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ERM is seeking highly motivated Principal Technical Consultant, Archaeologist to join our global consulting firm as part of our Cultural Resources Services team.
This is a full-time, salary-based position that can be based from a local ERM office or hybrid.
Applicants are preferred to be local to the Pacific Northwest or Alaska, as well as be familiar with the relevant regional regulatory processes (i.e., federal, state, and municipal).
Demonstrated Alaska and/or Pacific Northwest archaeological experience is required.
Successful candidates must be flexible and responsive to a challenging and changing work environment where schedules and tasks fluctuate according to the needs of the projects and clients.
Based in either Alaska or the Pacific Northwest, the successful candidate will also provide technical assistance for clients throughout the United States while also focusing on project needs and business development within their region.
RESPONSIBILITIES:
* Oversee a team performing literature review, field reconnaissance, field surveys, and excavation for archaeological studies and projects.
* Provide technical consulting skills to support the growth of ERM’s business and client base in the area of archaeology and cultural heritage.
* Interact with other ERM practice areas to share multi-disciplinary resources and best practices across the country.
* Represent ERM through communications and at meetings with state, federal and local agencies.
* Communicate regularly with clients via email and phone conferences.
* Oversee and manage subcontractors.
* Assist with preparing proposals to meet client needs.
* Manage multiple projects within scope/budget/schedule expectations and ensure quality standards on project deliverables.
* Lead, manage performance, hire and retain, inspire and mentor personnel for overall success of the technical team.
* Capitalize on existing ERM client relationships to expand ERM’s profile and market share in the Cultural Resource market (through a combination of excellence in technical delivery and business development). Work with other ERM resources to deepen relationships with ERM key clients and establish new client relationships that result in significant net revenue growth.
* Support the general growth and development of ERM’s international technical community. Collaborate with other ERM global practitioners to execute impact assessment projects. Participate on teams comprised of impact assessment professionals from multiple offices around the global ERM organization.
* Interact with various State Historic Preservation Offices, the Washington Department of Archaeology and Historic Preservation, and access online cultural resource databases.
* Lead and supervise staff in an office setting and/or during fieldwork.
* Perform research and write technical reports.
* Provide technical consulting skills to support ...
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Type: Permanent Location: Portland, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-26 08:02:22
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Environmental Resources Management, Inc.
(ERM) is currently hiring field-based Wildlife Biologists for Impact Assessment and Renewable Energy projects located in Northern California.
The role of a wildlife biologist requires technical skills, as well as strong organizational and communication skills.
Wildlife biologists will work as part of a collaborative and dynamic team of environmental professionals, shaping a sustainable future in California.
Pay is commensurate with experience.
RESPONSIBILITIES:
* Develop and lead field surveys, biological assessments, and implement permit mitigation measures in the field.
* Lead nesting bird surveys, natural community assessments, rare plant surveys, preliminary aquatic resource evaluations.
* Mentor junior field staff and provide technical QA/QC assistance on deliverables.
* Data entry, data review, and expertise with ESRI fieldmaps and sub-meter GPS data collection.
* Support preparation of CEQA and NEPA documents, ESA Biological Assessments, CDFW 1602 permits, and more.
* Collaborate with project managers and clients to ensure compliance with environmental regulations and permitting requirements.
* Prepare proposals, including development of scopes and cost estimates, and participate in business development with existing clients.
* Work on multiple projects within scope/budget/schedule expectations and ensure quality standards on project deliverables and timely delivery of reports.
* Build strong collaborative relationships with other ERM employees.
* Other assigned duties as required.
REQUIREMENTS:
* This is primarily a field-based role.
* BSc or MSc.
degree in Biological Sciences, or related field.
* A minimum of 2-5 years in environmental consulting experience; prior experience in power sectors are considered assets.
* Preferred 2+ years field experience in addition to consulting experience with a focus on biota in Northern California.
* Expertise with federal and state regulations including ESA and CEQA, and guidelines pertaining to survey methodologies and environmental assessments.
* Expertise in sub-meter accuracy GPS technologies, fieldmaps, and GIS collection techniques in the field.
* Strong commitment to safety, including following established health and safety protocols.
* Ability to follow directions and take initiative.
* Excellent communication, organizational, and time management skills.
* Ability to prioritize and meet deadlines in a demanding work environment.
* Valid driver’s license and good driving record.
* Must be willing to travel to field sites, frequently on short notice, and overnight stays throughout northern California.
* Botanical expertise is preferred.
For the Consultant, Wetland Biology position, we anticipate the annual base pay of $71,764 – $81,320 USD. An employee’s pay position within this range will be based on several factors including,...
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Type: Permanent Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-26 08:02:16
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ERM is hiring an experienced Consultant, Wetland Ecology with consulting experience to play a key role in implementing our existing programs in Southern California.
The ideal candidate will have served as a task leader and has a track record of high quality outputs and excellent client communication skills and responsiveness.
This is a fast-track opportunity for a junior-level professional looking to advance their career with a global environmental leader, on existing contracts.
The role will be a mix of remote desktop and field work.
RESPONSIBILITIES:
* Oversee desktop and field tasks related to environmental clearance and regulatory compliance.
* Achieve client’s expectations for scope, schedule, and quality.
* Maintain positive relationships with clients and public agencies.
* Other duties may include natural resource surveys, biological monitoring (as necessary), field team management, and providing specialized site assessments.
REQUIREMENTS:
* BS or MS in biology, wetland science, plant ecology or similar field with experience pertaining to a specialized biological training or field.
* 2+ years of consulting experience that involves oversight, task management, team collaboration, QA/QC, technical writing, survey design, impact assessment and multi-media permitting.
* Basic grasp of the key biological or wetland ecology impact assessment and management issues within the public utility sector, as well as a high degree of technical competence and broad knowledge of impact assessment best practices.
* Knowledge of state and federal environmental regulations.
* Positive outlook, collaborative, and driven by the success of ERM as a global company.
* Expertise and experience in both
For the Consultant, Wetland Ecology position, we anticipate the annual base pay of $71,764 – $79,800 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 compensation may be outside of the range, based on the factors noted above. This job is also eligible for an annual discretionary based performance bonus.
We offer a comprehensive package of benefits including paid time off, paid parental leave, medical, dental, vision, life, disability and AD&D insurance, 401(k) or RRSP/DPSP, and any other benefits to eligible employees as applicable.
