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field_job_experience

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Job Summary:
We are seeking an experienced Chemical process engineer to oversee daily operations at our chemical manufacturing facility. The ideal candidate will have a strong background in chemical engineering, process management, and hands-on experience in formulating, scaling, and producing polymers. This position requires comprehensive knowledge of chemical handling, process safety, and production optimization.
Key Responsibilities:
· Lead, supervise, and coordinate all aspects of plant operations related to polymer synthesis and chemical processing.
· Manage day-to-day plant activities including production scheduling, equipment maintenance, quality control, and personnel oversight.
· Monitor and optimize production processes for efficiency, yield, and quality, particularly in the manufacture of water-based, solvent-based, or specialty polymers.
· Ensure compliance with OSHA, EPA, and other regulatory requirements, including proper chemical handling, storage, and disposal.
· Oversee raw material procurement and inventory control of monomers, catalysts, surfactants, solvents, and other chemicals.
· Work closely with R&amp;D and QA teams to scale up lab-developed polymers to full-scale production.
· Develop and maintain standard operating procedures (SOPs), batch sheets, and safety protocols.
· Train and mentor plant staff in chemical safety, operational procedures, and emergency response.
· Analyze data and implement continuous improvement strategies for process reliability, safety, and cost-effectiveness.
· Manage capital improvement projects, plant expansions, and equipment upgrades.
Qualifications:
· Bachelor’s degree (or higher) in Chemical Engineering, Chemistry, or Polymer Science.
· Minimum 5 years of experience in a chemical or polymer manufacturing plant, with at least 2 years in a supervisory or management role.
· Strong working knowledge of polymerization techniques (e.g., emulsion, suspension, solution, bulk).
· Familiarity with chemical process equipment (reactors, mixers, filtration units, etc.).
· Proficient in chemical handling protocols, hazard communication (GHS), and personal protective equipment (PPE) use.
· Experience with batch processing, process control systems (PLC/SCADA), and ISO/GMP standards is preferred.
· Excellent leadership, communication, and problem-solving skills.
Preferred Skills:
· Experience with waterborne acrylics, polyurethanes, styrene-butadiene, or specialty resin systems.
Work Environment:
· Manufacturing plant environment with regular exposure to chemicals, high temperatures, and production machinery.
· Must be able to wear required PPE and respond to emergencies when necessary.
Compensation &amp; Benefits:
· Competitive salary commensurate with experience
· Health insurance
· SIMPLE IRA (SIRA) retirement plan
· Paid time off and holidays
· Relocation assistance (if applicable)
Job Type: Full-time
Pay: $90,257.70+
Benefits:
<ul>
<li>401(k)</li>
<li>Flexible schedule</li>
<li>Health insurance</li>
<li>Paid time off</li>
</ul>
Schedule:
<ul>
<li>8 hour shift</li>
<li>Monday to Friday</li>
</ul>
Education:
<ul>
<li>Bachelor's (Required)</li>
</ul>

Chemical Process Engineer

<h3>Job Description</h3>
Job Descriptionjob summary: 
Radiochemist I or II - permanent FTE role fully onsite in Atlanta, GA. If you are a traditional chemist / nuclear chemist / radiochemist with radiation experience you could fit this role!
You will manufacture radioactive calibration standards, check sources and and check the proficiency of testing samples. Plans and organizes quarterly production of Performance Testing Samples, evaluates data, performs some troubleshooting, and provides support to the traceability program.
 location: Atlanta, Georgia job type: Permanent salary: $68,000 - 70,000 per year work hours: 8 to 4 education: Bachelors responsibilities: 
<ul>
<li>Manufactures calibration standards, check sources and PE samples.</li>
<li>Manufactures sources to support Counting Laboratory and NIST MAP / traceability program.</li>
<li>Produces mixed isotope batches e.g., MGS, TCC, GRS, A/F, and others.</li>
<li>Performs gas and solution calibrations, reviews, and signs Certificates of Calibration.</li>
<li>Maintains laboratory environment, equipment, radionuclide, and chemical inventories.</li>
</ul>
 qualifications: 
-- a 4-year degree in Chemistry with 5 years related experience in radiochemistry and standard preparation.
-- 3 years combining wet radiochemistry (analytical balance operation, dilutions, pipetting),
(basics of nuclear counting methodology and nuclear physics experience a plus)
-- GLP experience
-- Nuclear Data software
#LI-DM1
 skills: Nuclear Magnetic Resonance (NMR) Spectroscopy 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.

Radiochemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Provides support for assigned, on-market products within Rheumatology Spondyloarthritis (SpA)&nbsp;therapeutic area and is responsible for performing the accurate and detailed scientific review of medical content for promotional and non-promotional materials. Contributes to the creation of externally facing medical affairs and training materials in accordance with established polices and standards, including regulatory guidelines to meet customer needs. Acquires and maintains up-to-date therapeutic expertise necessary to serve as a scientific, medical, and clinical partner to field medical teams/affiliates, TA teams, brand teams and R&amp;D partners
Responsibilities:
<ul>
<li>Promotional Material Review: Responsible for performing the accurate and detailed medical review of advertising and promotional materials for assigned therapeutic area(s) within Medical Affairs. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs.</li>
<li>Maintain understanding of product knowledge and labeling, associated disease states, relevant literature, treatment guidelines, competitor information</li>
<li>Evaluate risk and elevate as appropriate within the therapeutic area to ensure materials are compliant with applicable regulatory standards across all communication channels.</li>
<li>Evaluate literature, interpret data, write effectively, articulate information to a variety of internal and external audiences and effectively negotiate with counterparts from cross-divisional functional areas</li>
<li>Identifies Insight Trends: Aids in the broader teams ability to address educational scientific gaps identified through the gathering of feedback from multiple field sources, compile and summarize to provide relevant insights.</li>
<li>Development of non-promotional field/affiliate resources: Develops non-promotional field/affiliate resources and ensures communications are supported by medical communication standards, pharmacovigilance standards, SOP’s and all other quality and compliance standards in Medical Affairs.</li>
<li>Provides input into externally facing materials for use as directed : (i.e. Congress Booth, Ad Boards, Med Ed) with HCP or EE interactions (Payer, Patients, Prescribers, and Providers); educational initiatives (medical education, data, guidelines, and value proposition)</li>
<li>As directed, identifies, designs and implements focused and impactful internal training programs aiming to shape scientific understanding and medical practice (e.g. for Sales Representatives, MSLs, MOSLs, Affiliates)</li>
</ul>
Qualifications 
<ul>
<li>Scientific degree required; advanced degree (e.g., MS, PhD, MD/DO, PharmD, NP, MSN) preferred.</li>
<li>2-3 years of clinical, scientific/research, or industry related experience required.</li>
<li>Understanding of relevant therapeutic area required.</li>
<li>Demonstrates strong leadership competencies and proven team-building skills with ability to lead in a global matrixed environment.</li>
<li>Basic knowledge of clinical trial design, results and methodology, regulatory and compliance requirements governing development of promotional and non-promotional materials is desirable.</li>
<li>Demonstrated analytical, conceptual and administrative skills. Excellent communication skills (written and presentation).</li>
<li>Flexibility and adaptability to organizational change and business priorities. Ability to work in a fast-paced corporate environment. High sense of urgency and commitment to excellence in the successful achievement of objectives.</li>
<li>Excellent planning and organizational skills. Ability to manage multiple priorities and demonstrate good business judgment.</li>
<li>Strong Project Management and Teamwork skills to address project risks and issues.</li>
<li>Ability to influence without direct authority to effectively deliver cross-functional projects</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientific Manager, Medical Affairs

