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<h3>Job Description</h3>
Job DescriptionJob Title: Microbiologist Location: San Jose, CaliforniaHire Type: Onsite, Long-term contract w/full employee benefitsTarget Pay Rate: $35.00 - $38.00/hour (W2)Work Schedule: Weds–Fri (2:30pm-11:00pm), Sat–Sun (10:00am-7:00pm) Overview:Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S. As a contract employee of Sterling, you are eligible to receive a Full Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental &amp; vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan.Job Summary: Our client, a leader in the life sciences industry, is seeking a Microbiologist to join their Research &amp; Development team. This position plays a key role in developing and testing instruments and consumables to support ongoing product development and commercialization efforts.Job Duties:
<ul>
<li>Perform microbiological testing to support study protocols and new product development (instruments, AST panels, consumables).</li>
<li>Analyze and interpret data from completed assays and experiments.</li>
<li>Inspect and process biological samples and consumables using aseptic techniques.</li>
<li>Prepare and present experiment reports, including results and failure investigations.</li>
<li>Collaborate with cross-functional teams to ensure project goals and timelines are met.</li>
<li>Support daily lab operations including equipment maintenance, cleaning, and documentation.</li>
<li>Perform additional lab-related tasks and projects as assigned by management.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Microbiology or a related scientific field required.</li>
<li>Strong knowledge of aseptic techniques, Good Documentation Practices (GDP), and Good Laboratory Practices (GLP).</li>
<li>Proficiency in Microsoft Office (Word, Excel, PowerPoint).</li>
<li>Excellent attention to detail, organization, and problem-solving skills.</li>
<li>Ability to work independently and manage multiple priorities in a fast-paced environment.</li>
<li>Effective written and verbal communication skills; strong team collaboration mindset.</li>
<li>Familiarity with ISO 9001 and FDA Quality System Regulations preferred.</li>
</ul>
 Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identify, national origin, disability, protected veteran status, or genetic information.

Scientist

<h3>Job Description</h3>
Job Description
Job Title: Chemist
Job Description
We are seeking a dedicated chemist to join our team. This role involves testing finished products, raw materials, in-process samples, components, and stability study samples. You will conduct tests on samples such as oral rinses and antiseptics using titrations, pH measurements, specific gravity assessments, and HPLC within Quality Control (QC) as needed.
Responsibilities
<ul>
<li>Conduct daily testing using HPLC, GC, TOC, FT-IR, UV-Vis, and pH meters.</li>
<li>Inspect supplies and ingredients for pharmaceutical production.</li>
<li>Review and ensure accuracy of SOPs and lab protocols.</li>
<li>Perform some instrument validation.</li>
<li>Adhere to GMP and FDA guidelines.</li>
<li>Maintain rigorous documentation for testing protocols and executed tests, ensuring data integrity.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Preferred 4 years of pharmaceutical industry experience with hands-on experience in GC, HPLC, FTIR, and wet chemistry (titration).</li>
<li>Familiarity with Agilent OpenLab software.</li>
<li>Good handwriting for laboratory notebook documentation.</li>
</ul>
Work Environment
Join a state-of-the-art QC Lab specializing in oral rinse and antiseptic solutions and pharmaceutical products. This is a first-shift position. Benefit from the opportunity to advance in your career as the company expands, with structured career growth opportunities and training metrics in place. The company is privately held and in excellent financial standing.
Pay and Benefits
The pay range for this position is $32.00 - $34.00/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 Mount Prospect,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.

Chemist

<h3>Job Description</h3>
Job DescriptionIMMEDIATE OPENING: Microbiology Laboratory Supervisor
<ul>
<li>APPLY NOW: Email or call/text Abby Vaughn directly with an updated resume at: abvaughn @actalentservices.com 317 - 567 - 6605</li>
</ul>
Job Description
The main role of the Microbiology Lab Supervisor is to oversee and coordinate the activities of production and operating workers, ensuring smooth and efficient laboratory operations.
Responsibilities
<ul>
<li>Implement measures to motivate employees and improve production methods, equipment performance, product quality, and efficiency.</li>
<li>Review operations and work with technical or administrative staff to resolve production or processing issues.</li>
<li>Develop and implement production tracking and quality control systems, analyzing production, quality control, and maintenance to identify production problems.</li>
<li>Hire, train, evaluate, and manage staff, and resolve any personnel grievances.</li>
<li>Set and monitor product standards to ensure high-quality finished products.</li>
<li>Prepare and maintain comprehensive production reports and personnel records.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology, or a related field.</li>
<li>10+ years of microbiology/chemistry experience working in a CLIA certified or CAP accredited lab.</li>
<li>4-6+ years of leadership or people management experience. Proven leadership of teams with 30+ staff members</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>ASCP or AMT certification is preferred.</li>
<li>Proficiency with computers and familiarity with laboratory information systems.</li>
<li>Ability to work independently and collaboratively within a team.</li>
<li>High attention to detail with strong communication and organizational skills.</li>
<li>Ability to pass a standardized color vision screen.</li>
<li>Flexibility to work overtime or other shifts as needed.</li>
</ul>
﻿INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:
Interview availability this week
<ul>
<li>I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Abby Vaughn</li>
<li>HOW TO APPLY DIRECTLY : Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to abvaughn @actalentservices. com or call me/text directly at (317-567 -6605)</li>
</ul>
Pay and Benefits
The pay range for this position is $50.00 - $70.00/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 Indianapolis,IN.
Application Deadline
This position is anticipated to close on Oct 29, 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.

