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About the Company
Vantage Group Holdings Ltd.
(Vantage) was established in late 2020 as a re/insurance partner designed for the future.
Driven by relentless curiosity, our team of trusted experts provides a fresh perspective on our clients’ risks.
We add creativity to tech-enabled efficiency and robust analytics to address risks others avoid.
Vantage provides specialty re/insurance through its operating subsidiaries in Bermuda and the U.S.
Vantage has approximately 350 colleagues in both the United States and Bermuda.
We have offices in Chicago, IL, Norwalk, CT, Arlington, VA, Boston, MA, New York, NY and Hamilton, Bermuda.
Additionally, we are a highly geographically diverse workforce with colleagues based in 35 states and counting.
We fully support work flexibility including remote and hybrid work arrangements.
Location: Bermuda Office (In Person / Hybrid Opportunity)
About the role:
At Vantage, the Senior Actuarial Analyst, Reserving will provide reserving support to a variety of insurance and reinsurance lines written out of Bermuda.
This role is pivotal in enhancing the reserving process and developing advanced analytical tools for precise reserve estimation.
You will report directly to the Head of Reserving, Bermuda.
This position will be integral in carrying out the reserving process and in building out the analysis and tools needed for robust reserve estimation.
This role is located in Bermuda and relocation is not provided.
Vantage offers its colleagues performance-based bonus potential, strong health & welfare benefits, retirement plan benefits, competitive time off plans, a highly flexible work environment, and much more.
Responsibilities & Accountabilities:
* Lead and perform comprehensive reserve analysis using both internal and external data sources.
* Collaborate with cross-functional teams such as pricing, claims, finance, and data/analytics to develop and validate sophisticated reserving assumptions and methodologies.
* Develop and enhance reserving methods, tools, and monitoring metrics to support business objectives.
* Prepare and deliver detailed quarterly reports, presentations, and materials for senior management and other key stakeholders.
* Ensure strict compliance with local regulatory requirements and maintain actuarial best practices in all reserving analyses.
* Innovate and implement new ways to leverage data and analytics to optimize the reserving function.
* Contribute to adherence to local regulatory requirements and actuarial best practices within reserving analysis.
Ideal Candidate Profile:
* Bachelor’s degree in actuarial science, mathematics, finance, statistics, economics, or a related field; or the equivalent in work experience.
* 3 - 5 years of actuarial experience required with a focus on reserving in the P&C insurance and/or reinsurance industry.
* Progress toward actuarial qualification with CAS or IFOA (other recognized actuarial societie...
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Type: Permanent Location: Hamilton, BM-BM
Salary / Rate: 127500
Posted: 2025-07-23 08:33:07
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Voyant Beauty believes our people are more than just employees; they’re the driving force behind everything we achieve.
Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual’s contribution is valued and celebrated.
We invest in their growth, providing opportunities for development and advancement within our dynamic team.
Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products.
We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs.
This can include skincare, haircare, bath and body products, fragrances, and more.
Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life.
Safety is a core value at Voyant Beauty.
We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel.
If you’re seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you.
Come join us and be a part of our journey.
A Brief Overview
The Plant Hygienist plays a critical role in ensuring that all hygiene-related processes, systems, equipment, and personnel adhere to the highest standards of efficacy, efficiency, and regulatory compliance.
This position is responsible for overseeing cleaning protocols, sanitation procedures, environmental and critical equipment hygiene monitoring programs and employee training to maintain a safe and compliant manufacturing environment.
What you will do
• Create and update cleaning and sanitization work instructions for production and manufacturing equipment to maintain compliance and operational excellence for existing product portfolio and new launch.
• Lead C&S validation protocols for all manufacturing cleaning and sanitization processes.
• Develop and manage the Site Cleaning & Sanitization (C&S) Master Plan, ensuring consistency and efficacy across all sanitation processes.
• Optimize cleaning recipes by collaborating with Research & Development, Plant Operations, and Customers to improve efficiency and effectiveness.
• Provide training to applicable employees.
• Standardize best practices for cleaning and sanitization by working closely with other hygienists across the network.
• Support improvement initiatives through continuous improvement projects focused on optimizing cleaning recipes, 10sanitization recipes, and enhancing environmental responsibility.
• Partner with cross-functional teams to investigate and resolve Out of Specification (OOS) microbiological issues, ensuring corrective actions align with quality standards.
• Configure, maintain, and optimize Clean-in-Place (CIP) recipes within processing equipment to ensure consistenc...
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Type: Permanent Location: Roanoke, US-VA
Salary / Rate: Not Specified
Posted: 2025-07-23 08:32:06
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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
Was macht unseren Bereich aus:
Im Bereich Production Chemistry innerhalb des Geschäftsbereichs Diagnostics Operations Penzberg stellen wir Einsatzstoffe und ADIs für die Diagnostik sowie die chemische Forschung her.
Als führender Hersteller für chemische und biochemische Einsatzstoffe sind wir einer der wichtigsten Knotenpunkte im weltweiten Roche Netzwerk.
Gestalte und entdecke deine Perspektive bei uns und bringe dein Know-how in einem der größten Biotech-Unternehmen der Welt ein.
Sorge mit deinem Beitrag für die Aufrechterhaltung der SHE- und GMP-Compliance in unserem Bereich!
Das Team:
Wir sind das Team der chemisch-biotechnischen Produktion und sind stolz darauf, für nahezu alle Einheiten der Division Diagnostics und unsere externen Partner wichtige und hochwertige Einsatzstoffe und Reagenzien liefern zu können.
Die neugegründete Gruppe Process Technology befindet sich gerade im Aufbau und wird zukünftig die Produktionsbetriebe bei technologischen, prozess- und
automatisierungstechnischen Fragestellungen unterstützen und Expertise in die großen CAPEX-Projekte einbringen.
