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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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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
Anchor role:
Manufacturing Engineer I
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.
Working together, we’ve become one of the world’s leading research-focused healthcare groups.
Our success is built on innovation, curiosity and diversity.
Roche at Penzberg, near Munich, employs more than 7,000 people.
The site is one of the largest biotechnology centers in Europe and the only Roche site with research, development and production for both Pharmaceuticals and Diagnostics under one roof.
From your beginning with Roche, our motivated team will welcome and support you.
Numerous opportunities for personal development, flexible work hours, attractive compensation packages and special family assistance programs are available.
Roche is an Equal Opportunity Employer.
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-05-01 08:07:06
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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 an Agricultural Monitor to oversee environmental compliance during the construction phase in Rochester, MN.
The Agricultural Monitor functions as an independent third-party inspector providing direct reports to the Minnesota Department of Agriculture (MDA) and will be responsible for auditing Client’s compliance with the provisions of the Plan.
This is a full-time (60 hours/week), limited-term role for a duration of 9 weeks.
RESPONSIBILITIES:
* Participate in preconstruction training activities.
* Monitor construction and restoration activities on Agricultural Land for compliance with provision of the Plan.
* Report instances of noncompliance to the Environmental Inspector.
* Prepare regular compliance reports and submit them to the MDA.
* Act as a liaison between Landowners and the MDA when necessary and requested by the Landowner.
* Serve as a resource to investigate compliances at the direction of the MDA and explain any proposed changes to this Plan during construction.
* Maintain a written log of communications from Landowners regarding compliance with this Plan as well as report Landowner compliances to Environmental Inspector or right-of-way representative.
REQUIREMENTS:
* BS or BA degree preferred, equivalent agricultural monitoring/environmental inspection or monitoring experience, or a minimum of 6 years of relevant construction experience.
* 4+ years of agricultural monitoring/environmental inspection or permitting experience specific to linear and/or other energy infrastructure projects.
* An understanding of construction (e.g., pipelines, power lines, compressor/pumping stations, gas storage fields, wind farms, solar facilities, offshore facilities) gained through field experience.
* Strong verbal and written communication skills.
* Strong negotiation and conflict resolution skills.
* Proficient technical skills, including, but not limited to, experience using Microsoft Office programs and digital cameras.
* Knowledge of environmental sampling methods; and
* The ability to travel extensively and to work 40 to 70+ hours per week in a physically demanding position on temporary assignments.
* Be physically fit and able to:
+ Walk/hike for up to 10 hours per day on possible uneven, steep, challenging terrain.
+ Be able to carry up to 10 pounds of equipment while walking/hiking.
+ Work in all weather conditions.
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 th...
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Type: Permanent Location: Minneapolis, US-MN
Salary / Rate: Not Specified
Posted: 2024-04-30 08:31:52
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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
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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 Operational Excellence Director is an integral part of the Walkersville Site Leadership Team as they endeavor to empower the team to eliminate waste, drive results and create value for Lonza and our customers.
The Director, OpEx will drive the transformation towards a lean organization with the overall development and deployment of site strategic and tactical plans leveraging OpEx-, PMO-, and training resources.
The successful candidate will create value by understanding process, flow and customer needs and aligning with Lonza methodologies and strategies.
See what we are all about: About Us | Lonza
The ideal Operational Excellence Director will be an experienced lean transformation leader with a proven track record of implementing positive change within a cGMP environment. This person will also be flexible to adapt to changing business priorities and will promote continuous improvement and lean initiatives to improve safety, quality, service, productivity, cost, and engagement.
