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Primary Function:
Makes decisions and recommendations that are recognized as authoritative within area of expertise and have important impact on extensive scientific activities.
May function as technical specialist and/or project manager on mid-size projects.
Makes decisions and recommendations that are recognized as authoritative within area of expertise and that have important impact on extensive scientific activities.
Will have demonstrated creativity, foresight, and mature scientific judgment in anticipating and solving unprecedented scientific problems.
As a project manager, responsible for supervising scientific design on several small to medium projects or for a single major project.
Primary Duties:
• In project management role, manages medium-sized projects or small multi[1]disciplinary projects or studies.
Plans, schedules, conducts, or coordinates detailed phases of the scientific work for a major project.
Advises project management regarding problem areas, scope changes or other events that could affect project completion and profitability.
• As a PM, identifies resources and manages staffing for small to medium projects.
• As a technical specialist, applies a highly sophisticated mastery n the specialty area and a working knowledge of related specialties.
Applies advanced theories, concepts, principles, and processes.
• Keeps abreast of new scientific methods and recommends changes and develops new methodologies.
• Fully understands and works toward meeting the client’s needs and how the project relates to the other elements of the client’s organization and to other projects.
• Work results, decisions and approvals impact the overall design of systems, programs and/or critical aspects of the final product.
• Uses technical software and equipment to design solutions to scientific problems.
• Leads or assists in the preparation or modification of reports, studies, and permits.
• As a client manager, initiates and maintains extensive contacts with key professionals and officials in own and other organizations, requiring skill in persuasion and negotiations of critical issues.
May make major contributions to business development and client relationships.
• May attend on and offsite client meetings.
Education and Experience Requirements:
Normally requires a 4-year degree in biology, environmental science, geology or related science and typically 11-15 years’ related experience, or a Masters degree and 10 years’ experience.
This includes proficiency in utilizing technical software and computers related to the discipline.
May specialize in environmental science, air quality, GIS.
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 ...
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Type: Permanent Location: Oviedo, US-FL
Salary / Rate: Not Specified
Posted: 2024-05-16 08:06:37
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Do you crave an intellectually stimulating job that allows you to leverage your clinical expertise while developing new skills and improving the lives of others? Then look no further! As a Clinical Biochemical Genetics or Clinical Molecular Genetics and Genomics Medical Director at eviCore, part of Evernorth Health Services, a division of The Cigna Group, you'll use your clinical know-how to provide evidence-based medical reviews for patient care.
Collaborate with healthcare providers and stay current on healthcare regulations and industry developments as you review a wide range of cases.
This role offers you the opportunity to build new skills while enhancing the health and vitality of others.
We're seeking a detail-oriented individual with good communication, technology, and typing skills, as well as strong clinical judgment.
Drive growth in your career with our innovative team.
How you'll make a difference:
* You'll start training remotely in a structured environment with support from trainers, mentors, and leadership to set you up for success.
* Complete time-sensitive, specialized evidence-based medical case reviews for medical necessity on eviCore's case management software.
* Conduct physician consultation (peer-to-peer) calls with referring providers to discuss evidence-based medical necessity and appropriateness of the requested service or treatment.
* Leverage your clinical expertise to recommend alternative services or treatments as necessary.
* Work collaboratively with over 500 eviCore physician colleagues to help ensure patients receive proper care via evidence-based decision making.
What you'll enjoy about working here:
* Benefits start on day one
* Predictable work schedules
* 100% work from home
* 8 Paid Holidays + 23 PTO Days
* 401(K) with company match
* Reimbursement for continuing medical education
* Career growth opportunities across the enterprise
* Networking with peers across multiple medical specialties
Requirements:
* M.D.
or D.O.
with a current, active, U.S.
state medical license and board certified in Clinical Biochemical Genetics or Clinical Molecular Genetics and Genomics , recognized by the American Board of Medical Specialties, or American Osteopathic Association
* Eligible to acquire additional state licensureas required
* Clinical experience required
* 5 years of relevant clinical experience post residency/fellowship
* Knowledge of applicable state federal laws
* Utilization Review Accreditation Commission and National Committee for Quality Assurance standards is a plus
* Ability to commit to a set, weekly work schedule (Monday through Friday)
* Strong computer skills: ability to work autonomouslywith automated processes, computer applications, and systems
* Meet physical demands of the role including, but not limited to, typing, speaking, and listening 100% of time
* In accordance with our HI...
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Type: Permanent Location: Bloomfield, US-CT
Salary / Rate: Not Specified
Posted: 2024-05-15 10:56:16
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Do you crave an intellectually stimulating job that allows you to leverage your clinical expertise while developing new skills and improving the lives of others? Then look no further! As a Pediatric Infectious Disease Medical Director at eviCore, part of Evernorth Health Services, a division of The Cigna Group, you'll use your clinical know-how to provide evidence-based medical reviews for patient care.
Collaborate with healthcare providers and stay current on healthcare regulations and industry developments as you review a wide range of cases.
This role offers you the opportunity to build new skills while enhancing the health and vitality of others.
We're seeking a detail-oriented individual with good communication, technology, and typing skills, as well as strong clinical judgment.
Drive growth in your career with our innovative team.
How you'll make a difference:
* You'll start training remotely in a structured environment with support from trainers, mentors, and leadership to set you up for success.
* Complete time-sensitive, specialized evidence-based medical case reviews for medical necessity on eviCore's case management software.
* Conduct physician consultation (peer-to-peer) calls with referring providers to discuss evidence-based medical necessity and appropriateness of the requested service or treatment.
* Leverage your clinical expertise to recommend alternative services or treatments as necessary.
* Work collaboratively with over 500 eviCore physician colleagues to help ensure patients receive proper care via evidence-based decision making.
