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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:
Pharmaceutical Product R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
San Diego, California, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for an Experienced Scientist, Discovery Pharmaceutics in San Diego, CA.
Purpose: J&J Innovative Medicine Research & Development develops treatments that improve the health and lifestyles of people worldwide.
R&D development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, diabetes, hematology, metabolic disorders, immunologic disorders, pulmonary hypertension and reproductive medicine.
Within Pharmaceutical Product Development & Supply (PPDS), we are recruiting a talented Experienced Scientist to our Discovery Pharmaceutics team, based in San Diego, CA.
We are seeking an Experienced Scientist for a laboratory-based position to generate high-quality data in support of Discovery programs within our Synthetic portfolio, which includes small molecules, degraders, peptides, and oligonucleotides.
In this role, the individual will conduct experiments and provide functional input to Discovery teams to influence molecular design and drug delivery, as well as assist in the identification and selection of solid-state forms of APIs.
Additionally, you will develop and manufacture formulations (both conventional and enabling) for pharmacological, pharmacokinetics, and toxicological studies.
The successful candidate will thrive in a multidisciplinary collaborative environment and is expected to make substantial contributions to our innovative drug discovery efforts.
You will be responsible for:
* Conduct routine and non-routine experiments while providing data interpretation and draw conclusion.
* Contribute to technical documentation and reports, and maintain an electronic lab notebook in compliance with internal policies.
* Proactively identify and troubleshoot issues r...
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Type: Permanent Location: San Diego, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-24 08:14:32
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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:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Provides statistical support to specific segments of a study/development program, including analysis, interpretation, design, and reporting or communication of data evidence for research, development, and/or marketed product needs in Janssen.
Demonstrates data analytics expertise based on a foundation of statistical principles and uses relevant computational tools for study, experiment, or trial research objectives.
Ensures application of appropriate statistical methods and generation of accurate and reproducible results working independently or by providing specifications to statistical programming colleagues.
Produces clear, concise, well-organized, and error-free computer programs and statistical reporting content.
Collaborates and communicates effectively with cross-department team members and senior colleagues to deliver on goals and objectives.
Proactively recognizes need for additional help for complexities or integration beyond on own expertise.
Coaches more junior colleagues in techniques, processes and responsibilities.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-04-24 08:14:23
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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:
Legal & Compliance
Job Sub Function:
Enterprise Compliance
Job Category:
People Leader
All Job Posting Locations:
BE009 Turnhoutseweg 30, BE012 Diegem, CH002 Gubelstrasse, Zug, CZ005 Walterovo Namesti, IE007 Castletroy Limerick, IE012 Liffey Valley
Job Description:
The Johnson & Johnson Global Trade Controls (GTC) function, part of Johnson & Johnson’s Technical Operations and Risk organization, is recruiting for a GTC EMEA Manager, located in Belgium, Czech Republic, Ireland or Switzerland, preferably near an EMEA Johnson & Johnson (J&J) site.
In GTC, we provide centralized cross-functional governance and advisory support to J&J Family of Companies, across the Innovative Medicine and Medical Technology segments.
As the GTC EMEA Manager, you will provide guidance & direction on global trade topics such as product classification, country of origin, duty optimization, customs valuation, export controls and will drive compliance with GTC Global Standards.
Are you ready for a new challenge? Are you motivated to join a diverse team delivering outstanding results? Apply now for this exciting opportunity!
Key Responsibilities:
Act as key contact for the deployment, regional implementation & governance of global customs data, processes and technology solutions across the EMEA region
Guide J&J businesses on emerging and existing import and export trade regulations
Participate in key projects to represent Trade Controls requirements and ensure efficient and compliant trade flows
Measure, monitor and govern compliance, operational performance and regional third-party providers per global process and scorecards
Collaborate across teams and functions, incl.
R&D, Finance, Operations and Supply Chain to build trust, influence, empower self and others, practice diversity and inclusion, and make informed and timely decisions
Qualifications
Education:
Bachelor or masters degree (Supply Chain, Transport & Distribution, Logistics, International Studies, Legal, Economics, Financial)
Experience and Skills:
Required:
* Minimum of 7+ years of business experience with focus in Customs or Trade Controls
* Experienced across trade compliance competencies including: HTS code determination, customs valuation principles, rules of origin, free trade agreements, incoterms, export control classification, AEO in EMEA, etc.
* Customer & result oriented and a can-do attitude
* Experience leading...
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-04-24 08:14:07
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ERM is seeking a Principal Technical Consultant, Climate Change to join our growing corporate sustainability and climate change advisory services practice in across North America.
In this role, you will be a key contributor to a team developing and growing ERM’s corporate sustainability and climate change business.
ERM delivers a wide range of climate change services including decarbonization strategy development, creation of Scope 1, 2, and 3 carbon inventories, Task Force on Climate-related Financial Disclosure (TCFD) analysis and reporting, strategy development, policy and regulatory analysis, target setting, and benchmarking.
We help clients, including global companies, electric and natural gas utilities, and financial institutions, develop and implement climate change programs across a broad range of industry sectors and contribute to climate, clean energy, and clean transportation policy development.
This is an excellent opportunity for an experienced professional looking to play a key role working with an expert consulting team on leading-edge climate advisory projects for Fortune 500 and privately held clients.
RESPONSIBILITIES:
Managing Clients and Projects
* Demonstrates expertise in the evaluation of oil and gas, chemical, and/or manufacturing processes to evaluate GHG emissions.
