-
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.
About the Role
In support of continuous improvement in Mining and Alcoa’s environmental performance, we have a unique opportunity for a suitably qualified Environmental Research Scientist to join the team that are driving improvements in rehabilitation processes and practices.
Reporting to the Environmental Research Superintendent, you will be working with a close-knit team of scientists based at Alcoa’s Huntly Central location and contributing to improving plant and soil aspects of rehabilitation performance.
The key aspects of the role will include:
* Designing, implementing, monitoring, analysing and writing up field trials to improve plant recruitment and survival in rehabilitation, e.g.
fencing, irrigation, ripping, and topsoil management.
* Investigating plant health to understand and overcome limitations to plant survival.
* Undertaking soil testing and analysis.
* Communicating results to internal and external stakeholders.
* Liaising with external research scientists to facilitate site access and field trials.
* Supervising higher degree by research students.
What’s on offer
* Career development opportunities to pursue your passion
* Performance related bonus (variable)
* Enjoy additional time off with a monthly Leisure Day
* 16 weeks paid primary parental leave scheme
* Paid annual volunteering hours
* Social and diversity focused engagement opportunities
What you can bring to the role
* PhD in restoration ecology, land rehabilitation, soil science or ecohydrology.
* Research experience post-PhD studies with exposure to soil testing.
* Capable in installing and monitoring large-scale field trials with minimum supervision.
* An analytical mind that can solve complex datasets using appropriate statistical methods.
* Skilled in publishing papers in peer reviewed journals.
* Previous experience in mining rehabilitation, knowledge of the WA flora and GIS will be considered desirable.
Application Closing Date
Sunday, 5 May 2024
Additional information
* Interviews may progress prior to the closing date, although all applications will be considered.
* You will only be contacted if you are shortlisted for an interview, this process can take up to four weeks from the closing date.
#LI-JR1
About the Location
As an Alcoan you are part of a global team committed to advancing sustainability and delivering excellence and innovation.
Join in and become an essential part of our purpose: to turn raw potential into real progress.
The power is in your hands to shape the things that matter to us all.
We are values led, vision driven and united by our purpose of transforming raw potential into real progress. Our commitments to Inc...
....Read more...
Type: Permanent Location: PINJARRA, AU-WA
Salary / Rate: Not Specified
Posted: 2024-04-10 08:23:07
-
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 MSAT (Manufacturing Science & Technology) Team Ibex Visp responsible for the successful transfer, scale up, supervision and optimization of biopharma processes.
As a very experienced professional, you are regarded as an expert in process science and manufacturing aspects.
In this role, you significantly contribute to the development of the MSAT toolbox and share the manufacturing responsibility as a long-term process owner.
Key Responsibilities
* Leading cross-functional teams as a process expert tasked with technology transfers (process design and up-scaling) and timely process implementation at manufacturing scale.
This includes the whole lifecycle of assigned projects from planning over coordination, implementation, control and project completion aligned with project management goals
* Act as the interface between the process donor (external customer, process development) and operations.
Responsible to ensure process scalability and manufacturability
* Securing success during technology transfer by applying formal processes and tools to manage the transfer of information, process related risks and change control
* Responsible for the resolution of process issues that may arise during manufacturing, considering all regulatory requirements.
This includes on call duty
* Responsible for execution of GMP risk analysis for the manufacturing processes
* Ensuring timely compilation of process related deviations, change requests and campaign reports as well as responsible for continuous improvement of process performance
Key Requirements
* PhD (preferred), Master’s/Master’s degree in biotechnology, chemical engineering or related disciplines
* Working experience in biopharma manufacturing and / or process development preferable in of Mammalian Manufacturing
* Deep understanding of GMP and bioprocess technology
* Very good communication skills and interaction with all kinds of interfaces within customers and the project organization
* Fluency in English
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new...
....Read more...
Type: Permanent Location: Visp, CH-BL
Salary / Rate: Not Specified
Posted: 2024-04-10 08:18:55
-
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there's no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that's the kind of work we want to be part of.
For Drug Product Services (DPS), our successful DP focused branch located in Basel, Switzerland and Stein, Switzerland, we have 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 Principal Scientist/Group leader Formulation Development.
Key responsibilities:
* Lead formulation development activities related to liquid and lyophilized parenteral drug products of large molecule biologics(e.g.
monoclonal antibodies, novel formats, ADCs, peptides), vaccines and small molecules.
* Design, plan, execute and deliver formulation studies as well as characterization studies based on contracted terms and scientific inputs relevant to product
* Supervises the analyses of formulations in context of the product development using analytical and pharmaceutical test methods
* Author technical documents and support preparation of regulatory documentation
* Manage group of technicians, engineers and/or scientists and collaborate across departments
* Ensure safety and health protection following lab and safety instructions as well as basic GMP qualification
* Contribute to improvements, explore new technologies and lead integration of activities
* Enable innovation and technical strategy projects, generate IP and evaluate and implement new methods and technologies
Key requirements:
* Ph.D.
in pharmaceutical sciences, chemistry, biochemistry, or related fields
* Significant work experience in biotech / pharma industry
* Experience with technical issues and requirements for development of drug product formulation and/or processes of biologics.
* Knowledge of lyophilization, primary packaging, aseptic product manufacture (protein or vaccine drug products and/or protein analytics is desirable)
* Excellent communication skills, excellent command of English both written and oral
* Excellent leadership and interpersonal as well as planning 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.
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, ...
....Read more...
Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-10 08:18:38
-
Your Job
We are currently building our in-house Engineering staff and are looking for a talented Signal Integrity Engineer to join our team.
If you are looking for a way to accelerate your career and be part of a great company, this may be the opportunity for you.
In this role, you will have the opportunity to perform characterization of high-speed connectors/cables and systems, using high-speed digital and electromagnetic measurements for automotive in-vehicle networks.
Our Team
CMS Team
What You Will Do
Concept Design and Development
•Complete PCB Electromagnetic simulations
•Provide Signal Integrity test board layout support for high speed applications
•Provide recommended connector pin-out configuration for optimized signal integrity performance
Design Verification & Product Validation
•Complete design validation plan & report (DVP&R) documentation.
•Oversee signal integrity testing of shielded and unshielded automotive interconnects systems.
•Update product technical documentation (such as Engineering, Application and Product Specs).
