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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:
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:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson is currently seeking a Quality Control – Micro analyst to join our CAR-T Hub located in Beerse.
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/.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, Janssen has built two CAR-T manufacturing centers in the Ghent area (Belgium).
The QC laboratories will be operated from the existing Janssen Beerse site.
The QC Micro analyst, CAR-T Europe is responsible for preparing and conducting testing of the different samples taken during the production process.
You are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
The candidate will be part of the weekend team, working on Saturday and Sunday.
Working hours will be from 6am to 6pm.
Possibly preceded by training period in week regime.
You will be responsible for:
* Perform analytical testing in compliance with all applicable specifications, procedures, GMP regulations.
* Maintain a safe work environment in compliance with all applicable environmental, health, and safety regulations.
* Perform peer review of laboratory data.
* Author and update SOPs, WIs and Protocols to support daily operations of the lab using the Document Management System.
* Support laboratory related investigation records and CAPAs.
* Assist in the execution of internal audits.
* Provide input to functional laboratory meetings.
* Provide input and take actions as a QC representative at cross-...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-30 08:41:02
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Accounts Payable Analyst I - (Global Business Services)
Job Description
Accounts Payable Analyst I - (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 flexibility work for both you and th...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-05-29 09:39:11
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Job Summary
Responsible for ensuring our patients, families, visitors, as well as employees have a wonderful experience by cleaning and maintaining your assigned area within Nicklaus Children's Hospital and its properties.
Working here is about making a difference in the lives of children every day.
Job Specific Duties
* Cleans/maintains assigned work area by gathering materials, refill carts, trash removal, disposing red bags, disinfecting bathrooms (including showers, sink and toilet) and dusting.
* Cleans/Disinfect emergency spills and debris immediately.
* Ensures equipment is in good working order.
* Removes and properly disposes of trash and soiled linen.
* Replenishes supplies and linen.
* Reports safety hazards and defects immediately.
* Provides excellent customer service to all patients, visitors, and internal customers.
* Performs special cleaning procedures such as terminal cleanings when needed (deep cleaning using bleach, wipe walls, clean underneath bed, high dust, change curtains).
* Pull supplies from shelf and prepare cart.
Minimum Job Requirements
* Level II Background Check
* Prior work experience.
Knowledge, Skills, and Abilities
* High school education or equivalent preferred.
* Housekeeping and/or maintenance experience preferred.
* Floor care experience preferred.
* Able to communicate to request supplies and writes identifying information.
* Able to comprehend verbal and written instructions in English.
* Able to relate cooperatively and constructively with clients and co-workers.
* Ability to follow simple instructions to accomplish repetitive tasks.
* Excellent customer service skills.
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Type: Permanent Location: Miami, US-FL
Salary / Rate: Not Specified
Posted: 2025-05-29 09:29:37
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Come grow with us! Georgia-Pacific has an immediate need for a Product Compliance Engineer at the Building Products Decatur Technical Center (DTC) in Decatur, GA.
The Product Compliance Engineer will lead product compliance administrative programs, manage product testing and support product standard and industry initiatives.
The product compliance engineer role will help transform the product compliance capability of building products division! Bring your skills, passion, and willingness to learn and grow in a dynamic team environment!
The Decatur Technical Center primarily focuses on Georgia-Pacific building products Research & Development, Technical Service, and Product Compliance efforts.
As a market leader, Georgia-Pacific has the resources, tools, assets, and commitment for you to be a successful contributor and create value.
At Georgia-Pacific, your unique abilities and contributions will be instrumental to our team & business.
If you aspire to use your skills and passion to create value as a Product Compliance Engineer, we are interested in learning more about you!
The successful Candidate will demonstrate:
* Strong processes development skills
* Strong interpersonal and communication skills
* Ability to balance multiple priorities.
* Strong decision making skills and highly self-motivation
* Strong attention to detail
* Ability and desire to learn and grow
What You Will Do
* Own and manage 3 rd party testing process & program
* Perform product testing needs assessment and establish Scope of Work for all new product testing programs
* Plan resource deployment for testing
* Mange test report document control system
* Support manufacturing facility 3rd party compliance audit program
* Manage renewals and submissions of product evaluations and certifications
Own and manage all existing product evaluation reports and product certifications
* Participate in select standards activities/org (e.g.
