsgeld)
* Du kannst bei uns sofort starten
* Ein krisensicherer Arbeitsplatz, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Ausführliche Einweisung (bezahlt) – wir machen dich fit für deine Tätigkeit
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Standortleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote wie z.B.
arbeitgeberfinanzierte betriebliche Altersvorsorge, Fahrradleasing, Rabatte bei Mobilfunkanbietern, etc.
Deine Aufgaben als Paketverteilkraft bei uns
* Ausladen von Roll-Containern oder lose verladenen Paketen
* Heben von Lasten bis maximal 31,5 kg (im Durchschnitt unter 10 kg)
* Sortieren von Paketen für die Zustellung
* platzsparendes Stapeln der Pakete zur optimalen Auslastung der Transportkapazität
* Beachtung von Vorschriften zur Ladungssicherung
Was du als Paketverteilkraft bietest
* Du kannst anpacken und bist körperlich fit
* Du hast vormittags im Zeitraum von 06:00-10:00 Uhr Zeit? Dienstag bis Samstag, 16 Stunden die Woche.
* Du arbeitest zuverlässig, hängst dich rein und bist flexibel
* Du arbeitest gern im Team
* Du kannst dich auf Deutsch unterhalten
* Du bist mindestens 18 Jahre alt
Werde Paketverteilskraft bei Deutsche Post DHL
Wir freuen uns auf deine Bewerbung, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#jobsnlwiesbaden
....Read more...
Type: Contract Location: Büttelborn, DE-HE
Salary / Rate: Not Specified
Posted: 2025-11-27 07:26:52
-
Werde Paketverteilkraft für Pakete in Hochheim
Was wir bieten
* 15,63 € Tarif-Stundenlohn (16,24 € inkl.
50% Weihnachtsgeld)
* Du kannst bei uns sofort starten
* Ein krisensicherer Arbeitsplatz, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Ausführliche Einweisung (bezahlt) – wir machen dich fit für deine Tätigkeit
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Standortleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote wie z.B.
arbeitgeberfinanzierte betriebliche Altersvorsorge, Fahrradleasing, Rabatte bei Mobilfunkanbietern, etc.
Deine Aufgaben als Paketverteilkraft bei uns
* Ausladen von Roll-Containern oder lose verladenen Paketen
* Heben von Lasten bis maximal 31,5 kg (im Durchschnitt unter 10 kg)
* Sortieren von Paketen für die Zustellung
* platzsparendes Stapeln der Pakete zur optimalen Auslastung der Transportkapazität
* Beachtung von Vorschriften zur Ladungssicherung
Was du als Paketverteilkraft bietest
* Du kannst anpacken und bist körperlich fit
* Du hast vormittags im Zeitraum von 06:00-10:00 Uhr Zeit? Dienstag bis Samstag, 15 Stunden die Woche.
* Du arbeitest zuverlässig, hängst dich rein und bist flexibel
* Du arbeitest gern im Team
* Du kannst dich auf Deutsch unterhalten
* Du bist mindestens 18 Jahre alt
Werde Paketverteilskraft bei Deutsche Post DHL
Wir freuen uns auf deine Bewerbung, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#jobsnlwiesbaden
....Read more...
Type: Contract Location: Hochheim am Main, DE-HE
Salary / Rate: Not Specified
Posted: 2025-11-27 07:26:47
-
Werde Paketverteilkraft für Pakete in Pfungstadt
Was wir bieten
* 15,63 € Tarif-Stundenlohn (16,24 € inkl.
50% Weihnachtsgeld)
* Du kannst bei uns sofort starten
* Ein krisensicherer Arbeitsplatz, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Ausführliche Einweisung (bezahlt) – wir machen dich fit für deine Tätigkeit
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Standortleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote wie z.B.
arbeitgeberfinanzierte betriebliche Altersvorsorge, Fahrradleasing, Rabatte bei Mobilfunkanbietern, etc.
Deine Aufgaben als Paketverteilkraft bei uns
* Ausladen von Roll-Containern oder lose verladenen Paketen
* Heben von Lasten bis maximal 31,5 kg (im Durchschnitt unter 10 kg)
* Sortieren von Paketen für die Zustellung
* platzsparendes Stapeln der Pakete zur optimalen Auslastung der Transportkapazität
* Beachtung von Vorschriften zur Ladungssicherung
Was du als Paketverteilkraft bietest
* Du kannst anpacken und bist körperlich fit
* Du hast vormittags im Zeitraum von 06:00-10:00 Uhr Zeit? Dienstag bis Samstag, 15 Stunden die Woche.
* Du arbeitest zuverlässig, hängst dich rein und bist flexibel
* Du arbeitest gern im Team
* Du kannst dich auf Deutsch unterhalten
* Du bist mindestens 18 Jahre alt
Werde Paketverteilskraft bei Deutsche Post DHL
Wir freuen uns auf deine Bewerbung, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#jobsnlwiesbaden
....Read more...
Type: Contract Location: Pfungstadt, DE-HE
Salary / Rate: Not Specified
Posted: 2025-11-27 07:26:34
-
Werde Paketverteilkraft für Pakete in Heppenheim
Was wir bieten
* 15,63 € Tarif-Stundenlohn (16,24 € inkl.
50% Weihnachtsgeld)
* Du kannst bei uns sofort starten
* Ein krisensicherer Arbeitsplatz, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Ausführliche Einweisung (bezahlt) – wir machen dich fit für deine Tätigkeit
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Standortleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote wie z.B.
arbeitgeberfinanzierte betriebliche Altersvorsorge, Fahrradleasing, Rabatte bei Mobilfunkanbietern, etc.
