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<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose:
Generate and analyze precise, reliable, and reproducible data in a timely manner, under the direction of a more senior scientific leader. Demonstrate experimental precision and should possess general understanding of core discipline.
Responsibilities:
<ul>
<li>Completely follow established experimental protocols and assess results with supervision.</li>
<li>Recognize and report experimental variances.</li>
<li>Apply basic scientific principles to research.</li>
<li>Learn and effectively implement new experimental protocols and/or techniques. Maintain laboratory equipment and optimize laboratory operations for efficient use of time and laboratory supplies and reagents, when appropriate.</li>
<li>Consult literature to understand scientific purpose of assignments. Impact projects predominantly through lab and/or pilot plant based activities.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree, or equivalent education.</li>
<li>Theoretical and practical knowledge to carry out job functions.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements understate or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it&nbsp;will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested,and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any otherform of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company'ssole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole andabsolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist, I

<h3>Job Description</h3>
Compunnel Healthcare is seeking a travel Physicist for a travel job in Mountain View, California.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 09/15/2025</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours</li>
<li>Employment Type: Travel</li>
</ul>
Requirement: •\tFive (5) years medical physics experience. •\tExperience with Stereotactic Radiation Surgery (SRS), Stereotactic Body Radiation Therapy (SBRT), Intensity-Modulated Radiation Therapy (IMRT), High and/or Low Dose Brachytherapy, superficial therapy, and external beam treatment planning. License/Certification/Registration Requirements : •\tBoard Certified American Board of Radiology in Radiation Therapy Physics and /or American Board of Medical Physics in Radiation Oncology Physics preferred. •\tBoard of Licensure for Professional Medical Physicists preferred. •\tValid Radioactive Material License.
Compunnel Healthcare Job ID #11209103. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined.
About Compunnel Healthcare
Compunnel Healthcare is at the forefront of the healthcare staffing industry,
offering personalized and affordable solutions to help you find your ideal job
within local, regional, and national healthcare organizations. We are dedicated
to providing you with the best opportunities that align with your career goals
while also meeting the specific needs of employers.
 
Our approach is centered on creating a mutually beneficial relationship
between job seekers like you and healthcare employers. We strive to ensure
that every placement is a perfect match, adhering to high standards of ethics,
credibility, and quality service. With a deep understanding of what employers
are looking for and what you need to succeed in your career, we tailor our
services to fit your unique specifications and goals.
 
By choosing Compunnel Healthcare, you gain access to a team of experts
who are committed to your professional growth and satisfaction. We work
diligently to place you in roles that enhance your skills and advance your
career.

Travel Physicist

<h3>Job Description</h3>
Job DescriptionDescription:
Description:
Attention all Hearing Conservationists! We are seeking dedicated professionals to join us in providing essential hearing conservation services to Military Service Members. With a focus on maintaining the health and readiness of our brave personnel, you’ll primarily work weekends with some occasional weekdays on an "as-needed" basis.
Why Join Us?
<ul>
<li>Serve with Purpose: Contribute to the health readiness of our military personnel across all branches, including the Army, Navy, Marine Corps, Coast Guard, and Air Force Reserves.</li>
<li>Flexible Scheduling: Enjoy the flexibility of weekend work with the possibility of occasional weekday shifts, allowing you to maintain work-life balance.</li>
<li>Critical Role: Your expertise will play a crucial role in ensuring our service members receive the highest quality hearing assessments.</li>
</ul>
Responsibilities:
<ul>
<li>Conduct automatic audiograms for military personnel.</li>
<li>Review test results to ensure quality control, accuracy, and thorough demonstration of hearing capabilities.</li>
</ul>
Requirements:
Requirements:
<ul>
<li>Certification: CAOHC certification is required.</li>
<li>Skills: Strong attention to detail, proficiency in manual audiometry, and ability to work effectively in a fast-paced environment. Experience with DOEHRS preferred but training is provided.</li>
<li>Availability: Must be able to work weekends with the flexibility for occasional weekdays.</li>
</ul>
About Us: At DOCS Health, we provide innovative health readiness services that ensure our military force is prepared for duty. With over three decades of experience, we are a trusted leader in delivering health services across various sectors. Our dedicated team of professionals strives to set a new standard of care, ensuring that service members receive the attention they deserve.
Join us today to make a lasting impact on the lives of those who serve. Together, we can be the bridge for better health!

