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<h3>Job Description</h3>
Job Description
About Us We are a modern plastic surgery and medical aesthetics clinic located in Summerville, South Carolina; committed to providing exceptional and personalized care to enhance the beauty and confidence of our clients. Our team of skilled professionals is dedicated to staying at the forefront of the industry, utilizing the latest technologies and techniques to deliver outstanding results.
The Role
We are seeking a talented and experienced Aesthetic Nurse Injector to join our dynamic team. As a key member of our clinic, you will play a crucial role in providing top-tier non-surgical aesthetic treatments to our diverse clientele. If you are passionate about delivering exceptional patient care and have a keen eye for detail, we want to hear from you! Collaborate with the medical team to ensure a seamless and positive patient experience.
What You’ll Do
<ul>
<li>
Perform injectable treatments including (but not limited to) Botox, dermal fillers, and other injectables.
</li>
<li>
Carry out patient consultations and create tailored treatment plans.
</li>
<li>
Deliver safe, natural-looking results with a focus on patient care and satisfaction through effective communication and personalized service.
</li>
<li>
Stay up to date on new products, trends, and techniques.
</li>
</ul>
What You’ll Need
<ul>
<li>
Active nursing license in South Carolina.
</li>
<li>
2+ years’ experience with injectables.
</li>
<li>
Strong knowledge of aesthetics and the ability to create natural-looking results.
</li>
<li>
Excellent communication and interpersonal skills.
</li>
<li>
A proven track record of `high-quality patient care in an aesthetic setting.
</li>
<li>
Ability to work independently and as part of a collaborative team.
</li>
</ul>
What We Offer
<ul>
<li>
Competitive pay + performance incentives.
</li>
<li>
Health, dental, and vision insurance.
</li>
<li>
Ongoing training and professional development.
</li>
<li>
State-of-the-art facilities and cutting-edge technologies.
</li>
<li>
A supportive and collaborative team environment.
</li>
<li>
Staff discounts on in-house procedures.
</li>
</ul>
Apply Now
If you are a skilled and passionate Nurse Injector looking to join a forward-thinking clinic in Summerville, we would love to hear from you.
We are an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences.
Join us in shaping the future of aesthetic care and making a positive impact on the lives of our clients!

Aesthetic Nurse Injector - Sweetgrass - Summerville

<h3>Job Description</h3>
Job Description
Valley View hospital is seeking a Lead MLS position to be in charge of the Microbiology department! Valley View has a full-service Microbiology lab with state-of-the-art technology and equipment!
This is a full-time, Microbiology lead, day shift with one weekend per month! 
SALARY RANGE
<ul>
<li>‎$38.43 to $57.64/hour</li>
<li>Entry salary dependent upon education, skill set, and experience.</li>
</ul>
BENEFITS
<ul>
<li>Medical, Dental and Vision coverage including coverage for eligible dependents</li>
<li>Employer paid basic life coverage with buy-up coverage options</li>
<li>Flexible Spending Account (FSA) for health care and dependent care.</li>
<li>Time away from work: paid time off (PTO), paid family and medical leave (inclusive of Colorado FAMLI), Paid Sick/Bereavement Leave under Colorado Healthy Families and Workplaces Act (HFWA), leaves of absence.</li>
<li>Tuition Assistance Available</li>
<li>Retirement Plan 401(a)</li>
<li>Retirement Plan 403(b) plans with employer matching contributions.</li>
<li>Employee Assistance Program</li>
<li>Employee discount on Valley View Medical Services</li>
<li>Employee voluntary benefits such as Discounted RFTA bus passes, discounted gym memberships, Corporate Ski passes, free car seat for new Valley View babies born or adopted by Valley View employee(s)</li>
<li>Free Use of Sunlight and Aspen SkiCo day passes, based on availability.</li>
</ul>
Loan Repayment:
Valley View is a qualifying employer for the federal Public Service Loan Forgiveness (PSLF) program!
APPLICATION SUBMISSION END DATE
This position will be open for a minimum of three days and until a top applicant is identified.
About Us Located between Aspen and Vail, along the Colorado River, Glenwood Springs is a mecca for outdoor adventures in our beautiful mountains. When you are looking to relax, we also have the largest hot springs pool in the world. As a community with a population of about 10,000, Glenwood Springs is an ideal size.
Valley View Hospital offers exceptional benefits, including a robust health and dental plan; vision and life insurance; defined contribution pension plan; 403(b); and generous accrual of vacation/sick days. Relocation and other financial assistance may apply, along with many more employee perks.
At Valley View, our mission is to provide convenient, connected care to the communities of Western Colorado with scope, technology, and expertise that are rarely found in regional hospitals.