Deine Aufgaben als Paketverteilkraft bei uns
* Ausladen von Roll-Containern oder lose verladenen Paketen
* Heben von Lasten bis maximal 31,5 kg (im Durchschnitt unter 10 kg)
* Sortieren von Paketen für die Zustellung
* platzsparendes Stapeln der Pakete zur optimalen Auslastung der Transportkapazität
* Beachtung von Vorschriften zur Ladungssicherung
Was du als Paketverteilkraft bietest
* Du kannst anpacken und bist körperlich fit
* Du hast vormittags im Zeitraum von 06:00-10:00 Uhr Zeit? Dienstag bis Samstag, 15 Stunden die Woche.
* Du arbeitest zuverlässig, hängst dich rein und bist flexibel
* Du arbeitest gern im Team
* Du kannst dich auf Deutsch unterhalten
* Du bist mindestens 18 Jahre alt
Werde Paketverteilskraft bei Deutsche Post DHL
Wir freuen uns auf deine Bewerbung, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#jobsnlwiesbaden
....Read more...
Type: Contract Location: Heppenheim an der Bergstrasse, DE-HE
Salary / Rate: Not Specified
Posted: 2025-11-27 07:26:27
-
IKEA Peterborough, Customer Distribution Centre are looking to welcome a People and Culture Manager.
Our team of over 1200 coworkers perform in a high volume, fast paced and agile environment to secure stock availability in our multi-channel market.
We are looking to recruit a People and Culture manager who is motivated to lead with purpose, who will shape and develop our people strategy with a business perspective.
WHAT WE OFFER
• The Start Date of employment will be: January 2027
• Starting salary from £45,000 per annum, based on competence and experience.
• 39 Hours working 5 days per week includes weekends and late nights.
• We can discuss flexibility to match your life and our business needs during the interview.
WORKING WITH US HAS ITS REWARDS
Our co-workers bring unique ideas and talent to work every day, and we offer a variety of benefits that suit their and their family's everyday needs.
• 15% IKEA discount & discount portal helping you save £100’s on High-street retailers.
• Life Assurance of 4 times your pay, enhanced statutory pension contributions & interest-free loans.
• First Day Of School Paid Leave for Parents.
• Enhanced Parental Leave.
..as well, so much more!
WHAT YOU'LL NEED TO HAVE
• Value & culture driven leadership experience, senior functional experience would be beneficial.
• Relevant experience in People and Culture within the distribution, retail or a related high-volume sector is beneficial but not essential.
• Relevant University degree is beneficial but not essential.
• Able to build positive relationships and create a culture where everyone feels valued.
• Experience of the following is beneficial:
- Strategy development and stakeholder relations
- Performance Management
- HR Issue Resolution and Policy Management
- Business Model Guidance
• Proven ability to prioritise and organise your workload to make the most efficient use of available time and meet agreed goals and deadlines.
• Confidence to express ideas and opinions effectively through clear communication to influence and build effective relationships across all levels.
• You have effective problem-solving and decision-making abilities, particularly when faced with operational challenges.
WHAT YOU'LL BE DOING DAY TO DAY
As part of the unit senior management group you will:
• Guide and implement operational requirements, collaborating with stakeholders to support the implementation of the full range of People and Culture (P&C) strategy, solutions and activities.
• Lead and coach the P&C Business Partners and Coordinators within the unit to provide support to the business and to build succession planning within the country.
• Identify, evaluate and monitor actual and potential labour issues evolving internally or externally that could create significant risks for IKEA.
• Su...
....Read more...
Type: Permanent Location: Peterborough, GB-CAM
Salary / Rate: Not Specified
Posted: 2025-11-27 07:25:37
-
• SMÅRT für deine Karriere: In deiner 3-jährigen Ausbildung bekommst du einen umfassenden Einblick, wie die Warenströme bei IKEA gesteuert werden – vom Lieferanten bis ins Verkaufsfach.
Dafür erlernst du ganz praktische Fähigkeiten, wie z.
B.
das Staplerfahren, aber auch das Verständnis dafür, wie unsere Logistik von Computersystemen gesteuert wird
• Du lernst, wie die zahlreichen Abläufe ineinandergreifen – von der Warenbestellung über das Entladen der LKWs bis hin zur Überprüfung der Lieferungen
• Du lernst Ziele gut organisiert zu erreichen
• Du lernst unseren Parcel Bereich kennen, wo Pakete verpackt und österreichweit verschickt werden.
• Du lernst die Kunst, Warenflüsse clever zu planen und zu optimieren
Wann planen wir deine Arbeitszeiten?
Montag-Donnerstag: 7:00-16:00 Uhr
Freitags: 7:00-14:00 Uhr
Und das ist nur der Start! Bei IKEA hast du die Möglichkeit, nach deiner Lehre in verschiedenen Bereichen zu arbeiten und Karriere zu machen: Ob Küchen oder Restaurant Manager:in, als Teamleiter:in oder in der Administration: es gibt viele Möglichkeiten, dich bei IKEA zu entwickeln.
• Du freust dich darauf, Neues zu lernen
• Du bist ein:e Teamplayer:in und deine Kolleg:innen können sich jederzeit auf dich verlassen
• Du packst in der Arbeit gerne richtig mit an - und das auch frühmorgens
• Du hast Spaß dabei, Dinge zu analysieren und arbeitest gerne mit dem Computer
SMÅRT für dein Konto: Bei IKEA zahlen wir über dem geltenden Kollektivvertrag.
Das heißt, du bekommst
• im 1.
Lehrjahr € 1.190,-
• im 2.
Lehrjahr € 1.310,-
• im 3.
