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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 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
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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 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
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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...
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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
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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!
Global Information Technology (IT) Procurement Team
Title: Associate, Global IT Category Strategy, Indirect IT Procurement
The strategic vision of Elanco Indirect Procurement is to optimize category strategy compliance, supplier innovation and reduce the supply base 50% by 2022.
As part of the Elanco Global IT Procurement team, the Global IT Category Strategy Associate is a critical interface with indirect procurement peers and IT business stakeholders to bring competitive advantage and innovation through marketplace category expertise, strategic sourcing and management of suppliers.
This role will be critical in influencing stakeholders to right size internal business requirements, analyzing spend data, and investigating the marketplace best practices. The Global IT Category Strategy Associate is responsible for:
* First line responder; pivots between strategy, operations and transactional sourcing activities and focuses
* Process IT hardware and software purchase requests from within IT and across the business, including quoting, requisitions, approvals, contracting, order processing, licensing, and delivery.
* Negotiate enterprise-wide IT supplier contracts, including master agreements, statements of work, and professional service agreements.
Interface with Legal, Info.
Security, Data Privacy and Risk Management divisions to broker terms with vendors and ensure holistic compliance with Elanco standard policies.
* Communicates pertinent information to both internal stakeholders and suppliers to keep parties informed and to prevent problems.
This role will interact, influence, and make an impact at all levels, especially with Elanco senior management due to the significant spend and strategic direction of Information Technology touching all aspects of the Elanco business.
* Drive reductions in total cost of ownership to achieve Procurement-led saving initiatives through supplier rationalization, value engineering, re-sourcing and negotiation.
* Execute ad-hoc/one off buys and general IT procurement inquiries, su...
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Type: Permanent Location: Hook, GB-HAM
Salary / Rate: 47000
Posted: 2024-04-29 07:55:33
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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!
Position Description: The Veterinarian Medical Affairs Specialist is responsible for coordinating and providing technical consulting and educational activities to support the company’s sales, marketing and R&D objectives.
This position will play a key role in supporting the next wave of innovation at Elanco and will play in outsized in contributing to the success of the company.
Within the Elanco US Pet Health Organization, the specialist serves as a companion animal veterinary technical anchor and provides support to the commercial affiliate for all pre-launch, launch, and post-launch activities as deemed appropriate for the department.
At the direction of the brand marketing team, the specialist delivers high-quality medical education via live and virtual events and serves as an important speaker at specialty, national, and international conferences.
They represent Elanco and their respective product category on boards, committees, and leadership teams of professional organizations.
They are an internal disease state and subject matter expert.
They are recognized internally and externally as a thought leader through their influence with key industry organizations, deep medical and scientific expertise, and experience delivering education to a wide range of audiences.
They maintain close working relationships with external specialty colleagues in private, academic, and corporate practice.
The specialist’s internal influence is extensive, and they are relied upon to deliver expert medical knowledge to marketing, field sales, field veterinary teams, R&D, business development, and senior leadership.
Their consultation is expected to drive today’s key marketing initiatives and ensure Elanco maintains the appropriate strategy for the future.
Frequent domestic travel (approximately 60%) and occasional international travel are required.
Candidates should have reasonable accessibility to a major airport.
Functions, Duties, Tasks:
* At the direction of the department director and brand and medical strategy teams, represent Elanco to veterinarians, pr...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 225000
Posted: 2024-04-29 07:55:32
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Your Job
As a Mold Flow Engineer, you will be integral to the connector product development process, collaborating with a multidisciplinary team that includes product design engineers, mold CAE engineers, and mold tooling engineers.
Your expertise in molding technology will be crucial throughout the product development cycle, from design inception through to tooling qualification.
You will apply your manufacturing acumen to drive design for manufacturability (DFM), high performing injection molds, and elevate the efficiency of molding production operations, while managing priorities to adhere to project timelines.
What You Will Do
* Deliver expert guidance on plastic molding behaviors to enhance product manufacturability, mold performance, and molding production efficiency for cross-functional product development teams.
* Engage with Product Design Engineers during preliminary design phases to provide DFM insights and proactively address manufacturability issues and optimize product manufacturability prior to OK-to-Tool.
* Partner with mold tooling engineers to craft and authenticate tooling strategies, ensuring optimal runner/gate/cooling designs, and refining mold tooling plans.
* Optimize molding process parameters in conjunction with process engineers.
* Leverage molding simulation tools to boost production operational efficiency, targeting cycle time reduction, material usage minimization, defect reduction, and PM frequency decrease.
* Collect and evaluate data on molding behavior and part performance for predicted versus actual comparison studies.
* Execute additional duties as directed by management.
Who You Are (Basic Qualifications)
* Bachelor's degree in Mechanical or Polymer Engineering; Master's degree preferred.
* Proven background in creating molding simulation models, specifically for connector products, utilizing software such as Moldflow, Moldex3D, HyperMesh, and CAD systems like NX.
* Proficiency in conducting Flow, Pack, Cool, and Warp analyses with simulation software like Moldex3D or Moldflow.
* Expertise in interpreting simulation results, diagnosing potential issues in molding and product performance, and suggesting solutions and risk mitigation for product design, tooling, and processing.
* Effective communication capabilities, adept at generating simulation project reports, leading simulation review sessions, and spearheading cross-functional problem-solving discussions.
What Will Put You Ahead
* Practical experience with connector or other electronic product design.
* Hands-on expertise in mold design, injection molding processes, and injection molding press controls.
