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Your Job
We are currently recruiting for a Lab Technical Specialist for our Technical Center in Neenah, WI.
This person will be responsible for performing physical testing of products received from mills and consumers to ensure compliance and quality throughout the product lifecycle.
Our Team
Our Neenah Technical Center® is the central site for research, development, and lab services for Georgia-Pacific North American Consumer Products division.
The research and development areas include: Commercial and Retail towels, tissues, napkins and dispensers, Dixie® products and process development.
What You Will Do
* Physically testing products submitted by lab's clients
* Physically testing products from the paper machine and converting lines in the pilot plants
* Inputting test results, verifying data and reporting out results to clients
* Assuming Primary Person Responsible duties for several instruments in the lab to include maintenance, training and measurement control charting
* Supporting trial work at the mill locations when necessary
Who You Are (Basic Qualifications)
* Previous experience in a lab setting
* Able to travel up to 20% of the time
What Will Put You Ahead
* Associate Degree or higher in a physical science discipline
* 1+ years of lab experience
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based packaging, cellulose, specialty fibers, building products and much more, Georgia-Pacific works to meet evolving needs of customers worldwide with quality products.
In addition to the products we make, we operate one of the largest recycling businesses.
Our more than 30,000 employees in over 150 locations are empowered to innovate every day - to make everyday products even better.
At Koch, employees are empowered to do what they do best to make life better.
Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.
Our Benefits
Our goal is for each employee, and their families, to live fulfilling and healthy lives.
We provide essential resources and support to build and maintain physical, financial, and emotional strength - focusing...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2024-05-02 08:14:52
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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
027437 EHS Manager (Open)
Job Description:
Manages colleagues who perform Environmental Health & Safety work.
Typically supervises professional colleagues who exercise latitude and independence in assignments.
Key Responsibilities
* Manages the EH&S function and ensures the effective operations of the Environmental Health and Safety units.
* Oversees EH&S programs to ensure safe operating and working environments.
* Directs and reviews policies to ensure compliance with established standards.
* Direct supervision of professional staff including, recruitment, training, and performance reviews.
* Establishes and manages accident statistical basses for internal and external reporting.
* Prepares and presents a variety of reports, communications, and other documents.
* Develops and implements inspection policies and procedures, and a schedule of routine inspections.
* Develops health and safety procedures for necessary areas of the company.
* Performs other duties as assigned.
Education and Experience
* Typically possesses a Bachelor's degree (or equivalent) and 10 or more years of relevant experience.
Knowledge and Skills
* In-depth knowledge of relevant safety regulations.
* Demonstrated administration, planning and organization skills.
* Takes an analytical approach to complex issues and problem solving.
* Excels at training and coaching professional level colleagues.
* Exceptional interpersonal, communication and leadership skills.
* Demonstrated ability to analyze data pertaining to program functions and interpret other management information.
#LI-NG1
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EEO Statement:
https://www.greif.com/wp-content/uploads/2023/04/HR-101-Equal-Employment-Opportunity-Policy-English.pdf
We offer a competitive salary, excellent benefits and opportunity for growth.
Greif, Inc.
is an equal opportunity employer.
We will not discriminate against any applicant or employee on the basis of sexual orientation, gender identity, race, gender, religion, age, national origin, color, disability, or veteran status.
EOE/Minority/Female/Disabled/Veteran.
For more information read Greif’s Equal Opportunity Policy.
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Type: Permanent Location: Delaware, US-OH
Salary / Rate: Not Specified
Posted: 2024-05-01 08:45:40
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Sr.
Analytical Scientist, API Characterization
As Sr.
Analytical Scientist, API Characterization, you will be a vital part of our global team, contributing to the advancement of new chemical entities to market through your expertise in analytical method development and validation.
Your Responsibilities:
* Lead technical efforts in small molecule API analytical development, enabling the design, development, and implementation of analytical methodologies for small molecule characterization and analysis, including peptides.
* Establish analytical control strategy and specifications for API that can be transferred into manufacturing and successfully registered globally, requiring cross functional collaboration with manufacturing, development, and regulatory affairs
* Oversee the development and validation of analytical methods in third-party organizations, ensuring adherence to quality standards.
* Design and implement VICH-compliant stability studies conducted by external partners.
* Author analytical submission documentation and coordinate the CMC sections of dossiers for worldwide registrations, including responding to technical questions from Health Authorities.
* Serve as the Analytical Subject Matter Expert for global project development teams.
* Ensure adoption of state-of-the-art technologies and QbD (Quality by Design) development concepts as well as adherence to quality standards
What You Need to Succeed (minimum qualifications):
* Education: PhD in a scientific discipline (e.g., Analytical Chemistry or equivalent)
* Required Experience: A minimum of 5+ years of related experience in industry
* Top 2 skills: Strong understanding of pharmaceutical analytical chemistry and analytical techniques, such as HPLC/UPLC, NMR, SSPC, GC, IR, UV.
Familiarity with ICH and/or VICH guidance and GMP regulations.
What will give you a competitive edge (preferred qualifications):
* Experience in planning, designing, and evaluating Health Authority registrat...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:33
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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!
In this position, the incumbent will be trained in the set-up, operations, and troubleshooting of the equipment in the production areas. Additional duties will include documentation of work and specific computer functions.
Must integrate company initiatives such as LEAN into work practices.
Responsible for safely producing vaccines which meet all product specifications in accordance with current Good Manufacturing Practice standards.
NOTE: This position is offering a $2,500 Sign-On Bonus!
Basic Minimum Qualifications:
* High School Diploma/GED plus 4 years relevant experience
* Basic computer skills with Word, Excel and Electronic Management Systems
* Ability to read, interpret and conform to batch records, Quality and Safety requirements.
* Ability to operate applicable ERP system.
* Requires basic knowledge of manufacturing function, acquaintance with and general understanding of aspects of the production process and ability to apply this knowledge to situations ordinarily encountered.