Unser aktuelles Team zeichnet sich durch Vielfalt, angefangen bei der Berufserfahrung über den Ausbildungshintergrund bis hin zur gemeinsamen Freizeitbeschäftigung aus.
Wir gehen gerne auch einmal die Extra-Meile, sind offen für neue Ideen und vergessen dabei nicht den Spaß an der Arbeit.
Deine Aufgaben
* Du unterstützt den Betriebsleiter bei anlagen- und prozesstechnischen Fragestellungen.
* Du koordinierst technische Maßnahmen im Betrieb sowie Fremdhandwerker in enger Zusammenarbeit mit dem Plantmanagement und dem Betriebsingenieur.
* Als Ansprechpartner aus dem chemischen Betrieb wirkst du bei der Validierung und Qualifizierung sowie der Erstellung von ECCs von Prozessanlagen mit.
* Bei Themen rund um Arbeitssicherheit, Prozess- und Analgentechnik vertrittst du die Abteilung in Besprechungen.
* Du schulst und unterweist Mitarbeiter in neuen Vorschriften und Vorgaben.
* Anlagen-Störungen (ZBSS) fallen ebenfalls in deinen Verantwortungsbereich.
Deine Qualifikationen
* Du verfügst über eine Ausbildung oder ein Studium in einem technischen Fachgebiet (z.B.
Verfahrenstechnik, Anlagen- oder Maschinenbau, Chemieingenieurwesen) oder eine abgeschlossene Ausbildung zum Chemielaborant / Chemikant mit Weiterbildung zum Chemietechniker mit mehrjähriger Berufserfahrung.
* Du bringst vertiefte Kenntnisse im Bereich chemischer Anlagen- und Prozesste...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-07-23 08:27:32
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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
Wir als Roche Automation Diagnostic Solutions mit Sitz in Ludwigsburg suchen einen hochqualifizierten und strategisch denkenden Senior Quality Partner (m/w/d).
In dieser Rolle setzt Du mit Deiner Erfahrung, Führungsstärke und Innovationsvermögen Maßstäbe im Qualitätsmanagement und trägst aktiv zur Steigerung der Geschäftsergebnisse sowie des Kundennutzens bei.
Das ist Dein Wirkungsfeld
Als Senior Quality Partner im Operations Quality Netzwerk stellst Du sicher, dass Roche- Vorgaben und regulatorische Anforderungen (wie FDA, IVDR, ISO 13485) in enger Zusammenarbeit mit Projekt-, Produkt- und Produktionsverantwortlichen auf höchstem Niveau umgesetzt werden.
Diese Position ist entscheidend für die Konzeption, Implementierung und kontinuierliche Optimierung umfassender Qualitätsprogramme und unterstützt innovative Projekte, während die globale und lokale Compliance gewährleistet wird.
Das erwartet Dich
Steigerung von Geschäftsergebnissen und Kundennutzen:
* Erreichung von Qualitäts- und Regulierungszielen, Initiierung/Umsetzung von Verbesserungen.
* Fungieren als Experte mit fundiertem Wissen.
* Coaching und Mentoring unerfahrener Kollegen.
* Eigenständige Erstellung, Prüfung und technische Kontrolle von Dokumentationen.
* Vorbereitung/Teilnahme an internen/externen Audits.
* Regelmäßige Schulungen und Schulung/Betreuung anderer Qualitätsmanager/Geschäftspartner.
* Entwicklung und Umsetzung zuverlässiger Problemlösungen, Wahrung regulatorischer Compliance.
* Proaktive Information der Führungskraft über kritische Qualitäts-/regulatorische Risiken.
* Förderung von Netzwerken, Innovation und funktionsübergreifender Zusammenarbeit.
* Eigenständige Planung/Bearbeitung täglicher Aufgaben mit minimaler Aufsicht, Initiierung von Aktivitäten, bereichsübergreifende Zusammenarbeit und Entscheidungsfindung.
* Entwicklung und Implementierung von Prozessverbesserungen in Abstimmung mit Standorten und globaler Qualitätsabteilung.
* Proaktives Vorantreiben von Innovationen und Optimierungen.
* Leitung oder aktive Teilnahme an funktionsübergreifenden Projekten und Arbeitsgruppen.
* Beitrag zur Lösung komplexer Herausforderungen mit Auswirkungen auf die Organisation oder das globale Netzwerk, inklusive länderübergreifender strategischer Projekte.
Fachübergreifende Führungsverantwortung:
* Verantwortung für Prozessrisikoanalysen (pFMEA) zur Identifizierung von Ri...
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Type: Permanent Location: Ludwigsburg, DE-BW
Salary / Rate: Not Specified
Posted: 2025-07-23 08:19:26
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ERM is seeking a Consultant, Safety and Industrial Hygiene with industry experience, to play a key role in supporting our clients and growing our business.
The ideal candidate will bring H&S technical capability and deep understanding of business processes to help our clients proactively address their EHS risks and challenges.
As a health and safety professional, you will be responsible for supporting on a range of health and safety management projects to build a sustainable business locally, while networking with ERM's global technical team to share best practices across the industry.
This is an excellent opportunity for a senior-level professional looking to advance their career with a global Sustainability leader, and work with a team of outstanding professionals in over 40 countries around the world.
RESPONSIBILITIES:
* Support development and implementation of Safety Management Systems and risk assessments to ensure effective risk control and regulatory compliance.
* Perform incident investigations, development of corrective actions, verification/validation of controls, and learning from incidents. Support root cause analyses in conjunction with client leadership.
