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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
Irvine, California, United States of America
Job Description:
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
About the Role:
The Clinical Data Science - Lead Biostatistician will serve as a technical expert within Johnson & Johnson MedTech’s Electrophysiology business, supporting critical evidence-generation activities through robust statistical analyses and innovative methodological applications.
Reporting to the Clinical Data Science – Associate Director of Biostatistics, this individual will contribute to study design, analysis, and scientific dissemination, ensuring the delivery of high-quality, compliant, and impactful clinical data.
This role offers an excellent opportunity to influence patient outcomes while working in a collaborative, fast-paced environment.
This is a hybrid role based in Irvine, CA
Key Responsibilities:
* Provide expert statistical input for clinical trial design, analysis plans, and reporting, ensuring scientific rigor, regulatory compliance, and strategic alignment in support of device evidence generation.
* Independently develop statistical analysis plans for diverse phases of clinical studies.
Review protocols and case report forms (CRFs) to ensure proper design and methodology.
* Perform data analysis, prepare statistical reports, and contribute to scientific publications and presentations, working closely with cross-functional teams and external partners.
* Support the preparation of documentation for regulatory submissions, including statistical sections, ensuring adherence to regulatory standards and guidelines.
* Stay current with advances in statistical methods, integrating them into study strategies as appropriate.
* Maintain high standards of scientific integrity across all analyses, reports, and publications, ensuring compliance with company policies, SOPs, and regulatory requirements.
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-25 08:23:48
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Primary Care Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Shijiazhuang, Hebei, China
Job Description:
工作职责：
* 利用专业的电生理知识和技能，为术者提供手术支持，确保手术安全顺利进行；
* 熟悉客户手术习惯，与术者高效沟通，不断精进专业技能，在区域独立完成从简单到复杂的心律失常手术支持
* 紧跟行业和公司发展趋势，主动学习和掌握行业内新理念、新技术，新产品的优势和使用，能够制定针对性、可拆解的推广沟通方案
* 熟练使用新产品、数字化等新工具以及新技术，协助专业教育团队提升术者理念，技能和信心
* 有效传递新产品、新技术的价值，不断提升客户对于新技术的接受度，以安全高效的方式开展手术，服务病患
* 承担团队内教学带教工作，与团队共同进步，通过理论授课、模拟器练习、术中导管室带教、病历复盘等，有效提升新同事/初阶同事的知识和手术支持能力
* 严格遵守公司的合规政策，完成上级交予的其他任务
* 接受一定程度出差
能力要求：
* 具有自驱力，不断精进专业水平，积极学习业内不断发布涌现的新产品、新技术知识，并进行应用；
* 乐于沟通协作，与团队共同进步，共同承担团队目标，互相协助
* 有坚韧不拔的精神，遇到困难不轻易放弃，
* 有创新思维，积极探索方案并解决问题
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Type: Permanent Location: Shijiazhuang, CN-13
Salary / Rate: Not Specified
Posted: 2025-09-25 08:22:52
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
Warsaw, Masovian, Poland
Job Description:
Poszukujemy magistra farmacji z minimum 2-letnim doświadczeniem w aptece lub hurtowni farmaceutycznej, który dołączy do naszego zespołu na stanowisko Commercial Quality Specialist.
Oferta jest idealna zarówno dla osób na początku swojej kariery zawodowej, jak i tych, które chcą rozwijać się w zakresie jakości i dystrybucji produktów leczniczych.
Rodzaj umowy:
Umowa na zastępstwo na okres urlopu macierzyńskiego do kwietnia 2026.
Główne obowiązki i odpowiedzialności:
Wykonywanie zadań zgodnie ze standardami i procedurami systemu jakości dotyczącymi dystrybucji, przechowywania i transportu produktów leczniczych (GDP).
Udział w procesach Systemu Zarządzania Jakością, w tym:
* Kontrola Zmian,
* Działania Korygujące i Zapobiegawcze (CAPA),
* zarządzanie odchyleniami, reklamacjami oraz dokumentacją.
Nadzór nad dokumentacją GxP, w tym aktualizacje, dystrybucja, archiwizacja i analiza zgodności.
Udział w audytach i kontrolach wewnętrznych.
Badanie problemów jakościowych, przeprowadzanie analiz ryzyka i przyczyn źródłowych.
Udział w procesach kwalifikacji dostawców.
Przeprowadzanie szkoleń dla pracowników dotyczących Systemu Zarządzania Jakością i wymogów GxP.
Angażowanie się w projekty rozwoju jakości oraz przegląd procedur i instrukcji dotyczących jakości.
Współpraca z partnerami wewnętrznymi i zewnętrznymi.
W przypadku nieobecności Osoby Odpowiedzialnej za Obrót Środkami Kontrolowanymi:
* Zarządzanie licencjami importowymi,
* Nadzór jakościowy nad produktami zawierającymi substancje kontrolowane,
* Zapewnienie wdrożenia i aktualizacji dokumentacji związanej z dystrybucją takich produktów.
Działania wymagające fizycznej obecności w hurtowni farmaceutycznej:
* Działanie zgodnie z delegowanymi obowiązkami Osoby Odpowiedzialnej lub Osoby Odpowiedzialnej za Obrót Środkami Kontrolowanymi.
* Zwalnianie produktów do dystrybucji na podstawie dokumentacji przychodzącej.
* Obsługa reklamacji i zwrotów we współpracy z Działem Obsługi Klienta.
* Codzienna współpraca z Operatorem Logistyki.
Wymagania:
* Wykształcenie: magister farmacji.