* In-depth knowledge of plastic materials and their properties, including glass fiber-filled grades.
* Familiarity with CT data analysis using Volume Graphics.
* Experience with structural FEA tools like Abaqus or Ansys, and integrating them with molding simulatio...
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Type: Permanent Location: ChengDu, Sichuan, CN-51
Salary / Rate: Not Specified
Posted: 2024-04-29 07:55:22
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Ardurra is currently hiring a Project Engineer in California to work on our water and sewer infrastructure projects.
* Prefer engineers local to California or open to relocating.
Able to work remotely and/or out of any of our California Ardurra offices.
* Need to have CA PE license or the ability to obtain within 12 months of hire date.
* Salary range: $80-120k (DOE)
Primary Function:
* Work with and manage, engineers and CAD designers working in highly effective teams.
* Under the Project Manager’s minimal supervision, the Project Engineer is the primary person who communicates project-related items directly with the client, project team-members, subconsultants, and construction managers.
* Coordinates multiple disciplines, including technical issues, implementation of Ardurra’s Quality Management Plan, and producing project deliverables.
* Responsible for developing proposals, including scopes, budgets, and schedules.
* Ardurra’s Project Engineers are mentored and trained by the Project Manager and are encouraged to participate in the company wide Ardurra Mentorship Program.
Education and Experience Requirements:
* Education: Bachelor's degree in Civil or related Engineering degree from accredited university
* Experience: 8+ years managing and designing water and sewer infrastructure projects.
* Licensure: Registered PE in the state of California
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers.
We nurture a family-like culture, striving to create a work environment that is enjoyable, challenging and rewarding but also fun.
We are acutely focused on developing our staff, whether through our internal Ardurra Academy or through our industry-leading Leadership program.
We have made a deliberate and focused commitment to nurture a people-centric culture where people are: valued as individuals; supported in their professional and career development with multiple, varied career paths; provided the tools and resources to be successful, engaged, and satisfied in their work; and positive benefits, time-off programs, and flexibility to help maintain a healthy balance between work and home.
Ardurra is an Equal Opportunity/ Affirmative Action Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, gender identity or sexual orientation.
NOTICE TO THIRD PARTY AGENCIES:
Ardurra does not accept unsolicited resumes from recruiters or employment agencies.
In the absence of a signed Agency Agreement, Ardurra will not consider or agree to payment of any referral compensation or recruiter fee.
If a resume or candidate is submitted to any hiring manager without a previously signed agreement, Ardurra reserves the right to pursue and hire those candidate(s) without any fi...
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Type: Permanent Location: Bakersfield, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-29 07:52:02
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Your Job
* NPI project development.
* Commercialization project engineering support.
* Chengdu Manufacturing engineering support.
* Engineering support for other design center.
* Department operation and improvement activities.
What You Will Do
* Review and interpret customer design requirements from Marketing, Sales or Customer drawings or specifications.
* Review Requirements (drawing, model and standard...), feasibility assessment, and any exceptions with the Product Development Team (PDT) to gain Approval.
* Technical discussion with customer regarding the design feasibility and primary test plan.
* Perform design verification activities including tolerance analysis, FEA, SLA and patent investigation.
* Release ok to tool drawings and models for tooling design and development.
* Establish test plan for product reliability testing and review with reliability lab to ensure all documentation, est samples, equipment, fixtures, etc are ready for testing.
* Lead FOT part review.
* Support tooling engineers in disposing First Article inspection reports.
And approve or disapprove product deviation requests.
* Problem solving using E8D.
* Provide training to customer and other Molex engineering personnel as assigned by the Product Development Manager.
* Provide design support for product modifications and/or extensions.
* Provide design support for manufacturing process improvements.
* Respond to customer complaints on design related issues.
Who You Are (Basic Qualifications)
* University Degree in Mechanical or Manufacturing Engineering or equivalent, and above.
* Able to communicate (reading, writing, speaking and listening) in English.
* Good knowledge of product design process.
* At least 1 year of connector design experience and application.
* Adopt a professional attitude towards work and assume full responsibility for any project or tasks assigned.
* Demonstrate good teamwork for overall success.
* CAD Software for drafting and modeling.
* Connector design and manufacturing technologies.
* Connector materials - resin and metal.
* Design problem solving skills - 8D, DFMEA, Tolerance Analysis.
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...
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Type: Permanent Location: ChengDu, Sichuan, CN-51
Salary / Rate: Not Specified
Posted: 2024-04-28 08:11:28
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Your Job
Works with the Product Manager to develop and implement the strategic direction for an assigned product family in support of Divisional goals.
Acts as a focal point for market knowledge, profitability, forecasts, and planning.
What You Will Do
* Supports the product manager by developing and implementing strategic product and annual business plants, targeting markets, industries, and customers.
* Increases sales and market share of assigned product line in support of Divisional Objectives.
Tracks progress to plan for revenue, profit, and backing.
* Works with product manager to improve profit and return on investment of assigned product line.
Undertakes and leads cost reduction, capacity planning, and quality improvement project.
* Under the direction of the product manager, reviews and approves special price requests, maintains price bands and price lists and develops pricing strategies for new and existing products.
* Manages new development activity or existing product lines associated with extending and growing the life of assigned product lines .
* Promotion plans including: sales tools, literature, distribution, stocking, training, and sampling.
* Performs other related duties as assigned by management.
Who You Are (Basic Qualifications)
* Bachelor degree in a technical or business discipline.
* Min 2 years experience in the areas of Engineering, Marketing, Project Management, Business, Financial/Data analysis OR relevant connector work experience .
