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Project Engineer- Automation
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.
Responsible for development, support, configuration, replication, modifications of automation systems while utilizing the following platforms: Programmable Logic Controllers (PLCs), Supervisory Control and Data Acquisition (SCADA) systems, drives and servo systems, Open Platform Communication (OPC) software, process historians, and Distributed Control Systems (DCS). Utilizes Lonza global standard software development life cycle methodology; Creates test plans necessary to verify software fitness for use; Carries out commissioning and supports validation of automation systems; Develops accurate time estimates for control software development tasks; Participates in team-based continuous improvement initiatives.
The Automation Engineer must have excellent communication skills and be able to participate or lead global collaborative projects, while applying advanced software engineering competencies (FS/DS, PLC or SCADA or Motion control development, software life cycle methodology).
Key responsibilities:
* Designs automation systems, or designs modifications to existing automation systems based on process diagrams, user requirements, functional requirements, Piping & Instrumentation Diagrams (P&ID), machine mechanical drawings.
* Collaborates effectively with global automation engineering team on development projects, standards development, selection and implementation of new technologies and automation systems.
* Supports, configures and replicates (including new releases and patching) PLC systems, SCADA, drive configuration, servo systems, and vision systems.
* Maintains software and hardware global configuration information, technical documentation, software backups, control software revision notes, knowledge base data records, generates FS/DS documentation and supports cGMP validation process.
* Regularly communicates with Automation Engineering Manager on project progress and potential issues.
* Based on a rotating schedule provides after-hours support for plant operations. Effectively collaborates with plant personnel, provides technical guidance to electronics.
Key requirements:
* Bachelor of Science Electrical Engineer / Mechatronics / Computer Science / Mechanical Engineer / Robotics all with emphasis on automation / Chemistry or related field required.
* Master of Science degree preferred.
* Automation Engineering experience.
Every day, Lonza’s products and services have a positive impact on millions of people.
For u...
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Type: Permanent Location: Greenwood, US-SC
Salary / Rate: Not Specified
Posted: 2024-02-14 07:23:18
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Posted Job Advert
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
We are looking for a (Senior) QA Specialist Qualification (f/m/d), who will support our team QA plant qualification.
Key responsibilities:
* Representative of QA Qualification in the project organization for new facilities or other projects in regard to qualification of facilities, utilities, equipment and systems
* Coordinating different QA interests during the project phase e.g.
process, cleaning or other relevant QA objectives
* Driving implementation of new qualification strategy and being a strong decision maker when needed
* Compiling, reviewing and releasing Qualification Documents (URS, Qualification Plan & Report, DQ/IQ/OQ/PQ Reports and more) as also supporting and approving quality risk analysis (e.g.
FMEA)
* Performing assessments and approvals of technical changes requests during the different phases of a project and lifecycle and their relevance to the qualification of facilities, equipment, utilities and systems
* Representing qualification topics during customer audits and regulatory inspections
* Being responsible to drive CAPA and Effectiveness Checks items to completion and timely closing as well ensuring deviations are appropriately investigated and recorded in Deviation Reports
Key requirements:
* Bachelor's degree in engineering, Chemistry, Biotechnology or a related field
* Significant experience in the pharmaceutical industry, ideally in a QA role would be an advantage
* Good understanding of the applicable cGMP regulations would be an advantage
* General knowledge of engineering and manufacturing processes
* Ability to oversee project execution to identify non-compliance from quality standards
* Fluent language skills in German and English is required
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.
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-02-14 07:23:15
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Are you looking to help transform a company and an industry? As a Stewart employee, you’ll be joining a company that is committed to helping you own, develop, and nurture your career while growing our company.
We invest in your career journey because we understand that as you grow so does our company.
You will be part of a diverse and equitable work environment that reflects the customers we serve.
You’ll be empowered to use your unique experiences, passion and skills to help our company constantly evolve and improve.
Together, we can achieve our vision of becoming the premier title services company.
More information can be found at https://www.stewart.com, subscribe to the Stewart blog at https://blog.stewart.com or follow Stewart on Twitter® @stewarttitleco.
Job Description
Job Summary
Promotes Stewart services and solutions through various outside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share.
Job Responsibilities
* Promotes Stewart services and solutions through various inside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share
* Typically follows existing procedures to perform routine assignments and to solve standard problems
* Analyzes basic information and standard practices to make decisions impacting work performed
* Individual contributor working with direct oversight
* Performs all other duties as assigned by management
Education
* Bachelor’s degree in relevant field preferred
Experience
* Typically requires 0-2 years of related work experience
Equal Employment Opportunity Employer
Stewart is committed to ensuring that its online application process provides an equal employment opportunity to all job seekers, including individuals with disabilities.
If you have a disability and need assistance or an accommodation in the application process, please contact us by email at careers@stewart.com.
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Type: Permanent Location: Wasilla, US-AK
Salary / Rate: Not Specified
Posted: 2024-02-14 07:23:14
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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.
The site in Visp, Switzerland is growing and for our Biologics organization, we are currently looking for MSAT Microbial or BioConjugates Process Experts.
Lonza has a strong track record in the microbial and bioconjugation manufacturing of Biologics from early clinical to large scale commercial supplies.
