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<h3>Job Description</h3>
Job Description
We have several opportunities for on-call Field Archaeologists to monitor for a project located in the Ontario area.
· Willing to work 6:30 am to approximately 3:30 pm (1 to 4 days per week for the next 3 weeks or longer).
· Willing to work on Saturdays if needed.
· Have a BA or higher degree in Archaeology/Anthropology.
· Have around 2 years’ experience in CRM, monitoring experience desired.
(Archaeologist, anthropologist, archaeology, anthropology, CRM, cultural resources management)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

On Call Field Archaeologist

<h3>Job Description</h3>
Job DescriptionActalent is Hiring a Team of Analytical Scientists // First and Second Shift!Job Description
We are seeking a dedicated Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. The role involves assays, chromatographic purity, and content uniformity analysis using UV and HPLC, and particle size distribution using various techniques. This position requires working in a regulated laboratory environment, adhering to in-house monographs and USP standards.
Responsibilities
<ul>
<li>Perform routine tests on finished products, stability samples, raw materials, and CV samples using UV and HPLC.</li>
<li>Evaluate test results and decide on the acceptability of samples.</li>
<li>Maintain accurate lab notebooks and complete analytical reports, summaries, and proper documentation in compliance with SOPs.</li>
<li>Ensure laboratories are maintained with good housekeeping practices and are in compliance with cGMP.</li>
<li>Ensure notebooks are reviewed promptly according to SOPs.</li>
<li>Analyze and interpret results in written and oral formats.</li>
<li>Assist in the training of new analysts.</li>
<li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li>
<li>Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, UPLC, and UV-Vis.</li>
<li>Strong experience in chemistry and analytical techniques.</li>
<li>Experience with SOPs and GMP compliance.</li>
<li>Ability to analyze and interpret data accurately.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry or related scientific field with 1-2 years of pharmaceutical analysis experience, or Master's degree with 1 year of experience.</li>
<li>Ability to manage problems involving several concrete variables in standardized situations.</li>
<li>Competence in performing necessary computations and interpreting graphs.</li>
<li>Working knowledge of instrumentation software used in laboratories.</li>
</ul>
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.
Pay and Benefits
The pay range for this position is $29.00 - $35.00/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 Coral Springs,FL.
Application Deadline
This position is anticipated to close on Sep 16, 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.

Associate Scientist

<h3>Job Description</h3>
Job DescriptionOverview
Actalent is supporting a leading pharmaceutical development and manufacturing organization in their search for a&nbsp;Principal Scientist&nbsp;with deep expertise in&nbsp;mass spectrometry&nbsp;and&nbsp;bioseparation techniques. This role is ideal for a seasoned analytical scientist who thrives in a fast-paced, collaborative environment and is passionate about advancing biologics and large molecule therapeutics.
Key Responsibilities
<ul>
<li>Lead the development and validation of analytical methods for biologics, peptides, proteins, and nucleic acids using&nbsp;HPLC,&nbsp;LC-MS/MS,&nbsp;UV spectroscopy, and&nbsp;capillary electrophoresis.</li>
<li>Perform advanced structural and functional characterization, including&nbsp;peptide mapping,&nbsp;amino acid analysis,&nbsp;glycosylation profiling, and&nbsp;disulfide bond identification.</li>
<li>Troubleshoot instrumentation and analytical workflows; maintain accurate documentation in electronic lab notebooks.</li>
<li>Interpret complex analytical data and prepare technical reports, SOPs, protocols, and client-facing summaries.</li>
<li>Collaborate with cross-functional teams in formulation, manufacturing, and quality to support product development and stability studies.</li>
<li>Participate in regulatory audits and contribute to IND filings and scientific publications.</li>
<li>Mentor junior scientists and lead technical investigations and root cause analyses.</li>
</ul>
Required Qualifications
<ul>
<li>Ph.D. in Chemistry, Biochemistry, or related field&nbsp;with a minimum of&nbsp;10 years of industry experience&nbsp;(Master’s with 11+ years or Bachelor’s with 15+ years also considered).</li>
<li>Demonstrated expertise in&nbsp;mass spectrometry,&nbsp;chromatography (RP, IEX, SEC), and&nbsp;protein characterization.</li>
<li>Strong working knowledge of&nbsp;cGMP regulations&nbsp;and pharmaceutical development processes.</li>
<li>Experience with&nbsp;Imaging Capillary Electrophoresis&nbsp;and&nbsp;Analytical Ultracentrifugation&nbsp;is highly desirable.</li>
<li>Excellent communication skills and ability to present findings to internal teams and external clients.</li>
<li>Proficiency in Microsoft Office and electronic lab documentation systems.</li>
</ul>
Preferred Skills
<ul>
<li>Experience with&nbsp;cell and gene therapy products,&nbsp;bioassays, and&nbsp;small molecule analysis.</li>
<li>Familiarity with&nbsp;gel electrophoresis,&nbsp;sequencing, and&nbsp;accurate mass identification.</li>
<li>Prior involvement in&nbsp;regulatory submissions,&nbsp;scientific conferences, or&nbsp;peer-reviewed publications.</li>
</ul>
 
