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<h3>Job Description</h3>
\n Clean Harbors in Poca, WV is seeking an Environmental Field Chemist (CleanPack Chemist) to handle, segregate, pack, and inspect chemical waste in accordance with Federal/State/Local regulations and our company policies and procedures.&nbsp; &nbsp;This position will work both indoors and outdoors at plants, labs, customer sites and are responsible for assisting with lab packs within customer facilities, household hazardous waste (HHW) collections and lab moves.&nbsp; This is a customer facing position, working at customer sites daily. The Environmental Field Chemist are (NOT) laboratory-based Chemist.\n\n\n &nbsp;\n\n\n Clean Harbors is the leading provider of environmental, energy and industrial services throughout the United States, Canada, Mexico and Puerto Rico.&nbsp; Everywhere industry meets environment, Clean Harbors is on-site, providing premier environmental, energy and industrial services. We are solving tough problems through innovation and proven methodology – come be part of the solution with us.\n\n\n &nbsp;\n\n\n Why work for Clean Harbors?\n\n\n
<ul>\n
<li>Health and Safety is our #1 priority and we live it 3-6-5!</li>
\n
<li>Focus on maintaining sustainability and cleaning the Earth&nbsp;</li>
\n
<li>Pay Range: 21.00 -24.00 per hour, BOE</li>
\n
<li>Monday–Friday, and Saturdays as needed, 5:00 AM–5:30 PM, with up to one week of overnight travel per month.</li>
\n
<li>Comprehensive health benefits coverage after 30 days of full-time employment including 401K with Company match</li>
\n
<li>Own part of the company with our Employee Stock Purchase Plan</li>
\n
<li>Opportunities for growth and development for all the stages of your career</li>
\n
<li>Company paid training and tuition reimbursement</li>
\n </ul>
\n
RESPONSIBILITIES
\n \n Key Responsibilities:\n \n
<ul>\n
<li>Ensure that Health and Safety is the number one priority by complying with all safe work practices, policies, and processes and always acting in a safe manner</li>
\n
<li>Prepare computer generated packing lists, labels, manifest, and land disposal restriction notifications</li>
\n
<li>Perform inspections of staging, accumulating and storage areas to ensure proper housekeeping procedures and compliance</li>
\n
<li>Inspect storage area and drums for leaks or spills</li>
\n
<li>Inspect drums for compliance with labeling regulations</li>
\n
<li>Collects, segregates, and properly packages waste chemicals for disposal to maximize efficiency and maintain compliance</li>
\n
<li>Executes Jobs at Clean Harbors customer locations including fortune 500 companies</li>
\n
<li>Responsible for final preparation and approval of all projects before shipment in accordance with OSHA, EPA, DOT and company policies</li>
\n
<li>Conducts projects/jobs according to site specific Federal, State, and local regulations and health and safety plans</li>
\n
<li>Understand customer specific disposal restrictions/special packaging requirements</li>
\n
<li>Sample and profile of new waste streams or any waste needing analytical testing</li>
\n
<li>Ensures drum count is correct and that drum conditions are shippable in accordance our company’s policies and procedure</li>
\n
<li>Follow all local, state (provincial) and federal compliance regulations and rules</li>
\n
<li>Safely operate vehicles in accordance with U.S. DOT, local, state (provincial) and federal requirements</li>
\n
<li>Safely observe all corporate operating guidelines and procedures</li>
\n
<li>Observe all company environmental health and safety operating guidelines</li>