What you'll enjoy about working here:
* Benefits start on day one
* Predictable work schedules
* 100% work from home
* 8 Paid Holidays + 23 PTO Days
* 401(K) with company match
* Reimbursement for continuing medical education
* Career growth opportunities across the enterprise
* Networking with peers across multiple medical specialties
Requirements:
* M.D.
or D.O.
with a current, active, U.S.
state medical license and board certified in Pediatric Infectious Disease, recognized by the American Board of Medical Specialties, or American Osteopathic Association
* Eligible to acquire additional state licensureas required
* Prefer one of the following state medical licenses but is not required: DC, MD or VA
* 5 years of relevant clinical experience post residency/fellowship
* Knowledge of applicable state federal laws
* Utilization Review Accreditation Commission and National Committee for Quality Assurance standards is a plus
* Ability to commit to a set, weekly work schedule (Monday through Friday)
* Strong computer skills: ability to work autonomouslywith automated processes, computer applications, and systems
* Meet physical demands of the role including, but not limited to, typing, speaking, and listening 100% of time
* In accordance with our HITECH Security Accreditation, compan...
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Type: Permanent Location: Bloomfield, US-CT
Salary / Rate: Not Specified
Posted: 2024-05-15 10:55:59
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Summary
The Data Science Advisor - Clinical Outcomes Research position is an opportunity to provide leadership on complex analytics projects and initiatives supporting the Integrated Pharmacy and Specialty Analytics team.
This role will work with an innovative team on setting and executing the vision for how advanced embedded analytics can lead Cigna to achieving our growth goals.
We are looking for a Data Scientist to conduct opportunity analyses, program evaluation and support Pharmacy Therapeutic Class Strategy/Clinical Condition analytics work to drive business decisions supporting Cigna's Pharmacy Integrated Medical business.
The candidate will have the opportunity to work on analytical projects supporting other benefit domains such as Behavioral Health and Specialty Solutions with the goal of performing Integrated Analytics to support the enterprise.
Responsibilities
* Work collaboratively with Rx Clinical stakeholders to advise on strategic analytics that helps drive data decision making to support formulary strategy, clinical program strategy and clinical product design
* Lead analyses related to Cigna's Total Cost of Care Strategy with a focus on clinical conditions and related medications/treatment (root cause analyses, Health Outcome Studies, Opportunity analysis including descriptive and multivariate statistics to identify patterns in the data.)
* Perform Causal inference Studies , Matched-case control studies and/or randomized control trials for determining the effectiveness of clinical programs and clinical outcome studies
* Execute and apply advanced analytics techniques to evaluate and inform initiatives that will help achieve improved affordability and drive membership growth
* Analytical/Synthesizing of large volumes of data into meaningful information that is communicated effectively to drive meaningful conclusions that help make informed decisions and future projections/recommendations
* Determine opportunities and identify solutions to increase analytical processing efficiency
* Extraction and analysis of large healthcare claims data using state of the art big-data tools and techniques in a largely tool agnostic environment
* Build models using machine learning tools and various statistical packages
* Explore and visualize data using advanced tools and libraries
Qualifications
* 5+ years' of industry experience in solving Health Plan or Pharmacy Benefit Manager business problems through the application of advanced analytic approaches
* Proven experience and competency with predictive analytics and forecasting future state needs is highly desirable
* Proven experience building clinical outcome studies and presenting the findings in a clear and comprehensive manner to an non-technical audience is highly desirable
* Experience in Healthcare analytics (preferably PBM Analytics), Clinical Outcomes, Real World Evidence, Care Management Programs
* Deep heal...
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Type: Permanent Location: Bloomfield, US-CT
Salary / Rate: Not Specified
Posted: 2024-05-15 10:55:53
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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
027546 Quality Specialist (Open)
Job Description:
The responsibilities of a Quality Specialist
As a Quality Specialist, you contribute to the implementation and continuous improvement of our production process.
With a critical eye, you enter the production environment to identify quality needs and shape improvement projects.
You design, integrate, and document quality programs and advise management on continuous improvement regarding quality.
Additionally, you conduct periodic tests for certification.
You are also responsible for handling quality complaints and addressing non-conformities according to our internal procedures to ensure excellent customer service.
Giving training and workshops to production workers to raise awareness of the importance of high-quality products is also part of your duties.
You prepare internal and external audits with your colleagues and guide them.
Moreover, you are always ready to answer questions about quality and provide support where necessary.
Who will you work with?
You will closely collaborate with our SQE, to whom you will also report.
In the entire Lier site there are a total of 85 colleagues working.
Required competencies:
* You have a technical diploma or have the necessary experience in a similar role.
Additionally, you are handy and willing to continuously learn.
* You take responsibility, are independent, and have a pragmatic approach.
* Some knowledge or experience with quality assurance/control in a production environment is necessary.
* You have strong written & verbal communication skills and project management skills.
* Prior knowledge of ISO 9001 standards and FSSC 22000 certification is a plus.
* Safety first is a priority, so you also place great importance on following safety instructions.
* A good knowledge of Dutch and English is required.
39
EEO Statement:
https://www.greif.com/wp-content/uploads/2023/04/HR-101-Equal-Employment-Opportunity-Policy-English.pdf
We offer a competitive salary, excellent benefits and opportunity for growth.
Greif, Inc.
is an equal opportunity employer.
We will not discriminate against any applicant or employee on the basis of sexual orientation, gender identity, race, gender, religion, age, national origin, color, disability, or veteran status.
EOE/Minority/Female/Disabled/Veteran.
For more information read Greif’s Equal Opportunity Policy.
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Type: Permanent Location: Lier, BE-VAN
Salary / Rate: Not Specified
Posted: 2024-05-15 10:55:04
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Classification:
Exempt
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The District Manager is responsible to meet or exceed Service goals in the management of a district of routes.
Reports to the Service Manager.
A DM may manage a service center and if the service center has more than 7 routes, the DM becomes classified as a Senior DM.
Our full-time employees enjoy:
401K Plan with Company Match
Medical, Dental, Vision, FSA/HSA
Life Insurance, Disability Insurance
Vacation, Sick Time, Holidays
Choice of Global Cash Card or Direct Deposit
Career Advancement
Learning & Development Opportunities
Inclusive and Diverse Team Environment
Essential Functions:
- Develop and motivate a district to be a highly productive team through continual training, regular meetings, daily check-in, fostering a positive work environment, route rides, and building strong relationships with each RSR.
- Ensure customer loyalty and outstanding customer service through customer visits, audits, new installs, problem solving, open communication and negotiating with customers.
- Ensure all company policies and procedures are followed in their district, including safety and Service SOP.
