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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: 2024-03-30 07:07:07
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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 Tampa is seeking a Research & Development Chemist II to perform scientific experiments with a medium-high level of technical difficulty and a medium-low level of supervision.
The R&D Chemist II will work cross functionally within the organization to provide analytical and technical support to facilitate the successful completion of projects.
Key Accountabilities:
* Planning and executing scientific assignments and problem-solving techniques to support projects in Product Development
* Demonstrates scientific/technical accountability for assignment completion at project level
* Expertise in analytical instrumentation
* Collects, summarizes and analyzes scientific data to prepare reports and make presentations, as appropriate, to disseminate best practice throughout the function.
* Authors and reviews study protocols, reports, SOPs and other internal guidance documents
* Ability to identify atypical results, collect data, and establish facts to support possible corrective measures.
* Assists with investigations, documentation review, and approves results of other team members
* Ensure training and documentation compliance with internal safety standards, SOPs, and cGMPs
* Maintain clean, safe, and compliant laboratory work environment
* Maintain a positive, professional and confidential relationship with internal and external clients.
* Provides on-the-job training/support to new team members and new technologies
* Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear
* Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible
* Stop work where deemed necessary to maintain safety
Key Requirements:
* Bachelor degree in science, preferably chemistry
* Minimum of 3 years' experience in a GMP pharma environment
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 developin...
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Type: Permanent Location: Tampa, US-FL
Salary / Rate: Not Specified
Posted: 2024-03-30 07:06:16
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Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.
Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission.
Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.
By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.
Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.
It’s our work, our passion, and our legacy.
We invite you to join us.
Hybrid
Employee Value Proposition:
Taiho Oncology is a Japanese company specializing in the development and commercialization of orally administered anti-cancer agents.
Our mission is to improve the lives of patients with cancer, their families, and their caregivers.
Whether it’s our patients or employees, people come first at Taiho.
The compassion we practice for our patients extends to our team, empowering and motivating them to do their best work for those who need it most.
Our culture is inclusive and our leadership ensures an environment which encourages employees to be accountable for their own successes.
We hold ourselves and each other to a high bar of executional excellence because patients are counting on us.
Collaboration and trust are additional core principles operating at Taiho which sets us apart from other organizations.
These principles foster open communication and fun atmosphere.
Respect, dignity, compassion and kindness are required of each of employee.
We believe that honesty and integrity are critical to our business and our actions earn each other’s trust and the trust of the community we serve.
For this position, the incumbent will be assigned to lead one or two high priority late-phase clinical development programs as Global Regulatory Lead (GRL), responsible for leading regulatory sub-team and all regulatory activities including marketing authorization filing and approval in US and Europe.
Position Summary:
The incumbent is the most senior regulatory person on project teams and is responsible for regulatory activities globally except for Japan and Asia. For assigned projects and products, the Senior Director, Regulatory Affairs Strategy is responsible for strategic definition/direction, and implementation of regulatory strategies, and ensures that these strategies are consistent with company objectives. The incumbent directs the project/product teams’ regulatory activities to ensure high...
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Type: Permanent Location: Pleasanton, US-CA
Salary / Rate: Not Specified
Posted: 2024-03-30 07:04:10
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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: 2024-03-30 06:59:12
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* Compile, sort and verify the accuracy of data before it is entered into the ERP system or distributed throughout the organization.
* Store completed documents such as but not limited to production reports and work orders in the appropriate locations and maintain per document storage policies.
* Verify and analyze production data for trend analysis.
* Using standard analysis tools, detect and verify outliers within the data.
* Prepare and distribute reports regarding such topics as OEE performance, variances, use of materials etc.
In this case it is necessary to know Shop Logix system or any other software defined or used on the floor to record accurate data.
* Enter all relevant information into the ERP system relating to the work order process: such as Materials, also add, Scrap, Labor Hours if needed.
* Audit the work order process in the manufacturing environment and provide feedback to the management team.
* Maintaining constant communication with the production leads to understanding the changes on the operation to reflect the physical changes in the system.
* Consider inventory accuracy to update the consumption methodology, based on trends and historical data.
* Target the reduction (Trending to 0%) of inventory adjustments.
Materials consumption as well as supplies should be completed under the exact process-product and what was consumed.
* Act as a liaison between manufacturing management, finance, and logistics.
* Analyze variances report and lead the action plan needed to improve the variances of top products.
* Support the projects undertaken by the organization, where the employee’s experience, data management and expertise can add value.
* Keep updated databases and documents under the employee responsibility.
Perform other related duties that contribute to the success of the operation as assigned by manager.
Administrative
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2024-03-29 07:43:08
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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: 2024-03-29 07:33:41
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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: 2024-03-29 07:33:22
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Are you ready to dive into the dynamic world of Support Analysis? Here at Cayenta; a division of Harris, support calls are an exciting puzzle, typically falling into one of three thrilling categories: Application issues, Environment and Database issues, and IT/Communications issues.
As a Support Analyst, your focus will be on the intriguing realm of software application issues.