* Advises and manages climate-related projects including the design and development of GHG inventories (Scopes 1, 2 and 3) analysis of emission reduction levers (e.g.
energy efficiency measures, renewable energy, decarbonized fuels), and strategic policy assessment and design.
* Supports development of climate change strategy, action planning, and/or modeling with regards to mandatory or voluntary drivers.
* Builds strong and trusted relationships with clients and/or business partners
* Thinks strategically in order to influence decision-makers and outcomes.
* Distills complexity from detail to effectively coach colleagues to deliver high-quality outputs.
* Demonstrates strong project management skills and oversight through the project lifecycle, including scoping, budget and delivery.
* Demonstrates strong analytical skills, excellent writing and presentation skills, and a mastery of impactful client communication.
Teamwork and Organization
* Demonstrates strong people management skills; particularly the ability to support, coach and celebrate others to advance employee engagement and achieve results.
* Mentors junior staff in the proper planning and execution of projects, and in directing or conducting independent technical reviews of deliverable work products.
* Manages a team of two to five junior consultants.
* Identifies, evaluates, cultivates and manages partnerships and relationships with senior clients, external stakeholders and key opinion leaders.
* Effectively collaborates internally to bring our services to existing clients.
* Enhances ERM’s capability to support s...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-24 08:13:23
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Company
Federal Reserve Bank of St.
Louis
The St.
Louis Fed hires several Research Associates each year.
Start dates for this search are in the Spring or Summer of 2025.
This is an excellent opportunity to work with, learn, and engage with our reputable economist staff, visiting fellows and scholars.
Former St.
Louis RAs have continued their careers in other Bank divisions, in PhD programs, and in the private sector.
More Information can be found in the RAjobs link below under the success stories tab.
Visit https://research.stlouisfed.org/RAjobs/ for a detailed overview of the RA position.
What are the day-to-day activities?
* Perform statistical, econometric, computational and analytical research that economists can use for publication in academic journals.
* Utilize Excel and statistical packages such as Stata, R, Matlab, Julia, Python, and SAS.
* Collect, organize and interpret economic and financial data.
* Review academic journals, market sources and government reports.
* Write short articles or assist economists in developing short articles and presentations on current economic and financial conditions and policy issues.
* Attend to additional assignments, including gathering and organizing survey data and anecdotal information and summarizing economic data for the Beige Book.
Qualifications
* A GPA of 3.5 or above
* Bachelor’s degree in economics, econometrics, or quantitative economics
* Strong background in mathematics and statistics, including coursework in Calculus II, Econometrics, Linear Algebra, and Differential equations
* Previous economic research experience, such as undergraduate research assistant, research-related internship or independent research project.
How to Apply
Interested applicants must submit the documents requested below at the following link: EJM - Econ Job Market
NOTE: Applications will not be considered without all of these materials or if they do not apply on EJM.
* Cover letter
* CV/Resume
* Copy of unofficial transcripts from all colleges and universities attended
* Technical writing sample
* Completed applicant summary file using the following file (.docx): https://www.stlouisfed.org/-/media/project/frbstl/stlouisfed/research/careers/2025-ra-applicant-summary-file-st-louis-fed.docx?sc_lang=en&hash=4B75599CB455E5DC21F4AFDCBA67BD37"
For questions or concerns, contact: ra.recruiting@stls.frb.org
Benefits
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.
In addition to great compensation package, we offer a comprehensive benefits package that includes tuition assistance, generous paid time off, top-notch health care benefits, child and family care leave, professional development opportunities, a 401(k) match, pension, and more.
All brought together in a flexible ...
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Type: Permanent Location: St. Louis, US-MO
Salary / Rate: Not Specified
Posted: 2025-04-23 08:35:26
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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: Applied Immunology Scientist
As a Applied Immunology Scientist, you will be part of Elanco’s Mechanistic Biology team, working to advance next-generation drug discovery in Animal Health.
In this role, you’ll be responsible for driving target identification and validation, derisking potential on- and off-target effects, building collaborations, and contributing to translational disease models for small and large animals.
Your Responsibilities:
* Identify and validate immune system targets for solutions in animal health, addressing on- and off-target risks in the context of the animal’s life stage and clinical setting.
* Address gaps in immunological assessments, immunogenicity risks, developing innovative solutions, tools, and collaborations to enhance capabilities.
* Provide expertise in translational and target animal models, leveraging knowledge of human, small, and large animal immunology.
* Design, implement, and oversee animal studies and experiments, ensuring scientific integrity, animal welfare, and regulatory compliance.
* Apply advanced immunological techniques, including flow cytometry, transcriptomics (bulk, single cell, and spatial), proteomics, and biomarker characterization, to support research and development projects.
* Contribute to the progression of projects by designing strategies, tracking budgets and timelines, and maintaining study documentation.
* Support clinical studies and safety evaluations, utilizing knowledge of PK/PD, diagnostics, and the clinical landscape across species.
* Serve as a recognized leader in applied immunology, advancing expertise in state-of-the-art immunological assessments and model development.
What You Need to Succeed (minimum qualifications):
Education:
* Doctor of Veterinary Medicine (DVM) and/or PhD in immunology (DVM with PhD preferred).