* Organizational skills to anticipate, plan, prioritize and self-monitor workload.
* Effective written and oral English communication skills that demonstrate the ability to express ideas, exchange information clearly and concisely, and deliver concise and effective presentations to customers and Molex personnel.
* High level of interpersonal skills to effectively work with co-workers and external contacts to respond positively to situations.
* Must be self-motivated and goal oriented.
* The candidate/incumbent must be proactive rather than reactive and must be able to demonstrate personal initiative.
* Travel to customers as needed.
What Will Put You Ahead
* MBA or other related graduate degree.
Connector Industry Experience.
* 3+ years experience / knowledge within the global automotive industry.
* Strong technical background, experience in automotive connectors.
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.
...
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Type: Permanent Location: ChengDu, Sichuan, CN-51
Salary / Rate: Not Specified
Posted: 2024-04-28 08:03:37
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Summary
The inQbator AI team has a mature ecosystem of solutions currently deployed to production that use state of the art natural language processing and machine learning techniques to bring tangible improvements to healthcare processes.
Our near-term focus is on building solutions to address problems within the domain of prior-authorization, and our long-term problem space is incredibly broad and open-ended.
As such, to identify the next generation of problems that we will tackle, we interact regularly with a diverse and highly matrixed group of stakeholders that includes teams from multiple divisions across the enterprise, as well as clinicians and hospital networks with whom we have partnerships and ultimately the patients we seek to help.
Responsibilities
* Work closely and interactively with our data science and product teams to build data pipelines which support the inQbator
* Migrate legacy data ETL pipelines to cloud-based data platforms (Databricks, Snowfake)
* Develop new data resources which can be used for ML/NLP or product innovation
* Collaborate with various data stakeholders to identify internal and external healthcare data resources which can be used by the inQbator
* Establish data engineering best practices for junior data engineers and data analysts
* Establish quality metrics which can be used for identifying value of inQbator projects
* Provide BI support for new inQbator innovations
* Keep current with industry advances in data engineering
* Solve problems that will have a positive impact on the health and well-being of many people
Qualifications
* 5+ years' of relevant experience building and managing sophisticated ETL pipelines
* High degree of proficiency with SQL
* Experience with cloud-based data platforms (Databricks, Azure)
* Familiar with git source control
* Experience with Python and Tableau is preferred
* Experience building and managing data model architecture is highly desirable
* Experience working with ML or NLP teams is highly desirable
* Experience with healthcare data (claims, EMR) and/or Healthcare Utilization Management is highly desirable
* Degree in Computer Science, Engineering, Information Systems, Math or related technical field highly desired; Master's degree preferred
If you will be working at home occasionally or permanently, the internet connection must be obtained through a cable broadband or fiber optic internet service provider with speeds of at least 10Mbps download/5Mbps upload.
For this position, we anticipate offering an annual salary of 121,400 - 202,400 USD / yearly, depending on relevant factors, including experience and geographic location.
This role is also anticipated to be eligible to participate in an annual bonus plan.
We want you to be healthy, balanced, and feel secure.
That's why you'll enjoy a comprehensive range of benefits, with a focus on supporting your whole health.
Star...
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Type: Permanent Location: Boston, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-27 10:01:46
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Position Summary:
The Quality Technician A assures adherence to nationally recognized standards through the implementation of sound metrological practices.
In addition, the individual in this role adheres to applicable quality procedures through sound auditing practices while maintaining compliance to internal standards related to the calibration and inspection of manufactured and test related products.
Objectives:
1.
Calibration of gauges and equipment.
2.
Audit finished product
3.
Repair gauges
4.
Audit manufacturing process
5.
Routine gauge maintenance
6.
Audit finished product test equipment
7.
Gauge R&R studies
8.
Perform measurements with gauges and equipment
9.
ISIR & custom measurements set up
10.
Material analysis
11.
Receiving and first piece inspections
12.
Maintaining quality records
13.
Quality systems maintenance
14.
Author new quality system procedures
15.
Liaison with hourly, supervisory and technical personnel
16.
Coach/Educate hourly personnel
17.
Use of computers to operate company systems
18.
Capable of creating and executing programs on the coordinate measuring machines CMM)
19.
Perform other tasks as required
Requirements:
Education: Must have a two-year Technical Certificate or Degree in a related field.
Experience: Over 1 year up to and including 3 years.
Skills: Requires the use of shop mathematics together with the use of complicated drawings, specifications, charts, tables, various types of adjustable measuring instruments and the training generally applicable in a particular or specialized occupation.
Use of considerable judgment to plan and perform unusual and difficult work where only general methods are available, and the making of broad decisions involving considerable initiative and ingenuity.
Location: Tallassee, Alabama
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.
However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
41 CFR 60-1.35(c)
Operations
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Type: Permanent Location: Tallassee, US-AL
Salary / Rate: Not Specified
Posted: 2024-04-27 09:52:52
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ERM is hiring a Field Safety Observer in Chico, CA.
In this critical role, you will be responsible for engaging with client and contractor team members in the field to facilitate safe work practices, embrace client safety culture expectations, and maintain compliance with the client’s Contractor Safety Program elements and other applicable safety regulations (e.g., Cal/OSHA).
The Field Safety Observer will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This position works to promote a safe work environment by confirming that contractors and the project team, at a minimum, clearly understand the roles and responsibilities related to reviewing drawings; identifying known hazards; and communicating policies, standards, and procedures applicable to the work.