This is your chance to deepen your expertise in the solutions used by our ERP customers.
Whether you're in Canada or the United States, we're looking for talented individuals like you to join us remotely.
Embrace the challenge and become a pivotal part of our support team from wherever you are!
This remote role welcomes candidates anywhere in Canada and the US.
What your impact will be:
* Provide timely and thorough resolution to customer issues.
* Monitor the support call queue and take ownership or re-assign new tickets.
* Interact with a range of internal departments (Environment Specialist, R&D, other analysts, etc.) for issue escalation.
* Assist in the problem solving of data, architecture, and interface issues.
* Respond quickly to customer calls and provide frequent updates so customers know their problems are being addressed.
* Develop a deep understanding of the functional and technical features of our applications and use this knowledge to address application-related issues and questions.
* Provide recommendations to customers and Product Management to prevent recurrence of the issue.
* Understand the support services agreement to know when requested services are outside the support agreement terms.
* Provide suggestions on enhancements to the product or process.
What we are looking for:
* A University degree or technical college degree in computer sciences, software engineering, software development or related field is preferred.
* Experience delivering solutions, services and/or support to the financial or accounting industry is preferred.
Customer Support Qualifications
* Familiarity and experience in a Customer Support environment.
* Excellent client communication skills. Ability to manage and shape customer expectations.
* Ability to work on multiple initiatives and/or support tickets simultaneously.
* Strong analytical problem-solving skills.
Must be able to analyze information to make independent decisions quickly and effectively.
* Ability to work independently, be flexible, be self-motivated and be a team player.
* Finance/Accounting industry experience is preferred.
Technical Qualifications
* Software experience in applications based in at least one of the following: Java, SQL, PL/SQL, Uniface, Web technologies (Node.js, Angular, JavaScript, JSP).
* Experience in troubleshooting APIs and/or web services.
* Knowledge of Apache Tomcat configuration and troubleshooting is preferred.
What we can offer:
* 3 weeks' vac...
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Type: Permanent Location: Burnaby, CA-BC
Salary / Rate: 85000
Posted: 2024-03-29 07:31:54
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The Associate Director is a key member of the Market Regulation Surveillance and Market Intelligence section’s leadership team and is responsible for the effective generation and progression of regulatory reviews conducted by the section.
This role communicates and innovates with peers across the organization to facilitate sharing of surveillance intelligence to improve our ability to meet FINRA’s mission.
The function of this role is to ensure that member firms are complying with applicable rules and regulations.
This role administers directives and policies established by MRTS to ensure the effective and efficient functioning of assigned teams.
Essential Job Functions:
* Manages a team of individual contributors and is accountable for conducting effective performance management and meaningful career development conversations.
* Develops and implements policies and procedures for the execution of the surveillance program to ensure progress toward the organization's goals and objectives.
* Communicates regulatory information to internal and external stakeholders.
* Identifies and escalates situations that may present significant regulatory risks that could adversely affect the organization and recommend remediation plans.
* Leads staff in the review and analysis of regulatory intelligence received through a variety of sources, including internal sources, regulatory tips, customer complaints, firm regulatory filings, arbitration filings, and referrals from other regulators.
* Manages operational aspects of their team (e.g., workflow, performance, and compliance), as well as ensuring achievement of team goals.
* Ensures that all regulatory requests are fulfilled in a timely and accurate manner.
* Represents FINRA in internal/external meetings.
* Demonstrates FINRA’s values of Responsibility, Innovation, Collaboration and Expertise, while embracing FINRA’s culture of diversity and inclusion, in interactions with colleagues, management, FINRA members, and outside parties.
* Monitors and implements solutions to achieve the section’s measures of success.
Other Responsibilities:
* Represents FINRA at speaking engagements with various internal and external constituencies
* Leads multi-level initiatives across Regulatory Operations
* Provides subject matter expertise in regulatory area to advance FINRA and industry initiatives (e.g., CAT, Notice to Members, rule filings, market events, congressional testimony preparation)
* Remains current on industry trends, practices, and regulatory impacts
Education & Experience Requirements:
* Bachelor’s degree and a minimum of eight (8) years of experience in the securities/financial services industry; or an equivalent combination of education and experience in positions of increasing responsibilities.
* Experience supervising projects and/or mentoring junior staff.
* Demonstrated project manag...
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Type: Permanent Location: Rockville, US-MD
Salary / Rate: Not Specified
Posted: 2024-03-29 07:17:41
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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.
As a member of the Lonza – Personalized Medicine Clinical Application Team, the Senior Clinical Application Scientist works in a high-performing, cross-functional team with the goal of developing, transferring and supporting scalable manufacturing processes for cell therapies using a novel manufacturing system.
The Senior Clinical Application Scientist works with various global Lonza groups, clinical and research centers within their geographical territory, to assure progress and stability of cell therapy projects.
The Senior Clinical Application Scientist evaluates and recommends new technologies to enhance efficiencies of processes and scale. Routine activities include instrument demonstrations, customer trainings, and technical transfer of cellular therapy processes, while providing technical support and assay guidance to Personalized Medicine’s partners and customers.
