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<h3>Job Description</h3>
Job DescriptionDescription:
Venesco, LLC., is seeking a Molecular Biologist to assist on a contract with a federal government client in [LOCATION].
US Citizenship and [CLEARANCE] is required for this position.
The successful candidate will work directly with the Client and support team members to:
<ul>
<li>Assist biological and medical scientists in laboratories, setting up, operating, and maintaining laboratory instruments &amp; equipment, monitoring experiments, making observations, and calculating/recording results.</li>
<li>Perform DNA extraction from samples, generate genomic data through molecular techniques, and characterize genomic variation using phylogenetic tools.</li>
<li>Perform next generation sequencing, PCR, and bioinformatics as needed in support of various projects research objectives.</li>
<li>Assist PHT staff in developing and optimizing procedures for pathogen and infectious disease testing. Including the design and synthesis of primers and probes for those procedures.</li>
<li>Update/conduct review of scientific literature relevant to the research initiatives.</li>
<li>Support experimental planning/design, protocol training and execution, and data collection and analysis.</li>
<li>Support pursuit of funding opportunities, and development, reporting, and editing of competitive, well-written, full drafts of research proposals, papers, and presentations as related to the project.</li>
<li>Assist with the preparation, coordination, and submission of protocol-related documents to Institutional Review Boards (IRB) or Institutional Biosafety Committee (IBC).</li>
<li>Support the preparation of reports of program initiatives as related to the project at the direction and input of PHT staff.</li>
<li>Support the laboratory with other tasks as required to ensure proper function of the laboratory, including but not limited to communal solid waste disposal, and general laboratory maintenance procedures.</li>
<li>Perform experiments within a high containment lab in support of ongoing BSL-3 level efforts, being able to don a power air purifying respirator and full body personal protective equipment, for multiple hours per day.</li>
<li>The Contractor shall abide by all Federal, State and USAFSAM directives concerning the confidentiality of records, as embodied in federal statutes including the Privacy Act of 1974 and Health Information Portability Accountability ACT (HIPAA).</li>
</ul>
Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.
For more information on Venesco, LLC., visit <a href="https://venesco.com" target="_blank">https://venesco.com</a>.
Requirements:
 
<ul>
<li>Experience with prioritizing and executing tasks in a high-pressure environment.</li>
<li>Experience with government contracting firms supporting the Federal government.</li>
<li>Ability to maintain confidentiality of sensitive information within and external to Venesco, LLC., using own judgment.</li>
<li>Exceptional analytical, conceptual, and problem-solving abilities.</li>
<li>Ability to quickly develop understanding of the organization’s goals and objectives.</li>
<li>Able to prioritize and execute tasks in a high-pressure environment.</li>
<li>Excellent verbal, written, and interpersonal communication skills.</li>
<li>Exceptionally self-motivated, directed, and detail oriented.</li>
<li>Proficient in Microsoft Office (word, Excel, Outlook) and Adobe Acrobat.</li>
</ul>

Molecular Biologist

<h3>Job Description</h3>
Job DescriptionDescription:
Week Nights (Mon - Thurs; 5:00PM - 5:00AM 
 
Description
Reporting to the Production Manager, Chemical Operator will be located at the company’s headquarters and primary manufacturing location in Medina, OH location. This individual is responsible for assisting mixing/blending of materials, operation of process equipment, and related duties. They will maintain production records and ensure standard operating procedures are being followed. They will be required to comply with all regulatory, safety, and environmental requirements. 
 
