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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.
Synaffix – A Lonza company is a Dutch biotechnology company focused on the advancement of our technology platform for best-in-class antibody-drug conjugates (ADCs).
As a leading innovator in the field, our vision is to become world-wide the most prevalent ADC technology for pharma and biotech companies and to realize our ambition – Connect to Cure.
As a result of the increasing number of external ADC collaborations, we are currently looking for a skilled and enthusiastic Research Associate Bioconjugation.
You will operate in a team that supports the preparation of ADCs for external collaborations with biotech/pharma companies with key tasks including; setting up experiments, running reactions and purifying intermediates and final products and interpretation of results.
In addition you will characterize the produced ADCs with various analytical tools.
Key responsibilities:
* Execution of experiments following established protocols (including but not limited to performing remodeling and bioconjugation experiments, product purification, product fill-finish and product analysis)
* Processing, analyzing & documenting of results in ELN
* Take assigned responsibilities in designated tasks & projects (such as setting-up shipments and performing process optimization)
* Preparation of production reports and product certificates
* Supervise other team members with day-to-day execution of the work
* Work as a team player and work with a high degree of flexibility
* Provide general support to lab operations
* Adhere to company policies and quality & safety standards
* Perform other duties as assigned.
Key requirements:
* MSc in the field of bioconjugation chemistry or closely related would not be suitable for Phd Candidates
* An ideal candidate has > 3 years of relevant experience in the field of bioconjugates
* Experience with various protein purification and analysis techniques including SEC, IEX, affinity chromatography (protein A/L, Ni-NTA), SDS-PAGE, RP-HPLC and MS
* Experience with handling antibodies, including modification, purification and analysis
* Hands-on experienced with various bioconjugation chemistry techniques
* Strong commitment to laboratory work and project delivery
* Attention to detail and accuracy
* Strong team-player
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 resu...
....Read more...
Type: Permanent Location: Oss, NL-NB
Salary / Rate: Not Specified
Posted: 2024-05-15 09:33:07
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Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist.
Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen.
Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen.
Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig.
Denn ihre Ideen, ob gross und klein, verbessern die Welt.
Und das ist die Art von Arbeit, an der wir Teil haben möchten.
Am Standort Visp wird ein/e Senior Scientist Analytical Development gesucht.
Als Mitglied unserer Forschungsabteilung sind Sie im Auftrag unserer Kunden verantwortlich für die Entwicklung, Implementierung, Transfer, Validierung und Koordination der Ausführung bioanalytischer Methoden.
Sie arbeiten im Rahmen der Entwicklung von Herstellungsprozessen für Biopharmazeutika und Biokonjugate nach aktuellen ISO- und GMP-Qualitätsrichtlinien und beherrschen wesentliche Aspekte der statistischen Datenerfassung und -auswertung.
Die abwechslungsreichen Verantwortlichkeiten beinhalten auch die fachliche und disziplinarische Führung und Weiterentwicklung von Mitarbeitern
Ihre Aufgaben:
* Fachliche Betreuung und Beurteilung der Arbeiten im Zuständigkeitsbereich (z.B.
Methodenentwicklung, -implementierung, -validierung, sowie Routineanalytik).
Optimaler Einsatz der zugeteilten Ressourcen
* Fachliche Betreuung und Mitarbeit an den Innovationsprojekten.
Verantwortlich für das Einhalten der allgemeinen und der projektspezifischen Sicherheits- und Qualitätsstandards (ISO 9001 und cGMP) sowie der Data Integrity Vorgaben im Labor
* Enge Zusammenarbeit mit Projektleitern mit dem Ziel einer langfristig effizienten Umsetzung der Projektanforderungen
* Verantwortlich für die termin- und kostengerechte Bearbeitung der zugewiesenen Aufträge
* Schulung, Weiterbildung, Förderung und Betreuung des Personals.
Kontinuierliche Optimierung der Prozesse
* Sie sind selbständig im Rahmen der zugewiesenen Aufgaben tätig und übernehmen Verantwortung.
Dabei sind Sie in engem Kontakt mit anderen Gruppen, der Forschung, Produktion und Qualitätssicherung
Ihr Anforderungsprofil:
* Sie verfügen über ein abgeschlossenes Studium im Bereich Biochemie, Biologie oder Chemie und haben optimalerweise erste Erfahrungen in der pharmazeutischen Industrie gesammelt
* Sie sind selbständig, verantwortungsbewusst und besitzen sehr gute Kommunikations- und Teamfähigkeit
* Sie haben Spass daran, sich in ein junges, dynamisches Team einzubringen, sind engagiert und besitzen Eigeninitiative
* Sichere Deutsch- und Englischkenntnisse runden Ihr Profil ab
Lonza’s Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar.
Wie wir unser...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-15 09:23:31
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Located in Stein/Basel, Switzerland our successful CDMO Business Unit Drug Product Services (DPS) currently offers exciting opportunities.
Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the position as QC Sector Head Bioassays for a new sterile Drug product facility to support quality control and manufacturing related project activities.
Key responsibilities:
* Establishment of infrastructure and services in frame of project ramp-up for commercial finished drug product Bioassay testing.
* Support of analytical method transfer and/or validation of bioanalytical assays (cell based Bioassay)
* Provide expertise and ensure adequate cGMP QC lab processes for cell based Bioassays
* Ensure laboratory and workforce planning in order to manage expected forecast
* Author for bioassay / bioanalytical related quality and cGMP documents e.g.
procedures (SOPs) or source documents, reports, deviations, change requests etc.
* Developing an effective and cohesive teamwork, fostering close collaboration with internal and external customers and stakeholders
* Ensuring an inspection readiness state for the site to meet expectations from customers and regulators
* Participate as Subject Matter Expert in internal and external audits, customer visits and inspections
* Oversee and manage departmental performance and quality metrics
* Driving a lean mindset and establish mechanisms for continuous improvement
Key requirements:
* Relevant experience in pharmaceutical industry, preferred with Academic degree, e.g.
