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Accounts Payable Analyst I - (Korean Speaker) - (Global Business Services)
Job Description
Accounts Payable Analyst I - (Korean Speaker) (Global Business Services)
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Role Overview & Primary Accountabilities:
* Execute payment for vendor and expense claims. Ensure expenditures are duly paid.
* Attend queries from Query Management Team
* To perform First Strike Report to prevent duplicate payment
* Review and coordinate vendor master maintenance, vendors payment, blocked payment, aging reports and supporting documents.
* Payment Forecast to Treasury Team
* Support back up plan & ad-hoc tasks.
* Ensuring appropriate internal controls in place.
* Support and execute continuous improvement (CI) initiatives to streamline existing accounts payable processes.
* Perform analysis & trouble shoot exceptions to drive KPI results.
* Support internal & external audit query to Team Leader.
* Support in operation meeting.
* Support SME for APAC (within team's portfolio)
* Responsibilities include issue resolution and engage in process improvement AP projects.
* AP Project sustainability with improvement idea.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact.
We’re founded on 151 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make ...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-05-31 08:54:44
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Health and Safety Team Leader
Job Description
As a person, you’re a learner – a natural leader – someone who is always taking initiative to make things better and bring others along with you.
You live your life in alignment with the highest values of integrity and quality, always ensuring your responsibilities become a long-term success story.
In this role, you’ll help us deliver better care for billions of people around the world.
Position Summary:
The incumbent reports to the EHS Site Manager and has the responsibility to implement the site safety and sustainability strategies in the Beech Island CTEC process system.
The incumbent must work collaboratively with the site EHS team, Global EHS leaders, and all mill leaders to identify and lead appropriate initiatives that deliver continuous improvement in environmental, health and safety results.
It starts with YOU.
In this role, you will:
* Provide organizational and functional leadership to ensure that EHS systems meet Kimberly-Clark Standards, Best Practices and federal and state regulatory requirements.
The incumbent will provide leadership for continuous improvement in all EHS activities in support of achieving an injury-free work environment.
Lead crisis response to events as appropriate, ensuring effective investigation and follow-up.
* Provide personal and organizational sensitivity, vision, inspiration, innovation, talent building, decisive, strong communication, collaborating and influencing skills. Knowledge of regulatory requirements of OSHA, NFPA, and other federal, state and local agencies.
* Analyze EHS data, providing insights regarding results and trends through investigation and thorough problem solving, making recommendations for improvements that address substandard acts or conditions.
* Catalyst for site safety culture initiatives (People-Based Safety) and programs focused on the positive impact of Mindsets and Behaviors required to deliver a zero-injury work environment.
* Support of Contractor Safety ensuring adherence to KC safety requirements of contractors, vendors and visitors.
* Contribute to an environment in which all team members are respected regardless of their individual differences and are motivated to improve their individual/team contributions so as to achieve desired business results.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opport...
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Type: Permanent Location: Beech Island, US-SC
Salary / Rate: Not Specified
Posted: 2025-05-31 08:54:27
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SUMMARY
The California Department of Public Health’s Microbial Diseases Laboratory Program is responsible for diagnostic and surveillance testing, applied research projects, and education and training for the identification and characterization of bacterial, mycobacterial, fungal, and parasitic pathogens of public health importance.
Under the direction of the Supervisor of the Quality, Safety & Support Unit, within the Microbial Diseases Laboratory (MDL) Branch, the Microbiologist II performs duties associated with method validation and routine testing of microbial pathogens using advanced molecular detection (AMD) methods, primarily including methods utilizing next generation sequencing (NGS). This position will provide programmatic support for a variety of priority AMD validation projects and assists with surge testing for AMD methods across MDL laboratories, as qualified and assigned.
The position is Monday-Friday, 40 hours per week; weekend, holiday, and overtime coverage may be required during a public health emergency.
The salary range is $36.53 - $49.15 per hour depending on experience and qualifications
If hired for this position, you will be required to provide proof that you are fully vaccinated for COVID-19 prior to your start date or have a valid religious or medical reason qualifying you for an exemption (that may or may not require an accommodation).
ESSENTIAL FUNCTIONS
* Specimen receipt and data entry into Laboratory Information Management System (LIMS).
* Cultivates bacterial or fungal pathogens and quality control strains.
* Develops and optimizes standard operating procedures (SOPs) for next generation sequencing using various sequencing platforms, including but not limited to the Illumina and Nanopore platforms.
* Performs DNA extraction, library preparation, and sequencing of microbial pathogens using various sequencing platforms.
* Implement protocols and workflows on liquid handlers as needed
* Analyzes genomic sequences using validated pipelines and software.
* Participates in proficiency testing and adheres to Branch QC/QA policies for laboratory operations including biosafety, chemical hygiene, and other applicable standards.