Key responsibilities:
* Collaborates with the local Walkersville operations team and the Bioscience network functions to design and build a capable, and agile organization with the technical skills, experience, behaviors and know-how to continually build the innovation funnel and sustainably deliver results
* Drives overall transformation towards a lean organization
* Oversee the development and implementation of fit-for-purpose, standardized project management, LBMS, and related training processes and tools to facilitate and assess project planning, program budgeting, risk identification and management, change management, program governance, prioritization and project status reporting
* Ensure all executed projects, programs, and related training are aligned with site objectives and adhere to all the defined processes and meet the required standards for planning and execution
* Generates and implements strategies to ensure optimal flow of materials & information to enable all activities across the value chain to consistently deliver to customer and business expectations
* Develops Walkersville capabilities for analytics and data science, from defining performance metrics and balanced scorecards that support the strategic aims of the Bioscience business, to establishing best practice for collecting, curating, and analyzing data to drive decision-making
Key requirements:
* Bachelor’s degree in Science, Business, Engineering or related field; MBA a strong plus
* Prior Supervisory exp...
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Type: Permanent Location: Walkersville, US-MD
Salary / Rate: Not Specified
Posted: 2024-04-30 08:13:00
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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 our site in Basel, we are looking for Project Lead Commercial QC:
Key responsibilities:
* Represent Lonza in internal and customer meetings as project champion
* Enable release and stability testing of late phase (PPQ and Commercial) Drug Product (MABs, ADC, mRNA) within Lonza QC by:
* Project coordination (timelines and deliverables are visible and maintained in planning tools), in collaboration with Program Manager
* Implementing the testing strategy (evaluation of method performance, suitability, control strategy, specifications setting)
* Acting as regulatory liaison for QC in collaboration with the Lonza regulatory expert team
* Leading discussions with customers and interface with SMEs
* Ensuring the de.g.
Bio-Chemical testing, Physico-Chemical testing, Forensic Chemistry, Microbiology, incoming goods control, manufacturing, MSAT (Manufacturing, Science & Technologies), QA, Regulatory)
* Supporting draft of proposals and manufacturing contracts (SoWs)
* Maintaining up-to-date knowledge of assigned projects (molecules, formulation, product presentation)
* Demonstrating knowledge of analytical testing by e.g.
compendial and generic methods, HPLC and (i)CE purity methods, content determination, Bio-chemical methods (ELISA, SPR, Cell based potency / binding / activity assays), qPCR, MS, dimension testing.
* Adhere to cGMP regulations
* QC Project SME for audits and inspections
Key requirements:
* Degree in Life science or management (Bachelor, Master, Ph.D., MBA or similar)
* Scientific and GMP experience, commercial and financial acumen
* Strong analytical and problem-solving skills
* Substantial experience in QC, project management, QA or similar
* Results oriented and able to prioritize workload to meet timelines
* Knowledge of pharmaceutical regulatory landscape (e.g.
ICH guidelines, PIC/s, US FDA, PMDA, EMA)
* Excellent communication skills, command of English, academic writing
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 probl...
....Read more...
Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-30 08:08:00
-
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 our site in Basel, we are looking for Lead Scientist Commercial QC.
Key responsibilities:
* Review analytical testing documentation according to SOPs for clinical and commercial samples.
* Support implementation, validation, transfer analyses to perform release and stability testing under GMP, following applicable SOP’s and all current documentation practices.
* Contribute to the establishment of DPS Commercial QC infrastructure and services for e.g.
parenteral clinical and commercial Drug Substance and Drug Products under GMP.
* Support QC release decision, including LIMS
* Support Empower 3.x
* Support to maintain the qualified state of analytical instruments for DPS QC in close alignment with current best practices and regulations
* Raise and progress laboratory investigations and quality events (e.g.
OOS, SST, deviations, CAPA, tasks)
* Contribute to the evaluation and establishment of analytical methods and technologies as required
* Ensure safety and health protection by following lab and safety instructions and all cGMP regulations.
Key requirements:
* Degree in life sciences or management (Bachelor, Master, Ph.D., MBA or similar)
* Scientific and GMP experience, commercial and financial acumen
* Strong analytical and problem-solving skills
* Substantial experience in QC, project management, QA or similar
* Results oriented and able to prioritize workload to meet timelines
* Knowledge of pharmaceutical regulatory landscape (e.g.