The role includes responsibility of timely notification to management and the safety team about any safety issues.
This is a full-time (40hrs/week), limited-term position for a duration of 3 months.
RESPONBILITIES:
* Manage the receipt, review, provide feedback for contractor safety related documents (e.g.
Programmatic Safety Plans, Project Specific Safety Plans [PSSPs], Job Safety Analyses [JSAs], Field Safety Observations).
* Inspect site activities specifically during the kick-off and implementation of medium and high-risk scope activities.
* Perform Field Safety Observations as established by the frequency and level for each contractor and subcontractor in accordance with the SSSP/PSP.
* Provide on-site occupational safety support to identify, prevent, and mitigate safety risks.
* Document and retain safety documents in accordance with client requirements.
* Take direction from client Supervisors and Management responsible for Contractor Safety.
* Participate in safety incident investigations, root cause evaluations, etc.
* Assign and/or coordinate with team members to address corrective actions and communicate as appropriate with team members to prevent repeat occurrences.
* Share safety information to all in an impactful, constructive, and results-oriented manner.
* Communicate safety trends and recommends safety corrective actions
* Support compliance with applicable programs (respirator, hearing, ergonomics).
* Capable of identifying existing and predictable hazards in the surroundings or working conditions that are unsanitary or dangerous.
* Has training, knowledge, or experience related to the work to be performed and knowledge of the appropriate mitigation measures for the associated hazards.
* Has formal training to identify and mitigate hazards associated with specific high-risk activities.
* Familiar with managing contractor safety for operations; and
* Familiar with Cal/OSHA safety regulations and requirements.
* Initiate and/or participate in safety kick-off, periodic or daily safety meetings with contractors;
* Function as Subject M...
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Type: Permanent Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:36:43
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What You Will Do
* 1.参与项目后端服务研发;
* 2.参与产品的设计、研发和技术服务;
* 3.协助项目经理或产品经理制定项目整体实施计划与评审;
* 4.对实施的产品版本进行开发管理、版本发布约定、缺陷修复。
Who You Are (Basic Qualifications)
* 1.本科或以上学历,5年以上后端开发经验,具备计算机相关专业,基本功扎实,熟练掌握计算机原理、算法、网络、数据库、安全等知识;
* 2.具备扎实的 Java 基础,有良好的编码习惯;熟练掌握 Spring、Springboot、SpringMVC、Mybatis 框架开发模式;
* 3.熟悉分布式架构,对Dubbo、SpringCloud分布式框架有较深了解和经验;熟悉主流中间件的使用,如Kafaka、RocketMQ、Redis;
* 4.熟悉Oracle/MySQL数据库,了解常用的sql优化技术,能编写较为高效的sql语句;
* 5.良好的学习能力、沟通能力和解决问题能力;
* 6.英语读写熟练。
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.
Additionally, everyone has individual work and personal needs.
We seek to enable the best work environment that helps you and the business work together to produce superior results.
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Type: Permanent Location: Shijie Town, Dongguan, CN-44
Salary / Rate: Not Specified
Posted: 2024-04-27 08:36:29
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Qualified Mental Health Specialist (QMHS)
Are you looking for an organization where you can grow while making a positive impact on people's lives? At Signature Health, our purpose is to provide integrated healthcare for our community specializing in patients with mental illness and/or addiction because we want people to realize their highest potential.
Our core values are the foundation of who we are:
* People First mindset where we honor our colleagues and patients
* Striving for Excellence in our work each day
* Can Do approach where we roll up our sleeves in response to opportunities and challenges
In addition to a rewarding career, as a full-time employee, you will have access to the following employer/employee paid benefits:
Full Time:
* Medical, Dental, Vision
* Robust earned paid time off program (PTO)
* 401k match
* Various Life Insurance Options
* Short- and Long-Term Disability (Not applicable for school-based employees)
* Federal Loan Forgiveness Program (available on eligible on roles)
* HealthJoy - no cost medical and mental health online resources available Day 1 (coverage extends to family members living in the same household)
* Tuition & Professional Development Assistance
If you value the people around you, strive to be the best version of yourself and have a can do mindset, then Signature Health could be the best place for your next career.
Read below on how you can make a difference in our community and apply today!
SCOPE OF ROLE
Reporting to the Supervisor and Manager, Behavioral Health Services, the Qualified Mental Health Specialist (QMHS) will be key in the development and execution of patient treatment plans.
You will provide patients and their families with ongoing community support resources including transportation for access to identified resources.
The QMHS acts as an outstanding subject matter expert related to patient needs and will foster positive relationships to all patients, their families, and Signature Health team members.
HOW YOU’LL SUCCEED:
* Diligently develop, prepare and present treatment program work material to patients.
* Plan, coordinate, and provide reliable transportation to patients to access identified resources as part of their treatment plans.
* Maintains clear communication and professional boundaries with all patients.
* Act as a subject matter expert and provide support in accessing and developing a sober support network.
* Collaborates effectively with a patient's treatment team.
* Create an outstanding experience for both adult and child patients (SMD/SED, CD/Dual DX) by identifying support needed in the following areas: educational, medical, vocational, housing, and daily living skills resulting in patients becoming successful in their communities.
* Encourage, monitor, and follow-up on client engagement and participation in all treatment plan activities.
* Serve as a liaiso...
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Type: Permanent Location: Beachwood, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-27 08:31:49
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Au sein d’Aliaxis, chaque salarié·e opère selon une vision commune : nous pouvons faire la différence en apportant des solutions aux défis mondiaux liés à l’eau et en accélérant la transition vers une énergie propre.