* Doświadczenie: minimum 2 lata w aptece lub hurtowni farmace...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-09-25 08:22:35
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ERM is hiring a EHS Manager in Valencia, CA.
This is a full-time (40 hours a week), limited-term position for a duration of four months, extendable.
RESPONSIBILITIES:
* Conduct health and safety risk assessments.
* Perform field EHS observations and inspections.
* Develop and deploy safety programs such as hot work, lockout tagout, fall protection, industrial hygiene and Management of Change.
* Assist with collection, review, and analysis of field data to evaluate conditions, present information, and implement effective solutions, especially in a laboratory environment.
* Provide safety coaching, including influencing safe behavior in a dynamic work environment with front-line staff, and influence safe decision-making with leadership.
* Assess continuous changes in a research and development setting.
* Identify and implement corrective actions.
* Support our clients desire to improve H&S performance by providing field coaching.
* Participate as an enthusiastic team member on various project teams and effectively complete assignments.
* Spend time onsite at the client location to help solve their H&S challenges.
MINIMUM REQUIREMENTS:
* BS in Safety, Occupational Health, Engineering, or related science degree preferred.
* Minimum of 10 years relevant experience with exposure to the manufacturing or research and development industries preferred.
* Experience conducting health and safety risk assessments and industrial hygiene monitoring.
* Working knowledge of federal, state, and local regulations, including CAL OSHA.
* Strong written and verbal communication skills and the ability to communicate effectively.
* Ability to work independently and in a team setting, with guidance and direction.
* Strong work ethic with a passion to learn, grow, and thrive.
* Ability to distill goals into plans, develop timelines, and work independently as well as part of a team, to achieve goals.
For the EHS Manager position, we anticipate the annual base pay of $91,998.40 – $109,990.40, $44.23/hr– $52.88/hr, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/Flexforce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including Flexfor...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-25 08:21:07
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Company
Federal Reserve Bank of Richmond
Federal Reserve Bank of Richmond
When you join the Federal Reserve—the nation's central bank—you’ll play a key role, collaborating with a dynamic team of mission-driven professionals to strengthen and protect our economy and our communities.
Bring your passion and expertise, and we’ll provide the opportunities that will challenge you and propel your growth—along with a wide range of benefits and perks that support your health, wealth, and life.
About the Opportunity:
The Federal Reserve Bank of Richmond and National IT are now hiring for our 2026 Summer Intern Program.
The Summer Internship Program provides outstanding students with the opportunity to gain valuable work experience at a unique institution.
Through advanced project work assignments and professional development activities, interns are provided with an extensive understanding of the work of the Federal Reserve. Interns will be given the opportunity to enhance their business skills through critical financial analysis, formal presentations, research and writing.
In addition to specific business area tasks, you will receive targeted leadership training, mentorship and exclusive networking opportunities.
What You Will Do:
* Utilizes established methods and tools to perform moderately complex analyses of business issues
* Works with clients and other resources to assess current capabilities, identify customer needs and assist in recommendation process improvements
* Provides support in gathering, analyzing and compiling information from end-users and stakeholders to ensure processes, software and/or applications meet business requirements
* Contributes to process improvement and solution discussions, may present outcomes to management
* May participate in cross-functional team initiatives, process improvement and/or technology-based projects
* Escalates non-routine or unusual problems to higher level support staff as appropriate
Qualifications:
* Pursuing degree or advanced certification with a STEM (Science, Technology, and Engineering, or Math) focused curriculum
* Demonstrated ability to influence and lead others
* Communication and interpersonal skills, including the ability to work effectively in a team environment
* Creative thinker who embraces change
* Strong project management skills, including organization, planning, and execution, analytical and problem-solving skills
Other Requirements and Considerations:
* Candidates should review the Bank’s Employee Code of Conduct to ensure compliance with conflict of interest rules and personal investment restrictions. The Code is available on the About Us, Careers webpage at www.richmondfed.org.
* US Citizenship status is required.
Sponsorship is not available for this role.
* Selected candidate is subject to special background check procedures.
* The hourl...
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Type: Permanent Location: Richmond, US-VA
Salary / Rate: Not Specified
Posted: 2025-09-24 09:35:28
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Company
Federal Reserve Bank of Philadelphia
Job Description Summary
Research assistants (RAs) at the Philadelphia Fed play a key role in the Economic Research Department.
Whether they are helping economists prepare briefings on current monetary policy issues, working on economic forecasts, writing some of our newsletters on economic conditions, or analyzing data for long-term research projects, RAs work as an essential part of our team and gain depth of experience.
The Bank’s RA program is structured as a two-year program, with most RAs continuing on to graduate programs or other careers in economics or related fields after two years with the Bank.
Employment is at-will.
NOTE: The start date for this position will begin in the Summer of 2025!
The job description below reflects the higher level of a dual grade job posting. Candidates who possess a slightly lower level of experience, education, or qualifications may also be considered.
The salary grade for this position is 8/10.
The Federal Reserve Bank of Philadelphia is one of the 12 regional Reserve Banks that, together with the Board of Governors in Washington, D.C., make up the Federal Reserve System. It helps formulate and implement monetary policy, supervises banks and bank and savings and loan holding companies, and provides financial services to depository institutions and the federal government. The Federal Reserve Bank of Philadelphia serves eastern and central Pennsylvania, southern New Jersey, and Delaware.
Job Description
Our department prides itself on its collegial atmosphere.
RAs help one another develop their statistical, data, and programming skills.
Our economists collaborate on research with academic and central bank colleagues from around the world; as a result, so do our research assistants.