Key Responsibilities
<ul>
<li>Responsible for assisting mixing/blending of materials, filling and labeling bulk containers, and operation of process equipment</li>
<li>Assisting in the unloading of rail cars and tank wagons</li>
<li>Operate a forklift to stage materials</li>
<li>Complete production reporting and quality control reporting in a timely and accurate manner</li>
<li>Maintains the cleanliness of the yard</li>
<li>Maintains the organization of the tote and drum storage area</li>
<li>Must follow all safety procedures and act in a safe manner at all times and have an understanding and awareness of chemicals and their nature, hazards, safety and health issues etc. (MSDS's, use of PPE etc.)</li>
<li>Performs scheduled cycle counts</li>
<li>Performs other related duties as assigned Requirements</li>
</ul>
Requirements:
<ul>
<li>High School Diploma or equivalent required, Associate’s degree or higher a plus.</li>
<li>Must have effective verbal and written English communication skills</li>
<li>Able to work overtime and nights as required</li>
<li>2 years of manufacturing experience. Preferably in a chemical plant.</li>
</ul>
Knowledge – Skills – Abilities
<ul>
<li>Ability to work well under minimal supervision</li>
<li>Attention to details, organization ability and ability to interact well with others.</li>
<li>Must be able to operate basic hand tools</li>
</ul>
Physical Requirements• Ability to work in a chemical manufacturing plant environment.• Ability to execute strenuous, sometimes repetitive physical work such as climbing, lifting objects up to 50 lbs and pushing/ pulling objects up to and including moving heavy drums weighing 440+ lbs.• Ability to stand for long periods of time.• Able work in extreme temperatures, indoors and out#Operator #Quality #Chemicals #Manufacturing #Batch #BatchSpray Products is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Spray Products is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Spray Products are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Spray Products will not tolerate discrimination or harassment based on any of these characteristics. Spray Products encourages applicants of all ages. 
 
ADA Compliance: The job requires long periods of standing in a production environment. The job requires long periods of sitting on a forklift in a warehouse environment.

Chemical Plant Operator

<h3>Job Description</h3>
The Chemist will play a key role in both routine quality testing and advanced product development projects. This role involves hands-on work with paints, coatings, and emulsions, as well as supporting new product formulations, color matching, and troubleshooting production challenges. The ideal candidate has experience in coatings chemistry, a strong technical foundation, and the ability to balance day-to-day testing with long-term R&amp;D initiatives.
 
Chemist Responsibilities:
<ul>
<li>Perform QC/QA testing on raw materials and finished products, including viscosity, pH, density, solids, unit weight, and color analysis.</li>
<li>Develop and standardize color matching procedures using spectrophotometers and related instrumentation.</li>
<li>Contribute to formulation adjustments and product development for coatings, paints, and water-based emulsions (acrylics, waxes, etc.).</li>
<li>Research and evaluate raw materials to improve quality, cost-efficiency, and sustainability.</li>
<li>Troubleshoot production issues related to color, formulation, or process variations, implementing root-cause and corrective actions.</li>
<li>Support R&amp;D initiatives to optimize formulations and bring new products to market.</li>
<li>Maintain accurate testing records and reports, and ensure compliance with industry regulations (e.g., VOC).</li>
<li>Research and evaluate new raw materials to enhance supply chain efficiency, elevate product quality, and drive cost savings.</li>
<li>Partner with vendors and internal stakeholders to ensure compliance with regulatory standards, sustainability goals, and strategic alignment with business objectives.</li>
<li>Collaborate cross-functionally with lab, operations, and sales teams to resolve customer issues and provide technical expertise.</li>
</ul>
 
Chemist Requirements:
<ul>
<li>Bachelor’s degree in Chemistry, Chemical Engineering, Materials Science, or related field.</li>
<li>2+ years of laboratory experience in paints, coatings, emulsions, or related chemical formulations (3–5 years preferred).</li>
<li>Proficiency in QC testing methods (viscosity, pH, specific gravity, solids, spectrographic/color analysis).</li>
<li>Hands-on experience with color matching and formulation development.</li>
<li>Strong problem-solving, data analysis, and technical reporting skills.</li>
<li>Ability to work independently and collaboratively in a fast-paced lab and production environment.</li>
<li>Familiarity with experimental design (DOE), Six Sigma, Batch Master, or formulation software a plus.</li>
<li>Proficiency with advanced color science principles (CIE Lab, Delta E) and instrumentation (spectrophotometers, colorimeters).</li>
</ul>