Expert reconnu sur le marché Européen, Aliaxis France et ses marques Nicoll, GIRPI et AUI, crée des systèmes innovants et durables en matériaux de synthèse pour les acteurs du bâtiment, de l’industrie et des infrastructures à travers le monde.
Aliaxis et ses filiales encouragent la diversité et l'inclusion sur le lieu de travail en promouvant l'égalité des chances.
Nos offres d’emploi sont ouvertes à toutes et tous.
Nous nous engageons à effectuer des recrutements aussi inclusifs que possibles car nous croyons que la diversité des profils est une source d’enrichissement collective et de bien-être au travail.
Nous vous proposons de rejoindre une équipe Production dynamique au sein d'une entreprise en pleine transformation en tant qu’Alternant.e Gestionnaire Production sur 1 ou 2 ans dès septembre 2024 à Harfleur (76) (15min du Havre).
Vos missions principales :
* Participer à l'élaboration des standards de l'injection
* Former les équipes et managers aux standards de production
* Participer aux différents audits et analyser les résultats
* Mettre en place des plans d'action en lien avec les résultats des audits
Ce que nous apprécierons chez vous :
* Vous préparez une formation de niveau Bac +2/+3 en alternance dans un cursus de type organisation/gestion de production ou production /plasturgie/assemblage
* Vous avez le goût des chiffres et de l’informatique, notamment pour l’utilisation d’Excel.
* Vous êtes dynamique, rigoureux.se et polyvalent.e.
* Votre disposez d’une bonne capacité d’analyse et faites preuve de rigueur.
* Vous avez le sens de l’organisation et aimez le travail en équipe.
Les plus de cette alternance :
Une opportunité unique de rejoindre un groupe mondial dont le siège est à Bruxelles.
Dans un environnement international et collaboratif, nous nous engageons pour construire la croissance future, promouvoir l’excellence de nos services et l’engagement des collaborateurs.trices.
Totalement intégré.e au service Production, vous êtes un.e interlocuteur.trice à part entière du service.
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Type: Permanent Location: Harfleur, FR-76
Salary / Rate: Not Specified
Posted: 2024-04-27 08:16:08
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Au sein d’Aliaxis, chaque salarié·e opère selon une vision commune : nous pouvons faire la différence en apportant des solutions aux défis mondiaux liés à l’eau et en accélérant la transition vers une énergie propre.
Expert reconnu sur le marché Européen, Aliaxis France et ses marques Nicoll, GIRPI et AUI, crée des systèmes innovants et durables en matériaux de synthèse pour les acteurs du bâtiment, de l’industrie et des infrastructures à travers le monde.
Aliaxis et ses filiales encouragent la diversité et l'inclusion sur le lieu de travail en promouvant l'égalité des chances.
Nos offres d’emploi sont ouvertes à toutes et tous.
Nous nous engageons à effectuer des recrutements aussi inclusifs que possibles car nous croyons que la diversité des profils est une source d’enrichissement collective et de bien-être au travail.
Nous vous proposons de rejoindre une équipe Qualité dynamique au sein d'une entreprise en pleine transformation en tant qu’Alternant.e Qualité sur 1 ou 2 ans dès septembre 2024 à Harfleur (76) (15min du Havre)
Vos missions principales :
* Améliorer le processus de gestion des réclamations internes et externes
* Garantir la gestion du système documentaire, assurer la création et mise à jour des standards et plans de contrôle y compris pour la qualité fournisseurs
* Analyser les retours qualité des ateliers, aider à formaliser les critères qualité avec les contrôleurs de l’atelier et accompagner la mise en œuvre de ces critères
* Gérer les NC et le suivi des actions correctives et/ou préventives
* Gérer les réclamations clients et apporter des actions d’amélioration
* Aide au déploiement du projet de transformation du site
Ce que nous apprécierons chez vous :
* Vous préparez un diplôme d’ingénieur ou BAC+5 QHSE, spécialité matériaux/chimie ou productique.
* Vous avez une appétence particulière pour la gestion de projet et avez une bonne capacité d’échange et d’écoute
* Une première expérience en qualité serait un plus.
Les plus de cette alternance :
Une opportunité unique de rejoindre un groupe mondial dont le siège est à Bruxelles.
Dans un environnement international et collaboratif, nous nous engageons pour construire la croissance future, promouvoir l’excellence de nos services et l’engagement des salariés·es.
Totalement intégré·e au département Qualité, vous êtes un·e interlocuteur·rice à part entière du service.
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Type: Permanent Location: Harfleur, FR-76
Salary / Rate: Not Specified
Posted: 2024-04-27 08:16:06
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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.
Am Standort Visp suchen wir aktuell mehrere Infrastructure & Utilities Ingenieure oder Techniker (m/w/d).
Als Ingenieur oder Techniker Infrastructure & Utilities sind Sie zuständig für den einwandfreien Betrieb, Wartung und Kontrolle der Systeme / Anlagen wie Clean Steam, Purified Water, Water for Injection, Heating Ventilation & Air Conditioning Systems (HVAC) und der Black Utilities unter Einhaltung der GMP-Anforderungen.
Zusätzlich sind Sie verantwortlich für die Bereiche Zutrittskontrolle und Abfall-Management, sowie für die Akustik- und Brandmeldeanlage.