Lehrjahr € 1.570,-
• und im 4.
Lehrjahr € 1.680 Lehrlingseinkommen.
Auf folgende Vorteile kannst du dich bei uns freuen:
• Gratis Essen für Lehrlinge im Mitarbeiter:innen Restaurant
• Nationale Lehrlingstage
• Prämien für sehr gute und gute Schulleistungen
• In- und Auslandspraktika bei guter Leistung
SMÅRT für deine Träume: weitere Vorteile bei IKEA
• 15% Rabatt für Mitarbeiter:innen
• IKEA Bonus, wenn wir unsere Jahresziele erreichen
• Egal ob Mode, Technik oder Reisen: exklusive Angebote bei unterschiedlichen
Marken und Anbietern auf dem Shopping- Portal „Corporate Benefits“
• Vergünstige Tarife für Mobilfunk, mobiles Internet, Festnetz-Internet und TV
• Mental Health ist uns wichtig! Externe Beratung in verschiedenen
Lebenssituationen und in Krisensituationen (kostenlos und anonym).
Für dich und
bei dir im Haushalt lebende Personen
Und mehr.
SMÅRT GANZ DU SELBST: WIR GLAUBEN AN KARRIERE OHNE BARRIERE
In Schubladen denken wir nur, wenn es um Kommoden geht.
Deshalb setzen wir auf die Förderung von Geschlechtergerechtigkeit, einen bunten Mix aus Generationen, die Inklusion von Personen mit Behinderungen und einen offenen Umgang mit Religion, Glaube und Weltanschauung.
Mehr zu Lehrstellen bei IKEA findest du unter:
....Read more...
Type: Permanent Location: Wels, AT-4
Salary / Rate: Not Specified
Posted: 2025-11-27 07:24:31
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Irvine, California, United States of America, Remote (US)
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
We are searching for the best talent for a Senior Clinical Research Specialist to support our Mentor business. The preferred location for this role is within a commutable distance of Irvine, CA however remote options within the US may be considered on a case by case basis. The role may also require up to 25% travel depending on the phase of the program.
Purpose: This Senior Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.
You will be responsible for:
* Serves as a Senior Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for operating company.
* Oversees/executes feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures.
* May serve as the primary contact for clinical trial sites (e.g.
site management).
* Contributes towards development of clinical trial documents (e.g.
study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports,etc.).
* Supports applicable trial registration (e.g.
www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed.
* Manages and oversees ordering, tracking, and accountability of investigational devices and trial materials.
* Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel.
* Interfaces, collaborates, and oversees Clinical Research Associates (CRAs).
* Oversees and supports the development and execution of Investigator agreements and trial payments.
* Is...
....Read more...
Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-11-27 07:24:12
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Beijing, China
Job Description:
Location: AP-wide (candidates across Asia-Pacific)
POSITION OVERVIEW:
The Senior Manager APAC Regulatory Leader is a member of the Global Regulatory Affairs organization.
The position resides in the AP Region and is responsible for working with local regulatory affairs departments, AP regional cross-functional teams, Global Regulatory Teams and other global functions to define and implement the regional strategy for assigned neuroscience products.
The position is accountable for leading and providing region or country strategic input into the global regulatory strategy and identifying regional requirements to optimize registration, and lifecycle management of marketed products, taking into consideration current and proposed changes in regulatory requirements and standards.
This position provides strategic regulatory support to all affiliates in the AP region for the J&J Innovative Medicine business. Markets in scope of responsibility are: China, Japan, South Korea, Taiwan, Hong Kong, Australia, New Zealand, South East Asia and India. As the position is also a core member of the AP regional cross functional team, there is also.
CORE RESPONSIBILITY:
· As a core member of the AP regional cross functional team, you will be leading the regulatory strategy and execution for pharmaceutical assets across the Asia-Pacific region, ensuring timely registrations, lifecycle management, and ongoing compliance.
You will partner with global/regional teams to translate development progress into region-specific strategic regulatory plans and deliverables.
WHAT YOU’LL DO:
· Define and drive end-to-end regulatory strategy for AP markets, aligning with global, regional and local objectives.
· Lead AP product registrations, including input into the preparation, compilation, and management of CMC and Registration dossiers to ensure submissions meet local requirements.
· Manage Health Authority interactions in AP (briefing documents, questions, responses, and post-submission activities).
· Oversee multiple regulatory projects concurrently; set milestones, timelines, and resource needs; mentor junior staff.
· Communicate regu...
....Read more...
Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-11-27 07:24:08
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Beijing, China
Job Description:
POSITION SUMMARY:
The Manager, Regulatory Affairs is a member of the Global Regulatory Affairs organization.
The position resides in the AP Region and is responsible for working with local regulatory affairs departments, AP regional cross-functional teams, Global Regulatory Teams and other global functions to define and implement the regional strategy for assigned products.
The position, under minimal supervision, is accountable for leading and providing region or country strategic input into the global regulatory strategy and identifying regional requirements to optimize registration, and lifecycle management of marketed products, taking into consideration current and proposed changes in regulatory requirements and standards.
This position provides regional affiliates with timely responses to Health Authority enquiries and gives general regulatory support to all affiliates in the region for the pharmaceutical sector business.
RESPONSIBILITIES:
Regulatory Strategy and Expertise
* Understands regional and local requirements and advises the Global Regulatory Team (GRT) and Compound Development Team (CDT) on applicable regulatory requirements, guidelines and processes, region-specific regulatory issues with impact on the product strategy or deliverables.
Keeps up-to-date on understanding of regional/regulatory environment.