\n
<li>Perform other duties as assigned</li>
\n </ul>
\n
QUALIFICATIONS
\n \n Required Qualifications:\n \n
<ul>\n
<li>Valid Driver’s license</li>
\n
<li>Strong customer service skills</li>
\n
<li>By position, obtain a CDL Class B with hazmat and tanker endorsement within 6 months of employment</li>
\n
<li>Perform physical functions per job requirements</li>
\n
<li>Successfully complete a background check, drug test, and physical, by position</li>
\n
<li>Per OSHA's Respiratory Protection Standard, 29 CFR 1910.34, employees in positions requiring respirators are required to meet facial hair standards.</li>
\n </ul>
\n\n\n Preferred Qualifications:\n\n\n
<ul>\n
<li>College degree in Chemistry or Natural Science</li>
\n
<li>Previous experience in Environmental Services (i.e. remediation, abatement, emergency spill response, etc.)</li>
\n </ul>
\n\n\n &nbsp;\n\n\n \n Our Environmental Field Chemist is an entry level position into an exciting and rewarding career at Clean Harbors. Transitioning Military, this is a great opportunity to leverage your skills, experience, and training as you return to civilian life.\n \n \n &nbsp;\n \n \n This position is an entry level management position.&nbsp; &nbsp;From this role, there are approximately 15 other roles one can be promoted into within Clean Harbors.&nbsp; A significant number of our middle and senior management staff all started in this role, from less than 5 years ago to 30 plus years ago.&nbsp; Many others who have started in this role have significant positions within our customers as Environmental Health and Safety staff members at significant universities, pharmaceutical manufacturers as well as other customers.&nbsp;\n \n \n &nbsp;\n \n \n We will accelerate your training, so you learn the skills and knowledge to succeed in this position and start your career.&nbsp; You can work in any of our 200+ branch locations and can transfer internally.&nbsp; After successfully learning this position in approximately 18 to 36 months, then you will have the opportunity to move into a Salary Management position.&nbsp;&nbsp;\n \n \n &nbsp;\n \n \n Clean Harbors Technical Services\n \n \n
<ul>\n
<li>Waste Disposal – Comprehensive disposal of hazardous and non-hazardous waste at Company-owned facilities</li>
\n
<li>Recycling Services – Extensive recycling, reuse and reclamation options for materials such as solvents, chemicals, oil and electrical equipment</li>
\n
<li>Chemical Packing – Safe, efficient handling and disposal of the widest range of chemicals, including reactives and compressed gases</li>
\n
<li>Household Hazardous Waste (HHW) Services – HHW collection programs of all types and sizes, facilitated by Clean Harbors expert personnel&nbsp;</li>
\n </ul>
\n \n \n &nbsp;\n \n \n
Clean Harbors is an equal opportunity employer.&nbsp;
\n
Clean Harbors is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation, contact <a href="mailto:ect@cleanharbors.com" target="_blank">ect@cleanharbors.com</a>&nbsp;or 1-844-922-5547.
\n \n
Clean Harbors is a Military &amp; Veteran friendly company.
\n
 &nbsp;
\n
Clean Harbors is committed to complying with applicable pay transparency laws and ensuring fair and equitable compensation. The posted salary range reflects the minimum and maximum target for this role. Final compensation may vary based on factors such as location, experience, skills, and business needs. In addition to the base salary, some roles may be eligible for bonus or incentive compensation and a comprehensive benefits package.
\n
#CH
\n \n