Chemist

<h3>Job Description</h3>
Job Description
Endeavour’s Pact group has an exciting opportunity for a Chemical Process Pilot Plant Operator. We are currently operating a small pilot plant of our patented catalytic cracking process, which cracks methane into green hydrogen and graphite, located in Wadsworth, OH. We are seeking an experienced, skilled and motivated Chemical Process Pilot Plant Operator. We are currently operating a small pilot plant of our patented catalytic cracking process, which to join our team. The successful candidate will be responsible for operating and maintaining the pilot system, ensuring efficient and safe production processes. This role is crucial in achieving our mission of making low cost zero carbon footprint hydrogen. In this position you will work directly with the project lead and will be responsible for building a team of operators for our commercial rollout expected next year. Key Responsibilities Include but are not limited to: • Operate pilot plant equipment and machinery in accordance with standard operating procedures (SOPs) and safety guidelines. • Monitor and control the process parameters to ensure optimal performance and product quality. • Perform routine inspections and maintenance of plant equipment to ensure smooth operation and prevent breakdowns. • Troubleshoot and resolve operational issues in a timely and effective manner. • Record and maintain accurate production data and logs. • Participate in continuous improvement initiatives to enhance plant performance and efficiency. • Assist in training and mentoring new plant operators. Skills &amp; Requirements Education / Experience • High school diploma or equivalent; technical diploma or degree in mechanical, chemical, or industrial engineering preferred. • Minimum 3 years’ experience as a plant operator, preferably in a chemical, gas processing, or industrial furnace environment. Specific Skills / Abilities • Strong understanding of plant operations, process controls, and safety protocols. • Ability to read and interpret technical manuals, diagrams, and schematics. • Capable of reading Ladder Logic software and using computerized control systems. • Excellent problem-solving skills and attention to detail. • Strong communication and teamwork abilities. • Willingness to work in shifts, including nights, weekends, and holidays as required. Great Place to Work Enjoy… A fast-paced, entrepreneurial culture focused on innovation. A flexible, autonomous work environment. A culture of respect, learning, and excellence. Experienced, highly talented experts as team peers. Growth and travel opportunities. A team of change-makers having a significant impact on people and the planet.
About Pact Pact is scaling novel technologies that reduce carbon emissions while making local hydrogen, graphite, and biofuels affordable anywhere in the world. Pact is part of the Endeavour Energy ecosystem, a purpose-driven organization helping innovators to develop and launch global solutions for global challenges in the areas of energy, water, and waste to guarantee renewable energy and clean water to everyone, everywhere. Endeavour companies are made up of passionate change-makers who want to leave the world better than the way we found it. Today, Endeavour is deploying solutions that are immediately scalable and profitable, including EV charging, data center cooling, and waste to fuel systems. As we look to the future, Endeavour and Pact intend to remain at the forefront of innovation, taking on grander challenges based on the needs of our clients and of local economies. Position: Chemical Process Pilot Plant Operator Full-Time or Part-Time: Full-Time Reports to: Senior Director, Business Development &amp; Strategy Location: Wadsworth, OH (On-Site)
Company DescriptionEndeavour is taking on global challenges, and to create the appropriate global solutions is not easy. Our teams work extremely hard because we believe in Endeavour’s mission: to guarantee clean water and renewable energy to everyone, everywhere by decentralizing infrastructure, developing new technologies, &amp; deploying energy, water, and waste treatment solutions that are more profitable than those that currently exist. We are a group of passionate change-makers who want to leave the world better than the way we found it. Endeavour prides itself on hiring talented, highly motivated people because that’s what our mission requires. There is a strong sense of camaraderie between good-natured people who bring their A-game to work every day to make a difference. To work at Endeavour is to know that you are part of something special—something bigger than yourself. Today, we’re deploying solutions that are immediately scalable and profitable, including EV charging, data center cooling, and waste to fuel systems. As we look to the future, Endeavour intends to remain at the forefront of innovation, taking on grander challenges based on the needs of our clients and of local economies. We hope that our Sustainable Habitat for Innovation with a Purpose (SHIP) will be a model that inspires people and businesses to #jointhejourney so that together we can combine the best of what technology and the natural world can offer to ensure a regenerative/sustainable world for generations to come. 
<h3>Company Description</h3>
Endeavour is taking on global challenges, and to create the appropriate global solutions is not easy. Our teams work extremely hard because we believe in Endeavour’s mission: to guarantee clean water and renewable energy to everyone, everywhere by decentralizing infrastructure, developing new technologies, &amp; deploying energy, water, and waste treatment solutions that are more profitable than those that currently exist. We are a group of passionate change-makers who want to leave the world better than the way we found it. Endeavour prides itself on hiring talented, highly motivated people because that’s what our mission requires. There is a strong sense of camaraderie between good-natured people who bring their A-game to work every day to make a difference. To work at Endeavour is to know that you are part of something special—something bigger than yourself.\r\n\r\nToday, we’re deploying solutions that are immediately scalable and profitable, including EV charging, data center cooling, and waste to fuel systems. As we look to the future, Endeavour intends to remain at the forefront of innovation, taking on grander challenges based on the needs of our clients and of local economies. We hope that our Sustainable Habitat for Innovation with a Purpose (SHIP) will be a model that inspires people and businesses to #jointhejourney so that together we can combine the best of what technology and the natural world can offer to ensure a regenerative/sustainable world for generations to come.