* Support life safety programs such as control of hazardous energy, fall protection, electrical safety, machinery safety, powered industrial vehicle, materials lifting, hot work, and fire safety.
* Support client industrial hygiene programs, including leading the qualitative and quantitative assessment of exposure risk.
* Assist in the development of solutions to complex technical and regulatory issues and concerns.
* Contribute to expanding ERM’s Safety Services business.
Identify and develop new opportunities, prepare effective technical proposals, and take active leadership role in developing new business with new and existing clients.
Develop and expand client relationships that generate repeat business.
* Develop and manage innovative, behavior and performance outcome-focused approaches and programs for a variety of clients with complex technical/regulatory issues.
* Design and direct corporate H&S strategies and programs in areas such as industrial hygiene, behavior-based safety, safety culture and leadership, serious injury and fatality risk reduction, compliance auditing, EHS management systems, process safety and risk management, construction safety, high-impact training, and general compliance support.
Achieve client’s expectations for scope, budget, schedule, and quality.
* Manage a variety of tasks to achieve scope, budget and schedule targets while ensuring we meet and exceed our clients' expectations on deliverables.
* Build client relationships and nurture repeat business by continuously striving to Build a network within and outside of ERM that will enable you to leverage your skills and solve challenging multi-disciplinary client challenges.
REQUIREMENTS:
* BS...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-07-23 08:17:49
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At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.â¯Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Sr.
Regulatory Affairs Specialist (Remote) â Shockwave Medical to join our team located in Santa Clara, CA and Remote US.
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, weâre developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team thatâs 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 OverviewÂ
The Sr.
Regulatory Affairs Specialist is an individual contributor that works closely and partners with internal departments to efficiently and effectively meet assigned regulatory requirements for Shockwave Medical, Inc.
(SWMI).
 The Sr.
Regulatory Affairs Specialist combines knowledge of scientific, regulatory and business issues to ensure that products are developed, manufactured and distributed to meet regulatory requirements with a focus on the United States and the EU.
Under direction of responsible Regulatory Affairs Management, acts as a decision-maker on regulatory issues, assures that registration/renewal deadlines are met, and supports new product development.
Â
Essential Job Functions
â¢Â   Collaboratively interface with a variety of levels on significant matters, often requiring the coordination of activity across organizational units.
â¢Â   Outline submission and approval requirements in assigned geographies.
â...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-23 08:16:13
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HPBX Technician
$27.63 - $34.00
Arvig: Committed to Service, Dedicated to You
Join one of the nation’s largest independent broadband service providers! At Arvig, we deliver leading-edge broadband and telecommunications solutions—including high-speed internet, TV, phone, and security—to residential and business customers across Minnesota and beyond.
Our success is driven by a team of nearly 900 talented employees who embody our core values: ownership, engagement, efficiency, and knowledge.
We believe our people are the driving force behind everything we achieve, and we foster a culture built on courage, humility, open-mindedness, integrity, respect, and safety.
At Arvig, our goal is clear: to provide exceptional service and reliable solutions, backed by the latest technology, in an environment where employees can thrive in growth and opportunity.
Discover the Arvig Advantage—a workplace where you can bring your whole self, feel a true sense of belonging, and see your skills, ideas, and ambitions make a meaningful difference.
What You’ll Do
As an HPBX Technician you’ll lead the installation, provisioning, repair, and maintenance of hosted services and telecom equipment.
You'll mentor junior technicians, direct project tasks, and ensure service quality from start to finish.
From structured cabling to customer support, you’ll play a key role in ensuring systems run smoothly and efficiently.
You’ll also participate in the on-call rotation and troubleshoot legacy systems when needed—all while modeling safety, professionalism, and leadership.
Qualifications
What You'll Bring
* Commitment to Safety: A strong dedication to maintaining a safe environment -both physically and mentally -for yourself, your colleagues, and customers
* 5+ years of experience installing and supporting hosted or legacy telecom systems
* 3+ years of experience configuring and provisioning hosted or premise-based systems
* 1 or more years of demonstrated experience on project leadership and independent working
* Practical knowledge of legacy PBX, and broadband products and services
* Valid Class D Driver's License with acceptable driving record
* Power Limited Technician License
* Strong troubleshooting, customer service, and communication skills
* Ability to manage multiple tasks independently and adapt to new technologies
Bonus points if you have:
* AAS degree in Telecommunications or related field
* Additional experience with legacy PBX systems
* 3+ years of experience in a leadership or mentoring role
* Broader telecommunications or network knowledge
Your Schedule
Monday-Friday, 8:00AM-4:30PM; it is required to frequently work outside of normal business hours to meet the demands of the customer.
Location
On site: New Hope, MN
Experience the Benefits of a Career with Arvig
At Arvig, we offer more than just a job—we provide a foundation for a fulfilling career, support...
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Type: Permanent Location: New Hope, US-MN
Salary / Rate: Not Specified
Posted: 2025-07-23 08:15:13
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
The Opportunity
At Roche pRED, we transform cutting-edge science into life-changing medicines, driven by curiosity, responsibility, and humility.
Our BioX Genetics & Genomics (G&G) team within Pharmaceutical Sciences (PS) is seeking a highly skilled and motivated Genetics & Genomics Biomarker Operations Scientist.
In this role, you will be crucial to the efficient and compliant execution of biomarker strategies for Roche clinical trials.
You'll serve as a vital operational point of contact, ensuring seamless collaboration with external partners and internal stakeholders to support all aspects of biomarker outsourcing.
Your Impact
* Serve as the primary operational contact between Roche G&G and external Contract Research Organisations (CROs).
* Provide operational support for CRO contracting, work order setup, timeline agreements, and budget tracking.
* Support the identification, selection, evaluation and onboarding of new CRO vendors.
