field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Preferred Experience:
<ul>
<li>Eclipse, and Oncentra treatment planning systems</li>
<li>HDR planning and treatment.</li>
<li>ARIA ROIS and Mosiaq ROIS</li>
<li>SBRT and SRS procedures</li>
</ul>
?The ideal candidate will have
<ul>
<li>CAMPEP Accredited Residency Program in Medical Physics</li>
<li>Valid Texas Medical Board license</li>
<li>American Board of Radiology certification or board eligible</li>
<li>Preferred two years of experience as a certified medical physicist</li>
<li>Working knowledge of SRS, SBRT, and HDR</li>
<li>Experience with Varian linear accelerators</li>
<li>Experience with Eclipse Planning system</li>
<li>Experience with Oncentra Planning system</li>
<li>Strong organization and oral / written communication skills</li>
</ul>
Required Citizenship / Work Permit / Visa Status US Citizen / Green Card holder
Must-Haves CAMPEP Accredited Residency Program in Medical Physics Valid Texas Medical Board license American Board of Radiology certification or board eligible Preferred two years of experience as a certified physicist Working knowledge of SRS, SBRT, and HDR

Medical Physicist - Plano

<h3>Job Description</h3>
About Civica:
Critical shortages of essential generic injectable drugs are an ongoing crisis in U.S. healthcare and have reached an all-time high. Over 300 essential medications are currently reported to be in shortage, according to industry and FDA reports.
Shortages put patients at risk and waste hospital resources.
Civica is a market-based nonprofit solution created in 2018 by health systems and philanthropies for the express purpose of preventing and mitigating drug shortages. Today, nearly 60 health systems have joined Civica, representing over 1,400 hospitals and approximately one-third of all U.S. hospital beds. Civica has also supplied the U.S. Department of Veteran's Affairs, the U.S. Department of Defense and the U.S. Strategic National Stockpile with essential medicines. Civica currently supplies medicines to health system members in 49 states.
Civica's mission has expanded beyond the hospital setting to reach consumers directly through CivicaScript, which is dedicated to making quality outpatient generic medicines affordable and available. CivicaScript works with trusted manufacturing partners to develop quality generic medicines and has forged partnerships with like-minded payors, pharmacy benefit managers and pharmacies to enable significant cost savings to be passed along to their customers.
Civica's new 140,000 square foot state-of-the-art manufacturing facility in Virginia will soon produce a steady supply of more than three dozen sterile injectables, all drugs that are currently in or near shortage. The plant will also produce affordable biosimilar insulins, ensuring all Americans have access to lower cost, quality insulins, regardless of their insurance status.
The Civica Foundation is a 501(c)(3) organization that fosters philanthropic support for Civica's work to manufacture and distribute affordable medications. The Foundation's first commitment is to support Civica's efforts to bring affordable insulin to all Americans. Leaders from nearly every corner of the diabetes ecosystem are partners in this initiative. 
Civica is leading a movement for patients, not profits. Because eliminating shortages and stabilizing high prices are in the best interest of patients.
Join us. Learn more at <a href="http://www.civicarx.org" target="_blank">www.civicarx.org</a>
Job Description:
The Microbiologist will join the Civica, Inc. ("Civica") organization and its newly created team at the Petersburg, Virginia site by bringing their knowledge and experience in service to patients and pursuit of excellence in quality and compliance. The Petersburg site serves as Civica's new fill-finish facility dedicated to the manufacture and supply of essential generic sterile injectable medications. The responsibilities of the position include supporting facility qualification and equipment validation. 
The role is essential to ensure that the Petersburg site's microbiology laboratory and testing comply with applicable regulatory standards (e.g., Current Good Manufacturing Practices and FDA Guidance documents) and expectations for the development and reliable supply of quality medicines. Responsibilities also include but are not limited to, the generation and/or review of procedures, reports, and other records necessary to support the implementation and maintenance of a microbiology laboratory that meets or exceeds FDA and EU Annex 1 requirements. 