* Participates as a standing member of the project related GRT if applicable; supports the GRT by providing strategic regional input into registration and life cycle management.
* Expedites commercialization of new indications and line extension by providing regional regulatory inputs to identify barriers and needs.
* Provides guidance to local affiliates on development of strategies to accelerate submissions/approvals
* Provides input in post-registration activities, including labeling changes
*
+ Provide regional implementation and regulatory-based advice on new and updated Core Data Sheets.
* Maintains expert knowledge in regional regulatory requirements and ensure that staff is expert in country and product-specific regulatory requirements
* Provides AP evaluation in licensing activities
Health Authority, Operating Companies, and Business Partner Interactio...
....Read more...
Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-11-27 07:24:07
-
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:
Quality
Job Sub Function:
Quality Systems
Job Category:
Professional
All Job Posting Locations:
Xian, Shaanxi, China
Job Description:
* å®æ½å
/å¤é¨GMP 审计ï¼ç¡®ä¿è´£ä»»é¨é¨æ§è¡ç¸å
³æ´æ¹æªæ½ï¼æ ¹æ®GMPè¦æ±åè¯ä¼°ç»ææ¹è¿è´¨éä½ç³»ï¼
* Perform internal and external GMP audit as a team member.
Make sure the responsible dept.
to implement related CAPA.
Improve quality systems based on internal & external assessments to align with GMP requirements;
* ç°åºè´¨éï¼GMPï¼ç®¡çï¼æ¹è®°å½å®¡æ ¸ï¼ä¸»æ°æ®æ¹åï¼ç©æçå¤ç½®å产åçå°±å°è¡å¨å³å®ï¼æç
§GMP è¦æ±ç®¡çãçæ§åé¤ååè¿å产åï¼ä¸æ¥ï¼ææ管çä¸ç¬¦åäºä»¶ï¼CAPAååæ´å®æ½ï¼ä»¥ç¡®ä¿äº§åå®å
¨ï¼ææï¼åä¸ãæ¯æ产åå¼è¿ï¼
* Onsite GMP supervision, MBR review, master data approval, Make decision for products field action and materials disposition.
Manage and monitor rejected and returned materials handling to meet GMP requirements.
Escalation.
Manage Non- conformance, CAPA closure and CoC execution, make sure products with safety, effective, and purity.
Support product technical transfer;
* ä¾æ®å¼ºçIQPç¨åºåGMPè¦æ±ææå¤çå¤é¨å®¢æ·çè´¨éæè¯ï¼æ»¡è¶³å®¢æ·æ½å¨éæ±ï¼æ¯æ并çæ§ç产è¿ç¨ï¼æ导ç¸å
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* Handle external customer quality complaint effectively aligned with J&J/IQP policy and GMP to meet & exceed customer potential requirements.
Monitor and support production process, and instruct operator to follow procedure requirements;
* ä¾æ®ç¨åºåGMPè¦æ±ï¼å®¡æ ¸æ¹åä¸GMPç¸å
³çç¨åºï¼ç³»ç»å¹´åº¦è¶å¿æ¥ååå°åå
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* Review and approve GMP related procedure and system annual trend report and art work to meet procedure and GMP requirements;
* 建ç«é¨é¨çå®å
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* Establish department environmental, safety and industry hygiene objectives. Help organize sufficient training and site inspection to ensure all operations comply with environmental, safety and industry hygiene regulations and J&J requirements;
* ç¡®ä¿æ¥å¸¸æä½ç¬¦åç¹æ®è¯åå®å
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* Ensure that daily operations comply with control substance safety management system and related document requirements.
* ç»ç»å...
....Read more...
Type: Permanent Location: Xian, CN-61
Salary / Rate: Not Specified
Posted: 2025-11-27 07:24:00
-
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 Affairs – Marketed Products
Job Category:
People Leader
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines, Petaling Jaya, Selangor, Malaysia, Singapore, Singapore
Job Description:
Scientific Affairs Manager, Medical Operations
(J&J MedTech, Southeast Asia)
Job Location: Any Southeast Asia Market (SG/MY/TH/PH/ID/VN)
Function: Medical/Scientific Affairs (MedTech)
Reports to: Head of Medical/Scientific Affairs, SEA
Career level: Manager (people & program leadership)
Team: Manages internal and external talents and vendors
Employment: Full-time
Role summary
Lead, manage, standardize, and continuously improve core Medical Affairs operations across SEA—Medical Information (MI) requests, copy review (MLR - Medical-Legal-Regulatory), patient safety/vigilance interface, and performance dashboards—so that decisions are compliant, timely, and insight-driven.
Orchestrate cross-functional partners (Regulatory, Quality, Legal/Compliance, Marketing, Commercial Excellence, Data/IT) and ensure processes meet regional regulatory and company standards.
General Responsibilities:
* Accountable for SEA processes, SOPs, RACIs, SLAs, and audit readiness in MI, MLR, Safety interface, and dashboards
* Approver for MLR process outcomes within delegated authority; escalates risk to Medical Director/Legal/RA
* Budget co-owner for operational spend (tools, vendors, training); responsible for vendor selection, contracting, and performance
* Talent leader for an external enabling team (analysts/coordinators) and matrix leader across country stakeholders
Key responsibilities
1.
Lead Medical Information (MI) Operations
* Set regional MI strategy (channel intake, triage, Standard Response Document (SRD) library governance, multilingual coverage) and own SLAs (acknowledge same day; resolve within 2 business days for standard)
* Run end-to-end MI intake → triage → response → documentation → close, covering all channels (email, phone, web forms, congress booths, field escalations)
* Ensure responses are evidence-based, balanced, and non-promotional; manage unsolicited off-label queries per SOP (appropriate routing/approval/escalation)
* Maintain a Standard Response Document (SRD) library (references, version control, country adaptations); coordinate approvals with MLR and archive ...