Also, generate reports, execute experimental studies, analyze data, support the execution of development and manufacturing activities, and provide additional support to other departments as required (Quality Assurance, Quality Control, Program Management).
This role is 100% remote with a significant amount of travel domestic and/or international travel.
Key responsibilities:
* Plans and performs demonstrations and trainings for the Cocoon® Platform, eventual tech transfer of cell therapy processes, and ongoing support of Personalized Medicine customers/collaborators
* Leads the build out of application based training regimen for use with newly onboarded clients
* Maintains up-to-date knowledge of the cell therapy field through continued research and trainings
* Critically analyzes processes for improvement and scalability and proactively suggests changes to protocol and assists customers in experimental design
* Facilitates scientific meetings between client and internal R&D teams in an effort to acquire VOC, clients specifications and build out customer profiles
* Utilizes expertise in upstream production, harvest, and recovery technologies to establish and optimize new processes for manufacturing
* Capable candidate troubleshoots processes, compiles and analyzes data, and summarizes results in high-quality reports supported with appropriate laboratory records.
* Independently designs and executes experiments.
Interprets results and proposes next steps.
* Helps create and revise task orders for contractual relationships.
Supports new client development.
* Delivers results in a timely f...
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Type: Permanent Location: Walkersville, US-MD
Salary / Rate: Not Specified
Posted: 2024-03-29 07:17:14
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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 Tampa is seeking a QC Chemist to join the Quality Control team.
The incumbent will be Conduct analysis of raw materials, In process items and finished products.
Key Accountabilities:
* Analysis of dry product stability and finished product samples according to the assigned specifications, analytical methodology and protocols in a GMP laboratory setting with emphasis on attention to detail and accuracy of execution.
* Documentation of results in accordance with cGMP
* Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner.
* Reports lab testing data and completes documentation accurately and in accordance with laboratory procedures and regulatory requirements.
* Reviews results for conformance to standards.
* Perform analytical testing of pharmaceutical products following analytical methodology.
* Read and interpret analytical methodology and the USP.
* Supports method development and validation of new methods.
* Performs investigations and completes CAPA in response to deviations.
* Develops and executes validation protocols for test methods and equipment qualification as requested.
* Meet fundamental cGMP requirements relating to conduct and work practices to ensure the SISPQ (Safety, Identity, Strength, Purity, and Quality) of all products manufactured/tested at Lonza Tampa.
* Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear.
* Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible
* Stop work where deemed necessary to maintain safety.
Key Requirements:
* Associate degree in science, preferably chemistry
* Minimum of 3 years' experience in a GMP pharma environment
* Actively participates in customer and regulatory audits.
* Demonstrated experience with peer review work and data of other analysts to ensure compliance with method and regulatory requirements.
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...
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Type: Permanent Location: Tampa, US-FL
Salary / Rate: Not Specified
Posted: 2024-03-29 07:17:13
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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.
Our team in Portsmouth NH is searching for a QC Environmental Monitoring (EM) Analyst to join us at Lonza.
As our QC Environmental Monitoring Analyst, you will support routine environmental monitoring of air, surface and clean utilities for manufacturing of in process and final product drug lots for customers.
* This position has a rotating 2-3-2 NIGHTS schedule (on 2 days, off 2 days, on 3 days) 7PM-7AM
*
While working this shift, the employee will receive a 20% shift differential
While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential
Key Responsibilities:
* Perform analysis of environmental monitoring test results according to SOPs and test methods
* Running test samples for In-Process, Lot Release and Stability studies
* Participate in quality testing for ongoing customer support
* Reviewing assays
* Provide guidance for training to junior staff or other departments
* Write Standard Operating Procedures, Deviations, CAPA, Change Control, Test Methods and other Quality documents
* Level of this role is dependent on experience
Key Requirements:
* Associate Degree or higher required.
Preferred area of study in Microbiology, Biochemistry or Related Science Fields
* Minimum 2 years of experience within industry in a quality control lab setting in environmental monitoring
* Ability to walk, bend, climb ladders consistently throughout the shift
* Ability to wear full gown for up to 50% of the shift when needed
* Previous experience using GMP Quality Systems (ex.
TrackWise, LIMS, iLab, and Empower) preferred
* Excellent communication skills with the ability to collaborate across multiple teams and projects
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 consideration for employment without regard to race, re...
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Type: Permanent Location: Portsmouth, US-NH
Salary / Rate: Not Specified
Posted: 2024-03-29 07:14:47
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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.
Our team in Portsmouth NH is searching for a QC Environmental Monitoring (EM) Analyst to join us at Lonza.
As our QC Environmental Monitoring Analyst, you will support routine environmental monitoring of air, surface and clean utilities for manufacturing of in process and final product drug lots for customers.