* Assist G&G Scientists with clinical study documentation, including compiling study documents and ensuring compliance checks.
* Oversee and manage timelines and deliverables for outsourced activities.
* Lead investigations and interactions with CROs on non-conformance issues.
* Support FAIR data storage and vendor onboarding for data ingestion.
* Proactively support and update guideline documentation related to outsourcing and clinical processes.
* Contribute scientific support to G&G Functional Biomarker Experts (FBEs).
* Oversee overall key performance indicators (e.g., Turnaround Times, number of samples) for outsourced activities across CROs
Your Profile:
* Master's or PhD level scientist with a strong molecular biology background.
* Proven experience in working with CROs.
* Experience in supporting vendor onboarding for data ingestion tools.
* Familiarity with clinical documentation processes (Work orders, study plans, ICFs, etc.) is a plus.
* Experience with data conformance checks, FAIR data storage, and CAPA tracking.
* Strong communication skills to keep teams updated.
Who You Are: You are a proactive, collaborative team player committed to scientific excellence and con...
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Type: Permanent Location: Welwyn, GB-HRT
Salary / Rate: Not Specified
Posted: 2025-07-22 08:39:00
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
$2,500 Sign-On Bonus! Apply Today!
Relocation Assistance Available
Your Role: Sr.
Specialist - Downstream Operations Technician (Night Shift)
The Downstream OpTech is technical process leader on the Downstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of the Clarification, Chromatography, and Tangential Flow Filtration operations.
Your Responsibilities:
* Executes the operation with team serving as process leader, coach, trainer, and responsible party
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Operations representative for cross-functional process support team, engaging in process
* Real-time problem solving, process intervention, and technical experiment delivery
* Ensures process documentation is prepared and completed with accuracy and concurrence
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: A minimum of 3 years of experience in Liquid Protein A Chromatography at manufacturing scale
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Proficiency with SAP
* GMP manufacturing
* Tangential Flow Filtration
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental wel...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: Not Specified
Posted: 2025-07-22 08:23:09
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Bacterins Operator
A Bacterin Operator (2nd Shift, Monday-Friday 2pm-10:30pm) will be responsible for the media addition, inoculation, down-streaming, dispensing and final filtration of live and inactivated Bacterial Antigen.
Must be able to work independently with minimal supervision in accordance with standard methods, standard operation procedures, and manufacturing directions using proper laboratory techniques.
Your Responsibilities:
* Perform aseptic operations for production processes performed within the Bacterin area.
* Proper operation of automated and semi-automated equipment used in relation to Antigen production.
For example, Sharples units and Concentrator Units
* Will be responsible for assembling, wrapping, sterilizing, delivery and maintaining inventory of Bacterins equipment and tanks and any other equipment/tank needs for the area as deemed necessary by department management.
* Routine and consistent attendance is necessary and important to the safety and operational policies and will be required to retain this bid.
What You Need to Succeed (minimum requirements):
* High school diploma or equivalent
* Excellent verbal and written communication skills and ability to train others.
* Must be able to read, understand, and follow written procedures.
Document operations with strict adherence to cGMP documentation practices.
* Must be able to lift up to 60lbs.
and hold above waist level while maintaining sterility.
What Will Give You the Competitive Edge (preferred qualifications):
* Knowledge and skill to recognize creative ideas that add value and can be implemented to improve efficiency, effectiveness and reduce complexity for department.
* Knowledge of Hazardous Waste Handling, Decontamination and Sterilization.
* Understanding of Basic GMP/Documentation practices
* Understanding of Basic Laboratory Practices, Measurements, Biology and Microbiology
* Understanding of operating in an aseptic environment
Elanco is an EEO/Affirmative Action Employer and does ...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: 31.86
Posted: 2025-07-22 08:23:04
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Harris Computers is hiring a Business Analyst for our Cognera Business Unit.
The successful candidate will be a key member in our Support Services Team ensuring we are able to meet and exceed on our business goals.
The Support Services team is responsible for revenue assurance, client invoicing, client billing rate changes, time allocation, and small project management.
This role requires you to multi-task, quickly adjust in a rapidly changing environment and work under pressure with tight deadlines.
You will be engaged in multiple initiatives simultaneously as part of internal and external projects.
This role will report to the Manager, Support Services.
You are passionate about Cognera’s overall success.
You are focused on meeting the needs of your internal and external Customers as you are committed to meeting all financial and performance targets.
You are able to work independently but enjoy being part of a team and contributing to the overall team results.
You are the head cheerleader when it’s time to celebrate the successes of your team and of Cognera.
This remote role welcomes candidates anywhere in Canada and the US and will be working in the MST timezone
What your impact will be:
* Work with stakeholders to understand their needs and translate them into clear, actionable requirements for projects or systems.
* Measure and report on project performance; analyze variances and initiate corrective actions
* Help support project management activities, such as planning, scheduling, and monitoring project progress
* Identify room for process efficiencies and implement appropriate analysis and enhancements
* Create clear and concise documentation of requirements, processes, and solutions for various stakeholders
* Contribute to team results by supporting all work activities
What we are looking for:
* Bachelor’s degree in Commerce, Economics, Computer Science or Mathematics with 3-5 years of related work experience
* Strong technical aptitude, especially working with complex datasets in applications such as MS Excel
* Ability to evaluate the information gathered from multiple sources, reconcile conflicts, and decompose high-level information into details
* Excellent verbal and written communication skills
* Strong attention to detail
* Ability to create a climate where people want to achieve; establish clear directions
* Measure performance against goals and evaluate results
* Love a challenge and enjoy problem solving
* Proactive, "can do" attitude
* Ability to work effectively in a team environment
* Ability to work well under pressure
* Excellent time management skills and ability to prioritize tasks
* Desire to work in, and help promote, a fun and exciting work environment
What would make you stand out:
* Project Management experience within the IT or Energy industry
* Experience in the Retail Energy industry
...