Lead Medical Laboratory Scientist- Microbiology

<h3>Job Description</h3>
Job DescriptionPay: From $16-$18.00 per hourJob description:
Dye and Chemical Weigher
<ul>
<li>Maiden, NC</li>
<li>$16-$18.00 per hour</li>
<li>12-hour shifts (7:00 AM – 7:00 PM or 7:00 PM – 7:00 AM)</li>
</ul>
Job Summary: Arthur Services is seeking an experienced Dye and Chemical Weigher to join a leading facility in Maiden, NC. This role is essential to production, ensuring accurate weighing, measuring, and preparation of dyes and chemicals used in the textile manufacturing process.
Responsibilities:
<ul>
<li>Weigh and measure dyes and chemicals according to production specifications</li>
<li>Mix and prepare chemical solutions for the dyeing process</li>
<li>Ensure accuracy of formulas and record all measurements and usage</li>
<li>Maintain a clean and organized work area, following all safety protocols</li>
<li>Monitor inventory levels of chemicals and assist with restocking as needed</li>
<li>Collaborate with production staff to meet daily production goals</li>
<li>Follow all company policies and OSHA safety regulations</li>
</ul>
Requirements:
<ul>
<li>Previous experience as a dye weigher, chemical weigher, or in a similar manufacturing role (required)</li>
<li>Strong attention to detail and accuracy in measuring/recording</li>
<li>Ability to follow formulas, recipes, and safety procedures</li>
<li>Must be comfortable working around chemicals and wearing proper PPE</li>
<li>Reliable transportation to and from work</li>
<li>Ability to stand, walk, bend, and lift up to 50 lbs throughout the shift</li>
</ul>

3rd Shift Dye and Chemical Weigher

<h3>Job Description</h3>
Job Title: Associate Scientist
Location: Cambridge MA – 100% Onsite
Duration: 3 Years Contract
Terms: Contract W2
 
Description:
 
Fully onsite 8-5. Cambridge site. Must be able to commute to site. Open to relocation candidates but must be willing to start ASAP.
 
Must have: HPLC expertise and hands on lab experience.
M.S. and 1 YOE would be ideal.
 
B.S. and 3 YOE would be acceptable but a M.S is preferred.
 
Managers ideal candidate: Someone who has a couple of years experience in biopharma working on bioanalytical assays such as SEC HPLC, Ion Exchange HPLC, and some basic assays like pH, osmolality, protein concentration etc. Good communication skills are also a must as they will work with a big group of people.
 
Job Details:
 
1+ Years w/ Relevant MS OR equivalent 3+ Years w/ Relevant BS
 
To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
 
Responsibilities include:
1 Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision,
2 Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data,
3 Effectively transfers experimental methods from literature to the lab and makes modifications as necessary,
4 Develops and implements new protocols with moderate review,
5 Works efficiently in a matrix team environment and collaborates with coworkers,
6 Communicates data and interpretation to work group,
7 Skilled at developing systems to ensure quality data,
8 Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques (HPLC, CE, physical property testing...),
9 Effectively trouble-shoots equipment and experimental difficulties,
10 Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents,
11 Participates in department-wide support efforts such as safety, recruiting and committees,
12 May train staff and/or supervise others,
13 Coordinates and organizes resources needed to complete the task,
14 Understands when to seek input and when to make independent judgments.
 
Requirements: Minimum BS degree (MS is preferred) in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, Biology or related discipline and at least 2 year experience in a Biopharmaceutical working environment.
 
Top 3 Must Have Skill Sets: 
BioPharma lab experience is a plus
HPLC expertise - able to operate, process data, and report findings into electronic lab notebook.
Good organizational skills - must be able to handle multiple tasks and communicate to different teams effectively and efficiently.
Experience working in a biopharmaceutical lab showing analytical skills (compendial assays such as pH, osmolality, protein concentration, particle sizing etc).
 
Day to Day Responsibilities: 
Analyze samples from Drug product related studies and process the data output according to known SOPs and protocols. All data is then transcribed into a lab notebook for compliance and communicated with the study owners.

Associate Scientist/Chemist (HPLC experience)

<h3>Job Description</h3>
Job description:
We are currently seeking a highly motivated and passionate scientist to join our team in Immunology Discovery based in Cambridge MA. In this role, the candidate will collaborate with multiple cross-functional teams to advance portfolio projects, with a particular emphasis on supporting in vitro data generation. Responsibilities include performing and adapting cell-based in vitro protocols in a timely manner across diverse cell systems, data analysis and effective communication of results, and collaboration across multiple teams. The position offers a unique opportunity for a talented scientist to work in a dynamic, innovative, and multi-disciplinary environment to develop their career at the interface of basic research and early drug discovery. The position requires ability to work independently, demonstrate excellent technical, written and oral communication skills and work very well in a collaborative team environment.
 
