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<h3>Job Description</h3>
Job DescriptionDescription:
The purpose of this role is to provide analytical chemistry support to Phlow. This is an exciting opportunity for graduates or individuals with analytical chemistry experience to develop and perform analytical experiments under the direction of the Director, Analytical Chemistry, or other team members. The candidate will support Phlow’s contract development and manufacturing services to ensure business objectives are met for execution of the internal Phlow API development as well as commercial projects. The candidate will personify Phlow’s shared values and culture, both internally and externally. The candidate will work with the highest standards of safety, integrity, transparency, and ethics to create win-win scenarios for patients, customers, partners, and colleagues. While not required, we appreciate you accompanying your application with 1-3 professional references if you are able to provide. 
Requirements:
Essential Job Duties &amp; Responsibilities
· Independently conduct analytical method development, validation, and project support
· Identify technical challenges during analytical method development and perform analytical method troubleshooting
· Manage CMO/CRO analytical project resources as required such as contractors and contract laboratories, as needed
· Manage technical direction of analytical projects; identify key deliverables and next steps and communicate to the team
· Responsible for data production, review, analysis, and interpretation from a variety of sources. Provide accurate summaries and make recommendations to stakeholders with scientific rigor.
· Author and review technical reports, regulatory submissions, SOPs, validation protocols, and other cGMP documents
· Performs the assigned analytical tasks with minimum supervision in support of product development and clinical trial material.
· Performs activities within the assigned timelines and in compliance with cGXP's, regulatory requirements, and company practices and procedures
· Responsible for the design and conduct of studies in accordance with company and regulatory standards to facilitate new product development
· Manage day-to-day laboratory activities for analytical equipment, including sourcing consumables, troubleshooting, maintaining equipment and calibrations with various vendors
 
Experience &amp; Qualifications
· Advanced degree in chemistry, pharmaceutics, or related field.
· 5+ years experience in analytical method development, validation and API and/or drug product development activities regulated by FDA
· Working knowledge of standard Office tools (MS Office, MS Project, Excel, Visio, SharePoint).
· Ability to work well both independently and with a team.
· Broad range of functional expertise in analytical chemistry, compound purification, spectral analysis/interpretation.
· Experience with common analytical techniques such as: HPLC, LC/MS, GC, GC/MS, KF, LOD, DSC, TGA, NMR, UV, LC-MS
· Excellent written and verbal communication skills
· Strong interpersonal skills 
 
Preferred Qualifications
· Ph.D. with a minimum 2 years of experience, M.S with a minimum 5 years of experience, or B.S. degree with a minimum 10 years of experience in Analytical Chemistry, Pharmaceutical Sciences, or a related scientific field
· Knowledge of ICH and cGMP requirements
· Experience working for a contract organization (CROs/CMOs/CDMOs) is a plus
· Experience with technical and operational risk assessments (e.g., process robustness, mutagenic impurities, nitrosamines, etc.) is a plus
· Experience with the development and implementation of Process Analytical Technology (PAT) is a plus
· Experience with Design of Experiments (DOE) is a plus
 
Physical Requirements
· Constantly required to see to utilize computer screens and monitors to perform job duties including reading &amp; writing, as well as when presenting information and communicating with others.
· Frequently required to talk or hear to communicate with employees, candidates, vendors, and others, including presenting information in front of groups.
· Frequently required to reach with arms and hands performing repetitive motions and using finger dexterity to work primarily at a computer keyboard and with a mouse.
· Frequently required to sit, and occasionally required to stand or walk to move around primarily in an office environment.
· Occasionally lift and/or move up to 10 pounds.
This position may require up to 5% travel with occasional increase in travel demands based on business needs.

Senior Analytical Chemist

<h3>Job Description</h3>
Job DescriptionDescription:
Position Summary:
The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs.
 