* Complies with MDL’s Quality Management system, including complete, timely and accurate recording of results and quality documentation.
* Reviews test results for completeness and accuracy.
* Maintains inventory of essential chemicals, reagents, and disposables.
* Prepares technical reports and compiles data related to applicable grants and projects.
* Communicate effectively with internal and external partners.
* Assists with planning for educational events and in training of public health microbiologist trainees and other partners
* Provides technical consultation to laboratory staff and other local, state, and federal partners
* Attends to training and informational meetings/webinars/conference.
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-31 08:53:40
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Surgeons (Commission)
Job Category:
Professional
All Job Posting Locations:
Madrid, Spain
Job Description:
About Cardiovascular
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
The Clinical Support Specialist will provide comprehensive technical support for medical product sales across both new and established accounts, collaborating with the sales team to achieve sales objectives and enhance market penetration.
Responsibilities:
* Deliver technical and clinical support to physicians, nurses, and other medical professionals regarding company products and services.
* Assist the sales team in preparing and delivering impactful sales presentations to customers.
* Demonstrate the correct usage of products to customers, ensuring clarity and understanding.
* Conduct regular visits to customer locations to gather essential information about company products and assess market conditions.
* Evaluate, diagnose, and repair malfunctioning equipment in response to service calls, ensuring timely resolutions.
* Provide technical support for upgrades and special service initiatives, aiding field service operations.
* Develop customer- and product-centric technical packages and documentation.
* Perform technical analysis and documentation as required; follow up with customers to resolve product usage issues and ensure high satisfaction levels.
* Respond to customer inquiries and provide information as needed.
Facilitate the understanding of clinical trial data to support customer education.
Qualifications
* Bachelor’s degree in biomedical engineering, electronics, or a related field, with a preference for specialization in physiology
* Fluent in English
* Exceptional oral (including group...
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Type: Permanent Location: Madrid, ES-M
Salary / Rate: Not Specified
Posted: 2025-05-31 08:36:06
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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:
Guatemala City, Guatemala, Guatemala, Panama, Panamá, Panama, San José, San Jose, Costa Rica
Job Description:
Essential Job Duties and Responsibilities
The MSL Mission is to, through customized interactions, discuss our treatments with physicians and other customers to shape behaviors and support informed decision making whilst identifying and bringing medical insights into the organization as inputs to medical strategy.
The main activities are:
• Build relationships with community and academic HCPs focusing on changing medical behavior through the exchange of scientific knowledge
• Convey the value of the attributes related to the innovation (ie, efficacy, safety, effectiveness, adherence, QoL) to gain attribute endorsement with stakeholders
• Shaping medical practice by changing behaviors within the HCP Community during product pre
launching phases - prepare the health care environment and medical community, accelerate adoption (PIs engagement and pre-approval access programs)
• Follow up on education, adoption of new knowledge, identifying barriers for medical practice change for innovative products
• Respond to scientific inquiries of HCPs/investigators/health care systems and population health decision makers
• Integrates scientific data into real life practice to meet customer/audience needs
• Identify potential sites and support sites recruitment when needed in alignment with the TA
Head/Senior medical manager
• Execute Medical Field Educational Events focused on pipeline close to launch and key in line products
• Gather insights from Field interactions regarding scientific knowledge, treatments paradigms, Competitors, medical needs and opportunities
• Draw and execute the territory and KOL engagement plan according to the strategy and validated by the other MAF stakeholders
• Deep scientific knowledge according to business/regulatory needs
Requirements:
* Any health care/biomedicine career, desirable post-graduation or MSc/PhD.
* It is required that the candidates have Intermediate / advanced English reading, writing and speaking skills.
* No experience of MSL is required.
* Skills Ability to learn and effectively convey clinical and non-clinical technical information; fast Learner; ability to network and matrix, a...
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Type: Permanent Location: Panama, PA-8
Salary / Rate: Not Specified
Posted: 2025-05-31 08:35:35
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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:
MedTech Sales
Job Sub Function:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States, Columbus, Ohio, United States
Job Description:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for the Associate Clinical Account Specialist position to be in Cleveland and Columbus, OH.
.
Purpose:
The Associate Clinical Account Specialist (ACAS) position is a 6-9 month training position for those with little to no electrophysiology (EP) experience.
Upon successful graduation from the program, the ACAS will be promoted to a Clinical Account Specialist (CAS).
As a CAS the candidate will provide expert clinical product and technical assistance and training to physicians and EP lab staff on the effective use of the Electrophysiology’s systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during case procedures within an assigned geography.
The expectation that is that this work leads to meeting and/or exceeding business goals.
You will be responsible for:
Under (e.g.
limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and corporate Johnson & Johnson, procedures and guidelines, the ACAS will:
* Attend all portions of the ACAS fellowship training program without exception.