The assignments in the Economic Research Department offer our RAs a number of ways to increase their knowledge of economics and their analytical skills.
Moreover, RAs have access to a number of training and education opportunities, including courses in computer software and programming languages, as well as undergraduate and graduate courses in economics, statistics, and mathematics.
Working as a RA at the Philadelphia Fed is a rewarding experience, whichever career path you ultimately choose to pursue.
Our RAs have gone on to top graduate schools in economics, public policy and law; some have found opportunities in other departments in the Bank; and others have moved into higher positions within the Economic Research Department.
The Bank’s RA program is structured as a two-year program, with most RAs continuing on to graduate programs or other careers in economics or related fields after two years with the Bank.
Employment is at-will.
To Apply: Please attach your cover letter, resume, and unofficial transcript to the Attachments tab.
We may ask for 2 letters of recommendation, but, please do not have them sent until requested by the hiring team.
Requirements:
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Type: Permanent Location: Philadelphia, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-24 09:35:27
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your role:
Procurement team engages Contract Manufacturers (CMs) and suppliers to manufacture and package Drug Products and APIs that are supplied around the globe.
The team is responsible for the strategic sourcing of goods and services in a way that adds value to the Elanco business, by delivering cost savings, reduced supply risks and improved manufacturing network capabilities that impact the business top and bottom line.
Your responsibilities:
The primary role of this position will be to manage the API suppliers or CMs globally.
Support will consist of:
Strategic Sourcing: Conduct projects (in conjunction with global Elanco procurement API, Drug Product category owners) –category strategy development, requests for information/proposals, negotiations and contracting, financial dispute resolution and ongoing project management to ensure implementation and performance.
Relationship Management: He/ She will work closely with internal clients and be involved in relationship management with existing China/AP Regional EEM CMOs/suppliers to assure the value targeted during negotiations is realized for the business.
Monitor suppliers’ financial and compliance conditions to determine if there is risk or impact to product supply.
Opportunity Assessment: assessing potential opportunities on a regular basis that will benefit Elanco.
Monitor suppliers’ financial and compliance conditions to determine if there is risk or impact to product supply.
Participate in meetings, due diligence and visits with the EEM joint supplier/CMO management teams.
Perform market intelligence: the selected candidate will conduct site visits to potential suppliers to do an initial screening to determine if they are capable of meeting Elanco's requirements and quality standards.
This position will report to the Director of API Global Procurement - Elanco External Manufacturing
What You Need to Succeed (minimum qualifications):
* Bachelor’s degree in science, Business, Supply Chain, or Engineering
* At least 5 years of experience in Procurement with a global company
* At least 3 years of experience supporting a pha...
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Type: Permanent Location: Liverpool, GB-LIV
Salary / Rate: Not Specified
Posted: 2025-09-24 09:18:04
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Business Intelligence Solution Architect
Overview:
We seek a skilled Business Intelligence Solution Architect to join our Research & Development (R&D) department, reporting to the Development Manager of our BI and Database Administration (DBA) teams at Ingenious Med.
This role involves hands-on architecture, designing and implementing new features, and optimizing existing BI solutions.
Responsibilities include data modeling, developing data ingestion and integration strategies, implementing best practices, and evaluating new BI platforms.
The Technical Lead will collaborate closely with developers and DBAs within a small Agile SCRUM team, providing technical leadership and mentorship.
Key Responsibilities:
- Gain a thorough understanding of existing Ingenious Med solutions.
- Take ownership as a technical lead, guiding existing solutions toward target architectures.
- Participate in team design discussions to address new BI requirements.
- Deliver quality code to meet assigned requirements and user stories.
- Thoroughly test functional units of code before committing to source control.
- Assist with system integration, regression, and performance testing as needed.
- Identify opportunities for new tools to improve integration processes.
- Troubleshoot production issues and provide third-tier support when necessary.
- Engage in continuous learning to stay current with new technologies.
Key Competencies:
- Strong work ethic and commitment to quality results.
- Excellent analytical and problem-solving skills.
- Outstanding written and oral communication abilities.
- Ability to manage multiple projects simultaneously in an organized manner.
- Capacity to explain complex technical concepts in simple terms when needed.
- Adaptability to shifting priorities and effectiveness in a fast-paced environment.
- Team-oriented and highly collaborative.
- Provide technical leadership and mentorship to BI developers.
- Ensure security, scalability, and performance optimization of BI solutions.
Required Qualifications:
- Bachelor’s Degree in Computer Science or a related field.
- 7+ years of experience in BI, data engineering, or analytics roles.
- 5-7 years of experience with SQL Server and T-SQL.
- 3-5 years of experience with ETL data ingestion pipelines.
- 2-4 years of experience with MicroStrategy.
- 2-4 years of experience with Power BI.
- 2-4 years of experience with SSRS.
- 2-4 years of experience with SSIS.
Preferred Qualifications:
- Experience with source control systems.
- Proficiency with Visual Studio and Azure DevOps (ADO).
- Experience with Azure or other cloud platforms.
- Coding experience in object-oriented languages such as Java or C#.
- Scripting experience with PowerShell or Python.
- Knowledge of HIPAA and healthcare industry standards.
This position offers an opportunity to lead and innovate within our BI initiatives, contributing significantly to our organization's success.
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: 138000
Posted: 2025-09-24 09:17:09
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Your day to day
* Collaborates with regional and global leaders to develop and implement environmental targets and strategies for the America's region.
* Manages key internal environmental initiatives, including energy reporting, single-use items reduction, water, and food waste programs.