* Ability to work Sunday - Thursday, 6pm-2:30am
Job Responsibilities:
* Perform duties associated with aseptic processes, weighing, measuring, counting, calculations, sampling, and verifications required for biological production processes in accordance with batch production records (BPR) and in compliance with current good manufacturing practice (cGMP) standards, all current safety standards and site procedures.
* Understands, performs and teaches others basic operation of production equipment and ensures all equipment, instruments and production materials are released and available for use.
Look up and perform transactions within the electronic inventory management system.
* To oversee production processes, cleaning, environmental monitoring and personnel and perform in-process batch quality checks per the written procedures.
Knows and follows safety rules, wears appropriate safety equipment and maintains proper safety practices at all times.
* Basic computer skills to create and update standard operating procedu...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:31
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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!
Primary Function
* 了解并满足客户的需求，为客户提供有竞争力和有价值的服务
* 执行公司的业务发展战略，完成公司在当地的销售计划，实现公司的利益.
Primary Accountabilities/Responsibilities
* 执行公司业务发展战略，完成/超越销售指标
* 拜访养殖单位/客户，提供有价值的服务，体现公司的服务理念
* 建立并保持良好的分销渠道（经销商、兽药店）
* 组织技术研讨会，主讲小型的技术讲座
* 调查、反馈市场信息，与公司相关部门合作进行市场推广及市场分析
* 拓展公司在当地的业务，建立公司品牌和产品品牌
* 制定区域市场发展计划
* 管理当地销售团队和第三方销售员(TPS)，如有
Minimum Qualification:
* 动物科学、动物医学、动物营养及相关专业本科以上学历
* 3年以上农场或动保行业销售工作经验
* 熟悉猪饲料添加剂，功能性添加剂，饲料和动保市场
* 普通话流利，基本英语听、说、读、写能力
* 熟练操作电脑
* 居住在广西和湖南为尤佳
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:29
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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!
Chemielaborant Analytische Entwicklung SMTD (Small Molecule Technical Development) (m/w/d)
Wir suchen zum nächstmöglichen Termin eine/n Chemielaborant/in/Chemotechniker/Bachelor in der Chemie in der analytischen Entwicklung SMTD (m/w/d) am Standort Monheim am Rhein, Deutschland.
Die Position:
Als Chemielaborant der analytischen Entwicklung von Small Molecules Technical Development ist man Teil eines funktionalen Teams und arbeitet eng mit angrenzenden Disziplinen zusammen (Formuliertechnologie, Verpackungstechnologie, Wirkstoffentwicklung).
Zentral ist hierfür das eigenständige Umsetzen von wissenschaftlichen Protokollen unter Anwendung verschiedener analytischer Techniken mit dem Schwerpunkt Chromatographie.
Zu den Kernaufgaben zählen die analytische Methodenentwicklung, Methodenvalidierung und -transfers, sowie die Durchführung von Entwicklungsstabilitätsstudien und registrierrelevanten Stabilitätsstudien unter GMP.
Ihre Aufgaben und Verantwortlichkeiten:
* Praktische Versuchsdurchführung zur Entwicklung/Validierung analytischer Prüfverfahren für die Qualitätskontrolle neuer Tierarzneimittel
* Analytische Begleitung der Formulierentwicklung
* Prüfung von Stabilitätsmustern unter Berücksichtigung der relevanten Richtlinien
* Eigenständige Planung, Organisation, Durchführung und Dokumentation von Versuchsreihen
* Datenanalyse zur weiteren Versuchsplanung sowie Unterstützung bei der Ergebnisinterpretation
* Unterstützung beim Erstellen von Berichten, Arbeits-, Prüf- und Verfahrensanweisungen
* Präsentation von Ergebnissen bei Team-, Projekt- oder Gruppenbesprechungen
* Intensive Zusammenarbeit mit Kollegen im F&E Umfeld zum Wissensaustausch
* Berücksichtigung externer und interner Richtlinien (z.B.
SOPs, GxP, HSE).
* Pflege der Laborinfrastruktur und der organisierten, sauberen und sicheren Arbeitsumgebung.
* Planung / Durchführung der Wartung von Instrumenten / Geräten sowie Evaluierung neuer Laborgeräte
* Arbeiten unter Verwendung der entsprechenden Sicherh...
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Type: Permanent Location: Monheim, DE-NW
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:29
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Global Clinical Development Scientist
Join our innovative team and take the lead in developing groundbreaking parasiticide products for pet health! As the Global Clinical Lead, you'll spearhead the planning, coordination, and implementation of top-tier clinical effectiveness and target animal safety programs.
Dive into exciting pilot and pivotal studies, ensuring compliance with global regulatory standards like GLP, vGCP, and VICH guidelines.
Play a pivotal role in driving the future of pet health innovation!
Your Responsibilities:
* Serve as Global Clinical Lead, representing Global Clinical Development on R&D Project Teams.
* Formulate comprehensive clinical development plans for new products, fostering cross-departmental relationships.
* Focus primarily on parasiticide product development, with potential involvement in therapeutics.
* Execute clinical programs, designing protocols for efficacy studies in collaboration with other teams.
* Coordinate study monitoring to ensure compliance with regulations and company policies.
* Analyze and interpret study results, collaborating with Regulatory Affairs for submission to regulatory agencies.
* Ensure quality assurance and regulatory compliance through administrative activities and process development.
What You Need to Succeed (minimum qualifications):
* Education: DVM or Ph.D.
in an animal health related field preferred, MS with experience considered.
* Required Experience: Three or more years of experience in product development within or closely associated with the pharmaceutical industry preferred.
* Top 2 skills: Proficient in strategic planning and forward-thinking, with a consistent focus on achieving desired outcomes.
Basic understanding of research and development processes.