* Engage in dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during training.
* Understand the dynamics of an EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.
* Prioritize and appropriately respond to re...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-31 08:35:09
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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:
Marketing
Job Sub Function:
Marketing Insights & Analytics
Job Category:
Professional
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
We are searching for the best talent for an Associate Director, Integrated Analytics – Pulmonary Arterial Hypertension, to be based in Titusville, NJ.
About Pulmonary Hypertension
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 Pulmonary Hypertension team is focused on transforming the disease into a long-term manageable condition.
Bringing your passion for health to this team will help discover and develop effective treatments that help patients live their best possible life.
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
Purpose: The Associate Director, Integrated Analytics – Pulmonary Arterial Hypertension (PAH) position is responsible for generating, integrating, and translating insights into growth opportunities that shape decisions and drive organizational action for the PAH portfolio (OPSUMIT®, OPSYNVI® and UPTRAVI®). This position will partner closely with cross functional brand partners and serves as an internal consultant to the Sales & Marketing team and senior leaders.
This position plays a leading role in advising and counseling management in the development and evaluation of new and existing business strategies and tactics and as a result, shares accountability for business results.
Key Responsibilities:
* Develop insights and actionable recommendations influencing business partners at all levels to incorporate in decision making
* Leverage disparate data sources to address key business questions and uncover business opportunities
* Serve as a leader in integrating data and analytics (national, subnational, payer) with cross functional findings and insights developed by peers across the organization
* Integrate payer data and insights into ongoing business analytics to drive a holistic view of the customer and market
* Serve as a champion for the implementation of cross-functional capabilities to drive impact for brand or franchise and drive organiza...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-31 08:35:06
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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:
The Principal Statistical Programming Lead is a highly experienced Statistical Programmer with expert knowledge of Statistical Programming languages, tools and data structures, proven technical and analytic abilities and strong capabilities in leading Statistical Programming activities and programming teams in accordance to departmental processes and procedures.
This position is accountable for the planning, oversight and delivery of statistical programming activities in support of one or more clinical projects, compounds and/or submissions generally of high complexity/criticality.
In addition, this position leads and/or contributes expert knowledge and technical skills to Therapeutic area and/or departmental innovation and process improvement projects.
In this role, the Principal Statistical Programming Lead is responsible for making decisions and recommendations that impact the efficiency, timeliness and quality of deliverables with a high degree of autonomy and provide leadership, direction and technical and project specific guidance to programming teams.
Accountable for Statistical Programming team delivery for 1 or more clinical projects of high complexity, scope and/or criticality.
Provides matrix leadership to 1 or more programming teams, coordinating and overseeing programming team activities.
May act as a section lead of programming activities supporting a clinical development program, compound or submission.
Contributes to and applies strategic decisions and recommendations, developing and maintaining detailed programming strategy and plans.
Provides technical and project specific guidance to programming team members to ensure high quality and on-time deliverables in compliance with departmental processes.
Coaches and trains junior colleagues in techniques, processes and responsibilities.
Integrates Johnson & Johnson’s Credo and Leadership Imperatives into team goals and decision making.
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-05-31 08:34:38
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Clinical Development & Research – MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Lisbon, Portugal
Job Description:
Johnson & Johnson is recruiting for a Global Medical Safety Physician Fellow. This position will be located in Lisbon, Portugal.
The Global Medical Safety Physician Fellowship is an 18 month program designed to provide qualified physicians the opportunity to gain specialized and in-depth training in key areas of pharmacovigilance within the pharmaceutical industry.
This Fellowship does not provide certifications of any kind.
Principal Responsibilities:
* Participate and complete training in several areas of pharmacovigilance, which include the following: safety surveillance and signal evaluation; identification of new potential safety concerns; characterization of emerging and known product safety profiles; the design and implementation of risk minimization strategies.
* Provide medical expertise in the evaluation of safety data from a variety of sources (interventional and noninterventional clinical studies, post-marketing data, literature reports, and other sources of safety data) as part of the overall pharmacovigilance surveillance process; this includes medical review of individual case safety reports (ICSRs) and evaluation of aggregate safety data.
* Ensure communication of potential new safety concerns and trends to the Medical Safety Officer (MSO) and the Safety Management Team (SMT).
* Support SMT activities such as the evaluation of safety issues to characterize any emerging or known product safety profiles, preparation of aggregate safety reports, such as Periodic Benefit Risk Evaluation Reports (PBRERs), ad-hoc regulatory reports, and interpretation of surveillance and product quality data.
* Work in a cross functional, matrix team environment.
* Contribute to, when appropriate, the design and implementation of risk mitigation strategies to ensure the safe and appropriate use of Janssen Research & Development, LLC products.