* This position has a rotating 2-3-2 NIGHTS schedule (on 2 days, off 2 days, on 3 days) 7PM-7AM
*
While working this shift, the employee will receive a 20% shift differential
While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential
Key Responsibilities:
* Perform analysis of environmental monitoring test results according to SOPs and test methods
* Running test samples for In-Process, Lot Release and Stability studies
* Participate in quality testing for ongoing customer support
* Reviewing assays
* Provide guidance for training to junior staff or other departments
* Write Standard Operating Procedures, Deviations, CAPA, Change Control, Test Methods and other Quality documents
* Level of this role is dependent on experience
Key Requirements:
* Associate Degree or higher required.
Preferred area of study in Microbiology, Biochemistry or Related Science Fields
* Entry level to working experience within industry in a quality control lab setting
* Ability to walk, bend, climb ladders consistently throughout the shift
* Ability to wear full gown for up to 50% of the shift when needed
* Previous experience using GMP Quality Systems (ex.
TrackWise, LIMS, iLab, and Empower) preferred
* Excellent communication skills with the ability to collaborate across multiple teams and projects
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 consideration for employment without regard to race, religion, color, national ...
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Type: Permanent Location: Portsmouth, US-NH
Salary / Rate: Not Specified
Posted: 2024-03-29 07:14:46
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Are you passionate about video games? Want to create software that makes a difference? At the Virtual Heroes Group of Applied Research Associates, our goal is to improve your safety, security, and way of life.
Join us!
We're looking for dedicated, hard-working programmers with a passion for using game technology to develop state-of-the-art training applications.
You will be a key member of a team that is solving real-world problems for customers in the military, medical, commercial, and intelligence industries.
Ideal candidates will have broad programming experience on one or more published/deployed projects.
You must be able to serve multiple projects simultaneously with agility, poise, and focus.
Our games are award-winning, reflecting the creativity, dedication, and vision of every member of our studio.
You can be part of our team!
Why Work For Us?
* The opportunity to make a real impact.
Virtual Heroes has been making quality serious games for over 18 years.
Everyone who works here is important, from new faces to those who have worked here since the beginning.
Your contribution matters—you won’t be just a number!
* Flexible, reasonable hours.
We encourage all employees to have a good work/life balance.
We do not believe in burning you out! We invest in our people and want you to be happy with us for the long haul.
+ For additional information, please visit our benefits page at https://www.ara.com/benefits/.
Senior Game Programmer Requirements:
* US Citizenship is required
* Candidates selected may be subject to a government security investigation and must meet eligibility requirements for access to classified information
* BS (or higher) in Computer Science, Game Development, or a similar discipline, plus at least 8 years of relevant professional experience OR at least 13 years of experience will be considered for talented candidates without a degree
* Experience with Unreal Engine 4 C++ programming and Blueprints AND/OR Unity programming
* C++ experience and demonstrated knowledge of good software engineering practices
Preference to applicants with one or more of the following:
* Experience serving as project technical lead
* Experience developing multiplayer game/training applications
* Experience with mobile platform development (iOS, Android)
* Experience with databases (MySQL, sqlite, spatialite) or xAPI LMS integration
* Experience with VR development
* Experience with AR development
Senior Game Programmer Additional Requirements:
Please provide a resume that includes a link to code samples.
Salary Range: $96,555 - $150,000 dependent upon experience, education & skills as determined during the interview process.
Company Information:
At Virtual Heroes, we leverage simulation and digital-games-based paradigms to create applications that teach critical skills.
As a group of Applied Research Associates (ARA), we work with scientists and engineers...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2024-03-29 07:12:41
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Augenoptikermeister (m/w/d) für Graz
Kennst du das? Es gibt die besten Wachstumsgeschichten von Unternehmen und du denkst dir immer wieder "Da hätte ich auch gerne von Anfang an mitgewirkt".
Dieser Moment ist jetzt! Wir leiten unsere Zukunft ein und können sie nur mit dir erreichen.
Mister Spex hat weiterhin Großes vor, die 70 eröffneten Retail Stores waren erst der Anfang!
Unterschütze uns als Augenoptikermeister (m/w/d) mit deiner augenoptischen Expertise, positioniere Mister Spex als Retailer am Standort und gewinne die Kund
*innen deiner Stadt für uns!
Du möchtest bereits jetzt Großes mit uns bewegen und bist aber finanziell noch gebunden oder derzeit in der Weiterbildung zum Meister? - Wir haben auch dafür eine Lösung.
*
Das erwartet dich bei uns
* Du bist im Store für interne Trainings rund um die Augenoptik zuständig und arbeitest mit modernster Technik
* Du berätst Kund
*innen und unterstützt Kollegen hinsichtlich augenoptischer Belange
* Du refraktionierst und stellst sicher, dass Refraktionen im Team standardgemäß durchgeführt werden
* Du bist verantwortlich für die gesamte technische Ausstattung und ergänzt das Store Management mit Deinem fachlichen Know-How
Was du mitbringst
* Einschlägige Erfahrungen in der Refraktion und/ oder der Kontaktlinsenanpassung
* Abgeschlossene Ausbildung als Augenoptikermeister (m/w/d)
* Durch Dein Kommunikationstalent und Deine positive Energie liebst du es unsere Kund
*innen von unseren Produkten zu begeistern
* Als Teamplayer arbeitest Du gerne in einem motivierten Team, mit dem Du zusammen unsere Unternehmensziele erreichst
Deine Benefits bei uns
* On Top zu deinem Gehalt erhältst du einen Bonus für eure Store Perfomance
* Deine persönliche Entwicklung ist uns wichtig – wir bieten dir ein umfangreiches Onboarding, 360°- Feedback, eine digitale Lernplattform und Schulungen
* Du erhältst zum Start einen Gutschein über 200€ für eine Brille aus unserem eigenen Sortiment, sowie jährlich zu deinem Jubiläum einen Gutschein für eine Brille deiner Wahl
* Zum Start, sowie jährlich, erhältst du außerdem einen Zuschuss i.H.v.