ASTM)
* Lead compliance document control projects
Who You Are (Basic Qualifications)
* Bachelor Degree (BS) in engineering (chemical, civil, etc.), environmental studies/policy, chemistry or science field OR building products experience in one or more of the following areas:
* Lab / Product / Quality testing
* Product Stewardship
* Building code interpretation
* Product renewals
* Compliance audits
Experience with Microsoft Office Suite (i.e.
Teams, Word, PowerPoint, Outlook, Excel)
What Will Put You Ahead
* Project Management experience
* Gypsum board manufacturing knowledge, or Gypsum product knowledge, or
Building Code & building product compliance knowledge
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
Th...
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Type: Permanent Location: Decatur, US-GA
Salary / Rate: Not Specified
Posted: 2025-05-29 09:28:36
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
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 Director, Global Commercial Strategy, Precision Medicine to be base in Raritan, NJ.
Purpose:
The Director, Global Commercial Strategy, Precision Medicine will have responsibility for supporting the design & execution of J&J’s global commercial Precision Medicine (PM) strategy in close collaboration with key cross-functional stakeholders in the global and regional pharmaceutical organization.
The successful candidate should have diagnostic commercial experience and, preferably, pharma experience, be a strong leader with excellent communication and collaboration skills, possess scientific/technical aptitude and be able to translate the commercial PM strategy into execution for our therapeutic portfolio and pipeline.
Key focus will be to partner with R&D translational biomarker and diagnostic teams across therapeutic areas (TAs) on precision medicine assets in development to help ensure and accelerate their commercial success.
You will be responsible for:
Primary responsibilities for this position will include but not limited to:
* Support the design and implementation of Global Commercial PM strategy for various biomarker-driven assets in collaboration with the Global Brand Teams, Medical Affairs, Market Access, Regulatory, and Research & Development (R&D) teams across various Therapeutic Area’s (TA’s).
* Develop and implement plans for successful launch of PM programs and partnerships, ensuring seamless global access to strategic solutions that support pharmaceutical brand strategies in collaboration with internal global and regional pharmaceutical and PM partners as well as external experts and partners.
* Provide day-to-day oversight of diagnostic partnerships with testing laboratories or test manufacturers, including providing J&J input, coordinating cus...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-29 08:57:07
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Product Submissions and Registration
Job Category:
Professional
All Job Posting Locations:
Beijing, China
Job Description:
* Share the key information with all internal stakeholders in a timely manner.
Professionally interprate and analyze the impacts of new policies and regulations for product full lifecycle.
Represent JNJ to join policy-making discussion, and follow-up the development.
* Familiar with policy/ regulation developing procedure and timely involve in the development.
Timely capture the new regulation or regulation in drafting stage.
Actively contribute to the Medical Device industry associations, especially AdvaMed, Eucomed/COCIR and CAMDI, US & EU Chambers in China; and leading industry discussions on regulations & policies, closely follow-up updates from NMPA.
* Proactively work on China Medical Device regulations and policy, understanding on the relevant overseas regulations (USA, EU, Japan, and IMDRF), provide comprehensive and reasonable regulatory policy proposals, share policies and interpretation with peers and internal/external stakeholders if appropriate.
* Maintain good relationships with internal partners, including global RA, QA, R&D and Manufacture; and connect with medical device healthcare authority, such as NMPA, CMDE, etc.
and industry associations such as AdvaMed, EUCCC, etc.
Facilitate Policy workshops with NMPA and CMDE, follow up the project proposal completion, working on the process and project finalization’s evaluation.
* Lead and delivery internal policy training per needs to improve the registration process.
Participate in the review and revision of SOP and/or working guideline, to improve the process efficiency and effectiveness.
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-29 08:56:56
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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:
Project/Program Management Group
Job Sub Function:
R&D Project Management
Job Category:
Professional
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
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 the role of Director, Global Functions, Data Science Digital Health. We have a strong preference for this hybrid position to be located at one of the following offices; Titusville, NJ; Raritan, NJ; New Brunswick, NJ; Spring House, PA; Horsham, PA; Cambridge, MA; or San Diego, CA.
Remote work options in the US may be considered on a case-by-case basis and if approved by the Company.
At Johnson & Johnson Innovative Medicines R&D, the Data Science & Digital Health (DSDH) function is charged with applying analytic approaches to drug discovery and development across Therapeutic Areas.