PhD in Cell biology, Molecular biology, Biochemistry, or e.g.
Analytical Chemistry
* Excellent working knowledge in relevant analytical techniques related to testing of biological drug products
* Knowledge of pharmaceutical regulatory landscape (cGMP, ICH guidelines and pharmacopeias e.g.
USP, EP, JP)
* Strong analytical and problem-solving skills
* Substantial experience in Quality Control in pharmaceutical industries and cGMP controlled environment
* Ability to effectively prioritize and direct tasks in a fast-paced environment
* Excellent communication skills, command of English, academic writing
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference.
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-05-15 09:12:05
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Today Lonza is a global leader in life sciences.
We are more than 15,000 employees in more than 100 locations around the world.
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 currently looking to recruit a Senior Scientist to join our Manufacturing, Science, and Technology (MSAT) Pilot team.
This role will be part of a dedicated pilot batch execution team, to support the execution of the technical transfer of new or existing processes downstream (DSP) into the pilot plant.
As a Senior Scientist, you will be responsible for planning all batch execution logistics with technical hands on support for downstream (DSP) operations.
You will work with external customers as well as other cross functional teams to provide assurance of suitability to scale to cGMP manufacturing.
This role will give you the opportunity to develop hands on experience within biotech processes in a highly team focused, fast paced environment and would be suitable for candidates who thrive in a fast paced situation.
Please note: that this role will require 70% hands on laboratory work, and 30% desk based practical planning duties.
Key Responsibilities:
* Responsibility for the preparation of associated process descriptions, batch records for pilot batch execution, include ordering raw materials for downstream (DSP) operations working closely in communication with process development, R&T and New Product Introduction scientists within the MSAT team.
* With developed training and proficiency, understand prioritize and contributes to the work of the team daily tasks in set-up, operating plant equipment and associated process analytical technologies without direct supervision
* Ensuring relevant transfer documentation is written and followed such that projects meet the required deadlines/customer outcomes.
* Establish relationships with Process Development and R&T scientific peers to effectively challenge and participate outcomes in project discussions/meetings
* Will use existing knowledge to resolve routine process issues and suggest improvements.
Be proficient in structured data analysis identifying trends and offering solutions with the NPI scientists for batch data for preparation of process summary reports for the customer.
* Working independently will write and implement department EHS protocols, leads completion of continuous improvement activities to reduce costs, increase yield and productivity
* Working with the team, leads the completion of continuous improvement activities reducing costs, and increase yield and productivity
Key Requirements:
* BSc/BEng degree in a Scientific field or equivalent means of demo...
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Type: Permanent Location: Slough, GB-SLG
Salary / Rate: Not Specified
Posted: 2024-05-15 09:03:27
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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.
Role Purpose:
Working as part of a dedicated pilot batch execution team the primary purpose is to support the execution of the technical transfer of new or existing processes (either USP or DSP) into pilot from both external and internal customers using a defined structured approach according to standard procedures
Key Accountabilities and Duties:
Qualifications/Skills:
The role involves working closely with Process Development/R&T scientists and peers in the NPI team prior to and throughout the batch execution to resolve problems, provide effective communication and provide assurance of suitability to scale to cGMP manufacturing
•The role will be contribute to planning of batch logistics while acquiring experience in operating equipment and technical knowledge of USP or DSP operations.
•Following written process documentation/procedures prepared in collaboration with internal cross functional project team members to provide assurance of suitability of successful scale up to cGMP manufacturing Responsible for the preparation of associated process descriptions, batch records and ordering raw materials for either USP or DSP operations.
Will be supported communication with process development / R&T and New Product Introduction scientists within the MSAT team.
•Responsible for working as part of a dedicated pilot execution team following defined processes to plan and manage daily tasks in operating plant equipment and associated analytical technologies.
Will ensure relevant transfer documentation is written and followed daily such that projects meet the required deadlines/customer outcomes.
•With support will develop knowledge to resolve routine process issues and identify trends in data reviews.
•Responsible with support of the NPI/senior pilot scientists for collating and analyzing batch data for preparation of process summary reports for the customer
•Responsible for writing and executing EHS protocols and improving pilot operations through on the job training and experience of pilot plant operations working with others
•Contributes to identifying and completing continuous improvement activities to reduce costs, increase yield and productivity for the area
•Will begin developing key relationships with Process Development, R&T and MSAT TT peers to effectively communicate and understand project discussions and objectives
Degree (required)
*BSc/BEng Field of Study Biological science or biochemical engineering disciplines.
Every ...
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Type: Permanent Location: Slough, GB-SLG
Salary / Rate: Not Specified
Posted: 2024-05-15 09:01:41
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ERM is hiring Field Biologists to conduct nesting bird surveys, surveys for special status species, and biological surveys for a large construction project in Madera and Merced, CA.
Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of a field biologist requires technical skills, as well as strong organizational and communication skills.
This is a full-time (40 hours/week), limited-term role with a duration of one year, and the possibility of renewal.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction nesting bird and other special status species surveys and construction monitoring across the client’s territory.
* Work locations are often remote and require Biologist to work independently.
* Monitoring involves coordination with construction crews and providing advice for maintaining compliance with client requirements.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* At least 2+ years of Biology + Other Special Status Species Experience required.
In addition to nesting birds, expertise should include more than one of the following species: San Joaquin Kit Fox, California Tiger Salamander, Swainson's hawk, Crotch Bumble Bee, Branchiopod (Fairy Shrimp).
* Familiarity with nesting bird survey protocols and/or general bird identification skills required.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Demonstrated independent and effective problem solving and decision-making skills.
* Possess a valid driver’s license.
* Fluency in English and Spanish highly preferred.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solutions for our clients.
Our diverse team of world-class expert...
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Type: Permanent Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2024-05-15 08:40:41
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Ardurra is currently hiring a remote Engineer III to join our team our California design team working 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: $100-120k (DOE)
Primary Function:
Performs engineering assignments with limited direction from supervisor and increasing difficulty.