Enviromental Field Chemist

<h3>Job Description</h3>
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
Job Title: Analytical Lab Supervisor (3rd shift)
Working at Abbott&nbsp;
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:&nbsp;
<ul>
<li>Career development with an international company where you can grow the career you dream of.</li>
<li>Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.</li>
<li>An excellent retirement savings plan with a high employer contribution.</li>
<li>Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.</li>
<li>A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.</li>
<li>A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.</li>
</ul>
The Opportunity&nbsp;&nbsp;
This position works out of our Sturgis, MI location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives.&nbsp;
For over 70 years, Abbott’s Sturgis, Mich., has been impacting its community while producing products that provide essential nutrition to millions of families around the world. Working here, you’ll feel part of a family that is dedicated to making a difference and helping others.&nbsp;
What You'll Work On
The&nbsp;Analytical Laboratory Supervisor is responsible for and is an active leader in ensuring major objectives are met.&nbsp; Major objectives include:&nbsp; assuring regulatory compliance, meeting production schedules, creating and maintaining a high level of employee relations, satisfying all customer service needs&nbsp;and ensuring budgetary and financial goals are met.&nbsp; An excellent understanding of the manufacturing&nbsp;of products is required, as well as expert knowledge of the Processing and Analytical batch work orders.
<ul>
<li>Responsible for the overall results of a single shift of a 7-day multi-shift laboratory operation</li>
<li>Model and promote the behaviors that ensure delivery of high-quality products for our customers while championing compliance with Abbott policies and procedures, meeting all local and statutory requirements&nbsp;and adhering to the regulatory requirements of countries to which products are shipped</li>
<li>Initiate, manage and make decisions which impact product quality</li>
<li>Manage financial statements and budgetary responsibilities; share accountability for line budgetary decisions with direct manager.&nbsp; Track, trend, and continuously improve budgetary performance for overtime(OT), direct expenses, HPL, labor, year over year CIP and material usage&nbsp;(Note: This list is not all inclusive)</li>
<li>Understand all key performance indicators, developing, driving and leading the execution of plans through utilization and involvement of all team and support resources</li>
<li>Develop plans and execute efforts required to train and develop employees to improve overall laboratory capability to deliver performance results</li>
<li>Create a learning environment and support individual's learning and development plants.&nbsp; Coach and direct individuals and teams to meet performance goals and objectives</li>
<li>Directly supervises team and leads staffing activities</li>
<li>Assist in maintaining an operating budget for the Analytical and Incoming Material QA laboratories</li>
<li>Manage laboratory personnel&nbsp;including staffing, performance reviews,&nbsp;train and develop personnel&nbsp;and maintain safe lab environment</li>
<li>Assist in problem solving efforts related to laboratory issues</li>
<li>Provide technical guidance and support to plant</li>
<li>Assure lab test results reflect compliance to plant, division&nbsp;and corporate guidelines and procedures</li>
<li>Assure test methods are followed</li>
</ul>
You’ll be accountable for meeting our compliance standards including FDA, OSHA and Abbott policies and procedures.&nbsp;
Required Qualifications
<ul>
<li>High School Diploma / GED</li>
<li>Bachelor’s degree in science, food technology;&nbsp;technical OR 5+ years of experience in a laboratory in a regulated industry with preference being for food, pharmaceuticals, medical devices, cosmetics, etc.</li>
<li>Proven performance in leading a high volume manufacturing support laboratory</li>
<li>Proven leadership capabilities</li>
<li>Project planning &amp; execution experiences</li>
<li>Process control knowledge</li>
<li>Proven plant financial understanding</li>
<li>Experience with working on Continuous Improvement Projects</li>
</ul>
Preferred Qualifications
<ul>
<li>Advanced degree in science, food technology;&nbsp;technical</li>
<li>7+ years or experience in a laboratory in a regulated industry with preference being for food, pharmaceuticals, medical devices, cosmetics, etc.</li>
<li>Previous experience working in a laboratory in a regulated manufacturing work environment with emphasis on infant formula manufacturing experience</li>
<li>Experience utilizing project planning and execution tools</li>
<li>Knowledge of FDA – 21 CFR and other regulatory requirements for Infant Formula</li>
</ul>
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. Pre-Employment Inquiries and Citizenship | U.S. Equal Employment Opportunity Commission (eeoc.gov)&nbsp;
Apply Now&nbsp;
* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.&nbsp;
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  <a href="http://www.abbottbenefits.com&nbsp;&amp;nbsp" target="_blank">www.abbottbenefits.com&nbsp;&amp;nbsp</a>;
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity and Military/Veteran friendly Employer, committed to employee diversity.&nbsp;
Connect with us at <a href="http://www.abbott.com" target="_blank">www.abbott.com</a>, on Facebook at <a href="http://www.facebook.com/Abbott" target="_blank">www.facebook.com/Abbott</a>, and on Twitter @AbbottNews.
 