Hearing Conservationist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Biologics CMC Development team at AbbVie in the Bay Area has a long and rich history of biologics development. Now located in a new state of the art facility in South San Francisco, the team leverages its comprehensive end-to-end CMC capabilities to work collaboratively through all phases of CMC development with a primary focus on advancing complex biologic therapies, such as bi-specifics and novel modalities, to human clinical studies and eventual licensure.&nbsp;This role is within a team of highly experienced scientists and managers who have directly enabled the development/IND submissions of 20+ novel biologics and successfully filed two BLAs.
As one of CMC purification development group members, you will apply your strong expertise in CMC purification to develop robust, phase-appropriate processes for drug substance GMP production to enable human clinical studies and eventual licensure. You will be responsible for all aspects of CMC purification program deliverables and help drive drugs substance purification development strategy though program lead assignments in cross-functional CMC teams. &nbsp;
This position is an onsite role in a lab-based function. To be successful candidates must enjoy and thrive in an onsite, highly collaborative lab environment with daily face-to-face cross-functional interactions between scientists.
Responsibilities&nbsp;include:&nbsp;
<ul>
<li>Development, optimize, and scale-up purification processes for biologics candidates to support early and late stage&nbsp;development&nbsp;</li>
<li>Transfer processes to GMP manufacturing for clinical material production&nbsp;</li>
<li>Work with contract labs and carry out viral clearance&nbsp;studies&nbsp;</li>
<li>Conceive and evaluate novel, advanced bioprocess technologies that are in line with the group’s strategy&nbsp;</li>
<li>Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall&nbsp;program&nbsp;</li>
</ul>
<ul>
<li>Seize opportunities to pursue project relevant leads that are in line with the group’s strategy&nbsp;</li>
<li>Maintain a high level of productivity in the lab&nbsp;</li>
<li>Write technical&nbsp;publications,&nbsp;reports, presentations, and regulatory filings&nbsp;including publishing&nbsp;research in peer-reviewed journals and presenting&nbsp;work at scientific&nbsp;conferences&nbsp;</li>
</ul>
<ul>
<li>Work&nbsp;efficiently,&nbsp;collaboratively,&nbsp;and cross-functionally toward project timelines and goals&nbsp;&nbsp;</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, and GxP compliance, where applicable</li>
<li>Participate on&nbsp;cross-functional project&nbsp;teams&nbsp;</li>
<li>Mentor and train junior scientists&nbsp;</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Degree in Chemical Engineering, Biochemistry, Chemistry or other sciences</li>
<li>Bachelor’s degree + 10 or more&nbsp;years of experience OR Masters + 8 or more years of experience, OR a PhD&nbsp;</li>
<li>Must have CMC protein purification experience with standard bioprocess unit operations such as chromatography separations and filtration</li>
</ul>
Preferred Qualifications:&nbsp;
<ul>
<li>Proficient in writing methods and operating&nbsp;AKTA chromatographic instruments (such as AKTA Avant, AKTA Purifier, AKTA Pure, AKTA Ready&nbsp;or similar)&nbsp;</li>
<li>Has a strong understanding of analytical techniques, such as HPLC and&nbsp;ELISA&nbsp;</li>
<li>Has hands on experience with monoclonal antibody or antibody-like molecule purification process development at laboratory, pilot and/or&nbsp;GMP scale</li>
<li>Proven experience in mechanistic modeling of downstream purification unit operations including chromatography separations and/or membrane separations</li>
</ul>
Other Required Skills:
<ul>
<li>Able&nbsp;to independently design, execute, use and reference literature publications, and interpret laboratory experiments&nbsp;to answer scientific&nbsp;questions&nbsp;</li>
<li>Able to manage and organize large data sets to help interpret results using data visualization tools</li>
<li>Must be forward-thinking and be able to lead and contribute to scientific/technical&nbsp;discussions&nbsp;and innovation</li>
</ul>
<ul>
<li>Able&nbsp;to&nbsp;independently&nbsp;learn, understand and execute&nbsp;novel, advanced&nbsp;scientific&nbsp;techniques&nbsp;</li>
<li>Must have&nbsp;excellent attention to detail and ability to keep detailed written&nbsp;records&nbsp;&nbsp;</li>
<li>Proven record of authoring publications, technical reports, regulatory documents, and/or&nbsp;presentations&nbsp;</li>
<li>Has&nbsp;strong communication&nbsp;skills including&nbsp;verbal, written,&nbsp;and&nbsp;scientific data&nbsp;presentation&nbsp;</li>
<li>Has excellent&nbsp;understanding of&nbsp;biochemistry&nbsp;and&nbsp;bioprocess engineering&nbsp;concepts&nbsp;</li>
</ul>
<ul>
<li>Able&nbsp;to work collaboratively within and outside of the&nbsp;group&nbsp;</li>
<li>Has&nbsp;proficiency&nbsp;with Microsoft Office software, ability to learn new software&nbsp;applications&nbsp;</li>
<li>Has a strong understanding of statistical&nbsp;analysis&nbsp;&nbsp;</li>
<li>Demonstrated scientific aptitude through authorship of peer-reviewed&nbsp;publications&nbsp;</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist I - CMC BioProcess Purification Development