Chemical Process Pilot Plant Operator

<h3>Job Description</h3>
Job Description
Currently hiring for an Entry-Level Chemist in the north Dayton, OH area! This is a long-term career opportunity for someone looking to get their foot in the door and grow in the field. An ideal candidate will have a Bachelors degree in a science such as Biology, Chemistry, Biochemistry, Food Science, Microbiology, or a relative degree.
Shift: 3rd shift, 6pm - 6am. Will be working just 3-4 days per week (so total hours will be 36 or 48 hours in any given week)
Job Description:
This role is an entry-level Chemist position performing quality control testing on raw materials and finished products to meet cGMP requirements. This role will also participate in various lab activities and audits. You will primarily be testing on beverage related products.
<ul>
<li>Analyze samples including raw materials, finished products, process equipment, and environmental samples.</li>
<li>Test raw materials and finished products in accordance with cGMP standards.</li>
<li>Participate in lab investigations and operate laboratory equipment.</li>
<li>Engage in internal and external quality audits.</li>
<li>Maintain personal lab work area and assist with general lab cleaning tasks.</li>
<li>Participate in training sessions to enhance skills and knowledge.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's Degree in a Science discipline with chemistry coursework</li>
</ul>
Pay and Benefits
The pay range for this position is $21.00 - $21.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in COVINGTON,OH.
Application Deadline
This position is anticipated to close on Sep 17, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

QC Chemist

<h3>Job Description</h3>
Job Title: Manager, Pilot Facility, Chemical Research&nbsp;&nbsp;
Reports To: Executive Director, Polymer Industry Cluster&nbsp;
Location: PIC Polymer Innovation Pilot Plant – Akron, Ohio (specific location TBD)&nbsp;
Status: Salary, Exempt&nbsp;
 
POSITION OVERVIEW:&nbsp;&nbsp;
The Polymer Industry Cluster (PIC) is seeking an experienced and highly motivated Pilot Facility Manager to lead the operation of a new state-of-the-art facility dedicated to polymer research, product development, and scale-up. This role is essential to ensuring safe, efficient, and innovative operations that support the development and commercialization of advanced polymer materials. The Manager, Pilot Facility, Chemical Research will oversee day-to-day plant operations, supervise technical staff, and coordinate projects with internal and external stakeholders.&nbsp;
 