A master’s degree (e.g., in immunology, veterinary sciences, or a related field) plus 4 years of relevant experience
Experience:
* Expertise in human, small animal, an...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 141000
Posted: 2025-04-23 08:28:24
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The Harris Public Sector Group's Schools' division is looking to hire a Financial Analyst accountable for providing financial assistance and examine for the division.
You will work with fellow Analysts, AR/AP Clerks, the Controller, and the business unit's Vice Presidents.
You will have a chance to join a fast-paced organization with a large, stable, and growing presence in the vertical market software industry!
We are looking for a candidate on the CPA path with accounting experience and proven data-based skills with attention to detail.
Reporting to the Controller, you will perform month, quarter, and year-end closing tasks, in addition to working with the Business Unit on various ad hoc projects.
WHAT WILL BE YOUR NEW ROLE
* Build relationships with and providing excellent customer service to the business unit(s)
* Completing the month-end and quarter-end close processes by breaking down results, preparing journal entries and detailed reconciliations, and reporting for senior management
* Tracking & breaking down deferred maintenance, hardware, software, and professional services revenue streams
* Forecast benefits, payroll taxes and depreciation and updating actual results for headcount, bookings, and backlog
* Calculate commissions owed based on invoicing/bookings
* Assisting with special projects & ad hoc reporting as needed by divisional Controller, EVP, and VP's
WHAT WE ARE LOOKING FOR
* 3+ years of progressive experience in Financial and accounting fields.
* CPA designation (or in pursuit of)
* Business or Finance degree
* Effective communicator that has the experience and the ability of working with all levels of management
* Solutions focused mindset with a desire to improve processes
* Exceptional data-based skills with an attention to detail
WHAT WILL MAKE YOU STAND OUT
* Experience with IFRS accounting standards and project accounting and software revenue recognition
* Positive attitude and a passion for continuous learning
* A dynamic personality with the ability to manage the expectations of many stakeholders
WHAT WE OFFER
* Three weeks' vacation and five personal days
* Comprehensive Medical, Dental, and Vision coverage from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Flexible work options
* And more!
About us:
Harris is a leading provider of mission critical software to the public sector in North America.
As a wholly owned subsidiary of Constellation Software Inc.
(“CSI”, symbol CSU on the TSX), Harris has become the cornerstone for CSI’s investment in utility, local government, school districts, public safety, and healthcare software verticals.
Our success has been realized through investments in our proprietary software and market expertise.
This focus, combined with acquiring businesses that build upon or complement our offerings, has h...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 55000
Posted: 2025-04-23 08:28:08
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Are you a trailblazing Sales Director with a knack for charting new territories? NorthStar Utilities is on the hunt for a sales hunter like you to drive our net new sales in western North American while growing our existing account business in Ontario
This isn't just any role.
We need a sales maverick who can craft breathtaking presentations, write compelling pitches, and manage a whirlwind of projects with ease and precision.
Your attention to detail will be key in weaving together the big picture and fine intricacies of our sales strategy.
We need more than a Sales Director - we need a Hunter.
If you've got a proven track record of crafting winning responses to municipal RFP requests, working closely with marketing to boost top-of-funnel opportunities, and leveraging data to refine sales approaches and market strategies, then you're just the pro we're looking for.
Imagine a role where your insights have the power to increase sole-source wins or ramp up RFP response conversion rates.
Sounds exciting? Then let's shape the future of utility sales together.
Apply now and let's get ready to break new ground!
This remote role welcomes candidates anywhere in Canada and the US.
What your impact will be
* Develop and execute a sales prospecting plan to penetrate target accounts and capture significant market share within the North American utilities market.
* Source new sales opportunities through creative outbound prospecting and inbound lead generation programs
* Effectively deliver product demonstrations to prospects/customers to showcase the value of NorthStar solutions
* Serve as a trusted advisor to prospects/customers to achieve desired business outcomes
* Drive event attendance for webinars, trade shows/conferences, executive dinners and other events
* Manage the RFP sales motion from identification to win loss analysis
* Work cross functionally with the RFP Bid-Manager and subject matter experts from other departments to develop and maintain our library of RFP content
* Disciplined use of Salesforce.com to record all communication with each lead, contact and account
* Travel between 15%-30% may be required
What we are looking for
* Bachelor's degree, preferably in business administration, marketing, or a technical discipline
* 5+ years in an enterprise sales role responding to municipal RFP’s
* Experience delivering product demonstrations to create value
* Experience generating RFP responses
* Experience using Salesforce, Microsoft Office and RFP.io or another automated RFP application (nice to have)
* Proven track record of quick learning and exceeding set goals
What will make you stand out
* Exceptional verbal and written communication skills
* Organized, detail-oriented
* Proven success in executing outbound targeted sales programs to achieve desired results
* Experience engaging with prospects through social selling efforts
...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 131000
Posted: 2025-04-23 08:28:07
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Safety Manager Knoxville Plant
• Provide guidance and oversight to ensure compliance to all applicable Fresenius Policies.
Advise management and takes actions to ensure compliance with OSHA, EPA, DOT, and Company EHS requirements
• Measure site’s performance against requirements.
For all deficiencies, identify a plan for the site to implement and fix all identified deficiencies.
Drive accountability for the plan
• Analyze metrics and review incident trends to justify the allocation of appropriate resources to areas where the site risk is highest.
• Perform frequent site audits to identify all non-compliant equipment and/or processes at the site.
Implement solutions to eliminate exposure to these risks and prevent injury.