Responsibilities: Responsibilities include, but are not limited to: 
<ul>
<li>Follow all laboratory SOPs, including but not limited to laboratory safety, chemical handling and storage, gowning, equipment use, cGMP, GDP, data integrity, DEA requirements, etc. </li>
<li>Perform routine laboratory chemical analysis on finished product, stability, raw material, and/or investigation samples, as assigned, using HPLC, UPLC, GC, UV-vis, FTIR, ICP, TOC and other wet chemistry techniques in accordance with the prescribed approved analytical test method.</li>
<li>Maintain a clean and organized laboratory working environment.</li>
<li>Dispose of used/expired/excess chemicals, solutions, solvents, etc. in dedicated waste receptacles.</li>
<li>Report well-written, accurate and timely results.</li>
<li>Review data, calculations, notebooks, and reports.</li>
<li>Assist in laboratory investigations, as assigned.</li>
<li>Assist in Cleaning, Method and Process validation testing and protocol/report review, as assigned.</li>
<li>Assist in maintaining and troubleshooting laboratory equipment.</li>
<li>Suggest improvements to existing testing methods when possible.</li>
<li>Mentor and give guidance to entry-level personnel on techniques performed in the lab and assist with laboratory related questions as needed.</li>
<li>Assist with routine Metrology functions, including instrument cleaning/ preventive maintenance/ calibration/ verification activities.</li>
<li>Monitor and assist with maintaining proper inventory levels of all laboratory supplies.</li>
<li>Assist with sample receiving, chemical inventory, document filing, housekeeping, etc.</li>
<li>Other responsibilities as assigned by Management.</li>
</ul>
Requirements:
Education and Experience:
<ul>
<li>Bachelor’s degree in a science related field.</li>
<li>Between 1 and 9 years of work experience in a laboratory setting.</li>
</ul>
Skills, Knowledge, and Abilities:
<ul>
<li>Knowledge of laboratory chemistry and cGMPs.</li>
<li>Proficient in Microsoft Word, Excel, graphs/charts and databases.</li>
<li>Proficient in HPLC/UPLC, ICP, Dissolution, IR, UV/VIS, and wet chemistry testing.</li>
<li>Proficient with analytical laboratory software.</li>
<li>Able to multitask and meet tight deadlines.</li>
<li>Excellent organizational skills with attention to detail.</li>
<li>Able to effectively present results.</li>
<li>Able to perform testing on many methods and troubleshoot minor method issues. May require some guidance/supervision as needed. </li>
<li>Able to troubleshoot basic instrument issues independently and complex instrument issues under supervision.</li>
</ul>
Physical Demands:
<ul>
<li>Required to sit and stand for long periods of time. </li>
<li>Frequently reaching with arms/hands up to 2 feet. </li>
<li>Good hand eye coordination. </li>
<li>Occasionally required to walk and kneel.</li>
<li>Must be able to lift and/or move up to 50 pounds.</li>
<li>Must be able to use close vision, distance vision, peripheral vision, color vision and the ability to adjust focus. </li>
<li>Required to reach with arms and use hands and fingers to handle or feel objects, tools and computer controls.</li>
<li>Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs.</li>
</ul>
Work Environment:
<ul>
<li>Work environment in laboratory and production operations facilities include close proximity to heavy machinery and pharmaceutical powders.</li>
<li>Potential to move between production operations sites/areas to complete job functions. </li>
<li>Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion.</li>
<li>Required to be present in the laboratory to perform daily testing and collaborate with department director, manager, and peers.</li>
<li>Responsible for compliance with all rules and regulations pertaining to safety policies with the proper attitude toward safety and health, helping to ensure that all department operations are performed with the utmost regard for the safety and health for all personnel.</li>
</ul>
Supervisory Responsibilities:
<ul>
<li>None</li>
</ul>
Personal Protective Equipment or Attire Required for Position:
<ul>
<li>Gowning as required by GMPs and/or SOPs.</li>
</ul>
Pay Range:
$50,000 - $80,000 per year

Chemist; Quality Control

<h3>Job Description</h3>
Job DescriptionDescription:
Title: Senior Peer Mentor - Transportation Services 
Department: Behavioral Health 
Reports To: Transportation Services Coordinator 
Location: 56 Bay Street, 1st Floor, Staten Island, NY 10301 
Position Status: Part Time (20 hours per week) 
FLSA Status: Non-Exempt 
Pay &amp; Benefits: The pay range for this role is generally $17.79- 19.00 per hour, commensurate with relevant experience and qualifications and in alignment with internal equity. 
 
Community Health Action of Staten Island (CHASI) drives dramatic improvements in the health of New Yorkers by feeding people who are hungry, healing families broken apart by violence, and bridging the gaps between people and the compassionate health care they deserve. CHASI provides outreach, education, prevention, and direct support services for populations most affected by health disparities – people with low or no income, low-income people with chronic illnesses, people with criminal justice involvement, people who use drugs, domestic violence survivors, people of color, and the LGBTQ community.
 
POSITION SUMMARY:
The Senior Peer Mentor (SPM) will support the Transportation Coordinator in managing a grant-funded rideshare transportation program for individuals with a history of substance use disorder. The SPM will be responsible for documenting all transportation services utilized on a weekly and monthly basis and escorting participants to necessary locations across Staten Island when warranted. This role is ideal for a compassionate and detail-oriented individual committed to supporting people in recovery by ensuring they have reliable access to essential services. 
 