Ihre Aufgaben:
* Kontrolle, Betreuung und Organisation des fortlaufenden Monitorings der Reinstmediensysteme
* Bearbeitung entstandener Abweichungen in Zusammenarbeit mit QA, QC und dem Betrieb, sowie Definition entsprechender Massnahmen und Erstellung der Monatsberichte
* Koordination der Schnittstellen zum Betrieb, dem Betriebsengineering, sowie QA und QC
* Verantwortliche Teilnahme in Audits und Inspektionen die Abläufe und Prozesse der Reinstmediensysteme vorzustellen
* Verantwortlich für die Koordination des Membranwechsels und der visuellen Kontrolle der relevanten Systeme, Untersuchungen von Abweichungen, sowie Definition und Umsetzung von Massnahmen zusammen mit QA, QC und dem Betrieb
* Verantwortung für alle Medien im Schwarzbereich, dem Abfallmanagement sowie der korrekten Entsorgung der anfallenden Abfälle
* Tägliche Überwachung der Störmeldungen und Erstellung der Aufträge, sowie aktive Teilnahme bei der Lösungsfindung
Ihr Anforderungsprofil:
* Weiterbildung an einer Technikerschule (HF) oder Bachelor im Bereich Maschinenbau oder Verfahrenstechnik, alternativ eine abgeschlossene industrielle Ausbildung mit mehrjähriger Berufserfahrung
* Berufserfahrung in einem GMP regulierten technischen Bereich, sowie Verständnis und Wissen im Bereich Utilities und von GMP-Anforderungen
* Erfahrung im Bereich Change Management
* Gute IT-Kenntnisse, insbesondere in Office, SAP, DeltaV (Prozessleitsystem)
* Gute Deutschkenntnisse (Niveau B2) in Schrift und Wort, sowie gute Englischkenntnisse.
Bereitschaft dazu Deutsch- und Englischkenntnisse noch weiter auszubauen
Lonzas 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 Verantwor...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-27 08:15:52
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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 Bioscience has an exciting opportunity for an Executive Administrative Assistant to join our team in Walkersville, MD. The role exists to provide key support to the business unit SVP, leadership team, and some support at the site level.
Responsibilities include calendar management, planning travel, expense management, meeting arrangements, taking minutes, and preparing reports and presentations.
The position requires strong computer and internet research skills.
This position will assist with organizing and coordinating special projects from conception to completion, and must be able to work under pressure at times to handle a wide variety of activities and confidential matters with discretion, speed, and efficiency.
The successful candidate thrives in a fast-paced and challenging environment, has a passion for keeping team members well-prepared for projects/meetings, handles confidential information with professionalism, and pivots quickly when priorities change.
Key responsibilities:
* Completes a broad variety of administrative tasks, which require extreme confidentiality
* Organize events, guest visits and welcome visitors to the site
* Arranging sometimes complex detailed travel plans, itineraries, reservations, presentation creation/review, and agendas and compiling documents for meetings
* Assisting with pre-, during, and post-meeting action item follow-up
* Manage the schedules of SVP and other senior leaders, ensuring a balance of availability to stakeholders and time to work on projects and deliver on deadlines
* Researches, prioritizes, and follows up on incoming issues and concerns addressed to the executives, including those of a sensitive or confidential nature, determining the appropriate course of action or response
* Prioritize conflicting needs; handle matters expeditiously, and proactively, and follow through on projects to successful completion, often with deadline pressures
* Supports expense management and orders supplies and materials, as needed
* Files and organizes documents in electronic systems
* Perform other duties as assigned
Key requirements:
* Associate or Bachelor’s degree, plus 5 or more years of Administrative Assistance experience
* Proficient with Microsoft 365, including PowerPoint, Word, Excel, Teams, and other MS apps
* Strong experience with and comfort using technology and programs
* Strong organizational skills that reflect the ability to perform and prioritize multiple tasks seamlessly with...
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Type: Permanent Location: Walkersville, US-MD
Salary / Rate: Not Specified
Posted: 2024-04-26 08:16:49
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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 opening for a Microbiology Supervisor at our Bend, OR location.
The Microbiology Supervisor will report to the Sr.
Manager, Quality Control and provide leadership guidance to execute analytical development and quality control functions across the drug product lifecycle (in support of animal studies, clinical studies and commercial distribution).
Key Responsibilities:
* Create and manage schedules for day-to-day lab activities
* Write, review and approve test notes, specifications, and analytical test reports
* Represent the group at client and regulatory inspections
* Primary point of communication with client team
* Distribution of projects and continuous improvement tasks and track progress
* Review and approve lab employee training
* Continuously identify more effective ways to drive performance
* Effectively manage performance of direct reports
* Assist in microbiological testing as needed
Key Requirements:
* Must possess a minimum of a Bachelor’s Degree in Science
* Significant experience as a Microbiologist is required
* Some experience in a GMP environment is required
* Demonstrated ability to perform hands-on, detailed work, in a fast-paced manufacturing environment
* Demonstrate high standard of ethics, integrity and professionalism
* Will handle hazardous materials and occasionally work in confined spaces
* Must be able to work while wearing personal protective equipment
* Occasional heavy lifting
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 consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
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Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-26 08:16:40
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About us
Bringing True Hospitality to the world.
We want to welcome you to a world of bringing True Hospitality to everyone.
When you join us at IHG®, you become part of our global family.
A welcoming culture of warmth, honesty, and a passion for providing True Hospitality.
We pride ourselves on letting your personality and passions shine, recognizing the individual contribution you make and supporting your ambition to learn and create your own career path.