Essential Duties and Responsibilities:
<ul>
<li>Support establishing and maintaining the microbiological testing laboratory to ensure compliance with cGMPs and industry standards for best practices.</li>
<li>Perform microbiological testing methods consistent with USP testing requirements. Including but not limited to the following microbiological testing and procedures: bioburden, bacterial endotoxin, identification of microbial isolates and objectional organisms, viable/non-viable particulate monitoring, and growth promotion studies.</li>
<li>Conduct and maintain qualifications of laboratory equipment as well as ongoing maintenance and calibration.</li>
<li>Establish and coordinate test sampling plans.</li>
<li>Perform microbiological testing and sample collection to support environmental monitoring (EM) and utility systems.</li>
<li>Author and participate in the verification of microbiological methods and method transfers.</li>
<li>Participate in the development of training programs for microbiologists.</li>
<li>Lead and/or participate in investigations related to laboratory operations and non-conforming results.</li>
<li>Identify, track, and facilitate resolution of technical issues.</li>
<li>Proactively identify and work collaboratively to resolve problems, taking risk-based and compliant approaches to solutions.</li>
<li>Author and/or review SOPs, protocols, reports, test methods, and product specification documents as applicable.</li>
<li>Create and/or revise Risk Assessments.</li>
<li>Promote a quality mindset and quality excellence approach to all activities.</li>
<li>Travel (up to 10%) may be required.</li>
</ul>
Basic Qualifications and Capabilities:
<ul>
<li>Bachelor's degree in a scientific discipline (microbiology degree preferred) with a minimum of 4 years of Quality/cGMP experience in the pharmaceutical industry. </li>
<li>Strong project management, organization, and execution skills.</li>
<li>Microbiology testing and environmental monitoring experience.</li>
<li>Participation in activities to support regulatory agency inspections required.</li>
<li>Excellent interpersonal and written communication skills and experience using various software/electronic applications required.</li>
<li>Self-motivated, flexible, and able to work in a small, fast-paced, dynamic environment.</li>
<li>Ability to work autonomously and within established guidelines, procedures, and practices.</li>
<li>Committed to delivering high-quality results, working with others to overcome challenges, and focusing on what matters.</li>
<li>Continuously look for opportunities to learn, build skills and share knowledge with others.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience in sterile injectable manufacturing, aseptic processing, and facility qualification.</li>
<li>Environmental monitoring in isolators and cleanrooms per Annex 1 requirements.</li>
<li>Experience with the following microbiological testing and procedures.</li>
<li>Sterility testing and method suitability testing per USP &lt;71&gt;.</li>
<li>Acceptance testing and use of biological indicators.</li>
</ul>
Physical Demands and Work Environment:
The physical demands described here are representative of those that an employee must meet to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions.
While performing the essential duties of this position, the employee is regularly required to speak or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls, and stand, walk, sit, and reach with hands and arms. Specific vision abilities required by this position include color vision, close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate. 
The employee must have the ability to lift approximately 40 lbs, stand for 2 to 3 hours at a time, and walk long distances. Vision screening may be required.
The employee must have the capability to don gowning/PPE for entry into the aseptic core and supporting areas for extended periods of time. This will include standing, bending, reaching, kneeling, etc.
The company is an equal opportunity employer, a drug-free workplace, and complies with ADA regulations as applicable.
PandoLogic. Keywords: Microbiologist, Location: Petersburg, VA - 23803