KEY RESPONSIBILITIES:&nbsp;
<ul>
<li>Lead the safe and effective operation of pilot-scale chemical and polymer processing equipment.&nbsp;</li>
<li>Manage daily pilot plant operations, including scheduling, maintenance, and resource allocation.&nbsp;</li>
<li>Provide technical leadership in polymer process development and scale-up of novel materials.&nbsp;</li>
<li>Ensure compliance with EH&amp;S regulations and company safety protocols.&nbsp;</li>
<li>Collaborate with R&amp;D, engineering, and external partners to design and execute pilot campaigns.&nbsp;</li>
<li>Supervise and mentor a team of technical operators, engineers, and support staff.&nbsp;</li>
<li>Oversee commissioning, validation, and troubleshooting of new process equipment.&nbsp;</li>
<li>Develop and maintain standard operating procedures (SOPs) and documentation systems.&nbsp;</li>
<li>Track and report key performance indicators (KPIs) related to plant operations and project outcomes.&nbsp;</li>
<li>Support continuous improvement initiatives and implement best practices in pilot operations.&nbsp;</li>
</ul>
 
QUALIFICATIONS:&nbsp;
<ul>
<li>Bachelor’s degree in Chemical Engineering or a related field required.&nbsp;</li>
<li>Advanced degree (MS or PhD) a plus but not required.&nbsp;</li>
</ul>
 
EXPERIENCE:&nbsp;
<ul>
<li>Minimum of 5 years of relevant experience in process development, scale-up, or manufacturing within the chemical or polymer industry.&nbsp;</li>
<li>Demonstrated experience in operating and managing chemical process laboratories or pilot plants.&nbsp;</li>
<li>Hands-on knowledge of polymerization processes, mixing, extrusion, or other relevant chemical processing operations.&nbsp;</li>
<li>Experience commissioning new pilot equipment and implementing new technologies preferred.&nbsp;</li>
</ul>
 
SKILLS &amp; COMPETENCIES:&nbsp;
<ul>
<li>Strong leadership and team management skills.&nbsp;</li>
<li>Excellent troubleshooting and problem-solving capabilities.&nbsp;</li>
<li>Deep understanding of process safety, regulatory compliance, and risk management.&nbsp;</li>
<li>Effective communication and interpersonal skills for working with multi-disciplinary teams and external partners.&nbsp;</li>
<li>Proficient in technical documentation, data analysis, and project management tools.&nbsp;</li>
</ul>
 
OTHER CONSIDERATIONS:&nbsp;
<ul>
<li>May be required to work more than 8 hours during a workday.&nbsp;</li>
<li>Must be able to remain in a stationary position 50% of the time.&nbsp;</li>
<li>Occasionally moves office materials and/or supplies weighing up to 25 pounds throughout the office.&nbsp;</li>
</ul>
 
SCHEDULING REQUIREMENTS:&nbsp;
<ul>
<li>Must be available to work occasional off-hours.&nbsp;&nbsp;</li>
<li>Must be available during standard business hours.&nbsp;</li>
<li>While this position will be based in the plant facility in Akron, OH in the GAC’s main office, aspects of this role may be fulfilled through periodic telecommuting as determined appropriate and in conjunction with project supervision.&nbsp;&nbsp;&nbsp;&nbsp;</li>
<li>Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.&nbsp;&nbsp;</li>
</ul>