In making a difference to our guests and owners, colleagues and communities, every day is a chance to create great and unique experiences, in your own way.
With over 370,000 colleagues in nearly 100 countries sharing our values, there’s countless opportunities at your fingertips.
We’re growing; grow with us.
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*This is a Remote role and will be needed in the Atlanta, GA office on a quarterly basis
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*Working experience in Global Complex Organizations is needed for this role
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Role Purpose
This role will own and manage the HCM system release schedule including the monitoring of release communications, identifying release changes both required and optional, working with subject matter SMEs and stakeholders to identify, test, and migrate updates to production.
This includes all releases and deployment of additional functionality for all Oracle modules (core HR, recruiting, talent management, time & labour, payroll, absence, benefits, compensation).
Ensuring the use of HR technology to its full potential to support user friendliness and IHG’s competitiveness within the industry.
This position also serves as SME for core HCM functionality and cross module integration and drives continuous improvement to deliver standardised HR process, efficiency and effectiveness.
Key Accountabilities
•Coordinate the release schedule and resources required in close coordination with HRIS, defect backlogs, planned releases, and infrastructure updates.
•Support the adoption of the people technology roadmap with facilitation of release deployment and adoption of additional functionality, considering global process improvements to deliver increased HR process standardization, efficiency and effectiveness.
•Time management - plan the release of project deliverables and release life cycle working closely with involved teams, including planning, testing, and implementation in production environment.
•Project planning - create detailed project plans for implementation and deployment as per the release schedule.
•Identify product opportunities, drive strategic planning, and articulate topline business requirements.
•Lead the cross-functional working teams to design, develop, and implement release development and prioritized product roadmap elements.
•Ensure progress as per plan and give regular updates on the release activities and plans for leadership teams.
•Communication - communicate the project-related tasks such as plans, timelines, requirements, etc.
between differ...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2024-04-26 08:08:58
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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
Deine Abteilung
Als Learning Team im Bereich Pharma Technical Manufacturing verantworten wir die Ausführung von lokalen und globalen Prozessen in einer Vielzahl von IT Systemen und deren Messung mit aussagekräftigen Kennzahlen.
Damit unsere Prozesse visualisiert, optimiert und deren Ausführung mit Kennzahlen verfolgt werden, suchen wir Dich für 6 Monate Vollzeit (37,5h/Woche) als Unterstützung in unserem Team!
Deine Aufgaben
* Du interviewst verschiedene Stakeholder, um stets den Ist-Zustand des Prozesses adäquat darzustellen
* Du führst Prozessmappings in Tools wie bspw.
Lucid Chart aus
* Du entwickelst Vorschläge für die Optimierung und Standardisierung unserer Prozesse
* Du unterstützt uns dabei, aussagekräftige Kennzahlen zu evaluieren und im Team für einen kontinuierlichen Review zu implementieren
* Du setzt eine Kennzahlenstrategie für die Abteilung auf (Welche Kennzahlen werden auf welche Art an welche Zielgruppe kommuniziert)
Dein Profil
* Du bist immatrikulierter Student (m/w/d) des Wirtschaftsingenieurwesens, der Wirtschaftswissenschaften, Betriebs-/ Volkswirtschaftslehre oder Du befindest Dich in Deinem GAP-Year zwischen Bachelor- und Masterstudium
* Du hast Dich bereits mit Kennzahlen (idealerweise der Unterscheidung zwischen Leading- und Laggingindikatoren) und Prozessmappings auseinandergesetzt und ein Talent für das Strukturieren von Informationen
* Du verfügst über eine ausgeprägte Planungs- und Organisationsfähigkeit sowie eine selbstständige und eigeninitiative Arbeitsweise und überdurchschnittliches Engagement
* Du hast gute Englisch und MS Office Kenntnisse oder mit den vergleichbaren Google-Produkten
Deine Vorteile:
* Flexible Zeiteinteilung, Homeoffice ist möglich
* 2025 € Vergütung im Monat für ein Vollzeitpraktikum
* Vernetzung mit anderen Studierenden (online/offline)
* Ermäßigte Preise (-50 %) in unserer Kantine
* Fitnessstudio auf dem Roche Campus
* Weiterbildungsmöglichkeiten und spannende Gastvorträge
* Möglichkeit der Unterbringung im Roche Boardinghaus
* Gut organisierte Verkehrsanbindung nach München mit unserem Roche-Shuttle
Deine Bewerbung
Bitte lade nur Deinen Lebenslauf online hoch.
Denke daran, daß sich dieses Praktikum an Studierende (m/w/d) bei laufender Immatrikulation richtet oder alternativ an Personen im GAP-Year.
Zeitraum: ab 1.
Juni 2024 für 6 Monate oder nach Vereinbarung für die Dauer von 6 Monaten
Wir freuen uns auf Deine Bewerbung!
Your contact to us! With people.
For pe...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-04-26 08:08:23
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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.
Located in Stein, Switzerland our successful CDMO Business Unit Drug Product Services (DPS) currently offers exciting opportunities.
Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the position as MES Modeler DPS Growth Project 80 – 100% supporting a new sterile Drug product facility.