150€ für deine Arbeitskleidung
* Da wir unseren Beitrag zum Klima leisten möchten - 50% Zuschuss für öffentliche Verkehrsmittel Du erhältst 25 Tage Urlaub pro 5 Tage-Woche
* Bis zu 40% Rabatt auf unser Sortiment und attraktive Mitarbeiterrabatte über die Plattform Corporate Benefits
Deine Persönlichkeit ist unsere Stärke! Unabhängig der ethnischen Herkunft, des biologischen oder sozialen Geschlechts, der Religion oder Weltanschauung, einer Behinderung, des Alters oder der sexuellen Identität, freuen wir uns auf jed...
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Type: Permanent Location: Seiersberg, AT-6
Salary / Rate: Not Specified
Posted: 2024-03-29 07:12:36
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Augenoptiker / Augenoptikermeister als Store Manager/Filialleiter (m/w/d) in Graz
Kennst du das? Es gibt die besten Wachstumsgeschichten von Unternehmen und du denkst dir immer wieder "Da hätte ich auch gerne von Anfang an mitgewirkt". Dieser Moment ist jetzt! Wir leiten unsere Zukunft ein und können sie nur mit dir erreichen.
Mister Spex hat weiterhin Großes vor, die mehr als 70 eröffneten Retail Stores waren erst der Anfang!
Daher suchen wir dich! Du liebst es, andere zu motivieren, stets ihr Bestes zu geben? Du koordinierst und steuerst gerne Prozesse, bringst gleichermaßen die Leidenschaft für die Augenoptik mit und gibst diese durch Trainings gerne an dein Team weiter? Dann haben wir die passende Stelle für dich.
Als Store Manager mit augenoptischer Expertise agierst du als Vorbild und lebst mit einer positiven sowie motivierenden Kommunikation unsere Mister Spex Werte vor.
Du hast alles im Blick und stellst sicher, dass alle für den Store relevanten Vorgänge und Aktivitäten korrekt umgesetzt werden.
Und zusammen mit deinem Team positionierst du Mister Spex am Standort und gewinnst die Kund
*innen deiner Stadt für uns! #WeStayHungry! Wir freuen uns von dir zu hören.
Das erwartet dich bei uns
* Du trägst die Umsatzverantwortung für den Store, analysierst die unternehmensinternen KPI’s und leitest die entsprechenden verkaufsfördernden Aktionen ab
* Du refraktionierst und stellst sicher, dass Refraktionen im Team standardgemäß durchgeführt werden
* Du stellst sicher, dass unsere Customer Journey inklusive der augenoptischen Beratung nach Mister Spex Standards durchgeführt wird
* Du verantwortest mit Deinem Team das Einhalten von Prozessen und Guidelines und lieferst mit Deinen Ideen wertvollen Input für die weitere Expansion des Unternehmens im Retail
* Zusätzlich stehst du unseren Kund
*innen beim Kauf ihrer Lieblingsbrille mit Rat und Tat Zur Seite
Was du mitbringst
* Du besitzt Führungserfahrung im Store Management
* Du hast eine abgeschlossene Ausbildung zum Augenoptiker/ Augenoptikermeister (m/w/d)
* Du bist es gewohnt Retail-Prozesse auf Storeebene zu definieren und zu implementieren
* Du arbeitest eigenständig und ergebnisorientiert & führst monatliche Business Auswertungen mit dem Area Management durch
* Du erkennst Talente in Deinem Team, motivierst und entwickelst sie kontinuierlich & leitest gegebenenfalls auch disziplinarische Maßnahmen ein
* Du hast eine herausragende Kommunikationsfähigkeit und lebst sowie förderst eine Feedbackkultur in Deinem Store Team
Deine Benefits bei uns
* On Top zu deinem Gehalt erhältst du einen Bonus für eure Store Perfomance
* Deine persönliche Entwicklung ist uns wichtig – wir bieten dir ein umfangreiches Onboarding, 360°- Feedback, eine digitale Lernplattform u...
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Type: Permanent Location: Seiersberg, AT-6
Salary / Rate: Not Specified
Posted: 2024-03-29 07:12:34
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
The Manufacturing Science and Technology (MSAT) Associate Director is accountable for the Lonza-Tampa commercial drug product portfolio throughout the product lifecycle and for technical operations within the GMP manufacturing operation.