<h3>Job Description</h3>
&nbsp;
OLON USA LLC&nbsp;is seeking a qualified candidate to operate chemical process equipment in a pilot plant and laboratory environment. This is a 3rd shift opportunity.
 **Competitive salary, great benefits: 2 medical plans, dental, vision, company-paid + supplemental life &amp; income replacement benefits, 401k with company match-JOIN US!!**&nbsp;
Essential Job Functions:
This position will involve the operation of chemical process equipment in support of first-time scale-ups, process optimization and small-lot production of chemical-based materials in compliance with FDA’s current Good Manufacturing Practice guidelines. &nbsp;The successful candidate will execute processing activities according to specific procedures, make observations, record data and maintain accurate documentation. &nbsp;The position is hourly and the Technician will work 12 hour night shifts.
Educational Requirements:
High school diploma, basic knowledge of chemistry and math, mechanical aptitude, communication skills and teamwork skills. &nbsp;Must be able to work with and move drum quantities of chemicals. &nbsp;Previous experience, as a chemical plant/pilot plant operator is desirable. Knowledge of chemical hazards, forklift operation and college courses in chemistry considered a plus. &nbsp;
 
We offer a competitive salary along with a comprehensive benefit plan and a great workplace with really smart people, so join us!
--------------------------------------
Olon USA LLC. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.
 
 
 
 
PIad36359bb4cd-25405-37857420

Technician 2

<h3>Job Description</h3>
Job Description
Supports the enrollment of patients into clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements.
• Collaborates with the principal investigator to meet or exceed study enrollment.
• Reviews the study design and inclusion/exclusion criteria with physician and patient.
• Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements/compliance and provides close monitoring of subjects while on study.
• Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review. Monitors data for missing or inaccurate data and respond to queries.
• Creates study specific tools for source documentation when not provided by sponsor.
• Collects, completes, and enters data into study specific case report forms or electronic data capture systems.
• Generates and tracks drug shipments, device shipments and supplies as needed.
• Assists with sample collection to include environmental sample collection, packing and shipping of samples.
• Assists with study relevant forms required for various regulatory and oversight committees.
• Reports and follows up on serious adverse events as necessary.
• Implements study-specific communications.
• Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, device utilization logs, subject logs and study-related communications.
• Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations.
• Attends study specific on site meetings, Investigator meetings, conference calls and monthly CRC meetings as required or asked to do so.
• Apprises principal investigator of all study specific medical issues for guidance.
• Assists Sponsor, VA, FDA, IRB and other audit teams as needed.
• Reviews and responds to any monitoring and auditing findings
• Maintains patient confidentiality according to ethical and legal requirements.
• Assists in providing coverage for other projects and investigators as necessary or when asked to do so.
• Practice and adhere to the "VA Rules of Behavior."
• Performs other related duties as assigned by management.
 SUPERVISORY RESPONSIBILITIES:
• This job has no supervisory responsibilities.
QUALIFICATIONS:
• Bachelor's Degree (BA) from four-year college or university, or four years of related experience and/or training, or equivalent combination of education and experience.
• Certificates, licenses and registrations preferred but not required:
o Specialty research certification such as ACRP’s CCRA, CCRC, ACRP-CP or SOCRA’s CCRP.
• Computer skills required: Microsoft Office Suite
• Other skills required:
o Working knowledge of medical and research terminology.
o Working knowledge of federal regulations for human subject protections and Good Clinical Practices (GCP).
o Ability to communicate and work effectively with a diverse team of professionals.
o Excellent organizational and prioritizing capabilities.
o Strong computer skills with demonstrated abilities using clinical trial database, electronic data capture.
o Excellent interpersonal skills, detailed oriented and meticulous.
o Excellent professional writing and communication skills.
o Ability to demonstrate proficient achievement of ‘Intermediate CRC’ based on ACRP Core.
o Specimen and/or tissue collection, handling &amp; processing.
o Phlebotomy experience
 Monday - Friday 7am - 4pm on-site 40 hours per week