What will give you a competitive edge (preferred qualifications):
* Keen interest in parasitology or significant practical experience in the discipline.
* Experience working with regulatory authorities.
* Knowledge of GCP/GLP/GMP and quality sta...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:28
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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!
Position Description:
Drive and influence for successful identification and design of novel small molecule drug candidates for clinical development, utilizing a complementary set of in silico, in vitro and in vivo tools and datasets within a matrix environment inclusive of internal and external collaboration partners.
Actively support the research portfolio, project strategies, and initiatives that contribute to the success of Elanco R&D.
Functions, Duties, Tasks:
* Generate, support or lead global projects focused on the design and progression of small molecule drug candidates across Elanco research activities (multi parameter optimization)
* Manage allocation and capacity of the external chemistry resources to ensure timelines and key milestones.
* Work with the head of small molecules discovery to ensure resource alignment with project prioritization schemes (scope - SAR plans, timelines, resources & risk/mitigation/contingencies).
* Ensure constant flow of new research projects aligned with R&D strategy, by reviewing literature and external sources of innovation (academia, biotech/phama and agricultural companies) for new chemistry targets or platforms; contribute to Elanco Research strategies and goals.
* Provide scientific input and guidance to external project sources for portfolio entry into the companion and food animal research efforts.
* Identify and implement relevant technologies, methods and strategies in the respective discipline.
Continuously improve technical expertise in the function.
Proactively initiates value-added work to simplify processes, build capabilities and/or drive the portfolio.
* Maintain and foster sound working relationships within Research and to other functions such as Computational Science / Pharmacokinetics, Pharmacology/ Parasiticides, Safety, and External Innovation.
Ensure compliance with internal and external guidelines regarding quality and safety (quality manuals, good research principles, health authority guidance and SOPs).
Minimum Qualification (education, experience an...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:20
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
This is your opportunity to help share the future of sustainability with world-changing innovations and low-carbon technologies.
Become a valued part of the team that’s shaping the future of aluminium, revolutionising the way the world lives, builds, moves and flies.
Be part of it and shape your world.
About the Role:
We are seeking a dedicated and proactive Health Resource Officer to join our team at the Portland smelter on a 12 hour rotating days/night shift roster.
This pivotal role supports our commitment to maintaining the highest standards of health, safety, and emergency response, ensuring a safe and secure environment for all staff and visitors.
Joining a collaborative and supportive team your key responsibilities will include:
* Lead and coordinate the site's emergency response program, responding swiftly and effectively to any site emergencies.
* Deliver first aid treatment and manage ongoing care, keeping detailed records in line with legal and company requirements.
* Oversee safety and emergency response training programs, including firefighting, hazardous chemical control, and rescue operations.
* Manage and operate plant communication systems, alarms, and ensure efficient access control to the plant.
* Conduct safety inspections, equipment maintenance, and contribute to safety management programs such as confined space and hot work protocols.
* Act as the first point of contact for plant visitors, ensuring compliance with safety regulations from induction to exit.
* Develop and maintain critical emergency management documentation and training materials.
This role is more than a job—it's a commitment to safety and excellence.
At Alcoa, we provide a dynamic work environment where you can truly make a difference.
Help us keep our workplace safe and respond with precision and care to any challenge that arises.
What’s on offer:
* Career development opportunities to pursue your passion
* Five weeks annual leave
* Shift allowance
* Benefits allowance
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
To play a part in our ongoing success we are seeking someone with:
* Prior experience in First Aid or Emergency Response.
* Certificate III in Emergency Response and Rescue (RII30715) or similar qualification preferred.
* Skills in drug specimen collection (HLTPAT005) are desirable.
* Must have a current police clearance.
* Class A and HR licenses are desirable, with additional qualifications in security considered advantageous.
* Strong proficiency in Microsoft Office and gene...
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Type: Permanent Location: PORTLAND, AU-VIC
Salary / Rate: Not Specified
Posted: 2024-05-01 08:18:28
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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.
For Ibex™ Solutions (www.ibex.lonza.com), our unique biological manufacturing and development concept in Visp, Switzerland, we have multiple openings.
Become part of this exciting opportunity and join our team by applying for the position as MSAT (Manufacturing Science and Technology) Process Validation Expert.
In this role, you will be responsible for successful validation of process transfer, scale up and optimization in the biopharmaceutical plants, including process characterization, validation activities at scale, continued process verification and Product Quality Reviews (PQRs).
You will significantly contribute to the development of the MSAT Bio validation group and share the responsibility as a long-term process validation expert.
Key Responsibilities
* Designing process validation strategy for bio processes at Lonza
* Preparation of validation documents (study design / writing protocols and reports) according to Lonza procedure and in compliance with regulatory guidance
* Leading the process validation teams including communication with customers
* Supporting R&D teams during the process characterization phase.
Reviewing and approving of process characterization documents
* Responsibility for the validation assessment on changes and deviations (approval of deviation and changes)
* Preparation and maintenance of a documented continued process verification plan
* Assessing and approving of Product Quality Reviews
Key Requirements
* Master in Chemistry, Biotechnology, Life Sciences or related field
* Experience in project management, preferable in MSAT, Quality and Compliance
* Experience in interaction with different stakeholders within an organization and with regulatory agencies (Swissmedic, FDA etc.) would be an advantage
* Fluent communication in English (written and spoken), additional fluent communication in German is appreciated
* Ability to work on different tasks simultaneously and to work towards deadlines
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 not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, w...
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Type: Permanent Location: Visp, CH-BL
Salary / Rate: Not Specified
Posted: 2024-05-01 08:17:19
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Are you looking to help transform a company and an industry? As a Stewart employee, you’ll be joining a company that is committed to helping you own, develop, and nurture your career while growing our company.
We invest in your career journey because we understand that as you grow so does our company.
You will be part of a diverse and equitable work environment that reflects the customers we serve.