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 amount is earned, vested, and determinable.
The amount and availability of any bonus, commission, or any other form of compensation that are alloca...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-26 08:02:15
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Ashland Specialty Ingredients, GP
Are you the kind of person that is always thinking, sketching, seeking, and adjusting? Who needs to understand how things work and then figure out how they can work better? Are you a passionate, tenacious, solver who loves to work with others who share your drive? Are you positive, constructive, and ingenious?
Are you always solving?
Then we’d like to meet you and bet you’d like to meet us.
Ashland has an exciting opportunity for a Scientist I (Analytical Chemist) to join our Ashland Specialty Ingredients G.
P.
business at our Bridgewater, New Jersey location.
This is a very visible, significant role within the Company and the Global Measurement Science function.
This position will report to the analytical team lead.
The responsibilities of the position include, but are not limited to, the following:
* Perform a range of measurements and analyses including, titration, pH, UV-Vis, Karl-Fischer, nitrogen analysis, etc.
* Accurately record, interpret, and document results of laboratory experiments.
* Summarize and present results to internal/external audiences.
* Perform basic maintenance and troubleshooting for laboratory equipment.
* Maintain laboratory notebook in accordance with company policy.
* Comply with company procedural guidelines, laboratory procedures, and safety programs.
In order to be qualified for this role, you must possess the following:
* A Bachelor’s degree in Chemistry or related field with 0-2 years of experience.
* Relevant academic laboratory experience.
* Strong written and oral communication skills.
* Ability to work independently and part of a team.
* Proficiency in Microsoft Word, Excel, and PowerPoint.
* Basic knowledge or ability to learn of LIMS, various analytical instrument software, and other databases.
* Strong foundational knowledge in analytical and organic chemistry.
The following skill sets are preferred:
* Experience in method development, method transfers and validation/verification.
In more than 100 countries, the people of Ashland LLC.
(NYSE: ASH) provide the specialty chemicals, technologies and insights to help customers create new and improved products for today and sustainable solutions for tomorrow.
Our chemistry is at work every day in a wide variety of markets and applications, including architectural coatings, automotive, construction, energy, personal care and pharmaceutical.
Visit www.ashland.com to see the innovations we offer.
At Ashland our vision is to be a leading, global specialty chemicals company whose inspired and engaged employees add value to all we touch.
In fact our people, employees, customers and vendors define who we are.
They are the driving force behind everything we do.
Not only do we value our customers but we value our employees, and we work to offer them a dynamic and challenging environment.
We hold ourselves to high standards at Ashland, and we ...
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Type: Permanent Location: BRIDGEWATER, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-26 08:01:55
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Accounting Analyst II - RTR Operations - (Global Business Services)
Job Description
Accounting Analyst II - RTR Operations - (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 your Accounting Analyst II - RTR Operations - (Global Business Services) 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’re driven to 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’re also a university graduate with a Degree in Accountancy or Finance or other related field and have at least 10 Years of continuous work experience.
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 profe...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2024-04-25 08:29:40
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QA Manager Position Description
KeyLogic is looking for a part-time QA Manager to help develop and revise quality-related policies and procedures and to coordinate activities of an environmental QA Program.
This opportunity will include collaborating with partners within this and other Federal science agencies to revise existing policies and procedures of the QA program and coordinate subsequent reviews.
You will assist the Director of QA in identifying opportunities for improvement, provide recommendations, and implement strategies that effectively improve the program's ability to meet Agency requirements.
You will support the development and management of an organization-wide quality program effectively coordinating and communicating across all levels of the organization.
You should be independent and demonstrate strong organizational skills.
Objectives:
* Develop materials and resources such as summary reports, training or briefing materials, forms, templates, etc.
necessary to support the quality program, including the design and development of a website that leads to centralized program content in one streamlined web area.
* Lead or participate in QA-related Agency workgroups, meetings, or initiatives which may include research planning, data management, records management, system interoperability, etc.
* Plan and coordinate activities of the QA Program and related projects with implementation of other research modernization efforts such as remote temperature monitoring, Electronic Laboratory Notebooks and Laboratory Information Management Systems.
* Participate in relevant meetings, including monthly or annual meetings of the QA Community and QA training sessions that are agency wide.
Required Qualifications:
* Degree in a scientific field such as biology, toxicology, physical science, chemistry, engineering, social science, and/or environmental public health.
* 5+ years of work experience applying QA/QC principles to a scientific field.
* 5+ years of experience developing, managing, and implementing quality management systems.
Desired Experience:
* Knowledge of the principles, theories, inquiry, problem-solving, research, and practices in one of these scientific fields: biology, toxicology, physical science, chemistry, engineering, social science, and/or environmental public health.
* Knowledge of QA management theories, practices, methods, analysis, and evaluation techniques in Federal Agency and organizational policy and practices, sufficient to identify areas for improvement and develop and implement solutions.
* Knowledge of national and international standards for quality management systems (e.g.
ANSI E-4, ISO 17025, etc.).
* Knowledge of federal regulations, Good Laboratory Practices (GLP), and policies and procedures governing or impacting QA and QC.
* Knowledge of analytical methods and associated QA/QC requirements used in environmental research.
* Kn...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-25 08:24:27
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Position Overview:
As an Analytical Chemist you specialize in analyzing substances.
You would use complex equipment and procedures such as chromatography, electrophoresis, mass spectrometry, and optical spectroscopy to test samples and identify and quantify their components.
The work of the Analytical Chemist is of paramount importance to our organization, as it generates information about the make-up and possible interaction of substances that might be turned into a wide array of different products.
Responsibilities:
· Using a range of software, techniques, and equipment to carry out research and analysis.
· Analyzing and interpreting data.
· Perform routine maintenance of equipment and daily quality control testing of analytical methods.
· Calibrate laboratory equipment according to maintenance schedules.
· Design sampling protocols.
· Prepare standards, reagents, and solvents for experiments.
· Prepare reports identifying samples, explaining testing methods, documenting findings, and outlining conclusions of analyses.
· Design and execute experimental procedures, including qualitative and quantitative testing of complex samples.
· Validate and troubleshoot analytical methods.
· Plan, coordinate, and oversee laboratory analyses for compliance actions, emergency response, site studies, health and safety studies, investigations, and remediation.