The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

Analytical Laboratory Supervisor (3rd shift) - Sturgis, MI Plant

<h3>Job Description</h3>
Job Description
Help us change lives
At Exact Sciences, we’re helping&nbsp;change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.
Ready to kickstart your journey in healthcare and science? Join Exact Sciences as a Lab Processing Associate and become part of a team that’s changing lives through early cancer detection.
What You’ll Do:
<ul>
<li>
Be hands-on with cutting-edge lab technology—mixing samples, operating automated equipment, and keeping things running smoothly.
</li>
<li>
Support your teammates with essential tasks like racking samples, cleaning, and routine maintenance.
</li>
<li>
Help ensure every sample is processed with precision and care—because every one of them represents a real person counting on us.
</li>
</ul>
Why It Matters: You’ll play a key role in helping patients get accurate, timely results. It’s more than lab work—it’s purpose-driven science that makes a difference.
What’s In It for You:
<ul>
<li>
Learn on the job with guidance from experienced supervisors.
</li>
<li>
Build skills in biotech, automated lab operations, and teamwork.
</li>
<li>
Be part of a mission-focused company that values innovation, collaboration, and growth.
</li>
</ul>
Who You Are:
<ul>
<li>
A detail-oriented team player who’s curious, reliable, and ready to learn.
</li>
<li>
Someone who thrives in a fast-paced, supportive environment.
</li>
<li>
Looking for a meaningful role where your work truly matters.
</li>
<li>
Reliability starts with showing up—be the teammate others count on
</li>
</ul>
Minimum Qualifications
<ul>
<li>High School Degree/General Education Diploma.</li>
<li>Must be 18 years of age or older.</li>
<li>Experience using computers to include Internet navigation, email, Microsoft Office Suite.</li>
<li>Demonstrated ability to perform the Essential Duties of the position with or without accommodation.</li>
<li>Authorization to work in the United States without sponsorship.</li>
</ul>
Preferred Qualifications
<ul>
<li>Associate degree or Bachelor’s degree in Life Sciences, Physical Sciences, or field related to the essential duties of the job.</li>
<li>Experience in a laboratory or similar environment with maintaining sample integrity, following procedures and protocols, and sample collecting/handling.</li>
<li>Knowledge and understanding of CAP, GLP, GDP, CLIA, New York State Department of Health (NYSDOH), and HIPAA.</li>
<li>Experience in troubleshooting automation and performing instrument maintenance.</li>
<li>Lean experience (Kaizen, Kanban, root cause analysis, countermeasure implementation, etc.).</li>
</ul>
Physical Requirements
<ul>
<li>
Ability to lift and move up to 40 pounds for approximately 25% of a typical working day.
</li>
<li>
Ability to work seated for approximately 50% of a typical working day.
</li>
<li>
Ability to work standing for approximately 50% of a typical working day.
</li>
<li>
Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 75% of a typical working day.
</li>
<li>
Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.
</li>
<li>
Ability to comply with any applicable personal protective equipment requirements.
</li>
<li>
Ability to perform repetitive motions.
</li>
</ul>
#LI-JB1
Salary Range:
$31,000.00 - $52,000.00

The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible.
Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits.
Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here.
Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences.
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law.
To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub. The documents summarize important details of the law and provide key points that you have a right to know.
PandoLogic. Keywords: Medical Laboratory Technician (MLT), Location: Madison, WI - 53725 , PL: 600840043