Health Science Specialist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose
Performs laboratory testing and uses scientific education and experiences to generate results in accordance with good manufacturing practices, procedural requirements, and scientific principles. Interprets reviews, verifies, approves, and releases data generated by others to determine conformance with product specifications.
Responsibilities
<ul>
<li>Understands, implements, and maintains a safe work environment and good manufacturing practices with respect to procedural requirements and laboratory records and requirements.</li>
<li>Maintains training certificates as needed for assigned job tasks.</li>
<li>Performs analytical or microbial test methods and data verification of lab results to support product and material release with minimal error.</li>
<li>Interprets experimental data for conformance with product and material specifications.</li>
<li>Initiates appropriate exception documents in accordance with procedural requirements.</li>
<li>Accepts responsibility for acquiring knowledge and experience to support continual personal development.</li>
<li>Can work in multiple laboratory functional areas as assigned and can effectively perform a multitude of laboratory techniques for which they are trained on with minimal error and the ability to adjust to unforeseen obstacles to accomplish assignments.</li>
<li>Budget time effectively to carry out assigned tasks and takes initiative to be involved in team activities and decision making.</li>
<li>Makes suggestions for improvement based upon scientific and good manufacturing practices understanding.</li>
<li>Works with others to maintain a positive atmosphere to accomplish business objectives and is an active participant in the work structure and fosters positive working relationships with all levels of the organization.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree minimally required, Associate’s Degree with at least 2 years of lab experience, High School Diploma with at least 5 years of directly related lab experience.</li>
<li>Ability to effectively manage their own time to multi-task based upon their completed training matrix.</li>
<li>Accountable to supervisor and assigned teams to meet broader business objectives.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements understate or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that theCompany believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job gradefor this position. Individual&nbsp;compensation paid within this range will depend on many factors includinggeographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may bemodified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested,and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any otherform of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company'ssole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole andabsolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Lab Analyst I