Primary Duties:
* Work with and manage, engineers and CAD designers working in highly effective teams.
* Write reports, complete engineering calculations, draft specifications, complete engineering designs, prepare cost estimates, research codes, design procedures, and design standards.
* Under the Project Manager or Project Engineer’s minimal supervision, an Engineer III is the primary person who communicates project-related items directly with the CAD drafters, lower-level engineers, utility companies, subconsultants.
* Oversees the implementation of Ardurra’s Quality Management Plan and working with staff to produce project deliverables.
* 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: 5+ 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 an...
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Type: Permanent Location: Bakersfield, US-CA
Salary / Rate: Not Specified
Posted: 2024-05-15 08:40:31
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Ardurra is now hiring a remote CAD Designer to join our team our California design team working on our water and sewer infrastructure projects.
* Prefer Designers local to California or open to relocating.
Able to work remotely and/or out of any of our California Ardurra offices.
* Salary range: $80-100k (DOE)
Primary Function:
Oversees the implementation and completion of all phases of assigned projects, and independently performs the most difficult design assignments requiring the application of advanced design techniques in accordance with company and industry standards.
Primary Duties:
* Establishes design criteria for all phases of a project requiring the application of basic engineering principles, material properties, and a familiarity with construction, installation, and maintenance procedures.
* Takes the lead with multi-disciplinary projects to apply design criteria, establish project standards and requirements, and prepare deliverables.
* Also responsible for estimating project budgets, project schedules, and executing project to said budgets and schedules.
* Provides conceptual input to projects during the planning stages, proposal phases, and preliminary phases.
* Regularly assigns tasks to lower-level designers and engineers, provides technical guidance, and reviews completed assignments for accuracy and quality.
* Participates in performance reviews by conducting periodic coaching and progress review sessions with employees assigned to projects.
* Prepares detail and layout drawings and sketches of unusual, complex, or original designs requiring the application of theoretical and practical engineering knowledge.
* Assignments regularly include determining material needs and performing necessary calculations using accepted formulas and references.
* Supports field assignments and leads field investigations as required.
* Regularly interfaces with other departments, clients, vendors, and project engineers in order to support project production and to resolve conflicting priorities.
* Performs other related tasks in support of project engineer that are non-CAD related and complex in nature, such as preparing specifications, analyzing bids, compiling, computing, and analyzing various engineering design and/or test data, preparing engineering estimates, etc.
* Participates in the interviewing, selection, and training of new employees.
Education and Experience Requirements:
* 8+ years of design experience utilizing Basic AutoCAD, Civil 3D, Pressure Pipe, Pipe Networks, Autodesk Construction Cloud (ACC).
* Should have a background in transmission and distribution water and wastewater design.
* Water and wastewater plant design experience.
(a plus / not required)
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-lik...
....Read more...
Type: Permanent Location: Bakersfield, US-CA
Salary / Rate: Not Specified
Posted: 2024-05-15 08:40:27
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ERM is looking for a motivated, hands-on Managing Consultant, Project Manager Geologist, Engineer or Hydrogeologist (Senior Level) to join our growing Liability Portfolio Management & Remediation team in the West Virgina area.
Working under the direction of senior directors and Partners, the successful candidate will work on and manage a variety of site investigation and remediation projects under CERCLA, RCRA and state programs, as well in other US locations. You will have the opportunity to work with technical experts on these projects and learn how to implement innovative and sustainable site investigation and remediation technologies. As a Project Manager, you will be responsible for safely performing project work, supervising and mentoring junior staff, branding ERM in the marketplace through technical presentations and papers, working with ERM Partners to grow client relationships and develop new opportunities with those clients, and preparing winning proposals. Your experience at ERM will enable you to develop your career along with your leadership, client relationship building, and technical consulting skills. Ultimately, you will be able to support the growth of our business by delivering exceptional value to clients across multiple industry sectors.
RESPONSIBILITIES:
* Perform and coordinate project work involving site investigation, utility location and clearance, risk assessment oversight and remediation of soil, groundwater, and sediments with moderate to complex technical/regulatory issues with manufacturing, power, chemical, oil & gas, and technology sector clients.
* Plan and coordinate field work including sampling, drilling, well installation, soil, groundwater and LNAPL/DNAPL assessment; vapor intrusion assessment; and high-resolution site characterization (e.g., passive soil gas surveys, MIP, Waterloo Profiler), and remedial construction and O&M.
* Plan, install, and implement vapor intrusion investigations and remediation efforts in both commercial/industrial spaces and residential locations.
* Review and interpret environmental data; evaluate quality assurance/quality control data; develop conceptual site models; identify data gaps; prepare or peer review a variety of work plans and reports; and develop scopes of work, schedules, costs and health and safety plans for projects under RCRA, CERCLA and other state programs.
* Support internal and external projects utilizing new technologies to improve efficiency, quality and achieve project objectives, including electronic field data collection, management, and reporting.
* Evaluate remedial alternatives and assist clients in developing cost-effective closure strategies and negotiating them with regulatory agencies.
* Design, bench-scale testing and pilot testing remedies for contaminated soil, groundwater and sediments using traditional and/or innovative and emerging remediation technologies, and monitoring and optimizing their pe...
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Type: Permanent Location: Hurricane, US-WV
Salary / Rate: Not Specified
Posted: 2024-05-15 08:40:25
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ISP Chemicals LLC
Are you the kind of person that is always thinking, sketching, seeking, and adjusting? Who needs to understand how things work and then figure out how they can work better? Are you a passionate, tenacious, solver who loves to work with others who share your drive? Are you positive, constructive, and ingenious? Are you always solving? Then we’d like to meet you and bet you’d like to meet us.
Ashland has an exciting opportunity for a Quality Systems Associate to join our Ashland business at our Columbus, OH plant.
This is a very visible, significant role within the Company and the Quality Control/Quality Assurance function.