Launch Your Career in Science: Lab Processing Associate

<h3>Job Description</h3>
Date Posted:
2025-10-06
Country:
United States of America
Location:
AZ204: RMS Rita Road Bldg 9020 9000 South Rita Rd Building 9020, Tucson, AZ, 85747 USA
Position Role Type:
Onsite
U.S. Citizen, U.S. Person, or Immigration Status Requirements: 
Active and transferable U.S. government issued security clearance is required prior to start date.​ U.S. citizenship is required, as only U.S. citizens are eligible for a security clearance​
Security Clearance: 
DoD Clearance: Secret
At Raytheon, the foundation of everything we do is rooted in our values and a higher calling – to help our nation and allies defend freedoms and deter aggression. We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today’s mission and stay ahead of tomorrow’s threat. Our team solves tough, meaningful problems that create a safer, more secure world.&nbsp;&nbsp;
Systems Engineering &amp; Test Capabilities (SE&amp;TC) integrates, verifies, and validates our products. We put our systems together, exercise them in the lab or in the field, measure and analyze performance, and make sure our products work the first time and every time. To accomplish this, we develop plans and procedures, debug and evaluate system functions and interfaces, develop test environments, and work together with our customers&nbsp;
In this role, you will be supporting the successful completion of lab developmental test events, platform integration laboratory testing events, and the associated analysis of test data. &nbsp;The position is located in Tucson Arizona.
What You Will Do
<ul>
<li>Perform integration, verification, and testing to ensure the system under test performs according to design, specs and/or requirements.</li>
<li>Perform data collection activities, including review and assessment of data elements, and provide detailed reports of results.</li>
<li>Trace and/or correct faults in mechanical or electronic systems.</li>
<li>Create/modify documentation in support of reviews associated with formal testing, which include Test Readiness Review (TRR), Consent to Ship (CTS), and Test Data Review (TDR) packages.</li>
<li>Support field testing, which includes occasional travel.</li>
<li>Monitor / manage upcoming tasks; assign resources.</li>
<li>Collaborate actively with CAM, IPT, TA, CE, attend weekly meetings to provide status, needs.</li>
<li>Champion teammates, foster respect, and communication, and serve as mentor to newest team members.</li>
</ul>
Qualifications You Must Have
<ul>
<li>Typically requires a Bachelor’s in Science, Technology, Engineering, or Mathematics (STEM) and a minimum of 5 years of prior engineering experience.</li>
<li>Experience leading a Design Verification test.</li>
<li>Experience with troubleshooting and failure root cause definition.</li>
<li>Knowledge of Lab / test equipment</li>
<li>Active and transferrable US Government issued security clearance is required prior to start date. US Citizenship is required as only US Citizens are eligible for a security clearance.</li>
</ul>
Qualifications We Prefer
<ul>
<li>Circuit card testing experience</li>
<li>cPDM and data package review and approval processes</li>
<li>Familiarity with failure reporting, analysis, corrective action and/or fault tree analysis</li>
<li>Technical leadership with capture/pursuit experience, including contribution or authoring of white papers, RFI responses, proposal of technical volumes, or related experience.</li>
<li>Experience managing and presenting technical data to Stakeholders and Customer community, in design reviews and technical interchange meetings.</li>
</ul>
What We Offer:
Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Safety, Trust, Respect, Accountability, Collaboration, and Innovation.
Additional Information:
* Please consider the following role type definitions as you apply for this role.
Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products.
Location Information 
<ul>
<li>Tucson, AZ - <a href="https://jobs.raytheonmissilesanddefense.com/living-in-tucson" target="_blank">https://jobs.raytheonmissilesanddefense.com/living-in-tucson</a></li>
</ul>
The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate’s work experience, location, education/training, and key skills.Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company’s performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window.
RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans’ Readjustment Assistance Act.
Privacy Policy and Terms:
Click on this link to read the Policy and Terms