Manager, Pilot Facility, Chemical Research

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Assurance Chemist Pay: 60k+ Shift: 1st
Job Description
The Quality Assurance Specialist is responsible for supporting quality system processes and maintaining quality assurance standards, processes, and controls. This role involves close collaboration with Manufacturing, Quality Control, Maintenance, Shipping, and Receiving departments. The position requires the ability to perform in a fast-paced environment and demands a self-starter attitude. While the standard working hours are Monday through Friday, there may be a need for overtime on weekends and/or holidays to support Manufacturing and Lot Release activities.
Responsibilities
<ul>
<li>Generate, review, facilitate corrections, and archive documents used to support Good Manufacturing Practice manufacture of Final Product.</li>
<li>Perform internal and external audits as assigned.</li>
<li>Review and release raw materials, intermediate products, and finished products; assist in incoming material and tote inspection.</li>
<li>Perform review and approval of OOS, deviations, nonconformance, and investigations as required.</li>
<li>Coordinate CAPA, OOS, deviations, nonconformance, and investigations.</li>
<li>Ensure systems are in compliance with current SOPs.</li>
<li>Assist and perform investigations to resolve potential product quality issues.</li>
<li>Assist with writing, revising, and approving standard operating procedures and work instructions.</li>
<li>Review and approve SOPs, protocols, and reports as necessary.</li>
<li>Coordinate and/or conduct GMP training and SOP training.</li>
<li>Generate, publish, and manage quality systems metrics to drive continuous improvement.</li>
<li>Scan and archive GMP documents.</li>
<li>Conduct QMS related functions including calibration tracking and product release.</li>
<li>Assist Environmental and Safety functions as necessary.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in a scientific discipline or equivalent experience.</li>
<li>At least 2 years’ experience in a cGMP/FDA environment and ISO 9001 within relevant Quality Assurance/Compliance functions.</li>
<li>Strong knowledge in ISO 9001-2015, cGMP, CFR 210/211, FDA, Pharmaceutical, HACCP, Food Safety Management, and ICHQ7 requirements.</li>
<li>Knowledge of statistical process control (SPC).</li>
<li>Strong project, time management, and conflict resolution skills.</li>
<li>Proficient with Microsoft Office tools, especially Excel.</li>
<li>Excellent written and verbal communication skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in a manufacturing environment, with a strong preference towards chemical manufacturing/processing.</li>
<li>Training experience is a plus.</li>
<li>Experience with QT9 is a plus.</li>
</ul>
Work Environment
This position operates in a manufacturing setting and professional office environment, utilizing standard office equipment such as computers, phones, photocopiers, filing cabinets, and fax machines. Some work requires exposure to loud noises or fumes in the plant facility, collaborating with officials, plant managers, and employees. Physical demands include occasionally sitting, climbing, balancing, stooping, kneeling, crouching, or crawling, and frequently lifting/moving up to 10 pounds and occasionally up to 25 pounds.
Pay and Benefits
The pay range for this position is $60000.00 - $72000.00/yr.
Medical, Dental, Vision, Life/AD&amp;D, 401K, and vacation
Workplace Type
This is a fully onsite position in Ashtabula,OH.
Application Deadline
This position is anticipated to close on Sep 17, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Assurance Chemist

<h3>Job Description</h3>
Job Description Medical Physicist PhD Cert - Troy - Radiation Oncology - FT/First Shift US-OH-Troy Job ID: 2024-50824 Type: Full-Time # of Openings: 1 Category: Physicist KH Troy Overview 
Kettering Health is a not-for-profit system of 13 medical centers and more than 120 outpatient facilities serving southwest Ohio. We are committed to transforming the health care experience with high-quality care for every stage of life. Our service-oriented mission is in action every day, whether it’s by providing care in our facilities, training the next generation of health care professionals, or serving others through international outreach.
 Responsibilities 
Key Responsibilities:
<ul>
<li>Clinical Support: Provide expert medical physics support for Radiation Oncology procedures, ensuring optimal performance and safety of all equipment. Opportunity to contribute to Gamma Knife and HDR procedures located at main campus.</li>
<li>Equipment Management: Oversee the acquisition, installation, calibration, and acceptance of radiation treatment equipment, maintaining meticulous records and documentation.</li>
<li>Quality Assurance: Ensure compliance with quality measures and standards as set by the State of Ohio, documenting all quality assurance activities.</li>
<li>Professional Development: Maintain up-to-date knowledge and skills within the field, pursuing ongoing professional development and adhering to legal and ethical standards.</li>
<li>Patient Advocacy: Advocate for patient safety and high-quality care, actively participating in performance improvement initiatives and utilizing organizational resources effectively.</li>
<li>Mission Alignment: Uphold the organization’s mission, vision, values, and philosophies in all aspects of work and collaboration with the Radiation Oncology department.</li>
</ul>
 Qualifications 
Qualifications:
<ul>
<li>Education: PhD, DMP, or MS in medical physics or a related field. Board certification in Therapeutic Medical Physics is preferred, but we encourage board-eligible candidates to apply and continue to pursue certification.</li>
<li>Experience: A minimum of two years of recent clinical medical physics experience in Radiation Oncology is preferred.</li>
<li>Certification: Board certification in Therapeutic Medical Physics preferred. Must obtain BLS certification upon hire.</li>
<li>Candidates: MS, DMP, or PhD board-certified or board-eligible candidates are strongly encouraged to apply.</li>
</ul>
#PM21
 