* Provides expert advice and knowledge management on sustainability issues such as carbon, energy, water, and waste.
* Leads data collection, analysis, and reporting to support environmental performance tracking and target achievement.
* Facilitates cross-functional collaboration with internal partner teams to advance environmental goals.
* Oversees regional engagement through webinars, workshops, and communication on sustainability efforts.
* Supports broader corporate responsibility programs and shares best practices with global and regional counterparts.
What we need from you
* Bachelor’s or Master’s degree in statistics, environmental science, or a related field.
* 3-5 years’ experience in environment, sustainability, carbon, or energy management.
* Strong communication skills to simplify complex concepts and engage stakeholders effectively.
* Proven project management skills for efficient program delivery and multitasking.
* Experience in environmental sustainability within the hotel sector or built environment preferred.
* Proficient in handling and reporting environmental data (energy, waste, water, GHG emissions) and skilled in Microsoft Office.
* Knowledge of environmental management systems and certifications such as ISO14001, LEED, or BREEAM.
Travel - 3 domestic trips per year
Location - Our hybrid work structure is an expectation of three (3) days a week in the ATLANTA office.
This expectation may be adjusted to evolve with the changing needs of the business.
The salary range for this role is $58,844 to $110,000.
This role is also eligible for bonus pay.
We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance, 401K, and other benefits to employees.
#LI-SM1
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-09-24 09:00:59
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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
Ensures accuracy and reliability in laboratory testing and analysis.
The QC Analytical Chemist is responsible for conducting quantitative and qualitative analysis of raw materials and products, developing analytical methods, and ensuring compliance with industry standards.
What you will do
* Conduct quantitative and qualitative analysis of raw materials and products.
* Collaborate with production teams to troubleshoot production issues.
* Ensure compliance with industry standards and regulations.
* Prepare technical documents and reports.
* Develop and validate analytical methods.
* Calibrate and maintain analytical instrumentation.
* Manage standard chemical inventory and safety protocols.
* Some duties may vary slightly by location.
Education Qualifications
* Bachelor's Degree in Chemistry or related scientific discipline (Preferred)
Experience Qualifications
* 1-3 years Analytical chemistry in a manufacturing environment (Preferred)
* 1-3 years Method development and validation (Preferred)
Skills and Abilities
* Analytical Chemistry (High proficiency)
* Quality Control (Medium proficiency)
* Laboratory Safety (Medium proficiency)
* Technical Documentation (Medium proficiency)
* Regulatory Compliance (Medium proficiency)
* Data Analysis (Low proficiency)
* Instrumentation Calibration (Low proficiency)
* Method Validation (Low proficiency)
* Chemical Handling (Low proficiency)
* Collaboration (Low proficiency)
To Staffing and Recruiting Agencies:Our company does not accept unsolicited curriculum vitae’s or applications from agencies.
We are not responsible for any fees related to unsolicited curriculum v...
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Type: Permanent Location: Elkhart, US-IN
Salary / Rate: Not Specified
Posted: 2025-09-24 08:53:56
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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
Das Clinical Manufacturing Network (PTDN) stellt bahnbrechende Therapien aus den klinischen Phasen her, um Patienten in aller Welt zu versorgen – und dies jeden Tag.
Unser Kerngeschäft ist die Produktion sicherer, innovativer und wirksamer Arzneimittel, wobei hochmoderne Technologien in Herstellungsverfahren für Wirkstoffe und Arzneimittel zum Einsatz kommen.
Innerhalb unserer Sektion Science & Technology streben wir nach prozesstechnologischer Exzellenz, um höchste Qualität und regulatorische Compliance im Drug Product Clinical Supply Center (Parenterals) in Basel zu gewährleisten.
Gemeinsam zeichnen wir uns verantwortlich für die Herstellung und Abfüllung von sterilen Darreichungsformen aus dem globalen Forschungs- und Entwicklungsportfolio.
Für die Belieferung klinischer Studien der Phasen I–III stehen zukunftsorientierte Fertigungsanlagen in einem modernen Gebäude zur Verfügung.
Wir streben eine fürsorgliche und empathische Netzwerkorganisation an, die eine Kultur des Vertrauens und der Zusammenarbeit lebt.
Unsere engagierten Mitarbeitenden treiben Innovationen durch ihr Fachwissen, ihre Leidenschaft und ihre "Get-it-done"-Mentalität voran.
Dabei steht der Nutzen für den Patienten im Mittelpunkt unserer Überlegungen und Bemühungen.
Was Dich erwartet
Als CCS Manager & Operational Aseptic Assurance Lead spielst du eine entscheidende Rolle bei der Wahrung der Integrität aseptischer Herstellungsprozesse und der Aufrechterhaltung von Contamination Control Standards, die die Sterilität unserer Arzneimittel gewährleisten.
Eine effektive CCS-Implementierung in allen Abteilungen und Produktionseinheiten einschließlich regelmäßiger Schulungen ist hierfür unerlässlich.
Du stellst eine CCS Governance Structure sicher, die eindeutige Zuständigkeiten vorsieht sowie klare und nachvollziehbare Prozesse zur Aufrechterhaltung und Verbesserung des Kontaminationskontrollstatus garantiert.
Als Senior Expert gehst du fachlich in Führung, berätst die Organisation und lebst Ownership vor.
In dieser Rolle berichtest du direkt an den Section Lead Science & Technology.
Du wirst in deinem Aufgabengebiet die folgenden Verantwortlichkeiten übernehmen:
* Pflege und kontinuierliche Verbesserung der standortweiten Contamination Control Strategy (CCS) gemäss regulatorischer Anforderungen (u.a.