* Provide (2) presentations concerning Pharmacovigilance and/or pertinent medical topics to your team.
* Provide assistance in the Medical Affairs team's activities concerning pharmacovigilance, quality, and regulatory affairs.
* Assist in the planning and execution of Medical Affairs activities, both in-office and ...
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Type: Permanent Location: Lisbon, PT-11
Salary / Rate: Not Specified
Posted: 2025-05-31 08:34:37
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Business Enablement/Support
All Job Posting Locations:
Beijing, China
Job Description:
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-31 08:34:31
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Business Enablement/Support
All Job Posting Locations:
Shanghai, China
Job Description:
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-05-31 08:34:31
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As Global Director of Product Management you will be responsible for steering the product roadmap, achieving market growth and participation gains, orchestrating campaigns that drive specific product growth, deploying high quality standards and embedding a getting things done culture.
In this role, your responsibilities will be:
Participation on the Leadership Team
* Working collaboratively to craft and develop the business strategy.
* Drives business growth consistent with that of an innovative technology / business model aligning with the MSOL vision.
* Works to integrate the Corrosion and Erosion business and products into the broader Emerson organizations where appropriate in an expeditious manner.
Strategic
* Develop the vision, mission, and goals for delivering value to customers via data and analytics as well as through the entire system – both hardware and software
* Steer the product management and marketing team to influence end users and to understand future industry requirements.
* Maintain and strengthen collaborative capacity with key universities and research facilities.
* Coordinate and seek alignments within Measurement Solutions and Emerson through global forums, Emerson centres of excellence and through peer contacts.
* Collaborate with Engineering Managers to establish the Product Development strategy, objectives, and metrics aligned with overall CE strategic goals.
Functional Management and Technical Leadership
* Collaborate with sales leadership, world area marketing and business development and marketing/promotional teams to achieve growth goals.
* Direct pricing and discount structure strategy and execution.
Navigate competitive and market forces to understand and respond to changing market conditions.
* Defining and achieving product line financial targets of revenue, unit growth, profitability, and market participation (P&L).
* Ensure delivery of product releases to time and budget and engage with and steer the group NPD pipeline management processes.
Who you are:
Pushes self and helps others achieve results.
Encourages the open expression of diverse ideas and opinions.
For this role, you will need:
* Considerable experience at a senior level leading large multi-disciplinary engineering teams, new product development, research, and production support
* Proven strong people, leadership skills and track record to perform strategic analysis.
* Successful track record of product development projects and experience in sales management and leadership.
* Strong interpersonal, communication and collaboration skills with ability to work with all levels of the business, from diverse technical and functional subject areas.
* Degree in Engineering, Marketing or Business, coupled with a strong technical orientation acquired either through an Engineering degree or years of experience.
* Travel is required.
Preferred Qualifications...
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Type: Permanent Location: CRAWLEY, GB-WSX
Salary / Rate: Not Specified
Posted: 2025-05-31 08:32:25
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Ardurra is seeking a full-time Senior Ecologist to join our team in Orlando, FL.
This role focuses on environmental permitting, regulatory compliance, and database management for transportation-related projects.
The ideal candidate will possess strong ecological assessment skills and a solid understanding of permitting requirements for both state and federal agencies.
Primary Function:
We are seeking a motivated and knowledgeable Sr Ecologist to play a key role in the planning, execution, and management of wetland and natural resource projects throughout our Orlando Projects.
This is an exciting opportunity to work on diverse watershed projects in a collaborative and supportive work environment.
Primary Duties:
* Review roadway plans to determine permitting requirements for minor and major transportation projects, including identification and assessment of wetlands and protected species affected, and assessment of stormwater impacts
* Prepare state and federal permit application packages that describe the site assessments, stormwater data, agency jurisdiction, the measures necessary to satisfy permit requirements, and summaries of meetings with the regulatory agencies
* Conduct wetland inventories and Environmental Assessments, including a focus on protected species
* Assist in preparing and reviewing reports in support of projects, including protected species, natural habitat, environmental impacts, biological evaluations, minor NEPA/NMSA, and related regulatory requirements and compliance guidelines
* Review documents for projects prepared by others, including pre-design environmental documents, permit application packages, exemption verifications, or need for additional wildlife surveys
* Perform QA/QC reviews to ensure completeness, accuracy, and conformity to established industry standards and local, state, or federal criteria
* Provide practical solutions to project challenges by applying accepted procedures and methodologies and collaborating with others
* Support the preparation of draft environmental scope, units, and staff hours for projects based on existing transportation permitting policies and guidelines
* Monitor project budgets and schedules to ensure profitability and timeliness of deliverables
* Mentor junior-level team members while being a positive leader for the team
* Contribute to business development efforts by supporting proposals and identifying new opportunities
Education and Experience Requirements:
* Bachelor’s degree in physical or natural sciences or a related field such as Environmental Science, Biology, or Ecology
* 10+ years of prior practical experience (or 7+ with a relevant Master’s degree)
* Familiarity or established relationships with FDOT, regulatory agencies, and other municipal clients is strongly preferred
* In-depth knowledge of FDOT and regulatory agency criteria, standards, and plans preparation requirements
*...