This position will report to the Quality Control Manager.
The responsibilities of the position include, but are not limited to, the following:
* Testing of raw materials, in-process control samples, and final products
* Analytical controls are placed on raw materials to verify identification and required quality.
* Understanding the equipment cleaning specifications are critical to prevent cross contamination.
* Communicating results to production and process engineers.
* The use of the laboratory iLIMS tracking system (raw material samples, in-process samples, final samples, instrumentation calibration, and stability samples).
* Secondary responsibilities include process development support, process troubleshooting, analytical method development support, environmental samples, and quality systems support.
* Documentation consistent with good manufacturing practices (GMP).
* Calibration of analytical instrumentation.
* Scheduled testing associated with the stability program.
* Provide analytical support of the Ashland Columbus waste treatment facility, raw material qualifications and standard qualifications.
* Provide non-routine testing associated with corrective action preventative action (CAPA) investigations such as customer complaints, out of specification (OOS) investigations, product failures, and shelf-life extension requests.
* Other Quality Control Responsibilities
+ Maintaining the raw material and final product retain systems.
+ Assisting QC Supervision with maintaining laboratory supplies.
+ Managing lab, sample, and chemical waste disposal.
+ Following the Chemical Hygiene Plan, practice good housekeeping, and general maintenance of the lab.
In order to be qualified for this role, you must possess the following:
* Preferably Bachelor’s Degree in Chemistry or related field
* Knowledge and understanding of analytical chemistry
* Knowledge and understanding of good manufacturing practices (GMP)
* Preferably 1-3 years in a chemical manufacturing environment
* Attention to detail
* Strong communication skills
* Strong computer skills which include application knowledge of Microsoft Excel and Word
* Good organizational and documentation skill...
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Type: Permanent Location: COLUMBUS, US-OH
Salary / Rate: Not Specified
Posted: 2024-05-15 08:40:22
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Your Job
The Project Engineer will be responsible for the development of new and existing Cable products (Twinax) that meet or exceed customer expectations.
Coordinating project transfers from design center to volume manufacturing in either Molex Guadalajara or Molex Philippines.
Supports all projects in development, product testing, engineering changes and other technical documents.
Our Team
This role is part of Copper Solutions Business Unit and will collaborate with different projects across the company maintaining regular communication with our design center in Arkansas.
What You Will Do:
* Leads new raw cable development efforts from development of the product concept through volume production.
* Ownership of critical path technology items - plans and oversees progress of projects against schedules.
* Tooling Design
* Develops Solid and foam extrusion process design for polyethylene, polypropylene, PVC and other compounds.
* Work with process engineers to consider new or improved methods of manufacturing twinax resulting in higher yields, quality, and cost effectiveness.
* Work closing with design, quality, and manufacturing to develop and execute DFMEAs, PFMEAs, and verification plans for new twinax processes in development.
* Raw material evaluation and development.
* Provide technical direction for twinax manufacturing processes when necessary for facilities located in GDL and PHL.
* Responsible for SAP loading of BOM's (Bill of Material) and Material Master data sheets.
* Understand, support, and contribute to current Molex Total Quality Management (TQM), Six Sigma, International Standards Organization (ISO) and Environmental, and/or Health and Safety (EH&S) Management Systems by following stated policies and procedures.
* Leads new raw cable development efforts from development of the product concept through volume production.
Who You Are (Basic Qualifications):
* B.S in Mechanical, Electrical or Mechatronics engineering.
* Strong experience in similar position acting as point of contact for product design, development and improvement.
* Wire and cable experience with focus on extrusion process of foam polymers.
* Good & demonstrated knowledge of Geometric Dimensioning & Tolerancing (GD&T)
* Knowledgeable about mechanical PCB design parameters as they pertain to high speed circuits and manufacturing.
* English language proficiency is required.
What Will Put You Ahead:
* Experience working within a Global organization.
* Tooling Design experience.
* CAD experience required.
(NX siemens, Solidworks)
* Experience working with SAP system.
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 high...
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Type: Permanent Location: El Salto, MX-JAL
Salary / Rate: Not Specified
Posted: 2024-05-14 08:37:42
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Your Job
Product Design Engineer is responsible for all phases of the product development, from concept to pre-production, including the multi-disciplinary actions necessary to meet customers' requirements.
What You Will Do
• Together with Engineering team, perform all related Engineering work such as design concept proposal, technical solutions to meet customer`s requirements in terms of technical performance, schedule, quality, and cost.
• Liaise with other operational functions in Molex (manufacturing plants, supply chain, quality) to make sure proposed design can go seamlessly in production.
• Perform all related Engineering work on RFQ, such as analyzing customer requirements and communicate them with Molex global development team.
• Communicate with Molex laboratory on product validation.
• Maintain relationships with Engineering organizations of our customers, suppliers
• Assist with any quality issues on current production parts including our response to customer concerns/complaints on parts performance.
• Handle other Engineering activities that are assigned by Engineering Management.
Who You Are (Basic Qualifications)
• Bachelor's in mechanical / Electrical / Industrial engineering.
• 5 Years+ Experience in Automotive products Design and development (especially with a foreign company).
• Good communication skills internally within Molex Group and externally towards Customers and suppliers.
• Experience in design and development process of automotive parts from concept to production.
• Proven experience to create all required documentations (FTA, DFMEA, DR , DV/DP ...etc.)
• Experience in 3D CAD software and 2D drawings.
• Computer skills: Power point, Excel.
• Chinese : Native level or at least Business Level of communication
• English : Fluent (ability to read, write, and lead technical discussions)
What Will Put You Ahead
• 5 years+ of Working experience in design and development of high-speed cable assemblies.
• knowledge in automotive connectors requirements.
• Working experience with global companies.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Who We Are
As a Koch company, Molex is a leading supplier of connectors and interconnect components, driving innovation in electronics and supporting industries from automotive to health care and consumer to data communications.
The thousands of innovators who work for Molex have made us a global electronics leader.