Annex 1), interner Vorgaben und Industry Best Practices mittels kontrolliertem Änderungsmanagement
* CCS-Wirksamkeit bewerten, sichtbar unter Kontrolle halten, r...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-09-24 08:53:12
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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
Das Clinical Manufacturing Network (PTDN) stellt bahnbrechende Therapien aus den klinischen Phasen her, um Patienten in aller Welt zu versorgen - und dies jeden Tag.
Unser Kerngeschäft ist die Produktion sicherer, innovativer und wirksamer Arzneimittel, wobei hochmoderne Technologien in Herstellungsverfahren für Wirkstoffe und Arzneimittel zum Einsatz kommen.
Innerhalb unserer Sektion Science & Technology streben wir nach prozesstechnologischer Exzellenz, um höchste Qualität und regulatorische Compliance im Drug Product Clinical Supply Center (Parenterals) in Basel zu gewährleisten.
Gemeinsam zeichnen wir uns verantwortlich für die Herstellung und Abfüllung von sterilen Darreichungsformen aus dem globalen Forschungs- und Entwicklungsportfolio.
Für die Belieferung klinischer Studien der Phasen I–III stehen zukunftsorientierte Fertigungsanlagen in einem modernen Gebäude zur Verfügung.
Wir streben eine fürsorgliche und empathische Netzwerkorganisation an, die eine Kultur des Vertrauens und der Zusammenarbeit lebt.
Unsere engagierten Mitarbeitenden treiben Innovationen durch ihr Fachwissen, ihre Leidenschaft und ihre "Get-it-done"-Mentalität voran.
Dabei steht der Nutzen für den Patienten im Mittelpunkt unserer Überlegungen und Bemühungen.
Was Dich erwartet
Als Team Lead Cleaning & Biodecontamination Validation übernimmst du die fachliche und disziplinarische Führung einschlägiger Expert:innen.
Du verantwortest die Sicherstellung des cGMP-Status unserer validierten Reinigungs- & Dekontaminationsprozesse zur Herstellung klinischer Prüfpräparate zur parenteralen Applikation.
Dir obliegt die Ressourcenplanung des Teams hinsichtlich allfälliger (Re-)Validierungen.
Du fokussierst dich auf System- & Prozessoptimierungen und bist fachlicher Ansprechpartner für prozesstechnische wie regulatorische Fragestellungen.
Durch deine konzeptionelle Arbeit stellst du regulatorisch konforme Prozesse und Verfahren sicher und vertrittst diese bei Inspektionen.
Du vernetzt dich intern wie extern in fachspezifischen, globalen Gremien, um strategische Entscheidungen, harmonisierte Standards und prozesstechnologische Entwicklungen zu initiieren und aktiv mitzugestalten.
Dein fundiertes Verständnis für cGMP-Compliance bildet die Basis deiner Bemühungen.
Du wirst in deinem Aufgabengebiet die folgenden Verantwortlichkeiten übernehmen:
* Disziplinarische wie fachliche Führung eines Teams von 5-10 Expert:innen im Bereich Dekontaminationsvalidierung und Reinigungsv...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-09-24 08:52:30
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Spring 2026 Co-Op in Downstream Bioprocessing, located in Malvern, PA.
Research & Development Co-Op Overview:
J&J R&D encompasses the development of sophisticated materials, process improvements, risk management and mechanical testing through the development process across all sectors including Pharmaceutical, Medical Device, Consumer and Corporate/Enterprise.
We offer a fast-paced cross-functional, technologically advanced, corporate environment, passionate about developing individual engineering and scientific skills.
You will have the opportunity to learn about anatomy, disease states, deformities and the surgical procedure/products used to address these conditions.
Life as an R&D Co-Op:
The R&D Co-Op program provides each student with real-life hands-on experience, coaching and mentoring, networking opportunities, as well as the opportunity to meet people from various schools throughout the country.
Each Co-Op will be assigned to a single function with a specific project for the 6-month term.
The typical Co-Op term is from Jan 2026– Jun 2026.
Key Responsibilities:
The TDS Proteins Development API organization is seeking a candidate interested in protein process development.
Various chromatography methods are utilized in the downstream sphere to purify protein molecules from process impurities and aggregates.
Assessing the impact of product- and process-related impurities such as high molecular weight species (HMWS) and host cell impurities, respectively, on final drug substance (DS) stability is crucial for development of potent biopharmaceutical products and for establishing downstream bioprocesses to effectively balance yield with product quality.
In this role, the Co-Op will...
* Study the impact of variable levels of HMW content and co-associated host impurities on stability-indicating attributes across two model antibody products.
* Purify biopharmaceutical products to achieve variable levels of HMW content through targeted control of cation exchange (CEX) and multi-modal anion exchange (MMAEX) process operating conditions.
* Evaluate stability-indicating quality attributes of drug substance across different HMWS experimental test ...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-24 08:44:55
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Notting Hill,, Victoria, Australia
Job Description:
* Great Place to Work® Certified - 2024
* Competitive salary package, flexible work practices, award winning benefits
* Role based in Melbourne
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 VIC 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 co...
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Type: Permanent Location: Notting Hill,, AU-VIC
Salary / Rate: Not Specified
Posted: 2025-09-24 08:44:19
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PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) process.
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Type: Permanent Location: West Monroe, US-LA
Salary / Rate: Not Specified
Posted: 2025-09-23 13:48:23
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PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) proces...