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Type: Permanent Location: Camrose, CA-AB
Salary / Rate: Not Specified
Posted: 2025-07-22 08:22:49
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Voici l’occasion de vous joindre à l’équipe d’ACCEO Solutions, une division de Harris Computer, là où les employés sont au cœur de nos priorités! ACCEO Solutions vous offre un environnement de travail qui reflète concrètement nos valeurs tel que la qualité, la créativité, le respect, la responsabilité, l’honnêteté et l’intégrité.
Relevant de l’assistant contrôleur, l’agent de recouvrement qui se joindra à notre équipe se démarquera par sa débrouillardise, sa curiosité, sa proactivité, sa motivation, son entregent, ses habiletés en communication et son souci du détail.
Ce qu’on attend de vous :
* Effectuer le suivi et la collection des comptes clients pour les unités ACCEO Estimation, Gestion CMEQ et Service de Garde;
* Préparer des dépôts et mettre à jour des comptes clients avec les paiements reçus;
* Répondre aux demandes d’information des clients et collaborer étroitement avec vos collègues à l’interne;
* Participer à la facturation des clients pour les unités ACCEO Estimation et Gestion CMEQ;
* Participer à la préparation d’analyses, dont certains rapports Excel quotidiens;
* Apporter votre support au reste de l’équipe des finances;
* Effectuer toutes autres tâches administratives connexes.
Ce qu’il vous faut :
* Formation post-secondaire en comptabilité, administration ou toute autre formation jugée équivalente;
* Bonne connaissance des logiciels Microsoft Office Excel & Outlook;
* Connaissance générale des logiciels comptables et modules clients;
* Aisance à naviguer dans plusieurs systèmes informatiques différents;
* Bonne maîtrise du Français et connaissance de l’anglais.
Points bonis si :
* Expérience en comptabilité;
* Expérience en recouvrement;
* Expérience avec un logiciel ERP intégré, particulièrement Microsoft D365 (atout).
En plus d’une équipe incroyable, nous vous offrons :
* Télétravail à 100% avec équipements fournies;
* 3 semaines de vacances + 5 congés mobiles par an au prorata de la date d’embauche;
* Assurances collectives payées par l’employeur, dès le premier jour;
* Programme Lifestyle Rewards, prime de 325$ par an dès l’embauche;
* Programme de REER Matching, programme d’actionnariat, de référencement et beaucoup plus;
* Un environnement de travail stimulant et en constante évolution;
* Et bien d’autres encore … !
Veuillez noter que seules les personnes retenues seront contactées.
Harris souscrit à un programme d’accès à l’égalité en emploi et les candidatures des membres des groupes visés à savoir les femmes, les personnes handicapées, les personnes autochtones et les minorités visibles sont encouragées à soumettre leur candidature.
Si vous êtes une personne handicapée, vous pouvez recevoir, sur demande, de l’assistance pour le processus de présélection et de sélect...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-07-22 08:22:48
-
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
Über die Abteilung:
Die Hauptabteilung „Core Lab Operations“ (DOM) am Standort Penzberg (DOMMB) sieht sich in der Verantwortung, dass Patienten präzise medizinisch-diagnostische Resultate erhalten.
Hierfür beliefern wir Patienten, Labore und Krankenhäuser mit diagnostischen Reagenzien und Teststreifen und agieren mit größter Sorgfalt und Leidenschaft.
Für uns steht „DOM“ für Zuverlässigkeit, Qualität und Wachstum.
Mit unserer zupackenden, optimistischen Einstellung gestalten wir unsere Zukunft zum Wohle der Patienten, unserer Mitarbeitenden, für uns als Organisation, Global Operations und für Roche.
In der Position als Ansatztechniker Produktion (m/w/d) erwartet Dich ein umfangreiches Aufgabengebiet mit interessanten Verantwortlichkeiten:
* Du bist zuständig für die termingerechte Herstellung von diagnostischen Reagenzien, entsprechend der Herstellanweisungen unter Einhaltung der geltenden GMP-Regeln
* Die GMP gerechte Dokumentation der durchgeführten Prozessschritte sowie die Erstellung und regelmäßige Pflege von Arbeitsanweisungen gehören ebenso zu Deinen Aufgaben
* Deine Erfahrung und Flexibilität in einem agilen Umfeld bringst Du zusätzlich, bei der Herstellung in unterschiedlichen Produktionsstätten innerhalb der Abteilung, mit ein
* Die Planung, Durchführung und Dokumentation von Qualifizierungen und Validierungen gehört ebenso zu Deinen Aufgaben, wie die Erstellung von Vorgabedokumenten
Und dafür wollen wir dich!
Wenn Du folgendes Profil hast, bist Du die richtige Person für uns und kannst im Bereich „Diagnostics Operations“ durchstarten und Deine Kompetenzen in einem der größten Pharmaunternehmen der Welt noch weiter ausbauen:
* Du hast eine Weiterbildung als Chemie- oder Biotechniker erfolgreich abgeschlossen oder hast alternativ eine erfolgreiche Ausbildung als Chemielaborant, Biologielaborant, Chemikant oder Pharmakant mit zusätzlicher relevanter Berufserfahrung (> 5 Jahre)
* Du bringst Erfahrung in einer ähnlichen Position in einem Produktionsbetrieb der chemischen Industrie speziell im GMP-Umfeld mit
* Darüber hinaus hast Du ein gutes technisches Verständnis
* Neben PC-Kenntnissen der gängigen Microsoft- und Google cSuite-Anwendungen besitzt du sicherem Umgang mit SAP
* Du sprichst Deutsch auf muttersprachlichem Niveau und hast Grundkenntnisse der englischen Sprache in Wort und Schrift
* Dein Arbeitsstil zeichnet sich durch Eigenständigkeit, Verantwortungsbewussts...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-07-22 08:13:46
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country (s) that align with your preferred location (s):
United States – Requisition Number: R-018519
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
We are searching for the best talent for an Associate Director, CAR-T Analytical Scientific Integrator - Advanced Therapies to be located in Malvern, PA or Leiden, Netherlands.