· Select methods and laboratory procedures and schedule, conduct, and supervise analytical tests.
· Keeping up to date with scientific and technical developments.
· Ensuring that health and safety standards are adhered to.
· Preparing product license documentation.
· Liaising with customers, suppliers and research/scientific staff.
· Developing new analytical methods.
· Assist in special projects and other issues as they arise.
· Other skills and duties as assigned.
Skills and Qualifications:
· Bachelor’s degree in chemistry.
· A master's degree or Ph.D.
viewed very favorably.
· 3-5 years’ experience in a similar role.
· Strong attention to detail.
· Exceptionally strong communication skills, both written and verbal.
· Able to challenge conventions in a constructive way.
· Ability to work efficiently under tight timelines and achieve results, while maintaining high quality
· Excellent analytical, teamwork, customer service and leadership skills.
Physical Requirements:
The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of position in order to successfully undertake the essential duties and responsibilities of this position.
In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.
While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, type and...
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Type: Permanent Location: Elkhart, US-IN
Salary / Rate: Not Specified
Posted: 2024-04-25 08:24:06
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Liberty POST is currently seeking a motivated and energetic School Psychologist for per diem employment to work with children who are birth-5 years old through Early Intervention and Preschool Special Education programs.
Immediate positions are available throughout Hudson Valley.
Liberty POST has offered its clients a range of high-quality and individualized services since 1994. Backed by Liberty Resources Inc.
and part of a large social services circle, originally POST was a speech-language practice in Syracuse NY, and has grown to provide a range of services throughout all of New York State and New Jersey.
We employ over 500 professionals in a variety of settings and offer a collaborative team approach to provide evaluation, direct therapy, and family education through child-directed play.
We are focused on the importance of a child’s natural learning environment, a family’s unique strengths and needs and the diverse population we serve.
Job Duties and Responsibilities:
* Evaluate, monitor and track child’s progress and adjust treatment plans accordingly.
* Test and evaluate child’s abilities to determine realistic goals.
* Record information on the initial evaluation, treatment, and progress in a timely manner using Electronic Medical Record system.
* Proficient at writing detailed analysis and reports.
* Effectively organize and maintain confidentially of child’s records and other documentations.
* Follow all state laws and regulations as it pertains to Early Intervention, CPSE/CSE special education.
Qualifications, Knowledge and Experience:
* Master's degree in School Psychology required; along with minimum of two years working with children in special education.
Certification in NYS as a School Psychologist required.
* Knowledge and experience administering standardized testing in the following areas: cognitive, achievement, behavioral/social-emotional and adaptive skills.
* Experience using Frontline (formerly IEP Direct) to assist in developing IEPs.
Benefits for this position:
· Health Benefits and Retirement packages available for FT positions
· Accrual of sick time based on NYS Sick time Laws
· Mentoring is offered to all providers
· Access to unlimited CEU courses offered that are accredited through ASHA, AOTA, APTA and CTLE
· Flexible scheduling
· Work with a Team of professionals that care about making a difference
· Payment is biweekly with direct deposit
Pay Rate:
* Evaluations - Psychological - $180
* Social History $125
* Observation $40
* Lead Evaluator $25/evaluation
* CPSE meetings $25
Liberty POST cares about your safety. We are following all CDC guidelines to ensure safety for clients, families and employees.
Liberty POST is an Equal Opportunity Employer.
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Type: Permanent Location: Goshen, US-NY
Salary / Rate: Not Specified
Posted: 2024-04-25 08:20:55
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Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Who we are:
At Roche, we are passionate about transforming patients’ lives, and we are fearless in both decision and action - we believe that good business means a better world.
That is why we come to work each day.
We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all.
We do this today to build a better tomorrow.
The OPEX Team creates and drives concepts to ensure operational health of the Serum Work Area diagnostic Roche reagent portfolio through:
* Providing product specific knowledge and education
* Safeguarding the quality, legal and regulatory compliance of our products
* Owning cross Lifecycle Team projects in Core Lab Reagents
* Optimizing and harmonizing processes
Our team is offering a development opportunity as an Intern in International Product Management for Core Reagent Portfolio & Cross-Lifecycle-Projects in the Core Lab Customer Area.
In this role, you are working closely with the responsible product managers and project leads for the respective products and projects.
Thereby you support them in their daily business as well as contributing in overarching Life Cycle Team projects.
You will experience to be a key interface in translating customer and business needs, as well as strategy, into clear priorities.
This includes an active contribution in driving projects and product launches.
We are looking for an ambitious person with an operational, diagnostics or life science background who wants to experience the tasks of global product management by supporting the members of the International Business Operational Excellence Team.
Key responsibilities:
* Assist product managers with product management along the complete lifecycle:
+ requirement collection and assay development
+ responsibility for defined project tasks
+ launch preparation and roll out
+ on market support including creation of marketing, technical and educational material
+ activities to drive profitability and serviceability
+ ensure compliance to quality, regulatory and legal
+ conversion and phase-out of products
* Assist product managers and project leads with x-LCT projects
* Close collaboration with internal stakeholders like Operations, R&D, Regulatory, Quality, Legal, CIR, Finance, other Core Lab LCTs
Who you are:
* You are currently enrolled as a Master student or have recently graduated your Bachelor degree (within the last 12 months) in the field of operational, diagnostics or life scienc...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-04-25 08:19:28
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
We are looking for a Operations Planner (m/f/d) for our location in Visp.
You are responsible for the holistic operations planning in BioAtrium.
This includes the coordination of all operational activities (long, mid and short term) within BioAtrium, including resources and materials, as well as the coordination of large and small investment projects including qualification activities.
The medium and long term planning is done in collaboration with the BioAtrium Leadership Team, the short term planning is done by the local planning team reporting to you.
Your tasks:
* Responsible for the holistic operations planning BioAtrium.
Develop the planning strategy for BioAtrium Operations
* Support the Production Operations Planner to maintain the integrated operational plan (coordination all operational activities within BioAtrium)
* Maintenance of existing integrated schedules helping BioAtrium to deliver activities, support of Project Management Office Planner
* Coordination and planning of the tasks and requirements of the different areas such as Procurement Planning, BioAtrium Leadership Team and Production, Quality, Maintenance and Engineering, Global Engineering and Lonza Services.