We are building a brand new and unique facility in the Lonza’s Vibe-X dedicate model, in which the two technologies of microbial and bioconjugates production are combined in one project.
In the position as a MSAT Bioconjugates or Microbial Upstream (USP) or Downstream (DSP) process expert, you will make a difference by being responsible for the successful ramp-up, tech transfer and commissioning of the new facility as well as supervision, support and life cycle management of the Bioconjugate or Microbial process.
You will play a crucial role in the network between the different departments such as manufacturing, development, quality assurance and control.
Become part of this exciting opportunity and apply now!
Key Responsibilities:
* Participation in and/or process owner of the technical transfers, ramp-up and the commissioning of the facility currently in construction
* As an MSAT process expert, act as the interface between the process donor (customer, process development) and operations.
In this function, responsible to ensure process scalability and manufacturability
* Plan and supervise MSAT activities on project level to ensure that the processes deliver the required products with the required quality in a safely, timely and in a cost effective manner
* Directly communicate with customers during campaign execution and closure including daily reporting of batch status and performance
* Responsible for leading process troubleshooting on the manufacturing floor as needed
* Change control management
* Supporting process validation activities
* Participation in annual product review (APQR)
* Representing the facility during process specific inspections and audits as SME for area of responsibility
* Preparation of validation and commercial campaigns as part of a project team (tech transfer, scale up, GMP documentation, equipment)
Key Requirements:
* Master or PhD (preferred) in Bioconjugation, Biotechnology, chemical engineering, organic chemistry or related disciplines
* Significant experience in Bioconjugation or Microbial, biopharma manufacturing and / or process development, preferably in the area of BioConjugates or USP/DSP (Mammalian or Microbi...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-02-14 07:22:46
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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.
This role is based in BioAtrium, which is a joint venture and part of Ibex® Solutions (www.ibex.lonza.com).
Ibex® is a modular build complex to develop and manufacture biological products.
It enables companies to get access to a complete solution, gaining speed and achieving a simplified value chain.
The Ibex® Complex is our contribution to the medicine of tomorrow and possibly the next step in your career? Start your career with Lonza today.
Apply as QA Contamination Prevention Manager (f/m/d)!
Key responsibilities:
* Ensuring the development of an end-to-end microbial control concept for the biotechnological drug substance manufacturing facilities and capturing it in local documents (incl.
specifications, SOPs, etc.)
* Ensure that practices within the manufacturing facility are compliant and support microbiological control of the product
* Ensuring a robust contamination control strategy is in place
* Supporting the Quality Oversight on activities of Environmental Monitoring and activities related to the assessment of disinfectants from microbiological expertise point of view
* Writing, Reviewing and approving SOPs, deviation reports and change requests, associated with the above-mentioned topics
* Supporting the preparation and follow-up of customer audits and regulatory inspections
* Acting as an expert during audits / inspections, presenting aspects related to the microbial control and sterility strategies
* Enhancing the quality knowledge by following the quality standards and by visiting specific training courses / conferences
Key requirements:
* University degree (Bachelor, Master or PhD) in pharmacy, engineering, natural science, or related life sciences discipline - preferably microbiology
* Substantial experience in the area of biopharmaceutical manufacturing and a strong background in cGMP
* Broad knowledge related to hygiene topics, environmental monitoring, disinfectant testing and microbial control strategies
* Previous Contamination Control experience, would be an advantage
* Good communication skills and interaction with all kind of interfaces within the organization and regulatory agencies (e.g.
US FDA, EMA, etc.)
* Working knowledge with MS Office, Excel, data trend creation/analysis, TrackWise®, LIMS and SAP is an advantage
* Fluent in English, German is an advantage
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 grea...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-02-14 07:21:56
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
The site in Visp, Switzerland is growing and we are currently looking for (Senior) Program Managers for our Mammalian, Bioconjugates and Microbial BUs (Drug Substance manufacturing).
In this role, you will be the Key interface between Sales and Operations in order to deliver and execute customer contracts.
You are an advisor along the whole life cycle and will propose the optimal package to successfully deliver the drug to the patients together with the project team.
Key responsibilities:
* Drive the complete life-cycle of all projects (including tech transfer and GMP production) with a large and complex portfolio from signing of the contract to delivery
* Manage a team of experts in a matrix organization and drive the successful delivery in terms of quality, costs and time
* Acts as single point of contact for the customer and function as the customer advocate on-site
* Drive the communication within Lonza as well as between Lonza and the customer in regards to risks and issues and proactively manage resolutions
* Control Project scope and in conjunction with Proposals Team, prepare amendments and/or scope changes.
In conjunction with Sales/Commercial Development, provide input into mid-long term program strategies
* Coaches and mentors other team members
Key requirements:
* Bachelors- or Master’s Degree with technical background (chemistry, biology, biotechnology or similar), PhD preferred
* Previous work experience in Project Management – ideally in the pharmaceutical or CMO industry
* Proven knowledge of technical, commercial and organizational issues that impact project strategy and planning
* Successfully managed programs over several years in relevant business environment
* Able to analyze and solve complex problems that do not have routine solutions
* Have great communication- and leadership skills
* Fluency in English is required, German is a plus
Every day, Lonzas 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 improvi...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-02-14 07:21:21