DUTIES &amp; RESPONSIBILITIES:
Transportation Support &amp; Documentation:
<ul>
<li>Maintain accurate records of all rides provided through the program, including dates, times, destinations, and participant details. </li>
<li>Prepare and submit weekly and monthly transportation utilization reports to the Transportation Coordinator. </li>
<li>Assist with tracking program performance and identifying trends in transportation needs. </li>
<li>Communicate with participants about their scheduled rides, ensuring they understand pickup times and locations. </li>
</ul>
Peer Support &amp; Escorting Services:
<ul>
<li>Provide in-person escort services for participants who require additional support traveling to appointments, treatment programs, or other essential locations across Staten Island. </li>
<li>Offer peer-based support and encouragement during transit, helping participants navigate barriers to accessing care. </li>
<li>Act as a liaison between participants, transportation providers, and the program team to ensure smooth service delivery. </li>
</ul>
Collaboration &amp; Advocacy:
<ul>
<li>Work closely with the Transportation Coordinator and case management staff to address transportation-related concerns. </li>
<li>Advocate for participant needs and provide feedback on ways to improve the program’s accessibility and effectiveness. </li>
<li>Uphold confidentiality and ethical standards while supporting individuals in their recovery journey. </li>
<li>Perform all functions in alignment with CHASI’s Mission, Vision, and Core Values. </li>
</ul>
Requirements:
QUALIFICATIONS:
<ul>
<li>New York State Certified Recovery Peer Advocate-Provisional (CRPA-P), at minimum. </li>
<li>Prior experience in peer support, case management, or human services preferred. </li>
<li>Strong attention to detail with the ability to maintain accurate records and reports. </li>
<li>Excellent interpersonal skills with the ability to engage and support individuals in recovery. </li>
<li>Must be dependable and able to meet participants at designated locations on time. </li>
<li>Familiarity with Microsoft Office (Excel, Word) or Google Docs/Sheets for reporting. </li>
</ul>
PREFERRED:
<ul>
<li>Experience working with individuals in recovery and/or navigating transportation challenges. </li>
<li>Knowledge of Staten Island’s public transit system and local recovery resources. </li>
<li>Valid driver’s license and reliable transportation (not required but a plus). </li>
</ul>
COMPETENCIES: 
<ul>
<li>Works independently following receipt of instructions on a task, demonstrating the ability to understand and execute the task with minimal supervision.? </li>
<li>Takes initiative on future tasks by identifying potential areas for improvement and proactively addressing them.? </li>
<li>Ability to work independently, establish priorities, and handle multiple tasks simultaneously. </li>
<li>Models ethics and integrity? </li>
<li>Manages and accepts change to ensure successful growth and changes within the organization. </li>
<li>Evaluates obstacles and contributes alternative solutions. ? </li>
<li>Demonstrates strategic, conceptual, and critical thinking skills. </li>
</ul>
CHASI is an equal opportunity employer and is committed to hiring and supporting a diverse staff. All qualified applicants will be afforded equal employment opportunities without discrimination because of race, religion, color, national origin, sex, sexual orientation, gender identity, age, genetic information, disability or marital status.

Senior Peer Mentor - Transportation Services

<h3>Job Description</h3>
Job DescriptionDescription:
NON-EXEMPT. This position is responsible for providing professional level technical assistance for Special Projects in support of Perma-Fix Business Center activities on an as-needed basis. Such technical support may include, but is not limited to, radiation protection and health &amp; safety areas such as dosimetry, bioassay, instrumentation, program/procedure development, survey design and performance, dose assessment, regulatory compliance, and data analysis. Perform such other duties and responsibilities as may be assigned.
Duties
· Provide assistance for specific special projects.
· Directs activities of technical and administrative personnel assigned to support the task.
· Coordinates activities with Perma-Fix program management for the functional areas covered by the special project.
· Perform other duties as assigned.
Requirements:
· Minimum of 5 years of experience in relevant technical or applied activities. An advanced degree (1 year) or relevant certification (2 years) may be substituted in lieu of experience.
· BS degree in engineering, science, or related field.
· DOE “L” or “Q” security clearance or the ability to obtain the same, as required.
· Nationally recognized certification preferred (e.g., NRRPT, CHP, CIH).
· Strong general knowledge of radiation protection fundamentals, including internal and external dosimetry, shielding design, ALARA evaluation, regulatory requirements, program development, instrumentation, health effects of radiation, hazard assessment, survey design and implementation, laboratory analysis and quality assurance. 
· Demonstrated ability to implement and apply technical knowledge and theory to practical field situations. The individual may have equivalent knowledge and skills in a technical area other than radiation protection if that is the primary area that he/she will provide expertise in.
 
Working Conditions
In addition to office assignments, may need to have frequent visits to project locations which may include hazardous waste treatment facilities, environmental remediation projects, radioactive contaminated areas, etc. May require ability to don and use respiratory protection and other personal protective equipment. Visit facilities and projects throughout the United States and possible international locations.

Health Physicist

<h3>Job Description</h3>
Job DescriptionDescription:
WABG-TV, Greenville, MS and The Delta News is looking for a Chief Meteorologist who will lead our team in weather coverage. We are The Delta’s most trusted source for news, sports and weather information. 
 