The MSAT Associate Director leads a team of scientists and engineers that use their expertise of the technology, operation, and regulatory requirements to ensure that processes are reliable and capable of delivering safe and high-quality products to patients.
Key Accountabilities:
* Manage a portfolio of commercial drug products and intermediates throughout the drug product life cycle, including technology transfer, process validation, and commercial manufacturing.
* Understands the requirements for commercialization of a product and leads the commercialization of products at the Lonza – Tampa site.
* Develop the manufacturing facility’s systems and capabilities to enable the product portfolio in clinical development.
* Designs and implements projects to build or modify systems for improvements in safety, quality or operational efficiency.
* Balance technical, operational, and regulatory requirements to implement strategic business initiatives within manufacturing operation.
* Develop colleagues within the MSAT team by providing leadership and mentorship to identify growth areas and growth plans for the team members.
* Provide leadership and manage interactions between the client and internal cross-functional project teams.
Act as the project lead for commercial products guiding and overseeing the technical strategy for process validation and continuous improvements.
* Understand and apply chemical and engineering fundamentals including chemistry, materials science, heat and mass transfer, fluid mechanics, thermodynamics, conservation of mass and energy, and basic mathematical modeling.
* Leads process and/or technical-related investigations to support root cause analysis, product impact assessment, and effective Corrective Action and Preventative Action definition.
* Use risk management methodology and tools to drive reliable product quality and supply.
* Supports Pre-Approval Inspection (PAI) or other client and regulatory audits as product and process subject matter expert.
* Independently assesses impact of changes to the product, process, equipment, procedures or materials.
* Leads cross departmental teams to drive Operational Excellence by identifying projects to improve yield, lower costs, and impr...
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Type: Permanent Location: Tampa, US-FL
Salary / Rate: Not Specified
Posted: 2024-03-29 07:12:15
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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
Roche in Kürze:
Wir bringen die Wissenschaft voran, damit wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Was Dich erwartet:
Der Bereich Produktion Chemie innerhalb des Geschäftsbereichs Diagnostics Operations Penzberg ist für die termingerechte Produktion von chemischen und biochemischen Einsatzstoffe zuständig.
Als Teil unserer Teams gehören unter anderem die folgenden Tätigkeiten zu Ihrem Aufgabengebiet:
Dein Team:
Wir sind das Team der chemisch/biotechnischen Produktion und sind stolz darauf, für nahezu alle Einheiten im Roche Konzern viele wichtige Produkte liefern zu können.
Wir sind aktuell in der Abteilung über 40 Mitarbeitende, 3 Teamleiter, ein Gruppenleiter und ein Abteilungsleiter.
* Du arbeitest gerne praktisch und vorausschauend? Dann betreust Du die Produktionsansätze von A bis Z, indem Du in einem ersten Schritt die benötigten Geräte und Anlagen in Abstimmung mit Deinen Kollegen und anderen Arbeitsgruppen reservierst und in einem zweiten Schritt die Produktionsansätze durchführst und überwachst
* Des Weiteren bist Du auch an einem breiten Methodenspektrum interessiert? Dann vertrauen wir Dir verschiedene Anlagen und Geräte an, wie z.B.
Reaktoren, Korbzentrifugen, Extraktoren, Chromatographie- und Lyo-Anlagen und Verdampfer, die Du selbstständig für die Produktion der verschiedenen Substanzen bedienen kannst
* Du kannst Dich für klassisch organisch chemische Arbeitstechniken begeistern? Dann zeig Deine Affinität zu diesen Themen z.B.
bei der Durchführung von exothermen Reaktionen oder diversen Aufarbeitungsmethoden (Destillationen, Extraktionen oder Kristallisationen)
* Du bist gut im Organisieren? Dann stell die Verfügbarkeit aller erforderlichen Arbeitsmittel sicher, indem Du sowohl die Rohstoffbestellung als auch -vorbereitung durchführst und verantwortest
* Du verstehst die Wichtigkeit einer Prozessdokumentation, auch GMP? Dann erfasse Deine Arbeitsschritte gemäß gültiger Herstellungsvorschriften in Chargendokumenten, Reinigungsplänen und Betriebsbüchern
Was noch wichtig ist:
* Du bewegst Lasten von bis zu 15 kg mehrmals wöchentlich
* Du trägst Schutzausrüstung
* Wir bieten gute Entwicklungsmöglichkeiten
* Wir achten auf Deine Gesundheit
Dein Profil:
* Du stehst kurz vor Abschluss Deiner Ausbildung zum Chemielaborant/Chemikant (m/w) und/oder
Du verfügst über Kenntnisse der oben genannten Arbeitstechniken und hast Erfahrung im Umgang mit den dafür notwendigen Geräten
* Du verfügst darüber hinaus über K...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-03-29 07:10:47
-
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
Roche in Kürze:
Wir bringen die Wissenschaft voran, damit wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Was Sie erwartet:
Der Bereich Produktion Chemie innerhalb des Geschäftsbereichs Diagnostics Operations Penzberg ist für die termingerechte Produktion von chemischen und biochemischen Einsatzstoffe zuständig.