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Type: Permanent Location: Bastrop, US-LA
Salary / Rate: Not Specified
Posted: 2025-09-23 13:48:21
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Your Job
Georgia-Pacific is seeking a Lab Services Intern to join our teams in Summer 2026 at our Technical Center in Neenah, WI! This paid internship will provide the ideal opportunity for an early career student in the Science Field to work in a multi-lab environment.
The intern will be responsible for performing testing of products received from mills and consumers to ensure compliance and quality throughout the product lifecycle.
The focus will be in physical testing with possible exposure to another lab testing if needed.
Our Neenah Technical Center® is the central site for research, development, and lab services for Georgia-Pacific North American Consumer Products division.
The research and development areas include Commercial and Retail towels, tissues, napkins and dispensers, Dixie® products, and process development with the following lab capabilities: Physical Testing Lab, Analytical Lab, Microbiology Lab, Microscopy Lab, and Fiber Lab
Georgia-Pacific, a Koch company, is one of the world's leading manufacturers and marketers of building products, tissue, packaging, paper, cellulose, and related chemicals.
The company employs more than 30,000 people at approximately 300 locations in North and South America.
Georgia-Pacific creates long-term value by using resources efficiently to provide innovative products and solutions that meet the needs of customers and society, while operating in a manner that is environmentally and socially responsible and economically sound.
Our Team
We believe that everyone should be an entrepreneur no matter what role they are in.
As an intern, co-op, or full-time hire, there are countless opportunities for you to be challenged, have your voice heard, and gain real experience within our companies.
Sound exciting? Do you want to be a part of meaningful work? Kickstart your career with us by applying today!
What You Will Do
* Test products submitted by lab's clients
* Input test results into a database, verifying data and reporting out results to clients
* Opportunity to work on projects in different lab environments
At Koch, interns gain real-world, hands-on experience, with the opportunity to tackle significant projects, solve problems, and take ownership of their work.
Alongside your day-to-day role, the Koch Intern Program offers an opportunity to learn more about Koch, our people, Principle Based Management, and the local community you will be working in, all while growing your network.
Through weekly learning sessions, location-specific programming, and professional development, we aim to help every individual grow and learn how they can best contribute.
This 12-week program will allow you to experience Life at Koch , as you start your career and go anywhere within our network of companies.
Who You Are (Basic Qualifications)
* Enrolled in a Science degree program
* Able to work full-time in the summer
* Ability to relocate per program requirements
* Legal autho...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-23 13:47:02
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Position Summary:
We are seeking a highly motivated and detail-oriented Global Pricing and Data Administrator. In this role, you will be asked to use your judgement and discretion to create the architecture for, and maintenance of the accuracy, consistency, and integrity of customer pricing and product data.
This role involves collaboration with multiple global departments, including product management, sales, and IT, to ensure effective pricing execution and data governance.
Responsibilities Include:
* Customer Pricing Administration – Generate customer pricing based on market, supplier, commodity pricing, and input from sales and product management.
Work closely with global divisions to create and maintain pricing in our ERP and PIM system for use in software integrations and printable Pricebooks.
Create and update OEM customer price books based on indexing agreements and product material makeups.
Ensure implementation of pricing across platforms and customer systems. Assure consistent pricing for global customers across all regions.
* Classify Product Data – Accurately classify and categorize product information in the PIM software (Perfion) to meet business requirements and standards.
* Data Enrichment and Quality Assurance – Enhance product data by adding attributes, perform regular audits for accuracy and consistency, and develop standardization practices in partnership with Product Managers.
* Reporting and Analysis – Generate interpret and publish reports on customer, product, and segment gross margin and sales/price variance data to identify trends, gaps, and opportunities.
Recommend strategic adjustments based on findings.
* Translation Support – Collaborate with local users to ensure accurate multilingual attribute translations across regions.
Nature and Scope:
* Exercises discretion in developing pricing strategies and in interpreting complex data to recommend commercial actions.
* Makes independent decisions regarding the structure, classification, and maintenance of large datasets with commercial impact.
* Identifies data inconsistencies and proactively recommends process improvements or policy updates to management.
* Acts as a key contributor in shaping pricing implementation processes and data management standards across departments and regions.
Knowledge, Skills, and Abilities:
* Technical Skills: Advanced Excel skills a must.
Power Query and Power BI preferred.
* Product Information Management (PIM) systems, data management tools, and database models.
Perfion preferred.
* Experience with ERP and CRM systems, especially LN (BaaN) and D365, preferred.
Minimum Requirements:
* Bachelor’s degree minimum.
* 2 years experience working with pricing and data systems.
* Must be able to speak, read, and write English at high school level minimum.
* Permanent work authorization for the USA preferred.
* Familiarity with Mic...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-22 08:06:13
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Your Job
INVISTA, a Koch company, are seeking a motivated and detail-oriented Plastics / Polypropylene Intern to join our R&D team and support our polypropylene manufacturing processes.
This role provides hands-on experience in the formulation, testing, and optimization of resin products within a dynamic and collaborative product development environment.
Throughout the internship, you will deepen your understanding of polymer development, processing, and manufacturing while working closely with experienced professionals who will mentor and guide you through real-world challenges in the resin industry.
Additionally, you will play an active role in driving innovation by contributing to the creation of sustainable and cutting-edge material solutions, gaining valuable insights into advanced industry practices and technologies.
The Product Development Internship will be for an initial duration of 90 days with potential to extend as business needs permit.
The R&D Development Intern offers flexible scheduling options M-F to balance our needs with the selected individual's school schedule.