ICH guidelines, PIC/s, US FDA, PMDA, EMA)
* Excellent communication skills, command of English, academic writing
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.
....Read more...
Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-30 08:07:58
-
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 our site in Basel, we are looking for Scientist QC Commercial Physico Chemistry:
Key responsibilities :
* Implement, validate, transfer analyses to perform release and stability testing under cGMP, following applicable SOP’s and all current documentation practices.
* Focus area: compendial testing, pH measurement, osmolality, purity testing HPLC, iCIEF, CE-SDS
* Perform sample analysis and review according to SOPs for clinical and commercial samples.
Contribute to the establishment of DPS Commercial QC infrastructure and services for e.g.
parenteral clinical and commercial Drug Substance and Drug Products under GMP.
* Maintain the qualified state of assigned instruments for DPS QC in close alignment with current best practices and regulations
* Contribute to the evaluation and establishment of analytical methods and technologies as required
* Contribute to timely execution of assigned development projects, including monitoring timelines, proper execution and reporting.
Draft validation plans and reports.
* Ensure safety and health protection by following lab and safety instructions and all cGMP regulations.
Key requirements :
* Completed apprenticeship (Laborant EFZ, CTA, BTA or equivalent) or B.Sc.
in analytical chemistry, biochemistry, Pharmaceutical Sciences or related subject
* Basic knowledge of physico chemical analytical techniques (e.g.
pH measurement, osmolality, HPLC, iCIEF, CE-SDS)
* Strong working knowledge in relevant analytical techniques in the lab
* At least 2 years experiences in GMP environment, preferably commercial
* Experienced in large molecule analytics (advantageous)
* Thorough and accurate scientific attitude, strong analytical, reporting, and documentation skills
* Good knowledge of written and spoken English
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.
....Read more...
Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-30 08:07:49
-
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 our site in Basel, we are looking for Scientist Commercial QC Bio Analytics.
Key responsibilities:
* Analyses for DP (DS) batch release, stability and related samples under cGMP within DPS Commercial QC using biochemical assays such as
* cell based assays, ELISA, SPR/Biacore
* Documentation according to GDP standards and following applicable EHS regulations.
* Review analytical raw data for assays
* Act as method trainer and instrument responsible person in area of expertise
* Support transfer and validation activities and investigations
Key requirements :
* Completed apprenticeship (Laborant EFZ, CTA, BTA or equivalent) or B.Sc.
in analytical chemistry, biochemistry, Pharmaceutical Sciences or related subject
* Basic knowledge of bioanalytical techniques (e.g.
cell based assays, ELISA, SPR/Biacore)
* Strong working knowledge in relevant analytical techniques in the lab
* At least 2 years experiences in GMP environment, preferably commercial
* Experienced in large molecule analytics (advantageous)
* Thorough and accurate scientific attitude, strong analytical, reporting, and documentation skills
* Good knowledge of written and spoken English
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.
....Read more...
Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-30 08:07:47
-
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.
At our sit in Visp, Switzerland we are looking for a Biology Laboratory Technician (m/w/d) for our biochemistry laboratory.
Your responsibilities:
* Implementation of bioanalytical methods in the GMP environment using ELISA and qPCR
* Collaboration in the transfer and validation of new methods
* Supervision of laboratory equipment and associated equipment responsibility
* Investigation of deviations and unexpected results, troubleshooting
* Data extraction, data evaluation
Job requirements:
* Apprenticeship diploma as laboratory assistant, BTA, or Bachelors degree in biology, biochemistry or similar field
* Practical laboratory experience with Elisa and/or PCR
* Experience in GMP environment is a plus
* Very good knowledge of English and basic understanding of German
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.
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-30 08:07:33
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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
Our health is a great treasure - join us safe guarding it.