- Manage retention and growth by motivating their district to solicit new customers, up-sell/cross-sell/sample all lines of service or product and ensure a profitable product mix.
Monitor and report competitive activity.
Oversee promotions, contests and continued excellent customer relationships.
- Leading their district to success, communicate changes and policies, oversee route organization, project a professional image and require of their district likewise, and cooperatively work with other departments in the branch.
- Complete general route responsibilities when necessary.
Safely operate a delivery vehicle, following all applicable laws and company policy.
- Follow written and verbal instructions and perform other tasks as directed by supervision.
- A Senior DM performs the above functions as well as oversees a service center.
This includes securing the facility, managing inventory to ensure sufficient s...
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Type: Permanent Location: Palm Desert, US-CA
Salary / Rate: Not Specified
Posted: 2024-05-15 10:54:49
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POSITION SUMMARY:
The Quality Specialist is primarily responsible for management and oversite of subcontractors on behalf of Vallourec NA entities.
The Quality Specialist is responsible for qualifying and auditing subcontractors to get them onto the approved supplier list for the entities in addition they will be involved in and managing the order placement to subcontractors.
To ensure that orders are produced as per order requirements.
Along with this they will support the quality teams in projects, audits, and system management as required.
KEY RESPONSIBILITIES:
Subcontracting
* Manage subcontractors and suppliers within the Quality function for Vallourec NA entities
* Support the process of aligning different legal entities
* Perform audits to qualify potential suppliers, as per ISO 9001, API Q1, API 5CT, API 5L and internal specifications.
* Perform audits as per the requirements from the entities to ensure continued compliance to the standards and process and procedures from the entities.
* Report to the entities on the findings of audits, and support follow-up on corrective actions from the audits.
* Travel to different facilities (mills, subcontractors, suppliers) within USA
* Organize and manage inspection of ongoing orders at subcontractors through either witnessing the orders and/or supporting
* Provide regular reporting on the status of the subcontractors and orders ongoing
* Support any issues ongoing and supporting NCRs management raised with suppliers
* Manage and lead the supplier Quality Systems audit program for NA entities.
* Host external Quality System audits (ISO 9001, API Q1, API Q2 or Customer specific criteria)
* Support all areas of the business as well as across the supply chain.
* Collate quality data for monitoring targets
* Assist with training of quality awareness
* Report on Key Performance Indicators (KPIs) to adhere to process and prevent occurrence of any non-conformity relating to product, process, or system
* Conduct benchmarking studies to determine best practices/designs and future trends
* Manage the NCR / Corrective Action program
* Perform document review to internal impact of changes to industry standards
Supplier Management
* Undertake special projects as required
* Contribute, support, and lead continuous improvement activities
* Quality control of work by appropriate reviews
* Write reports and present progress at project meetings
* Achieve goals within budget and time
* Plan projects or subtasks so they may be tracked and presented
* Attend various meetings and action/communicate instructions
* Undertake continuous training and development
* Perform root cause analysis and resolve problems
* Promote effective communication vertically and horizontally within the organization.
* Must follow all company policies, practices, and regulations to incl...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2024-05-15 10:44:29
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As an In-Home Installation and Health Technician, you’ll be responsible for the delivery, installation, integration, and troubleshooting tech products such as home theater, computing, smart home, networking and health technology.
This role also requires technical expertise in health device installation and support including all appropriate HIPAA and health-related requirements Outside of delivery and installation, you’ll find the right solutions for customers’ lifestyles and technology needs based on your conversations.
You’ll partner with other Geek Squad Agents, service partners, retail employees and supply chain employees to drive performance to meet Best Buy’s strategy and yearly initiatives.
What you’ll do
* Provide a seamless customer experience by advising and fulfilling on lifestyle recommendations regarding products and services
* Maintain phone and in-person contact with customers to reveal diagnostic discoveries and make recommendations
* Provide feedback, coaching and training to Best Buy store teams
* Provide a variety of fulfillment duties including delivery, installation, integration, networking and troubleshooting consumer electronics devices
* Take the lead on two-person jobs and perform other work alone
* Manage inventory and vehicle maintenance, process paperwork and payment, provide feedback and training opportunities, and follow safety guidelines
Basic qualifications
* Must be at least 21 years old
* Current, valid driver’s license
* Have and maintain a driving record which meets Best Buy safety standards
* Ability to acquire and maintain any state or local licensing, as required to perform job effectively
* Ability to acquire any health-related certifications (e.g., HIPPA), as required to perform the job effectively within 90 days of hire
* Ability to lift weight up to 75 pounds with or without reasonable accommodation and up to 150 pounds as part of a team with or without reasonable accommodation
* Ability to lift weight up to 250 pounds as part of a team with the support tools such as harnesses or lifts
* 2 years of consumer electronics delivery, installation, integration and troubleshooting experience
* 1 year of customer service experience
Preferred qualifications
* 1 year of experience in installation, integration and troubleshooting of advanced or complex consumer electronics products
What’s in it for you
We’re committed to helping our people thrive at work and at home.
We offer generous benefits that address your total well-being and provide support as you need it, especially during key moments in your life.
Our benefits include:
* Competitive pay
* Generous employee discount
* Financial savings and retirement resources
* Support for your physical and mental well-being
About us
As part of the Best Buy team, you’ll help us fulfill our purpose to enrich lives through technology.
We bring...
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Type: Permanent Location: Columbia, US-SC
Salary / Rate: Not Specified
Posted: 2024-05-15 10:21:44
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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!