Anticipated hours are 15-20 hours per week.
What You Will Do
* Demonstrate and develop strong analytical.
problem-solving skills, communication and teamwork.
* Partner with the R&D team to explore and refine new resin formulations through hands-on testing and experimentation.
* Collaborate on analyzing the physical and chemical properties of resin samples to enhance product performance.
* Work alongside technical and customer-facing teams to address and resolve customer challenges effectively.
* Coordinate lab testing activities by facilitating requests, managing data, and interpreting results.
* Engage and collaborate with cross-functional teams, including Quality, Manufacturing, and Sales, to foster alignment and drive innovation.
* Contribute to the preparation of technical insights by assembling reports and delivering presentations.
* Support operational excellence by partnering in areas such as quality improvement, process changes, and project initiatives based on business priorities.
Who You Are (Basic Qualifications)
* College Junior or Senior currently pursuing a Bachelor's degree in Chemical Engineering, Materials Science, Polymer Science, Chemistry, or any Science, Technology, Engineering or Mathematics (STEM) discipline.
* MS Office Experience (Outlook, Word, Excel, PowerPoint).
* 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
* Experience applying polymer chemistry or material testing methods.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount ...
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Type: Permanent Location: Longview, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-22 08:03:36
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
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: 2025-09-22 07:59:37
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Bray Commercial is seeking an experienced and detail-oriented Quality Control Inspector to join our team in a fast-paced industrial manufacturing environment.
This role offers an exciting opportunity to contribute to a global leader in industrial valve and actuator solutions.
If you are passionate about quality assurance and have a strong background in inspection within a manufacturing setting, we encourage you to apply.
Job Summary
The Assembly Line – Quality Control Inspector is responsible for ensuring that assembled products meet all applicable quality standards, work instructions, checklists, and customer-specific requirements prior to final packaging and shipment.
This includes performing in-process inspections during assembly, final verification, proper labeling, and documentation.
The role is vital to maintaining product integrity, customer satisfaction, and reducing costly errors or rework.
Key Responsibilities
* Conduct in-process and final inspections of assembled products for conformance to engineering drawings, work instructions, and customer requirements.
* Review special instructions and order-specific checklists to ensure consistent compliance throughout the assembly process.
* Identify, document, and report defects or quality concerns to the Quality Manager.
* Provide feedback to production leadership regarding assembly personnel who may require retraining or process reinforcement.
* Maintain accurate inspection records and ensure traceability of inspected units.
* Support and participate in continuous improvement initiatives.
* Suggest and implement process or procedural enhancements as appropriate.
* Communicate clearly and professionally with team members across multiple departments.
Core Competencies
Knowledge
* Basic understanding of mechanical and electrical assembly principles.
* Familiarity with standard quality inspection practices (visual, dimensional, and functional).
* Ability to interpret engineering drawings, assembly procedures, and work instructions.
* Awareness of quality tools such as checklists, non-conformance logs, and corrective action reports.
Skills & Abilities
* Strong observational skills with high attention to detail.
* Effective interpersonal and communication skills.
* Proficient in Microsoft Excel; experience with ERP systems is a plus.
* Ability to multitask and prioritize in a fast-paced production environment.
* Self-motivated and capable of working independently with minimal supervision.
* Competent in basic math and measurement using inspection tools (e.g., calipers, rulers).
* Physically able to stand or walk for extended periods.
Qualifications & Experience
* High School Diploma or equivalent (required).
* Minimum of 2 years of experience in quality control or quality assurance in a manufacturing environment, preferably with both mechanical and electrical assemblies....
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-21 08:16:59
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role:
As a Principal Engineer, you will be a key member of our software engineering team, driving the modernization of Elanco Knowledge Solutions (EKS).
You will partner with product managers, architects, and platform teams to design and deliver modern, scalable, and secure digital products that enable data-driven insights and improve customer outcomes across the animal health ecosystem.
Your Responsibilities:
* Develop full-stack solutions, building scalable distributed systems that support business growth and positive user experiences.
* Implement and support modern digital products, ensuring compliance, security, and stability.
* Partner with product managers to shape backlogs, size initiatives, and design engineering approaches.
* Collaborate with Platform Engineering to influence product direction and improve developer efficiency.
* Contribute to Elanco’s engineering community by sharing best practices and coaching peers.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree in Information Technology.
* Experience: 10–15 years of engineering experience, including 8 years of technical leadership.
* Skills: Strong organizational and communication skills with the ability to convey complex technical topics; demonstrated stakeholder engagement and vendor management experience.
What Will Give You a Competitive Edge (preferred qualifications):
* 5–10 years working with modern application architecture methodologies (SOA, API-centric, 12-Factor, FAIR).
* 5+ years designing cloud-native solutions (Azure or Google Cloud preferred).
* 5+ years delivering digital solutions using product-mindset and Agile/iterative methods.
* Proven hands-on software engineering expertise with modern web technologies (TypeScript, JavaScript, Node, React/Next.js).
* Experience with DevSecOps practices, CI/CD pipelines, TDD, Kubernetes, Terraform, and Ansible.
* Knowledge of modern data practices (Databricks, ML models, Lakehouse architectures).
* Experience with API-first integration patterns and...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 158000
Posted: 2025-09-21 08:11:45
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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
The position will include routine testing of in process antigens and final product samples for the release of veterinary vaccines. The individual will be responsible for ensuring all methods are performed as written and filed with regulatory agencies and standard operating procedures.
Your Responsibilities:
* Perform required tests for bulk antigens, final products, and raw materials, as well as other procedures necessary to support company and laboratory objectives to meet specified timelines.