•Approve Test lab best practices for internal and external signal integrity lab usage.
•Prepare presentation material for internal and customer design reviews.
Production Support
•Support product engineers with internal & customers
Who You Are (Basic Qualifications)
Experience in EM and CAD/CAE tools, such as Channel Designer, HFSS, CST, FDTD tools, MoM tools, Sigrity PowerSI, PAKSI-E, Power-grid, Agilent ADS and Mentor Hyperlynx
• Working knowledge of Altium or any PCB design tool
• Understanding of high-speed data applications
• Working Knowledge of multi-port network analyzers, BER testers, Eye pattern analyzers, digital sampling scopes and TDRs.
• Ability to apply signal integrity concepts to laboratory data for analysis and troubleshooting.
• Experience in correlating simulation results with lab measurements using oscilloscopes, TDRs and VNAs is essential.
• Strong knowledge of high-speed material properties and behavior during data transmission.
• In depth understanding of electromagnetics and transmission line theory
What Will Put You Ahead
Proficient in using simulation to drive optimizations of a connector design.
•Familiarity with PCB technologies (HDI, Substrate, etc.) and their DFM rules
•Demonstrated ability to work with cross-functional teams in providing design feedback which provides optimal signal integrity performance without sacrificing mechanical integrity and/or manufacturability.
•Demonstrated ability in information analysis problem solving, sound judgment, and leadership.
•Good verbal and written skills for exchange of information in a clear and concise manner.
Demonstrated ability to work effectively within a team environment.
•Good analytical ability to resolve signal integrity issues and apply logical reasoning, test assumptions, observe results and make corrections.
At Koch companies, we are entrepreneurs.
T...
....Read more...
Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2024-04-10 08:17:06
-
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 MSAT (Manufacturing Science & Technology) Team Ibex Visp responsible for the successful transfer, scale up, supervision and optimization of biopharma processes.
As a very experienced professional, you are regarded as an expert in process science and manufacturing aspects.
In this role, you significantly contribute to the development of the MSAT toolbox and share the manufacturing responsibility as a long-term process owner.
Key Responsibilities
* Leading cross-functional teams as a process expert tasked with technology transfers (process design and up-scaling) and timely process implementation at manufacturing scale.
This includes the whole lifecycle of assigned projects from planning over coordination, implementation, control and project completion aligned with project management goals
* Act as the interface between the process donor (external customer, process development) and operations.
Responsible to ensure process scalability and manufacturability
* Securing success during technology transfer by applying formal processes and tools to manage the transfer of information, process related risks and change control
* Responsible for the resolution of process issues that may arise during manufacturing, considering all regulatory requirements.
This includes on call duty
* Responsible for execution of GMP risk analysis for the manufacturing processes
* Ensuring timely compilation of process related deviations, change requests and campaign reports as well as responsible for continuous improvement of process performance
Key Requirements
* PhD (preferred), Master’s/Master’s degree in biotechnology, chemical engineering or related disciplines
* Working experience in biopharma manufacturing and / or process development preferable in of Mammalian Manufacturing
* Deep understanding of GMP and bioprocess technology
* Very good communication skills and interaction with all kinds of interfaces within customers and the project organization
* Fluency in English; German nice to have
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 proble...
....Read more...
Type: Permanent Location: Visp, CH-BL
Salary / Rate: Not Specified
Posted: 2024-04-10 08:16:03
-
SUMMARY:
The person in this role will oversee all Safety Activities and be responsible for the field training and mentoring of Engineering Services employees as it relates to MOW technical procedures, specifications, safety guidelines as required by FRA, OSHA, MSHA and company policies regarding machinery and hand tools to ensure safe and efficient operating procedures, usage, and maintenance.
RESPONSIBILITIES:
* Be familiar with all state, federal, and local safety regulations governing all aspects of the rail industry.
* Establish a safety culture foundation based on compliance with GWI safety rules, regulations and environmental responsibilities
* Supervise and set the example for all safety training and work with the Corporate Safety Team.
* Create a professional and safe environment that is conducive to the development of all employees
* Respond to reported incidents to evaluate current best practices and recommend changes where necessary.
* Ensure the safety of the workplace by coordinating, administering and implementing comprehensive training programs in occupational, industrial and environmental safety.
Support the design, delivery and continuous improvement of equipment training programs as well as ongoing learning opportunities across the organization, in support of the organization’s needs
* Assist in the administration of the company's On-The-Job Injury Policy and return to work issues.
* Implement regional and corporate safety initiatives and policies.
Conduct audit assessments and provide feedback to regional leadership.
* Participate in corporate and regional safety calls with the ability to intercede in any operational activity that may be deemed an improper/unsafe job procedure.
* Conduct safety audits and inspections to ensure compliance with occupational and environmental health and safety requirements.
* Evaluate employees to measure their progress in achieving proficiency in specific tasks.
Ensure accurate record keeping of training conducted
* Deliver training via oral and hands on demonstration in a field and classroom environment
* Conduct initial and follow up training sessions with employees and provide feedback on developmental needs
* Other projects and duties as assigned.
REQUIRED SKILLS AND/OR EXPERIENCE:
* Demonstrate an ability to lead and direct, plan work schedules, assign or delegate work on a daily basis, develop and mentor employees and take corrective actions when necessary.Creates and maintains a positive and professional learning environment.
* Ability to identify problem safety areas and set up a solution to resolve.
* Good oral and written communication skills.
Excellent communication, team building, and leadership skills.High level of interpersonal skills to work effectively with others, motivate employees and elicit work output.
* Must have a good understanding of rail industry and its goals and object...
....Read more...
Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2024-04-10 08:11:41
-
Classification:
Non-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 Soil Counter/Sorter handles, counts, sorts and records incoming soiled textiles from the customer.
Identifies damaged or abused textiles.
Prepares and transfers textiles to other departments.
Performs other tasks as needed.
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:
- Open bag of soiled textiles, then sort them by type, size and color.
- Count textiles manually or electronically, and transfer them into sorting systems.
- Identify damaged or abused textiles and record into sorting systems.
- Meet efficiency and safety standards for the position.
- Follow instructions as directed by supervision.
Additional Functions:
- Work in other production positions as needed.
Qualifications:
- Recognize colors and sizes, count accurately.
- Comprehend and follow direction.