You’ll be empowered to use your unique experiences, passion and skills to help our company constantly evolve and improve.
Together, we can achieve our vision of becoming the premier title services company.
More information can be found at https://www.stewart.com, subscribe to the Stewart blog at https://blog.stewart.com or follow Stewart on Twitter® @stewarttitleco.
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.
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Type: Permanent Location: San Antonio, US-TX
Salary / Rate: Not Specified
Posted: 2024-05-01 08:14:09
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
About the Role:
Exploration operates large annual exploration drilling programs with multiple rigs working across very large areas, generating thousands of data points per day.
The efficient and secure collection and processing of this data is critical to the success of the programs and requires the coordinated and innovative application of technology and software (currently the Microsoft Power Platform).
The primary function of the Exploration Systems Specialist role is to design, implement and maintain the data collection, processing, and reporting systems for Exploration.
This includes the selection of hardware, customising of firmware in collaboration with vendors and the development of user interfaces (Power Apps) and reports (Power BI).
The incumbent will apply their working knowledge of SQL and Python to ensure the maintenance and optimisation of these field-based collection and display systems, the associated workflows and linkages to the central databases, AcQuire and GIS.
What’s on offer:
* Career development opportunities to pursue your passion
* Monthly Leisure Day
* Benefits allowance
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
To play a part in our ongoing success we are seeking someone with:
* Ideally a Computer Science Degree (geospatial or similar) with Minimum 5yrs experience in a mining or exploration environment, with demonstrated experience in the application of GPS technologies.
* Experience with Power Platform Developer – PowerApps, Power BI, and Power Automate (Flows).
* Experience with database management, primarily SQL Server and T-SQL.
* Experience with ArcGIS Enterprise/Pro desired but not essential.
* Experience with C# .NET Framework desired but not essential.
If you feel that you meet some of the criteria above but would need help and training to develop some aspects, please apply, training and support will be available.
About the Location
Huntly is one of our two bauxite mines in Western Australia and it is the world’s second largest bauxite mine, supplying ore to Alcoa’s Pinjarra and Kwinana alumina refineries.
Established in 1976 and located east of North Dandalup in WA.
Bauxite ore from Alcoa’s Huntly and Willowdale mines helps to produce almost half of Australia’s alumina and approximately 19 per cent of Australia’s aluminium.
Our workplace is an inclusive and respectful environment, where we embrace change, new ideas and equal opportunity to succeed.
Come shape your career with us!
We are values led, vision driven and united by our purpose of transforming raw potential i...
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Type: Permanent Location: PINJARRA, AU-WA
Salary / Rate: Not Specified
Posted: 2024-05-01 08:13:41
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Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist.
Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen.
Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen.
Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig.
Denn ihre Ideen, ob gross und klein, verbessern die Welt.
Und das ist die Art von Arbeit, an der wir Teil haben möchten.
Für unserer Standort Visp suchen wir eine/n QC Senior Laboratory Technician / Laborant (all genders).
Ihre Aufgaben:
* Als Mitglied unseres QualitätskontrolleTeams sind Sie unter Einhaltung der GMP- und Sicherheitsrichtlinien verantwortlich für die Durchführung von analytischen Methoden, mit Schwerpunkt in der HPLC Analytik
* Neben der Durchführung von Routine-Analytik umfassen Ihre Aufgaben Methodenimplementierung, -validierungen und Methodentransfers
* Sie arbeiten nach Qualitätsrichtlinien und führen neben der praktischen Laborarbeit auch die notwendigen administrativen Tätigkeiten durch, wie z.B.
die Dokumentation der Resultate und das Erstellen von Arbeitsanweisungen durch
* Dabei unterstützen Sie gleichzeitig den Laborunterhalt (Geräteverantwortlichkeit) und geben Acht auf Sauberkeit und Ordnung im Labor
* Die abwechslungsreichen Verantwortlichkeiten beinhalten auch die enge Zusammenarbeit mit Schichtmitarbeitenden, Betreuung von Lehrlingen sowie Pikettdienst
Ihr Anforderungsprofil:
* Sie verfügen über eine abgeschlossene Ausbildung als Laborant/in Fachrichtung Chemie oder Biologie oder gleichwertig
* Sehr gute Kenntnisse mit HPLC wird vorausgesetz
* Erfahrung mit GMP ist von Vorteil
* Fließende Sprachkenntnisse (Wort und Schrift) in Deutsch wird vorausgesetzt.
Gute Kenntnisse in Englisch sind ein Plus
* Sie sind selbständig, gewissenhaft und verantwortungsbewusst und besitzen eine gute Kommunikations- und Teamfähigkeit sowie Freude an interdisziplinärer Zusammenarbeit
* Sie besitzen die Fähigkeit abstrakt zu denken, sind gut organisiert und bleiben in stressigen Situation ruhig
* Ihre Lern- und Einsatzbereitschaft runden Ihr Profil zudem ab
Lonza’s Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar.
Wie wir unsere Geschäftsergebnisse erreichen, ist für uns genauso wichtig wie unsere Erfolge selbst.
Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt.
Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.
Zu Lonza kommen Menschen, die Herausforderungen annehmen und mit ihrer Kreativität im Bereich Life Science neue Ideen für komplexe Problemstellungen entwickeln.
Zusammen leisten wir ein...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-01 08:07:10
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Your Job
A TSBU MIE is the technical lead for all manufacturing process disciplines and serves as the liaison to the core PDT and is responsible for the overall manufacturing process development.
This involves leading the technical efforts with the mold& die tooling, plating, automation groups, CAE, Packaging, and plant process engineers to assure effective "design for manufacturing" with that the technical goals of the program are achieved and drive competitive manufacturing solutions under economical thinking and decision-making framework.
MIE is the constant contact with the product engineers, product managers also often in direct contact with customers to ensure the customer understands the process and help in support of product managers and product engineers to facilitate strong compromise and then success for all.