Purpose: The Associate Director, CAR-T Analytical Scientific Integrator will provide analytical, technical and strategic leadership to a matrixed team, in addition to representing Advanced Therapy (BioTD-AD) on the CMC team(s).
This role is also responsible for working with teams in the preparation of technical documents and regulatory submissions, participating in review, and contributing to development of strategies to follow global requirements.
You will be responsible for:
* Representing analytical development to provide strategic and scientific guidance to CMC project teams for all analytical topics including method development, control strategy and regulatory filings supporting FIH through commercial licensure.
* Leading the development and execution of analytical strategy, including shaping the strategy to meet global health authority expectations.
* Leading the analytical review of each program at governance meetings with support from subject matter experts.
* Ensuring the submission of complete, consistent, comprehensive, high-quality dossiers.
...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-07-22 08:13:37
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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:
Professional Medical Education
Job Category:
Professional
All Job Posting Locations:
North Ryde, New South Wales, Australia
Job Description:
* Great Place to Work® Certified - 2024
* Competitive salary package, flexible work practices, award winning benefits
* Role based in Sydney
ABOUT THE COMPANY
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
Brief role intro…
THE OPPORTUNITY
We have an exciting opportunity for an Associate Clinical Specialist to join our NSW team supporting our dynamic Biosense Webster business.
As an Associate Clinical Specialist, you will provide expert clinical products and technical assistance to physicians and EP lab staff.
You will be assisting in the effective use of Biosense Webster’s systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during Cardiac Electrophysiology procedures.
RESPONSIBILITIES
* Attend all portions and successfully complete the ACS training program without exception, including co-travel case coverage.
* Collaborate and support team members and other internal and external partners.
* Understand the dynamics of an EP lab, including, but not limited to physicians, nurses, technicians, clinical, hospital administrators and staff.
* Prioritize and appropriately respond to requests in a high-stress environment.
* Additional duties include performing administrative work, including managing account documentation, compliance training requirements, expense reporting, and company system input.
ABOUT YOU
* Hold a Tertiary education within Medical Science, Biomedical Engineering or related fields.
* Possess a natural aptitude and passion for technology.
* Exhibit an ability to troubleshoot and remain calm under pressure.
* Be passionate about delivering exemplary patient outcomes.
* Love working as part of a c...
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Type: Permanent Location: North Ryde, AU-NSW
Salary / Rate: Not Specified
Posted: 2025-07-22 08:13:33
-
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:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, 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
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country (s) that align with your preferred location (s):
Netherlands – Requisition Number: R-020291
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
We are searching for the best talent for an Associate Director, CAR-T Analytical Scientific Integrator - Advanced Therapies to be located in Malvern, PA or Leiden, Netherlands.
Purpose: The Associate Director, CAR-T Analytical Scientific Integrator will provide analytical, technical and strategic leadership to a matrixed team, in addition to representing Advanced Therapy (BioTD-AD) on the CMC team(s).
This role is also responsible for working with teams in the preparation of technical documents and regulatory submissions, participating in review, and contributing to development of strategies to follow global requirements.
You will be responsible for:
* Representing analytical development to provide strategic and scientific guidance to CMC project teams for all analytical topics including method development, control strategy and regulatory filings supporting FIH through commercial licensure.
* Leading the development and execution of analytical strategy, including shaping the strategy to meet global health authority expectations.
* Leading the analytical review of each program at governance meetings with support from subject matter experts.
* Ensuring the submission of complete, consistent, comprehensive, high-quality ...
....Read more...
Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-07-22 08:13:25
-
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:
Beijing, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% in compliance.
Stra...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-07-22 08:13:19
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Sr.
Analytical Scientist, Biologics
As an Sr.
Analytical Scientist, Biologics you will be part of Elanco’s R&D team, driving the development of chromatographic, electrophoretic, and LC/MS analytical methods for biopharmaceutical products.
In this role, you’ll be responsible for advancing analytical techniques for therapeutic proteins and vaccines, supporting bioprocesses, and leading method development, validation, and transfer efforts across global sites.
If you are passionate about advancing analytical methodologies and playing a key role in biopharmaceutical development, we invite you to apply and join our innovative team!
Your Responsibilities:
* Develop and optimize chromatographic, electrophoretic, and LC/MS analytical methods for vaccine and therapeutic protein products.
* Innovate and implement analytical solutions for diverse drug formulations and bioprocess support.
* Lead method validation, verification, and transfer activities across global sites and CROs.
* Train and mentor associates and scientists globally to ensure consistency in analytical practices.
* Author technical reports, review scientific documents, and maintain laboratory safety standards.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree with 12+ years or Master’s Degree with 10+ years of experience in Analytical Chemistry, Biochemistry, Biophysics, or a related scientific field.
* Experience: Extensive hands-on experience developing HPLC/UPLC-based, electrophoretic, and LC/MS analytical methods for large molecule characterization.
* Top 2 skills: Strong expertise in analytical method development and validation, with excellent problem-solving and communication skills.
What will give you a competitive edge (preferred qualifications):
* Expertise in recombinant proteins, monoclonal antibodies, oligonucleotides, and peptides.