Typical Physical Activity:
- Physical Demands consist of standing, walking, reaching overhead, pushing, pulling, grasping, lifting up to 50 lbs.
and stooping.
- Physical Requirements consist of being able to meet the physical demands for the entire shift.
Typical Environmental Conditions:
- Production areas of a typical industrial laundry facility, which includes variations in temperature, odors, humidity, lint and dust.
Soiled linens come from a variety of customers such as restaurants, hotels, medical facilities and shops.
Travel Requirements:
- none.
Education:
- none.
For a general description of benefits that are being offered for this position, please visit alsco.com/benefits.
Alsco is an Affirmative Action/Equal Employment Opportunity Employer.
Revised: 04/29/2022
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applic...
....Read more...
Type: Permanent Location: Anchorage, US-AK
Salary / Rate: Not Specified
Posted: 2024-04-10 08:06:43
-
Counselor, School Based
Are you looking for an organization where you can grow while making a positive impact on people's lives? At Signature Health, our purpose is to provide integrated healthcare for our community specializing in patients with mental illness and/or addiction because we want people to realize their highest potential.
Our core values are the foundation of who we are:
* People First mindset where we honor our colleagues and patients
* Striving for Excellence in our work each day
* Can Do approach where we roll up our sleeves in response to opportunities and challenges
In addition to a rewarding career, as a full-time employee, you will have access to the following employer/employee paid benefits:
Full Time:
* Medical, Dental, Vision
* Robust earned paid time off program (PTO)
* 401k match
* Various Life Insurance Options
* Short- and Long-Term Disability (Not applicable for school-based employees)
* Federal Loan Forgiveness Program (available on eligible on roles)
* HealthJoy - no cost medical and mental health online resources available Day 1 (coverage extends to family members living in the same household)
* Tuition & Professional Development Assistance
If you value the people around you, strive to be the best version of yourself and have a can do mindset, then Signature Health could be the best place for your next career.
Read below on how you can make a difference in our community and apply today!
SCOPE OF ROLE
Reporting to the Supervisor, BH Services the Counselor, School Based will provide an array of services to support school students and staff.
These services may include education, consultation/training, prevention, crisis intervention, and ongoing treatment.
Ongoing treatment services will be developed in response to a student's needs, including complete diagnostic assessment, case management, and individual, group, and family counseling. You will be relied on to provide excellent and complete diagnostic client assessment.
You will formulate treatment plans by providing community, home, and school based counseling services to children and their families.
HOW YOU’LL SUCCEED:
* Working primarily in the school environment, will demonstrate excellent outreach and engagement skills, forming positive relationships with school staff, students, and parents.
* Conduct comprehensive diagnostic assessments for referred students, incorporating input from students, parents and educational staff. These will be conducted at a location convenient for the family, including school, office or home.
* Develop treatment plans to meet assessed needs, including specific goals, objective and interventions.
* Facilitate referrals to other Signature Health services and community resources as needed.
* Work with school staff to plan and implement early intervention activities, including screenings, classroom...
....Read more...
Type: Permanent Location: Willoughby, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-09 08:28:29
-
Company
Federal Reserve Bank of Atlanta
As an employee of the Atlanta Fed, you will help support our mission of promoting the stability and efficiency of the U.S.
economy and financial system.
Your work will affect the economy of the Southeast, the United States, and the world.
The work we do here is important, and how we do it is just as important as what we do.
We live our values of integrity, excellence, and respect every day.
We do the right thing, we do things right, and we treat people right.
A career at the Federal Reserve Bank of Atlanta gives you the chance to do work that touches lives and helps communities prosper.
In addition to competitive compensation, we offer a comprehensive benefits package that includes tuition assistance, generous paid time off, top-notch health care benefits, child and family care leave, professional development opportunities, a 401(k) match, pension, and more.
All brought together in a flexible work environment where you can truly find balance.
Position Summary:
You will support the design, implementation and execution of the Division’s operational strategies by interacting with Division, Bank and/or System stakeholders.
Interact with and provide support for key Division, Bank and/or System projects.
Develop working relationships within the team, department, division and other business partners throughout the Bank.
Develop knowledge of multiple disciplines and participate on projects related to business operations, quality management, and operational controls.
Assist in delivering products and services that create efficiencies and improve business processes.
Anticipate potential issues or problems that arise in day-to-day operations and responds appropriately to meet stakeholders’ needs.
You will report to Supervision & Regulation's (S&R) Information Technical Director.
We are a hybrid work environment.
Key Responsibilities:
* Coordinate projects related to business and operations, quality management and operational controls while obtaining knowledge of multiple disciplines; deliver products and services to create efficiencies and improve business processes; contribute to and participate in process improvement and solution discussions
* Maintain and create reports, documents and other correspondence to stakeholders.
Create, maintain, collect and distribute key materials such as tracking spreadsheets, metrics and/or documentation
* Work on problems or projects of limited scope and basic complexity; exercise sound judgment within defined procedures and practices; follow standard procedures in analyzing situations or data from which answers can be readily obtained; receive detailed instructions on routine work and on new projects or assignment
* Identify best practices and suggest how to improve current business practices; assist in efforts to improve operations efficiency, and department services; working with others, prepare reports and materials to support proposed recommenda...
....Read more...
Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2024-04-09 08:25:54
-
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...
....Read more...
Type: Permanent Location: Onalaska, US-WI
Salary / Rate: Not Specified
Posted: 2024-04-09 08:19:05
-
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Located in Stein, Switzerland our successful CDMO Business Unit Drug Product Services (DPS) currently offers exciting opportunities.
Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and apply for the position as MSAT Expert where you will be responsible for successful drug product and manufacturing process transfers as well as implementation at the manufacturing site.
Join us to lead projects to improve and expand manufacturing capabilities across our DPS network.
Key Responsibilities:
* Participate in GMP risk analysis for the manufacturing processes and Contamination Control Strategy of the facility
* Contribute to the development and implementation of standardized MSAT procedures and processes (e.g.
qualification standard and strategy, single use system…)
* Partake in cross-functional teams as MSAT Expert tasked with technology transfers (process implementation and transfer) and timely process implementation at manufacturing scale
* Support new product introduction by evaluating/developing ‘fit for purpose’ processes
* Take care of process monitoring and process control strategy as well as complex data analysis
* Own concepts on site or across the DPS network continuously improving in quality and efficiency in compliance to cGMPs, SOPs, EHS and applicable guidelines
* Lead Performance qualification activities for new equipment, filling line or a facility and support Process Performance Qualification of Biologics License Application projects
* Lead complex product and process related investigations and deviations including complaints actions and resolve technical challenges within area of expertise.