What You Will Do
* Lead and coordinate technical communications among mfg.
engineering and liaison to product development team and customers, assuring technical resources fully understand customer's needs and get feedback in between to enable strong compromise of feasibility review and DFM (Design for manufacturing) solutions.
* Partner with Product Managers, product engineering, procurement, quality, and to strengthen the technical success opportunities and competitive manufacturing proposals which customers preferred and deliver excellent processes to our organization under economical thinking and DMF (Decision Making Framework).
* Responsible for building the manufacturing quote summary based on inputs from the technical teams and preparing manufacturing deliverables phase reviews and be the face and voice of the technical team members by presenting to the management team, having humility and open to challenges and feedback.
* Be an advocate for both the design and manufacturing groups.
Facilitate strong compromise and success for all.
* Lead the technical resources in investigations, discovery and solving of manufacturing problems.
* Depth engaged in process qualification plans and runs which leading to successful production release.
* Support Make and Buy decision making, provide support outsourcing feasibility assessment.
* May require some global travel to codevelop product designs and discover process improvement opportunities.
* Will directly exposure to global communications with English.
Who You Are (Basic Qualifications)
* Bachelor's degree in science engineering or equivalent with qualified certification, or above.
* 5 years+ experiences in manufacturing process/tooling development, e.g., molding, insert molding, automation, stamping, plating, SMT, etc.
or direct exposure to product engineering development, quality planning and improvement etc.
* Experience around pFMEA/Lean/Six sigma is a plus.
* Strong integrity and PBM virtues with the strength to face difficult situations with transparency and a sense of urgency and hold accountability.
...
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Type: Permanent Location: ChengDu, Sichuan, CN-51
Salary / Rate: Not Specified
Posted: 2024-04-30 08:31:57
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ERM is hiring a Construction Safety Specialist for a key construction client in Columbus, OH.
In this critical role, you will be responsible for establishing, implementing, managing, and continuously improving the safety programs for several ongoing construction projects.
The Construction Safety Specialist will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a full-time (40 hours), fixed-term position for a duration of one year, renewable.
RESPONBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Provide timely, high quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments.
And pre-task plans
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze Safety performance and initiate action to support or correct trends.
* Coordinate local business continuity, emergency response, and crisis management plans.
Develop and test the plans.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree is preferred.
* Minimum 3 years’ experience with H&S in the construction industry, preferably with data center construction or large projects.
CHST certification a plus.
* Proficient with the management of high-risk activities including electrical safety, excavation, fall protection, material handling, and crane operations.
* Experienced in communicating and problem solving as a team with sub-contractors is required.
* A background and knowledge working with specific trades such as electricians, ironworkers, pipefitters etc.
is a plus.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
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 ...
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Type: Permanent Location: Columbus, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-30 08:31:49
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We are seeking a Senior Manager of UX Research who will lead a small but influential team of mixed-method researchers who work with cross-functional product, design, and engineering teams as they plan, design, build and deploy Tricentis products for our customers. You will collaborate with the leadership team to define and execute the vision for the UX Research team as it informs long-term strategy and refines product experiences for near-term delivery.
As a player-coach you will leverage user research to shape how the business understands and prioritizes the user’s experience, as well as partnering with cross functional teams to ensure a seamless experience across our Desktop and SaaS products.
You will help drive a consumer-driven mindset across the org by instilling an understanding of the end-to-end user experience and advocating for the consumer across the org.
You possess a strong understanding of quantitative and qualitative user research methods and can leverage insights to make actionable recommendations to improve the digital experience.
You are an excellent communicator with high emotional intelligence, and a great collaborator committed to high-quality and rigorous research in a fast-moving organization.
Responsibilities:
* Collaborate with senior stakeholders to understand business opportunities and to identify and prioritize projects for the UX research team.
* Collaborate with leadership to define UX and product improvement opportunities.
* Set goals, measure success of research projects, and implement ways to continually improve.
* Forecast resource needs and grow the team to provide necessary capabilities and expertise.
* Manage, mentor and develop the abilities of our UX Researchers who support our strategic vision.
* Partner with Design, Product, Engineering to build in research at multiple stages of the product development process.
Requirements:
* 7+ years of experience as a UX Researcher, combining quantitative and qualitative methodologies.
* 3+ years of experience managing and developing a UX Research team (or cross functional design organization).
* Excellent communication, negotiation and collaboration skills.
* Excellent coaching and mentoring skills.
* Expertise in both quantitative and qualitative research methods with the ability to determine the right methodology for the question at hand.
* Track record of discovering, synthesizing, and socializing actionable insights that have influenced real product decisions and produced true business impact.
* Experience working in an international company, managing teams and research across different geographies is a plus.
Tricentis Core Values: Knowing what we need to achieve and how to achieve it is important.
Tricentis core values define our ways of working and the behaviors we model that create an enjoyable and successful Tricentis life.
* Continu...
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2024-04-30 08:29:29
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POSITION SUMMARY:
The main focus will be to improve product quality and reduce cost through optimization of practices and standards, trials of the new processes, methods and materials, stabilization of improvements gained and strong collaboration.
This position has responsibility for all Vallourec Star locations.
KEY RESPONSIBILITIES:
Oversee NDT inspection requirements of outsourced inspection company.
Review, write and standardize NDT practices as it relates to API and customer requirements.
* Review customer specifications to evaluate capability.
Develop quality plans based on customer need.
* Use knowledge of product and testing requirements to perform field service evaluation when customer issues arise.
* Utilize 8D problem solving to reduce customer claims.
* Technical support for heat treating, threading and inspection operations to resolve multi-discipline problems.
Maintain and improve standard procedures, train the operators on use of procedures.
Reduce variation of key process indicators.
•Manage quality parameters for Level 3 IT mill system.
Develop test plans and assure customer and quality requirements are correctly applied to meet customer orders.