Senior DVT Lead P3

<h3>Job Description</h3>
Job DescriptionAt Houston Methodist, the Radiation Physicist is responsible for performing measurements and providing data for quality assurance of radiation sources and treatment plans, under the supervision of a fully licensed therapeutic medical physicist, to ensure that patients receive the physician prescribed radiation dose for accurate treament of disease as well as protecting patients, staff and public from radiation harm. The incumbent will monitor the performance of radiation producing devices as well as ensure that patient-specific quality assurance, including initial and periodic treatment plan checks, and measurements are performed appropriately and in a timely manner.PEOPLE ESSENTIAL FUNCTIONS 
<ul>
<li>Works with therapy staff to ensure that periodic machine quality assurance is routinely and appropriately performed.</li>
</ul>
<ul>
<li>Works with engineering/vendor staff to ensure machine repairs and upgrades are adequately performed and machine performance verified.</li>
</ul>
<ul>
<li>Provides consultation to physicians and guidance to dosimetrists and therapists regarding best approaches to simulate, plan, image and treat patients to assure accurate delivery of prescribed radiation dosage to a specific human patient, and the associated risks.</li>
</ul>
<ul>
<li>Participates in training of departmental personnel as needed to effectively and safely utilize equipment for patient care and in the didactic education and hands-on training for radiation oncology and medical physics residents and other trainees.</li>
</ul>
 SERVICE ESSENTIAL FUNCTIONS 
<ul>
<li>Participates in the development of procedures for testing and evaluating performance levels of radiotherapy treatment and simulation equipment. This includes assisting in the development and execution of plans for acceptance and commissioning of new radiotherapy and dosimetry equipment and software.</li>
</ul>
<ul>
<li>Provides documentation that radiotherapy treatment, simulation and measurement equipment meet accreditation and regulatory compliance requirements.</li>
</ul>
<ul>
<li>Participates in the development and management of the quality control program for a radiation treatment facility that includes applicable facility accreditation and regulatory requirements, and the review of policies and procedures pertaining to therapeutic radiation and its safe and appropriate use.</li>
</ul>
 QUALITY/SAFETY ESSENTIAL FUNCTIONS 
<ul>
<li>Performs quality assurance to verify proper functioning after installation, repair or upgrade of radiation treatment equipment and software. It includes acceptance testing of radiotherapy treatment and simulation equipment, calibration and characterization of radiation beams from therapeutic equipment including radiation quantity, quality, and distribution characteristics, and assessment of the mechanical and geometric optics for proper placement of the beam. It also includes calibration and/or verification of the physical and radiological characteristics of brachytherapy sources.</li>
</ul>
<ul>
<li>Supports the implementation and management of dosimetric and beam delivery aspects of external beam delivery, brachytherapy irradiation and special procedures. External beam delivery aspects include treatment aids, beam modifiers, and geometrical arrangements. Special procedures are included for both external beam (e.g. radiosurgery, total body irradiation, total skin irradiation, intraoperative therapy) and brachytherapy (e.g. high dose rate, intravascular brachytherapy).</li>
</ul>
<ul>
<li>Participates in acceptance testing, management, and supervision of computer systems used for treatment planning and calculation of treatment times or monitor units. This includes measurement and input of dosimetry data base and verification of output for external beam radiotherapy and brachytherapy.</li>
</ul>
<ul>
<li>Ensures that patient-specific quality assurance, including initial and periodic treatment plan checks, and measurements if required, are performed on a timely manner.</li>
</ul>
<ul>
<li>Participates in the development and/or evaluation of a radiation safety program in a therapeutic radiation facility including written procedures for the protection of patients, workers, and the public, as well as in the protective shielding design and radiation safety surveys in a radiotherapy facility.</li>
</ul>
 FINANCE ESSENTIAL FUNCTIONS 
<ul>
<li>Supports the development of specifications for radiotherapy treatment and simulation equipment, including software. Provides equipment and software evaluations of value and performance on possible equipment and software purchases.</li>
</ul>
 GROWTH/INNOVATION ESSENTIAL FUNCTIONS
<ul>
<li>This position is eventually expected to grow into a senior physicist position (Radiation Physicist II) and manage all aspects of the clinical medical physics program.</li>
</ul>
<ul>
<li>Participates in clinical research and development projects as well as other research projects that are consistent with departmental goals.</li>
</ul>
 This job description is not intended to be all-inclusive; the employee will also perform other reasonably related business/job duties as assigned. Houston Methodist reserves the right to revise job duties and responsibilities as the need arises.EDUCATION 
<ul>
<li>M.S. degree in physical science required.</li>
</ul>
 WORK EXPERIENCE 
<ul>
<li>Minimum of two years of experience in therapeutic medical physics in a hospital/clinic based environment, including educational training.</li>
</ul>
LICENSES AND CERTIFICATIONS - REQUIRED 
<ul>
<li>MPHYS - Medical Physicists - State Licensure -- in Therapeutic Medical Physics OR</li>
<li>MPHYS-Temp - Temporary Medical Physicists - State Licensure AND</li>
<li>ABR-TMP - Therapeutic Medical Physics (ABR) -- or eligible for certification </li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES 
<ul>
<li>Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going skills, competency assessments, and performance evaluations</li>
</ul>
<ul>
<li>Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security</li>
</ul>
<ul>
<li>Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles</li>
</ul>
SUPPLEMENTAL REQUIREMENTS 
WORK ATTIRE 
<ul>
<li>Uniform No</li>
<li>Scrubs Yes</li>
<li>Business professional Yes</li>
<li>Other (department approved) No</li>
</ul>
ON-CALL* *Note that employees may be required to be on-call during emergencies (ie. DIsaster, Severe Weather Events, etc) regardless of selection below. 
<ul>
<li>On Call* Yes</li>
</ul>
TRAVEL** **Travel specifications may vary by department** 
<ul>
<li>May require travel within the Houston Metropolitan area Yes</li>
<li>May require travel outside Houston Metropolitan area No</li>
</ul>
Company Profile:
Houston Methodist Specialty Physician Group is an integral part of Houston Methodist’s overall strategy to become one of the nation’s leading academic medical centers. Established as a nonprofit corporation certified by the Texas State Board of Medical Examiners, the Specialty Physician Group enables physicians to maintain autonomy with respect to clinical practice while growing their practice within an academic environment.
Houston Methodist is an Equal Opportunity Employer.
Equal employment opportunity is a sound and just concept to which Houston Methodist is firmly bound. Houston Methodist will not engage in discrimination against or harassment of any person employed or seeking employment with Houston Methodist on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, status as a protected veteran or other characteristics protected by law. VEVRAA Federal Contractor – priority referral Protected Veterans requested.
]]&gt;