<h3>Job Description</h3>
Job Description
Calgon Carbon | A Kuraray Company is growing—and so can your career. Be part of a global leader in environmental solutions, where your work directly impacts the quality of air and water around the world.
Position: Chemical/Environmental Senior Applications Engineer Location: Remote - Western US
Excellent Benefits:&nbsp;Medical, dental, prescription &amp; vision, HSA &amp; retirement savings (401k) –&nbsp;Generous Company Match! Perks:&nbsp;Incentives/bonus plans, competitive pay, dress for your day, hybrid schedules, paid time off (vacation starting at 3 weeks), tuition reimbursement, wellness programs, fun events, learning &amp; development opportunities.&nbsp;&nbsp;
Hours of work:&nbsp;Full-time position with hours Monday-Friday 9:00-5:00 PM
 The Senior Applications Engineer provides the lead technical support for the sale of carbon, equipment, and service in domestic or international markets. This role interfaces with Equipment Engineering, Research and Development, Equipment and Assembly, Product Management, and Sales to provide the technical justification for the use of activated carbon technology in customer applications. The Senior Applications Engineer will assist in the technical development of emerging markets/applications as it pertains to their area of focus, as well as providing lead technical and business support for key global business development groups. This role can also include supervision of entry or intermediate applications engineers &nbsp; &nbsp;Duties and Responsibilities (not limited to) &nbsp;
<ul>
<li>Uses gained technical expertise, know-how and supplied computer models to select appropriate carbon and equipment for liquid and vapor phase applications, and predict performance based upon customer conditions</li>
<li>Set-up and monitor pilot trials in the field and provide design information for future full-scale systems</li>
<li>Interpret data from the lab and the field trials for pilot and full-scale systems to provide technical design and operational recommendations</li>
<li>Trouble shoot customer problems such as short filter run-times or unexpected breakthrough</li>
<li>Provide application engineering support for a geographic region(s) or set of Technical Sales Reps</li>
<li>Called to work with R&amp;D on the development / testing of new carbon products / applications</li>
<li>May also provide technical guidance to engineers with less experience and to overseas colleagues when called upon</li>
<li>Prepares and provides technical training for TSR when new topics, applications, etc. are encountered</li>
<li>Responsible for other general training and assuring consistency of technical messages from TSRs to customers</li>
<li>In coordination with the Technical Director, Market Development Director, and Sales Director, develop strategies and market-specific approaches to expand existing base business and develop new business opportunities through CCC technology adoption</li>
<li>Regularly review and evaluate actual results, report/troubleshoot variances, adjust strategy as appropriate</li>
<li>Provide technical lead for the Business Unit on CCC global initiatives / cross-business segment groups</li>
<li>Working closely with other CCC global regions on projects covering multiple geographic territories</li>
<li>Acts as technical support and back-up contact related to specific projects for Sales team</li>
<li>Serves as liaison between Sales team and internal support teams including Product and Project Management</li>
<li>Review bid specifications for clarity, accuracy and acceptance</li>
<li>Provide recommendations to improve technical quality of bid specifications and prevent undue risk to Calgon Carbon</li>
<li>Serve as main Calgon Carbon contact to customer when Technical Sales Rep is unable to respond to customer</li>
<li>Participate in Industry forums related to emerging markets and existing applications</li>
<li>Attend technical conferences and trade shows to gain technical knowledge and represent Calgon Carbon as a leader in the activated carbon market</li>
<li>Prepare and present papers/posters at conferences, trade shows and virtual opportunities, e.g. webinars</li>
<li>Develop and present technical presentation / training to engineering consultants, clients, regulators, legislators and others to influence selection of treatment solutions</li>
<li>Attendance at conference would be as lead technical personnel &nbsp;</li>
</ul>
Qualifications
<ul>
<li>A bachelor’s degree (B.A. or B.S.), or equivalent from four-year college or university is required (Chemical Engineering or related engineering/chemistry field)</li>
<li>10+ years&nbsp;of experience in the application of carbon adsorption technology to address customer requirements in liquid and gas purification, including carbon modeling, equipment design and development, and equipment functionality is required</li>
<li>5-7 years&nbsp;of experience in the use and troubleshooting of adsorption equipment at customer sites is required</li>
<li>Experience with business/marketing is preferred.</li>
</ul>
 About Calgon Carbon
At Calgon Carbon, we are scientific innovators with a proud legacy of over 80 years and more than 205 patents to our name. Since pioneering the first activated carbon products from bituminous coal in the 1940s, we’ve been at the forefront of developing cutting-edge technologies and solutions to meet the world’s evolving air and water purification needs.
Today, our portfolio includes more than 700 direct market applications across a wide range of industries. Headquartered in Pittsburgh, Pennsylvania, Calgon Carbon employs approximately 1,685 professionals and operates 20 facilities worldwide dedicated to manufacturing, reactivation, innovation, and equipment fabrication. In Europe, we operate under the name Chemviron.
In March 2018, Calgon Carbon became part of the Kuraray Group. Together, we offer complementary products and services, united by a shared commitment to delivering the highest quality and most innovative activated carbon solutions to customers around the globe.
Calgon Carbon is an Equal Opportunity Employer, including disabled/veteran
 
PI94efdfc0921a-25405-37796249

Chemical/Environmental Senior Applications Engineer

<h3>Job Description</h3>
Job DescriptionQuality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to perform testing and evaluations of raw materials, bulk, and finished products following written procedures. The role involves ensuring compliance with GMP requirements and maintaining accurate documentation records. You will develop an understanding of various testing methodologies and maintain neat and organized work areas.
Responsibilities
<ul>
<li>Perform testing and evaluations of raw materials, bulk, and finished products in accordance with written procedures.</li>
<li>Ensure test results meet current specifications prior to completion and approval.</li>
<li>Troubleshoot out-of-specification situations and perform batch adjustments as needed.</li>
<li>Maintain compliance with current regulatory expectations and practices, such as USP.</li>
<li>Document monthly Key Quality Incidents and out-of-specification situations, determining root causes and suggesting solutions.</li>
<li>Utilize data to focus improvement efforts, ensuring customer requirements and regulatory regulations are met.</li>
<li>Understand and maintain a culture of 'lean action' within the department.</li>
</ul>
Essential Skills
<ul>
<li>4-year degree in Chemistry.</li>
<li>0-2 years of quality control industry experience in pharma, cosmetics, or food.</li>
<li>Proficiency in laboratory techniques such as wet chemistry, FTIR, and quality control.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with solution preparation, wet chemistry titrations, HPLC, GC, and UV is a plus.</li>
</ul>
 Pay and Benefits
The pay range for this position is $25.00 - $26.00/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 Minneapolis,MN.
Application Deadline
This position is anticipated to close on Sep 1, 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 Control Chemist