Microbiologist

<h3>Job Description</h3>
Job DescriptionHeadquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO).&nbsp; As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services&nbsp;to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project – including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! The QC Microbiologist I/II supports the microbiological control program in a sterile injectable (parenteral) manufacturing facility. This position plays a key role in&nbsp;maintaining&nbsp;the facility’s aseptic control state by performing environmental and utility monitoring, microbiological testing of raw materials, in-process samples, and finished drug products. The role also includes data review, investigation support, and ensuring compliance with regulatory requirements and cGMP standards.&nbsp;Responsibilities
<ul>
<li>Perform viable and non-viable environmental monitoring in ISO Class 5–8 cleanrooms, including aseptic filling areas (isolators and RABS).</li>
<li>Conduct personnel monitoring to assess aseptic technique compliance.</li>
<li>Collect and test utility samples (WFI, Purified Water, compressed gases) per approved sampling plans.</li>
<li>Trend and assess environmental and utility data to support cleanroom control and sterility assurance.</li>
<li>Perform microbiological assays including bioburden, endotoxin, and growth promotion testing.</li>
<li>Support and handle samples for media fills/aseptic process simulations.</li>
<li>Test raw materials, in-process, and finished products per USP, EP, and internal methods.</li>
<li>Maintain and verify microbial culture stocks, control strains, and reference organisms.</li>
<li>Document all work per cGMP and ALCOA+ principles.</li>
<li>Review, interpret, and ensure accuracy and traceability of analytical data.</li>
<li>Author, revise, and review SOPs, test methods, qualification protocols, and reports.</li>
<li>Summarize data trends and prepare monitoring review reports.</li>
<li>Provide microbiological input for environmental excursion and deviation investigations.</li>
<li>Support equipment and laboratory qualifications (e.g., autoclaves, incubators, isolators, particle counters).</li>
<li>Assist with method validations, verifications, and transfers.</li>
<li>Maintain a clean, compliant, and organized laboratory.</li>
<li>Follow biohazard and waste-handling procedures.</li>
<li>Participate in internal/external audits and provide technical support.</li>
<li>Identify and support laboratory process improvements and automation initiatives.</li>
</ul>
Requirements
<ul>
<li>Bachelor’s degree in Microbiology, Biology, Biotechnology, or a related life science discipline.&nbsp;</li>
<li>Microbiologist I: 0–2 years of experience in a GMP-regulated microbiology laboratory within sterile drug manufacturing.&nbsp;</li>
<li>Microbiologist II: 2–4 years of experience supporting QC Microbiology operations for sterile injectables or other aseptically manufactured products.&nbsp;</li>
<li>Hands-on experience with environmental monitoring of cleanrooms and isolators&nbsp;as well as aseptic technique&nbsp;&nbsp;</li>
<li>Working knowledge of compendial methods (USP &lt;61&gt;, &lt;62&gt;, &lt;71&gt;, &lt;85&gt;, &lt;1116&gt;) and regulatory guidance (FDA, EMA, ICH Q7/Q9/Q10).&nbsp;</li>
<li>Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).&nbsp;</li>
<li>Strong attention to detail and commitment to data integrity.&nbsp;</li>
<li>Effective communication skills (written, verbal, and presentation).&nbsp;</li>
<li>Demonstrated initiative, accountability, and ability to work both independently and in cross-functional teams.&nbsp;</li>
<li>Flexibility to support off-shift or weekend sampling and testing based on manufacturing needs.&nbsp;</li>
<li>Ability to work in cleanroom gowning and controlled environments for extended periods.&nbsp;</li>
<li>Frequent standing, bending, and walking.&nbsp;</li>
<li>Ability to lift up to 25 lbs and handle routine laboratory equipment and sampling tools.&nbsp;</li>
</ul>
Shift Hours
<ul>
<li>This is a weekend-only position with two shift options available:</li>
<li>Weekend Night Shift: Friday–Sunday, 7:00 PM–7:00 AM</li>
<li>Weekend Day Shift: Saturday–Monday, 7:00 AM–7:00 PM</li>
</ul>
At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule – from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment. &nbsp;We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team! August Bioservices &nbsp;is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.

Microbiologist I/II (Weekend Shift)