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Type: Permanent Location: Orlando, US-FL
Salary / Rate: Not Specified
Posted: 2025-05-31 08:30:09
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Strategic Healthcare Programs (SHP) is a leader in analytics and performance management solutions serving the post-acute market. We are an industry leader in helping Home Health, Hospice, and Skilled Nursing providers improve their financial and quality performance while complying with many regulatory requirements Additionally, we connect the post-acute world to the broader provider markets to allow for optimal management across the continuum of care.
The Survey Processor plays an integral role in the timely and accurate processing of survey data.
Duties and Responsibilities:
* Receive inbound mail delivery
* Sort and cut received mail
* Set up the mail cart of the day
* Handling mail accurately by opening, extracting and classifying the content of each envelope
* Scanning of surveys along with documentation
* Operation of a PC and a scanner for data input and review
* Archive completed survey trays
* Move shred bins to shredding area when scheduled
Knowledge, Skills and Abilities
* Able to follow specific instructions and procedures without deviation
* Excellent attention to detail
* Excellent communication is a must
* Proficient in core computer skills (Excel, Word, etc.)
* Be able to lift up to 40 lbs.
and push a 65-gallon shred container on wheels.
* Maintain an acceptable level of work quality
Pay:
$19.00 per hour.
Benefits
We value work/life balance.
Temporary part-time employees are not eligible for health benefits, but are eligible for paid vacation, sick time, and holidays.
This is an on-site temporary part-time position this Summer, working approximately 5 days in June, 10 days in July, and 10 days in August.
The hours are 8am – 1pm, on the days of scheduled work.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
Administration
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Type: Permanent Location: Goleta, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-30 09:31:32
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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: Technical Consultant, Swine
As a Technical Consultant within Elanco’s SBU team, you will be a trusted technical partner to customers and internal teams across the food animal health space.
You will position Elanco as the partner of choice by delivering exceptional technical expertise, market-leading product solutions, scientifically sound research, and value beyond product - including consulting, diagnostics, analytics, and market access support.
This role is field-based and requires travel up to 50%.
You will work cross-functionally within account teams, train Elanco colleagues, engage with industry stakeholders, and influence the long-term direction of our food animal portfolio through research, innovation, and customer-centric solutions.
Your Responsibilities:
Sales and Marketing Support
* Collaborate directly with customers and account teams to support Elanco’s commercial goals
* Identify opportunities and position Elanco products as solutions for customer challenges
* Participate in account planning and help implement Elanco’s value strategy at the customer level
* Support training efforts and contribute to product launch readiness
* Develop and deliver educational events and technical materials for internal and external stakeholders
Customer and Technical Leadership
* Train and coach Elanco teams on disease, product knowledge, and industry practices
* Build strong relationships with external veterinarians, consultants, and academic partners
* Serve as a technical authority to influence decisions at customer and industry levels
* Represent Elanco in key industry organizations and maintain thought leadership presence
Research and Innovation
* Conduct applied research with Elanco-approved products to generate field-relevant data
* Align technical research with business priorities and lifecycle planning for key brands
* Contribute to peer-reviewed publications and present at scientific meetings
* Support R&D efforts, including product line extensions and innovation ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-05-30 09:20:53
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Actus Nutrition is an industry-leading manufacturer of innovative dairy-based nutritional ingredients designed to optimize health and nutrition.
We are currently seeking a Quality Assurance Technician to be based out of our facility in Visalia, CA.
This is a 12-hour shift working on a rotating schedule.
Wages $22.50 - $25.00
QA Techs are responsible for:
Environmental sampling, performing microbiological tests for a dairy food production facility
Reporting results, validations, data entry and general sanitation for the lab
Requirements:
Individuals who would like to be considered for this opportunity will have at lease 1-2 years of manufacturing experience, preferably in a food grade facility and/or quality/auditing department.
Experience with petrifilm plating, moisture, Mojonnier fat testing, yeast/mold, ash and kjeldahl testing is a plus.
Ideal candidates will have excellent analytical, organizational and leadership skills with proven ability to manage multiple priorities in a fast-paced environment.
Must be detail oriented and customer focused with exceptional communication and computer skills.
The company is committed to identifying and recruiting only the highest caliber of talented individuals to join its team of passionate and dedicated employees.
It offers a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
OPEN
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Type: Permanent Location: Visalia, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-30 08:51:10
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What We’re Looking For:
Michael Baker International is seeking a Transportation Planner for our Harrisburg, PA office.