* Development of detailed plans for production planning, maintenance planning, resource planning and availability of plant and equipment
* Proactive development of strategies to anticipate or counteract possible future supply bottlenecks
* Active development of measures to improve planning accuracy (process and system optimizations)
Your Profile:
* Bachelor's or Master's degree in supply chain or biotechnology or corresponding training qualification
* Several years of experience in supply planning in pharmaceuticals or biotechnology, or in planning other complex projects (e.g.
CAPEX)
* Professional experience in production environment (GMP)
* English business fluent and German at least intermediate
* Experience in leading smaller teams of advantage
* Good SAP knowledge in the area of production planning in the pharmaceutical/process industry
* Proficient knowledge of Office programs, especially MS Project
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if n...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-25 08:18:20
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ERM is hiring Inspectors to perform inspections of water service lines, and work in field teams of two to determine the service line material.
Work will occur in properties in Scranton—Wilkes-Barre, PA, and the surrounding areas.
The projects we work on and the services we provide demand teams of multi-disciplinary professionals working collaboratively to meet our clients’ needs. The role of an Inspector working within this program requires the use of multiple methods to perform detailed inspections of customer-side water service lines to identify the service line material.
This is a part-time (20 hours/week), limited-term role for the duration of 6 months, renewable.
RESPONSIBILITIES:
* Conducting field inspections to determine water service line material,
* Interacting with, and serving as a point of contact for ERM with landowners, contractors, clients, and other project team members,
* Reviewing and implementing project documents and data entry,
* Providing technical leadership, support, and direction to field staff. This includes the coordination of daily inspections, schedules, and meetings,
* Distributing water sampling test kits and contracts to landowners, as needed,
* Documenting service line material findings by preparing daily written inspection reports that provide up-to-date, consistent written and photo documentation of activities observed in the field,
* Participating in various meetings,
* Performing additional tasks as assigned or required.
REQUIREMENTS:
* High School Diploma, GED, or equivalent,
* A basic understanding of building construction and the ability to locate a water meter/shutoff is preferred but not required.
Necessary training will be provided,
* Strong oral and written communication skills,
* Proficient technical skills, including, but not limited to, experience using Microsoft Office programs, digital cameras, and other handheld data collection devices,
* The ability to travel on temporary assignments with short notice,
* Must possess a valid Driver’s License,
* Must be able to comply with ERM health and safety procedures,
* Must have a good driving record.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solutions for our clients.
Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, hea...
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Type: Contract Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-25 08:09:55
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ERM is hiring Inspectors to perform inspections of water service lines, and work in field teams of two to determine the service line material.
Work will occur in properties in Pittsburgh, Sharon, and New Castle, PA; and Youngstown, OH and the surrounding areas.
The projects we work on and the services we provide demand teams of multi-disciplinary professionals working collaboratively to meet our clients’ needs. The role of an Inspector working within this program requires the use of multiple methods to perform detailed inspections of customer-side water service lines to identify the service line material.
This is a part-time (20 hours/bi-weekly), limited-term role for the duration of 6 months, renewable.
RESPONSIBILITIES:
* Conducting field inspections to determine water service line material.
* Interacting with, and serving as a point of contact for ERM with landowners, contractors, clients, and other project team members.
* Reviewing and implementing project documents and data entry.
* Providing technical leadership, support, and direction to field staff. This includes the coordination of daily inspections, schedules, and meetings.
* Distributing water sampling test kits and contracts to landowners, as needed.
* Documenting service line material findings by preparing daily written inspection reports that provide up-to-date, consistent written and photo documentation of activities observed in the field.
* Participating in various meetings.
* Performing additional tasks as assigned or required.
REQUIREMENTS:
* High School Diploma, GED, or equivalent.
* A basic understanding of building construction and the ability to locate a water meter/shutoff is preferred but not required.
Necessary training will be provided.
* Strong oral and written communication skills.
* Proficient technical skills, including, but not limited to, experience using Microsoft Office programs, digital cameras, and other handheld data collection devices.
* The ability to travel on temporary assignments with short notice,
* Must possess a valid Driver’s License.
* Must be able to comply with ERM health and safety procedures,
* Must have a good driving record.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solutions for our clients.
Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in ...
....Read more...
Type: Contract Location: Cranberry Township, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-25 08:09:55
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ERM is hiring a Field Biologist to conduct nesting bird surveys and surveys for special status species for a large vegetation management compliance program in Sacramento, San Jose, Livermore, Oakland, Ventura, and Orange or Los Angeles County, CA.
Successful candidates must be flexible and responsive to a challenging and 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 1 year and the possibility of renewal.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction nesting bird and other special status species surveys and construction monitoring across the client’s territory.
* Work locations are often remote and require Biologist to work independently.
* Monitoring involves coordination with construction crews and providing advice for maintaining compliance with client requirements.
* 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 Avian Biology + Other Special Status Species Experience required.
In addition to nesting birds, expertise should include more than one of the following species: Southwestern Willow Fly Catcher, Burrowing Owl, Spotted Owl, Eagles/raptors, Least Bell’s Vireo, California Gnatcatcher, Yosemite toad, Ca Red-Legged Frog, Yellow Legged Frog subspecies, San Bernardino Kangaroo Rat, Stephen’s Kangaroo Rat, Western Pond Turtle or Desert Tortoise.
* Familiarity with nesting bird survey protocols and/or general bird identification skills required.
* 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 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.
* Demonstrated independent and effective problem solving and decision-making skills.
* Possess a valid driver’s license.
* Fluency in English and Spanish highly preferred.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a di...
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Type: Permanent Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-25 08:09:54
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Your Job
Georgia-Pacific is searching for a Senior Innovation Engineer to support the Neenah Technical Center in the Papermaking Technology department.
The Process Development Engineer will be principally responsible for areas within our converting technology development team.
Designs, develops, prototypes, and tests all aspects of converting components, equipment, and machinery.
Develops specifications for new parts or prototypes.
Identifies appropriate materials and processes to ensure the quality, performance, and manufacturability of products.
Develops strategies to inform organizational investment decisions, using sound experimentation, landscape studies and understanding equipment solutions from OEM's in the space.
Conducts analysis and tests to determine weaknesses and failures in prototypes, processes and/or products.
Requires a bachelor's degree in chemical/mechanical engineering.