Review all changes to ensure new equipment and process are compliant.
• Audit recordkeeping practices entries to ensure compliance to global standards and regulations.
Complete and timely submittal of required safety and environmental reports (internal and external).
• Audit the workplace organization and Associate behaviors to ensure that training, auditing and scoring methods are accurate and consistent
• Ensure site leadership and Associates are trained and knowledgeable of their responsibilities under each policy.
Audit the quality, delivery (including qualifications of the trainer), and effectiveness of all required training.
• Develop and revise site EHS policies, procedures and programs as required.
• Manage safety and environmental regulatory processes, trainings, and programs to ensure compliance and to improve safety culture.
• Develop, coordinate and deliver EHS training to address regulatory standards and corporate environmental policies, programs and procedures.
• Conduct required EHS inspections and assist with internal EHS auditing programs.
• Develop/Coordinate Emergency Response activities.
• Maintain necessary EHS-related documentation and reporting requirements.
• Manage accident and hazard investigations and recommend and/or implement corrective actions.
• Manage workers comp injuries, worker comp claims, and return to work on injured employees.
• Inspect workplaces, and minimize or eliminate hazards from processes and materials.
• Maintain Hazard Communications Programs.
• Champion permitting and regulatory compliance efforts for new processes and equipment installations
• Manage hazardous waste generation, storage and shipment in accordance with procedure.
• Excellent people skills, with the ability to manage, motivate, coach and work with other people to accomplish Company objectives.
• Strong problem-solving, negotiation and follow-up skills.
• Experience with technical writing for procedures, work instructions, guides and manuals.
• Auditing and training skills.
• Experience working with Federal, state and local environmental regulations.
• Excellent communications skills; both oral and
PURPOSE AND SCOPE:
Educate and advise staff on theory of operat...
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Type: Permanent Location: Knoxville, US-TN
Salary / Rate: Not Specified
Posted: 2025-04-23 08:27:07
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SUMMARY
The Epidemiology and Laboratory Capacity (ELC) Program addresses emerging infectious disease threats and is one of the Center for Disease Control and Prevention’s (CDC) key nationwide cooperative agreements for supporting state epidemiology, laboratory and health information systems capacity to address infectious diseases.
The ELC Laboratory-Epidemiology (Lab-Epi) Coordinator will be housed under California Department of Public Health (CDPH)’s Center for Laboratory Science (CLS).
This individual will work closely with ELC Program Manager and support communication between CLS laboratory staff and Center for Infectious Diseases (CID) epidemiologists as well as clinical lab partners.
This individual will address cross cutting needs of both labs and epidemiologists.
They will assess laboratory gaps and coordinate lab-epi stakeholder meetings.
Under the direction of the CLS Deputy Director, the ELC Lab-Epi Coordinator will develop and implement processes, collaborate with key partners to evaluate program activities, and manage day-to-day program operations.
The ELC Lab-Epi Coordinator will assist with the coordination of federal grant deliverables including progress reports, and monitoring program budgets.
If hired for this position, applicant will be required to provide proof of full vaccination for COVID-19 prior to the start date; or have a valid religious or medical reason qualifying the applicant for an exemption (that may or may not require accommodation).
Salary range: $70,000 to $85,000 annually depending on experience/qualifications.
ESSENTIAL FUNCTIONS
* Coordinate ELC-project conference calls and meetings, track progress, and provide administrative and fiscal updates.
* Analyze project operations and implement strategies to improve effectiveness and efficiency.
* Develop project budgets, in collaboration with CDPH CLS and CID project staff, and Heluna Health.
* Review budgets with ELC CLS Principal Investigators to forecast progress and potential challenges, in collaboration with the ELC Program Manager.
* Assist in monitoring and tracking of performance measures.
* Write and compile fiscal or programmatic reports for submission to CDC, meeting critical deadlines.
* Oversee and review the development of duty statements, hiring, onboarding, and performance evaluations of project staff, ensuring consistency with ELC Enhancing Detection project mandates and objectives.
* Maintain excellent working relationship with CDPH CLS and CID, Heluna Health, and other partners.
* Conducts other duties as requested or assigned.
JOB QUALIFICATIONS
Education/Experience
* Bachelor’s degree, required.
* Graduate degree in Public Health or related field, preferred.
* A minimum of two years’ experience in program and federal grant management, required.
* Experience working collaboratively with diverse groups with multiple activities, timelines, and de...
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: 70000
Posted: 2025-04-23 08:25:28
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As a Environmental Health and Safety (EHS) Specialist, you will support the development, implementation and maintenance of the Company’s safety, health and environmental policies and standards.
This role has Environmental, Safety and Health responsibilities for large special order engineered manufacturing facility located in Marshalltowann, Iowa.
In this Role, Your Responsibilities Will Be:
* Coordinate and ensure compliance with all environmental regulations, permits, and reporting requirements.
* Maintain compliance with site air permits, monitor required data, and own the Minor Source Emission Inventory Questionnaire (MSEIQ).
* Prepare and submit environmental reports for regulatory agencies, including IDNR and EPA (e.g., NPDES DMRs, Tier II, and EPCRA Form R).
* Develop and implement environmental programs to ensure compliance with federal, state, and local environmental regulations.
* Conduct environmental inspections to ensure proper waste management, pollution prevention, and regulatory compliance.
* Be responsible for hazardous waste management, ensuring proper storage, handling, and disposal in compliance with environmental laws.