Pharmaziepraktikum Formulation Development (m/w/d)
(betrifft die Beschäftigung einer Person ab November 2024 und einer zweiten Person ab Mai 2025)
Ihre Aufgaben und Lernfelder
* Absolvierung des Pharmaziepraktikums gemäß § 4 der Approbationsordnung für Apotheker (m/w/d) in der Abteilung Formulation Development, Small Molecule Technical Development
* Unterstützung bei der Entwicklung und Charakterisierung unterschiedlicher Veterinärarzneistoffzubereitungen unter besonderer Berücksichtigung physikalisch-chemischer und biopharmazeutischer Parameter
* Einbindung in das Tagesgeschäft und Unterstützung des Teams
* Mitarbeit bei der Erstellung von Versuchsplänen sowie deren Ausführung
* Durchführung von physikalisch-chemischen Messungen im Rahmen der Formulierungsfindung
* Umfangreiche computergestützte Aufbereitung von Versuchsergebnissen
* Erhalt von Einblicken in die Entwicklungsschritte eines Arzneimittels und regulatorischer Verfahren sowie Voraussetzungen für die Arzneimittelzulassung und weitere angrenzende Bereiche
* Erstellung eines Berichts am Ende des Praktikums
Was Sie mitbringen
* Erfolgreich abgeschlossenes zweites Staatsexamen im Studiengang Pharmazie zum Praktikumsbeginn
* Schwerpunktinteresse an analytischen oder formuliertechnologischen Fragestellungen
* Sicherer Umgang mit Microsoft Office
* Eigenverantwortliche und zielorientierte Arbeitsweise sowie gute kommunikative Fähigkeiten
* Zuverlässigkeit und Freude an der Arbeit im Team
* Sehr gute Englischkenntnisse in Wort und Schrift
WEITERE INFORMATIONEN:
* Wir bieten Ihnen die Möglichkeit eines Pflichtpraktikums für die gemäß Prüfungs-/Studienordnung vorgeschriebene Dauer, beginnend ab November oder Mai.
* Ihr Praktikum bei Elanco dient dazu, Erfahrungen und neue Kenntnisse zu sammeln und sich beruflich zu orientieren.
Bei der praxisnahen Arbeit werden Sie umfangreich durch erfahrene Mitarbeiter betreut und können so das theoretische Wissen vertiefen.
Elanco is an EEO/Affirmative Actio...
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Type: Permanent Location: Monheim, DE-NW
Salary / Rate: Not Specified
Posted: 2024-05-15 10:14:58
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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!
Making animals' lives better makes life better- join our team today!
Your Role:
Responsible for performing Work in Process (WIP) testing of all antigens, and batch release testing in accordance with approved Outlines of Production and GMP.
In addition, the QC technician is responsible for stability testing, environmental and utility testing, and qualification/validation activities as required.
Your Responsibilities:
* Performing all WIP and Final Product batch release tests within the scope of the Outlines of Production, according to GMP principles
* Methods include, but are not limited to microbiology, cell culture, and molecular biology techniques
* Update / maintain / create relevant SOPs, SOs, MDFs and forms
* Recognize and report any OOS or deviations to QC Manager
o Initiate and complete investigations where applicable
* Occasional after-hours work, on-call schedule, and weekend work
* Ability to work within all Quality systems
What You Need to Succeed (minimum qualifications):
* Minimum Bachelor of Science or Technical Diploma (Biotech or Lab technologist)
* 2 years lab experience, GMP training are preferred
* Developed analytical skills
* Flexible work schedule
What will give you a competitive edge (preferred qualifications):
* Excellent problem-solving skills
* Communication and decision-making skills
* Advanced time management skills
Additional Information:
* This is an onsite position Monday-Friday with responsibilities to have an on-call phone from time to time including requirements to occasionally work outside working hours.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benef...
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Type: Permanent Location: Charlottetown, CA-PE
Salary / Rate: Not Specified
Posted: 2024-05-15 10:14:57
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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!
A Bacterin Operator (2nd Shift, Monday-Friday 2PM-1030PM) will be responsible for the media addition, inoculation, down-streaming, dispensing and final filtration of live and inactivated Bacterial Antigen.
Must be able to work independently with minimal supervision in accordance with standard methods, standard operation procedures, and manufacturing directions using proper laboratory techniques.
The operator must adhere to the policies.
Requirements:
* High school diploma or equivalent
* Excellent verbal and written communication skills and ability to train others.
* Must be able to read, understand, and follow written procedures.
Document operations with strict adherence to cGMP documentation practices.
* Demonstrated ability to effectively convey information in an appropriate and effective manner.
* Demonstrated analytical skill / problem solving skills – identifies problems; recognizes symptoms, causes, and alternative solution.
* Knowledge and skill to recognize creative ideas that add value and can be implemented to improve efficiency, effectiveness and reduce complexity for department.
* Must be able to lift up to 60lbs.
and hold above waist level while maintaining sterility.
Preferences:
* Knowledge of Hazardous Waste Handling
* Knowledge of Decontamination and Sterilization
* Understanding of Basic GMP/Documentation practices
* Understanding of Basic Laboratory Practices, Measurements, Biology and Microbiology
* Understanding of operating in an aseptic environment
Job Responsibilities:
* Perform aseptic operations for production processes performed within the Bacterin area.
* Proper operation of automated and semi-automated equipment used in relation to Antigen production.
For example, Sharples units and Concentrator Units
* Will be responsible for assembling, wrapping, sterilizing, delivery and maintaining inventory of Bacterins equipment and tanks and any other equipment/tank needs for the area as deemed necessary by department management.
* Routine and consist...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: 30.3
Posted: 2024-05-15 10:14:50
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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.
Chez Alcoa :
Vous contribuez à façonner le futur de la durabilité avec des innovations révolutionnaires et des technologies à faible émission de carbone.
Faites partie dâune équipe qui façonne le futur de lâaluminium, révolutionnant la façon dont le monde vit, se construit, se déplace et vole.
Faites-en partie et façonnez votre monde.
Ce qui est offert :
Pour vous soutenir, vous et votre famille, au-delà du travail, Alcoa offre un ensemble dâavantages sociaux exceptionnels à compter du premier jour dâemploi.
En plus des avantages médicaux, nous offrons des groupes de ressources, des options de plans de retraite et un plan de vacances de premier ordre pour un meilleur équilibre travail-vie personnelle.
* Horaire flexible du lundi au vendredi;
* Rémunération globale attirante;
* Régime de retraite à cotisation déterminée;
* Programme de rémunération incitative (bonis);
* Télémédecine (Dialogue);
* Plan dâaide aux employés;
* Cafétéria et Service santé sur place;
* Possibilité dâavancement au sein de lâentreprise;
* Ãvénements corporatifs et activités sociales.
à propos du rôle :
Relevant du Superviseur dâexploitation Santé et Sécurité, le titulaire du poste devra assurer la réalisation au niveau usine des activités et objectifs santé-sécurité reliés aux champs de spécialisation qui lui seront dévolus.