Michael Baker is an industry leader in leveraging data and technology (using open-source, commercial, and in-house applications) as we develop transportation and municipal planning solutions that are innovative, sustainable, and resilient.
We value candidates who have project and client experience with transportation software platforms, AI, and smart data applications.
This includes data, technology, and AI experience with geospatial applications (including ArcGIS, Experience Builder, StoryMap, CityEngineer, UrbanFootprint), data visualization (Power BI, Tableau), predictive transportation analytics (including Replica), traffic management platforms, transportation modeling and forecasting (including transportation land-use integrated models).
The successful candidate’s experience may also include regional transportation models, network modeling (including Remix), long range transportation planning, corridor planning, safety solutions (using applications such as Urban SDK), scenario planning, Smart City solutions (including Digital Twins), active transportation planning, environmental compliance, customer and stakeholder engagement leveraging data, and interactive platforms such as Social Pinpoint.
A Hybrid working arrangement is available requiring 2-3 days in the Harrisburg, PA office
SPONSORSHIP IS NOT AVAILABLE FOR THIS POSITION
What You’ll Do:
* Gathers field data from site visits
* Compiles and analyzes data on economic, social, and physical factors affecting land use, and prepares or requisitions graphic and narrative reports on data
* Analyzes data to determine arrangements of land and physical facilities for residential, commercial, industrial, and community uses
* Researches regulations affecting land use, public utilities, community facilities, and housing and transportation to control and guide community development and renewal
* Reviews and evaluates environmental impact reports applying to specified private and public planning projects and programs
What You Need to Succeed:
* Bachelor's degree in Planning, Environmental Sciences, Engineering, Architecture, Landscape Architecture, Urban Design, or related discipline
* 1-3 years of related experience
* Project and client experience with transportation software platforms, AI, and smart data applications as specified above
* Solid writing, communication, technical analysis, computer and field research skills
Compensation:
The approximate compensation range for this position $67,049 - $96,819 per year.
This compensation range is a good faith estimate for the position at the time of posting.
Actual compensation is dependent upon factors such as education, qualifications, experience, skillset, and physical work location.
Why Choose Us:
* Medical, dental, vision insurance
* 401k Retirement ...
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Type: Permanent Location: Harrisburg, US-PA
Salary / Rate: Not Specified
Posted: 2025-05-30 08:51:06
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POSITION SUMMARY:
The Chemical Process Operator is responsible for assisting in the repair process and production of manufactured parts of exceptional quality.
PRIMARY DUTIES AND RESPONSIBILITIES: The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The duties and responsibilities regularly performed for this position are:
* Blending of surfaces and applying or removing excess material with hand tools or machinery
* Set-up and use of various machines, fixtures and tools.
* Part modification to specifications
* Mixing production materials
* Must follow production specifications at all times
* Embrace/implement continuous improvement and lean principles in all activities
* Maintain department safety and housekeeping standards
* Ensure compliance with Quality Control Manual (QCM)
* Must be aware of ISO – Total Customer Satisfaction (TCS) quality requirements
* Ensure compliance with Company RSM, must be aware of ISO/TCS quality requirements
* Adhere to all Company health, safety and environmental policies while performing job duties
* Adhere to and promote Corporate Code of Ethical Standards
* Regular and reliable attendance
* Performing other tasks in the facility as needed
QUALIFICATIONS:
* Ability to use handheld measuring tools.
* Ability to work effectively individually or as part of a team.
* Must be able to read, write and speak in English
* Must be able to follow oral and written instructions.
* Previous metal working experience preferred but not required
* High School Diploma or GED preferred
COMPUTER SKILLS
Basic computer skills including Microsoft Outlook and familiarity with Microsoft packages.
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Type: Permanent Location: Carson City, US-NV
Salary / Rate: Not Specified
Posted: 2025-05-30 08:50:59
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Intertek (BML) is a commercial laboratory which specializes in recovery of base and precious metals from raw mineralization.
We are looking for dedicated technicians to join our team.
General Responsibilities
To ensure that all required tasks are performed safely, accurately and on schedule.
Specific Responsibilities:
* Carry out method statements for all required assays and equipment
maintenance/operation in an efficient manner, including proper documentation.
* Analyze and report data in a safe and timely manner.
* Uphold quality control standards to ensure accuracy of analyses.
* Perform fire assaying duties as required.
+ These include fluxing, fusing, deslagging, cupelling, digesting and reading
samples.
* Troubleshooting instruments/equipment as needed.
* Other duties as assigned.
Skill Experience Requirements
* Bachelor of Science, BCIT Assayers Certification or equivalent.
* 1 year lab experience.
* Ability to work independently or as a team.
* Working knowledge of Excel and Word.