Key responsibilities
<ul>
<li>Human colon organoid culture, passaging, and plating for experiments to support the group</li>
<li>Perform cell-based assays using cell lines and mammalian primary cells</li>
<li>Test biologic and small molecules in cell-based assays for functional readouts including cell proliferation, cytokine release, and gene expression</li>
<li>Perform advanced molecular and cellular biology techniques (including but not limited to FACS, ELISA, MSD, HTRF, qPCR)</li>
<li>Responsibilities may include processing animal tissue ex vivo and isolation of immune cells from human and animal tissue or blood</li>
<li>Work independently on the design, execution and interpretation of experimental results to validate hypotheses related to the project need</li>
<li>Maintain close communication with multiple groups to support human colon organoid cell needs</li>
<li>Implement and innovate new experimental protocols/techniques as needed</li>
<li>Analyze, interpret, document and report data consistently, concisely and rigorously, both to individual stakeholders and in group settings</li>
<li>Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment</li>
<li>Impact projects mostly through lab-based activities</li>
</ul>
 
Qualifications and requirements:
<ul>
<li>Bachelor’s degree in Biological Science or related field with 2+ years of experience in biotech or pharma setting (industry experience)</li>
<li>Experience with human organoid culture</li>
<li>In vitro assays with primary human immune cells (ie myeloid, PBMCs)</li>
<li>Molecular and cellular analysis techniques including qPCR, MSD, ELISA, flow cytometry</li>
</ul>

Biologist

<h3>Job Description</h3>
Job Description
Overview: We're seeking a motivated Project Manager to lead environmental projects involving contamination investigations, regulatory reporting, and remediation oversight. This role prepares and manages reports such as ESA, MOP, NAM, PARM, RAP, SAR, and TCAR, ensuring projects meet client and regulatory requirements efficiently and accurately.
Key Responsibilities:
<ul>
<li>Manage environmental assessment and remediation projects from start to finish.</li>
<li>Conduct field investigations, sampling, and data analysis.</li>
<li>Prepare technical reports, regulatory submissions, and client communications.</li>
<li>Coordinate with clients, agencies, and internal teams to ensure timely, compliant deliverables.</li>
<li>Apply dewatering and contamination assessment principles, including Sichardt's equation.</li>
<li>Use MS Office, ArcGIS, Adobe, and related software to prepare professional documentation.</li>
</ul>
Qualifications:
<ul>
<li>Education: Bachelor's in Construction, Earth Sciences, Engineering, or Mathematics (or equivalent experience) preferred.</li>
<li>Experience: 2+ years in environmental consulting (air, groundwater, soil, asbestos, or mold testing preferred).</li>
<li>Skills: Strong analytical, communication, and project coordination abilities; proficiency in Microsoft Office, ArcGIS, Adobe Acrobat, and Google Earth Pro.</li>
<li>Other: Valid driver's license; ability to travel locally; must pass background and drug screening.</li>
<li>Language: English required; Spanish preferred.</li>
</ul>
Compensation &amp; Benefits:
<ul>
<li>Competitive salary (commensurate with experience)</li>
<li>Paid time off</li>
<li>Health insurance &amp; retirement plan</li>
<li>Professional development and license reimbursement</li>
</ul>