Radiation Physicist- West

<h3>Job Description</h3>
Job Description
JOB SUMMARY
<ul>
<li>Under indirect supervision, provides professional medical physics services for Radiation Oncology in accordance with the highest standards of practice and as required by regulatory agencies. Collaborates with medical providers in the design, evaluation and modification of effective radiation treatments for patients; oversees and monitors treatment plans developed by dosimetrists, participates in the evaluation, acquisition and operation of equipment or systems to include equipment monitoring, calibration, and safety surveys. Supervises staff physicists and dosimetrists.</li>
</ul>
GENERAL REQUIREMENTS
<ul>
<li>Adheres to the hospital and departmental attendance and punctuality guidelines</li>
<li>Performs all job responsibilities in alignment with the core values, mission and vision of the organization</li>
<li>Performs other duties as required and completes all job functions as per departmental policies and procedures</li>
<li>Maintains current knowledge in present areas of responsibility (i.e., self-education, attends ongoing educational programs)</li>
<li>Attend staff meetings and complete mandatory in-services and requirements and competency evaluations on time.</li>
<li>Demonstrates competency at all levels in providing care to all patients based on age, sex, weight, and demonstrated needs. For non-clinical areas, has attended training and demonstrates usage of age- specific customer service skills.</li>
<li>Wear protective clothing and equipment as appropriate.</li>
<li>Must possess and maintain a valid Georgia Driver's License and meet auto insurability requirements as approved by Phoebe Putney Health System's insurance company.</li>
</ul>
WORKING CONDITIONS
<ul>
<li>General environment: Works in a well-lighted, air-conditioned area, with moderate noise levels.</li>
<li>May be exposed to high noise levels and bright lights.</li>
<li>May be exposed to limited hazardous substances or body fluids, or infectious organisms.</li>
<li>May be required to change from one task to another of different nature without loss of efficiency or composure.</li>
<li>Periods of high stress and fluctuating workloads may occur.</li>
<li>Long-distance or air travel as needed - not to exceed 10% travel.</li>
</ul>
EDUCATION REQUIREMENTS
<ul>
<li>Master’s degree in medical physics (Required)</li>
<li>Doctorate Degree in Medical Physics (Preferred)</li>
</ul>
 EXPERIENCE REQUIREMENTS
<ul>
<li>6 - 7 years Clinical Radiation Oncology (Required)</li>
</ul>
 CERTIFICATIONS AND LICENSURES
<ul>
<li>Required Certifications/Licensures: Certified Health Physicist (CHP)</li>
</ul>
 GENERAL SKILLS
<ul>
<li>Organizational Skills</li>
<li>Communication Skills</li>
<li>Interpersonal Skills</li>
<li>Customer Relations</li>
<li>Mathematical</li>
<li>Analytical</li>
<li>Grammar / Spelling</li>
<li>Read / Comprehend Written Instructions</li>
<li>Follow Verbal Instructions</li>
<li>Transcription</li>
<li>Mechanical</li>
<li>Basic Computer Skills</li>
<li>Microsoft Office Suite</li>
<li>General Clerical Skills.</li>
</ul>
 PHYSICAL REQUIREMENTS
<ul>
<li>Have near normal vision - Clarity of vision (both near and far), ability to distinguish colors</li>
<li>Have good - manual dexterity and eye-hand-foot coordination</li>
<li>Ability to perform - repetitive tasks/motion</li>
</ul>
 PHYSICAL DEMANDS
<ul>
<li>Standing - Occasionally within shift (1-33%)</li>
<li>Walking - Occasionally within shift (1-33%)</li>
<li>Sitting - Frequently within shift (34-66%)</li>
<li>Bending/Stooping - Occasionally within shift (1-33%)</li>
<li>Pushing/Pulling - Occasionally within shift (1-33%)</li>
<li>Lift/carry up to 20 lbs - Occasionally within shift (1-33%)</li>
<li>Lift/carry &gt; 20 lbs with assistance - Occasionally within shift (1-33%)</li>
<li>Reaching above shoulder - Occasionally within shift (1-33%)</li>
</ul>
]]&gt;