We drive and shape internal and external collaborations, working across Janssen’s Therapeutic Areas and R&D functions, including Global Development and other areas.
The Global Functions, Data Science & Digital Health (GF, DSDH) group within the R&D Data Science organization has the accountability for full scale impact across the Development pipeline via AI/ML-driven site recommendation trial design optimization, real-world evidence (RWE) generation, digital endpoints, decentralized trials, and external policy, with the key pillars being:
* Manage the development of solutions for the purpose of driving Trial Acceleration & Optimization using data science, including but not limited to:
* Enrollment modeling, feasibility analytics, country footprint expansion, advanced AI/ML modeling for predictive site recommendations
* Leverage real-world data for pat...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-29 08:55:45
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ERM is hiring Field Biologists to conduct surveys and monitoring for special status species for large construction projects in Fresno/Tulare, California.
Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of a field biologist requires technical skills, as well as strong organizational and communication skills.
This is a full-time (40+ hours/week), limited-term role with a duration of one year, and the possibility of renewal.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction special status species surveys across the client’s project area.
* Work locations are often remote and require biologists to work independently.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* At least 2+ years of Biology + Other Special Status Species Experience required.
Expertise should include more than one of the following species: Fisher.
* Must have experience with delineation, installation, or maintenance of wildlife exclusion fence, environmentally sensitive areas, no work buffers, or wildlife exclusion zones.
* Familiarity with nesting bird survey protocols and/or general bird identification skills is required.
* Experience with San Joaquin Kit Fox (SJKF), California Tiger Salamander (CTS), Swainson's hawk (SWHA) a plus.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in the documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Flexible availability: willingness to work weekends, holidays, and evenings as needed by the project.
* Demonstrated independent and effective problem-solving and decision-making skills.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Fluency in English and Spanish is highly preferred.
Pay Transparency:
For the Field Biologist position, we anticipate the annual base pay of $74,825 – $96,901, $35.97/hr – $46.58/hr USD, limited-term, non-exempt limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant ...
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Type: Permanent Location: Carpinteria, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:55:08
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ERM is hiring Field Biologists to conduct surveys and monitoring for special status species for large construction projects in San Jacinto, California.
Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of field biologist requires technical skills, as well as strong organizational and communication skills.
This is a full-time (40+ hours/week), limited-term role with a duration of one year, and the possibility of renewal.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction special status species surveys across the client’s project area.
* Work locations are often remote and require Biologist to work independently.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* At least 2+ years of Biology + Other Special Status Species Experience required.
Expertise should include more than one of the following species: Kangaroo Rats.
* Minimum experience requirements for these species are as follows:
+ Kangaroo Rats – Resume demonstrates ability to differentiate Kangaroo Rats from other Dipodomys species (e.g., coursework/training/experience).
* Must have experience with delineation, installation, or maintenance of wildlife exclusion fence, environmentally sensitive areas, no work buffers, or wildlife exclusion zones.
* Familiarity with nesting bird survey protocols and/or general bird identification skills is required.
* Experience with San Joaquin Kit Fox (SJKF), California Tiger Salamander (CTS), Swainson's hawk (SWHA) a plus.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in the documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Flexible availability: willingness to work weekends, holidays, and evenings as needed by the project.
* Demonstrated independent and effective problem-solving and decision-making skills.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Fluency in English and Spanish is highly preferred.
Pay Transparency:
For the Field Biologist position, we anticipate the annual bas...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:55:07
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ERM is looking for a motivated, detail-oriented Managing Consultant, Hydrogeologist to join our growing team in Boston, Massachusetts.
Working under the direction of project managers and partners, the successful candidate will work on interesting site investigation and remediation projects in the northeast region and throughout the United States.
You may also have the opportunity to work on international site investigation and remediation projects. This is a great opportunity to work with ERM's technical experts to implement the latest site investigation and remediation technologies.
RESPONSIBILITIES:
* Plan and oversee field data collection, including sampling, drilling, well installation, aquifer hydraulic conductivity testing, remedial pilot tests, and remedial system operation and maintenance.
* Compile and evaluate site investigation and remedial system monitoring data.
* Synthesize site characterization and remediation information to develop and refine conceptual site models.