Lab Supervisor (Microbiology)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Responsibilities include, but are not limited to, the following:
<ul>
<li>Perform routine analytical testing of medium to high complexity drug substance/drug product and/or method verification/characterization using instrumentation including, but not limited to, HPLC, GC, UV spectrophotometer, dissolution apparatus, pH meter, water activity meter, Karl Fischer titrators.</li>
<li>Participate in conducting investigations</li>
<li>Document test results in notebooks and reports</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree in biology, biochemistry, chemistry or other related degree concentration</li>
<li>At least 10-15 years of related laboratory experience</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and&nbsp;a&nbsp;positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Proficiency in IT related skills such as Microsoft excel, word, PowerPoint, etc.&nbsp;</li>
<li>Candidates located within a commutable distance of Indianapolis, IN are encouraged to apply.&nbsp;</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, Monday-Friday, 8:00 am - 5:00 pm.&nbsp;</li>
<li>Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply</li>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>#LI-EB1</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Senior Chemist

<h3>Job Description</h3>
Job DescriptionOur mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care. We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine’s greatest challenges. GRAIL is headquartered in Menlo Park, California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, please visit grail.com. The Senior Scientist, Process Integration, is responsible for the scientific and technical advancement associated with introducing new assays and diagnostic products into Grail’s high-throughput, regulated laboratory environment. This individual contributor role focuses on supporting key activities in process integration, improvement, monitoring, and troubleshooting, in close partnership with cross-functional teams such as MSAT, Engineering Operations, and Clinical Lab. The ideal candidate brings deep expertise in the full laboratory workflow—from pre-analytical to post-analytical phases—process optimization, and comprehensive knowledge of clinical laboratory regulatory frameworks. Responsibilities:
<ul>
<li>Support the transfer and implementation of new assays and diagnostic products from development into production, ensuring robust performance across all workflow phases.</li>
<li>Develop, optimize, and document validation protocols and procedures in compliance with CLIA, CAP, NYS, ISO 13485, FDA, and other applicable standards.</li>
<li>Provide scientific and technical support to MSAT, Engineering Operations, and Clinical Lab teams.</li>
<li>Evaluate, qualify, and implement alternative reagents and vendors to maintain continuity and strengthen lab operations.</li>
<li>Monitor process performance, analyze data and metrics, and contribute to process monitoring and improvement strategies to sustain high-quality, efficient operations.</li>
<li>Identify process gaps and contribute to or lead process improvement initiatives to enhance efficiency, reliability, and quality.</li>
<li>Lead or assist in process troubleshooting activities, including root-cause analysis and impact assessments, resolving technical challenges.</li>
<li>Prepare comprehensive technical documentation, scientific reports, and regulatory submission materials as required.</li>
<li>Maintain high standards of scientific rigor, quality, and regulatory compliance in all process integration activities.</li>
</ul>
Preferred Qualifications:
<ul>
<li>PhD in Life Sciences, Molecular Biology, Biochemistry, Bioengineering, or a related field.</li>
<li>Proven experience in technology transfer of assays and launching new products in a regulated diagnostic laboratory.</li>
<li>Direct, hands-on experience with end-to-end clinical workflows (pre-analytical, analytical, and post-analytical).</li>
<li>Strong knowledge of high-throughput laboratory automation and advanced instrumentation.</li>
<li>Deep understanding of clinical laboratory regulatory standards, including CLIA, CAP, NYS, ISO 13485, and FDA.</li>
<li>Experience with or understanding of reagent manufacturing and alternative vendor qualification processes.</li>
<li>Experience participating in audits (internal, regulatory, or client-driven).</li>
<li>Excellent skills in technical documentation and scientific writing.</li>
<li>Demonstrated ability to collaborate effectively across MSAT, Engineering Operations, and Clinical Lab teams.</li>
<li>Six Sigma certification or significant experience with Lean, Kaizen, or other process improvement methodologies.</li>
<li>Hands-on experience with data analytics tools and platforms (e.g., JMP, Minitab, R, Python, Tableau) for process monitoring, analysis, and reporting.</li>
<li>Experience with laboratory information management systems (LIMS) or MES.</li>
<li>Advanced data analysis skills applied to laboratory operations and quality improvement.</li>
<li>Experience supporting laboratory scale-up, automation, or operational excellence projects.</li>
</ul>
Expected full time annual base pay scale for this position is $119K - $142K. Actual base pay will consider skills, experience and location. Based on the role, colleagues may be eligible to participate in an annual bonus plan tied to company and individual performance, or an incentive plan. We also offer a long-term incentive plan to align company and colleague success over time. In addition, GRAIL offers a progressive benefit package, including flexible time-off, a 401k with a company match, and alongside our medical, dental, vision plans, carefully selected mindfulness offerings. GRAIL is an Equal Employment Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. We will reasonably accommodate all individuals with disabilities so that they can participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. GRAIL maintains a drug-free workplace.