The successful candidate will be a Certified Broadcast Meteorologist and is expected to have the ability to forecast accurately, to live storm track, create and develop detailed and easy to understand graphics and to ad lib flawlessly on TV and across social media and radio. 
 
Job Responsibilities: 
· Degreed Meteorologist must create and deliver The Delta News weather forecast following researched formats and action plans.? 
· Work with and lead a team of meteorologists to deliver life-saving weather information to our audiences 24/7. 
· Must have the ability not only to forecast in weather market, but live storm track, using your skills?to communicate not just data, but a forecast and its impact, in a way viewers and listeners will understand, and also record forecasts for our Alexandria, Louisiana station. 
· Qualified candidates will be proficient in creating digital videos, social media engagement, ad-libbing live on TV, radio, live streams and Facebook Live. 
· Must be willing to work extended hours during impactful, severe weather events 
· Must be able to pitch and create original weather content and environmental investigative journalism for television and digital platforms. 
Requirements:
· Degree in Journalism, Communications, Science, or Other 
· 2+ years television weathercaster, live storm tracking experience 
· Completion of Certified Broadcast Meteorology (CBM) program 
· Requires strong computer skills, communication skills, social media skills 
 
If you are motivated, goal-oriented and wish to work for a company that rewards excellence, please submit your application and provide a link to your reel. 
 
Imagicomm Communications, LLC is an equal opportunity employer and does not discriminate against applicants on the basis of race, color, creed, religion, genetic information, ancestry, age, sex, gender, marital status, national origin, disability or handicap, veteran status, or any other status or characteristics protected by federal, state and/or local laws. Applicants may notify the appropriate local, state or federal agency if they believe they have been the victims of discrimination.

Chief Meteorologist NE

<h3>Job Description</h3>
Job DescriptionDescription:
FLSA Status: Non-exempt/Hourly
Schedule: 8:00AM – 4:30PM, Monday – Friday. Occasional 2nd shift work required
Location: 400 Street Road, Bensalem PA 19020
 
Position Summary: Are you interested in growing your laboratory career at a fact-paced and expanding environmental testing laboratory? If so, we may have a great role for you; Criterion's Laboratory Analyst (PLM) role primarily performs precise and timely analysis of asbestos bulk samples using polarized light microscopy techniques. This role is responsible for adhering to quality assurance and quality control standards, following Criterion Laboratories’ Laboratory Safety Procedures, ensuring a clean work environment, and fostering effective collaboration within a team environment.
 
Essential Duties and Responsibilities:
<ul>
<li>Uses polarized light microscopy to conduct detailed analysis of bulk samples for the identification and quantification of asbestos fibers.</li>
<li>Adheres to established analytical protocols and procedures to ensure reliable and reproducible results.</li>
<li>Maintains rigorous quality assurance practices to uphold data integrity and compliance with regulatory requirements.</li>
<li>Adheres to safety protocols to ensure a secure work environment for all personnel.</li>
<li>Maintains cleanliness and organization of the workspace to prevent contamination and ensure optimal working conditions.</li>
<li>Collaborates effectively with team members to achieve departmental objectives and contribute to a positive team culture.</li>
<li>Participates in training programs and stays abreast of advancements in polarized light microscopy techniques and asbestos analysis methodologies.</li>
</ul>
Requirements:
Required Knowledge and Experience:
<ul>
<li>At least six (6) months experience performing analyses via polarized light microscopy</li>
<li>Familiarity with regulatory requirements and standards pertaining to asbestos analysis is preferred.</li>
<li>Strong attention to detail and the ability to maintain accuracy under tight deadlines.</li>
<li>Excellent organizational and communication skills, both verbal and written.</li>
<li>Demonstrated ability to work both independently and collaboratively within a team environment.</li>
<li>Commitment to maintaining high safety standards and promoting a culture of safety in the workplace.</li>
</ul>
 
Required Education, Certifications, and Licenses:
<ul>
<li>Bachelor’s degree in a relevant scientific field (e.g., Geology, Biology, Chemistry, Environmental Science) and/or an equivalent amount of education and experience.</li>
</ul>
 
Physical and Mental Requirements:
<ul>
<li>Ability to perform microscopy work for extended periods, including sitting or standing.</li>
<li>Capability to lift and handle sample containers and equipment (up to 25 pounds).</li>
</ul>

Laboratory Analyst (Polarized Light Microscopist: Asbestos)

<h3>Job Description</h3>
Job DescriptionDescription:
Manufacturing QC Lab Analyst – Where Science Meets Impact!
(This is not an IT position)
 
Location: Red River Plant | Team: Manufacturing | Shift: Variable 12-hour shifts (includes nights, weekends &amp; holidays)
Are you a lab lover with a passion for precision? Do you geek out over instruments, take pride in chasing down out-of-spec results, and find satisfaction in helping teams turn great into excellent? If you're nodding your head, read on — this just might be your next adventure.
 