* Utilize conceptual site models to communicate findings, identify data gaps, and focus additional data collection efforts.
* Review investigation and remediation data developed by other consultancies and develop recommendations for additional investigation and remediation activities.
* Work closely with geographic information system experts to develop visually compelling and informative graphics.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Communicate with subcontractors, regulatory agents, tenants, and clients during field activities.
REQUIREMENTS:
* Master's degree in hydrogeology, geology, environmental engineering or related degree.
* Minimum 5 years of experience.
* Strong written/verbal communication and organization/analytical skills; experience writing detailed technical reports.
* Willingness/interest in travel for field assignments.
* Environmental field work experience and 40-hour OSHA HAZWOPER certification a plus.
* Strong commitment to safety, including following established Health and Safety protocols.
* Valid driver’s license and a good driving record.
* Ability to work independently and as part of a team.
* Detail-oriented with mechanical aptitude and hands-on trouble-shooting/problem-solving skills.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
For the Managing Consultant, Hydrogeologist position, we anticipate the annual base pay of $83,318 – $98,209 USD. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based...
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Type: Permanent Location: Boston, US-MA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:54:43
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Accounting Analyst II - RTR Operations (Korean Speaker) - (Global Business Services)
Job Description
Accounting Analyst II - RTR Operations (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:
* Maintain assigned SAP systems by ensuring that all relevant RTR Finance master data changes for SAP security, system tables, chart of accounts, internal orders, cost centers and profit centers are appropriate, authorized and documented.
* Ensure Finance security roles are in compliance with global segregation of duties matrix.
* Provide a source of system expertise, business knowledge and problem solving capabilities to ensure sound analysis, recommendations and action programs in the maintenance and development of RTR module
* Perform period end closing for CO-PA (customer and product profitability analysis) for management reporting purposes.
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 flexibility work for both you and the business.
In one of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.
To succeed in this role, you will need the following qualifications:
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-05-28 08:30:58
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At Stewart, we know that success begins with great people.
As a Stewart employee, you’ll be joining a company that was named a 2024-2025 Best Company to Work For by U.S.
News & World Report, and a 2025 Top Workplace by USA Today.
We are committed to helping you own, develop, and nurture your career.
We invest in your career journey because we understand that as you grow, so does our company.
And our priority is smart growth – by attaining the best people, investing in tools and resources that enable success, and creating a better home for all.
You will be part of an inclusive work environment that reflects the customers we serve.
You’ll be empowered to use your unique experiences, passion and skills to help our company and the communities we serve constantly evolve and improve.
Together, we can achieve our vision of becoming the premier title and real estate services company.
Stewart is a global real estate services company, providing title insurance, settlement, underwriting, and lender services through our family of companies.
To learn more about Stewart, visit stewart.com/about.
More information can be found on stewart.com.
Get title industry information and insights at stewart.com/insights.
Follow Stewart on Facebook @StewartTitleCo, on Instagram @StewartTitleCo and on LinkedIn @StewartTitle
Job Description
Job Summary
Promotes Stewart services and solutions through various outside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share.
Job Responsibilities
* Promotes Stewart services and solutions through various inside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share
* Typically follows existing procedures to perform routine assignments and to solve standard problems
* Analyzes basic information and standard practices to make decisions impacting work performed
* Individual contributor working with direct oversight
* Performs all other duties as assigned by management
Education
* Bachelor’s degree in relevant field preferred
Experience
* Typically requires 0-2 years of related work experience
Equal Employment Opportunity Employer
Stewart is committed to ensuring that its online application process provides an equal employment opportunity to all job seekers, including individuals with disabilities.
If you have a disability and need assistance or an accommodation in the application process, please contact us by email at careers@stewart.com.
Benefits
Stewart offers eligible employees a competitive benefits package that includes, but is not limited to a variety of health and wellness insurance options and programs, paid time off, 401(k) with company match, employee stock purchase program, and employee discounts.
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Type: Permanent Location: Bloomington, US-MN
Salary / Rate: Not Specified
Posted: 2025-05-28 08:28:41
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Title: Intelligence Analyst IV
Location: Washington D.C., Merrifield, VA
Security Clearance: Secret
Schedule: Due to the nature of law enforcement work and operation, position may require occasional support outside of core working hours, as well as intermittent weekend support, mission dependent.