* Experience with method validation, transfer, and qualification under GMP conditions.
* Strong statistical knowledge and proficiency with statistica...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 123500
Posted: 2025-07-21 08:04:58
-
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:
Hefei, Anhui, China, Zhengzhou, Henan, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% in c...
....Read more...
Type: Permanent Location: Zhengzhou, CN-41
Salary / Rate: Not Specified
Posted: 2025-07-21 08:00:44
-
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:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
People Leader
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
Basic purpose of the role
* Leading the EH&S organization for Janssen Biologics (JBV) site in the Netherlands (NL).
This consists in deploying, leading, and implementing EH&S strategies, policies, plans, procedures for JBV.
Key outcome is ensuring the EH&S team has taken all needed EH&S precautions to assure continuous, EH&S reliable & compliant supply chain, research & development activities, and is continuously improving in the field of EHS.
* Familiar with the annual company /division goals and aware of how he/she can influence these through his/her performance.
* Results achieved through effective leadership of the JBV EH&S team and through effective collaboration / influencing key leadership teams on the JBV EHS team as well as with J&J global EH&S.
All their needs/ improvements to be balanced with global/ local context.
The EH&S lead decides how to convert these in a lean, results oriented, compliant EHS approach.
* Responsible for developing and coordinating site EHS&S infrastructure to help GM & Site Management to ensure compliance with legislative and J&J requirements.
* Partner with Site LT to establish and implement site EHS&S strategy and Management Action Plan (MAP) in alignment with the J&J requirements.
* Responsible for site EHS&S department including budget (OPEX &CAPEX)
* Coach and mentor line management to take ownership of EHS&S.
* Ability is to reach outside J&J and represent the JBV EH&S team when meeting with governmental inspectors for the site.
Key Responsibilities
* Shared responsibility with site General Manager for EHS&S performance at the site.
Responsibility to provide advice to Site Manager for EHS&S performance at the site.
* Partner with local Management to develop and implement a site MAP to address EHS&S program deficiencies and ensure EHS&S regulatory compliance.
* Build effective working relationships with staff and key stakeholders including corporate EHS&S function and regulatory authorities.
* Develop EHS&S objectives for the site - auditing, analyzing, documenting, reporting on their implementation / effectiveness to management via dashboards, reports & management re...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-07-21 08:00:43
-
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 – Rare Diseases (Commission)
Job Category:
Professional
All Job Posting Locations:
Portland, Maine, United States
Job Description:
Johnson & Johnson Innovative Medicine is searching for the best talent for a Rare Disease Account Manager (RAM) for Immunology Autoantibody Diseases to cover the Portland, ME Territory.
This position is field based.
About Immunology
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.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases. 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 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 on patient access and affordability options.
* Analyze qualitative and quantitative market data to assess business opportunities and priorities.
* Build LHM-specific business plan and account plans to drive growth.
* Be the quarterback of...
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Type: Permanent Location: Portland, US-ME
Salary / Rate: Not Specified
Posted: 2025-07-21 08:00:40
-
Your Job
Georgia-Pacific, LLC (GP) is now hiring a R&D Process Engineer for its Tolleson, Arizona Mailers facility.
The R&D Process Engineer supports manufacturing on site including equipment installation, training, acceptance testing, performance testing, and process and equipment upgrades.
The R&D Process Engineer must be able to present data in a concise way to both technical and non-technical audiences.
We believe in the challenge process and this person must be open to the ideas and recommendations of others to create the best outcome for both the site, R&D and i2.
Typical work schedule would be weekdays from 8am-5pm.
Our Team
The GP Tolleson facility employs about 115 people and serves converting customers throughout the Southwest with sustainable packaging products.
This position provides opportunities for promotion within GP Tolleson, as well as many other Georgia-Pacific and Koch facilities across the country.
Come join our team!
You know us already! Georgia-Pacific is one of the nation's leading corrugated sheet and box manufacturers.
Check out these videos/links to learn more about the Corrugated Business at Georgia-Pacific:
www.gppackaging.com
What You Will Do
* Actively engage with Operations, Maintenance, and R&D to identify opportunities for evolutionary changes to the process and equipment
* Update process control and troubleshooting procedures and train plant personnel on current and updated process procedures
* Identify and lead process improvement projects to improve OEE (Overall Equipment Effectiveness)
* Translate learnings and technology upgrades from other sites and work with EHS and site operations to deploy on site
* Support new customer and product trials and production campaigns
* Employ process control best practices and strategies to centerline the process
Who You Are (Basic Qualifications)
* Bachelor's degree in engineering or science
* Previous experience using Microsoft Office programs and other software programs to present data (Word, Excel, Outlook, Teams, Power Bi, etc.)
* Previous experience in a manufacturing facility
* Previous experience moderating meetings and training sessions
* Must be willing and able to travel up to 25%
* 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
* Bachelor's degree or higher in Mechanical, Chemical or Electrical Engineering
* 2+ years of hands-on experience in a manufacturing facility interfacing with quality, operations leadership, maintenance and hourly employees
* Previous experience within a corrugated and/or converting manufacturing facility
* Previous experience developing and executing experiments and monitoring process data
* Previous experience leading process improvement initiatives
* Previous experience in data analysis and/or statistical software (JM...
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Type: Permanent Location: TOLLESON, US-AZ
Salary / Rate: Not Specified
Posted: 2025-07-19 10:17:37
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POSITION SUMMARY
The Safety & Training Specialist serves as a key technical resource to develop and implement the health and safety program. Ensures that working conditions at the site meet applicable federal and state laws.
Develops and implements procedures and activities that will control and reduce losses at the site.