Senior Scientist Process Integration # 4375

<h3>Job Description</h3>
Job Description
As a Genealogist at Lauth Investigations International Inc, you will play an essential role in uncovering and documenting family histories and lineage for our clients. This position involves comprehensive research, data analysis, and investigative strategies to trace ancestry and build familial connections. You will utilize various resources, technologies, and methodologies to collect and verify information, providing clients with accurate and thorough genealogical reports. 
Key Responsibilities:
<ul>
<li>Conduct in-depth genealogical research using various resources, including public records, databases, and archival materials.</li>
</ul>
<ul>
<li>Analyze historical documents and data to construct family trees and lineage charts.</li>
</ul>
<ul>
<li>Verify, cross-check, and validate historical information to maintain accuracy in genealogical records.</li>
</ul>
<ul>
<li>Prepare comprehensive genealogical reports that summarize findings and provide clients with actionable insights.</li>
</ul>
<ul>
<li>Utilize technology tools and genealogical software for data organization and presentation.</li>
</ul>
<ul>
<li>Communicate effectively with clients to understand their genealogical goals and keep them updated on progress.</li>
</ul>
<ul>
<li>Collaborate with other team members and departments to enhance research strategies and share best practices.</li>
</ul>
<ul>
<li>Stay current on genealogical standards, methodologies, and best practices to improve research outcomes.</li>
</ul>
<ul>
<li>Participate in relevant workshops, conferences, and training to enhance professional knowledge and skills.</li>
</ul>
<ul>
<li>Occasionally assist in training junior genealogists or interns.</li>
</ul>
Requirements
<ul>
<li>Strong research and analytical skills with attention to detail</li>
</ul>
<ul>
<li>Proficiency in genealogical tools and methodologies</li>
</ul>
<ul>
<li>Excellent written and verbal communication skills</li>
</ul>
<ul>
<li>Experience with genealogical databases and archival research</li>
</ul>
<ul>
<li>Ability to interpret historical documents and data effectively</li>
</ul>
<ul>
<li>Prior experience in genealogy, history, or a related field preferred</li>
<li>Experience in obtaining court documents</li>
<li>Understanding the document process</li>
</ul>
<ul>
<li>Familiarity with data management and presentation software</li>
</ul>
Benefits
This is a temp-to-hire position. It is remote with onsite training to start.