Key responsibilities:
* Work closely with MES manager, system users and process owners to develop and revise MES recipes in a timely manner
* Configure production recipes using a library of objects, and conduct basic troubleshooting on all related systems and provide ongoing end user support
* Assist in fulfilling requirements of quality records such as process change controls, CAPA and deviations
* Draft and execute test script for the validation of recipes (IQ, OQ, PQ)
* Manage MES master data like Products, Locations, Equipment, Materials
* Support floor activities as required to bring running records to successful process conclusion
* Work closely with Process Automation and MES Analysts to develop and revise Controls Logic, batch records and other MES records in a timely manner
* Support production via the Helpdesk, assisting with production issues
Key requirements:
* Academical degree minimum Bachelor degree preferred in a technical field and/or engineering
* Proven process understanding in Sterile Manufacturing (Pharma, regulatory aspects)
* Familiarity with GMP requirements, quality procedures and SOP execution
* Previous exposure to any of the commercial MES systems (Rockwell PharmaSuite, Werum Pas-X, POMS, Emerson Syncade).
* Good communication skills and interaction with a variety of interface within the organization and the shop floor
* Strong team orientation
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: Stein, CH-AG
Salary / Rate: Not Specified
Posted: 2024-04-26 08:08:06
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ERM is seeking highly motivated Senior Consultant, Archaeologist to join our global consulting firm as part of our Cultural Resources Services team.
This is a hybrid full-time, salary-based position that can be based from a local California ERM office or remote if 100 miles away from an ERM office.
Applicants are preferred to live in California, as well as be familiar with the relevant regional regulatory processes (i.e., federal, state, and municipal).
California archaeological field experience is highly desired.
Successful candidates must be flexible and responsive to a challenging and changing work environment where schedules and tasks fluctuate according to the needs of the projects and clients.
Based in California, the successful candidate will also provide technical assistance for archaeological desk and field studies for clients within the United States.
RESPONSIBILITIES:
* Conduct research and writing for cultural resource heritage components of CEQA, NHPA Section 106, and NEPA documents for projects for private and government sector clients.
* Perform literature review, field reconnaissance, field surveys, and excavation for archaeological studies.
* Interact with various State Historic Preservation Offices, federal agencies, and access online cultural resource databases.
* Lead and supervise staff in an office setting and/or during fieldwork.
* Perform research and write technical reports.
* Provide technical consulting skills to support the growth of ERM’s business and client base in the area of archaeology and cultural heritage.
* Interact with other ERM practice areas to share multi-disciplinary resources and best practices across the country.
* Represent ERM through communications and at meetings with state, federal and local agencies.
* Communicate regularly with clients via email and phone conferences.
* Assist with preparing proposals to meet client needs.
REQUIREMENTS:
* Bachelor’s degree in Anthropology, Archaeology, or closely related field of study.
* 4+ years of related professional experience.
* Knowledge of California and Great Basin cultural areas.
* Demonstrated experience completing inventory, survey, testing, and/or data recovery.
* Experience as primary author on agency-reviewed technical reports.
* Must have strong attention to detail in documentation of work.
* Experience interacting with regulatory agency personnel.
* Excellent communication and computer skills.
* Demonstrated business development abilities.
* Ability to work within a team as well as independently.
* Strong proficiency in Microsoft Office Suite.
* Must be locally available for projects.
* Ability and willingness to frequently travel to field sites that will be located in and out of state.
* Must be able to walk long distances (up to ten miles per day) in varying terrain under adverse conditions, including inclement w...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-26 08:02:24
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ERM is seeking highly motivated Senior Consultant, Archaeologist to join our global consulting firm as part of our Cultural Resources Services team.
This is a full-time, salary-based position that can be based from a local ERM office or hybrid.
Applicants are preferred to be local to the Pacific Northwest, as well as be familiar with the relevant regional regulatory processes (i.e., federal, state, and municipal). Pacific Northwest archaeological field experience is required.
Successful candidates must be flexible and responsive to a challenging and changing work environment where schedules and tasks fluctuate according to the needs of the projects and clients.
Based in the Pacific Northwest, the successful candidate will provide technical assistance for archaeological desk and field studies for clients within the United States.
RESPONSIBILITIES:
* Conduct research and writing for cultural resource heritage components of Washington SEPA and Governor’s Executive Order 21-02 (formerly 05-05), NHPA Section 106, and NEPA documents for projects for private and government sector clients.
* Perform literature review, field reconnaissance, field surveys, and excavation for archaeological studies.
* Interact with various State Historic Preservation Offices, the Washington Department of Archaeology and Historic Preservation, and access online cultural resource databases.
* Lead and supervise staff in an office setting and/or during fieldwork.
* Perform research and write technical reports.
* Provide technical consulting skills to support the growth of ERM’s business and client base in the area of archaeology and cultural heritage.
* Interact with other ERM practice areas to share multi-disciplinary resources and best practices across the country.
* Represent ERM through communications and at meetings with state, federal and local agencies.
* Communicate regularly with clients via email and phone conferences.
* Assist with preparing proposals to meet client needs.
REQUIREMENTS:
* Master’s degree in Anthropology, Archaeology, or closely related field of study.
* 5+ years of related paid experience.
* Oregon SHPO-qualified Archaeologist (must have approval in hand).
* Knowledge of Great Basin, Northwest Coast, and Columbian Plateau culture areas.
* Demonstrated experience completing inventory, survey, testing, and/or data recovery.
* Experience as primary author on agency-reviewed technical reports.
* Must have strong attention to detail in documentation of work.
* Experience interacting with regulatory agency personnel.
* Excellent communication and computer skills.
* Demonstrated business development abilities.
* Ability to work within a team as well as independently.
* Strong proficiency in Microsoft Office Suite.
* Must be locally available for projects.
* Ability and willingness to frequently travel to field sites that...
....Read more...
Type: Permanent Location: Portland, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-26 08:02:23