* Maintain aseptic laboratory technique at all times and ensure accuracy of test results through precision and attention to detail.
* Maintain accurate and concurrent testing records and ensure compliance with Company SOPs and specifications, USDA, and cGMP regulations. Assist with updating, writing, and maintaining SOP’s, bench records and data entry for the department.
* Environmental monitoring of clean rooms and personnel: assisting in and/or performing microbial and particulate tests (air sampling).
* Provide effective training as requested, confirming that individuals are trained on the procedure at hand and all required training documentation has been completed.
What you need to succeed (minimum qualifications):
* High School Diploma or equivalent required.
* Experience in working in a team environment and handling multiple tasks simultaneously.
* Proficient in Microsoft Word and Excel, capable of using a controlled informatics system.
What will give you the competitive edge (additional preferences):
* Bachelor of Science degree in Microbiology, Virology, Bacteriology, Biology, or related field
* Laboratory experience including cell culture, viral and/or bacterial propagation.
* Experience in biotechnology and aseptic technique.
Other Information:
* Location: Winslow, ME (Onsite)
* Shift: Monday-Friday, 7am-3:30pm (evening, weekend, and holiday hours may be required)
* Must be able to pass a background check and gain Select Age...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: 25
Posted: 2025-09-21 08:11:44
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ERM is seeking a self-starting, dynamic Consulting Associate, Biological Technician to join our Capital Project Delivery team in Overland Park, KS.
As part of our team, you will provide high-quality field data collection for ERM client projects while working closely with project managers, task managers, field team leaders, and other team members.
Assignments will primarily involve field work and will include domestic travel 50% or more of the time.
This is an excellent opportunity for a junior professional looking to advance his or her career level with a global sustainability leader.
The individual selected to fill this full-time position will perform biological and environmental field surveys to gather data for a range of client projects.
The Environmental Technician will also assist project managers, staff scientists, and senior scientists with data management and report writing related to various environmental tasks.
RESPONSIBILITIES:
Field data collection for various surveys, including:
* Eagles and raptor surveys;
* Threatened/Endangered wildlife/plant surveys;
* Bat mist-netting and acoustic surveys;
* Wetland delineations and habitat assessments;
* Field data collection for permit applications and environmental reports;
* GPS data collection and mapping support;
* Assisting project and task managers with and preparing portions of written reports, tables, spreadsheets, databases, and maps.
REQUIREMENTS:
* BS in biology, ecology, natural resources, wildlife management, soil science or related field.
MS degree a plus.
Or equivalent experience.
* 1+ years (3+ preferred) of experience.
* Excellent writing and grammar skills
* Ability to walk at least 10 miles per day in rough terrain and lift up to 50 lbs.
* Willingness to work in team environments or independently.
* Willingness to travel and conduct fieldwork in potentially remote areas for extended periods (1-4 weeks)
* Knowledge of ARGIS Field Maps and Survey 123
* US citizenship or permanent US residency
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Must be able to pass a pre-employment drug screen
* This position is not eligible for immigration sponsorship.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us crea...
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Type: Permanent Location: Overland Park, US-KS
Salary / Rate: Not Specified
Posted: 2025-09-21 08:03:17
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Job Description
We are seeking a highly motivated researcher to join our team for conducting cutting-edge theoretical and experimental research on super-resolution imaging for two- and three-point sources.
The candidate will also explore the enhancement of super-resolution techniques using machine learning methods.
This position offers the opportunity to collaborate with a dynamic team of researchers and contribute to advancements in imaging technologies.
Responsibilities:
Theoretical and Experimental Research:
* Design and execute theoretical models, collaborate on experimental setups and measurements, for super-resolution imaging of two- and three-point sources.
* Analyze and interpret experimental data to validate theoretical predictions.
* Develop innovative methods to push the boundaries of super-resolution imaging.
Machine Learning Integration:
* Investigate and implement machine learning algorithms to enhance super-resolution imaging techniques.
* Collaborate with machine learning experts to integrate advanced computational methods into experimental workflows.
Technical Proficiency:
* Utilize LaTeX for the preparation of technical documents, research papers, and presentations.
* Employ Python and Matlab for data analysis, simulation, and algorithm development.
* Use PowerPoint for creating engaging presentations.
Dissemination of Research:
* Prepare and submit research findings to high-impact conferences and peer-reviewed journals.
* Present research outcomes at national and international conferences, workshops, and seminars.
Qualifications
* Doctoral degree in Quantum Physics, Optics, or related fields.
* Strong research background in quantum physics.
* Experience with optical imaging.
* Experience with machine learning techniques.
* Proficiency in LaTeX, Python, Matlab, Microsoft Word, and PowerPoint.
* Excellent written and verbal communication skills.
* Ability to work collaboratively in a multidisciplinary team environment.
Application Process
Interested candidates should submit the following materials:
* A detailed CV highlighting relevant experience and publications.
* A cover letter describing your research interests and how they align with this position.
* Application Deadline: November 15th 2025.
For detailed information, please contact Prof.
Xiaofeng Qian at xqian6@stevens.edu
Department
Physics
Compensation Range
In compliance with the New Jersey Wage Transparency Act, the annual base range for this position is $45,000- $48,500 .
This range represents the University’s good faith estimate of possible compensation at the time of posting.
Stevens Institute of Technology determines compensation based on factors including the position’s scope and responsibilities, the candidate’s experience, education, skills, internal equity, market data, and organizati...
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Type: Permanent Location: Hoboken, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-20 08:43:53