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About KACE:
When you make the decision to join KACE, you are choosing to work alongside talented professionals that have one thing in common; the passion to make a difference! KACE employees bring their diverse talents and experiences to work on critical projects that help shape the nation’s safety, security, and quality of life.
The desire to have a career that is purposeful and forward thinking is woven into every KACE employee…it’s The KACE Way.
KACE employees are; purpose driven, forward focused, open-minded, trustworthy, and invested.
The KACE Way is our commitment to our employees, to our customers, and to our communities.
Join KACE and make a difference!
Job Summary:
Serves as a technical authority in one or more intelligence disciplines.
Is responsible for planning, coordinating, and synthesizing research from other Intelligence Analysts to prepare and disseminate all-source intelligence products and responses.
Determines research methodology and work approach and revises as appropriate.
Evaluates incoming intelligence and determines pertinent data that should be directed to the attention of the Senior Intelligence Officer.
Assesses progress of research efforts and redirects efforts.
Evaluates correctness and accuracy of researched material.
Essential Functions and Responsibilities:
* Briefs intelligence assessments and positions to principals and subordinates.
* Ensure team products fulfill National-level intelligence requirements.
* Provides technical guidance to staff principals and subordinates.
* Conducts complex research and analysis of intelligence, counterintelligence, counternarcotic, organized crime operations, capabilities, and trends supporting all source intelligence and threat production.
* Leads the preparation, coordination, and implementation of intelligence production and analysis activities in support of OCDETF operations.
* Develops intelligence estimates and projections.
Presents, advocates, and defends OCDETF positions effectively within the intelligence, planning, and operational communities.
* Coordinates, develops, drafts, writes, produces, revises, and ensures completeness of intelligence plans, annexes and associated appendices that require management input.
* Formulates and prepares the intelligence plans and security portions of exercises.
* Plans and coordinates intelligence support of joint and combined exercises.
Serves as intelligence representative, liaison, site survey officer, and focal point staff officer for exercises and real-world crisis operations.
* Maintains close liaison with counterparts in other intell...
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Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2025-05-28 08:28:01
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Post Doc – Drug Discovery & Pre-Clinical/Clinical Development
Job Category:
Career Program
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
We are seeking a highly skilled and motivated postdoctoral scientist, with a fixed term of 2 years, o join the team of Global Safety Pharmacology located in Beerse, Belgium.
The postdoctoral scientist will focus on de-risking drug-induced peripheral neuropathies (DIPNs) to support our drug discovery and development programs.
The successful candidate will apply their expertise in neuroscience to establish translatable human in vitro models of peripheral neuropathies with robust read-outs for functional and molecular biomarkers of DIPNs and perform intricate data analyses.
Responsibilities include experiments such as 2D co-culture of hiPSC-derived sensorimotor neurons and Schwann cells, multi-electrode array recordings, and various gene and protein expression analyses.
Collaboration with cross-functional teams and a commitment to ethical research practices aligned with the 3Rs principles will be essential.
Proficiency in English and strong communication skills will facilitate effective collaboration and dissemination of findings through scientific writing and presentations.
Major Duties & Responsibilities
* Establishing in vitro platforms of drug-induced peripheral neuropathies (DIPNs) using co-culture models of hiPSC-derived peripheral neurons and human Schwann cells
* Identification, testing and validation of human-relevant biomarkers for DIPNs in the in-vitro platforms
* Define strategies whilst collaborating with cross-functional teams and establish in-vitro screening tools to assess DIPN liabilities
* Data analysis and reporting
* Development, training, conferences and writing scientific papers for publication in relevant journals
Required Knowledge, Skills, and Abilities:
* PhD in Neuroscience, Physiology, Cell Biology, or a relevant field focused on CNS and PNS safety pharmacology/toxicity
* In-depth knowledge and experience in the mechanisms of peripheral neuropathies (up to the molecular level), electrophysiology, and hiPSCs, with a proven track record
* Hands-on experience in the experimental techniques mentioned below
* hiPSC-derived sensory or motor neurons co-cultured with human Schwann cells (or other human glial cells) on microfluidic platform...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-28 08:22:28
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
ES024 Janssen Madrid Oficinas
Job Description:
Position Summary:
Manager Clinical Operations is accountable for the operational management and successful country execution of all phases of clinical trials within assigned therapeutic area(s) or specific role(s), including resource allocation, adherence to timelines and budget, compliance with relevant Standard Operating Procedures (SOPs), policies, Health Care Compliance (HCC) and local regulatory requirements.