* Maintain processes at Inspection readiness level and to provide the necessary support in any internal or external audits as well as in Back/Front office or in facility tours
Key requirements:
* University degree preferably in Biotechnology, Chemistry, Pharmacy, Engineering, Pharmaceutical Technology or equivalent scientific degree / equivalent experience
* Working experience in aseptic drug product manufacturing (clinical product and/or commercial product)
* Proven process and regulatory understanding in Sterile Manufacturing, cGMP and writing SOPs
* IT knowledge in SAP or MES is an asset
* Good communication skills and interaction with a variety of interfaces within the organization and on the shop floor
* Experience in international inspection / audit is an asset
...
....Read more...
Type: Permanent Location: Stein, CH-BL
Salary / Rate: Not Specified
Posted: 2024-04-09 08:12:01
-
PURPOSE AND SCOPE:
The Sr.
Financial Analyst provides analytical support and focus on the economic research and study in areas of financial analysis within the assigned function(s). The incumbent performs in-depth and complex analysis in compliance with company policies and procedures and applicable regulatory requirements. The Sr.
Financial Analyst facilitates accurate systems which gather, analyze, prepare and summarize recommendations for financial plans, acquisition activity, trended future requirements and operating forecasts for management review.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Utilize knowledge of accounting and/or financial principles by reviewing, reconciling and consolidating submitted financial data of complex scope on a routine basis; collaborating with cross-divisional teams on the accurate and timely resolution of outstanding issues.
* Serve as a subject matter expert (SME) by providing in-depth analysis, review and presentation of diverse financial reports.
* May provide a contribution to financial close processes on a routine basis.
* Provide essential contributions to the efficacy of operations through identification, analysis and maintenance of data; supporting management in the development and implementation of process improvements and initiatives.
* May participate in process reviews, business process analyses and internal control testing; ensuring compliance with Generally Accepted Accounting Principles (GAAP), Sarbanes-Oxley Act (SOX), and other regulatory requirements within the assigned function(s).
* May serve as a contact for cross-divisional teams.
* Mentor other staff as applicable.
* Assist with various projects as assigned by a 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.
Travel may be required including but not limited to regular department meetings in person
EDUCATION:
Bachelor’s degree required; Advanced degree desirable
EXPERIENCE AND REQUIRED SKILLS:
* 5 – 8 years’ related experience; or a Master’s degree with 3 years’ experience; or a PhD without experience.
* Excellent computer skill with strong demonstrated proficiency in Microsoft 365 suite of products - word processing, spreadsheet, business intelligence, presentation and email applications.
* Working knowledge of SAP enterprise resource planning (ERP) and financial system reporting (e.g., SAP Business Warehouse).
* Working knowledge of Anaplan budgeting and forecasting system
* Working knowl...
....Read more...
Type: Permanent Location: Waltham, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-09 08:06:04
-
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:
We have a newly created opportunity for an experienced bioprocess media development and optimization scientist with managerial experience to join our team of experts in Cell Culture Media Development as a Director of Media R&D.
This is a fast-growing team that is purely focused on innovation and a unique opportunity to help define cell culture media strategy and build a team.
Key responsibilities:
* Working closely with business development, manufacturing, operations and technical leaders from R&D to develop and execute on a bioprocess media development strategy which addresses the needs for the business units for both internal and external customers
* Lead the development and drive the implementation of the technical approach to media development and optimization
* Provide scientific and technical guidance for new bioprocess media development and optimization projects
* Manage the portfolio of bioprocess media development and optimization projects
* Provide leadership to direct reports through pro-active performance management, mentoring and coaching
* Organizing the Media R&D team in Slough UK and ensuring that it functions independently but cohesively within the Bioprocess R&D organization at Slough, UK, and engaging in cross-site collaborations with the Media R&D team in Rockville, MD, USA
Key requirements:
* Demonstrated experience and expertise in designing, developing and optimizing bioprocess cell culture media for biologically active proteins, monoclonal antibodies and biosimilars
* Deep understanding and knowledge of cell biology and the current best practices for developing bioprocess cell culture media including metabolomics and media chemistry
* Demonstrated innovative skills, experience leading complex technology projects and proven track record of successful project completion and product launches
* Strong leadership skills with demonstrated managerial experience
* Demonstrated interpersonal, presentation, time management, organizational and written/ oral communication skills.
* Demonstrated experience leading cross-matrixed/functional teams and ability to work effectively and collaboratively in a matrixed environment
* Demonstrated experience working with program management and phase/stage-gate processes to evaluate, monitor and report on progress on projects to senior leadership
* An understanding of business and financial fundamentals with a strong focus on customer-oriented solutions
Qualifications:
* PhD...
....Read more...
Type: Permanent Location: Slough, GB-SLG
Salary / Rate: Not Specified
Posted: 2024-04-09 08:05:44
-
ABOUT THE ROLE
Amsted Automotive, Piston Pin Geneva, IL is looking for a Quality Gauge Technician to perform duties to maintain gauge systems and issue gauges to production personnel.
WHAT YOU'LL DO
* Work from instructions, prints, product certifications, standards and process
specifications.
* Issues and sets tolerances on gauges for production personnel according to print or
instruction sheets.
* Repair mechanical gauges and determine when gauges need to be replaced.
* Perform gauge and standard calibrations in accordance with the prescribed schedule.
* Perform equipment and standards calibrations.
* Train and assist operators on gauging applications.
* Perform necessary recordkeeping and paperwork.
* Participate in team problem solving as part of the departmental continuous improvement
* process.
* Understand and performs ISO 14001 work instructions as identified in, “ISO 14001
* Work Instruction Assignments.
* Follow all safety rules and keep work area clean and in an orderly condition.
* Wear all personal protective equipment as required by the safety policy.
* Be responsible and accountable for the professional use of assigned work periods, machinery, equipment and tools.
* Understand and perform to the BN Quality Policy taking pride in the products produced.
* Perform other miscellaneous duties as assigned.