At Arq, Inc., we’re redefining what’s possible in the environmental technology space. Our mission is to enable a cleaner and safer planet. And you? You’ll be the one making sure the science behind it all is spot on.
 What You’ll Do
As our QC Lab Analyst, you won’t just run tests — you’ll own quality. You’ll be part of the team that ensures our raw materials, in-process samples, and finished products are nothing short of exceptional.
You’ll:
<ul>
<li>Conduct routine and special chemical &amp; physical analyses (yes, that includes real chemistry!). </li>
<li>Keep our lab running smoothly — from instruments to sample inventory and lot tracking. </li>
<li>Be the hero who troubleshoots tricky instrumentation issues before they become big problems. </li>
<li>Create clear, compelling reports that make complex data easy to understand. </li>
<li>Collaborate with production and R&amp;D teams to drive continuous improvement. </li>
<li>Handle hazardous materials (like H2S) safely and confidently — your commitment to safety is as strong as your science. </li>
<li>Help develop new testing methods and ensure all our equipment is calibrated and audit-ready. </li>
</ul>
What You Bring
<ul>
<li>Solid foundation in chemistry — think: titrations, chromatography, spectroscopy, or similar. </li>
<li>Experience working with analytical instrumentation and a love of troubleshooting. </li>
<li>Strong critical thinking and data interpretation skills. </li>
<li>A can-do attitude and ability to work independently (but also pitch in when teamwork is needed). </li>
<li>A passion for safety, quality, and process improvement. </li>
</ul>
The Fine Print
<ul>
<li>You’ll work with hazardous chemicals and gases — this role is hands-on and high-impact. </li>
<li>Shifts are 12 hours and may include nights, weekends, and holidays. Flexibility = key.</li>
</ul>
Benefits That Have Your Back
At Arq, we take care of our team — in and out of the lab. Our benefits package includes:
<ul>
<li>Medical, dental, and vision insurance </li>
<li>Company-paid Short-Term and Long-Term Disability </li>
<li>Company-paid Life and AD&amp;D insurance </li>
<li>401(k) plan with a competitive employer match </li>
<li>Generous Paid Time Off — because recharging matters </li>
</ul>
Why Arq?
Because here, your work really matters. We’re on a mission to reduce waste, support cleaner air and water, and create high-performing carbon products. When you work with us, you’re helping solve real-world environmental challenges — one sample at a time.
Ready to get your gloves on and make a measurable impact? Apply now and bring your inner lab superhero to Arq.
Requirements:
Education and experience
<ul>
<li>Education: Bachelors of Science degree in Chemistry, , or other relevant, science – related field. Academic or industrial laboratory experience required.</li>
<li>Experience: 2-5 years manufacturing QA/QC laboratory experience preferred</li>
<li>Experience in an industrial laboratory setting or equivalent academic research is highly preferred.</li>
</ul>
Sign-on bonus available for highly qualified candidatesWork authorization required — Arq is not currently sponsoring employment visa
 
Physical Requirements
<ul>
<li>Must be willing and able to work with hazardous chemicals and gases, including acids, solvents, and other reagents commonly used in laboratory testing.</li>
<li>Must be able to lift, move and carry heavy sample buckets, containers, and equipment (up to 50 lbs).</li>
<li>Occasional climbing of stairs or ladders may be required.</li>
<li>Ability to stand for long periods and perform tasks at laboratory workstations.</li>
<li>Required to wear personal protective equipment (PPE), including lab coats, gloves, safety glasses, respirators, and hearing protection as needed.</li>
<li>Exposure to chemicals and fumes may occur, so adherence to safety guidelines and use of required PPE is essential.</li>
<li>Ability to work in a fast-paced, high-stress environment while maintaining a focus on quality and safety.</li>
<li>Work in varying environmental conditions, including occasional exposure to heat, humidity, and noise in an industrial setting.</li>
<li>Ability to work rotating 12-hour shifts, including evenings, weekends, and holidays as required by production schedules.</li>
</ul>
 Arq is an Affirmative Action, Equal Opportunity Employer. Reasonable accommodations may be made to enable individuals with disabilities to apply and to perform the essential functions of the position. For application assistance, please contact Lorrie Lang at 720.235.2871 or <a href="mailto:lorraine.lang@arq.com" target="_blank">lorraine.lang@arq.com</a>.

Manufacturing QC Lab Analyst I

<h3>Job Description</h3>
Job DescriptionDescription:
Committed to our Team, Craft &amp; Community, Since 1910
Join the always-growing Team at Ellsworth Creamery as we work with our cooperative of local farmers to create award-winning cheese!
 