....Read more...
Type: Permanent Location: Singapore, SG-01
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:59
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Irvine, California, United States of America
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
We are searching for the best talent for a Clinical Research Specialist to support our Mentor business. This role will work a Flex/Hybrid schedule with 3 days per week on-site and must be located within a commutable distance of Irvine, CA. The role may also require up to 25% travel depending on the phase of the program.
Purpose: The Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.
You will be responsible for:
* Serves as a Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Operating Company under supervision.
* Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures.
* May serve as the primary contact for clinical trial sites (e.g.
site management).
* Assists in the development of clinical trial documents (e.g.
study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports).
* Supports applicable trial registration (e.g.
www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed.
* Coordinates and executes ordering, tracking, and accountability of investigational devices and trial materials.
* Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel.
* Interfaces and collaborates with Clinical Research Associates (CRAs).
* Assists in overseeing and supports the development and execution of Investigator agreements and trial payments.
* Assists in clinical data review to prepare ...
....Read more...
Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:31
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Project Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Irvine, California, United States of America
Job Description:
Biosense Webster, a part of J&J MedTech, is recruiting for an NPI/LCM Senior Engineer located in Irvine, CA.
Atrial fibrillation (AFIB) is a quivering or irregular heartbeat (arrhythmia) that can lead to blood clots, stroke, heart failure and other heart-related complications.
20 million people around the world suffer from AFIB each year.
Biosense Webster, Inc.
is the global leader in the science of diagnosing and treating heart rhythm disorders.
The company established its leadership in electrophysiology with the development of the first real-time, 3D cardiac mapping and navigation technology, as well as the first electrophysiology catheter.
The introduction of the company’s CARTO® 3 System in 2009 revolutionized 3D mapping technology by increasing the accuracy, speed, and efficiency of the cardiac ablation procedure.
About the Role:
The successful candidate will be working within a cross-functional project team through all phases of the product development process, planning and executing projects through the product launch and support of product after launch.
The candidate will work closely with members of the project core team (R&D, Quality Engineering, Marketing, Finance, Sourcing, Plan, External Manufacturers etc.,) to define user needs, generate design concepts and prototypes, perform design evaluations (such as tolerance analysis, FEA, DOE's, simulated use testing, etc.), and support development of product and process validation plans and testing during the development and full life cycle of the product.
The candidate will also be involved in test method development and evaluation of the proposed design.
The NPI/LCM Senior Engineer will work with cross functional team and suppliers to optimize designs for manufacturability and produce prototypes.
The candidate should demonstrate an understanding in the application of design controls and development processes.
The candidate should have the ability to prioritize tasks and manage a varied workload, exhibit strong written and verbal communication skills and interface effectively with others in the project team.
The NPI/LCM Senior Engineer will be responsible for:
* This NPI/LCM Senior Engineer will be responsible for collaborating with R&D, Qua...
....Read more...
Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:29
-
Werde Lagermitarbeiter / Sortierer für Briefe in Straubing (Hafen)
Was wir bieten
* 16,60 € Tarif-Stundenlohn inkl.
50% Weihnachtsgeld
* + 25% Nachtzulage steuerfrei schon ab 20:00 Uhr (bis 6:00 Uhr)
* Weitere 50% Weihnachtsgeld im November
* Bis zu 332 € Urlaubsgeld im Juli ab dem 2.
Jahr
* Ein krisensicherer Arbeitsplatz, bezahlte Einarbeitung, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Du kannst sofort befristet in Teilzeit starten, 5,0 Stunden/Woche
* Kostenlose Ausstattung, wie z.B.
Sicherheitsschuhe und Schutzhandschuhe
* Entwicklungsmöglichkeiten (bspw.
Teamleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote, wie z.B.
Rabatte bei Mobilfunkanbietern, Fitnessstudios, Modemarken etc.
Deine Aufgaben als Sortierer bei uns
* Sortieren der Briefsendungen nach verschiedenen Kriterien
* Bedienen der Sortieranlagen
* Heranholen der zugeführten Briefbehälter
* Leeren der Fächer und Abtransport der Briefbehälter
* 5 Tage/Woche
* Unsere Schichten:
+ Nachtschicht Samstags von 00:00 bis 07:00 Uhr oder Tagschicht Samstags 10:00 bis 14:00 Uhr
Was du als Briefsortierer bietest
* Du arbeitest zuverlässig und bist engagiert
* Du kannst anpacken und hast Spaß an körperlicher Arbeit
* Du kannst dich auf Deutsch unterhalten
* Du arbeitest gern im Team
Werde Sortierer bei Deutsche Post DHL
Als Briefsortierer sorgst du dafür, dass unsere Briefe pünktlich ankommen.
Bei uns sind auch Quereinsteiger oder Studenten herzlich willkommen, denn du zählst, wie du bist!
Wir freuen uns auf deine Bewerbung als Sortierer, am besten online.
Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#werdeeinervonunssortierer
#werdeeinervonunslagerhelfer
#jobsnlstraubing
#nlstraubing
#F1Lager
....Read more...
Type: Contract Location: Straubing, DE-BY
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:23
-
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:
Technology Enterprise Strategy & Security
Job Sub Function:
Security & Controls
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for TS Manager BTP Security Lead located in Raritan, New Jersey.
The Digital Platform Transformation Program is a critical component of the Innovative Medicine strategy to become a digital first company.
Innovative Medicine is investing significantly to transform our core ERP landscape through the implementation of a single global instance of SAP’s S4 Hana platform and BTP Platform.