WHAT YOU NEED TO SUCCEED
* Blueprint reading, metrology
WHAT ELSE YOU'LL NEED TO KNOW
* The physical requirements described here are representative of those that must be met by an employee to successfully perform the functions of this job.
Reasonable accommodations will be considered for those with specific physical restrictions.
* Physical requirements include good speaking, hearing and vision ability, excellent
manual dexterity, ability to lift and carry up to 25 pounds occasionally.
* Work is performed in a typical manufacturing environment with exposure to noise and heat with several elements continuously present to the extent of being objectionable.
* Full-time position.
May require overtime and weekend hours.
Experience
Required
* 1 year(s): Working with quality gauges
Education
Required
* High School or better
See job description
....Read more...
Type: Permanent Location: Geneva, US-IL
Salary / Rate: Not Specified
Posted: 2024-04-09 08:05:17
-
Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Roche in Kürze:
Wir bringen die Wissenschaft voran, damit wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Über die Abteilung:
Die Hauptabteilung „Diagnostics Operations Mannheim“ am Standort Penzberg sieht sich in der Verantwortung, dass Patienten präzise medizinisch-diagnostische Resultate erhalten.
Hierfür beliefern wir Patienten, Labore und Krankenhäuser mit diagnostischen Reagenzien und Teststeifen und agieren mit größter Sorgfalt und Leidenschaft.
Und dafür brauchen wir Dich!
Wenn du folgendes Profil hast, bist du der Richtige für uns und kannst in der Abteilung „Diagnostic Operations“ durchstarten, Dein Wissen an uns weitergeben und Deine Kompetenzen in einem der größten Pharmaunternehmen der Welt noch weiter ausbauen:
* Du hast eine Ausbildung als Chemie- oder Biotechniker erfolgreich abgeschlossen oder hast alternativ eine erfolgreiche Ausbildung als Chemielaborant oder Biologielaborant mit zusätzlicher relevanter Berufserfahrung von > 5 Jahren hinter dir
* Alternativ hast du ein Bachelorstudium abgeschlossen
* Du bringst Erfahrung in einer ähnlichen Position in einem Produktionsbetrieb der chemischen Industrie speziell im GMP-Umfeld mit
* Neben PC-Kenntnissen der gängigen Microsoft-Anwendungen und dem sicheren Umgang mit SAP besitzt du Grundkenntnisse der englischen Sprache in Wort und Schrift
* Du sprichst fließend Deutsch
In der Position als Facharbeiter Produktion (m/w/d) erwartet Dich ein umfangreiches Aufgabengebiet mit interessanten Verantwortlichkeiten:
* Du bist zuständig für die termingerechte Herstellung von diagnostischen Reagenzien, entsprechend der Herstellanweisungen unter Einhaltung der geltenden GMP-Regeln
* Die GMP gerechte Dokumentation der durchgeführten Prozessschritte sowie die Erstellung und regelmäßige Pflege von Arbeitsanweisungen gehören ebenso zu Deinen Aufgaben
* Die Produktprüfung durch produktionsbegleitende Sonderuntersuchungen und die anschließende Auswertung und Dokumentation der Prüfergebnisse liegt ebenfalls in deiner Zuständigkeit
* Die Planung, Durchführung und Dokumentation von Qualifizierungen und Validierungen gehört ebenso zu deinen Aufgaben, wie die Erstellung von Vorgabedokumenten
Deine Bewerbung
Wir machen’s.
Einfach.
Bitte lade nur Deinen Lebenslauf online hoch.
Zum aktuellen Zeitpunkt benötigen wir kein Motivationsschreiben, Zeugnisse oder Ähnliches.
Wir freuen uns auf deine Bewerbung!
Your contact to us! With people.
For people.
Do you need further support?
Please have a...
....Read more...
Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-04-09 08:04:10
-
The Environmental Health and Safety (EHS) Technician will assist with management of the safety and environmental programs.
The role will provide oversight of site safety and environmental compliance activities and programs and will lead/support EHS initiatives and inform management of critical issues.
The EHS Technician will perform safety risk management as well as EHS compliance audits, EHS incident investigations, problem solving and overall policy/program training.
The EHS Technician will participate in continuous improvement initiatives, as required.
This position will report directly to the EHS Manager and is located at the VAM USA - Miller Road facility in East Texas.
RESPONSIBILITIES:
* Ensure consistent adherence to, and execution of, Company safety and environmental standards.
* Provide technical support in management of EHS related topics including: Lockout, Confined Space, Emergency Response, Hazard Communication, Overhead Cranes, Mobile Equipment, Cardinal Safety Rules, Waste Management, Spill Response, Storm Water etc.
* Perform onsite safety audits of employees, processes, contractors, vendors, etc.
* Recognize process safety conditions and coach operations staff accordingly.
* Manage HSE incident investigations and reporting, including root cause analysis, development of corrective action strategies, maintaining statistical information, recommending program revisions as appropriate and issue required reports to management.
* Provide technical support and problem solving in troubleshooting safety and environmental issues
* Coordinate and instruct safety-related training classes, and act as subject matter expert for Safety meetings.
* Vendor interface for company policy communications & expectations
* Know and follow all Health, Safety and Environmental (HSE) policies always.
* Always know and use appropriate Personal Protective Equipment (PPE).
* Exercise stop work authority in the event of unsafe conditions or situations.
* Assist in writing technical and management systems reports and documents
* Establish and maintain EHS controls and documentation procedures
* Assist with internal compliance audits and program evaluations
* Oversee department sub-contractor support as needed
* Support the EHS department as a valuable and knowledgeable resource
* May conduct other tasks as required
EXPERIENCE, SKILLS, AND KNOWLEDGE:
* HSE regulatory knowledge
* Environmental regulatory knowledge
* Outstanding communication skills
* Highly organized and able to successfully manage multiple projects
* Capable of working independently in a self-directed environment
EDUCATION, TRAINING, AND CERTIFICATIONS:
* Associate of Science degree in Safety or any HSE-related discipline required
* First responder/CPR trained (desired)
* Experience with OHSAS 18001, ISO 14001, ISO 45001, Integrated Management Systems, and associated ...
....Read more...
Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2024-04-08 08:00:12
-
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!