Compensation details: 108.29-151.61
 
PI3fc1de845092-25405-35498376

Medical Physicist PhD Cert - Troy - Radiation Oncology - FT/First Shift

<h3>Job Description</h3>
Staff Scientist:
 
Manage the primary responsibilities for the Research and Development processes associated with a specific ASK product line which contributes to the North American (USA, Canada, &amp; Mexico) business unit. A Scientist’s key roles are both strategic (50%) and tactical (50%). Strategic elements include identification of possible technology paths, project governance, etc. while tactical elements include technology screening, technical bench work, and some administrative activities.
 
Primary Roles &amp; Responsibilities: 
 
<ul>
<li>Act as the technology gatekeeper within ASK’s governance process to screen potential development projects for technical feasibility. Plan, design, and administer projects while ensuring project objectives are well defined and resulting outcomes / deliverables meet those requirements.</li>
<li>Lead a defined team of scientists and technicians in conducting research &amp; development for existing technology platforms and manufacturing processes according to defined business priorities. Manage product line development personnel and budgetary resources while coordinating work group.</li>
<li>Manage and perform technical bench work on both a commercially driven portfolio of projects as well as a defined number individual projects of their choosing while investigating new / alternative technology platforms and manufacturing processes.</li>
<li>Hire, train, coach, supervise and develop technical personnel. Review and appraise subordinate performance while recommending adjustments in role and / or compensation.</li>
<li>Provide technical oversight, expertise, problem solving, and data driven analysis while developing solutions to complex technical problems. Gather, manage, and analyze regional competitive product intelligence.</li>
<li>Maintain a high level of knowledge in the field of specialty. Prepare, distribute, and present scientific reports and papers for internal communication.</li>
</ul>
 
Secondary Roles &amp; Responsibilities: 
<ul>
<li>Submit periodic monthly reports summarizing the status of individual projects and resources applied.</li>
<li>Submit individual final project reports to global peer group summarizing project objective, technical paths evaluated, and resulting success or learnings.</li>
<li>Collaborate with research and development peers, plant engineers, foundry process engineers, design services engineers, and technical service personnel in commercialization / implementation of new products and processes.</li>
<li>Collaborate with internal EH&amp;S and IP functions to maintain regulatory compliance, achieve health and safety goals, and establish patent position for new developments.</li>
<li>Assist in the generation of specific product line technology strategies as they relate to the overall business unit strategy.</li>
<li>When appropriate prepare, distribute, and present a limited number of scientific reports and papers for external communication to the professional community.</li>
<li>Any other duties as assigned by the Director of Research &amp; Development.</li>
</ul>
 
Required Education &amp; Experience Levels: 
<ul>
<li>Masters or Bachelors Chemistry, Chemical Engineering, Material Science, or Metallurgy with 2-3 years of applied research and development or industrial experience required</li>
</ul>
 
Preferred Skills &amp; Know How: 
<ul>
<li>Strong interpersonal skills and ability to work in a team and project driven environment.</li>
<li>Attention to detail while demonstrating the ability to see the big picture.</li>
<li>Utilization of standard MS Office tools.</li>
<li>Utilization of advanced statistical tools (MiniTab®, MatLab®, SAS®, etc.).</li>
<li>Familiarity with ERP and Document Management platforms (SAP®, Entropy®, etc.).</li>
</ul>
 
ASK Chemicals is a new and growing company with a history of attracting the best people and keeping them. The reasons are simple: industry competitive salary and benefits, pay-for-performance incentive plans and a diverse work environment where employees feel challenged and valued. As a growing global specialty chemical company, we offer opportunities for development and advancement throughout our organization. If you are looking for a relationship with a company instead of simply a job, this may be a great fit.
 