Genealogist

<h3>Job Description</h3>
Job Description
Job Title: Research Support Assistant II
Grade: 10
Salary: $42,843-$51,079
The Research Foundation for Mental Hygiene is seeking a qualified full-time research assistant to contribute to the Anacker lab's ongoing studies on the neurobiology underlying stress-induced psychiatric disorders in mouse models of chronic psychosocial stress and early life adversity. The research assistant will contribute to all aspects of the projects, including pharmacological treatment of mice with novel antidepressant compounds, in vivo calcium imaging of neural activity in freely moving mice, biosensor imaging of neurotransmitter signaling in the in vivo brain, rodent behavioral experiments of cognitive flexibility and fear generalization, stereotactic surgery, mouse colony maintenance, brain tissue processing, and microscopy of brain tissue markers of activity-regulated genes
Duties and Responsibilities:
Responsibilities include:
<ul>
<li>Mouse handling and transgenic mouse colony maintenance, </li>
<li>Genotyping, </li>
<li>Behavioral experimentation, </li>
<li>Rodent models of stress and early adversity, </li>
<li>Intraperitoneal injections, </li>
<li>Stereotactic brain surgery in mice, </li>
<li>In vivo calcium imaging of neural activity using miniature microscopes and fiber photometry in freely moving mice,</li>
<li>Transcranial perfusions,</li>
<li>Brain extractions,</li>
<li>Brain tissue processing, </li>
<li>Immunohistochemistry,</li>
<li>Microscopy and data analysis.</li>
</ul>
 Minimum Qualifications:
<ul>
<li>Bachelor's degree in neuroscience</li>
<li>At least (6) months cumulative experience working in a laboratory environment </li>
<li>At least (6) months of experience with rodent behavioral experiments, transcranial perfusions, brain tissue processing, and data analyses</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with in vivo Ca2+ imaging techniques and advanced data analysis approaches (e.g. using R or Python)</li>
</ul>
Work Location: 1051 Riverside Drive, New York, NY-10032
To Apply: Submit an application through our website at <a href="https://rfmh.applicantpro.com/jobs/" target="_blank">https://rfmh.applicantpro.com/jobs/</a>. Please note only applications submitted through our website will be considered.
The Mission of the Research Foundation for Mental Hygiene, Inc. (RFMH) is to promote the mental health of all New Yorkers, with a focus on providing hope and supporting recovery for adults with serious mental illness and children with serious emotional disturbances. Applicants with lived mental health experience are encouraged to apply. RFMH is deeply committed to supporting underserved individuals, organizations, and communities. To this end, RFMH is focused on implementing activities and initiatives to reduce disparities in access, quality, and treatment outcomes for underserved populations. A critical component of these efforts is ensuring that RFMH is a diverse and inclusive workplace where all employees' unique attributes and skills are valued and utilized to support the mission of the Agency. RFMH is an equal opportunity/affirmative action employer.
The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits. Excellent Benefits Package. Affirmative Action/Equal Opportunity Employer - Disabled/Veteran, 41 CFR 60-741.5(a) and 41 CFR 60-300.5(a) compliant.
 
 Job Posted by ApplicantPro

Research Support Assistant II

<h3>Job Description</h3>
Job Description
Job Details:
Job Title: Medical Device Assembler
Location: 829 Towne Center Drive, Pomona, CA 91767
Contract: 12 Months Contract
Shift: 1ST Shift (6 am to 2:30 pm)
Pay Rate: $ 20/Hr.
Job Description
<ul>
<li>Responsible for setting up and performing adjustments to equipment used in support of manufacturing. Ability to diagnose and perform routine technical troubleshooting is required.</li>
</ul>

Job Duties
<ul>
<li>May be tasked with completing set-up operations for one of the following: assembly, packaging and prep operations in compliance with approved documentation, and QSR.</li>
<li>This will include but not limited to line clearance, equipment preventative maintenance and housekeeping.</li>
<li>Performs routine tasks working from detailed written or verbal instructions.</li>
<li>Assembles, repairs, inspect and/or test products following written instructions.</li>
<li>Assist the Engineering and Maintenance teams with trouble shooting, maintenance, and repair of equipment.</li>
<li>May be tasked with the completion and accuracy of documentation associated with the manufactured product and equipment maintenance.</li>
<li>May be tasked with cleaning, performing and documenting routine equipment maintenance and minor repair.</li>
<li>Disposes hazardous waste material on corresponding hazardous waste areas.</li>
<li>Required to support continuous improvements activities, (e.g. 5S and OEE, etc.).</li>
<li>Support new equipment installation and validation.</li>
<li>May be required to assist with problem-solving related to product quality.</li>
<li>Ability to read and comprehend basic instructions and other work related documents.</li>
<li>Demonstrate strong customer service skills while maintaining product Quality.</li>
<li>Participate in root cause analysis and implement corrective actions under the guidance of Supervisor or Manager.</li>
<li>Collaborates with Engineers, Maintenance Technicians, QC Technicians and Management to identify and help implement process improvements.</li>
<li>Works on assignments that are semi-routine in nature where judgment is required in resolving problems and making routine recommendations.</li>
<li>Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.</li>
<li>Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships.</li>
<li>Carries out duties in compliance with established business policies.</li>
<li>Other duties as assigned, according to the changing needs of the business. </li>
</ul>

Assembler (Cleanroom) - $ 20/Hr.