Director - Occupational Health Services
The Director - Occupational Health Services provides strategic direction for US Occupational Health Services and operational oversight of the US Occupational Health Services team located within manufacturing sites in Indiana, Iowa, Maine, and Kansas and the corporate headquarters, which includes Worker’s Compensation and Workplace Accommodations for the US.
Primary Functions, Duties, Tasks:
* Partners with HR/HSE leaders at US locations on OHS processes and procedures to ensure consistency of practices.
* Oversight of Elanco’s Medical Surveillance programs and procedures.
* Leads or actively participates in projects as US OHS subject matter expert.
* Responsible for coordinating, managing, planning, and developing policies and procedures to provide high quality occupational health services that meet all internal and external requirements.
* Provides consultation for HR, EEO, legal, absence management, corporate health and safety, benefits, line management, corporate communication, Elanco Health Plans, and community health projects and programs, and international employee health programs.
* Partnership and collaboration with Health, Safety, Environmental (HSE) on development, implementation and continuous improvement of processes and procedures related to employee health and wellbeing.
* Provides medical consultation for emergency medical response teams in the US.
* Ensure clinics are appropriately staffed and resourced at all times.
* Ensures clinic staff are appropriately trained and act in accordance with privacy and OSHA regulations.
* Oversight of Elanco’s case management program, ensuring consistency and compliance with all applicable laws and regulations. This includes evaluating claims to ensure disability duration guidelines are maintained when applicable and leading continuous improvement initiatives within case management.
* Oversee the performance of Elanco’s workers’ compensation third-party administrator.
* Develop OHS polici...
....Read more...
Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 135000
Posted: 2024-04-07 07:59:22
-
What Will Your Job Look Like?
The Manager, Safety and Training is responsible for implementing safety and training programs as defined by the Leadership of Safety Administration and will ensure compliance with State and Federal regulations, as well as corporate, client guidelines and policies.
This position will sit in Colorado Springs, CO and is contingent upon contract award.
What You’ll Do:
* Manage a consistent safety culture that incorporates various departments, such as operations, safety and maintenance
* Oversee Corporate Safety Incentives and programs effectively and consistently, including assignment of Safety Points
* Implement and support the company and client’s safety management system (SMS) safety plan and initiatives Manage and monitor the FTA’s drug and alcohol DAMIS reporting requirements
* Monitor and support all location insurance claims activities to ensure effective communication with claimants, to help control claims costs and support claims closure
* Lead and support the local safety committee and SMS Ambassador group
* Oversees the locations worker compensation program to ensure compliance and effectively reduce/eliminate claims
* Deliver proper classroom, behind the wheel and mobility management training in accordance with contractual and company requirements
* Promote employee self-responsibility to achieve all safety goals and training requirements
* Ensures all new hires meet minimum qualifications for each division including, background and DMV checks
* Ensure all safety manuals, programs and policies and practices are current and meet the needs of the operating divisions; updating as appropriate
* Successfully complete all related audits including those conducted by the Company, the Client, internal staff members, and state and federal regulatory agencies
* Review, determine and respond to all vehicular, passenger and employee accidents/incidents, indicating the cause and preventability, identifying potential trends to be addressed in future training efforts
* Provide functional expertise in safety regarding hiring of safety department employees
* Collaborate with local Leadership to deliver comprehensive safety meetings and plans
* Act as the location drug program manager, ensuring compliance of FTA/DOT regulations
What You’ll need:
* High School Diploma or G.E.D.
* Bachelor’s Degree (or equivalent combination of education and experience) in a related field
* Minimum 5 years of transit safety management experience
* Previous management experience in a union environment
* Thorough knowledge of all applicable safety rules, regulations – ADA, FTA and DOT to include all corporate programs
* Must have completed the Public Transportation Safety Certification Training Program (PTSCTP) Bus Track curriculum
* Must possess a valid driver’s license
* Must be able to pass a pre-e...
....Read more...
Type: Permanent Location: Colorado Springs, US-CO
Salary / Rate: Not Specified
Posted: 2024-04-07 07:58:39
-
PURPOSE AND SCOPE:
The Clinical Project Manager is a high impact, leadership role responsible for key elements of program execution within Frenova's Team.
The CPM role requires a talented individual with proven expertise in leading cross functional teams and driving the study planning, startup and execution. The CPM in partnership with the Frenova team members, Sponsor, CRO staff, vendors and Study sites, will drive study management and ensure clear and timely communication of project strategy implementation plans and program progress.
The CPM will work to ensure the cross functional teams operate effectively with Positive team dynamics driving study progress. The CPM is expected to be knowledgeable about the overall indication, study product and over all development in order to be strategic in planning, program progress, oversight, communication and site management, delivering high quality project management expertise, leadership and other high value services that support the team and improve the probability of study success.
The CPM acts as the team leader, ensuring that assigned studies are delivered successfully, on-time, within budget and with the highest level of quality possible.
The CPM monitors and tracks the progress of clinical study activity at research sites ensuring compliance with all local, state and federal regulatory requirements.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Responsible for the routine cross-functional operations of the assigned study or studies for one or more clients.
* Ensures the Trial Master File documents for assigned sites is maintained and ready for inspection.
* Provides support with regulatory agency and sponsor inspections/audits.
* Provides leadership and assistance to Project Assistant/Associate level staff with complex tasks that require a high level of understanding of functions.
* Motivates cross-functional project teams, facilitating the team's ability to fulfill their responsibilities in accordance with project contracts, contract amendments, applicable regulatory, ICH GCP and Standard Operating Procedure (SOP) requirements and company policies and procedures.
* Functions as a liaison between Sponsor/CRO and the project team for project issues, including initiating, planning, executing, overseeing, and closing out of assigned studies.
* Coordinates and manages day to day operational aspects of multiple concurrent projects with competing timelines independently and as defined in each project's scope.
* Develops and maintains project metrics, timelines, budgets and deliverables including project plans, trackers and tools for assigned projects.
* Utilizes defined guidelines and checklists, supports the coordination, oversight and tracking of clinical research studies, and ensures clinical activity receives appropriate regulatory approvals and is conducted in compliance with the protocol and OHRP, ICH/GCP guidelines, FDA regulations, an...
....Read more...