This will unlock significant value and establish a best of breed foundation for our S4 Digital Core.
This role will be accountable for the delivery of security solutions for the BTP Platform. This role will deliver the overall BTP security design and setup for Security by ensuring progress to the plan, by reporting progress status and metrics to Management and by driving issue resolution.
This role is also responsible for assessing functional requirements, guide the group as per Application Security guidelines and Compliance standard methodologies, and ensure transparent security design.
Major Duties & Responsibilities
Security solutioning and delivery and program oversight
* Assess functional requirements and provide recommendations per Application Security guidelines and Compliance standard methodologies.
Translate functional specifications into a technical design for Data level Security
* Responsible for MedTech S4 Security Support in accordance with Global Security Strategy and Administration
* Crafting and building security groups and permissions.
* User administration with Active Directory or Identity Access Management.
* Solid understanding of NetWeaver and Data level security, S/4 HANA, ability to craft data level security concerns and to work with technical team to ensure such concerns are addressed.
* Detailed experience with ERP Security, Enterprise S/4 HANA Security, BW/4 HANA Security
* Identify Risks and compliance issues by running segregation of duties checks
* Experience with Security Weaver – Separation Enforcer and Emergency Repair.
* Develop and implement Application Data Security policies and procedures.
* Strong conceptual, analytical, problem-solving, troubleshooting and resolution skills
...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:18
-
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:
Kibbutz Shefayim, Center District, Israel
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
Join Our Team as a Clinical Trial Assistant (CTA) Intern!
We are looking for a motivated and fast learner intern to support our GCO Israel team.
Position Summary:
6 months internship program, located in Kibbutz Shefayim.
The program includes rotation between 2-3 different teams in our GCO Israel organization.
During the program you will join 2-3 on-site monitoring visits.
Principal Responsibilities:
* Assists and Contributes to assigned team for duration of temporary internship.
* Receives guidance, training, and mentoring from colleagues in planning and carrying out activities and assignments.
* Support trial documentation and study start-up, ensuring timely collection of necessary materials.
* Provide logistical support throughout the study execution and closure phases.
* Maintain communication with internal teams and external partners including investigators and ethical committees.
Education and Experience Requirements:
* A minimum of a BA or BS degree in Life Sciences, Nursing, or a related field.
* Proficiency in English and strong knowledge of MS Office.
* Excellent organizational and interpersonal skills.
If you are ready to contribute to impactful clinical trials and gain invaluable experience, we want to hear from you!
Apply now to join our innovative team
....Read more...
Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:11
-
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:
Communications & Corporate/External Affairs
Job Sub Function:
Internal Communications
Job Category:
People Leader
All Job Posting Locations:
North Ryde, New South Wales, Australia
Job Description:
Location: Macquarie Park, NSW
Type: Full-Time, 12-Month Fixed Term Contract (Parental Leave Cover)
Johnson & Johnson MedTech ANZ is seeking a dynamic Manager, Communications & Public Affairs to lead strategic internal and external communications that drive business growth and strengthen our reputation across Australia and New Zealand.
In this role, you will be responsible for managing internal and external communications to drive business objectives for Johnson & Johnson MedTech ANZ, with a key focus on:
1. Drive growth for the business units
* Develop and implement communication strategies to support the key priorities, based on the ANZ J&J MedTech strategy.
* Act as integrated business partner to the MedTech business units to provide communication consul in support of critical and priority business growth / objectives.
2. Build J&J MedTech’s leadership through creating compelling communication programs for new product launches, patient education, disease awareness and other related activities
* Partner with business stakeholders to create innovative programs to generate SOV and impact for product launches, market entry of new technologies and innovations.
* Create on-going stories through effective PR efforts to raise awareness of diseases. Partner with Marketing team to develop effective patient education activities by driving high quality media coverage and content.
* Explore new / creative ways to engage HCPs and patients to raise the awareness of disease treatments.
3. Internal communications to cultivate culture and engage employees across all levels
* Partner with HR and leadership to develop internal communication strategy and programs to support the needs of business and culture development across the J&J MedTech ANZ organization & respective business units.
* Lead key employee engagement activities by designing relevant and impactful content, which include but not limited to Townhalls, kick off meetings, global executive visits and etc.
4. Raise and protect J&J MedTech’s reputation in Australia and New Zealand by proactively developing a highly impactful corporate communication strategy ...
....Read more...
Type: Permanent Location: North Ryde, AU-NSW
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:10
-
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:
Technology Enterprise Strategy & Security
Job Sub Function:
Security & Controls
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson Active ERP is recruiting for a TS Manager BTP Security Lead located in Raritan, New Jersey.
The Digital Platform Transformation Program is a critical component of the Active ERP, Medtech and Innovative Medicine strategy to become a digital first company.
Johnson & Johnson is investing significantly to transform our core ERP landscape through the implementation of a single global instance of SAP’s S4 Hana platform and BTP Platform.
This will unlock significant value and establish a best of breed foundation for our S4 Digital Core.
This role will be accountable for the delivery of security solutions for the Active ERP and BTP Platforms. This role will deliver the overall security design and setup for Security by ensuring progress to the plan, by reporting progress status and metrics to Management and by driving issue resolution.
This role is also responsible for assessing functional requirements, guide the group as per Application Security guidelines and Compliance standard methodologies, and ensure transparent security design.
Major Duties & Responsibilities:
Security solutioning and delivery and program oversight
* Assess functional requirements and provide recommendations per Application Security guidelines and Compliance standard methodologies.
Translate functional specifications into a technical design for Data level Security.