<h3>Job Description</h3>
Job Description
Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant to our direct client, a global medical device company in Johns Creek, GA.
 
Job Title: Research Scientist I (Contract)
Pay Rate: $36.23/hr
40 hours/week, Mon-Fri, 1st shift
 
Job Summary: Research Scientists to work in a laboratory environment, conducting research and experiments for academic, industrial or commercial ends. They may help develop new products for their company, for example, or help contribute to scientific understanding within their field.
 
Responsibilities:
• Lead the formulation, development, and optimization of new programs, designs, and prototypes.
• Participate in research formulating and writing with other staff.
• Assess new technologies and future applications of technologies.
• Propose, plan, and manage research projects, report preparation, and presentation of findings.
• Apply for grants to continue their research.
• May be required to mentor, train and/or coach junior research scientists.
• Stay up to date on developments within their field through methods such as reading academic journals, attending training programs and attending conferences within their field.
 
Education:
• Bachelor's degree or higher in a scientific discipline with adequate experience (MS with 0-2 yrs; BS with 2-4 yrs)
 
Experience:
• Background in Chemistry, Material Science, Chemical Engineering, Process Engineering
• Formulation and process experience with hydrogel and contact lens care are desired
• Must be able to write reports and communicate well to internal customers
Company DescriptionA WBENC (woman owned) certified company; Source One provides a full range of professionals to the Pharmaceutical &amp; Healthcare, Defense, Technology, Financial Services, Retail &amp; Manufacturing, and Energy &amp; Transportation industries nationwide. 
<h3>Company Description</h3>
A WBENC (woman owned) certified company; Source One provides a full range of professionals to the Pharmaceutical &amp; Healthcare, Defense, Technology, Financial Services, Retail &amp; Manufacturing, and Energy &amp; Transportation industries nationwide.

Research Formulation Scientist I

<h3>Job Description</h3>
Job Description
Join Our Team at Rock Solid Geotechnical, Inc.
Are you a skilled geologist or engineer with a passion for geotechnical work? Rock Solid Geotechnical, Inc. is seeking a talented Staff Geologist/Engineer and/or Project Geologist/Engineer to join our growing team in beautiful downtown Laguna Beach!
About Us: Though Rock Solid Geotechnical, Inc. is just 3 years old, our team has deep local roots with over 25 years of experience in the community. We pride ourselves on providing exceptional geotechnical services across South Orange County to North San Diego County, with some occasional outlier projects.
Position: Staff Geologist/Engineer to Project Geologist/Engineer
Key Responsibilities:
<ul>
<li>Perform subsurface investigations and geotechnical fieldwork.</li>
<li>Prepare detailed geotechnical reports and draft cross-sections.</li>
<li>Conduct construction observations and inspections.</li>
<li>Assist in creating and maintaining a comprehensive geotechnical database.</li>
</ul>
What We’re Looking For:
<ul>
<li>Relevant experience in geotechnical.</li>
<li>Strong analytical skills and attention to detail.</li>
<li>Proficiency in drafting cross-sections and preparing geotechnical reports.</li>
<li>Ability to work effectively both independently and as part of a team.</li>
<li>Enthusiasm for contributing to a dynamic, community-focused company.</li>
</ul>
What We Offer:
<ul>
<li>Competitive pay and benefits. Pay will be commensurate with experience.</li>
<li>401K plan to help secure your future.</li>
<li>Health Insurance</li>
<li>A vibrant work environment in downtown Laguna Beach.</li>
<li>Opportunities to work on diverse projects across South Orange County and North San Diego County.</li>
</ul>
Why Rock Solid Geotechnical, Inc.?
<ul>
<li>Be part of a growing company with a strong community presence.</li>
<li>Collaborate with an experienced team dedicated to excellence.</li>
<li>Enjoy working in a picturesque location with exciting and varied projects.</li>
</ul>
Ready to make an impact? Apply now to join Rock Solid Geotechnical, Inc.!
Send your resume and cover letter to [email address] or visit our website at [website URL] to learn more about this exciting opportunity.
Rock Solid Geotechnical, Inc. – Laying the foundation for the future, one project at a time.
Company DescriptionWe are a passionate team of geologists/engineers. We have been in this area and working this field for more than 25 years. We are all hands-on deck kind of a team and you will definitely learn all aspects of the geotechnical field with our company. 
<h3>Company Description</h3>
We are a passionate team of geologists/engineers. We have been in this area and working this field for more than 25 years. We are all hands-on deck kind of a team and you will definitely learn all aspects of the geotechnical field with our company.

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