Chief Physicist

<h3>Job Description</h3>
Job DescriptionToday, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
We are thrilled to announce an outstanding opportunity for a Senior Biotechnologist at Lonza AG, based in New Hampshire, USA. As one of the world's largest healthcare manufacturing organizations, Lonza is committed to encouraging a safe, controlled work environment and promoting continuous growth. The Senior Biotechnologist will play a vital role in ensuring the outstanding implementation of our daring projects within the Cell Gene Therapy network.
Key responsibilities:
<ul>
<li>
Ensure site safety objectives are strictly communicated and understood.
</li>
<li>
Demonstrate flexibility by supporting other sites within the Cell Gene Therapy network, including necessary travel.
</li>
<li>
Act as the Subject Matter Expert in the assigned area (e.g., Cell Growth, Drug Product Filling) during manufacturing operations.
</li>
<li>
Assume a lead role during manufacturing operations such as harvest, vial filling, and visual inspection.
</li>
<li>
Collaborate with customer SMEs to successfully implement and maintain customers' processes in the production facility.
</li>
<li>
Represent manufacturing in technical and project meetings during campaign preparation.
</li>
<li>
Provide and arrange effective training for manufacturing staff on new processes, batch records, or quality systems used in Cell Therapy.
</li>
<li>
Work with the CT Manufacturing project specialist team to incorporate process and operational improvements into new customer processes.
</li>
<li>
Collaborate with the CT Manufacturing team to determine and procure necessary equipment and materials for process execution.
</li>
</ul>
Key requirements:
<ul>
<li>
High School Diploma or equivalent experience is required; a bachelor’s degree or equivalent experience is preferred.
</li>
<li>
5-10 years of proven experience in a related field.
</li>
<li>
Outstanding communication and collaboration skills.
</li>
<li>
Strong ability to compete and thrive in a fast-paced, dynamic environment.
</li>
<li>
Demonstrated ability to successfully coordinate and lead all aspects of complex biotechnological processes.
</li>
<li>
Proven track record of leadership and expertise in relevant manufacturing areas.
</li>
<li>
Willingness to travel and support other manufacturing sites as needed.
</li>
</ul>
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
]]&gt;

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