Typically reports to a supervisor or manager.
Occasionally directed in several aspects of the work.
Gaining exposure to some of the complex tasks within the job function.
Typically requires 5 - 7 years of related experience.
What You Will Do
* Provide engineering guidance in a R&D environment, supporting day-to-day trials and project design, installation/mill trials, and optimization of processes/equipment.
* Lead assigned projects/tasks to meet unit objectives within applicable corporate policies.
* Develop and implement products, processes, materials, and systems that improve process capabilities to deliver a reduction in defects and variability.
* Use engineering principles, knowledge, and/or scientific analysis to develop equipment and industrial processes that meet safety codes, policies, and guidelines, and promote the safety and well-being of mill personnel.
* Use Georgia Pacific systems to document projects and day to day work to ensure the retrieval of data and protection of proprietary information.
* Define and solve technical issues that impede the achievement of unit objectives, as well as identifying opportunities to improve.
Who You Are (Basic Qualifications)
You're driven to 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.
To succeed in this role, you will need the following qualifications:
* Bachelor's or advanced degree in Chemical Engineering or equivalent from an accredited college or university.
* 5-7+ years relevant experience in an industrial/manufacturing environment.
* Sufficient computer skills to use or learn Word, Excel, PowerPoint, and SAP.
* Strong written and oral communication skills.
* Ability to work closely and communicate well with trades people and key stakeholders in leadership roles.
* Ability to work in an industrial environment (noise, dust, moving equipment).
May include long peri...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2024-04-24 08:41:22
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About the Company:
Merz is a family-owned medical device and pharmaceutical company headquartered in Germany.
Our Global Technical Operations based in WI manufactures, packages and ships several innovative products so that people all over the world can live better, feel better, and look better.
Key Responsibilities:
Change Control:
* Support/Lead Change Control Activities (Operations, Engineering, Design, etc.). Support updates to operating procedures, process, product / specifications, risk management files, etc through the Change Control process.
* Support/Lead 3rd party supplier management activities such as review 3rd party design control activities.
Support NCR and CAPA:
* Support / lead corrective/preventive actions and product non-conformance including capturing data and investigations associated with product deviations, product non-conformances, CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement and reporting.
Design Control:
* Support operations, sustaining engineer, R&D and NPI departments in the development, verification and validation of product changes and introduction of new.
products.
Risk Management:
* Support / Lead Risk Management activities including review and coordination of quality activities related to risk.
Inspections:
* Support/Lead with federal, state, and local regulatory officials during regulatory inspections.
* Support/Lead in internal and vendor quality system audits as applicable.
Quality Initiatives:
* Identifies and implements new quality improvement initiatives / projects in accordance with cGMP expectations to improve compliance, quality levels (reducing defects), and improve operational efficiencies.
* Works with manufacturing and other functional groups on manufacturing regulatory compliance issue
* Support/Lead training program by developing, coordinating, and delivering assigned training tasks.
Adherence to Regulations:
* Assist with adherence to all Federal, State and Local Regulations controlling the manufacture of Electromechanical Devices (EMD) and non-EMD medical devices.
Management:
* For those who manage or supervise staff: Manage staff including interviewing, hiring, training, and developing employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.
Other duties as assigned:
* Provides support to Quality Management personnel and perform other duties as assigned
Education:
Sr.
Quality Engineer
* BS in a Physical Science or Engineering, or equivalent experience.
- Required
* ASQ Certification as a Quality Engineer or equivalent.
- Preferred
* BS Engineering.
- Preferred
Quality Engineer
* BS in a Physical Science or Engineering, or equivalent experience.
- Required
* ASQ Certification as a Quality Engineer or equivalent - Preferred ...
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Type: Permanent Location: Racine, US-WI
Salary / Rate: Not Specified
Posted: 2024-04-24 08:40:49
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Who We Are:
Managed Health Care Associates, Inc.
(MHA), provides care communities with access, solutions, and insights to help them run their businesses more effectively.
Our members include post-acute providers across the care continuum including long-term care, home infusion, and specialty pharmacies, as well as senior living and other group living facilities.
Our team of associates are passionate about our common mission of helping people age with grace, and champion our core values of being Curious Learners, Selfless Advocates, and Relentless Finishers.
Who we’re looking for:
You’re engaged and self-motivated with a superior analytical approach to solving problems, constantly driving for improvement and innovation.
Your strong communication and organizational skills make you an excellent team player that adds meaningful contributions to our collaborative and fast-paced work environment.
As curious learners, we question the status quo and so should you.
The Vice President will provide executive leadership and operating management for MHA’s specialty, brand, and other product portfolios as necessary. He/she shall utilize strategic contracting, client relationship/development knowledge, and executive leadership to drive new contracting opportunities and increase revenue and ongoing contract performance.
The VP will provide the follow-through necessary to add products to MHA contracts and expand currently contracted products to contribute significantly to top-line growth, customer satisfaction, and profitable performance of Managed Health Care Associates (MHA).
The VP will report to the SVP of Trade Relations.
The Division works with the senior management team to execute strategic and tactical activities to enable the organization to achieve short- and long-term objectives. In addition, by way of the candidate’s prior training and experiences, the VP will play a significant role in further creating and implementing contractual growth strategies that will enable MHA to continue to build a nationally recognized MHA brand.
What You’ll Be Doing:
* Adheres to all company policies and procedures, including, but not limited to, those identified within the Standards of Business Conduct and the Employee Handbook, as may be amended occasionally.
Adheres to all applicable laws and regulations and the company's governance/compliance program.
* Responsible for reporting violations of the company's policies and procedures, Standards of Business Conduct, governance program, laws, and regulations through the company or other mechanisms that may be available during the violation.
Assists with internal control failure remediation efforts.
* Becomes knowledgeable of internal control responsibilities through training and instruction.
Responsible and accountable for internal control performance within their area of responsibility.
Participates in the internal controls self-assessment process.
* Ensures internal control...
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Type: Permanent Location: Parsippany, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-24 08:34:17
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As an In-Home Installation and Health Technician, you’ll be responsible for the delivery, installation, integration, and troubleshooting tech products such as home theater, computing, smart home, networking and health technology.
This role also requires technical expertise in health device installation and support including all appropriate HIPAA and health-related requirements Outside of delivery and installation, you’ll find the right solutions for customers’ lifestyles and technology needs based on your conversations.