<h3>Job Description</h3>
Job DescriptionCompany Description 
At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit <a href="https://global.allerganaesthetics.com/" target="_blank">https://global.allerganaesthetics.com/</a>. Follow Allergan Aesthetics on LinkedIn.
Job Description 
The Neurotoxin Research Group at Allergan/AbbVie is seeking a highly motivated and independent Associate Scientist II to join our Toxin Innovation Pharmacology Group. This individual will execute in vivo neuromuscular and sensory pharmacology studies, contributing to the design, execution, and communication of novel research in our highly collaborative neurotoxin discovery and innovation program.
The successful candidate for this position will contribute to projects aimed at in vivo pharmacological characterization of biotherapeutics. He/she/they will be required to work on a variety of in vivo pharmacology models to help characterize and evaluate biological compounds. The successful candidate will organize, analyze, and interpret results, come forward with recommendations, and present the findings to senior personnel or in team meetings. Experience with rodent models is required. A background in neurobiology is highly desirable but not required.
Key Responsibilities
<ul>
<li>Design, execute, and analyze in vivo assays to answer scientific questions and contribute to conceptual and experimental protocols</li>
<li>Work with cross-functional team members to accomplish the goals and requirements of the organization, including excellence in execution, and workload prioritization</li>
<li>Hands-on experimentalist: perform small animal handling, dosing of molecules through a variety of delivery routes, conduct behavioral studies, and post-mortem tissue harvest</li>
<li>Demonstrate critical thinking to troubleshoot and provide creative solutions to address experimental challenges</li>
<li>Effectively organize and present scientific plans and data to functional leaders</li>
<li>Demonstrate flexibility and a commitment to scientific excellence</li>
<li>Meet experimental timelines and impact projects through lab-based contributions</li>
<li>Understand and adhere to corporate standards regarding conduct, safety, material handling, CDC compliance, and animal care</li>
<li>Learn, understand, and become proficient at new experimental techniques</li>
</ul>
<ul>
<li>Effectively prepare and communicate presentations to multidisciplinary teams</li>
</ul>
Qualifications 
Minimum Education and Experience:
<ul>
<li>Bachelor’s Degree with&nbsp;3+ years of experience OR Master’s Degree&nbsp;</li>
<li>Experience with small animal/rodent handling is required</li>
<li>Experience with behavioral assays (sensory or motor)</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with small animal dosing and post-mortem tissue harvest is highly desirable.</li>
<li>Familiarity with in vivo behavioral or pharmacological assays is highly desirable.</li>
<li>Working knowledge of neuroscience and animal anatomy is a plus</li>
<li>Experience with histological techniques, including immunohistochemistry, microscopy, and other laboratory techniques, is a plus.</li>
<li>Experience with in vitro assays including cell culture techniques is a plus.</li>
<li>Knowledge of graphing software (e.g., GraphPad prism) and basic understanding of statistical analyses is a plus.</li>
</ul>
Other Required Skills:
<ul>
<li>Exhibit flexibility and a commitment to scientific excellence</li>
<li>Highly motivated, hands-on experimentalist who thrives in a collaborative, multidisciplinary environment</li>
<li>Willing and able to conduct various in vivo behavioral and pharmacological assays in small animals</li>
<li>Independently design and conduct critical experiments that advance project goals in a timely manner</li>
<li>Proactively seek advice from others when developing new models or when troubleshooting</li>
<li>Possess strong interpersonal skills and able to collaborate with diverse groups within the organization.</li>
<li>Meticulous attention to detail and diligence in record keeping</li>
<li>Interpret results and draw conclusions from own multistage experiments</li>
<li>Note significant deviations and suggest, design, and pursue relevant experiments</li>
<li>Present findings in team meetings and to senior personnel using precise written and oral communication</li>
<li>Possess basic understanding of standard statistical analysis of scientific data</li>
<li>Excellent writing and communication skills.</li>
<li>Computer skills: working knowledge of MS-Office (Excel, Word, PowerPoint) is required.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist II - In Vivo Pharmacology

<h3>Job Description</h3>
Job Description
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for an Associate Scientist I in our GBA group. In this role, you will play a pivotal part in QPS’ continued expansion of our bioanalytical capabilities to support small molecule, antibody drug conjugate, protein, and gene therapy drug development. 
As an Associate Scientist I in our Bioanalytical department, you will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations.
No visa sponsorship (e.g. H‑1B, L‑1, E) will be provided for this active position, now or in the future. Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis.
 