* Internal and Supplier management system audits.
* Benchmark the existing and evaluate new technologies, processes, materials.
* Use advanced problem-solving techniques such as Design of Experiments, process capability, SPC and FMEA to isolate and reduce sources of variation and to resolve production and quality issues.
* Implement root cause analysis and corrective action of non-conformance to mitigate rework, reduce cost and improve quality.
* Coordinate Project activities with Vallourec R&D centers, external research organizations and universities.
* Promote effective communication vertically and horizontally within the organization.
EXPERIENCE, SKILLS, AND KNOWLEDGE:
The position will require a strong statistical and metallurgical background to problem solve.
API product and specification background is required.
The ability to work in diverse groups to achieve a common goal is critical to the success of this position.
The individual must be proficient in Microsoft Excel, Access and PowerPoint.
Also, knowledge in statistical software, such as Minitab, is beneficial.
EDUCATION, TRAINING, AND CERTIFICATIONS:
* BS in engineering discipline with a preference in metallurgy/material science.
* Prefer: Training or Certifications of either UT and/or EMI principles.
ASNT Level Il or level Ill.
If level Il, willing to complete ASNT Level Ill certification.
CRITICAL COMPETENCIES & CAPABILITIES:
The position will require demonstrated leadership experience and the ability to concisely communicate objectives and results to reach targeted goals.
Flexibility to work in R&D, process control, quality assurance (lab testing and quality systems) and technical service.
Quality
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2024-04-30 08:27:36
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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!
Responsibilities:
* Responsible for your own safety and in ensuring safe working practices are followed in the laboratory to create a safe working environment for all staff by wearing correct Personal Protective Equipment at all times and any identified risks are reported.
* Analyze samples in a timely manner to meet laboratory key performance indicators and customer needs by performing analysis according to the laboratory schedule and relevant Quality Control documentation and prompt review of results.
* Provide a prompt investigation of all Quality Control out of specification results to enable the release of test results within agreed timeframes by ensuring investigations and corrective and preventative actions are completed by their due date.
* Conduct all routine analysis and with adherence to Quality Control procedures to remain in compliance and deliver accurate results by following local standard operating procedures, Good Manufacturing Practice, Good Laboratory Practice and site Quality Systems.
* Assist in the development of standard operating procedures and test methods to ensure the Quality Control documents are accurate and within their review date by drafting documents and reviewing documents as assigned.
* Assess that all equipment is qualified and calibrated according to standard to ensure accurate test results are generated by reviewing equipment status before use and reporting any deviations to the Quality Control Manager.
* Maintain microbiological reference cultures to agreed standards.
* Perform media preparation, validation and quality control checks to agreed standards.
Basic Qualification:
* Minimum Bachelor's Degree in Microbiology or related field.
* 3 years of work experience in a microbiology laboratory in Pharmaceutical industry.
* Must have work experience in GMP and knowledge in GLP.
* Experience in media/method validation would be an advantage.
* Strong problem-solving skills, including Out of Specification investigations.
* Candidates must be legally a...
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Type: Permanent Location: Auckland, NZ-AUK
Salary / Rate: Not Specified
Posted: 2024-04-30 08:19:43
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
At Alcoa, you’re an essential part of our purpose: to turn raw potential into real progress.
This is an opportunity for you to bring your wealth of experience to the team and help shape our future - You have the power to shape things to make them better.
About the Role
We have 3 positions within our Kwinana health & safety team for Emergency Services Officers, based on a 12-hour shift position - Working in a team of two officers on shift, you will be responsible for on-site medical and emergency response co-ordination by providing medical services to employees requiring treatment for emergency and non-emergency incidents.
You will co-ordinate and integrate with the site Emergency Response Team to ensure timely and effective response to incidents for the protection and well-being of all site personnel, company assets, and the environment.
Site security access forms a part of this role.
Your main responsibilities include, but are not limited to:
* Emergency Management for the Prevention, Preparedness, Response and Recovery of incidents and risks to site personnel, the Refinery, and the Business.
* Medical Emergency response site wide for the treatment application of emergency and non-emergency medical conditions in accordance with approved clinical practice guidelines.
* Site access control and security co-ordination, inclusive of all supporting systems, reporting, administration, and area access management.
* Co-ordination of the Emergency Response Team to ensure readiness and availability for response prior to commencement of site high risk works.
* Fire protection systems monitoring, response co-ordination and maintenance reporting.
* Engagement with internal business units for the delivery, implementation, approval, and maintenance of emergency management and security services and systems.
* Lead, advise, and train as required contract Emergency Services Officers.
* Conduct AOD specimen collection for suspicion/cause/FFW or random testing
* Skill specific training enabling improvement and maintenance for individual, team, and Emergency Response Team members.
What’s on offer:
* Career development opportunities to pursue your passion
* Shift allowance
* Five weeks annual leave
* Benefits allowance
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
To play a part in our ongoing success we are seeking someone with:
* Cert IV Health Care and Cert III Mines Rescue.
* Emergency Management experience in high risk environments.
* A background in heavy industrial or resources se...
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Type: Permanent Location: KWINANA, AU-WA
Salary / Rate: Not Specified
Posted: 2024-04-30 08:19:20
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
WA Mining Biodiversity Advisor will provide on-ground and project management support for flora, fauna and vegetation surveys and monitoring, and provide advice on biodiversity to WA mining.
Reporting to the Environmental Specialist- Biological Assessments, the position has a strong project management and contractor liaison focus and will be required to communicate the importance of processes related to biodiversity across WA mining.
This is your opportunity to shape your career through the skills and experience you bring to the role now and by training for the roles you may want in the future.
Our success depends on great teams, where you can thrive and do your best work in a supportive environment. This is an exciting opportunity to develop and implement biodiversity programs across Alcoa’s Mining Operations.
The position will be offered as on a Monday to Friday roster based at Pinjarra hub offices, with site travel to our WA mining operations at Willowdale and Huntly.