ASK Chemicals is proud to be an Equal Opportunity Employer.

Staff Scientist

<h3>Job Description</h3>
The Ohio State University College of Medicine is seeking applicants to join our General Internal Medicine team as Director of Research.&nbsp; This is a full time, tenure track position at the Associate or Full Professor level. The position is expected to dedicate the majority of their time to research, but also to make significant contributions to the clinical and education missions of the Division.
Recognized for providing personalized comprehensive patient care, innovative educational opportunities for students and residents and a developing research environment, our aim is to develop long-term healing relationships with patients and help them navigate their care within a complex medical system. The Division is leading efforts for the medical centers Comprehensive Primary Care Plus (CPC+) and Million Hearts programs while also leading innovative services in Pediatrics, Geriatrics, Transitional Care for Young Adults and various other research collaborations.
&nbsp;The position will lead and direct the research activities of GIM. The position will have the oversight responsibility for implementation of processes and ongoing development of research infrastructure, programs, recruitment, clinical integration, as well as development of metrics and tracking mechanisms to ensure steady growth of the research enterprise. The successful applicant could also direct a specified research program related to their area of expertise.
&nbsp;Requirements: MD or DO; Completion of Internal Medicine Residency from ACGME accredited program; Board-certified/eligible in Internal Medicine; at least 5 years experience post training; Associate Professor/Professor rank.
&nbsp;All academic appointments are commensurate with experience. *Physicians will have privileges at The Ohio State University Wexner Medical Center, University Hospital East, The James Cancer Center and Solove Research Institute, Richard M. Ross Heart Hospital.
Why work for The Ohio State University Wexner Medical Center:
<ul>
<li>Central Ohios Academic Leader</li>
<li>One of the largest and most diverse medical centers in the country; only academic medical center in central Ohio and Columbus (Ohios largest and most rapidly growing metropolitan region)</li>
<li>Ranked one of &nbsp;Americas Best Hospitals" by U.S. News and World Report for over 30 consecutive years</li>
<li>Voted one of Central Ohios Best Places to Work by Columbus Business First newspaper</li>
<li>For over 30 years, recognized as a national leader in quality outcomes and patient safety</li>
</ul>
Our planned growth at The Ohio State University Wexner Medical Center:
<ul>
<li>Main campus:&nbsp; New construction of a state-of-the-art biomedical research tower, 880-bed hospital tower, ambulatory center and Health Sciences building that will house the College of Medicine</li>
<li>Around the city:&nbsp; Construction of 2 Newly designed Ambulatory Centers COMPLETED AND NOW OPEN in addition to 5 established ambulatory care centers up and running today</li>
</ul>
Why live in Columbus, Ohio:
<ul>
<li>1.8 million population base and diverse cultural, sports, dining and recreational opportunities: Cost of Living is LOW</li>
<li>Recently voted the #1 IT city in the nation surpassing Silicon Valley</li>
<li>Home to several Fortune 500 companies</li>
<li>Ranks in Money magazines picks as one of the ten best big cities</li>
<li>Second fastest growing major metropolitan area in the Midwest :&nbsp; 14th largest city in the nation</li>
<li>Booming real estate market</li>
<li>Consistently ranked in the top ten in nearly every category: Economic growth, things to do, affordable cost of living, great place to raise a family</li>
</ul>
To join our team, please email your cover letter and CV to: Kam Carlberg, Faculty Recruitment The Ohio State University Wexner Medical Center <a href="mailto:kamala.carlberg@osumc.edu" target="_blank">kamala.carlberg@osumc.edu</a>
The university is an equal opportunity employer, including veterans and disability.

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