* Lead the Storm Water Pollution Prevention Plan (SWPPP) and Spill Prevention, Control, and Countermeasure (SPCC) program, including inspections and corrective actions.
* Perform environmental risk assessments and audits to identify potential issues and implement corrective measures.
* Coordinate air emissions monitoring, recordkeeping, and reporting to meet environmental standards.
* Develop and implement sustainability initiatives to reduce the environmental impact of operations.
* Conduct training programs for employees on environmental policies, procedures, and standard processes.
* Work with internal teams and external agencies to ensure compliance with environmental regulations and permits.
* Investigate environmental incidents, resolve root causes, and develop corrective actions to prevent recurrence.
* Maintain records and documentation related to environmental compliance, inspections, and corrective actions.
* Support the safety team by assisting in safety initiatives, compliance efforts, and training programs to promote a safe and environmentally responsible workplace.
Who You Are:
You step up to handle tough issues. You carefully consider all relevant factors and use appropriate decision-making criteria and principles. You understand that different situations may call for different approaches. You partner with others to get work done.
For This Role, You Will Need:
* Bachelor Degree (B.A./B.S) from four-year college or university in Occupational Health and Safety, Industrial Hygiene/Safety, Environmental Mgmt./Engineering, Safety engineering or related field
* Experience with environmental management in a manufacturing environment and facility
* Knowledge of manufacturing safety elements
* ...
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Type: Permanent Location: Marshalltown, US-IA
Salary / Rate: Not Specified
Posted: 2025-04-23 08:20:58
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PA Device Security Evaluator is involved with cybersecurity evaluations of payment devices to various Payment Card Industry (PCI) requirements including:
* PIN Transaction Security (PTS) Point of Interaction (POI)
* PIN Transaction Security (PTS) Hardware Security Module (HSM)
* Software-based PIN Entry on COTS (SPoC)
* Contactless Payments on COTS (CPoC)
* Mobile Payments on COTS (MPoC)
Evaluations can include the following types of assessments:
* Physical device security
* Tamper detection mechanisms (e.g., the electrical/electronic components)
* Side-channel analysis
* Secure boot
* Cryptographic key management
* Source-code review
* Firmware/OS hardening
* Secure software development lifecycle
* Malformed input (i.e., fuzzing)
* Vulnerability assessment and penetration testing
* Reverse engineering
* Mobile application testing (e.g., OWASP MASVS/MSTG)
* Policy, process, and procedure review
It is expected that a candidate will have expertise in a few of the above areas with at least an interest in the remaining areas.
Skills in the remaining areas can be gained through on-the-job training.
Device security analysis and assessments can require the use or knowledge of:
* Standard hand tools
* Drilling and rotary tools
* Soldering
* Heat and solvents
* Electronic circuits
* PCB design
* File formats
* Communication protocols
* Secure coding and common weaknesses
* iOS and Android application protections
The work is being done on client devices and as such, communicating the results of testing is necessary and done through technical reports.
In order to produce high quality reports, the following is needed:
* Attention to detail including consistency and completeness
* Ability to communicate effectively in English
* Good use of figures, images, and tables
* Effective use of the Office suite (Word and Excel in particular)
Additional skills that are sought in a candidate include:
* Communicating and working effectively within a small team
* Communicating with clients
* Being able to work in a shared lab environment
* Being able to work independently
* Being able to identify and understand limitations in tests
* Being able to come up with new test plans or improvements on existing test plans
For this position, work is mainly in the office with potential for on-site client visits.
In addition to the assessment work, there will be opportunities to develop and deliver training and consulting to clients, which could be done virtually or on-site.
While the position is for the Payment Assurance area of the company, work in other related areas of the company (e.g., IoT security) may be assigned as needed.
The work requires a mixture of hardware, software (firmware/OS level), and communications knowledge.
A post-secondary degree or diploma, or equivalent wo...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2025-04-23 08:14:33
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
People Leader
All Job Posting Locations:
Shanghai, China
Job Description:
* Please kindly note this is an Individual contributor role.
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...
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-04-23 08:12:35
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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:
R&D Product Development
Job Sub Function:
Multi-Family R&D Product Development
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
We are searching for the best talent for a R&D Associate Director of Global Product Stability Science & Compliance located in Raritan, NJ.
Purpose: As an Associate Director, you will play a pivotal role in shaping the future of surgical solutions by leading a team of scientists in accordance to world-wide product stability regulations on a wide diversity of cutting-edge research and development programs.
Your expertise will drive the introduction of new products, the improvement and cost reduction of existing products and processes, and the development of innovative business applications for core technologies.
In this dynamic role, you will collaborate with senior management to set organizational goals and manage projects that meet business objectives.
You will ensure regulatory compliance in research strategies and protocols and stay ahead of emerging technologies and market trends in the global field of product stability.
Your leadership will guide a team of professionals, providing them with the necessary tools and guidance to excel in their roles supporting a large number of stakeholders across MedTech. You will also closely partner with the Associate Director of R&D Global Product Stability Operations to ensure that forecasted demand is contemplated in his/her department’s plans for capacity.
You will be responsible for:
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Participates with senior management in developing organizational goals and recommending projects and/or initiatives to achieve these goals.
* Responsible for communicating business related issues or opportunities to next management level
* Remains current in all appropriate regulations, emerging new technologies and market trends which may affect the organization's business or result in new opportunities.