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control Chemist Job Description
We are seeking a dedicated Quality Control Chemist to maintain the Quality Control Laboratory in compliance with cGMP standards. This role involves supporting Quality Assurance during audits, executing laboratory qualifications and validations, and revising material specifications. The successful candidate will perform QC testing for various processes, write and update standard operating procedures, and participate in laboratory investigations.
Responsibilities
<ul>
<li>Maintain the Quality Control Laboratory in compliance with cGMP according to procedure.</li>
<li>Support Quality Assurance during customer and regulatory audits.</li>
<li>Support the execution of laboratory qualifications and validations, including performing testing, data review, or protocol revisions.</li>
<li>Revise material specifications in collaboration with Quality Assurance.</li>
<li>Write and update standard operating procedures.</li>
<li>Perform QC testing in support of raw material, in-process, intermediate, cleaning verification/validation, and release testing.</li>
<li>Review laboratory control records.</li>
<li>Participate in OOS laboratory investigations and provide analytical support to QA.</li>
<li>Perform cleaning verification/validation activities as needed.</li>
<li>Ensure that retention samples are prepared and stored appropriately.</li>
<li>Manage reagents, standards, and reference materials.</li>
<li>Assist in the maintenance of the stability program, including stability testing and evaluation of trends.</li>
<li>Issue Certificates of Analysis.</li>
<li>Assist in the management of calibration, qualification, and maintenance of laboratory equipment.</li>
<li>Develop independence through mentoring with QC and QA staff.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor’s degree in chemistry or related discipline.</li>
<li>4 years of experience in GMP pharmaceutical/biopharmaceutical industry, with at least 2+ years in a QC environment.</li>
<li>Excellent oral and written communication skills.</li>
<li>Strong laboratory technique to avoid cross-contamination or misidentification of samples.</li>
<li>Ability to independently perform testing samples and document results.</li>
<li>Capacity to quickly learn new skills and techniques.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with HPLC and analytical chemistry.</li>
<li>Proficiency in method validation and QC processes.</li>
</ul>
Work Environment
Work in a smaller lab environment where you will engage in more than just routine testing, including method development, method validation, and data review. The setting is a pharmaceutical, GMP, quality-focused laboratory.
Job Type &amp; Location
This is a Contract to Hire position based out of Kalamazoo, Michigan.
Pay and Benefits
The pay range for this position is $31.25 - $33.65/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 Kalamazoo,MI.
Application Deadline
This position is anticipated to close on Nov 8, 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>
Job DescriptionJob Title: Microbiology Laboratory Technologist IV
Job Description
The Lab Technologist IV will process and analyze patient samples, monitor quality control, ensure all instruments are maintained properly, and enter patient results in their department. This role requires experience and training in the relevant department. The Lab Technologist IV may also conduct training for new employees and work closely with departmental personnel to maintain effective workflow. Compliance with regulatory standards is essential.
Responsibilities
<ul>
<li>Read and follow Departmental Standard Operating Procedures (SOPs).</li>
<li>Demonstrate proficiency in the performance, interpretation, and troubleshooting of assays.</li>
<li>Judge acceptability of quality control results and participate in proficiency testing.</li>
<li>Review performed work for accuracy before releasing it to clients.</li>
<li>Communicate sample issues within and outside the department to ensure proper client communication.</li>
<li>Assist in the evaluation and development of new procedures.</li>
<li>Achieve training goals as established by Human Resources.</li>
<li>Assist supervisors in the daily operation of the department.</li>
<li>Perform maintenance on departmental equipment.</li>
<li>Collaborate with other departmental personnel and the Product Development Department.</li>
<li>Maintain adequate supplies in the department.</li>
<li>Participate in the training of new employees.</li>
<li>Assist in maintaining year-round inspection readiness.</li>
<li>Understand and follow all safety rules and regulations.</li>
<li>Apply value statements and quality principles to work.</li>
<li>Assist in research projects as needed.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in clinical microbiology testing/assays, including blood, wound, and urine cultures.</li>
<li>Experience with microbial identification techniques such as bench biochemicals, Vitek, and MALDI-ToF.</li>
<li>Parasitology microscopic analysis and identification with trichrome and concentrate preparations.</li>
<li>Experience in molecular biology, PCR, and DNA extraction.</li>
<li>Ability to troubleshoot routine issues and train others on sample quantification.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s or Master’s Degree in Biological or Chemical Science, or a degree in Medical Technology.</li>
<li>For an MS degree, 4 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>For an MT degree, 6 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>For a BS degree, 7 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>Passage of a colorblind test for the Microbiology position.</li>
<li>Strong supervisory skills including mentoring, training, and leadership potential.</li>
</ul>
Work Environment
The work environment is a CLIA-compliant clinical diagnostics laboratory. The role requires meeting educational requirements and maintaining compliance with regulatory standards. Employees benefit from a collaborative culture that values innovation, diversity, and inclusion. Opportunities for professional growth are supported through ongoing training, mentorship programs, and career advancement. The role involves meaningful work that contributes to advancing personalized healthcare.
Pay and Benefits
The pay range for this position is $52000.00 - $79040.00/yr.
Benefits would be available to them after they complete their time through protouch and would have a waiting/probationary period of 60 days once they are an employee. Once they meet their 60-day waiting period with the company they are eligible for health, dental, and vision benefits. We offer PPO and HDP plans through Aetna.
After 90 days of employment you are eligible for 401k. There is an employer contribution. For each dollar you contribute, we will match dollar for dollar up to a maximum of 3% and $0.50 on the dollar for the next 2% of compensation. That is 100% vested.
Vacation- When employees are hired, they begin accruing vacation at a rate of 3.08 hours per pay period and up to 80 hours per year.
Personal Leave- Employees will receive personal leave after 6 months of employment. Full time employees will receive 40 hours.
Holidays-After 60 days employees are eligible for paid holidays. The company’s seven paid holidays are: New Year’s Day, Easter, Memorial Day, July 4th, Labor Day, Thanksgiving, Christmas.
Workplace Type
This is a fully onsite position in Greensboro,NC.
Application Deadline
This position is anticipated to close on Oct 30, 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.