Fight the pesky monster of diabetes and its cronies!
Being a global leader in integrated Personalized Diabetes Management (iPDM), Roche Diabetes Care collaborates with pioneers around the globe, including people with diabetes, caregivers, healthcare professionals, and payers.
We aim to transform and advance care provision and foster sustainable care structures.
Under the brands RocheDiabetes, Accu-Chek and mySugr, comprising glucose monitoring, insulin delivery systems, and digital solutions, we unite with our partners to create patient-centered value.
By building and collaborating in an open ecosystem, connecting devices, and digital solutions as well as contextualizing relevant data points, we aim to support the optimization of therapy and enable better-informed therapy decisions.
For a behind-the-scenes look, check out our Roche code4life to see what makes Roche Diabetes Care tick.
Here’s what we’re looking for:
We’re looking for a hands-on software engineer (m/f/d) who will have a significant impact on some of the most cutting edge software powering connected devices that help millions of people manage their diabetes on a daily basis.
In close collaboration with device firmware engineers you will be responsible for the design and management of our development toolchain, fostering automation and increasing efficiency.
Your tasks will include application development, scripting, testing, troubleshooting problems and a bunch of creativity to speed us up with your ideas.
Your upcoming mission:
* Ensure high quality and consistent software development using our CI/CD DevOps toolchains
* Design and implement applications for testing, analyzing and configuring our device under development.
* Improve CI/CD-toolchain to provide our FW developers the best possible support
* Collaborate on design, development and integration of unit tests and related SW infrastructure
* Create and maintain dashboards of results and reports
* Investigate the use cases, system-level operation, and performance requirements for our firmware team
Essential skills for this mission:
* Solid programming experience using C#, Java, .net Framework
* Great Experience in automation: Continuous Integration and Continuous deployment process for different technologies (for example Embedded, Desktop (Windows, MacOS), API, Android, iOS, Databases
* Knowledge on Datadog/Prometheus/Grafana/PowerBI
* Knowledgeable on structured software development and/or obje...
....Read more...
Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2024-04-30 08:05:18
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Your Job
At Molex, you could discover the latest trends in disruptive technologies ushering in a new connected world of possibilities.
You will be a member of new product design group focusing on the hybrid high speed connector in automotive industrial.
What You Will Do
* Evaluate product design on its SI performance.
Using the HFSS to build up analytical models and simulate the signal integrity.
Deep understand on the simulation report and give out the professional advise on design of connector.
* Test coaxial connector performance including, but not limited to, SI, EMC, eye diagram with VNA, TDR, CoMeT, etc.
Deep understanding on the report is required and share your findings to your design group.
* Analyse SI failure and lead DFMEA research.
* Collaborate with design group to optimize the signal performance.
Who You Are (Basic Qualifications)
* University Degree in Electrical/Electronic Engineering or equivalent, and above.
* Experience of signal integrity and signal simulation software (HFSS, CST)
* Good knowledge of high-speed connector.
* Good Knowledge and Experience of signal integrity.
* Good Knowledge and Experience of signal simulation software (HFSS, CST).
* Knowledge of high-speed connector.
* Capability of realizing 2D/3D design independently.
* Self-motivated and good learning ability.
* Good English level.
What Will Put You Ahead
Familiar with terminal metal, injection plastic and manufacturing process, including plating, injection, or crimping.
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.
Who We Are
As a Koch company, Molex is a leading supplier of connectors and interconnect components, driving innovation in electronics and supporting industries from automotive to health care and consumer to data communications.
The thousands of innovators who work for Molex have made us a global electronics leader.
Our experienced people, groundbreaking products and leading-edge technologies help us deliver a wider array of solutions to more markets than ever before.
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.
....Read more...
Type: Permanent Location: ChengDu, Sichuan, CN-51
Salary / Rate: Not Specified
Posted: 2024-04-30 08:03:59