<h3>Job Description</h3>
Planet Healthcare is seeking a travel Physicist for a travel job in Augusta, Maine.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: ASAP</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 10 hours, days</li>
<li>Employment Type: Travel</li>
</ul>
Job Profile Summary: Ensures the safe and effective delivery of radiation to achieve a diagnostic or therapeutic result as prescribed in patient care plan.
Equipment: Two 4.1 true beam, with 6dof couch, both held at srs and SABR tolerance.
Planet Healthcare Job ID #71209423. Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined.
About Planet Healthcare
Delivering Vital Healthcare Talent. Today.
Planet Healthcare is a global leader in clinical staffing because we take a candidate-first approach. We pride ourselves on a consultative method and help to create the right opportunity, at the right time, with each healthcare professional. The recruitment engine at Planet Healthcare is driven by leaders in this market, who understand the market demands and trends within your specialty. With a wide array of job opportunities and geographic diversity in our client base, we are your advocate and will work to find the best position for you. We are ready to go to work. Welcome to Planet Healthcare.
Our Methodology
Let’s face it; finding a new job can be scary. Whether you’re currently employed or in between positions, the search can feel overwhelming. If you’re looking for support, guidance and an upper-hand on the competition, you’ve come to the right place. We know that not every job, company or commute is right for everyone, so Planet Healthcare recruiters are trained to not only discuss our open job orders, but to find out about your search and take a proactive approach to the market. Our recruiters are experts in this industry and we are your advocate and partner during your job search. We look forward to working with you soon.
CLEVELAND | CHICAGO | RALEIGH | BOSTON | PHOENIX

Benefits
<ul>
<li>Medical benefits</li>
<li>Vision benefits</li>
<li>Dental benefits</li>
<li>401k retirement plan</li>
<li>Weekly pay</li>
<li>Referral bonus</li>
</ul>

Travel Physicist

<h3>Job Description</h3>
Job Description
KEY RESPONSIBILITIES:
Strategic Leadership
<ul>
<li>Define and execute the company’s electrochemistry R&amp;D strategy in alignment with the company strategy</li>
<li>Anticipate industry trends, emerging technologies, and competitive developments to maintain innovation leadership</li>
<li>Lead the development of intellectual property (IP) portfolios, patents, and trade secrets in battery chemistry</li>
<li>Develop strategic relationships with key material suppliers to understand what raw materials are available and how they can be integrated or adapted into our products</li>
<li>Work with suppliers to understand their development and industrialization plans</li>
</ul>
Technical Program Oversight
<ul>
<li>Direct research on electrode, electrolyte, and separator chemistries for high-performance, cost-effective, and safe energy storage solutions (lithium-ion, solid-state, advanced chemistries)</li>
<li>Oversee advanced materials characterization, electrochemical testing, and performance modeling</li>
<li>Ensure successful scale-up of new chemistries from lab prototypes to pilot production and mass manufacturing</li>
<li>Execute root-cause analysis of failures and corrective actions for issues occurring during development and launch</li>
</ul>
Organizational Leadership
<ul>
<li>Build, develop, and mentor a high-performing electrochemistry R&amp;D organization, including senior scientists, engineers, and technicians</li>
<li>Develops best practices, characterization plans, design and group standards</li>
<li>Foster a culture of technical excellence, collaboration, and innovation</li>
<li>Manage R&amp;D budgets, resources, and external research partnerships</li>
</ul>
Cross-Functional Collaboration
<ul>
<li>Partner with cell design, manufacturing engineering, supply chain, and quality teams to ensure smooth technology transfer from R&amp;D to production</li>
<li>Collaborate with external partners, suppliers, universities, and research institutions on joint development programs</li>
<li>Communicate technical strategy and progress to executive leadership, investors, and stakeholders</li>
</ul>

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