* Good communication and interpersonal skills.
Salary & Benefits Information
The base wage or salary range for this position is $22.00 to $28.00 per hour.
Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons.
In addition to competitive compensation packages, Intertek (BML) employees are eligible for a variety of benefits including vacation, paid sick days, medical benefits and more.
Intertek’s Commitment
Intertek (BML) is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts.
With passion, pace, and precision we work to exceed our customers’ expectations, while engaging with our employees to be 10X in their performance and professional growth.
Our Culture of Total Quality Assurance
Intertek (BML) promotes a culture where motivated, customer-oriented employees can flourish, experience professional fulfillment, and reach their highest potential.
At Intertek (BML) we exercise our spirit of innovation, the passion of our people and our unmatched customer commitment to realize our purpose of making the world an ever better, safer, and more sustainable place for all.
A career with Intertek (BML) offers rewarding opportunities to help companies around the world develop products that are used safely by millions of people every day.
Intertek (BML) is the trusted advisor to many of the world’s leading brands, companies, and governments, and has earned a reputation for accuracy, reliability, integrity, and technical competence.
Working at Intertek (BML) means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustai...
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Type: Permanent Location: Kamloops, CA-BC
Salary / Rate: Not Specified
Posted: 2025-05-30 08:42:39
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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 Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Madrid, Spain, Porto Salvo, Portugal, Warsaw, Masovian, Poland
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Mexico & Brasil - Requisition Number: R-015573
United Kingdom - Requisition Number: R-014669
Portugal, Spain, Poland - Requisition Number: R-015574
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
The Medical Affairs – Delivery Unit, Lead, Trial Delivery Manager (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, vendor oversight & delivery, compound training, and other activities.
The TDM is responsible for country and regional oversight of local operational delivery, including the alignment of the feasibility strategy and target setting, risk reviews and local challenges that could impact overall study delivery.
The TDM might have responsibilities cross different trial types (such as Company Sponsored, Investigator Initiated, and Collaborative Studies), within different Therapeutic Areas, in a local, regional, or global setting, depending on the business need.
Principal Responsibilities:
* Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
* Manage vendor set up and management of day-to-day study vendor activities, including set-up, SOW
* creation and budget oversight.
* Responsible for country / regional coordination of trial management activities and oversight (e.g., ...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-05-30 08:41:33
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Mexico City, Mexico, São Paulo, Brazil
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Mexico & Brasil - Requisition Number: R-015573
United Kingdom - Requisition Number: R-014669
Portugal, Spain, Poland - Requisition Number: R-015574
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
The Medical Affairs – Delivery Unit, Lead, Trial Delivery Manager (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, vendor oversight & delivery, compound training, and other activities.
The TDM is responsible for country and regional oversight of local operational delivery, including the alignment of the feasibility strategy and target setting, risk reviews and local challenges that could impact overall study delivery.
The TDM might have responsibilities cross different trial types (such as Company Sponsored, Investigator Initiated, and Collaborative Studies), within different Therapeutic Areas, in a local, regional, or global setting, depending on the business need.
Principal Responsibilities:
* Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
* Manage vendor set up and management of day-to-day study vendor activities, including set-up, SOW
* creation and budget oversight.
* Responsible for country / regional coordination of trial management activities and oversight (e.g., aligns feasibility stra...
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Type: Permanent Location: Mexico City, MX-CMX
Salary / Rate: Not Specified
Posted: 2025-05-30 08:41:31
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Primary Care Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Beijing, 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: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-30 08:41:22
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
* Perform the inspection for raw material/component/WIP/final product as required ; / 根据需要对原材料/零部件/生产过程中产品/成品进行检验；
* Perform inspection activities for NPI/PVE/PVA product as required; / 根据需要对新产品导入/过程验证/过程确认产品进行检验；
* Monitor and report on the quality of product received through inspection; / 通过检验监控和汇报接收的产品质量；
* Report non-conformance information during inspection to Quality engineer; provide the suggestion to disposition of non-conforming products; / 在检验期间，向质量工程师汇报不合格信息，提供不合格产品的处理建议；
* Control the Non-conformance products in specific area.