Type: Permanent Location: Waltham, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-07 07:58:05
-
PURPOSE AND SCOPE:
Under general supervision, the Credits Representative identifies, analyzes and resolves credit balances within the assigned portfolio of accounts. The credit representative applies acquired job skills in the performance of credit responsibilities in compliance with company policies and procedures.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Perform assigned responsibilities in compliance with company policies and procedures; meeting or exceeding goals within company-defined timelines.
* Principle responsibility to work credit balances to resolution by identifying type of credit and taking the appropriate action to resolve.
* Identify, analyze, and research refund requests from Commercial, Government and Patient for accuracy and submission for refund to be submitted.
* Submit appropriate Cash Corrections and adjustments in system to resolve posting issues that are causing credit balances.
* Perform insurance verifications and take appropriate action to resolve COB issues that are causing credit balances.
* Contact insurance to verify that credit balance is still outstanding with Insurance and follow appropriate steps to resolve credit on account based on Insurance response.
* Ability to identify credits caused by trends and report to team lead/manager for appropriate action to resolve issue.
* Assist with various projects as assigned by direct supervisor.
* Other duties as assigned.
Additional responsibilities may include focus on one or more departments or locations.
EDUCATION:
High School Diploma required.
EXPERIENCE AND REQUIRED SKILLS:
* 1 - 2 years' related experience in the medical field for credit or insurance collections.
* Knowledge of state statute limitations helpful.
* Good computer skills with demonstrated proficiency in word processing, spreadsheet, database and email applications.
* Detail oriented with good analytical and organizational skills.
* Good time management skills with the ability to multitask concurrent priorities in an organized manner.
* Must be able to work independently with minimal supervision as necessary, and alternately work cohesively within a team environment.
* Possess a positive, enthusiastic and energetic attitude.
* Strong oral and written communication skills to effectively communicate with 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.
....Read more...
Type: Permanent Location: Kennesaw, US-GA
Salary / Rate: Not Specified
Posted: 2024-04-07 07:57:54
-
PURPOSE AND SCOPE:
The professional registered nurse Inpatient Services RN CAP 1 is an entry level designation into the Clinical Advancement Program (CAP). This position is accountable and responsible for the provision and coordination of clinically competent care including assessment, planning, intervention and evaluation for an assigned group of patients.
This may include delegation of appropriate tasks to direct patient care staff including but not limited to RNs, LVN/LPNs and Patient Care Technicians.
As a member of the kidney disease health care team, this position participates in decision-making, teaching, leadership functions, and quality improvement activities that enhance patient care outcomes and program operations.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
All duties and responsibilities are expected to be performed in accordance with Fresenius Kidney Care, policy, procedures, standards of nursing practice, applicable contractual service agreements, state and federal regulations.
* Performs all essential functions under the direction of the Supervisor and with guidance from the Educator, Preceptor or in collaboration with another Registered Nurse.
* Performs ongoing, systematic collection and analysis of patient data pre – during – post treatment for assigned patients and documents in the patient medical record, makes adjustments and modifications to treatment plan as indicated and notifies Supervisor, Physician, patient’s primary nurse and others as may be indicated.
* Assesses, collaborates and documents patient/family’s basic learning needs to provide initial and ongoing education to patients and family.
* Recognizes aspects and implications of patient status that vary from normal and reports to or collaborates with appropriate health team members for input including but not limited to Supervisor, appropriate physician, and the contracted facility primary Nurse.
* Directs and provides safe effective patient care for assigned patients as prescribed for all modality specific treatment procedures.
* Assesses daily assigned patient care needs and collaborates with direct and ancillary patient care staff as needed.
* Initiates and coordinates communication with FKC and Non-FKC dialysis providers and appropriate contracted facility personnel as needed to provide continuity of patient care.
* Performs the implementation, administration, monitoring, and documentation of patient's response to prescribed intradialytic transfusions, including appropriate notification of adverse reactions to physician and appropriate blood supplier.
* Administers medications as prescribed and documents appropriate medical justification and effectiveness.
* Initiates and assists with emergency response measures.
* Serves as a resource for health care team, participates in staff training and orientation of new staff as assigned.
* May be asked to provide specialized nursing care instruc...
....Read more...
Type: Permanent Location: Baltimore, US-MD
Salary / Rate: Not Specified
Posted: 2024-04-07 07:56:44
-
Qualified Mental Health Specialist (QMHS)
Are you looking for an organization where you can grow while making a positive impact on people's lives? At Signature Health, our purpose is to provide integrated healthcare for our community specializing in patients with mental illness and/or addiction because we want people to realize their highest potential.
Our core values are the foundation of who we are:
* People First mindset where we honor our colleagues and patients
* Striving for Excellence in our work each day
* Can Do approach where we roll up our sleeves in response to opportunities and challenges
In addition to a rewarding career, as a full-time employee, you will have access to the following employer/employee paid benefits:
Full Time:
* Medical, Dental, Vision
* Robust earned paid time off program (PTO)
* 401k match
* Various Life Insurance Options
* Short- and Long-Term Disability (Not applicable for school-based employees)
* Federal Loan Forgiveness Program (available on eligible on roles)
* HealthJoy - no cost medical and mental health online resources available Day 1 (coverage extends to family members living in the same household)
* Tuition & Professional Development Assistance
If you value the people around you, strive to be the best version of yourself and have a can do mindset, then Signature Health could be the best place for your next career.
Read below on how you can make a difference in our community and apply today!
SCOPE OF ROLE
Reporting to the Supervisor and Manager, Behavioral Health Services, the Qualified Mental Health Specialist (QMHS) will be key in the development and execution of patient treatment plans.
You will provide patients and their families with ongoing community support resources including transportation for access to identified resources.
The QMHS acts as an outstanding subject matter expert related to patient needs and will foster positive relationships to all patients, their families, and Signature Health team members.
HOW YOU’LL SUCCEED:
* Diligently develop, prepare and present treatment program work material to patients.
* Plan, coordinate, and provide reliable transportation to patients to access identified resources as part of their treatment plans.
* Maintains clear communication and professional boundaries with all patients.
* Act as a subject matter expert and provide support in accessing and developing a sober support network.
* Collaborates effectively with a patient's treatment team.
* Create an outstanding experience for both adult and child patients (SMD/SED, CD/Dual DX) by identifying support needed in the following areas: educational, medical, vocational, housing, and daily living skills resulting in patients becoming successful in their communities.
* Encourage, monitor, and follow-up on client engagement and participation in all treatment plan activities.