You’ll partner with other Geek Squad Agents, service partners, retail employees and supply chain employees to drive performance to meet Best Buy’s strategy and yearly initiatives.
What you’ll do
* Provide a seamless customer experience by advising and fulfilling on lifestyle recommendations regarding products and services
* Maintain phone and in-person contact with customers to reveal diagnostic discoveries and make recommendations
* Provide feedback, coaching and training to Best Buy store teams
* Provide a variety of fulfillment duties including delivery, installation, integration, networking and troubleshooting consumer electronics devices
* Take the lead on two-person jobs and perform other work alone
* Manage inventory and vehicle maintenance, process paperwork and payment, provide feedback and training opportunities, and follow safety guidelines
Basic qualifications
* Must be at least 21 years old
* Current, valid driver’s license
* Have and maintain a driving record which meets Best Buy safety standards
* Ability to acquire and maintain any state or local licensing, as required to perform job effectively
* Ability to acquire any health-related certifications (e.g., HIPPA), as required to perform the job effectively within 90 days of hire
* Ability to lift weight up to 75 pounds with or without reasonable accommodation and up to 150 pounds as part of a team with or without reasonable accommodation
* Ability to lift weight up to 250 pounds as part of a team with the support tools such as harnesses or lifts
* 2 years of consumer electronics delivery, installation, integration and troubleshooting experience
* 1 year of customer service experience
Preferred qualifications
* 1 year of experience in installation, integration and troubleshooting of advanced or complex consumer electronics products
What’s in it for you
We’re committed to helping our people thrive at work and at home.
We offer generous benefits that address your total well-being and provide support as you need it, especially during key moments in your life.
Our benefits include:
* Competitive pay
* Generous employee discount
* Financial savings and retirement resources
* Support for your physical and mental well-being
About us
As part of the Best Buy team, you’ll help us fulfill our purpose to enrich lives through technology.
We bring...
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Type: Permanent Location: Boulder, US-CO
Salary / Rate: Not Specified
Posted: 2024-04-24 08:19:50
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Your Job
Responsible for proactively implementing and maintaining Global Reliability and Test Solutions (GRTS) quality assurance team initiatives and strategies related to performance and conformance at site/location.
Our Team
This role will collaborate across the facility with different areas to ensure the suitability, adequacy, and effectiveness of laboratory policies and procedures.
What You Will Do
* Providing oversight of laboratory test execution activities to ensure accurate and consistent testing procedures.
* Review and approval of testing methods, techniques, and equipment to ensure compliance with industry standards and regulations.
* Collaboration with laboratory personnel to address and rectify any identified issues or deviations from established procedures.
* Conducting regular internal audits and inspections of laboratory practices, equipment, and documentation to ensure compliance with quality standards.
* Participating in the development and validation of new testing methods, processes, and protocols
* Delivering training programs to laboratory staff on quality assurance procedures, practices, and requirements
* Collaborating with external accreditation bodies, clients, and stakeholders to address quality-related concerns and ensure compliance with requirements.
* Providing guidance and support to laboratory staff during quality audits and inspections conducted by external bodies.
* Maintain oversight of the testing laboratory document control system (aka quality management system) to ensure continued compliance.
* Ensure the accuracy, reliability, and compliance of testing procedures and results.
* Maintain corrective action status review process.
* Provide corrective action subject matter guidance/review root cause analysis and track corrective actions to maintain integrity and impartiality.
* Review impartiality and conflict of interest risk assessments for appropriate resolution.
* Approve test run/customer satisfaction survey revisions.
* Participate in customer complaint resolution process.
* Track requirements and maintain testing laboratory accreditations/certifications by way of continued correspondence with accreditation/certification bodies facilitating external audits.
* Oversight of the management review process, including intra-laboratory comparison (ILC)/proficiency testing (PT) plan compliance.
* Schedule, perform, review, and manage internal audits at defined frequency; providing laboratory management risk assessments, ensuring action is taken when required.
* Prepare monthly critical-to-quality (CTQ) key performance indicators/metrics.
Who You Are (Basic Qualifications)
* Bachelor's degree (Engineering with expertise in lab test).
* Strong experience in quality assurance or quality control positions within manufacturing industry.
* Good understanding of quality management systems and standards ...
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Type: Permanent Location: Zacoalco de Torres, MX-JAL
Salary / Rate: Not Specified
Posted: 2024-04-24 08:13:13
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Global Machine Safety Program Leader, (Roswell, GA./Remote))
Job Description
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.
At Kimberly-Clark, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands and take our future to the next level.
In this role with K-C's procurement team, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Kimberly-Clark is looking for an ambitious, self-driven and talented individual to lead our Global Machine Safety program.
In this role, you will use your expertise in machine safety to drive meaningful change through the development and execution of global tactical improvement plans across impacting performance at the site level across the enterprise.
You will actively partner with internal teams, including Research & Engineering and Supply Chain Operations to develop and deploy creative solutions aimed at reducing the risk of injury to our people during the manufacturing process.
It will be critical that you are able to effectively collaborate, communicate, and influence without authority within a heavily networked environment, including with senior leaders.
This role is an individual contributor with no direct reports.
Role Accountabilities:
* Provide leadership and subject matter expertise in the identification and analysis of trends, technologies and processes, and applying insights into deployment of machine safety opportunities to minimize personal injury and property loss.
* Develop, drive and maintain the machine safety roadmap and strategy plans across the enterprise by partnering with our supply chain operations and engineering groups.
* Deploy machine safety metrics (KPI’s) and supporting data management/analytics platforms that identifies performance gaps and drives improvement actions that reduce risk.
* Implement machine risk reduction and compliance plans, leveraging risk prioritization that informs annual resource planning.
Tracking and driving delivery of these plans for both capital and non-capital initiatives.
* Drive global compliance to machine safety standards across the enterprise and develop action plans to remedy substandard conditions.
* Lead safety assessment activities across the enterprise to drive compliance with governmental, industry and K-C standards.
* Use insights from assessments and identified compliance gaps to establish minimum control standards and compliance requirements across the enterprise.
* Develop and execute an enterprise-wide training and education curriculum by leveraging various learning processes and embedded operating systems, ensuring that all sectors and regions develop and maintain the required Machine Safety skills ...