Pay and Benefits
The pay range for this position is $110000.00 - $125000.00/yr.
Competitive health benefits Bonus program 401(k) with match Paid time off College loan reimbursement
Workplace Type
This is a fully onsite position in Durham,NC.
Application Deadline
This position is anticipated to close on Sep 18, 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.

Principal Scientist

<h3>Job Description</h3>
Virology Scientist Location: Rochester, Minnesota Join a pioneering team dedicated to advancing the future of medicine! At our cutting-edge facility near the prestigious Mayo Clinic, we're seeking a Scientist skilled in virology and molecular cloning. Dive into projects that revolutionize treatments for cancer patients and push the boundaries of cell, gene, and virus therapies. Your work will directly contribute to defining and delivering tomorrow's healthcare solutions. Why You Should Apply 
<ul>
<li>Engage in innovative scientific research with real-world impact.</li>
<li>Be part of a driven team of experts passionate about excellence in science.</li>
<li>Opportunities to lead and collaborate on cross-functional projects.</li>
<li>Competitive salary commensurate with experience and qualifications.</li>
<li>Comprehensive benefits package including health, dental/vision insurance, and more. </li>
</ul>
What You'll Be Doing: 
<ul>
<li>Designing, rescuing, and characterizing novel viral vectors.</li>
<li>Executing and optimizing molecular cloning and cell-based assays.</li>
<li>Independently planning and leading scientific research projects.</li>
<li>Analyzing and presenting data, contributing to strategic project development. </li>
</ul>
About You: 
<ul>
<li>Hold a Ph.D. or master's in Molecular/Cellular Biology, Biochemistry, Virology, or related.</li>
<li>Proficient in molecular cloning and lentiviral vector production.</li>
<li>Experienced in optimizing experimental procedures. </li>
</ul>
How To Apply We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to <a href="mailto:genna@scientificsearch.com" target="_blank">genna@scientificsearch.com</a> and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19435.

Scientist Virology

<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 DescriptionDescription:
Measurement Technician wanted now! If you are talented in flooring and customer service, click to apply now! You have the opportunity to travel and meet new people – best of all – help them meet their flooring needs and be your own boss! This is a 1099 contract position. *Not a remote position*
Looking for talented "sub-contractors" to measure flooring installations in your area that can start ASAP!
We will provide:
<ul>
<li>The job assignments</li>
<li>Tablet to use (with training - two weeks of training)</li>
<li>Paid per measure and weekly</li>
</ul>
Requirements:
Duties:
<ul>
<li>Listen to the customer’s needs and expectations</li>
<li>Create detailed digital floor diagrams</li>
<li>Inspect the job site to determine the need for products in the flooring installation process.</li>
<li>Take before photographs</li>
<li>Make detailed notes for the quoting process</li>
<li>Can travel frequently for an hour or more one way to get to site</li>
</ul>
Requirements:
<ul>
<li>Active listening skills.</li>
<li>Friendly, customer-oriented, and professional.</li>
<li>Math proficiency</li>
<li>Detailed oriented</li>
<li>Have and able to maintain a valid driver's license with personal vehicle insurance.</li>
<li>Reliable transportation.</li>
<li>Smart phone, no flip phones, and basic computer skills/tablet skills.</li>
<li>Able to pass a background check</li>
<li>Construction experience preferred (flooring knowledge a bonus)</li>
<li>Have availability to see customers in their homes Monday – Saturday.</li>
</ul>