Als Teil unserer Teams gehören unter anderem die folgenden Tätigkeiten zu Ihrem Aufgabengebiet:
* Im Rahmen der Durchführung und Überwachung von Produktionsansätzen reservieren Sie die dafür benötigten Geräte in enger Abstimmung mit anderen Kollegen/Arbeitsgruppen
* Die zur Produktion benötigten Anlagen bzw.
Geräte wie zum Beispiel Reaktoren, Korbzentrifugen, Extraktoren, Chromatographie-Anlagen oder Verdampfer bedienen Sie selbstständig
* Dabei wenden Sie organisch-chemische Arbeitstechniken an wie zum Beispiel die Durchführung von exothermen Reaktionen oder diverse Aufarbeitungsmethoden (Destillationen, Extraktionen oder Kristallisationen)
* Sie stellen die Verfügbarkeit aller erforderlichen Arbeitsmittel sicher, indem Sie sowohl die Rohstoffbestellung als auch -vorbereitung durchführen und verantworten
* Sie dokumentieren Ihre Arbeit in Chargendokumentationen, Reinigungsplänen und Betriebsbüchern gemäß gültiger Vorschriften
Diese Tätigkeit erfordert das Heben und Bewegen von Lasten bis zu 15kg mehrmals wöchentlich.
Diese Position ist auf 2 Jahre befristet.
Wer Sie sind:
* Sie bringen eine erfolgreich abgeschlossene naturwissenschaftliche Ausbildung (z.B.
Chemielaborant, CTA, BTA, Pharmakant, Chemikant, o.ä.) mit mehrjähriger Berufserfahrung und eine Weiterbildung als Techniker/Meister
* Idealerweise konnten Sie bereits praktische Berufserfahrung in einem chemischen/pharmazeutischen Produktionsbetrieb erwerben
* Sie besitzen darüber hinaus vertiefte Kenntnisse der oben genannten Arbeitstechniken und haben Erfahrung im Umgang mit den dafür notwendigen Geräten
* Die für Ihre Arbeit relevanten Regularien aus den Bereichen Arbeitssicherheit, Umweltschutz, Qualitätssicherung, etc.
sind Ihnen bestens vertraut
* Sie besitzen sehr gute Deutsch- und gute Englischkenntnisse
* Sie sind in der Lage, sich mit diversen Arbeitsgruppen nachhaltig abzustimmen und schätzen eine partnerschaftliche, offene Zusammenarbeit im Team
Starten Sie Ihre Bewerbung jetzt und werden Sie ein Teil unseres Teams!
Bitte laden Sie hierfür nur Ihren Lebenslauf sowie Ihr letztes Zeugnis hoch.
Zum aktuellen Zeitpunkt benötigen wir keine weiteren Dokumente, w...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-03-29 07:10:42
-
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.
Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow.
Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.
We have a number of great opportunities for Biotechnologists to join our Large Scale Manufacturing Team at our Tuas site in Singapore.
Reporting to the Section Lead/Manager, you will be responsible for the manufacturing of therapeutic proteins under cGMP conditions.
You will be working in 12-hour rotating shift in a 2-2 3-2 2-3 pattern and will be compensated with shift premium and allowances!
Key responsibilities:
* Learn and perform well-defined procedures within a GMP manufacturing setting
* Perform equipment monitoring & and basic 6S housekeeping
* Perform basic laboratory tasks (e.g.
sampling, pH/ conductivity/ osmolality measurements etc.)
* Perform routine sanitization tasks to maintain facility standards
* Trained & signed off on Performance Measures (PMs) relating to CIP/ SIP/ basic tank & instrument operations
* Demonstrate aseptic technique in the handling of product/ materials
* Perform basic process & equipment troubleshooting
* Multi-task on equipment preparations & operations to ensure adherence to schedule
* Attain full competency in the performance of all operations relevant to manufacturing areas assigned.
* Display basic process & equipment troubleshooting ability under routine scenarios.
* Become a technical process expert by exhibiting basic understanding of critical process/operational parameters and target/acceptable ranges, as well as interactions between different process parameters.
* Use Standard Operating Procedures (SOPs), logbooks & Batch Records (BRs) effectively & competently
* Submit samples via Laboratory Information Management System (LIMS)
Cell Culture (Upstream large scale)
* Skill and knowledge of aseptic technique for subculture stages example using culture flask, spinners, wave bioreactors, etc.
* Technical knowledge on the bioreactor culture control example pH/DO control, CO2/O2 control, cell performance, and metabolites analysis.
Purification (Downstream large scale)
* Skill an...
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Type: Permanent Location: Singapore, SG-05
Salary / Rate: Not Specified
Posted: 2024-03-29 07:10:26
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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: 2024-03-29 07:09:19
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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: 2024-03-28 07:42:53
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Environmental Service Technician
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 Part-Time/PRN employee, you will have access to the following benefits:
Part Time and PRN
*
* Employer Paid
+ 401k match
+ HealthJoy - no cost medical and mental health online resources available Day 1 (coverage extends to family members living in the same household)
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!