Ãtre la référence en termes dâexigences légales et de connaissance des standards dans une approche de responsabilisation. Supporter la direction dans le déploiement des standards usine, de la mise en pratique des outils dâanalyse de risques et des processus dâanalyse des événements.
Les principales responsabilités du poste comprennent :
* Gérer la santé-sécurité afin dâassurer la conformité aux politiques corporatives et aux règlements provinciaux et fédéraux qui peuvent sâappliquer;
* Participer au développement, à lâorganisation, à la promotion et à la coordination de lâensemble des programmes de santé-sécurité et des activités de prévention;
* Conseiller les gestionnaires sur les orientations, les plans dâaction et objectifs en santé-sécurité;
* Conseiller et soutenir les services/secteurs dans leurs décisions et le choix des moyens les plus appropriés à lâatteinte de leurs objectifs et ceux de lâusine;
* Assurer une uniformité des différents programmes santé-sécurité mis en place dans les secteurs;
* Vérifier lâefficacité, la conformité et la qualité des diverses activités de prévention qui sont liés à ces domaines de compétence, via des activités de prévention ou autres outils de gestion;
* Animer des analyses et enquÃ...
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Type: Permanent Location: Becancour, CA-QC
Salary / Rate: Not Specified
Posted: 2024-05-15 10:14:34
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PURPOSE AND SCOPE:
Under the general direction of the VP of Compliance, this position assists with the development, implementation, and continuous monitoring of an enterprise-wide Compliance Investigations Program and leads the Company’s Compliance Investigations for all Business Units and Corporate functions within North America.
Supports FMCNA’s mission, vision, core values, and custom service philosophy.
Adheres to the FMCNA Compliance Program, including following all regulatory and company policy requirements.
Collaborates with the appropriate personnel on selected Compliance related projects and processes.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Leads and conducts compliance investigations within North America, including, but not limited to, assessment of allegations, review of relevant documents, witness interviews and written summaries of same, analysis of facts, and preparation of investigation reports.
* Utilize subject matter expertise in the areas of healthcare laws and compliance to support the business.
* Accountable for outstanding customer service to all external and internal customers.
* Develops and maintains effective relationships through effective and timely communication.
* Assists with the implementation, and continuous monitoring of an enterprise-wide Compliance Investigations Program.
* Adheres to Compliance Investigation work plans and protocols, assembles and manages the necessary internal and external resources, and conducts the investigation in compliance with protocols.
* Provides timely reports, both orally and in writing, to the Director of Compliance Investigations and/or senior management regarding the status of investigations.
* Provides input into investigation best practices and recommendations for continuous improvement to the Compliance Investigation Program.
* Collaborates with other departments, including the Finance, Human Resources, and Patient Care on investigations and the investigation process.
* Maintains current knowledge of laws, regulations and market changes that impact all aspects of the business, including, but not limited to, FCPA, Stark Law, Anti-Kickback Statute, Patient Inducement Statute, Health Insurance Portability and Accountability Act, relevant Office of Inspector General Model Guidance, and applicable advisory opinions.
* Complies with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations while maintaining the highest degree of personal ethics and integrity.
* Assist with various projects as assigned by Director of Compliance Investigations.
* Other duties as assigned.
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 enab...
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Type: Permanent Location: Waltham, US-MA
Salary / Rate: Not Specified
Posted: 2024-05-15 10:13:03
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As an Advanced Research Programs Lead, you will not only have an opportunity to build your own technical team but will also be a creative catalyst to help drive innovative development across the company. You will be a valued member of a team of passionate, service-focused professionals, located all around North America.
Ideally, you will work from our office in Ballston, Arlington, VA but we are open to other ARA office locations and teleworking with the right candidate.
What you’ll do as the Advanced Research Programs Lead
* Pursue advanced research projects within your area of expertise to drive innovation and build work in new business areas with an emphasis on DARPA.
* Work across the company to help ARA staff members and subject matter experts prepare innovative concepts and ideas, and set-up and facilitate face-to-face meetings to present the concepts to X-ARPA PMs.
* Develop and maintain business relationships with DARPA PMs and senior leadership as well as key industrial partners
* Provide input into a long-range business plan and develop a detailed associated marketing/business plan, to include a marketing strategy(s) to develop work within the “ARPAs”, DARPA, IARPA, ARPA-E, and ARPA-H.
* Capture and interpret market intel (directly from customers and indirectly from publications, trade shows, and other sources) and share intel with others through regular communications and through entry into ARA’s customer resource management (CRM) system
* Serve as the ARA Customer Portfolio Manager (CPM) for DARPA
* Assist with preparation/delivery of briefings to ARA senior leadership
* Assist ARA business units with X-ARPA marketing activities to ensure professional and compelling marketing/proposal offerings.
* Lead ARA’s Advanced Concepts Team (ACT); evaluate internal creative research and development ideas. Make seedling awards for promising concepts and provide feedback and guidance to researchers.
Desired Advanced Research Program Manager Qualifications
* Ph.D.
degree or equivalent in physics, engineering, mathematics, chemistry, biology, or other hard science
About ARA
ARA is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems in the physical sciences.
The company, founded in Albuquerque, NM, in 1979, currently employs over 1,500 professionals and continues to grow.
ARA offices throughout the United States and Canada provide expertise across a broad range of engineering and science technologies.
Our Better Fuels Group develops and deploys innovative fuels technologies, converting waste products to renewable fuels, and creating high value products for a sustainable future.
ARA employs traditional refinery equipment and novel water-based technologies to make fuels and chemicals, including sustainable jet fuel that meets petroleum specifications without blending and diesel...
....Read more...
Type: Permanent Location: Alexandria, US-VA
Salary / Rate: Not Specified
Posted: 2024-05-15 10:09:43
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Staff Position Description
Position Title: Specialist Position Code: SpecEVS-8240
Department: Environmental Services Safety Sensitive: YES
Reports to: Environmental Services Lead/Supervisor Exempt Status: NO
Position Purpose:
All KHI employees are expected to perform their respective tasks and duties in such a way that supports KHI’s vision of providing the region’s best clinical care and patient service through an environment that fosters respect for others and pride in performance.