Job Title: Laboratory Supervisor 
Reports To: Quality Assurance Manager 
Status: Exempt/Salary 
Supervises: Intake Operators 
 
General Description: The Laboratory Supervisor is responsible for the day-to-day supervision and operation of the State Licensed Milk, Food and Water Laboratory. This role oversees all aspects of lab testing, including patron, product, and environmental testing. The Lab Supervisor ensures accurate and timely test results, maintains compliance with regulatory and internal standards, and upholds the integrity of all laboratory records. This position also plays a key role in maintaining laboratory certifications, coordinating lab evaluations, and ensuring adherence to Good Manufacturing Practices (GMPs), Safe Quality Food (SQF) standards, Hazard Analysis and Critical Control Points (HACCP) programs, and Halal policies. Responsible for overseeing and coordinating weekend laboratory operations, ensuring proper coverage and continuity of testing and documentation. 
 
Duties and Responsibilities:
<ul>
<li>Ensure compliance with all regulatory standards including but not limited to: Human resources, current Good Manufacturing Practices, Occupational Safety and Health Administration, Food and Drug Administration, Wisconsin Department of Agriculture Trade and Consumer Protection, Safe Quality Food, United States Department of Agriculture and Halal.</li>
<li>Maintain and oversee operations of the WDATCP-licensed Milk, Food, and Water Laboratory, ensuring compliance with licensing requirements and timely renewals. Oversee analyst training and ensure compliance with 2400 forms and individual analyst licensing.</li>
<li>Oversee the Intake Screening Laboratory, including certification and performance of Appendix N analysts. Supervise the Intake Department, train personnel, and ensure compliance with internal policies and external regulations (WDATCP, FDA, USDA, HACCP, and SQF).</li>
<li>Oversee Grade A silo operations and report inventory and usage data to the Finance Department.</li>
<li>Lead WDATCP Grade A Receiving Station audits and ensure timely follow-up and resolution of any corrective actions.</li>
<li>Oversee, interpret, and report microbiological and analytical testing of cheese, whey, cream, milk, water, and environmental samples.</li>
<li>Manage patron milk quality testing and the patron dairy water testing program; download and review daily external lab results for accuracy. Work with field representatives to address and correct issues. </li>
<li>Oversee monthly official state patron testing; manage recheck testing and ensure timely submission to the state within regulatory deadlines.</li>
<li>Verify patron test results each pay period and collaborate with payroll to finalize and lock results for accurate payment.</li>
<li>Oversee and manage European Union certification status, including preparation and distribution of monthly reports and certificates of conformance. </li>
<li>Place product on hold when necessary; complete required documentation and update Hold/Finished Product Quality (FPQ) tracking systems; release product in DSI and generate Certificates of Analysis (COAs).</li>
<li>Oversee calibration and routine maintenance of laboratory equipment.</li>
<li>Manage lab supply ordering, inventory control, and ensure a clean, sanitary, and GMP-compliant workspace.</li>
<li>Maintain accurate and complete laboratory records and documentation.</li>
<li>Assist with internal audits, third-party inspections, and regulatory agency reviews.</li>
<li>All other duties as assigned. </li>
</ul>
Requirements:
Required Skills and Abilities:
<ul>
<li>Bachelor’s degree in operations management, food science, or related technical field and 2-5 years of related experience; or 5-10 years of progressively responsible related experience; or a combination of education and experience. </li>
<li>Must gain full certification for the following and all appropriate State testing standards within one year:</li>
</ul>
<ol>
<li>Charm SL Drug Screening and confirmation </li>
<li>Delvotest P 5 Pack screening and Confirmation</li>
<li>Petrifilm Plate Loop Count </li>
<li>Petrifilm Aerobic Count</li>
<li>Petrifilm Coliform Count </li>
<li>Phosphatase Test-Fluorophos</li>
<li>Total Coliform Water Analysis </li>
<li>Certified Industry Supervisor</li>
</ol>
<ul>
<li>Must complete HACCP, PCQI and Internal Auditor training and certification </li>
<li>Proficient computer skills and strong written/verbal communication.</li>
<li>Ability to read and follow directions, interpret scales, and perform basic math.</li>
<li>Strong attention to detail, accuracy, organization, and reliability.</li>
<li>Skilled in interpreting and creating GMPs, SOPs, safety rules, schedules, and technical documentation.</li>
<li>Capable of writing clear reports, procedures, and correspondence.</li>
<li>Effective communicator with all levels of staff, auditors, and customers.</li>
<li>Strong analytical and problem-solving abilities.</li>
<li>Self-motivated with a high level of integrity and accountability.</li>
</ul>
Physical Requirements:
<ul>
<li>Ability to lift 50+ lbs. repetitively.</li>
<li>Stand for up to 8 hours per shift.</li>
<li>Pass a drug &amp; alcohol screen as well as a general background check.</li>
</ul>
Work Environment / Environment Condition:
<ul>
<li>Food plant environment. Must adhere to all food and plant safety policies and regulations.</li>
<li>Atmosphere may be humid, hot, and is dependent on weather. </li>
</ul>
 
ABOUT ELLSWORTH CREAMERY:At Ellsworth Creamery, our team members are more than employees; you are like family and we want you to succeed. This culture has contributed to the longevity of our staff, whose careers at Ellsworth Creamery span 10, 20 and even 50 years! Our Ellsworth, Wisconsin facility specializes solely in the production of our world-famous All Natural White Cheddar Cheese Curds, both natural and flavored, our All Natural Cheddar Cheese Curd Crumbles and sweet whey powder.
 