The Manager Clinical Operations supports Country Head in shaping and managing local organizational structure to ensure its optimal efficiency and demonstrates effective issue management.
This individual is responsible for line management of Local Trial Managers (LTM), Site Managers (SM), Clinical Trial Assistants (CTA) and/or other GCO staff, as required.
Oversees staff performance, development, training, project assignments, workload distribution and supports issue resolution with direct reports.
Ensures alignment of local goals with organizational objectives.
Drives innovative solutions and process improvements for the assigned therapeutic area(s), country, and GCO/Global Development (GD) overall.
Principal Responsibilities:
1.
Provide line management to direct reports including setting goals and objectives, performance evaluation and talent development.
2.
Evaluate and forecast resource needs for assigned portfolio and/or other specific area of responsibility, as required and agreed with local GCO management accordingly.
3.
Responsible for deployment of the One Delivery Model through collaboration and oversight of vendors.
4.
Accountable for the acquisition of new talents and development of human resources.
5.
Guide direct reports in issue resolution and communication with involved stakeholders.
6.
Lead organizational changes and effectively communicate on priority shifts as required.
7.
Review and approve expenses in compliance with the company policies.
8.
Demonstrate leadership behaviors in alignment with J&J Leadership Imperatives.
9.
Foster an environment that encourages sharing of ideas, information and best practices (internal and external to the organization).
10.
Provide coaching and mentorship as needed, including conduct of accompanied site visits as appropriate.
11.
Define, execute or support of long ...
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Type: Permanent Location: Madrid, ES-M
Salary / Rate: Not Specified
Posted: 2025-05-28 08:22:20
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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:
Market Access
Job Sub Function:
Health Economics Market Access
Job Category:
People Leader
All Job Posting Locations:
Beijing, China, Shanghai, China
Job Description:
Key Responsibilities:
Lead product value proposition and access.
Working closely with Sales/Marketing/Strategical Key Account/Government Affairs team to identify key business challenges then to provide appropriate HEMA solution to help addressing access related challenges.
Lead and coordinate HEMA project development, design, planning and delivery of HEMA projects to agreed timelines, quality and budget, using appropriate data, analytical expertise, and rigorous methodology.
Support products HEMA assessment and actively involved in evidence generation discussion then prepare HEMA evidence to support launch.
Lead and Influence cross functional internal stakeholders and multi-disciplinary matrix functions to incubate collaboration in (but no limit to) internal education, strategic project, etc.
Proactively identify, initiate and manage collaborations with external stakeholders and execute environment shaping program.
Provide technical review support for team members’ study protocol and appropriate consultant in related field.
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-27 08:07:54
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Shanghai, China
Job Description:
工作内容（Job Description）：
* 协助真实世界研究
* 数据整理与分析
* 撰写流行病学研究报告
职位要求（Job Requirement）：
* 对真实世界数据研究有浓厚兴趣
* 有相关医学科研背景
* 流行病学或统计学本科在读及以上
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-05-27 08:07:48
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
$2,500 sign-on bonus eligible!
Why Work at Elwood?
The Elanco Elwood, Kansas facility was acquired from Kindred Biosciences in 2021 which offers a strong pipeline of innovative drugs for companion animals within the monoclonal antibody space.
Working at a monoclonal antibody start-up facility in Elwood, Kansas presents an exciting opportunity to contribute to cutting-edge research: Monoclonal antibodies are an innovative type of biologic drug that can target specific molecules in the body to treat a variety of diseases, including cancer and autoimmune disorders.
Working at a start-up facility that is developing these drugs is an opportunity to be on the forefront of medical research and contribute to developing treatments that can have a significant impact on pets' lives.
Shift: This role currently operates on an 8-hour shift schedule.
Starting in July 2025, the position will transition to a 12-hour shift schedule.
Further details about the specific 12-hour shift schedule (days of the week, start/end times) will be discussed during the interview process.
Please note that weekend work will have a 4% premium and work outside of your shift hours will have 10% premium.
Your Role:
An operator is responsible for performing and documenting all tasks and activities associated with biologics manufacturing at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility.