Project Manager - Staff Scientist

<h3>Job Description</h3>
Job DescriptionLoureiro Engineering Associates is seeking a Project Scientist to join our Environmental Division in Connecticut. This role is ideal for a motivated professional with strong technical and organizational skills who is ready to support and lead environmental projects, contribute to client solutions, and grow with a collaborative, experienced team. At Loureiro, you won’t just work for the company—you’ll own a part of it. As a 100% employee-owned company, our Employee Stock Ownership Plan (ESOP) gives you a company-funded ownership stake that grows over time—so when we succeed, you share in the rewards. What You'll Do:
<ul>
<li>Assist in preparation of proposal estimates of time and expense required to complete the project.</li>
<li>Participate in presenting the proposal to the client as needed</li>
<li>Participate in major project design decisions in conjunction with the Project Manager.</li>
<li>Assign duties to Project Team, answer their questions, and monitor their progress.</li>
<li>Provide the technical expertise for projects to which assigned.</li>
<li>Support or maintain client communication throughout the development of the project</li>
<li>Serve as Project Manager on select projects as needed</li>
<li>Perform other related work as apparent or as assigned and performs all such work in a safe manner, consistent with the firm’s policies and procedures.</li>
</ul>
Who You Are:
<ul>
<li>A proactive learner who thrives in a fast-paced, team-driven environment</li>
<li>Technically skilled with excellent attention to detail</li>
<li>Highly organized with the ability to manage multiple tasks and priorities</li>
<li>A strong communicator—both written and verbal</li>
</ul>
 What You Bring:
<ul>
<li>Bachelor’s degree in Engineering, Geology, or Environmental Science (Master’s or Doctorate a plus)</li>
<li>5+ years of relevant experience in environmental project design and implementation</li>
<li>Strong proficiency in Microsoft Office</li>
<li>Excellent organizational and problem-solving skills</li>
</ul>
 Physical Requirements:
<ul>
<li>Prolonged periods of sitting at a desk and working on a computer</li>
<li>Must be able to lift up to 15 lbs.</li>
<li>Ability to operate standard office equipment and keyboards.</li>
<li>Able to push, pull, and place materials on level surfaces and overhead cabinets.</li>
<li>Must be able to work in a variety of weather conditions and terrains.</li>
<li>Adherence to safety protocols and proper use of personal protective equipment</li>
</ul>
 Why Loureiro?
<ul>
<li>Employee Ownership, Real Impact: Through our ESOP, you gain a meaningful financial stake in the company’s success.</li>
<li>Diverse Expertise: Partner with specialists across engineering, environmental, construction, and EH&amp;S disciplines.</li>
<li>Opportunity to Advance: We’re serious about your growth, offering hands-on learning, coaching, and clear career paths.</li>
<li>People-First Culture: You’ll be part of a respectful, team-oriented environment that values your voice.</li>
<li>And of Course…Exceptional Benefits: From health coverage to financial wellness, our benefits are built to support you in and out of the workplace. &nbsp;</li>
</ul>
We are committed to delivering high-quality engineering and construction solutions that make a lasting impact, and we take pride in fostering an empowering workplace. If you’re looking to take ownership of impactful work and grow your career in a supportive environment, we’d love to hear from you! Loureiro Engineering Associates, Inc. (Loureiro) is an employee owned (ESOP), full-service multi-disciplinary consulting firm with operations in Connecticut, Massachusetts, Rhode Island, New Hampshire, North Carolina, and Missouri. Loureiro’ s areas of expertise include the integration of the highest quality engineering, construction, environmental health &amp; safety, energy, and waste management services. EEO/AAP Statement: Loureiro Engineering Associates Inc., 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. &nbsp;
Loureiro Engineering Associates Inc. 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.
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Project Scientist

<h3>Job Description</h3>
Job Description
Position Purpose:
Signature Science, LLC is seeking highly motivated Forensic Scientists with specific expertise in human DNA analysis to contribute to our laboratory operations throughout the Mid-Atlantic region. These positions are contingent upon contract funding.
The primary responsibility of this role is to perform DNA analysis on forensic casework samples, from initial sample processing to final report generation. This includes a range of tasks, such as DNA extraction, quantification, amplification, and genetic analysis. Additionally, the Forensic Scientist will contribute to research and validation efforts, ensuring the accuracy and reliability of our laboratory procedures.
*This position can be located in Dover, DE*
Essential Duties &amp; Responsibilities:
Laboratory Operations:
<ul>
<li>Adhere to strict laboratory protocols and quality assurance standards.</li>
<li>Utilize appropriate personal protective equipment (PPE) to maintain a safe working environment.</li>
<li>Practice rigorous contamination control techniques to prevent sample cross-contamination.</li>
<li> Handle and safeguard DNA samples and data in accordance with established procedures.</li>
<li>Perform DNA analysis on diverse sample matrices, including touch DNA samples.</li>
<li>Employ various DNA extraction methods, quantification techniques (e.g., Real-Time PCR), and amplification protocols.</li>
<li>Utilize advanced genetic analyzer platforms to generate high-quality DNA profiles.</li>
<li>Interpret complex DNA profiles, including single-source and mixture samples, using both manual and probabilistic genotyping methods.</li>
<li>Prepare clear and concise forensic reports, summarizing findings and conclusions.</li>
<li>Conduct technical reviews of casework to ensure accuracy and completeness.</li>
<li>Collaborate with team members to efficiently process a high volume of casework.</li>
<li> Adapt to changing priorities and deadlines to meet client needs.</li>
<li>Maintain and troubleshoot laboratory equipment, such as Real-Time PCR instruments, thermocyclers, and genetic analyzers.</li>
<li>Participate in validation studies of new DNA methodologies and established procedures.</li>
</ul>
Required KSA's
<ul>
<li>Strong understanding of forensic DNA analysis principles and techniques.</li>
<li>Proficiency in using laboratory equipment and software (e.g., GeneMapper ID-X, STRmix).</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Attention to detail and ability to follow precise protocols.</li>
<li>Strong written and verbal communication skills.</li>
<li>Ability to work independently and as part of a team.</li>
<li>Strong organizational and time management skills. </li>
<li>Ability to obtain and maintain a security clearance.</li>
</ul>
Education/Experience:
<ul>
<li>Bachelor's degree in biological sciences, forensic science, or a related field.</li>
<li>Minimum of 6 months of full-time laboratory experience, preferably in a forensic laboratory.</li>
<li>Experience with DNA analysis techniques, including extraction, quantification, amplification, and genotyping.</li>
<li>Adherence to FBI Quality Assurance Standards (QAS) for DNA analysis.</li>
</ul>
Clearance:
US Citizenship required; candidates will be subject to security screening.
Working Conditions/Equipment/Travel:
<ul>
<li>Laboratory environment requiring the use of PPE.</li>
<li>Potential exposure to hazardous materials, including biological fluids.</li>
<li>Ability to lift up to 20 pounds independently and 40 pounds with assistance.</li>
<li>Limited (&lt;5%) travel may be required.</li>
</ul>
 Powered by ExactHire:160583