Benefits Package:
<ul>
<li>Full Time employees are eligible for benefits on the 1st of the month, following 30 days of employment.</li>
<li>Medical, Health Savings Account, Dental, Vision, Accident, Critical Illness and Hospital insurances available.</li>
<li>Employee Assistance Program (EAP) and other free resources.</li>
<li>401k match, Paid Time Off &amp; Holiday Pay!</li>
</ul>

Lab Supervisor

<h3>Job Description</h3>
Job DescriptionDescription:
A Senior Research and Development Chemist is an experienced researcher/formulator who combines technical knowledge and innovation when formulating a variety of personal care products, cosmetics and OTC (lip balms and sunscreens) from concept to finished product based on customers’ requests. Shows the ability to look at different brands’ gaps and develop products based on those gaps or customer specification. The Senior R&amp;D Chemist II demonstrates strong leadership and communication skills that are utilized within the organization and with external customers.
Requirements:
Responsibilities
<ul>
<li>Responsible for initiating project concepts, developing objectives, planning and assigning priorities, and completing multiple projects under minimal supervision.</li>
<li>Independently investigate/resolve research problems/scale up issues.</li>
<li>Ability to communicate with customers on technical aspects as well as regulatory and performance.</li>
<li>Utilize and follow relevant legal requirements, regulations and product development standards.</li>
<li>Determine and perform appropriate cost reductions (raw materials).</li>
<li>Scale-up of approved formulations, to include identification of critical process variables.</li>
<li>Ability to troubleshoot production issues and address batch variations.</li>
<li>Set product specifications and write compounding procedures.</li>
<li>Supervise and coordinate pilot batches.</li>
<li>Provide paperwork for new formula and new raw materials to operations.</li>
<li>Provide specifications and other information to QC to receive and test new ingredients and finished goods.</li>
<li>Test stabilities and monitor testing statuses.</li>
<li>Research product formulations and properties and interactions of raw materials.</li>
<li>Vendor research for raw materials.</li>
<li>Compose and check ingredient lists, QQs and artwork</li>
<li>Interpret results of laboratory findings and assess risks involved in new products and communicate findings to sales and upper management.</li>
<li>Remain up to date and current on trends in the retail market and trends on formulations materials, ingredients, etc.</li>
<li>Training and supervising lab staff (permanent and temporary).</li>
<li>Notebook documentation</li>
<li>Other duties as assigned.</li>
</ul>
 
Required Skills/Abilities
<ul>
<li>Working knowledge of laboratory equipment set-up and operation, common laboratory techniques and safe chemical handling</li>
<li>Advanced formulation skills and technical knowledge</li>
<li>Thorough understanding of FDA regulations and cGMP’s</li>
<li>Excellent written, verbal and interpersonal communication skills</li>
<li>High level of initiative, innovation, critical thinking and problem-solving skills</li>
<li>Ability to work cross-functionally &amp; at all levels within the organization including senior leadership</li>
<li>Ability to prioritize multiple responsibilities and manage deadlines accordingly.</li>
<li>Communicate effectively and professionally with clients and vendors</li>
<li>Exceptional attention to detail and high level of accuracy &amp; organization</li>
<li>Ability to work as part of a team and excel independently in fast-paced environment</li>
<li>Ability to adapt quickly to changing policies and procedures</li>
<li>Demonstrated leadership skills</li>
<li>Proficient with Microsoft Office</li>
</ul>
 
Required Education and Experience
<ul>
<li>BS in Chemistry, Cosmetic Science, Physical Chemistry, Chemical Engineering or related sciences with 8+ years of formulating personal care products</li>
<li>-OR- advanced degree in cosmetic chemistry and more than 6 years’ experience.</li>
</ul>
 
Preferred Education and Experience
<ul>
<li>Master’s Degree in Chemistry, Cosmetic Science, Chemical Engineering or related field</li>
<li>10+ years of experience in formulation of personal care products</li>
</ul>
 
EEO Statement
<ul>
<li>Bell International Laboratories provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</li>
<li>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.</li>
</ul>

Senior R&D Chemist

<h3>Job Description</h3>
Job DescriptionDescription:
An excellent opportunity exists to work for a government contractor with competitive compensation and work-life balance. Posterity Group is seeking experienced Therapeutic Medical Physicist at the G.V. Sonny Montgomery VAMC.
 