About the Role:
* Project manage fauna pre-clearance works, including liaising with mining clearing supervisors to track harvesting and clearing schedules and requirements.
* Manage consultants completing specialist fauna pre-clearance monitoring works.
* Ensure complete and timely record keeping and data collection.
Ensure standardisation of all data, records, and reports received.
* Maintain fauna sightings register and associated database.
* Support WA Mining in flora, vegetation, and fauna survey requirements and consultant management.
* Support WA Mining in change management, effectively communicating and ensuring processes and procedures are followed across sites.
What’s on offer:
* Career development opportunities to pursue your passion
* Monthly Leisure Day
* Benefits allowance
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
To play a part in our ongoing success we are seeking someone with:
* A Bachelor's degree, in Environmental Science, Zoology, Conservation Biology or related disciplines, or a Post-graduate qualifications in Ecology or relevant field experience.
* Minimum of 2 years’ experience in fauna or flora related work.
* Strong communication and interpersonal skills.
* Minesite experience desirable.
* Demonstrate experience in ensuring safe working practices.
* Project and Contractor Management desirable.
* Strong self-management skills/well organised.
About the Location
As an Alcoan you are part of a global team committed to advancing sustainability and delivering excellence and innovation.
Join...
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Type: Permanent Location: PINJARRA, AU-WA
Salary / Rate: Not Specified
Posted: 2024-04-30 08:19:20
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Fresenius Clinical Leadership opportunities including Clinical Manager, Facility Administrator, Home Therapy Clinical Manager & Inpatient Services Program Manager within the Midwest Group including the states of:
Indiana
Illinois
Minnesota
Missouri
Wisconsin
About this role: As a Clinical Manager with Fresenius Medical Care, you will ensure that quality patient care is delivered while maintaining clinical operations. As the facility leader, you will be part of a close-knit, collaborative team responsible for delivering unique care plans and providing dialysis treatment to patients facing end stage renal disease or chronic kidney disease.
Training and advancement: You will enter our Clinical Leadership Program that creates and supports a culture of continuous learning for our managers.
The curriculum will cover onboarding, essential functions, leading your business, and advanced leadership. As a Clinical Manager, you may advance your career into an Area Team Lead or Director of Operations role.
Our culture: We believe our employees are our most important asset — we value, care about, and support our people.
We are there when you may need us most, from tuition reimbursement to support your education goals, granting scholarships to family members, delivering relief when natural disasters strike, or providing financial support when personal hardship hits, we take care of our people.
Our focus on diversity: We have built a nurturing environment that welcomes every age, race, gender, sexual orientation, background, and cultural tradition.
We have a diverse range of employee resource groups (ERGs) to encourage employees with similar interests, goals, social and cultural backgrounds, or experiences to come together for professional and personal development, discussion, activities, and peer support.
Our diverse workforce and culture encourage opportunity, equity, and inclusion for all, which is a tremendous asset that sets us apart.
At Fresenius Medical Care, you will truly make a difference in the lives of people living with kidney disease.
If this sounds like the career and company you have been looking for, and you want to be a vital part of the future of healthcare, apply today.
PRINCIPAL RESPONSIBILITIES AND DUTIES
CLINIC OPERATIONS:
* Manages the operations of the clinic, including costs, processes, staffing, and quality standards.
* Provides leadership, coaching, and development plans for all direct reports.
* Partners with internal Human Resources, Quality, and Technical Services departments.
* Collaborates with or functions as the Home Therapies Program Manager to oversee the facility’s Home Therapies Program.
* Maintains integrity of medical and operations records and complies with all data collections and auditing activities.
* Accountable for completion of the Annual Standing Order Review and Internal Classification of Disease (ICD) coding.
* Manages clinic financials including ...
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Type: Permanent Location: Downers Grove, US-IL
Salary / Rate: Not Specified
Posted: 2024-04-30 08:19:16
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Lead Scientist - Analytical Science
Job Description
We are seeking an Analytical Lead Scientist to support projects utilizing Chromatography and various techniques, with Mass Spectrometry (MS).
Candidates should have primarily scientific and industrial experience in Liquid Chromatography (LC) and LC-MS aided by sample preparation techniques.
Candidates will have demonstrated abilities in sample preparation techniques, analytical methods development and solving chemical, quality, and material problems for Consumer Packed goods (CPG) products.
The focus of this role is on early to mid-stage development of Family Care, Personal Care, and Kimberly-Clark Professional materials and products, with demonstrated ability to drive projects and function as part of a larger team to accomplish project goals.
This position will interface with internal Kimberly-Clark customers across the globe such as researchers, quality, product safety and mill personnel.
Excellent collaborative skills across functional areas are necessary.
The incumbent will report to the Global Research and Engineering Senior Manager-Analytical Sciences and will receive direction in documented project objectives.
Responsibilities:
Apply LC and LC-MS analytical knowledge to solving customer problems involving formulations, new products, process problems, failure analysis, customer complaints, and intellectual property.
Perform necessary sample preparation using techniques as required for LC, LC-MS, including established sample extraction methods.
Apply knowledge in UV spectroscopy and classical wet lab techniques such as titration and gravimetric analysis.
Conduct and develop analytical test methods to support various internal customer projects.
Provide protection to internally developed methodologies and technologies through the appropriate use of patents and trade secrets.
Accurately record, analyze, and interpret analytical data with limited assistance and direction.
Document work in a laboratory E-notebook and publish analytical and/or formal technical reports.
Participate in interdisciplinary and cross functional project teams to obtain practical solutions for our internal customers.
Effectively communicate project plans and results to internal customers.
Be able to work safely in a lab environment, complying with all rules and regulations.
Perform routine and in-depth maintenance and troubleshooting to keep instruments functioning properly.