* Execute and monitor critical processes for mAb manufacture such as media and buffer preparation, upstream expression, downstream purification, formulation, fill/finish, and/or secondary packaging.
* Operate in a USDA / FDA / EMA cGMP regulated environment, maintaining strict adherence to all applicable regulations.
* Accurately follow SOP’s and batch production records in operation of production equipment, performance of processing steps, and execution of daily tasks.
* Perform aseptic manipulations and demonstrate knowledge and experience of aseptic techniques.
* Interface with the Quality Control department to submit in-process samples and coordinate en...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 24
Posted: 2025-05-26 08:00:28
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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:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
Warsaw, Masovian, Poland
Job Description:
For J&J Innovative Medicine we are looking for a Commercial Quality Specialist (CQS) reporting to Quality Head Poland and to be hired with a fixed-term contract (until April 2026).
Essential Duties and Responsibilities
* Perform tasks according to quality system standards and procedures for distribution, storage, and transportation of medicinal products (GDP).
* Participate in Quality Management System processes, including Change Control, Corrective and Preventive Actions (CAPA), deviations, complaints, and documentation management.
* Oversee GxP documentation, including updates, distribution, archiving, and compliance analysis.
* Participate in internal audits.
* Investigate quality problems, conducting risk and root cause analyses.
* Participate in supplier qualification processes.
* Conduct staff training on the Quality Management System and GxP requirements.
* Engage in quality development projects and review quality procedures/instructions.
* Collaborate with internal and external partners.
* In the absence of Responsible Person for Controlled Substances:
- Manage end-to-end import licenses and quality oversight for controlled substances.
- Ensure documentation related to controlled substances distribution is implemented and updated.
Activities Requiring Physical Presence at Distribution Center
* Act in the absence of the Responsible Person or Responsible Person for Controlled Substances as per delegated duties.
* Finalize product releases for distribution based on inbound documentation.
* Handle complaints & returns in collaboration with Customer Service.
* Collaborate with Logistics Operator on daily basis.
Requirements
* Education: Must be a pharmacist.
* Experience: Minimum of 2 years of experience working in a pharmacy or pharmaceutical wholesale.
* Language Skills: English (good knwoledge), fluent in Polish.
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-05-26 07:56:36
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WK Dickson (an Ardurra company) is seeking an Environmental Scientist/Wetland Scientist to join our team in our Charlotte, NC office!
We are a trusted leader in providing reliable and innovative water resource solutions across the Southeast.
We offer tailored and cost-effective approaches to improve watershed functions, protect public safety, and enhance quality of life.
As advisors to municipal clients, we guide communities in developing sustainable stormwater programs focusing on nature-based solutions.
Our expertise includes watershed planning, ecosystem restoration, regulatory permitting, water quality and quantity control, and capital design projects.
Primary Function:
We are seeking a motivated and knowledgeable Wetland Scientist to play a key role in the planning, execution, and management of wetland and natural resource projects throughout the Southeast.
This is an exciting opportunity to work on diverse watershed projects in a collaborative and supportive work environment.
Primary Duties:
* Conduct wetland and stream delineations per USACE Manual and applicable Regional Supplements
* Prepare technical documents: delineation reports, jurisdictional determination packages, mitigation plans, and environmental permits
* Manage the environmental permitting process (404/401, NPDES, etc.) at the federal, state, and local levels to support various practice areas firmwide
* Conduct site evaluations and assist in environmental impact assessments.
* Collaborate with senior engineers and multidisciplinary teams to develop innovative watershed planning and nature-based stormwater
* Lead fieldwork efforts, data collection, and ecological assessments with a strong emphasis on collaboration and safety
* Coordinate directly with clients, regulatory agencies, and multidisciplinary project teams
* Mentor junior staff and contribute to the professional growth of our team
Education and Experience Requirements:
* Bachelor’s or Master’s degree in Environmental Science, Biology, Ecology, or a related field
* Approximately 7+ years of experience in wetland science and delineations
* Proficiency in ArcGIS, GPS data collection, and technical writing
* Understanding of the Clean Water Act, USACE protocols, and Section 404/401 permitting
* PWS (Professional Wetland Scientist) is preferred but not required
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers.
We nurture a family-like culture, striving to create a work environment that is enjoyable, challenging and rewarding but also fun.