<h3>Job Description</h3>
Job Description

Job Title: Associate Scientist, Drug Metabolism and Pharmacokinetics (DMPK) Location: Exton, PA Reports To: Vivarium Manager / Study Director
 
Company
Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
Position Summary: A dedicated and detail-oriented Vivarium Associate Scientist to support studies. This role involves the routine care and handling of laboratory animals, preparation for in vivo studies, and collaboration with scientific staff to ensure timely and high-quality data and sample collection in compliance with study protocols and animal welfare regulations.
Key Responsibilities:
<ul>
<li>Perform daily husbandry tasks including feeding, watering, cage changing, and health monitoring.</li>
<li>Assist with in vivo dosing procedures (e.g., oral, intravenous, subcutaneous) under supervision or upon training certification.</li>
<li>Conduct biological sample collection (e.g., blood, urine, feces, tissues) following approved protocols and SOPs.</li>
<li>Maintain accurate records of animal health, treatments, and study-specific procedures.</li>
<li>Prepare and label dosing and sampling materials and ensure proper sample storage and tracking.</li>
<li>Perform minor vascular and major surgical procedures</li>
<li>Monitor animals for clinical signs and report any abnormalities to the study team or veterinary staff.</li>
<li>Ensure vivarium cleanliness and compliance with IACUC and AAALAC standards.</li>
<li>Collaborate with DMPK scientists and project teams to coordinate study timelines and logistics.</li>
<li>Assist with inventory and ordering of animal care and dosing supplies.</li>
</ul>
Qualifications:
<ul>
<li>Associate’s or Bachelor's degree in Animal Science, Biology, or a related field preferred.</li>
<li>ALAT certification or willingness to obtain preferred.</li>
<li>Experience working with laboratory animals in a research or CRO environment (rodents required).</li>
<li>Familiarity with in vivo DMPK study procedures is a plus. </li>
<li>Ability to follow SOPs, protocols, and regulatory guidelines (GLP, IACUC).</li>
<li>Strong organizational skills and attention to detail.</li>
<li>Ability to work occasional weekends and holidays as study needs require.</li>
</ul>
Physical Requirements:
<ul>
<li>Ability to lift up to 50 lbs and perform physical tasks such as bending, stooping, and prolonged standing.</li>
<li>Comfortable working in a controlled environment with laboratory animals.</li>
</ul>

Salary and Benefits:
Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability

Associate Scientist

<h3>Job Description</h3>
Job Description
EnSafe continues to grow, and we are adding an Environmental Project Geologistto our Memphis office.
***Up to $5,000.00 igning bonus offered, depending on experience. Relocation assistance will be provided, if needed, for the right candidate***
EnSafe is an employee-owned global environmental consulting and engineering firm. We strive to provide innovative, creative solutions for our clients. EnSafe specializes in Environmental Management and Planning, Civil Design Engineering, Environmental Restoration, Natural &amp; Water Resources, Health &amp; Safety, and Technology, with offices operating within the US. 
What We Are Looking For
A Project Geologist who is driven to contribute to a wide range of projects, ranging from site investigations, feasibility studies, and remedial design and implementation for both common and emerging (i.e., PFAS) contaminants. 
Joining our team means immersing yourself in an atmosphere that nurtures creativity, encourages collaboration across all levels, embraces a supportive culture, and facilitates professional development. 
What You Will Be Doing:
• Preparing work plans, Environmental Site Assessment (ESA) reports, and safety plans.
• Coordinating and performing site assessments, including collecting groundwater, soil, surface water, and soil gas samples.
• Providing design support for small—and large-scale remedial systems to address soil, groundwater, and vapor contamination at sites regulated under CERCLA, RCRA, and state programs.
• Documenting field work and drafting technical reports.
• Developing technical recommendations for site assessment/remedial activities.
• Assisting with client management.
What You'll Need:
• A bachelor’s degree from an ABET-accredited college in geology or hydrology is required.
• 3-5 years of environmental field experience, assessments, sampling, remedial technology installation, and continuation monitoring. 
• Possess or be able to obtain a P.G. certification.
• 40-hour HAZWOPER training and certification.
• Experience with multi-media environmental sampling.
• Experience with Phase I and II Environmental Site Assessments.
• Experience with the TDEC VOAP program.
• Ability to travel, including occasional overnight travel.
• Excellent written and verbal communication skills (consulting skills preferred).
• Critical thinking and problem-solving skills.
• Must have a strong work ethic.
• Attention to detail.
• Valid driver's license to operate a vehicle in the U.S.
About EnSafe
EnSafe began as a two-person firm in 1980, navigating complex regulatory compliance issues on behalf of our clients. We nurture our people with growth and development opportunities. We build enduring, trustful relationships with each of our clients, with a focus on high ethical and safety standards. We build this reputation by attracting high-quality people and retaining them long-term.
At EnSafe, we are dedicated to building a diverse, inclusive, and authentic workplace. If you’re excited about this role but your past experience doesn’t perfectly align with every qualification in the job description, we encourage you to apply anyway. You may be just the right candidate for this role or others at our company.
EnSafe is committed to being an EEO employer and all qualified candidates will receive consideration without regard to race, color, religion, national origin, citizenship, age (except for bona fide occupational qualifications), sex, disability, sexual orientation, gender identity, marital status, military or veteran status, any other status protected by federal, state, or local law, or association with a person on the basis on one or more of the foregoing.
Check us out on the web at <a href="http://www.ensafe.com" target="_blank">www.ensafe.com</a>

Environmental Project Geologist

<h3>Job Description</h3>
Job Description
Job Title: Calibration Technician
Job Description
The Calibration Technician is responsible for performing calibrations, inspections, and measurements on test equipment to ensure measurement accuracy of s pressure, temperature, time, force, torque, speed, flow, electric current, voltage, and resistance. 
Responsibilities
<ul>
<li>Perform calibrations, inspections, and measurements on test equipment to ensure measurement accuracy.</li>
<li>Use assigned calibration standards and procedures.</li>
<li>Document all aspects of calibration events.</li>
<li>Evaluate contracts and work orders to ensure all work can be properly completed.</li>
<li>Assist customers with traceability or procedural questions in calibrations and resolve technical contract issues.</li>
<li>Develop and maintain preventative maintenance and laboratory safety/housekeeping programs and ensure team compliance.</li>
<li>Quantify sources of measurement error and determine measurement uncertainty.</li>
<li>Aid in the setup of processes and paperwork related to calibration.</li>
<li>Complete administrative tasks related to incoming calibrations as necessary.</li>
<li>Perform minor repairs as necessary.</li>
<li>Perform other duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>ISO experience.</li>
<li>Hands-on calibration experience.</li>
<li>Experience in metrology and calibration processes.</li>
<li>Ability to resolve technical contract issues.</li>
</ul>
Pay and Benefits
The pay range for this position is $22.00 - $32.00/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 Vernon Hills,IL.
Application Deadline
This position is anticipated to close on Oct 31, 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.

Metrology Technician

<h3>Job Description</h3>
Job DescriptionSalary: $80K - $90K, depending upon experience 
Cogent Scientific, an insourced contract research organization, is looking for the right people toaccomplish our Mission: to partner in the global effort to improve lives through innovative science with an experienced workforce. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation. 
 
Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.), and an exciting work environment. We aim to recruit the best people who stand out among their peers and embody our Core Values: 
 
Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. imble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients.
We currently have a role available for a Pharmaceutical Purification Chemist.
Job duties include, but are not limited to: 
<ul>
<li>Purifying small molecule samples using one or more of the following:
<ul>
<li>HPLC - Reversed phase purification using Agilent 1100/1200/1260/1290 series. Familiarity with ChemStation software recommended.
<ul>
<li>Prep-LC experience strongly preferred.</li>
</ul>
</li>
<li>ISCO Combiflash and ACCQPrep.</li>
<li>Chiral purification using LC and SFC systems.</li>
</ul>
</li>
<li>Performing purification instrument maintenance and troubleshooting as needed.</li>
<li>Providing critical feedback to improve workflow and chemistry performance and implementation of best practices.</li>
</ul>
Job requirements include, but are not limited to:
<ul>
<li>BS - Chemistry or related field with 3-6 years of industry experience (preferably pharma). MS - Chemistry with 1-3 years of industry experience would also be considered.</li>
<li>Excellent communication skills verbal and written.</li>
<li>Works well both within a team and as an individual.
<ul>
<li>Proven ability to work under high-pressure environments preferred.</li>
</ul>
</li>
<li>Demonstration of excellent team player and collaboration skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions.</li>
<li>The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery.</li>
</ul>
 
This job posting will close by 12/1/2025 or when a candidate is identified, whichever comes first.