Contribute to an environment in which all team members are respected regardless of their individual differences and are motivated to improve both their individual and team contributions to achieve desired business results.
Required Qualifications:
A bachelor’s degree in chemistry or a related field from an accredited college or university.
5+ years of direct work experience, with a BS degree, in an Analytical Lab with hands-on experience with liquid chromatography instrumentation.
Experience developing and conducting liquid chromatogr...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2024-04-30 08:16:48
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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's Small Molecules department is currently seeking a Senior Chemist to join our dynamic team.
This position is based at our Visp, Switzerland site, which stands as the largest and most historic location within Lonza's global network of more than 30 sites.
Renowned for its contributions to research, development, and manufacturing, our Visp site offers an unparalleled environment for professional growth.
As a Chemist in our MSAT (Manufacturing Science & Technology) team specializing in Chemical Manufacturing Pharma, you are responsible for scale-up, implementation, and optimization of chemical processes.
As a technical expert, you are the process owner for an assigned portfolio of commercial products and drive proactive life-cycle management through continuous and systematic optimization of production processes.
You also play a key role during new product introductions and are responsible for a smooth and complete process of knowledge transfer from the customer to Lonza.
Your work includes planning and supervising the execution of experiments as well as data analysis, writing reports, preparation of customer presentations, and documentation.
The diversified responsibilities of your role comprise also the supervision of lab professionals.
You will work in interdisciplinary teams committed to ensuring product profitability and sustainable business success.
This position presents an exciting chance for someone who has successfully completed their academic journey and is eager to make a mark in the industry.
Key responsibilities:
* Responsible for continuous optimization of production processes in terms of productivity (yield and throughput), quality, safety, and ecology: development and optimization of chemical processes in the lab and implementation of the elaborated improvements on a commercial scale.
* Responsible for process transfer and scale-up of customer processes and technologies from laboratory through pilot plant to commercial production scale.
* Resolves process issues that may arise during manufacturing (troubleshooting and production support).
* Plan and supervise experimental lab work.
* Manage, coach, and develop 1-2 lab technicians.
* Collects, summarizes, and analyses data to prepare reports and makes presentations, as appropriate, to disseminate best practices throughout the organization.
* Technical lead in customer meetings and supporting the development of sustainable customer relationships.
* The extended area of responsibility includes: the developm...
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Type: Permanent Location: Visp, CH-BL
Salary / Rate: Not Specified
Posted: 2024-04-30 08:15:37
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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.
The Associate Scientist’s core responsibilities involve the isolation and banking of human primary cells and the design and execution of various in vitro cell-based bioassays.
As part of your role, good record keeping and skilled presentation of data will be essential.
The role will involve leading multiple client projects as well as developing current and new bioassay platforms.
Key Responsibilities:
* Supporting existing bioassay platforms to assess the immune response to a wide range of therapies (biologics, cell & gene therapies, small molecules, nucleic acids).
* Isolation, banking and characterization of human PBMC (peripheral blood mononuclear cells).
* Performing lab and area inspections to maintain high levels of quality and safety.
Contribute to lab cleaning rotation and Operational Excellence initiatives.
* Effectively communicate with external customers and internal stakeholders across departments and sites.
Key Requirements:
* Degree in Biological Sciences/Biotechnology and/or relevant experience in an industrial lab environment
* 2+ years of Immunology cell line experience in a lab setting
* Strong knowledge of human immunology, primary cell culture and cell-based assays
* Familiar with some of the following techniques: flow cytometry, ELISpot/FluoroSpot, Luminex, ELISA and reporter gene assays
* A team player able to share knowledge with others and actively participate and lead scientific discussions with other members of the team and collaborators
* Able to work independently and diligently to an established plan, prioritize and work to tight deadlines.
* Excellent interpersonal skills, with good communication and attention to detail
* A demonstrable analytical approach to problem-solving
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 not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer.
All qualified applicants will receive consider...
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Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-30 08:13:34
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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.
Lonza Pharma & Biotech has an excellent opportunity for an experienced Computerized Maintenance Management System Administrator at their Bend, Oregon location.
This position is responsible for planning, scheduling, and coordinating proactive maintenance work performed at the site.
In this role, you will maximize the maintenance work force efficiently and productively with the objective of minimizing total maintenance cost and effort.
Key Responsibilities:
* Responsible for maintaining the master data within the CMMS (Computerized Maintenance Management System) and CMS (Calibration Management System) which includes equipment, hierarchy, work orders, maintenance plans, maintenance work scope, calibration functions and procedures, and bill of materials.
* Provide training to new users of the CMMS.
* Maintain and update CMMS training materials and SOPs.
* Lead improvement projects for the CMMS system and data to aid in more efficient work completion.
* Provide support to all CMMS users for day to day usage of the system.
* Coordinates with maintenance planners to ensure that all maintenance is scheduled appropriately for efficient work execution.
* Performs CMMS reporting on KPIs for compliance and management review.
* Document master data standards and document changes made to the master data.
* Perform all SME approved changes in the system as needed for new equipment, new maintenance plans, improvement projects, schedule updates, decommissioning, etc.
* Own the relevant job roles in the user access request portal.
* Perform admin closures of work orders and review completed work orders within the system.
* Attend internal user group meetings for best practice sharing.
* Complies with all safety rules and regulations
* Strong communication skills, both oral and written
* Ability to interpret blueprints and engineering drawings
* Knowledge of manufacturing processes and procedures
* High level of interpersonal skills to work effectively with others, motivate employees and elicit work output
* Knowledge of preventative maintenance programs with a grasp of financial factors in maintenance
* Read and interpret vendor manuals and drawings
* Communicate with shop floor personnel, vendors, OEM suppliers, and management personnel
* Perform other duties as needed
Key Requirements:
* High School Diploma or GED
* 2-year associate degree or 4-year BS degree preferred
* Demonstrated ability to perform hands-on...
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Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-30 08:13:05