Therapeutic Medical Physicists (TMPs) work in Radiation Oncology and have responsibilities that include: protection of the patient and others from potentially harmful or excessive radiation; establishment of adequate protocols to ensure accurate patient dosimetry; the measurement and characterization of radiation used for radiotherapy; the performance and supervision of treatment planning; the determination of delivered dose; advancement of procedures necessary to ensure delivered dose integrity; the assessment and monitoring of image quality; development and direction of quality assurance programs; assistance to other health care professionals in optimizing the balance between the beneficial and deleterious effects of radiation; and compliance with applicable federal and state regulations. The advanced level TMP can perform the most complex of these tasks, and has the experience to commission and clinically implement novel technologies. 
Specific tasks include but are not limited to the following:
<ul>
<li>Recommending an optimal modality and treatment technique for the patient.</li>
<li>Evaluating the quality, safety, and accuracy of radiation treatments planned and delivered to patients, thus ensuring that radiation dose is carried out correctly and completely.</li>
<li>Safely operating all radiation planning and delivery devices.</li>
<li>Implementing radiation therapy of outstanding technical difficulty and responsibility, providing knowledge-based solutions to resolving issues where no rule-based solutions exist.</li>
<li>Planning and directing a specialized program encompassing all physics and clinical aspects of external beam and brachytherapy (if applicable) treatment procedures from treatment simulation to treatment planning to the actual treatment delivery.</li>
<li>Providing technical oversight for the work of entry level TMPs, medical dosimetrists and radiation therapists.</li>
<li>Overseeing radiation therapy treatment planning.</li>
<li>Designing and approving treatment plans.</li>
<li>Monitoring the accuracy of treatment data recorded in the patient's medical records.</li>
<li>Providing consultation to the radiation oncologist regarding difficult treatment cases.</li>
<li>Performing patient-specific treatment validation measurements.</li>
<li>Developing medical physics policies and procedures for the delivery and quality assessment of advanced treatment modalities such as intensity modulated radiation therapy, stereotactic body radiation therapy, and brachytherapy.</li>
<li>Developing, operating and fully documenting the medical physics quality assurance program and ensures regulatory compliance within the Radiation Safety Officer's radiation safety program.</li>
<li>Safely utilizing and properly operating all radiation oncology equipment, and is therefore qualified and responsible for educating radiation oncology team members including radiation oncologists, radiation therapists and dosimetrists in safety issues that relate to radiotherapy planning and delivery.</li>
<li>The employee performs the following actions to assist in the implementation of new equipment and processes:
<ul>
<li>Assesses radiation therapy equipment needs</li>
<li>Performs acceptance testing and commissioning of new radiation therapy equipment</li>
<li>Evaluates the adequacy of room shielding</li>
<li>Performs radiation surveys</li>
<li>Develops and implements treatment processes.</li>
</ul>
</li>
<li>The advanced level TMP will be a knowledgeable user and subject matter expert in the use of the Pinnacle, Eclipse and Cyberknife Precision treatment planning systems, Truebeam and Cyberknife delivery systems, and Sun Nuclear QA equipment and software.</li>
<li>The advanced level TMP will also be an expert in the following special procedures: stereotactic radiosurgery, stereotactic body radiation therapy, and surface-guided radiation therapy.</li>
<li>Provide support for clinical research trials, including submission of radiation plans, DICOM datasets as needed. </li>
</ul>
Requirements:
<ul>
<li>United States Citizenship: Non-citizens may only be appointed when it is not possible to recruit qualified citizens in accordance with VA Policy.</li>
<li>Education: Master's degree or higher in a physics, science, or engineering discipline recognized by an accredited college or university with at least 30 semester hours in medical physics, health physics, radiological science, physics, engineering, chemistry, or biology; or an equivalent foreign degree and coursework substantiated by the National Association of Credential Evaluation Services.</li>
<li>Board Certification: Persons hired or reassigned to TMP positions in the VHA must be board certified in the field of therapeutic medical physics by an approved certifying body. The board certificate must be current and the applicant must abide by the certifying body's requirements for continuing education. Approved Certifying Bodies:
<ul>
<li>The American Board of Radiology (ABR) in any of the following field titles:
<ul>
<li>Therapeutic Medical Physics</li>
<li>Therapeutic Radiologic or Therapeutic Radiological Physics</li>
<li>Radiologic Physics or Radiological Physics</li>
</ul>
</li>
<li>The American Board of Medical Physics (ABMP) in the subfield of Radiation Oncology Physics.</li>
<li>The Canadian College of Physicists in Medicine (CCPM) in the subfield of Radiation Oncology Physics.</li>
</ul>
</li>
</ul>

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