* Responsible for S4 and BTP Security Support in accordance with Global Security Strategy and Administration.
* Crafting and building security groups and permissions.
* User administration with Active Directory or Identity Access Management.
* Solid understanding of NetWeaver and Data level security, S/4 HANA, ability to craft data level security concerns and to work with technical team to ensure such concerns are addressed.
* Detailed experience with ERP Security, Enterprise S/4 HANA Security, BW/4 HANA Security.
* Identify Risks and compliance issues by running segregation of duties checks.
* Experience with Security Weaver – Separation Enforcer and Emergency Repair.
* Develop and implement Application Data Security policies and procedures.
* Strong conceptual, analytical, problem-solving, troub...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:09
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Product Development
Job Sub Function:
R&D Software/Systems Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
JOB TITLE: Senior Systems Engineer - Robotics
LOCATION: Santa Clara, California, United States
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
Johnson & Johnson MedTech is recruiting for a Senior System Engineer -Robotics, located in Santa Clara, CA.
This is a great opportunity for a Robotics Engineer to use fundamental modeling and data-driven analysis techniques to bring together the needs of multiple partners, including end-user, regulatory, clinical, mechanical, electrical, controls, marketing, etc.
The candidate will be responsible for building and maintaining simulation tools for surgical robotic systems, enabling the model-based analysis framework to support technical trades and decisions.
The role requires a strong background in the kinematics/dynamics of multi-axis systems, robot manipulators, physics, data analytics, and simulation modeling.
Key Responsibilities:
* Develop and maintain computational and logical models for key system performance aspects and behaviors.
* Create and execute realistic robotic system simulations utilizing the NVIDIA technologies, including tools like Isaac Sim and Omniverse.
* Perform ad-hoc analysis of surgical robotics systems within cloud-based computational platforms.
* Collaborate closely with design teams to create solutions that align with requirements and mitigate risks.
* Lead technical discussions and multi-functional team meetings with a digital-first approach.
* Contribute to building a knowledge database for digital assets and techniques applicable across projects.
QUALIFICATIONS
* Minimum B.S (Mechanical Engineering, Robotics, Mechatronics, Computer Science, or other related Engineering field equivalent) and 4+ years of industry experience with proven success in Robotics Systems or M.S.
with 2+ years, or Ph.
D.
and 0+ years of industry experience with proven success in Robotics Systems.
* Solid foundation in kinematics, multi-body dynamics, and control of mult...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-11-27 07:23:03
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Athens, Georgia, 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 Senior Process Specialist! This onsite position will be located in Athens, Georgia.
The Senior Process Specialist is responsible for providing technical support for the Active Pharmaceutical Ingredient (API) and Monomer manufacturing processes.
Technical support includes safety, quality, efficiency improvements and issue resolution to ensure products are manufactured compliantly and efficiently.
They also support capital projects, site wide initiatives, or other projects as needed as a project lead or subject matter authority.
Key Responsibilities:
* Drive day-to-day manufacturing technical implementation focusing on safety, quality (manufacturability) and product cost.
* Implement processes and methodologies that support the sharing of standard processes.
* Own process improvements related to safety, environmental, quality, compliance, productivity, yield, and cost.
* Lead multi-functional teams in the identification and performance of cost and process improvements.
* Investigate complex technical problems and provide solutions for process improvement and cost reduction.
* Own corrective/preventative measures to improve compliance and reduce repeat occurrences.
* Serve as Subject Matter Authority during internal and external regulatory audits (including FDA, EMEA, DEA).
* Provide documentation support for SOP/ Batch Record revisions.
QUALIFICATIONS:
EDUCATION:
* Minimum of a High School Diploma or equivalent diploma/degree required; Associate's, Trade/Technical, Vocational, Bachelor's, or equivalent degree/diploma/certification strongly preferred
EXPERIENCE AND SKILLS:
Required:
* Minimum four (4) years of relevant work experience
* Experience within Chemical, Pharmaceutical, Me...
....Read more...
Type: Permanent Location: Athens, US-GA
Salary / Rate: Not Specified
Posted: 2025-11-27 07:22:59
-
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:
Technology Enterprise Strategy & Security
Job Sub Function:
Security & Controls
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for TS Manager, BTP Security Lead located in Raritan, New Jersey.
The Digital Platform Transformation Program is a critical component of the Innovative Medicine strategy to become a digital first company.
Innovative Medicine is investing significantly to transform our core ERP landscape through the implementation of a single global instance of SAP’s S4 Hana platform and BTP Platform.
This will unlock significant value and establish a best of breed foundation for our S4 Digital Core.
This role will be accountable for the delivery of security solutions for the BTP Platform. In addition, the manager will deliver the overall BTP security design and setup for Security by ensuring progress to the plan, by reporting progress status and metrics to Management and by driving issue resolution.
This role is also responsible for assessing functional requirements, guide the group as per Application Security guidelines and Compliance standard methodologies, and ensure transparent security design.
Responsibilities will include:
* Assess functional requirements and provide recommendations per Application Security guidelines and Compliance standard methodologies.
Translate functional specifications into a technical design for Data level Security.
* Responsible for MedTech S4 Security Support in accordance with Global Security Strategy and Administration.
* Crafting and building security groups and permissions.
* User administration with Active Directory or Identity Access Management.
* Solid understanding of NetWeaver and Data level security, S/4 HANA, ability to craft data level security concerns and to work with technical team to ensure such concerns are addressed.
* Detailed experience with ERP Security, Enterprise S/4 HANA Security, BW/4 HANA Security.
* Identify Risks and compliance issues by running segregation of duties checks.