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
 
Please visit our website (<a href="http://www.qps.com" target="_blank">www.qps.com</a>) for more information and to see all current openings.
The Job
<ul>
<li>Perform routine lab operations, such as sample extraction, preparing reagents, operating automatic liquid handling equipment, pipetting, weighing, monitoring, and recording, in a neat/clean manner</li>
<li>Assist Principal Investigator in performing quantitative analysis of drug and metabolites in biological samples utilizing validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods under GLP regulations</li>
<li>Document experiment details, calculations, results and observations in accordance with GLPs and SOPs</li>
<li>Basic math skills to perform routine calculations</li>
</ul>
Work Location
<ul>
<li>This job will be 100% QPS-office/facility based</li>
</ul>
Requirements
The successful candidate will hold a degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline as follows:
<ul>
<li>Bachelor’s degree </li>
<li>Associate's degree in Chemistry may be considered</li>
</ul>
Why You Should Apply
<ul>
<li>Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li>
<li>Structured Career Ladders that provide excellent growth based on your personal aspirations.</li>
<li>Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li>
<li>Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&amp;D and Short and Long-term Disability Insurance</li>
<li>Park-like setting in Newark, Delaware</li>
<li>Internal committees designed with the needs and enjoyment of QPS employees in mind.</li>
</ul>
QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Associate Scientist I - Bioanalytical Dept

<h3>Job Description</h3>
Job Description
R&amp;D Partners is seeking to hire aResearch Scientist I inFort Worth, TX.
Your main responsibilities as a Research Scientist I:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Be able to carry out experiments under the limited supervision, following GxP guidelines.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Capable of taking initiative, self-driven, capable of focusing on objectives, and strong ability for prioritization.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Detail oriented and hand-on is a must.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Contribute to DOE development in collaboration with supervising scientists
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Analyze, summarize, and present the data.
﻿What we are looking for in Research Scientist I:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;BS degree in chemistry, polymer science, surface science, colloid chemistry, or similar.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;MS or PhD degree with experience in polymer science, surface science, colloid chemistry, or similar. - Preferred
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Chemical lab experience, Ability to work following SOPs and instructions.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience working with polymer solutions and / or with emulsions, familiarity with rheology, microscopy, and particle size characterization methods.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience developing ophthalmic products

Why ChooseR&amp;D Partners?
As an employee, you have access to a comprehensive benefits package including:
<ul>
<li>Medical insurance – PPO, HMO &amp; HSA</li>
<li>Dental &amp; Vision insurance</li>
<li>401k plan</li>
<li>Employee Assistance Program</li>
<li>Long-term disability</li>
<li>Weekly payroll</li>
<li>Expense reimbursement</li>
<li>Online timecard approval</li>
</ul>

Pay Scale:
$68,540 – $85,675 (Dependent on Experience)
R&amp;D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research &amp; engineering.&nbsp;We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.&nbsp;&nbsp;
R&amp;D Partners is an equal-opportunity employer.&nbsp;&nbsp;&nbsp;
Company DescriptionR&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities. 
<h3>Company Description</h3>
R&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