Measurement Technician - 1099-Subcontractor

<h3>Job Description</h3>
Job Description
Apply Here: <a href="https://secure.onehcm.com/ta/RAUTAH.jobs?ShowJob=620938945&amp;TrackId=ZipRecruiter" target="_blank">https://secure.onehcm.com/ta/RAUTAH.jobs?ShowJob=620938945&amp;TrackId=ZipR…</a>
The Visual Acuity Examiner is primarily responsible for performing standardized refraction and visual acuity as
required by various study protocols and manual of procedures. Day-to-day activities may include all or some of the
essential functions listed below, depending upon individual experience / knowledge and the needs of the organization
which are subject to change from time to time. The research assistant is primarily responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Research Assistant

<h3>Job Description</h3>
Job DescriptionMicrobiologists are responsible for conducting microbiological on cannabis samples, interpreting results, and ensuring the accuracy, reliability, and compliance of testing procedures in an ISO 17025 accredited testing laboratory. • Perform routine microbiological tests on cannabis samples, including microbial enumeration, pathogen detection, and microbial identification. • Follow standard operating procedures (SOPs) and test methods to ensure consistency, accuracy, and compliance with ISO 17025 standards and regulatory requirements. • Prepare culture media, reagents, and samples for analysis, following established protocols and safety guidelines. • Operate and maintain laboratory equipment and instruments for microbial testing, including incubators, autoclaves, microscopes, and colony counters. • Document test results, observations, and deviations accurately and promptly in laboratory notebooks and electronic systems. • Assist with data analysis, quality control checks, and method validation studies as needed. • Adhere to health and safety protocols, including the proper handling, storage, and disposal of hazardous materials. Requirements• Bachelor's degree in microbiology, biology, or a related field. • Prior laboratory experience or coursework in microbiology is preferred but not required. • Strong attention to detail, organizational skills, and ability to follow instructions. • Excellent communication and teamwork skills. • Ability to work independently and collaboratively in a fast-paced environment. • Proficiency in Microsoft Office Suite. BenefitsHealth Insurance Stipend Phone Stipend PTO 401k with 6% match

Microbiologist

<h3>Job Description</h3>
Job Description
Chemical Plant Operator – Industrial Manufacturing (Confidential Employer)
Greensboro, NC
Up to $50/hr&nbsp;+ Full Benefits| Full-Time | Onsite
Are you someone who doesn’t mind getting your hands dirty? Do you take pride in doing hard work that matters? We’re looking for a dependable, safety-conscious&nbsp;Chemical Plant Operator&nbsp;to join a tight-knit production team working to shift the culture&nbsp;at a well-established American specialty chemical manufacturer serving critical industries.
What You’ll Be Doing:
<ul>
<li>Operating and monitoring chemical processing equipment, including&nbsp;chemical reactors and packaging systems.</li>
<li>Handling bulk raw materials such as oils, acids, and solvents</li>
<li>Recording process data and making routine operational adjustments</li>
<li>Loading and unloading tank trucks and railcars</li>
<li>Performing quality checks and keeping work areas clean and organized at all times</li>
<li>Supporting safe plant operations in a physically demanding environment</li>
</ul>
What You Should Know:
<ul>
<li>This is NOT light industrial work.&nbsp;</li>
<li>It’s hot in summer, noisy at times, and involves working around chemicals and high-temperature/pressure equipment.</li>
<li>You’ll be on your feet, climbing stairs, wearing PPE, and working with materials that require caution,&nbsp;precision, and attention to detail.</li>
<li>Shift work may include weekends or overnights.</li>
</ul>
Qualifications: (Do not apply if you do not have these qualifications -&nbsp;we will ignore you.)
<ul>
<li>High school diploma or GED required</li>
<li>Minimum 5 years of experience&nbsp;in chemical plant operations, including:</li>
</ul>
<ul>
<li>
<ul>
<li>Blending and mixing</li>
<li>Chemical reactions, packaging, material&nbsp;handling, shipping and receiving of bulk chemicals.</li>
</ul>
</li>
</ul>
<ul>
<li>Strong mechanical aptitude and a commitment to safety and cleanliness</li>
</ul>
Why Join Us:
<ul>
<li>Earn&nbsp;up to $50 per hour, depending on experience</li>
<li>Join a stable company with a strong reputation and opportunities to advance</li>
<li>Work in a team-oriented culture where reliability and hard work are recognized</li>
<li>Enjoy a full benefits package, including health, dental, vision,&nbsp;401(k), and paid time off</li>
</ul>
Pay Factors That Justify $50/hr:
<ul>
<li>Experience with&nbsp;hazardous or flammable materials</li>
<li>Direct experience in chemical reactions, blending, and bulk material handling.</li>
<li>Proven ability to operate&nbsp;multiple unit operations&nbsp;independently</li>
<li>Willingness to work&nbsp;rotating shifts or overtime</li>
<li>Familiarity with&nbsp;batch documentation, ERP systems, and safety compliance standards (OSHA, PSM, etc.)</li>
<li>A prove track record or desire to&nbsp;affect change among your peers&nbsp;and drive cultural shifts</li>
</ul>
Company DescriptionConfidential employer. 
<h3>Company Description</h3>
Confidential employer.