* Experience with Security Weaver – Separation Enforcer and Emergency Repair.
* Develop and implement Application Data Security policies and procedures.
* Strong conceptual, analytical, problem-solving, troubleshooting and resolution skills.
* Ability to supervise and lead t...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-11-27 07:22:54
-
Ce que tu feras au quotidien
Ton cadre de travail est un Atelier de conception et commande.
Il s'agit d'un point de contact de petit format, rattaché à un magasin IKEA (magasin mère).
Ici nos clients peuvent s’inspirer, concevoir, acheter, commander et rapporter de la marchandise ! Le service est axé sur l'accompagnement des projets de cuisine et de rangement.
Avec l'appui du Leader d'équipe de l'unité commerciale, voici tes principales missions :
• Maximiser les ventes en t'assurant que ta zone de responsabilité soit toujours en parfait état
• D'accueillir, renseigner, orienter et proposer aux clients des services en fonction de leurs besoins .
• Tu abordes avec respect les visiteurs pour en savoir plus sur leurs besoins et les guider dans leur choix grâce à ta connaissance approfondie de nos produits et services (Livraison, financement,…).
• Tu veilles à ce que ta zone soit impeccable et facilite le parcours client : modèles d’exposition en parfait état, propreté du rayon, étiquetage correct.
• Tu t'appropries les objectifs de ton magasin et tu sais comment y contribuer, notamment en pilotant les ventes.
• Tu enregistres en caisse les articles avec fiabilité
• Au retrait des marchandises/transport, tu t'assures du bon contrôle de la marchandise préparée avant la remise au client ou au transporteur dans le respect des procédures.
• Au comptoir du service après-vente, tu accueilles avec bienveillance les clients dans le cadre de la politique de retours et échanges et gères les réclamations.
Salaire : entre 26 364 € et 29 000€ /an selon expériences et compétences (salaire brut annuel incluant la prime de 13ème mois, sur la base d’un temps plein 35h).
Les avantages :
• Une prime de 13 ème mois versée en 2 fois.
• Une remise de 15% sur tes achats chez IKEA.
• Une part de rémunération variable liée à la performance économique globale.
• Des tickets restaurants.
• Une mutuelle d'entreprise avantageuse dès ton arrivée.
• Une prime d'ancienneté (au-delà de 2 ans).
• Des congés supplémentaires pour ancienneté (au-delà de 3 ans).
Qui tu es
• Tu aimes le contact avec les clients et tu es à l'aise pour les approcher de manière amicale et polie.
• Tu es curieux et souple et tu sauras t'adapter aux tâches diverses et variées.
• Tu apprécies le travail en équipe.
• Tu es l'interlocuteur des clients sur l'ensemble des services.
• Tu es organisé et tu fais preuve d’initiative pour gérer les priorités et t’adapter selon les situations.
• Tu as déjà travaillé dans la Vente ou la Relation clients, idéalement dans un environnement très dynamique.
....Read more...
Type: Permanent Location: Angoulins, FR-17
Salary / Rate: Not Specified
Posted: 2025-11-27 07:22:36
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ERM is seeking an experienced Senior Consultant, Permitted Bat Biologist, Natural Resources to play a key role in growing our business in our Charleston (WV), Indianapolis, Nashville, or Charlotte offices.
The ideal candidate will have experience leading bat presence/absence mist-netting survey tasks related to renewable energy, transmission, pipelines, or other capital project developments. Applicants must have a valid USFWS Section 10 permit to conduct bat mist netting surveys in the Midwest.
This is an excellent opportunity to advance your career with ERM’s experienced consulting teams in renewable energy permitting, with additional opportunities to contribute to onshore wind, electrical transmission, oil & gas, and technology infrastructure projects.
As a bat biologist, you will manage bat related tasks including development of proposal scope and budgets, task management, lead field survey efforts, development of survey protocols and level of effort, in-office data analysis, report writing, and quality control.
You will also be part of teams conducting National Environmental Policy Act (NEPA) compliance, Endangered Species Act (ESA) Section 7 & 10, state-level equivalent reviews, and environmental permitting for large-scale capital projects in the Great Plains, Midwest, and beyond.
This position will include opportunities for both field and office work in the Heartland Region, and potentially elsewhere in the United States.
RESPONSIBILITIES:
* Lead mist-netting and radio-telemetry surveys for protected bat species.
* Oversee acoustic bat surveys and review acoustic data.
* Perform background data and desktop site reviews.
* Submit environmental permit applications.
* Review endangered bat species resource records.
* Support GPS data collection and mapping.
* Record, enter, organize, manage, and analyze data.
* Lead and/or prepare portions written reports, tables, spreadsheets, databases, and maps for client and regulatory agency review.
* Complete quality control review for bat data and reports.
REQUIREMENTS:
* A bachelor’s degree in an environmental (biology, ecology, natural resources, soil science, or related field) discipline.
Or equivalent experience.
* Master’s degree in biology or related field from an accredited institution is a plus.
* 3+ years (4+ years preferred) of related experience.
* USFWS Collection Permit for protected bat species.
* Experience conducting bat surveys in Arkansas, Kansas, Missouri, Nebraska, and/or Oklahoma.
* Experience with bat radio telemetry and roost emergence counts.
* Familiarity with acoustic bat surveys and associated software.
* Comfortable with ArcGIS field maps and GPS-based survey equipment.
* Knowledge, understanding, and use of statistical analysis a plus.
* Experience working well both in a team setting and independently.
* Technical writing skills are necessary for this posit...
....Read more...
Type: Permanent Location: Nashville, US-TN
Salary / Rate: Not Specified
Posted: 2025-11-27 07:21:55