Forensic Scientist (hDNA Analyst)-Contingent

<h3>Job Description</h3>
Job DescriptionJob Description:&nbsp;Ninyo &amp; Moore Geotechnical &amp; Environmental Sciences Consultants has an immediate opening for a Project Environmental Scientist, Engineer or Geologist in Irvine, California. The successful candidate will conduct Phase I and Phase II Environmental Site Assessments, Preliminary Endangerment Assessments (PEAs), Removal Action Workplans (RAWs) and Remedial Action Plans (RAPs), and Risk Assessments. Responsibilities will include scheduling field work and subcontractors. The candidate will perform fieldwork activities, including drilling supervision, logging of borings, test pits, trenches and cores; evaluating geologic and hydrogeologic conditions; and sampling soil, soil gas, and groundwater; and will prepare environmental proposals and reports. Duties of the Project Geologist/Engineer will also include managing project scope, budgets and schedules.
Education:&nbsp;B.S. Degree in Environmental Sciences, Geology or Civil Engineering, M.S. preferred.&nbsp;
Required Skills:&nbsp;5-10 years experience performing all or most of the duties listed in the job description required. The ideal candidate will bring local experience and familiarity with the local geologic practice and a strong knowledge of local, state and federal regulations. The ideal candidate must be familiar with permitting acquisition, performing site assessment and soil and groundwater remediation activities and system operation and maintenance. The candidate should be a team player, detail oriented, and have excellent verbal and written communication skills.
Status:&nbsp;Full time
Location:&nbsp;Irvine, CA
Reference ID:PEEG-IRV
 
Compensation details: 100000-120000 Yearly Salary
 
PI9ddc54354198-25405-38827770

Project Environmental Scientist, Engineer or Geologist

<h3>Job Description</h3>
Job title: Quality Control Analyst II
Location: Fort Worth, TX (Onsite)
Duration: 12 months
 
Job Description:
 
The Quality Control Analyst II is responsible for maintaining high standards of laboratory operations and ensuring compliance with regulatory requirements.
Key responsibilities include:
• Performs microbiological validations for raw materials and finished products, including Bioburden, Endotoxin, Sterility, and PET.
• Provides support to QC Microbiology laboratories.
• Conducts equipment qualifications.
• Supports audits.
• Organizes and assists with Media Fill and Reads.
• Identifies ongoing quality issues, prevents potential problems, and suggests improvements.
• Interprets and evaluates analyses for accuracy and precision against established specifications, recommending and implementing corrective actions when necessary.
• May be responsible for analytical and protocol report writing, as well as standard operating procedures.
• Strictly adheres to Good Documentation Practices (GDP).
• Collaborates with and supports coworkers to enhance the organization's overall capabilities.
• Communicates effectively with production, maintenance, warehouse, and other relevant functions.
• Participates in problem-solving and troubleshooting.
• Supports training needs of team members and works cohesively with the team.
• Coordinates with and supports other departments to ensure smooth workflow execution.
• Ensures the availability of supplies and equipment to meet schedules and carries out tasks as defined by the schedule.

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