*PT/PRN hours are based on working 59 hours or less per two-week pay period
SCOPE OF ROLE
Reporting to the Director, Facilities, the Environmental Service Technician is responsible for maintaining a clean work environment in assigned areas with a commitment to service excellence. The Environmental Service Technician is proactive in identifying and attending to needs in the assigned area, strong attention to detail and communicates well with others.
Responsibilities may vary depending on location, site requirements and business needs.
HOW YOU’LL SUCCEED:
* Performs Environmental Services duties in an effective, efficient manner completing all steps in the 7 Step Cleaning Process.
* Performs assigned duties according to quality standards to ensure a clean and comfortable environment for patients, visitors and staff.
* Keeps cleaning cart, equipment and storage rooms clean and organized.
All cleaning materials properly labeled.
* Required to properly and safely use cleaning chemicals per manufacturer standards.
* Cleans offices, patients’/residents’ rooms, classrooms, common areas, restrooms, halls, food service areas and any other areas that may require attention.
* Sweeps, mops, and vacuums hallways, stairs and office space.
* Cleans light fixtures, ceilings and vents, walls, furniture, windows and window coverings.
* Empties trash and garbage containers, may transport waste to outside trash containers including recyclables.
* Replenishes supplies and materials.
* Moves furniture and sets-up tables and chairs.
* Notifies leaders concerning any need for any maintenance repairs.
* Participates in regular safety meetings, safety training and hazard assessments.
* Applies all applicable OSH...
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Type: Permanent Location: Lakewood, US-OH
Salary / Rate: Not Specified
Posted: 2024-03-28 07:39:55
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Registered Nurse (RN), Infectious Disease (ID)
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 Manager, ID Clinical Services, the Registered Nurse (RN), Infectious Disease (ID) will be instrumental in providing outstanding nursing support and assistance to patient treatment plan development.
The role will grow and build an excellent patient care experience everyday through assessment, evaluation and treatment services to patients and their families suffering from infectious disease diagnoses.
HOW YOU’LL SUCCEED:
* Assessment of ID patient care needs in office and in the community
* Consult and collaborate with patient, staff and providers to correctly execute appropriate plan of care.
* Arrange and diligently perform urine toxicology screens, routine lab draws, medication teaching, pill/film counts, observed dosing, medication management, prior authorizations, safe medication administration, and refill requests.
* Obtain vital signs for each patient prior to the provider visit.
* Provide client education regarding medication and health promotion.
* Build nursing evaluations and assist in the admission process for new clients.
* Serve as a subject matter expert for patients on calls when answering questions or gathering information.
* Track and review medical record and lab results.
* Assists with tracking in the Addiction Service Condition registry.
* Complete appropriate documentation in the medical record to comply wi...
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Type: Permanent Location: Lakewood, US-OH
Salary / Rate: Not Specified
Posted: 2024-03-28 07:39:53
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DataVoice, a leader in utility industry solutions, seeks a Remote GIS Support Analyst to join our dedicated team.
The successful candidate will investigate, manage, track and close client support issues, specifically related to the mapping and database functions of the DataVoice applications.
This remote role welcomes candidates anywhere in Canada and the US.
A valid driver's license and passport for travel is required for this role to travel within the USA.
This role will be working in the CST timezone.
What your impact will be:
* Operate as a frontline, primary support liaison between DataVoice and our client’s GIS technicians and dispatchers by effectively responding to inquiries of both a product and technical nature received by telephone or electronically submitted tickets
* Assess a variety of situations, reviewing software configuration, set-up and software code and identify the correct resolution or escalate according to departmental guidelines
* Report detailed information within the client tracking system and document processes, routines, and programs by following the defined guidelines and team goals & objectives
* Work closely with other team members as part of a cohesive group in exchanging knowledge through peer to peer interaction driving future product requirements
* Maximize and maintain current knowledge and awareness of GIS applications and related technologies
* Interpret requirements and recommend solutions that best address clients' needs
* Other duties as assigned by management
What we are looking for:
* Bachelors degree in a GIS, computer science, computer engineering or other related field
* Knowledge and working Experience with ESRI, PostGIS and Postgresql
* Experience with Linux OS and basic scripting
* Creative problem-solving skills
* Excellent interpersonal, written, and oral communication skills
* Strong work ethic and self-starter, able to work independently and as a team player
* Ability to effectively manage multiple priorities and adapt to change within a fast-paced business environment
* Desire to work collaboratively in cross-functional teams
* Ability to learn and navigate new software quickly
* Experience in the utility industry is a plus
* A valid driver's license and ability to travel as needed
* Occasional travel for In-Office events
What we can offer:
* 3 weeks' vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Remote work and more!
About us:
At DataVoice International, we tackle utilities' challenges head-on, from disruptive weather events to customer inquiries about outage restoration times.
Our cutting-edge solutions ensure seamless communication and efficient outage management, empowering the utilities, our customers...
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2024-03-28 07:36:45