* Responsibility for creating department budget and monitors expenses to ensure adherence to the budget.
* As people leader, manages resources to anticipate needs and trends.
* Hires, trains, and evaluates staff, leads a high performance team.
* Sets and communicates clear priorities, st...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-23 08:12:30
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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:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Job Description
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Associate Analyst Quality Control to be in Raritan, NJ.
Purpose: Entry to developing individual contributor, who works under close supervision.
Assists staff in various processes in the Quality Control function.
Supports day-to-day laboratory activities such as sample management, supply ordering and receipt, and general housekeeping.
Assists with analysis, qualification/validation activities, and lab investigations.
Supports data review and metrics reporting.
Executes continuous improvement projects with supervision.
May execute testing under supervision.
You will be responsible for:
* Ensure testing is completed in compliance with all applicable procedures, standards, and current Good Manufacturing Practices regulations.
* Conduct analytical testing of final product samples submitted to the QC laboratories.
* Perform peer review/approval of laboratory data.
* Use electronic systems (LIMS, iLAB) for execution and documentation of testing.
* Build, review, and approve relevant QC documents, SOPs, and WIs.
Qualifications / Requirements:
Education:
* Minimum of a Bachelor’s or equivalent University Degree required; focused degree in Biology, Biochemistry, Microbiology, or related scientific field is preferred
Experience and Skills:
Required:
* 0 - 2 years of relevant work experience
* Knowledge and understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
* Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, ELISA, Cell Culture, and/or Potency assays
* Experience with Manual Sample Processing
* Excellent written and verbal communication skills
Preferred:
* Experience in a Quality Control settin...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-23 08:11:49
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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
* Minimum of four (4) years of laboratory experience.
* Fundamental experience in 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 b...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: 27.12
Posted: 2025-04-22 08:35:47
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En tant que gestionnaire de produits, ce professionnel sera chargé de guider la découverte et le développement de solutions innovantes qui répondent aux besoins futurs du marché.
Il collaborera avec les ingénieurs, les chercheurs et les dirigeants pour définir la vision du produit, hiérarchiser les initiatives et piloter le développement du produit.
Responsabilités et tâches:
* Définir et gérer la feuille de route des produits de R&D, en veillant à l'alignement sur les objectifs et les stratégies à long terme de l'entreprise.
* Diriger la découverte et l'exploration des technologies et tendances émergentes afin d'identifier de nouvelles opportunités de produits.
* Collaborer avec les parties prenantes au sein de l'organisation.
Exigences:
* Baccalauréat en informatique, en ingénierie, en gestion de produits ou dans un domaine connexe, ou expérience pertinente.
* Plus de 4 ans d'expérience dans la gestion de produits, avec un accent sur les produits logiciels.
* Expérience technique et compréhension des processus de développement de logiciels.
* Expérience de la gestion du cycle de vie des produits, de la conception au lancement.
* Une bonne maîtrise du français et de l’anglais est requise, car le titulaire du poste aura à communiquer fréquemment dans les deux langues, tant oralement que par écrit, car nous avons des collègues, des clients et des partenaires au Québec, ainsi que dans le reste du Canada et aux États-Unis.
Un atout à ne pas négliger:
* Expérience de l'application des règles de stationnement, des paiements mobiles, des tribunaux et des recouvrements :
* Expérience des logiciels de stationnement, de circulation, d'application des règlements et des codes
* Expérience de l'application des règlements de stationnement, des paiements mobiles, des tribunaux, du recouvrement
* Expérience de la reconnaissance automatisée des plaques d'immatriculation (ALPR/ANPR).
*Seuls les candidats retenus seront contactés.
Harris est un employeur souscrivant au principe de l'égalité des chances et les membres des groupes cibles suivants sont encouragés à postuler : femmes, personnes handicapées, autochtones et minorités visibles.
Si vous êtes une personne handicapée, une assistance au processus de sélection est disponible sur demande.
L'équipe de Harris Talent Acquisition n'utilise pas de SMS pour contacter les candidats ou solliciter des informations confidentielles.
Nous encourageons tous les candidats à postuler aux postes annoncés.
Ils seront contactés soit par un responsable de Harris, soit par un membre de l'équipe d'acquisition de talents pour un entretien, une fois que les critères requis auront été remplis.
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As a Product Manager, this professional will be responsible for guiding the discovery an...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-04-22 08:35:27
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Job Category:
Intern
Job Family:
Student Intern
Job Description:
We are looking for motivated and talented engineering students to join us as interns for the upcoming 2025 Summer.
Our Engineering Internship Program offers an exciting opportunity to gain hands-on experience in a food manufacturing environment. Interns will work closely with skilled engineers, contributing to projects that have a direct impact on our operations and success. We offer internship opportunities in various areas of engineering, allowing you to specialize based on your interests and career aspirations.
Interns will also participate in our company Internship Program which includes Executive Speakers, Social & Networking Events and Career Branding & Professional Development.
Manufacturing Engineering:
* Focus on the optimization of manufacturing processes.
* Work on process improvements in efficiency, productivity, process capability, risk, and cost reduction.
* Collaborate with cross-functional teams to design and implement efficient manufacturing workflows.
Reliability Engineering:
* Participate in helping implement strategies to enhance the reliability and lifespan of equipment and systems.
* Interpret failure data and coordinate initiatives to reduce downtime.