Our experienced people, groundb...
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Type: Permanent Location: ChengDu, Sichuan, CN-51
Salary / Rate: Not Specified
Posted: 2024-05-14 08:37:34
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If you have at least four years' experience in the industrial manufacturing environment as a quality inspector, and you desire a growing and fast-paced environment, then you should apply for our Quality Control Inspector position in Houston, Texas.
Bray would rely on you to analyze and determine the best method and set up of inspection for measuring product on incoming parts to ensure that our customer needs and/or engineering drawings are met.
You would have the authority to evaluate problems and make initial recommendations for possible corrective action to supervisors.
Essential Duties and Responsibilities:
* Perform incoming inspection on incoming purchased parts, subassemblies or finished product according to the engineering drawing and/or customer standards.
* Perform in -coming inspection to engineering drawing and/or customer requirements.
* Review of Material Test Reports (MTR), and Certificate of Conformance(CofC), against relevant standards and specifications.
* Analyze NCR reports to look for Trends and send out CAR reports as required.
* Generate Non-Conformance Reports as well as other internal departmental reports as assigned.
* Evaluate problems and make initial recommendations for possible corrective action to supervisor.
* Investigating failures, determining root cause and proposing remedial actions.
Qualifications:
* At least four years' experience in the industrial manufacturing environment in a quality control area.
* Experience with (PMI) Positive Material Identification is preferred.
* Experience with computerized record-keeping (e.g., document, drawings)
* Computer literacy with standard software application and demonstrates excellent written and verbal communication skills.
* Experience using & calibrating precision measuring equipment such as micrometers, height gages, calipers, dial indicators, bore gages, etc.
is a must.
* Must have knowledge with ISO 9001-2008/2015 & API.
* Must have the ability to analyze and determine the best method/setup of inspection for measuring product conformity.
* Must be able to interpret engineering drawings and be able to read and understand Geometric Dimensioning and Tolerancing (GD&T).
* Must have experience with Coordinate Measuring Machine (CMM).
* Ability to perform multiple tasks in a fast-paced environment to assure delivery requirements are met in a timely fashion.
* Ability to follow documented procedures and standards.
* High School Diploma or equivalent is the minimum.
Physical Demands:
* Must have 20/20 (correctable) vision without color blindness.
* Must be able to life 20 pounds.
Please Note
* Immigration sponsorship not offered for this position
* Staffing and recruiting agencies are not invited to submit candidates for this job posting
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in an...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2024-05-14 08:37:13
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POSITION SUMMARY:
The Environmental Health and Safety (EHS) technician will assist with management of the safety and environmental programs. The position will support EHS initiatives and inform management of critical issues. The technician role is a hands-on position that supports production and performs immediate corrective actions to mitigate risks or hazards in the workplace. This position is expected work on site during scheduled production hours.
KEY RESPONSIBILITIES:
* Exercise stop work authority in the event of unsafe conditions or situations.
* Know and follow all Health, Safety and Environmental (HSE) policies always.
* Maintain records associated with environmental and safety regulations and standards and company management system.
* Participate in investigations of safety and environmental related incidents.
* Ensure proper removal and storage of chemicals and hazardous materials.
* Participate in the review and update of policies, procedures, and programs.
* Collect samples and conduct inspections to ensure compliance with environmental permits.
* Facilitate and arrange safety and environmental related training for employees and contractors.
* Evaluate the effectiveness of EHS policies and practices.
* Responsible for new hire orientation, safety training, and contractor management.
* LOTO program.
* Chemical storage and compliance.
* Maintain safety KPIs and lead incident investigations.
* Ensure proper PPE is being used.
* Ensure SDS logs are uploaded, and Risk Assessments are completed in Quarks.
* Support compliance and management system audits.
* Other assigned requirements as needed.
EXPERIENCE, SKILLS, AND KNOWLEDGE:
* Knowledge of environmental and safety regulations, standards and best practices.
* Effective communication skills: ability to interact with personnel at all levels of the organization with confidence, respect and integrity.
* Ability to analyze information, solve problems, work in a team environment as well as on your own, prioritize tasks & projects, mange time effectively and function effectively in stressful situations.
* Experience with 5S, continuous improvement processes and/or ISO management systems strongly preferred.
* Bilingual is a plus.
EDUCATION, TRAINING, AND CERTIFICATIONS:
* Associate degree or 2 years’ experience as a Military Field Medic.
* OSHA10
* First responder/CPR trained.
* Experience working within a manufacturing industry (preferred).
CRITICAL COMPETENCIES & CAPABILITIES:
* Sound Judgment
* Change Management
* Service Orientation
* Organizational Awareness
* Teamwork and Collaboration
Quality
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Type: Permanent Location: Muskogee, US-OK
Salary / Rate: Not Specified
Posted: 2024-05-14 08:32:20
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PURPOSE AND SCOPE:
The Patient Account Representative - Collections provides administrative support to the collections operations within the assigned function(s). Through ongoing database maintenance, the Patient Account Representative - Collections ensures the timely receipt of claim payments and minimizes bad debt accrual. In this capacity, the Patient Account Representative - Collections provides outstanding customer service to customers and vendors through effective and timely communication.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Under general supervision, identify and resolve routine outstanding claims.
* Generate and analyze diverse reports and work lists in the identification and resolution of general patient account issues.
* Assist in the resolution of outstanding payments from past due accounts.
* Ensure timely receipt of claim payments; processing payments accordingly and reconciling all necessary data.
* Perform all responsibilities in compliance with company policies and procedures; ensuring timely and complete documentation of activities performed.
* May serve as a point of contact for customers and/or external vendors in response to inquiries and unresolved issues.
* May mentor other staff as applicable.
* Assist with various projects as assigned by direct supervisor.
Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.
PHYSICAL DEMANDS AND WORKING CONDITIONS:
The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Occasionally lift and/or move up to 50 pounds.
EDUCATION:
* High School Diploma required
EXPERIENCE AND REQUIRED SKILLS:
* 1 - 2 years' related experience.