The Specialist assists in the assigned areas to maintain a safe and healthy environment for patients, visitors, and KHI personnel by meeting and maintaining established medical, sterilization, and cleanliness protocols.
Key Responsibilities:
All staff:
1.
Perform all duties, as assigned, for which employee is trained or qualified to perform.
2.
Wear appropriate Personal Protective Equipment (PPE) and follow all applicable safety regulations.
3.
Dispose of waste, including medical and biohazard waste, according to federal, state, organizational, and departmental guidelines.
4.
Manage supplies and equipment efficiently and keep cleaning supplies and equipment safely stored when not in use, and away from patients' access when in use.
5.
Use cleaning chemicals according to federal, state, organizational, and departmental guidelines.
6.
Comply with all federal, state, organizational, and departmental policies and procedures.
7.
Participate in on-going process improvement within the organization and department.
8.
Demonstrates regular attendance and participation at scheduled department and team meetings or calling in and personally notifying the supervisor or another member of management if going to be either absent or tardy, unless unforeseeable circumstances make it impossible to do so.
9.
Consistently demonstrates the ability to adapt to changes in the workload.
10.
Report problems to supervisor.
Housekeeping – Environmental Services
1.
Clean and sanitize assigned patient rooms and bathrooms daily.
2.
Clean, disinfect, and sanitize assigned areas, including moveable and stationary objects, as designated in procedures.
3.
Reset assigned areas to present an attractive and sanitary environment for all customers (patients, visitors, staff, etc.).
4.
Properly maintain the designated supply closet and work cart.
5.
Keep cleaning supplies and equipment safely stored when not in use, and away from patients' access when in use.
Laundry
1.
Maintain an adequate stock and flow of laundered materials, throughout the organization, per policies, processes, and regulatory guidelines.
2.
Maintain laundry area in a clean and sanitary condition.
3.
Use and maintain equipment safely, appropriately, and as efficiently as possible.
4.
Document accurate records of items delivered to ensure accurate reporting.
Qualifications:
· Must be able to communicate well with a variety of customers.
· Must be able to read and write well enough to respond ap...
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Type: Permanent Location: Kingman, US-AZ
Salary / Rate: Not Specified
Posted: 2024-05-15 10:06:05
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Lonza Pharma & Biotech has an opening for an Operations Material Handler at our location in Bend, Oregon.
Key Responsibilities:
* Read, understand and demonstrate proficiency on Standard Operating Procedures (SOPs)
* Required to work on a 12-hour shift schedule that may include nights/weekends and some holidays
* Read, write, and understand Standard Operating Procedures (SOP’s)
* Actively engage in departmental continuous improvement activities, questioning current practices to actively promote and improve the workspace area
* Membership in safety committee, sweep team, or ERT team
* Day to day operations of rooms 1060, 1070, 101, 121, 121 cold room, and area deliveries of solvents and removal of waste
* Maintain Hazardous waste manager status at the site
* Ensure the areas have adequate supplies of consumables, other in-house stock items and equipment.
This may include engineering stores items and industrial gases
* Manage equipment transfer process to and from Warehouses when required
* Be responsible for all area logbooks, ensuring current versions are in use, log books are completed/signed off, and logbooks are reviewed and returned to Quality Assurance Document Control
* Performance of area housekeeping activities, including the prompt reporting of problems, shortages, or equipment breakdowns
* Proficient in Master Control at reporting and completing change control, deviations, CAPA, and procedure changes
* Oversee and request work orders for facility upgrades, repairs, and maintenance in area of responsibility
* Manage bulk solvent and waste offloads and maintain bulk solvent and waste area
* Other duties as assigned
Key Requirements:
* High school Diploma or GED
* 2-year associate degree or 4-year BS degree preferred
* Previous experience maintaining and operating SAP Inventory control systems
* Certifications in Lean Manufacturing or similar Operations Excellence
* Experience with manufacturing equipment is preferred
* Promote safety and demand high quality standards for work being performed
* Team player, open and reliable character with good interpersonal and communication skills
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...
....Read more...
Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-05-15 10:05:58
-
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
The Regulatory Affairs CMC Manager II will support the site and customer related regulatory affairs and CMC project activities.
Work collaboratively with appropriate company personnel to coordinate the regulatory work stream elements for CMC activities for Portsmouth Lonza Pharma and Biotech customers.
Provide regulatory support and advice for internal and external customers in line with defined Regulatory plans and in response to ad-hoc questions.
Must be within (or able to relocate to) commuting range of our Portsmouth NH facility, as regular on-site presence is required for this role
Key Responsibilities:
* Preparation and/or review of scientific and technical information suitable for Health Authority submission in conformance with applicable Lonza procedures.
* Lead the submission preparation and/or review of customer clinical (e.g IMPD/INDs) and commercial (e.g.
MAA/BLAs) filings.
* Preparation and/or review of responses to agency submission review questions.
* Preparation and review of customer variation submissions.
* Support for scientific advice meetings and development of regulatory strategy with customers.
* Prepare documents for customer RoW submissions including certifications and attestations where applicable.
* Internal regulatory support for operation and control, including Interpretation of EU, US and other global regulatory requirements to support compliance in all phases of contract manufacturing of Mammalian products.
Maintain transparency of information across regulatory function.
* Site support for deviation and change control assessment for regulatory impact.
Support site-specific regulatory documentation and activities.
* Maintenance of Lonza site Facility registrations with regulatory agencies and plant-level documentation (e.g.
Site Master File and Japan FMA).
* Lead the creation and maintenance of Lonza Drug Master Files as appropriate for site activities.
* The individual in this role is an individual contributor and will not have any direct supervisory responsibilities.
* Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, and cGMP regulations.
Key Requirements:
* Bachelor’s Degree or higher required in applicable science field or equivalent
* Regulatory Affairs Certification (RAC) Preferred
* 10+ years of experience working in Pharmaceutical/ Biotechnology or related industries
* Minimum 7 years of experience preparing/authoring CMC DS s...
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Type: Permanent Location: Portsmouth, US-NH
Salary / Rate: Not Specified
Posted: 2024-05-15 09:59:35
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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:
Role Purpose: Biotechnologist 1 is an entry level position.