Pharmaceutical Preparative Purification Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiology Laboratory Technologist IV
Job Description
The Lab Technologist IV will process and analyze patient samples, monitor quality control, ensure all instruments are maintained properly, and enter patient results in their department. This role requires experience and training in the relevant department. The Lab Technologist IV may also conduct training for new employees and work closely with departmental personnel to maintain effective workflow. Compliance with regulatory standards is essential.
Responsibilities
<ul>
<li>Read and follow Departmental Standard Operating Procedures (SOPs).</li>
<li>Demonstrate proficiency in the performance, interpretation, and troubleshooting of assays.</li>
<li>Judge acceptability of quality control results and participate in proficiency testing.</li>
<li>Review performed work for accuracy before releasing it to clients.</li>
<li>Communicate sample issues within and outside the department to ensure proper client communication.</li>
<li>Assist in the evaluation and development of new procedures.</li>
<li>Achieve training goals as established by Human Resources.</li>
<li>Assist supervisors in the daily operation of the department.</li>
<li>Perform maintenance on departmental equipment.</li>
<li>Collaborate with other departmental personnel and the Product Development Department.</li>
<li>Maintain adequate supplies in the department.</li>
<li>Participate in the training of new employees.</li>
<li>Assist in maintaining year-round inspection readiness.</li>
<li>Understand and follow all safety rules and regulations.</li>
<li>Apply value statements and quality principles to work.</li>
<li>Assist in research projects as needed.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in clinical microbiology testing/assays, including blood, wound, and urine cultures.</li>
<li>Experience with microbial identification techniques such as bench biochemicals, Vitek, and MALDI-ToF.</li>
<li>Parasitology microscopic analysis and identification with trichrome and concentrate preparations.</li>
<li>Experience in molecular biology, PCR, and DNA extraction.</li>
<li>Ability to troubleshoot routine issues and train others on sample quantification.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s or Master’s Degree in Biological or Chemical Science, or a degree in Medical Technology.</li>
<li>For an MS degree, 4 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>For an MT degree, 6 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>For a BS degree, 7 years of clinical laboratory training or experience, with 2 years in the area of supervision.</li>
<li>Passage of a colorblind test for the Microbiology position.</li>
<li>Strong supervisory skills including mentoring, training, and leadership potential.</li>
</ul>
Work Environment
The work environment is a CLIA-compliant clinical diagnostics laboratory. The role requires meeting educational requirements and maintaining compliance with regulatory standards. Employees benefit from a collaborative culture that values innovation, diversity, and inclusion. Opportunities for professional growth are supported through ongoing training, mentorship programs, and career advancement. The role involves meaningful work that contributes to advancing personalized healthcare.
Pay and Benefits
The pay range for this position is $52000.00 - $79040.00/yr.
Benefits would be available to them after they complete their time through protouch and would have a waiting/probationary period of 60 days once they are an employee. Once they meet their 60-day waiting period with the company they are eligible for health, dental, and vision benefits. We offer PPO and HDP plans through Aetna.
After 90 days of employment you are eligible for 401k. There is an employer contribution. For each dollar you contribute, we will match dollar for dollar up to a maximum of 3% and $0.50 on the dollar for the next 2% of compensation. That is 100% vested.
Vacation- When employees are hired, they begin accruing vacation at a rate of 3.08 hours per pay period and up to 80 hours per year.
Personal Leave- Employees will receive personal leave after 6 months of employment. Full time employees will receive 40 hours.
Holidays-After 60 days employees are eligible for paid holidays. The company’s seven paid holidays are: New Year’s Day, Easter, Memorial Day, July 4th, Labor Day, Thanksgiving, Christmas.
Workplace Type
This is a fully onsite position in Asheville,NC.
Application Deadline
This position is anticipated to close on Oct 30, 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.

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