* General computer skills with working knowledge of word processing, spreadsheet, and email applications.
* Detail oriented with good analytical and organizational skills.
* Good interpersonal skills with the ability to work cohesively within a team environment.
* Excellent oral and written communication skills to effectively communicate with customers and all levels of management.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
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Type: Permanent Location: Plano, US-TX
Salary / Rate: Not Specified
Posted: 2024-05-14 08:15:58
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PURPOSE AND SCOPE:
The Patient Account Representative - Collections provides administrative support to the collections operations within the assigned function(s). Through ongoing database maintenance, the Patient Account Representative - Collections ensures the timely receipt of claim payments and minimizes bad debt accrual. In this capacity, the Patient Account Representative - Collections provides outstanding customer service to customers and vendors through effective and timely communication.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Under general supervision, identify and resolve routine outstanding claims.
* Generate and analyze diverse reports and work lists in the identification and resolution of general patient account issues.
* Assist in the resolution of outstanding payments from past due accounts.
* Ensure timely receipt of claim payments; processing payments accordingly and reconciling all necessary data.
* Perform all responsibilities in compliance with company policies and procedures; ensuring timely and complete documentation of activities performed.
* May serve as a point of contact for customers and/or external vendors in response to inquiries and unresolved issues.
* May mentor other staff as applicable.
* Assist with various projects as assigned by direct supervisor.
Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.
PHYSICAL DEMANDS AND WORKING CONDITIONS:
The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Occasionally lift and/or move up to 50 pounds.
EDUCATION:
* High School Diploma required
EXPERIENCE AND REQUIRED SKILLS:
* 1 - 2 years' related experience.
* General computer skills with working knowledge of word processing, spreadsheet, and email applications.
* Detail oriented with good analytical and organizational skills.
* Good interpersonal skills with the ability to work cohesively within a team environment.
* Excellent oral and written communication skills to effectively communicate with customers and all levels of management.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
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Type: Permanent Location: Metairie, US-LA
Salary / Rate: Not Specified
Posted: 2024-05-14 08:15:42
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Global HR Director, Digital Technololgy Solutions
Job Description
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
In this role, you will:
* Be a strategic partner who is responsible for setting people strategies that build the next diverse generation of leaders and ensure the DTS organization has the right capabilities and culture needed to deliver the strategic agenda.
* Develop and implement people strategies and successfully execute the talent agenda for DTS.Educate the business on people trends and impact to broader strategy work.
Uses data and metrics to drive decisions and build recommendations for future plans and actions.
* Create and implement plans for a working environment that encourages Inclusion & Diversity as part of KC's culture.
* Ensure leaders have the right skills/capabilities and tools to be able to manage their team members life cycle.
* Develop strategic talent plans and ensure the alignment with organizational strategy, data (e.g., attrition rates, hiring trends) and budgets.
Leverages Total Rewards to analyze the market competitiveness of the DTS organization’s compensation practices and identifies strategies to harness the appropriate fiscal levers for driving engagement and retention.
The role is consultative, giving support to KC executive level leaders by:
* Designing and managing the implementation of interventions that improve leadership and team performance to achieve strategic objectives.
* Drive and collaborate with a variety of functions on leadership capability and support effective leadership team and/or other decision-making bodies on critical issues.
Identify strategies and action plans to transform leaders and teams to embody our values and ways of working.
* Partnering with, and coaching, managers and leaders to facilitate organizational and cultural change, inclusive of our new company values, ways of working, and transformation agenda.
* Influencing peers, COE partners, and senior leaders across the company, as well as immediate manager to drive to the right outcome from a people perspective.
* Possessing strong executive presence and a successful track record of partnering with senior executives delivering superior business results.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, million of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark ...
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Type: Permanent Location: Irving, US-TX
Salary / Rate: Not Specified
Posted: 2024-05-14 08:15:30
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Job Description:
Location: 6500 Technology Center Drive Suite 200, Indianapolis, IN 46278
This is an on-site position.
No remote or hybrid options are available.
Summary
Manage and track all assets, including but not limited to fleet, computers, locating equipment and supplies, phones, and general purchases.
Troubleshoot computer issues in and out of the field.
Provide general administrative support to the region and travel to field locations as needed.
Requirements
* Associate degree and inventory tracking experience preferred.
* Must be detail-oriented and possess strong project, logistical, and time management skills.
* Basic knowledge of computer hardware preferred.
We are an Equal Opportunity Employer.
Veterans are encouraged to apply.
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Type: Permanent Location: Zionsville, US-IN
Salary / Rate: Not Specified
Posted: 2024-05-14 08:13:32
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Operations Technicians start out at $22 perhour + an additional 15% per hour for working the night shift.
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Lonza Pharma and Biotech is looking to add an Operations Technician to their growing team in Bend, OR.
As a new member of the Operations Technician team, you’ll follow Standard Operating Procedures (SOPs) in a structured environment, understand and apply Good Manufacturing Practices (GMP), and deliver results with high integrity.
This is an excellent advancement opportunity.
Lonza Bend does retain several long-term Operation Technician roles; however, most Technicians are expected to progress to the full Operator level.
Technical and management growth options exist.
Key Responsibilities:
* Read, understand and train on Standard Operating Procedures (SOP’s)
* Demonstrate understanding of basic GMP’s for facilities and operations
* Follow basic instructions within a structured environment
* Primarily responsible for completing routine cleaning and cleaning logs
* Primarily responsible for restocking consumables
* Sign for and understand GMP documentation, i.e.
room logs, equipment logs, balance logs, etc.