The Biotechnologist will be expected to learn and carry out the basic skills used in a GMP Manufacturing environment, progressing from supervised to unsupervised activities.
Key Accountabilities and Duties:
Responsibility Perform various duties which will ensure that products are manufactured within the manufacturing area at the Slough UK facility in accordance with schedule, safety requirements and Good Manufacturing Practices
Training Obtain a thorough knowledge of the production systems and the relevant LONZA systems to enable efficient production
Responsible for maintaining own training and ensure full training has taken place in all aspects of the production activities according to LSO.
Quality Systems Ensure that high standards of cGMP are adhered to both for self and others.
Gain familiarity with Lonza quality procedures eg change control, the deviation system and validation procedures.
Assist in batch disposition activities e.g.
correctons, datamart Ensure that high standards of documentation completion are adhered to both for self and others
Plant and Process Direct involvement in the manufacturing process.
Identify any Continuous Improvements to the process/equipment, and help with completion of projects .
Area Ownership
Ensure high standards of housekeeping are adhered to
Ensure that team values are adhered to
Ensure that the appropriate safety policies and systems are adhered to.
Highlight safety issues in the area and instill a safety attitude in the team.
Ensure that objectives given are met in the appropriate timescale
Skills:
Good command of both written and oral English
Good organizational skills
Strong problem solving skills
Interpersonal and coaching skills
Qualities & Attitude
Self Motivation Drive for Results
Attention to detail
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: Slough, GB-SLG
Salary / Rate: Not Specified
Posted: 2024-05-15 09:57:07
-
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
Wie sieht deine zukünftige Abteilung aus?
Unterstütze unser Team in der Zellkulturentwicklung als studentische Hilfskraft(m/w/d) im Bereich Pharma Late Stage Development.
Wir sind das Bindeglied zwischen der frühen Forschung und unserer großtechnischen Produktion.
Unser Kerngeschäft ist die zeit- und qualitätsgerechte Entwicklung von Prozessen und Technologien in der biopharmazeutischen Wirkstoffherstellung.
Damit unterstützen wir die Einführung von neuen Medikamenten zur Therapie in der Onkologie und andere Bereiche.
Das Team besteht aus 9 Mitarbeitenden, die mit Herz und Leidenschaft täglich mit Zellkulturversuchen im Maßstab von 1 bis 400 Litern Daten zur Prozessvalidierung und -charakterisierung erzeugen.
Dein Praktikum
Nach einer intensiven Einarbeitung in den Umgang mit tierischen Zellkulturen arbeitest du im Rahmen des Praktikums an der aktuellen Entwicklung einer neuen Messmethode.
Der Einstieg kann ist flexibel und wird an deine Bedürfnisse angepasst.
Die Dauer beträgt mindestens 3 - 6 Monate.
Wir bitten dich, den gewünschten Zeitraum bei deiner Bewerbung mit anzugeben.
Nach Absprache und Möglichkeit ist im Anschluss an dieses Praktikum auch eine Abschlussarbeit möglich.
Was beinhaltet deine neue Stelle?
* Die selbständige Versuchsplanung, -vorbereitung und -durchführung geben dir Spielraum zur Entwicklung neuer Erkenntnisse
* Du analysierst den Einfluss von Variablen auf das Puffergleichgewicht in Zellkulturmedien
* Du begleitest Zellkulturversuche im kleinen und großen Maßstab, in der Vorbereitung, sowie in der Durchführung
* Im Rahmen der Optimierung von bestehenden Prozessen bringst du dein chemisch-physikalisches Wissen ein
* Durch geschicktes Kombinieren von Technologien und Prozesswissen etablierst du neue Wege zur pH Sonden Kalibrierung
* Du dokumentierst deine Ergebnisse und präsentierst diese in einem geeigneten Rahmen
Du kannst dich mit folgenden Aussagen identifizieren?
* Du hast Grundkenntnisse von biopharmazeutischen Prozessen
* Du bist in einem Masterstudiengang der Fachrichtung Biologie, Chemie, Biotechnologie, Verfahrenstechnik, Medizintechnik, oder einem vergleichbaren Studiengang eingeschrieben
* Du verfügst über grundlegende theoretische oder praktische Kenntnisse in molekularbiologischen und proteinbiochemischen Methoden sowie im Bereich der Zellbiologie (Zellkultur)
* Du bist geübt im Umgang mit gängiger Software zur Präsentation von Daten und Ergebnissen
* Englischkenntnisse in Wort und Schrift sind von Vorteil
* Eigenständi...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-05-15 09:49:39
-
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 QA Operations Team, the QA Project Manager, Senior QA Specialist (f/m/d) supports in all matters of GMP compliance (e.g.
representation in local and global Quality Boards, contact person for customers and compliance questions), promotes the adherence and continuous improvement of Quality Systems and ensures Quality oversight in the specified area.
Key responsibilities:
* Representing the department Quality Assurance in cross-functional teams and ensuring and managing interfaces to different internal and external stakeholder
* Assesses, reviews and approves quality records such as deviations, change controls, CAPAs, investigations, effectiveness checks, and extensions in line with valid SOPs
* Authors, reviews and approves GMP-relevant documents and SOPs in the ownership of QA
* Supports and participates in internal, customer and regulatory audits
* Support customer communications, manage interactions in case of changes, deviations, out of specifications etc.
* Review and approval of executed batch records, prepares batch release package for the Responsible Person / FvP, including recommendation on disposition status
* Review and approval Master Batch Records
* Support continuous improvements programs to establish effective Quality Management Systems
Key requirements:
* Bachelor or Master Degree in life sciences (e.g.
chemistry, biotechnology or a related field)
* Significant work experience in the GMP-regulated industry; preferably in the following units: Production, QC or QA
* Broad knowledge in Quality standards (e.g.
ICH Q7, 21 CFR Part 11)
* Availability to occasionally provide quality support outside of working hours
* English language skills (written and spoken) are required, 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: 2024-05-15 09:48:59
-
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:
The role of the technologist is to organize and execute a variety of lab-based tasks to a high standard and degree of attention to detail within area expertise/ownership.
Work is performed according to protocol in compliance with rules and procedures and the employee contributes to problem solving activities.
The individual takes a proactive approach to their learning and development and is beginning to train others.