Chemical Plant Operator

<h3>Job Description</h3>
Job Description
Ironwood Cancer &amp; Research Centers has beautiful state-of-the-art integrated Cancer and Women's Centers, with locations strategically located throughout the Valley. Each one provides a superior cancer care environment with a full spectrum of cancer related services for patients. Our multi-disciplinary team approach includes surgical oncology, medical oncology, radiation oncology, women's centers, diagnostic imaging services, social service support, nutritionist, integrative services, and genetic counseling.
Mission Statement: To serve the community by providing quality, comprehensive cancer care which respects the values and needs of each individual.
Overview: We are looking for a qualified and experienced Physicist to work in our fast-paced out-patient oncology clinic. The Medical Physicist conducts all aspects of radiation therapy physics, including clinical medical physics support, equipment calibration and commissioning, maintenance of appropriate quality assurance programs for equipment and treatment delivery, compliance with radiation safety, licensing issues and other pertinent regulatory requirements. 
Schedule: Full-time, Monday through Friday day shift position. 
Essential Duties and Responsibilities: 
<ul>
<li>Responsible for all physics of radiotherapy treatments.</li>
<li>Responsible for Calibration and QA of all treatment devices.</li>
<li>Responsible for Calibration and QA of treatment simulators.</li>
<li>Responsible for Calibration and QA of treatment planning systems.</li>
<li>Responsible for Calibration and QA of the physics test equipment.</li>
<li>Review of treatment plan calculations.</li>
<li>Review of weekly chart checks.</li>
<li>Commissioning of new radiologic systems.</li>
<li>Establish new commission &amp; QA criteria for new radiologic programs.</li>
<li>Establish new treatment protocols for safe and effective treatment delivery.</li>
<li>Consult with and assist radiation therapists, dosimetrists and radiation oncologists.</li>
<li>Provide training for new clinical systems and programs.</li>
<li>Provide radiation safety training.</li>
<li>Provide treatment planning for special procedures like HDR and SBRT.</li>
</ul>
Knowledge and Skills:
<ul>
<li>Ability to communicate frequently with front office staff, radiation therapists, dosimetrists, other physicists and radiation oncologists. Must be able accurately exchange detailed information in each situation.</li>
<li>Must remain calm and solve problems in highly stressful situations with limited time.</li>
<li>Constantly working around occupational levels of radiation exposure and hazardous materials.</li>
<li>Constantly operates computer and office equipment.</li>
<li>Must be able to maintain stationary position for up 6 hours per day.</li>
<li>Must be able to read medical charts on a computer screen for up to 6 hours per day.</li>
<li>Ability to use office equipment, computer, and typing is essential.</li>
</ul>
 Education and Experience:
<ul>
<li>Master’s Degree or PhD in Medical Physics or closely related field.</li>
<li>2 years clinical experience.</li>
</ul>
We offer a competitive salary and a comprehensive benefit package including health/dental/vision and life insurance, 401K, and a caring work environment. We are an E.O.E.
Please visit our website at <a href="http://www.ironwoodcrc.com" target="_blank">www.ironwoodcrc.com</a>. "Outsmarting Cancer One Patient at a Time"

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