Research Scientist I

<h3>Job Description</h3>
Job Description
Triple Cities Metal Finishing is seeking a motivated Chemical Engineer to join our team! As a Chemical Engineer, you will be a vital part of our team, developing and managing our Chemical processes within a fast paced and dynamic organization. You play a crucial role in maintaining quality, safety, and productivity through a hands-on approach. Additionally, this role offers a fantastic opportunity to work directly with our Leadership Team, with a clear path for career advancement and professional growth. 
About Us
Triple Cities Metal Finishing provides a wide variety of surface finishing options to a multitude of industries including aerospace, agricultural, automotive, computer, electronics, household, industrial, medical, military, construction, and office parts. We are ISO 9001:2015, AS9100D &amp; NADCAP Certified!
Since 1945, TCMF has made innovative, as well as necessary changes in the way we conduct everyday business. From advanced surface preparation to highly technical finishing processes, we can handle the smallest pieces to large parts over 30 feet long.
Our three shifts of skilled professionals in our 125,000 square foot facility have made us the vendor of choice for metal finishing for Northeastern United States. Whether it is electroplating, electroless plating, wet paint, or powder coat, we finish it right the first time!
Position Overview
<ul>
<li>Participate in process optimization and troubleshooting operational issues.</li>
<li>Analyzes operating procedures, equipment and machinery functions to improve raw material efficiency and improve product quality.</li>
</ul>
<ul>
<li>Troubleshoot problems with chemical/plating processes.</li>
</ul>
<ul>
<li>Determine effective use of unit operations exercising judgment to compromise between process requirements, economic evaluation, operator effectiveness, and physical and health hazards.</li>
<li>Evaluate chemical equipment and processes to identify ways to optimize performance or to ensure compliance with safety and environmental regulations.</li>
<li>Manage technical projects for Chemical Processes to completion. </li>
<li>Direct activities of operators on equipment including condensers, absorption and evaporation towers, pumps, valves, tanks, boilers, compressors, pipelines, etc. to effect required chemical or physical change.</li>
<li>Perform testing on plating tanks, as well as assist with the cleaning and prepping of plating tanks.</li>
<li>Perform testing and measurements to determine degree of control over variables such as temperature, density, specific gravity, and pressure.</li>
<li>Manages and controls the movement, storage, and packaging of liquids and gases.</li>
<li>Provide technical assistance to resolve environmental or safety issues.</li>
<li>Promote a safe work environment - lead by example. Ensure staff is following established safety standards.</li>
</ul>
Qualifications
<ul>
<li>Experience:
<ul>
<li>3+ years of experience working as a chemical engineer or technician with a focus on testing preferred. </li>
<li>Bachelor's degree in chemical engineering or related field.</li>
<li>Knowledge of chemical unit operations/ equipment – reactors, distillation, condensers, adsorption, compressors, evaporators, pumps, piping, heat exchangers, etc. preferred. </li>
</ul>
</li>
<li>Skills:
<ul>
<li>Clear and concise communication skills, both verbal and written, to effectively convey information and/or ideas professionally across all levels of the organization.</li>
<li>Ability to create and maintain positive and professional relationships at all levels of the organization.</li>
<li>Strong attention to detail</li>
<li>Strong analytical skills</li>
<li>Ability to problem-solve issues to their root cause and work to implement corrective action.</li>
<li>Excellent organization skills.</li>
</ul>
</li>
</ul>
Total Compensation Package
<ul>
<li>Wage
<ul>
<li>$60,000 - $70,000 Compensation depends on the selected candidate's experience.</li>
</ul>
</li>
</ul>
<ul>
<li>Benefits - We recognize the value of a comprehensive benefits package and work vigorously to ensure our package meets the needs of our employees and their families. Eligible employees can elect and participate in variety of benefits including:
<ul>
<li>Paid Holidays</li>
<li>Paid Vacation / Sick Time</li>
<li>401 (k) Retirement Plan with Company Match</li>
<li>Medical, Dental &amp; Vision Insurance </li>
<li>Employee Assistance Program (EAP)</li>
<li>Health Savings Account (HSA)</li>
<li>Company Paid Life Insurance </li>
<li>Voluntary Insurance Benefits including Disability Insurance, Accident Insurance, Cancer Insurance, Critical Illness Insurance, Hospital Indemnity Insurance and Life Insurance </li>
<li>Free Fountain Soda Machine On-site!</li>
</ul>
</li>
</ul>
Triple Cities Metal Finishing is an Equal Opportunity Employer. We provide equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Chemical Engineer