We are acutely focused on developing our staff, whether through our internal Ardurra Academy or through our industry-leading Leadership program.
We have made a deliberate and focused commitment to nurture a people-centric culture where people are: valued as individuals; supported in their professional and car...
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Type: Permanent Location: Charlotte, US-NC
Salary / Rate: Not Specified
Posted: 2025-05-26 07:55:36
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
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: 2025-05-24 08:35:41
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ERM is hiring an Archaeological Field Technician to support future needs of survey efforts for projects located in Riverside, CA.
Archaeological Field Techs will assist with or conduct archaeological field surveys or monitoring.
This is a fixed-term consulting role with a duration of six months and the possibility of renewal.
RESPONSIBILITIES:
· Digging shovel tests and screening soil;
· Conduct intensive pedestrian surveys consisting of visually inspecting the land surface for presence of artifacts;
· Monitoring alongside construction crews to avoid impacts to resources;
· Bagging recovered artifacts and recording the provenience of the finds;
· Maintaining field notes;
· Compliance with corporate HSE; and
· Performing other duties as assigned or required.
REQUIRED:
· B.A.
in Anthropology
· 2 years of related experience
· Ability to travel extensively throughout Northern or Southern California
· Archaeological field school or prior archaeological field survey experience;
· Ability to work outdoors in variable weather conditions and on varied terrain;
· Ability to work weekends and over 40 hours per week when needed;
· Working knowledge of archaeological survey and monitoring protocols;
· Ability to work in the field for extended periods of time;
· Ability to work independently and as a part of a crew
· Must meet criteria identified in Job Demands & Conditions Analysis for Office and Field Positions.
· Permitted BLM Field Director preferred;
· Master’s in Anthropology preferred
For the Archaeological Field Technician position, we anticipate the annual base pay of $73,207 – $95,761 $35.19/hr – $46.03/hr USD, limited-term, non-exempt.
An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/Flexforce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including Flexforce) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible.
See your recruiter for more details.
You can apply for this role through https://www.erm.com/careers/apply/ or through the internal careers portal if you are a current employee.
Note: No amount of pay is considered to be wages or compensation until such a...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-24 08:35:18
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ERM is seeking a Managing Consultant, Environmental, Health & Safety Management Systems and Compliance to join our Sustainable Operations technical team in the Cincinnati, Ohio area.
In this role, you will manage and contribute technically to challenging environmental compliance, management systems, auditing, and compliance assurance projects and programs for clients locally, nationally, and internationally.
The successful candidate will also network with ERM's national management systems and compliance technical teams to share consulting opportunities, business relationships, and the application of best practices to address client needs.
This is an excellent career opportunity for a mid-level professional looking to advance their career with a global environmental leader, and to make a significant impact in successfully implementing ERM's global strategy.
RESPONSIBILITIES:
* Provide leadership and strategic direction for expanding ERM's management systems and compliance service area and client base. Identify and develop new opportunities, prepare effective technical proposals, and take active leadership role in developing new business with new and existing clients. Develop and expand client relationships that generate repeat business.
* Direct strategic management systems and compliance assurance programs for a variety of clients with complex technical/regulatory issues. Work closely with clients and develop strong relationships to understand specific processes and develop compliance strategy to help clients maintain maximum operating flexibility.
Achieve client’s expectations for scope, budget, schedule, and quality.
* Serve as a senior technical resource on management systems, compliance, and/or auditing programs.
* Capitalize on existing client relationships to expand ERM’s profile and market share in the regional and global management systems and compliance markets (through a combination of excellence in technical delivery and business development).
* Mentor junior and mid-level staff in the proper planning and execution of projects, and in directing or conducting independent technical reviews of deliverable work products.
* Support the general growth and development of ERM’s global services. Collaborate with other ERM global practitioners to execute projects, including participating on teams comprised of management systems and compliance professionals from multiple offices around the global organization.
REQUIREMENTS:
* BS/MS in engineering (chemical, mechanical, environmental), environmental science, or related degree.
Or equivalent experience.
* Experience or interest in supervising direct reports.
* Relevant consulting experience with multimedia environmental compliance and management systems.
* 4-6 years (7+ years preferred) of experience.
* Experience in managing projects, including scope, schedule and budgets, communications, and interactions with cli...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-24 08:34:30