/特定区域内不合格品的控制；
* Manage and maintain related documentation as required, keep quality records in good condition as required; / 按要求管理和维护相关文件，按要求保存好质量相关记录；
* Attend related training and get the certification related to inspection; /参加相关培训，获得和检验相关的证书；
* Help QE & supervisor train and assess other inspectors & operators for inspection criteria and method; / 帮助质量工程师或主管，对其他检验员进行检验标准和方法的培训与考核；
* Assurance team achieve the operation and quality target ; / 确保团队达到运营和质量目标；
* Assist project leader to finish the project timely; / 协助项目主管按时完成项目；
* Complete SAP transactions to dispose product(Only apply to IQC inspector); / 在SAP中完成产品处置的处理（仅适用于进料检验员）；
* Implement material disposition according to NR or follow procedure requirement when facing the change of drawing 、specification; /按照NR或当图纸/标准变更时按照程序文件要求执行对材料的处置；
* As a guide, take initiative behaviors in daily work base on the needs from both internal or external customer; / 作为一个指导，在日常工作中根据内外部客户的需求采取主动性行动；
* Responsible for minimizing both the Environmental and Health & Safety effects of the work that they perform; / 负责将所从事工作的环境健康和安全影响最小化
* Perform other work assigned by supervisor or inspection foreman or Inspection technician; / 执行主管或检验组长/检验技术员分配的其它工作；
* Perform all job duties in full accordance with: / 完成所有工作职责时参照：
* The J&J policies on Information, Assets protection, Maintain password(s) confidential, protect critical Business Information; / 强生关于信息，资产保护，维护密码保密性，保护关键业务信息的政策；
* JNJ Credo/ 强生信条
* All J&J policies and regulations; / 所有强生政策和规定；
* The policies of the Health Care and Environmental programs; /卫生保健和环境程序的政策；
* The code of conduct policies; / 行为准则政策；
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-05-30 08:41:11
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
Professional
All Job Posting Locations:
Limerick, Ireland
Job Description:
Job Title: Senior EHS Specialist
Company: Johnson & Johnson Vision Care, Limerick
Overview: Johnson & Johnson Vision Care is seeking a hardworking, highly-motivated and innovative individual to maintain and advance our EHS Program.
This role is essential for ensuring compliance with EHS Regulations and Corporate standards, driving best practice, developing our EHS Culture and ensuring the safety of all those who work on our site.
Key Responsibilities:
* Prepare and submit EHS reports, metrics, and documentation to management and regulatory agencies as the need arises.
* Support the site’s EHS Programs with a focus on compliance, risk management and continual improvement.
* Ensure adherence to EHS Regulatory requirements and Corporate EHS Standards.
* Design and Deliver EHS Training Programs.
* Collaborate with Senior Management and other partners to establish and achieve EHS Goals and Objectives.
* Support the maintenance of EHS Managements systems including the ISO14001 Environmental Standard.
* Function as site Administrator of the Corporate EHS Software System (CURVE) providing SME Support, oversight, and training.
* Provide Analysis of EHS Metrics and prepare and issue of Reports as the need arises.
* Coordinate EHS Audits with Regulators, Corporate and Certifying bodies as the need arises.
* Run the EHS Audit and Inspection program and conduct regular inspections and audits of the facility and Environmental, Health, and Safety (EHS) systems to confirm compliance and identify areas for improvement.
* Conduct workplace inspections and risk assessments to identify potential safety and environmental hazards; recommend corrective actions.
* Function as SME on assigned IOSS (Integrated Ownership of Safety Systems) Teams.
* Act as SME for and run the sites e-Permit and Contractor Management Systems.
* Function as EHS Partner for assigned Business units / departments/ Projects.
* Support the business in the Investigation of EHS Events to identify root causes and implement corrective and preventative actions to prevent re-occurrences.
* Run the Industrial Hygiene / Chemicals Programs
* Cultivate positive relatio...
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Type: Permanent Location: Limerick, IE-LK
Salary / Rate: Not Specified
Posted: 2025-05-30 08:41:07
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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:
Quality
Job Sub Function:
Business Process Quality
Job Category:
People Leader
All Job Posting Locations:
San Angelo, Texas, United States of America
Job Description:
Ethicon, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Process Quality Specialist to be located in San Angelo, TX.
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/ (https://www.jnj.com/
Under the direction of the Business Unit Manager and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
• Leads investigations and rapid response teams (RRT) of the negative trends, quality/product process investigations & product complaints.
• Provides technical leadership towards the identification of the causes for non-conformances & process' failures, and implementation of the immediate, corrective & preventive actions.
• Reviews & analyses quality trends with the manufacturing team & provides guidance for process enhancement setting work priorities, effective in-depth investigation.
• Provides training and education to the manufacturing team on tools for process evaluation and enhancement.
• Provides guidance to manufacturing supervisors or support groups to ensure that effective in-depth investigations are performed.
• Manages all preparation and execution for internal and external audits including audit observations and implementation of corrective actions.
• Analysis of data and based on the trends recommends actions for process, equipment and system improvement.
• Writes procedures, protocols and any other Documentation needed for the enhancement of processes and systems.
• Provides training and education to the manufacturing team on tools for process evaluation and enhancement.
(Analytical trouble shooting, FMEA, statistical concept application and Q...
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Type: Permanent Location: San Angelo, US-TX
Salary / Rate: Not Specified
Posted: 2025-05-30 08:41:03