* Perform tasks for Hazardous Waste worker as outlined in the Large Quantity Generator program
Key Requirements:
* Minimum High School diploma or GED
* Manufacturing experience desired
* Ability to work in an environment with a constant, low noise level during production
* Good standards of literacy and numeracy
* Ability to work nights, weekends, and holidays as required (12 hour shifts)
* Must have a valid driver’s license with ability to drive company vehicle as needed and pass a background and drug screen
* Must be able to successfully pass a pre-employment physical exertion and visual acuity test
* Performing work in a clean, secure and regulated environment
* Required to lift 50 lbs.
from floor and lift 25 lbs.
above head while working
* Perform cleaning with 20 foot wand above head height
* Wears powered air purifying respirator on occasion
* Wears personal protective equipment during shift (i.e.
coveralls, scrubs, booties, hair and beard covers, safety glasses, gloves, etc.)
* Able to move heavy equipment on casters or pallet jacks
* Manually manipulate drums onto carts and pallets
* Manually manipulate small parts
* Required to climb up and down ladders, bend, kneel, reach, squat, etc.
* Required to stand during majority of shift
Every day, Lonza’s products and services ...
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Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-05-14 08:13:16
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
.
Lonza Pharma & Biotech has an open position for a paid internship as a Marketing & Communications Intern at our location in Bend, OR.
The program duration is for a minimum of 6 months with potential to go longer.
We are offering significant flexibility in hours and working time to accommodate life and school schedules.
This is a part-time role (around 20 hours per week) with potential to grow into a fulltime opportunity.
Successful candidate will need to start onsite in Bend, Oregon before transitioning to a remote work-from-home role with occasional onsite time required.
Key Responsibilities
* Assists in the development of marketing and communications plans
* Create content for design/layout/web placement for internal announcements, updates, and activities
* Administer intranet website direction and content
* Work closely with outside vendors including advertising, design, public relations and website development
* Create and edit image and video content for internal website (CoLAB)
* Implement plan for increasing internal website engagement
* Maintain strong relationship with internal networking groups (Culture Club, Women's Professional Network...etc) to ensure updates on site media platforms
* Performs other duties as assigned
Key Requirements
* High School Diploma required along with some college courses related to Marketing & Communications
* Strong communication and interpersonal skills
* Experience creating content and design direction for digital/social media platforms
* A “take-ownership” attitude and mindset
* The Bend site includes multiple buildings throughout town and the successful candidate will need their own reliable transportation
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
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Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-05-14 08:13:12
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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
Was macht Unseren Bereich aus:
Im Bereich Reagents & Production Services innerhalb des Geschäftsbereichs Diagnostics Operations Penzberg (DOZ) verantworten wir die Quality Compliance gemeinsam mit den Bereichen Biotech Production, Chemistry Production, Reagents, Quality Control, Business Support und den Bereich Manufacturing Science & -Technology.
Durch kompetente und verantwortungsvolle Entscheidungen sichern wir unseren Produkten das "right to market".
In unseren Teams vor Ort, welche für die Themen Equipment-Qualifizierung, Validierung, Assets und Hygiene zuständig sind, bieten wir den direkten Support in den produzierenden Betrieben und der QC.
Unsere zentralen Teams für Prozesse & Systeme sowie Abweichungs- und Änderungskontrolle treiben Qualitätssicherungsprozesse voran und sind für Training sowie die Behandlung von Abweichungen und Änderungen (ECR) verantwortlich.
Gestalte und entdecke Deine Perspektive bei uns und bring Dein Know-how in einem der größten Biotech-Unternehmen der Welt ein.
Ergänze Unser Team:
Das Deviation & Change Control Team ist die zentrale Stelle rund um das Abweichungsmanagement und Änderungswesen in DOZ und unterstützt die Organisation bei Non Conformity (NC), Out-of-Specification (OOS), Corrective Action and Preventive Action (CAPA), Kundenreklamations- sowie Change Control (ECR) Prozess.
Dabei steht unsere Gruppe als starker Partner an der Seite unserer produzierenden & freigebenden Betriebe, unter anderem auch zur Erreichung unserer Quality-KPI Ziele und stellt durch risikobasierte, unternehmerische Entscheidungen eine erfolgreiche Vermarktung sicher.
Das Deviation & Change Control Team besteht aktuell aus 9 Mitarbeitenden mit einer Zielgröße von 12 Mitarbeitenden bestehend aus Specialists, Experts und einem Process Owner.
Die Abteilung hat aktuell insgesamt über 60 Mitarbeitende mit einer Abteilungsleitung, 4 Gruppenleitern und 6 Business Partnern.
Unterstütze unser Team mit deiner Leidenschaft, deinen hohen Koordinationsfähigkeiten und deinem Know-how für ein modernes und offenes Qualitätsmanagement.
Wie kannst Du dein Know-How bei Uns einbringen:
* Du bist ein hochqualifizierter Experte (w/m/d) für Non-Conformities, Out of Specification, CAPA, Kundenreklamationen und Change Control (ECR), der/die Qualitätsstandards von DOZ in Bezug auf Produkte und Prozesse gewährleistet und gem.
mQMS (modulares Qualitätsmanagement System) Anforderungen kontinuierlich weiterentwickelt
* Du bist verantwortlich für die effektive Koordination und Leitung von interdisziplinären Teams ...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-05-14 08:08:10
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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.
We are looking for a new team member to perform HPLC and CE analysis in the laboratory.
You will test and validate novel HPLC and Capillary Electrophoresis methods and transfer them to other labs.
You will also perform routine release testing according to GMP guidelines.
You will have the chance to work in a technically and scientifically state of the art environment within a fun and dynamic team.
Key responsibilities:
* Independent execution of laboratory experiments in the Quality Control laboratory
* Perform HPLC and CE analysis
* Documentation according to GMP guidelines
* Maintenance of the lab instruments
* Troubleshooting
Key requirements:
* Technical education as Laboratory Technician, e.g.
Berufslehre, CTA or BSc in Chemistry, Biochemistry or similar field
* You already have hands-on experience with HPLC and/or Capillary Electrophoresis (CE) or iCIEF
* You enjoy working in the lab and enjoy working with a team, in a dynamic environment
* Good communication skills in English.
Good communication skills in 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 great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference.