<h3>Job Description</h3>
Job Description
When you join Groundwater &amp; Environmental Services, Inc. (GES), you are not a number – you become the reason for our success. You’ll have the opportunity to carve your own career path while working shoulder-to-shoulder with some of the most talented and dedicated professionals in the industry. By combining our unique talents and expertise, we help the world’s leading organizations solve their most complex environmental challenges.
We work hard, and we have a lot of fun while we’re at it. Our core values are centered on doing what’s right – for our clients, our employees, and our community. Our employees benefit from a supportive, collaborative culture and an entrepreneurial spirit that promotes new ideas and shared learning. 
Groundwater &amp; Environmental Services, Inc. (GES), an industry leader with a reputation for excellence in providing environmental consulting, engineering, compliance, and technical field services to clients in diverse market sectors, seeks an experienced Geologist or Environmental Scientist to support environmental remediation project activities in Southern California. 
<ul>
<li>Under general supervision, provides project management support including client involvement, work plan and proposal preparation, project scheduling and deadline tracking, budget evaluation and analysis, and technical editing and report finalization. </li>
<li>Must be a detail-oriented team player able to multi-task, and possess strong communication, analytical, organizational, problem-solving, planning, technical writing, delegation, mentoring, and time management skills. </li>
<li>Executes, supervises, and documents field aspects of environmental site assessment and remediation activities using standard operating procedures (SOPs). Conducts compliance assessment (e.g., facility response plan compliance), remedial testing, operation, maintenance, and monitoring (OM&amp;M), short-term remedial events (e.g., chemical injection, groundwater and vapor extraction), and other project-support field activities.</li>
<li>Self-performs or directs junior staff in the installation of soil borings, monitoring wells, remediation activities, waste management and disposal, and other field requirements using standard operating procedures (SOPs). Self-performs and may direct junior staff in the performance of engineering design, permitting, OM&amp;M, remedy process optimization, and environmental compliance.</li>
<li>Acts as the primary author for site work plans and proposals for routine scopes of work on low/medium priority projects, and co-author for complex scopes of work including comprehensive site characterizations and remedial actions. Co-authors comprehensive site characterizations and remedial action plans. These reports contain multiple level and interrelated interpretations and conclusions as well as provide recommendations based upon conclusions with focus on conceptual site model development.</li>
<li>May manage various level priority projects by providing technical, regulatory, and financial project support. Technical responsibilities may include monitoring contaminant concentrations, fate and transport analysis, QA/QC of data collected and documents generated, and ensuring compliance with applicable regulations. </li>
<li>Provides technical, regulatory, and financial project support for O&amp;M sites. Technical responsibilities may include monitoring contaminant concentrations, site remediation activities, quality of data collected and documents generated, and ensuring compliance with applicable regulations. </li>
<li>Knowledgeable of pertinent regulations and their application to the compliance and progression of the projects. </li>
<li>Performs hydrogeological assessments regarding groundwater flows to identify contamination impact and related concerns. </li>
<li>Researches information relating to identifying geological formations and soil delineation studies and prepares reports and geological maps based on the findings.</li>
<li>Participates in the identification of viable remedial solutions consistent with all federal, state, and local regulations </li>
<li>Procures and manages subcontractors and vendors for completion of project tasks (e.g., trenching and excavation, system construction, and electrical work), including supplier bid package development.</li>
</ul>
Skills &amp; Requirements:
<ul>
<li>A Bachelor's degree or higher in geology, environmental science, engineering or related scientific discipline.</li>
<li>4+ years of related experience.</li>
<li>GIT or EIT a plus</li>
<li>Must be detail-oriented, and a team player with good communication, analytical, organization, and time management skills.</li>
</ul>
Our comprehensive benefits include: medical, dental, vision, prescription, 401k, FSA, LTD, STD, New Parent Leave, 529 CollegeBound Fund, Continuing Education/Training Course Assistance, Bonus Plan, and more.
Groundwater &amp; Environmental Services, Inc. (GES) believes that diversity and inclusion among our staff is critical to our success, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool. At GES, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and employees without regard to race, color, religion, gender, pregnancy, national origin, age, disability, marital status, sexual orientation, gender identity or expression, military and veteran status, and any other characteristic protected by law.

Mid-Level Environmental Scientist, Geologist, or Engineer

<h3>Job Description</h3>
Job Description
Chemical Operator
Nights 7pm-7am - Rotating 3-2-2 schedule
This position is engaged in the distillation, fermentation, and evaporation processes to produce ethanol from beverage and waste streams delivered to the plant. 
Job Duties
<ul>
<li>Recording readings on an hourly basis</li>
<li>Monitoring and/or adjusting liquid and steam levels for efficient operation</li>
<li>Monitoring the PH of the wastewater discharge and recording results of tests</li>
<li>Safely starting, monitoring, and shutting down the Evaporation System</li>
<li>Reacting to abnormal conditions, breakdowns, and emergencies</li>
<li>Unloading/loading of tanker trucks, railcars, syrup trucks, totes, barrels, and kegs</li>
<li>Submitting work orders on equipment and facilities requiring maintenance</li>
</ul>

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