Key Accountabilities and Duties:
•Operation of standard and non-standard, documented processes and techniques (e.g.
ELISA, HPLC, CESDS, qPCR, icIEF)
•Completion and peer review of laboratory documentation
•Reporting results to appropriate audience (presentations, data summaries, reports)
Execution of work of increased complexity and breadth in line with expected standards (safety, on time, right first time to the appropriate degree of quality)
•Undertake activities that contribute to the running of the department e.g.
equipment ownership and maintenance, documentation (add documentation to others as well)
•Deliver practical training
•Develop an area of technical expertise e.g.
equipment, system superuser
•Escalating issues in a timely fashion
•Requirement to join the out of hours call out rota to respond to alarms on cold storage units (or cell culture systems as appropriate)
Qualifications/Skills:
Required - Degree in relevant scientific/ technical discipline, 1-2 years relevant laboratory experience
Required: Word, Excel, PowerPoint, Outlook Desirable: Application of Continuous Improvement tools and techniques such as 6S, visual management, mistake proofing and the 8 wastes.
Ability to conduct basic process / data analysis (7 basic quality tools), interpret output and develop robust solutions.
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: Slough, GB-SLG
Salary / Rate: Not Specified
Posted: 2024-05-15 09:48:16
-
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 QA Operations Manager for Drug Product Services (DPS) in Visp, you will represent Quality Assurance in cross-functional teams, including but not limited to Manufacturing, MSAT, QC, Engineering, Supply, Qualification/Validation and others to effectively execute tasks related to Drug Product processes.
Key responsibilities:
* Act as point of contact for Drug Product QA related questions and issues related to the manufacturing operations
* Ensure shop floor QA oversight (regular presence in the cleanroom)
* Assess, review and approve GMP documents and quality records e.g.
SOPs, risk assessments, deviations, investigation, CAPAs, change controls, complaints, APR/PQRs, protocols, executed MBRs
* Act as QA representative during the conduction of internal / customer / regulatory inspections and audits
* Provide GMP-related trainings to Operations personnel
* Support continuous improvement programs to establish an effective Quality Management System for DPS Visp
Key requirements:
* Master of Science in biotechnology or a related field
* Significant work experience in the GMP regulated environment, in relation with aseptic manufacturing activities and preferably within a Quality Unit
* Experience working with stakeholders from different departments and management levels
* Fluent in English (written and spoken), German language 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: 2024-05-15 09:48:14
-
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 Senior Scientist (all genders) gesucht.
Sie arbeiten im Rahmen der Entwicklung von Herstellungsprozessen für Biopharmazeutika nach aktuellen ISO- und GMP-Qualitätsrichtlinien.
Das Arbeiten in interdisziplinären Teams macht Ihnen Spass und Sie behalten aufgrund Ihrer strukturierten Arbeitsweise auch in sehr komplexen Projekten den Überblick.
Als Mitglied unserer analytischen Forschungs- und Qualitätsabteilung sind Sie auch für die fachliche Weiterentwicklung der Mitarbeiter verantwortlich.
Die Ihnen zugeteilten Projekte bearbeiten Sie eigenverantwortlich und selbstständig.
Sie führen die finale Revision der komplexen Studienprotokolle, Arbeitsanweisungen und Berichte in multiplen Studien entsprechend den GLP-Richtlinien durch.
Sie repräsentieren die Abteilung gegenüber internen und externen Kunden und sind eine der Schnittstellen für technische und wissenschaftliche Aspekte.
Mit Ihrem Engagement tragen Sie zur stetigen Weiterentwicklung der Abteilung und zum Erfolg des Unternehmens bei.
Ihre Hauptaufgaben:
* Primäre Schnittstelle für technische und wissenschaftliche Aspekte der Entwicklung, Implementierung und Validierung von biochemischen und HPLC Assays (z.B.
ELISA, Enzyme Assays, RT-qPCR, Protein-PCR, UV/Vis, icIEF, RP-/SE-/IEX-HPLC etc.)
* Erstellung und finale Revision der komplexen Studienprotokolle, Arbeitsanweisungen und Berichte in multiplen Studien entsprechend den GLP-Richtlinien
* Training und Entwicklung von Laboranten und wissenschaftlichen Mitarbeitern
* Identifizierung und Implementierung neuer analytischer Technologien und Verantwortung für die Laborautomatisierung
Was Sie mitbringen:
* Hochschulabschluss in Biologie, Biochemie, Biotechnologie (oder vergleichbare Qualifikation)
* Mehrjährige Industrieerfahrung in der Bioanalytik für therapeutische Proteine ist von Vorteil
* Erfahrung in statistischer Versuchsplanung (DoE) als Voraussetzung für effiziente Methodenentwicklungen ist ein Plus
* Erfahrung mit ISO- und GMP-Standards
* Gute Kommunikationsfähigkeiten sowie ausgezeichnete Deutsch- und Englisch Kenntnisse
Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar.
Wie wir unsere Geschäftsergebnisse erreichen ist für uns genau...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-15 09:46:27
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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 Associate Principal Scientist (all genders) 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 mit Promotion im Bereich Biochemie, Biologie oder Chemie und haben 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 ...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-15 09:44:23
-
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 Associate Principal Scientist (m/w/d) 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:
* Primäre Schnittstelle für technische und wissenschaftliche Aspekte der Entwicklung, Implementierung und Validierung von biochemischen und HPLC Assays (z.B.
ELISA, Enzyme Assays, RT-qPCR, Protein-PCR, UV/Vis, icIEF, RP-/SE-/IEX-HPLC etc.)
* Erstellung und finale Revision der komplexen Studienprotokolle, Arbeitsanweisungen und Berichte in multiplen Studien entsprechend den GLP-Richtlinien
* Training und Entwicklung von Laboranten und wissenschaftlichen Mitarbeitern
* Identifizierung und Implementierung neuer analytischer Technologien und Verantwortung für die Labordigitalisierung und -automatisierung
Ihr Anforderungsprofil:
* Sie verfügen über ein abgeschlossenes Studium mit Promotion 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 unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst.
Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt.
Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.
Zu Lonza kommen Menschen, die Herausforderungen annehmen und mit ihrer Kreativität im Bereich
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-15 09:35:17