* Serve as a liaison wi...
....Read more...
Type: Permanent Location: Ashtabula, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-06 08:39:00
-
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.
This is your opportunity to help share the future of sustainability with world-changing innovations and low-carbon technologies.
Become a valued part of the team that’s shaping the future of aluminium, revolutionising the way the world lives, builds, moves and flies.
Be part of it and shape your world.
About the Role:
Do you love solving problems? Do you thrive working in a diverse role where every day presents new challenges and activities? Then we have just the position for you!
A rare opportunity exists for a Technician to join our Occupational Hygiene team supporting our smelter operations and the Environment, Health & Safety team.
Working across all levels of our operations, you will be a key contributor in carrying out the site exposure monitoring and assessment program which enables effective identification, evaluation and control of hazardous work-place exposures to prevent workplace injuries.
You will be required to produce reports and communicate your findings based on the sampling, analysis and interpretation of the results that you've acquired.
The data collected and information prepared is used to uphold Alcoa's values in health and safety and to comply with corporate EHS policies, standards and legislation.
Other duties and responsibilities will include:
* The development and periodic maintenance of a plant job/task dictionary.
* Conducting and completing the site quantitative base-line exposure assessment monitoring plan using air sampling, biological monitoring and physical measuring techniques.
* Working with the operating department supervisors and employees to ensure that personal exposure monitoring can be carried out with area cooperation.
* Interpreting exposure data collected to identify significant and unacceptable exposures for the areas and makes recommendations to identify means of controlling and minimising potentially hazardous exposures.
* Entering and maintaining relevant Occupational Health data into the computer data management systems.
* Responding to EHS related requests for help from areas within the plant in answering and resolving workplace health issues, including those relating to hazardous material mgt.
* Assisting the areas where significant exposure hazards have been identified and evaluate feasible control options in consultation with the Occupational Hygienist and EHS team.
What’s on offer:
* Career development opportunities to pursue your passion
* Monthly Leisure Day
* Benefits allowance
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
To play a part in our ongoing s...
....Read more...
Type: Permanent Location: PORTLAND, AU-VIC
Salary / Rate: Not Specified
Posted: 2024-04-06 08:19:53
-
Your Job
INVISTA is looking for a Research and Development Intern that is technology-driven and who continually develops new capabilities consistent with their innate abilities and evolving business needs.
The successful applicant will demonstrate initiative, challenge the status quo, prioritize work based on risk and value, be solution-oriented, and meet deadlines.
You will need to apply interpersonal skills and contribute positively to a team-oriented environment while using analytical thinking and problem-solving skills and have a commitment to ongoing learning and developing new skills.
INVISTA customers and employees are located across the globe.
In this role, you will collaborate with colleagues in our Kennesaw, GA office and globally.
The role will focus on driving testing of products through external and/or internal labs, analyzing results, comparing the properties of various products, and documenting the findings through presentations, reports, and articles.
Our Team
In this role, you'll be a part of the Downstream Fibers Team located in Kennesaw, GA.
We believe that the very best products start with the best ingredients, and that starts with the ingredients that make up our business: our people, our culture, our innovation, and our brand.
Together, these create our sustainable and superior fiber and fabric solutions for our customers and society.
What You Will Do
• Collaborate with external and/or internal labs to test textile products.
• Analyze large data sets to generate knowledge systems that present actionable information.
• Document test work through reports, program review presentations, and articles.
• Understand the state of the art in technology through literature searches, patent searches, and discussions with subject matter experts.
• Collaborate with colleagues across the business.
Embrace the peer challenge process with intellectual honesty to deliver best solution.
• Work with a sense of urgency and apply critical and economic thinking to create sustaining value solutions.
Who You Are (Basic Qualifications)
* Currently enrolled in a university program studying Chemical Engineering, Polymer Science, or Material Science
* Experience with statistical and data analysis
What Will Put You Ahead
• Interest in polymer, textile, or fiber applications
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.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgroun...
....Read more...
Type: Permanent Location: Kennesaw, US-GA
Salary / Rate: Not Specified
Posted: 2024-04-06 08:19:44
-
Your Job
INVISTA Nylon Polymer customers are located across the globe.
Centered in Shanghai, our Nylon Polymer Research and Development team is focused on delivering and commercializing innovative solutions to the global business.
With today's ever-increasing rate of change, we are transforming our R&D to be a competitive advantage for INVISTA.
Utilizing advanced development facilities in Shanghai, the role will focus on delivering innovative technical solutions to our global business and manufacturing facilities.
R&D will drive value through disciplined application, innovation, rapid experimentation, and critical economic thinking.
We are looking for a Research and Development Scientist that is technology-driven and who continually develops new capabilities consistent with their innate abilities and evolving business needs.
What You Will Do
* Identify and propose innovative research projects that will provide competitive advantage and have significant value creation potential.
* Lead and/or collaborate on new product developments for feedstock resins for new-to-market products and for products in our current portfolio.
* Deliver innovative solutions against business opportunities through planning and relationships with global teams, commercial development teams and operations.
* Conduct research and perform experiments using our advanced development facilities.
* Understand problems within the market to research potential applications; research market to ensure up to-date with relevant scientific and technical developments.
* Perform root cause analysis and critical thinking to develop a point of view on market opportunities and risks.
* Plan and execute laboratory and semi-works testing that demonstrates the commercial viability of new technologies that improve and broaden our portfolio.
* Support technology scale-up and commercialization in global production facilities.
* Build strong collaborative relationships with researchers and technicians as well and manufacturing and business leaders.
* Stay abreast of the competitive landscape and external polymer applications as sources of insight and inspiration.
* Execute responsibilities with excellence in EHS and compliance.
* Mentor and support coworkers to enhance their overall productivity and effectiveness.
Who You Are (Basic Qualifications)
* Degree in Chemical Engineering, Polymer Science, or Material Science
* At least 3 years of industrial research experience
* Experience with statistical and data analysis
* Interest in Polymer applications
What Will Put You Ahead
* Graduate level in Engineering, Chemical, Material Science or related discipline
* 5+ years of industrial experience in polymer processing
* 5+ years in Polymer Chemistry
* Experience in research and development of a wide range of materials or polymers.
* Experience in patent development and landscaping
At Koch c...
....Read more...
Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2024-04-06 08:15:32