* Work with maintenance teams to create predictive maintenance schedules.
Controls Engineering:
* Engage in the design, programming and testing of automated controls systems.
* Work with PLCs, HMIs and robotics to enhance system performance.
* Collaborate on projects involving system integration and optimization.
Process Excellence:
* Focus on continuous improvement initiatives across various operations.
* Utilize Lean Six Sigma methodologies to streamline processes.
* Drive efficiency projects aimed at reducing waste and improving productivity.
Schreiber Foods is seeking multiple summer Engineering Interns across our manufacturing plants in the U.S. Your desired interests and location will be discussed during our initial phone interview. Relocations benefits are available.
Qualifications:
* Completed Sophomore-level status or higher toward a BS degree in an Engineering or Engineering Technology program (Electrical, Automation, Mechanical, Chemical, Engineering Physics or Manufacturing preferred)
* Ability to work a minimum of 10 weeks during the 2025 Summer
* Ability to work 40 hours/week during the summer
* Strong analytical and problem-solving skills
* Excellent communication and teamwork abilities
* Interest in pursuing a fulltime career in of the areas listed above
* Ability to take ownership of assignments and complete them on time and accurately
* Desire to grow and take on new opportunities
* Reliable transportation
Schreiber Foods strives to do good through food every day.
Based in North America, we’re a customer-brand le...
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Type: Permanent Location: Mt. Vernon, US-MO
Salary / Rate: Not Specified
Posted: 2025-04-22 08:26:49
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Kibbutz Shefayim, Center District, Israel
Job Description:
About Oncology
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 Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for MSL to be in Shefayim.
Key Job Activities:
* Keeping abreast of medical and scientific knowledge
* Creating and fostering a network of partnerships with experts
* Working cross-functionally within the company to become a valuable team member
* Providing high level scientific engagement with experts, while utilizing multichannel platforms
* Initiator and coordinator of medical education activities and advisory boards, in alignment with Medical Manager
* Scientific support and training to company sales representatives and other peers
* Supports and initiates evidence generation via research and publications
* Gains valuable scientific insights contributing to the short & long-term strategic plans of the therapeutic area
* Skillful in implementing innovative solutions and ideas for multichannel engagement and data-collection
* Champions medical benefits of products and contributes to the fostering of innovative therapeutic approaches for patient's benefits
* Actively involved in strategy and action plans related to local reimbursement of products
The role is mainly field-based ( 85%) , requires agility with regards to travel & work hours
Requirements:
Education
MD, D.M.D, D.V.M, Ph.D.
(Pharmacy or Science)
Experience:
With preference for:
* Previous experience working in the pharmaceutical industry or research company- an advantage
* High-competency in project & customer-affairs management
Knowledge:
* Deep scientific & clinical kn...
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Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-04-22 08:14:54
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Company
Federal Reserve Bank of Dallas
PhD Dissertation Fellow – Federal Reserve Bank of Dallas Research Department
Advertiser: Research department, Federal Reserve Bank of Dallas
Field(s) of specialization: Any field
Position type(s): Other nonacademic
Location of job: 2200 N.
Pearl St., Dallas, TX, 75201, United States
Degree required: Doctorate
Job start date: Negotiable, but with a start date no later than August 1, 2025 and a termination date that should be no later than August 29, 2025
Job duration: Negotiable, with a minimum of 4 weeks and up to a maximum of 12 weeks
Letters of reference required: 1
Current search status: Position open
Posting end date: April 15, 2025
Call for candidates:
The Research Department of the Federal Reserve Bank of Dallas invites applications for two PhD Dissertation Fellow positions for the summer of 2025.
This program provides an excellent opportunity for PhD students in economics to engage in high-quality research and gain valuable exposure to scholarly work conducted at the Dallas Fed.
Fellows will have the opportunity to collaborate with the Bank’s research economists, visiting scholars, and other dissertation fellows, fostering a rich academic and research environment.
Qualifications/Skills:
* Open to PhD students from all PhD-granting institutions (both domestic and international).
* Applicants must have passed their qualifying exams and reached the dissertation stage of their program.
* Preference will be given to students expecting to complete their PhD in 2026.
* The program will be held in-person in Dallas, lasting from 4 to 12 weeks, during the summer of 2025.
* Fellows are expected to deliver a formal presentation at the Dallas Fed’s brownbag seminar series during the last two weeks of their fellowship.
To Apply:
We are currently accepting applications for 2 positions for the summer of 2025.
The deadline to apply is Tuesday, April 15, 2025.
Submit your application online.
Required documents include:
(1) Curriculum vitae
(2) Paper or writing sample
A letter from your principal academic advisor, commenting on your potential for producing high-quality research, the significance of your dissertation topic, and your progress to date, must also be uploaded with your submission.
For More Information:
Enrique Martínez García
Assistant Vice President and Head of the International Group
Email: enrique.martinez-garcia@dal.frb.org
Full Time / Part Time
Full time
Regular / Temporary
Temporary
Job Exempt (Yes / No)
No
Job Category
Internship Family Group
Work Shift
First (United States of America)
The Federal Reserve Banks are committed to equal employment opportunity for employees and job applicants in compliance with applicable law and to an environment where employees are valued for their differences.