Manages the completion of mandatory training and continuing education, maintaining accurate records.
KEY RESPONSIBILITIES
Responsibilities include but are not limited to the following:
* Comply with all company rules and regulations.
* Provide health and safety leadership and ensure a workplace free from serious hazards with a culture of health and safety across the facility.
* Research and stay well informed on new regulations and develop initial recommendations for their implementation.
Act as a resource to handle concerns regarding OSHA procedures and compliance.
* Train and work with supervisors to perform incident investigations, including root cause analysis and follow-up.
Administer and ensure compliance with IFG’s post-accident drug and alcohol testing requirements.
* Manage new employee safety training and integration into the workforce.
* Help maintain and update safety policies and procedures (such as Job Safety Analysis (JSA’s) and Safe Operating Procedures (SOP’s) and Lockout procedures (LOTO’s)), providing training to supervisors, managers, and employees.
* Help maintain chemical product inventory in the SDS management system and assist with plant environmental planning and compliance, including monthly inspections and audits.
* Update safety programs and ensure compliance with OSHA documentation requirements.
* Manage and facilitate the site safety committee.
* Initiate contact with and work with vendors to bring training to the facility and schedule offsite training.
* Utilize our Learning Management System (LMS) to develop, track, and maintain safety training records.
Regularly update supervisors, managers, and superintendent on employees’ training status.
* Other duties as needed.
REQUIRED QUALIFICATIONS
* High School diploma required
* Skills:
* Strong communication and presentation skills
* Organizational, planning, scheduling and problem-solving skills
Proficient in Microsoft Word, Excel, Outlook and PowerPoint
Intermediate proficiency in Learning Management System (LMS) administration.
Knowledge of safety principles and OSHA requirements.
* Knowledge of Industrial Hygiene including monitoring equipment (pumps, dosimeters, calibrators).
* Valid driver’s license.
* Ability to pass a drug and alcohol test, post-offer pre-employment physical, and background check.
PREFERRED QUALIFICATIONS
* Associate or bachelor’s degree in safety or related field
PHYSICAL DEMANDS
Ability to sit and/or stand for shift, reach with hands and arms, stoop, squat, bend at...
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Type: Permanent Location: Athol, US-ID
Salary / Rate: Not Specified
Posted: 2025-07-19 10:10:17
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Technician - Clinical Animal Testing
As a Quality Control Technician within our Clinical team, you will perform bio-analytical methods (immunological, in vivo, microbiological) for various Bio QC tests on raw materials, in-process, release, or stability samples in compliance with 9CFR, EU and VICH regulatory guidelines, Outlines of Production and Special Outlines. You will initiate, execute and complete assays as per approved procedures and within Quality and Compliance guidelines and communicates testing, compliance and/or scheduling issues to supervisors.
Your Responsibilities:
* Conduct animal potency and safety tests on large, small and laboratory animals such as: mice, hamsters, guinea pigs, rabbits, cats, dogs, cattle, and swine.
Testing includes animal handling, observation, vaccination, challenges, and blood collection.
* Perform potency assays with live bacterial and viral challenges such as Leptospira and Rabies.
* Maintain and prepare laboratory reagents, supplies and calibrated equipment
* Calculate results and communicate schedule, tests status and concerns.
* Revise and Standard Methods and Standard Operating Procedures (SOPs), and ensure they are up to date with current processes, as well as follow Good Manufacturing Practices (GMP) documentation.
What You Need To Succeed (Minimum Qualifications):
* High School degree and 2 years relevant experience.
* Knowledge of basic scientific principles and techniques.
* Ability to perform work following applicable methods and procedures with moderate supervision.
What Will Give You the Competitive Edge (Preferred Qualifications):
* Associate degree preferred with two years’ experience may be substituted.
* Work experience in USDA or regulated animal industry is beneficial.
* Understanding of small and large animal husbandry and handling, animal vaccination and bleeding, bacterial culture maintenance, serological assays, IACUC ACUP submissions and AALAS certification.
Additional Information:
* Location: ...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2025-07-19 09:59:19
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Global Innovation Strategy Lead – Pet Health Parasiticides & Infectious Diseases
The Global Innovation Strategy Lead – Pet Health Parasiticides & Infectious Diseases will play a critical role in defining and driving the innovation strategy of our Parasiticides and Vaccines businesses, including the refinement of innovation target areas and prioritization of pipeline assets for resource allocation.
He/she will be responsible for assessment of BD opportunities, pipeline asset forecasts at multiple milestones, as well as key inputs into the launch of global assets, including the development of global brand positioning statements, pricing recommendations and brand name selection.
Your Responsibilities:
* Lead strategic direction for assigned segments, with expertise in Elanco’s portfolio, market trends, competitive landscape, and future technologies to maximize global portfolio value.
* Oversee the commercial evaluation of Innovation Target Areas, Product Profiles, and Launch Labels, collaborating with regional marketing, R&D, and technical teams to align R&D priorities.
* Manage global brand development during launch preparations, including brand name, positioning, and pricing recommendations, while ensuring cross-functional execution.
* Develop business opportunities for pipeline entry and commercialization decisions, providing clear forecasts and scenarios to inform strategy and decisions.
* Establish governance mechanisms to ensure effective input from regional stakeholders and maintain strong cross-functional alignment across key processes and strategic initiatives.
What You Need to Succeed (minimum qualifications):
* Education: MBA preferred and/or bachelor's degree in marketing, business administration, or a related field.
* At least 10 years of experience in product marketing, brand management, project management, or product launch leadership roles.
* Minimum of 10 years of animal health experience with a detailed understanding of global dynamics in PH Prevention
* Proven understanding ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 193000
Posted: 2025-07-19 09:59:04