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-14 08:07:54
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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
Join our dynamic team at Roche and contribute to meaningful initiatives in sustainability and innovation.
Our Global Internship Programme in Innovation & Sustainability #IP2TIS offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.
As a sustainability and innovation intern, you will work on cutting-edge projects that align with our commitment to environmental responsibility, social impact, and forward-thinking solutions.
As part of Roche's commitment to crafting a more sustainable future, we are seeking an intern to join our packaging engineering team in Mannheim and be part of a major development project.
Your part will be to transform the current transportation process into a more sustainable and eco-friendly process by reducing plastic waste and greenhouse gas emissions.
Be part of a development team, have a glance behind the scenes at a leading firm in innovation and create something with a lasting impact.
This internship position is located in Mannheim as a hybrid.
At least two days per week on site are mandatory.
Key Responsibilities
* You will have the opportunity to transform a disposable transportation tray into a sustainable process.
* You will assess suitable methods to clean used trays to an ISO 8 clean room standard and prove its effectiveness.
* You will investigate all requirements to use circular trays on the production lines and estimate the implementation effort to switch to a circular system.
* You will conduct an experiment to determine how often a tray can be used.
* You will prepare geometrical suggestions to increase the tray’s life span.
Who You Are
You are enrolled or have completed your Bachelor’s or Master’s studies at a university, preferably in the field of Engineering (e.g.
Environmental Engineering, Mechanical Engineering, Industrial Engineering or similar) or (Material)-Sciences within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 3 months and getting to know the pharmaceutical industry.
Furthermore you are
* Expected to possess a very good technical knowledge
* Possess strong analytical thinking skills and creative problem-solving abilities
* Able to communicate optimally and collaborate well with diverse teams and stakeholders
* Self-motivated and able to work independently, while also being a proactive standout colleague
* Passionate about or knowledgeable in ...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2024-05-14 08:07:30
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
The Opportunity
Roche Diagnostics in Cape Town is seeking a Senior Scientist (Automation & Technology) to join their Sequencing Assay Development team.
You as the successful candidate for this role will use your technical expertise to assist with development and implementation of automated methods on various liquid handling and other platforms installed at the Roche DIA Cape Town site.
Key Challenges
* Act as a subject matter expert for automation-related efforts within and beyond the Development group at Roche DIA, Cape Town
* Participate in, and use, advanced scientific techniques during planning and analysis phases for new assay, process and/or product development.
* Participate in planning, execution, data analysis, protocol and report creation and reviews where required, including but not limited to assay, process and/or product development.
* Assumes responsibility for the accuracy, quality, and timeliness of results and deliverables.
* Support creating and driving a department-specific technology and automation strategy, with input from management.
* Support driving site-specific automation or technology strategies, by cooperating and interacting with site leadership and other stakeholders.
* Serves as representative on project teams as required, both at and outside of the site (within Roche).
* Communicates progress of programmes and projects to senior management and other stakeholders.
* Interacts with Quality, Regulatory, Operations and other functions to support improvement programmes, change management and CAPA activities.
* Ability to work independently within project teams, and manage their time, tasks and deliverables based on project or team priorities.
Who You Are as an Ideal Candidate
Qualifications and Education Requirements
* At least a Bachelor’s degree in Engineering, Science or a related field.
* At least 5 years’ experience in automated liquid handling in a biotechnology applications / process development / product development / technical manufacturing function.
* Expert level knowledge on at least one major liquid handling platform (e.g.
Hamilton or Tecan), including programming, workflow development, and support is required.
* Demonstrable programming capability wit...
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Type: Permanent Location: Cape Town, ZA-WC
Salary / Rate: Not Specified
Posted: 2024-05-14 08:05:45
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
Shape your career by joining Alcoa’s Vacation Student program! Based in WA at our Pinjarra refinery, you’ll have the chance to put your university knowledge into practice, propelling you toward a career path that exceeds your wildest expectations.
Throughout your 12-week paid summer placement, you’ll experience professional growth, technical expansion, and become an integral part of our vibrant community, where inspiration and daily challenges await.
With best-in-class bauxite mining and rehabilitation practices, the lowest-carbon alumina refining system on the planet, game-changing innovations in aluminium smelting, and the industry’s most comprehensive portfolio of low-carbon products, Alcoa is working to reinvent the aluminium industry for a sustainable future, and we want you to join us!
Throughout the program, you will be paired with a senior specialist that will provide you with the hands-on training, mentoring, and coaching to support you in becoming a creative problem solver, helping you towards completing the meaningful projects that you will be assigned.
What’s on offer?
* Exposure to industry and a future career at Alcoa.
* An attractive hourly rate of pay for the hours you work.
* Meaningful project work that provides you with valuable hands-on work experience
* Working locally, in an onsite environment enabling you to return home to friends or family every night.
* Inclusion and diversity networks; shaping a culture where everyone is welcome, respected and heard.
* Be part of our commitment to sustainability, delivering world class technology and innovations that lead the aluminium industry!
* A workplace culture that strongly values your safety.
* Increased opportunity to gain a place in the Alcoa Graduate Program after you have completed your degree
What you’ll be doing
As an Occupational Hygienist Vacation Student at Alcoa, you will be:
* based on site at our Pinjarra Alumina Refinery.
* assigned a project that both delivers real value to the business and provides you with hands-on industry experience.
* involved in conducting ongoing surveillance programs including workplace exposure monitoring.
* exposed to hazardous materials risk assessment and management.
* assisting in the identification and verification of exposure controls for chemical, physical and biological hazards.
You’ll receive a suitable level of responsibility to tackle assigned project(s), leveraging your innovative thinking, motivation to learn, and passion for growth to make meaningful contributions to the business.
In an open-minded workplace, your ideas will be highly valued within a supportive environment that encourages thinking outside the box.
If you are curr...
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Type: Permanent Location: Pinjarra, AU-WA
Salary / Rate: Not Specified
Posted: 2024-05-13 07:59:18