Always verify and apply to jobs on Federal Reserve System Careers (https://rb.wd5.myworkdayjobs.com/FRS) or through verified Federal Reserve Bank soc...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: 29
Posted: 2025-04-21 08:05:28
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
Job Description:
Job Description:
Janssen Sciences UC Ireland is recruiting for a QC Analyst - located in Ringaskiddy
Job Description
Performs advanced tests and analyses to assure that products align with established specifications.
Carries out complex calculations and documents test results.
This is a volume driven position that that directly touches product.
Compiles and analyzes data on reoccurring product defects to determine root cause.
Documents analysis results.
Analyzes raw material inspection logs for consistent failures.
Notifies purchasing and quality departments about suppliers that have provided inferior products.
Studies work processes, measurements and performance metrics to identify improvement areas.
Recommends new or modified procedures based on findings.
Collaborates with customers, suppliers and associates to define and improve quality standards and expectations.
Participates on process improvement teams.
Monitors and scrutinizes internal and external complaints and compiles data to be used in reports.
Performs analyses in order to achieve compliance with specifications using a wide variety of chemical, biological and physical standard procedures
Key Responsibilities:
* Attending daily meetings, working on own initiative.
* Testing and reviewing daily
* Training new analysts
* Always aim to meet site metrics
* Promoting 6S within the laboratories
Qualifications
Education:
A minimum of a bachelor’s degree in a science related discipline and 3 years of experience in a pharma company.
Experience and Skills:
* Experience in lab-based testing
* Proficient in Lab report writing.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
#RPOAMS
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-04-21 07:58:34
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Analyst Quality Control to be in Cork.
You will be responsible for:
* Achieves competency in laboratory methods and procedures.
* Trains other QC analysts in laboratory methods and procedures when required.
* Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
* Executes validation, operation, maintenance, calibration and troubleshooting of equipment and its associated software.
* Writes, executes, reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
* Performs routine and non-routine analytical testing activities.
* Review and approval (where appropriate) of laboratory test results.
Ensures that testing and results approval are completed within agreed turnaround times.
* Writes and reviews laboratory TMs, SOPs, TMDs and WIs as directed by company policy.
* Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
* Is an active member of the QC group and provide assistance with other group activities as required and communicates relevant issues to the QC Specialist, QC Team Leader and Manager.
* Deals with Quality Issues in an accurate and timely manner.
* Maintains and develops knowledge of analytical technology as well as cGMP standards.
* In process control testing and activities to support the production units.
Qualifications / Requirements:
* A third level qualification of a scientific/technical discipline is required.
* Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
Key Individual Contributor Competencies
* Builds ...
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-04-21 07:58:26
-
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 Writing
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Principal Scientific Communications - Shockwave Medical (Remote) to join our team located in Santa Clara, CA.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Principal, Scientific Communications, is responsible for the execution of high-quality scientific communications and medical information deliverables.
This high-impact role will ensure that all scientific communications are accurate and compliant and will provide expertise in support of the development of new scientific content. Scientific content includes the development of abstracts, posters, slide decks and scientific manuscripts in collaboration with cross-functional stakeholders to drive the execution of the overall scientific communications strategy.
This position will be expected to establish and maintain collaborative relationships with external healthcare providers (HCPs), ultimately leading to peer-reviewed evidence dissemination generated from studies.
This role requires a high level of autonomy to deliver on business priorities.
Essential Job Functions
* Responsible for successful execution of all activities related to the preparation...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-21 07:58:18
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Specialty Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States, Columbus, Ohio, United States, Detroit, Michigan, United States, Pittsburgh, Pennsylvania, United States of America
Job Description:
This is a field-based role available in multiple states within the US.
While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
We invite candidates from various locations to apply and encourage you to review the following states/cities where this opportunity is available:
Cleveland, OH
Columbus, OH
Pittsburg, PA
Michigan
Johnson & Johnson is recruiting for a District Business Manager to support our J&J Vision business, responsible for key distributor and direct accounts. The district for this position will include Cleveland OH, part of Columbus OH, Pittsburgh PA and Michigan.
This is a field-based position with the ideal candidate residing in Cleveland, OH.
About Johnson & Johnson
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/.
About Vision
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medte...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-04-21 07:58:07
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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:
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
We are searching for the best talent for a Principal Scientist, Analytical Comparability & Product Characterization – Advanced Therapies to be in Malvern, PA.
Purpose:
The Biotherapeutics Development - Analytical Development (BioTD - AD) group is seeking an upbeat, highly motivated Principal Scientist to focus on analytical comparability and product characterization for advanced therapy modalities. The individual would work with team to develop product comparability study approaches for advanced therapy modalities that will be endorsed by the health authorities. A successful candidate will have experience with the design, execution and optimization of a broad range of characterization assays and will have the opportunity to engage in multi-functional teams.
They will learn from and contribute to industry-leading drug discovery/development programs that has brought numerous quality therapeutics to patients and has made significant contributions to human health.
Primary Responsibilities:
·Design and lead the execution of analytical comparability studies for advanced therapy modalities across various stages of development.
·Lead the execution of the advanced methodologies associated with comparability and deep characterization of cell and gene therapy.
·Author or coordinate appropriate IND/IMPD/BLA/MAA sections & interact with regulatory agencies to address CMC-comparability and product characterization related inquiries.
·Optimally communicate comparability study plans, statistical justifications, and results and scientific data to cross-functional teams, project teams, and health authority as needed.
·Collaborate to develop innovative approaches to challenging solutions for analytical comparability strategy and product characterizati...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-21 07:58:03