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Type: Permanent Location: Roswell, US-GA
Salary / Rate: Not Specified
Posted: 2024-04-24 08:13:05
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This is a Remote position.
At Fresenius Medical Care, the well-being of our patients is our top priority.
Patient experience and employee engagement are closely intertwined.
While healthcare organizations that improve either patient experience or employee engagement see improvements in how patients rate their care, healthcare organizations that enhance both factors see compounding effects.
The Experience Team at Fresenius Medical Care is focused on measuring and analyzing the experiences of both our patients and our employees, and developing and implementing the programs and processes that will enhance patient care and employee engagement.
Our Experience Team is a part of our broader Global People Analytics Team within Human Resources, a strategic organizational design decision that was made to align our people-centric strategies and initiatives.
We are currently in the process of building out our Global People Analytics and Experience Team – which makes it an exciting time to join the organization.
The Analyst, Experience Surveys and Analytics will execute work in the employee and patient care experience space.
This individual will have a background in I/O Psychology or related field and be skilled in psychological theory, scientific research methods, survey design, advanced statistical analysis, and data visualization.
The Analyst, Experience Surveys and Analytics will leverage these skills to design measurement tools to collect employee and patient experience data, analyze the data to identify actionable insights, and develop and communicate critical business stories to stakeholders via data visualization.
Ultimately, this work supports programs that will drive measurable changes in attitudes and behaviors of employees and patients and improve the experience of both groups.
Please note that experience in healthcare is not required for this role.
Responsibilities
* Consult with stakeholders to understand business challenges involving our patients and employees and determine what data is needed to further explore and identify the root causes of those challenges (note that this is not always self-report survey data)
* Support the execution of employee and patient experience work globally
* Design tools such as surveys, focus groups or interviews, observational checklists, etc.
to reliably measure attitudes, perceptions, behaviors, or other constructs related to employee and patient experience
* Serve as a Qualtrics subject matter expert.
Examples include configuring surveys, building distribution lists, managing user access, building results dashboards, training HRBPs and business leaders to access/leverage dashboards, troubleshooting survey/dashboard/data integration issues, leveraging knowledge of directories, embedded data, ticketing systems to inform survey design/deployment methodology, support data feed integrations, etc.
* Manage and ensure the quality/accuracy of datasets by cleaning, joining, updating, re...
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Type: Permanent Location: Waltham, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-24 08:12:37
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Lonza Pharma and Biotech is looking to add an experienced Operator to their growing team in Bend, OR.
As an Operator, you’ll follow Standard Operating Procedures (SOPs) in a structured environment, understand and apply Good Manufacturing Practices (GMP), and deliver results with high integrity.
Daily tasks include activities such as cleaning, assembly, and system testing of manufacturing equipment, operation of stainless-steel tanks to mix powders and solvent, spraying solution into chambers, drying and collecting powder at the bottom of the chamber, recording mathematical computations, taking samples, weighing, packaging, and transferring powders, tablets, and capsules to storage.
Key Responsibilities:
* Read, understand, and demonstrate proficiency on Standard Operating Procedures (SOP’s)
* Assist in Deviations and CAPAs
* Execute steps of a Master Batch Records (MBRs)
* Follow instructions within a structured environment
* Operate, disassemble, clean, and assemble equipment
* Responsible for monitoring various spare parts of a processing system
* Sign for and understand GMP documentation
* Complete calculation section of MBRs
* Complete reviews of executed GMP documents
* Responsible for own work and will provide direction to Operators and Operator Trainees for GMP procedures, equipment operation, and MBR execution
* Can execute and verify steps in a MBR
* Allowed to make comments to the executed MBR worksheet with supervision
* Perform tasks for Hazardous Waste worker as outlined in the BRIM Large Quantity Generator program
* Perform other duties as required
Key Requirements:
* Minimum High School diploma or GED
* Manufacturing experience in a GMP environment required
* Ability to work in an environment with a constant, low noise level during production
* Good standards of literacy and numeracy
* Ability to work nights, weekends, and holidays as required (12-hour shifts)
* Must have a valid driver’s license with ability to drive company vehicle as needed and pass a background and drug screen
* Must be able to successfully pass a pre-employment physical exertion and visual acuity test
* Performing work in a clean, secure and regulated environment
* Required to lift 50 lbs.
from floor and lift 25 lbs.
above head while working
* Perform cleaning with 20-foot wand above head height
* Wears powered air purifying respirator on occasion
* Wears personal protective equipment during ...
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Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-24 08:11:55
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Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Lonza is hiring an Executive Director, for our Global Supply Chain team in Walkersville, MD.
This position will lead through all facets of supply chain management globally, including purchasing, logistics, warehousing, inventory management, capacity planning and sourcing, master scheduling, inventory control and financial costing, in support of all Lonza Bioscience’s production and distribution activities.
The Global Head, Supply Chain implements strategies within the Supply Chain organization to ensure: optimal flow of materials to enable operations/ laboratory activities to consistently deliver to customer and business expectations; financial and GMP audit/ inspection readiness at all times; appropriate management/ governance systems are implemented to achieve business unit and company goals.
This position is eligible for remote work based on the East Coast of the US
Key responsibilities:
* Builds a capable, agile, and global Supply Chain organization with the technical skills, experience and know-how to define the optimal supply chain for Lonza Bioscience and implement appropriate systems and controls to sustainably deliver results.
* Generates and implements Supply Chain strategies to ensure continuous flow of materials to enable operations/ laboratory activities consistently deliver to customer and business expectations.
* Designs, implements and leads an effective & efficient Sales and Operations Planning process (S&OP) for both made-to-stock and made-to-order business.
* Works to continually optimize forecast/ demand planning accuracy, inventory analysis, and capacity modeling to optimally schedule production and troubleshoot supply chain issues.
* Continuously identifies opportunities to optimize and risk mitigate the Lonza Bioscience supply chain through analytics and leveraging the full capability of appropriate tools/ systems (e.g., ERP).
* Develops plans for improving productivity, quality and efficiency of operations, in partnership with key stakeholders, to support the strategic aims of the business.
* Collaborate with Lonza Supply Chain Center of Excellence and other Division Supply Chains to drive best in class integrated business processes.
* Oversee make-or-buy decisions, in alignment with appropriate stakeholders.
Manage third-party manufacturing and distribution strategy and tactics.
* Responsible for ensuring appropriate management/ governance systems are implemented across the BU to achieve business unit and company goals.
* Coll...
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Type: Permanent Location: Walkersville, US-MD
Salary / Rate: Not Specified
Posted: 2024-04-24 08:10:34
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
The Site Quality Head CGT will lead the Quality organization (QA & QC) and will assure the site remains under control with respect to GMP, collaborating with Operations to solve quality issues.
Accomplishes corporate business objectives by developing site quality systems and enforcing Regulatory compliance.
Responsible for providing the strategic leadership and management for the Site`s Quality organization.
Provide leadership to the Site Quality organization to ensure that teamwork, high morale and innovation are fundamental components of a team.
Ensures alignment with customer needs and linkage with the overall Quality and business strategies.
Key responsibilities:
* Acts as Key Account Quality Manager for selected customers
* Leads & supports Audits & Regulatory Inspections at the Site
* Leads and directs staff in both QA and QC and ensures their development
* Develops compliance related manufacturing and process controls and improves quality systems
* Holds responsibility for Quality budget and driving Operational Excellence
* Member of the Site Leadership team
Key requirements:
* BS degree in a Life Sciences, Engineering or Quality Management or related science discipline
* Highly experienced in GMP manufacturing and Quality Management of products regulated by FDA CBER or CDER or EMA
* Proven experience in senior leadership positions
* Must have prior aseptic processing experience
* Proven experience implementing CI initiatives to drive Quality programs and ensure maximum productivity. Ensure systems meet the needs of all internal and external constituencies with an emphasis on process, quality, productivity, budget control, and profitability.
* Past experience developing, implementing and monitoring Quality programs, policies and procedures to ensure compliance with GMP standards, corporate policies, FDA, EMA and other regulatory body regulations and guidelines.
* Serve as the point person with industry partners regarding product quality matters, customer satisfaction levels and regulatory authority interaction.
* Evaluate all current Quality systems and processes and recommend and implement appropriate enhancements to ensure the achievement of Lonza’s long-term objectives.
* Create active training and development plans for Quality staff with the objective of driving the overall competence and professionalism of the Quality functions.
* Represent the Lonza on quality and cGMP compliance issues that are specific to the site...
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Type: Permanent Location: Portsmouth, US-NH
Salary / Rate: Not Specified
Posted: 2024-04-24 08:08:46
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At Milk Specialties Global, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios.
The human nutrition division focuses on industry leading whey and milk protein isolates, concentrates, and hydrolysates - backed by the speed, execution and passion it takes to exceed the expectation of our customers.
We are currently seeking Sanitation candidates to join our Jerome, ID team.
This is a rotating schedule position, 12 hr shifts 6am-6pm.
Starting wage $19.00 per hour.
Ideal candidates will have exposure to the manufacturing environment.
We are committed to identifying and recruiting dedicated and reliable candidates to join the team of passionate employees.
Milk Specialties Global prides itself of advancement opportunities for our current workforce to promote within.
We offer a comprehensive benefits package that includes medical, dental, vision and life insurance, as well as a healthy 401(k) match program.
OPEN
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Type: Permanent Location: Jerome, US-ID
Salary / Rate: Not Specified
Posted: 2024-04-24 08:08:43
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Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Was Dich erwartet:
Als Team Business Finance sind wir flexibel und halten das Business handlungs- und sprachfähig - global wie lokal - intern wie extern.
Der Fokus unserer Arbeit liegt darauf, als Sparringspartner Squads, Teams und Abteilungen der Roche Pharma AG in allen finanziellen und unternehmerischen Entscheidungen unter Einbeziehung vorhandener Informationen als auch zukünftiger, antizipierter Entwicklungen zu beraten und Impulse zu setzen.
Als Praktikant (m/w/d) erhältst Du Einblick in alle Themenbereiche des Controllings und der Vertriebssteuerung.
Dies umfasst unter anderem:
* Unterstützung von Monatsabschluss Aktivitäten
* Mitarbeit in Marktforschungs- und Targetingprojekten im deutschen Pharmamarkt
* Mitarbeit bei der Budgetplanung/-präsentation
* Erarbeitung und Aufbau interner Berichte (z.B.
Sales- und Kostenberichte) sowie Erstellen von Analysen und Auswertungen (z.B.
Sales, Kosten, Headcount, KPI’s)
* Enge Zusammenarbeit mit Kolleginnen und Kollegen in den Fachabteilungen und Mitarbeiter/Übernahme von Projekten
Wer Du bist:
Dein Studiengang ist idealerweise wirtschaftswissenschaftlich ausgerichtet und Du hast Lust darauf, das Erlernte praktisch anzuwenden.
Neben einer hohen Affinität für Zahlen zeichnest Du Dich durch analytische Fähigkeiten, eigenständiges Arbeiten und Engagement aus.
Darüber hinaus bringst Du folgende Qualifikationen mit:
* Hohe Lernbereitschaft und Interesse an neuen Aufgaben
* Sicheres und kommunikationsstarkes Auftreten
* Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift
* Sehr gute MS Office Kenntnisse (Outlook, Excel, Powerpoint); optional Kenntnisse in SAP S/4Hana, SAP/ERP, SAC sowie SAP/BW bzw.
Business Objects
Die Vorteile:
* Flexible Zeiteinteilung
* 2025 € Vergütung im Monat für ein Vollzeitpraktikum > 3 Monate
* Vernetzung mit anderen Studierenden
* Kostenfreier Aufenthalt in unserem Boardinghouse
Die Bewerbung:
Bitte lade nur den Lebenslauf online hoch.
Denke daran, dass sich dieses Praktikum an Studierende (m/w/d) bei laufender Immatrikulation richtet oder alternativ an Personen im GAP-Year.
Zeitraum: ab dem 01.08.24, spätestens zum 15.08.2024 für die Dauer von 6 Monaten.
Wir freuen uns auf Deine Bewerbung!
Your contact to us! With people.
For people.
Do you need further support?
Please have a look at our FAQs, you will find them via https://careers.roche.com/global/en/faq.
Who we are
At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare.
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Type: Permanent Location: Grenzach, DE-BW
Salary / Rate: Not Specified
Posted: 2024-04-24 08:06:13
