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<h3>Job Description</h3>
Job Description
Location: Remote/Lab Access Preferred Compensation: $180–260/hour
Job Summary Advance biomarker strategies in translational oncology and rare diseases.
Key Responsibilities
<ul>
<li>Biomarker identification/validation</li>
<li>Support assay and companion diagnostic development</li>
</ul>
Qualifications Ph.D. biology/biomed, 7+ years translational research.
What We Offer Highly competitive hourly compensation to reward your expertise. Ultimate flexibility to balance with other commitments. Opportunities to contribute to cutting-edge pharma innovations from anywhere. Remote work with collaborative virtual tools for seamless engagement.
How to Apply To apply, visit our career portal and complete the quick and straightforward application process: enter your details, upload your CV, add your LinkedIn (optional), answer a few qualifying questions. 
Apply Now
 (Or visit:&nbsp;<a href="https://www.pharmasmarket.com/signup/talent" target="_blank">https://www.pharmasmarket.com/signup/talent</a>)

Fractional Biomarker Scientist - Translational Medicine

<h3>Job Description</h3>
Job Description
Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.
For more information see: <a href="http://www.septerna.com" target="_blank">www.septerna.com</a>.
THE ROLE
The Associate scientist/Scientist will primarily be responsible for the development and conduct of in vivo, ex vivo, as well as in vitro studies in in vivo Pharmacology to support the advancement of Septerna's small molecule drug discovery pipeline. They will help develop preclinical models, generate robust data to support therapeutic development and contribute to the understanding of therapeutic mechanism of action. The successful candidate will add their passion, unique talents, and expertise to a dynamic team on the frontlines of innovative therapeutic development.
The position is based in South San Francisco, CA. Title and compensation commensurate with experience.
Key Responsibilities: 
<ul>
<li>Perform surgical procedures in rodents</li>
<li>Design and execute in vivo and in vitro studies in rodents</li>
<li>Generate, analyze, document, and help interpret data to establish functional PK/PD relationships</li>
<li>Contribute to the interpretation of experimental results in a broader biological and pharmacological context to progress our understanding of target biology and therapeutic hypothesis</li>
<li>Help in authoring in vivo pharmacology study designs, protocols, and reports to support regulatory filings</li>
<li>Follow all company policies/practices, and maintain accurate records and notebooks</li>
</ul>
Required education, skills and experience 
<ul>
<li>BSc or MSc in Pharmacology, Toxicology, or related biological science</li>
<li>At least 10 (or 8 years with MSc) direct experience with generating complex surgical models in rodents in academia or the biotechnology and pharmaceutical industries</li>
<li>Ability to collaborate in writing protocols and trouble-shooting biological experiments</li>
<li>Detail-oriented and organized, with strong interpersonal skills for clear and effective communication</li>
<li>Ability to proactively engage and collaborate with colleagues to integrate in vivo findings with in vitro pharmacology studies</li>
</ul>
Preferred skills and experience 
<ul>
<li>Experience working with rodent models of bone, kidney, and/or endocrine organs</li>
<li>Previous work on therapeutic discovery and development programs</li>
<li>Experience working with vendors and CROs to execute studies, analyze data, and generate reports</li>
</ul>
The anticipated salary range for candidates who will work in South San Francisco, CA is $100,000 - $125,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions.
We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Associate Scientist/Scientist, In Vivo Pharmacology (industry experience required)

<h3>Job Description</h3>
Job Description
Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.
For more information see: <a href="http://www.septerna.com" target="_blank">www.septerna.com</a>.
THE ROLE
We are seeking an experienced scientist and dynamic scientific leader. Reporting to the Sr. Director, in vivo pharmacology, this individual will be responsible for establishing and expanding the company's internal capabilities and be hands-on with running pre-clinical studies for programs in multiple therapeutic areas. The Scientist will be responsible primarily for the development and conduct of in vivo and/or ex vivo studies in o support and advance Septerna's small molecule drug discovery pipeline. They will work both independently and collaboratively as part of a matrixed inter-disciplinary team to develop preclinical in vivo models of disease to understand the therapeutic mechanism of action of Septerna's drug candidates. The successful candidate will serve as the biology lead on cross-functional project teams and may have opportunities to lead drug discovery programs from early discovery through IND filing.
The position is based in South San Francisco, CA. Title and compensation commensurate with experience.
Key Responsibilities include but are not limited to: 
<ul>
<li>Design and execute in vivo, ex vivo, and in vitro studies to inform therapeutic programs</li>
<li>Generate, analyze, and interpret complex data to establish functional PK/PD relationships and elucidate the therapeutic mechanism of action of drug candidates</li>
<li>Serve as Biology lead on multiple project teams, trouble-shoot experiments, analyze and interpret data and work cross functionally with colleagues to help advance therapeutic programs</li>
<li>Help build and expand in vivo pharmacology and biomarker discovery capabilities</li>
<li>Author in vivo/ex vivo protocols, and study reports to support regulatory filings</li>
<li>Follow all company policies/practices, and maintain accurate records and notebooks</li>
</ul>
Required education, skills and experience 
<ul>
<li>PhD or MSc in Metabolic Disorders, Endocrinology, Pharmacology, Immunology / Inflammation, or related biological science field</li>
<li>At least 8 years (or 12 years with MSc) direct hands-on experience in drug discovery and development leveraging in vivo metabolic and/or endocrine disease models in biotechnology and pharmaceutical industries</li>
<li>Ability to be hands-on, working in the vivarium and lab, writing protocols, and executing studies</li>
<li>Direct experimental experience and demonstrated expertise developing PK/PD, efficacy, and cell and tissue-based pharmacology or disease biology models</li>
<li>Experience working on project teams with functional responsibility to organize, analyze, interpret, and present data</li>
<li>Experience working with vendors and CROs to execute studies externally, analyze data, and generate reports</li>
<li>Detail-oriented and organized, with strong interpersonal skills for clear and effective communication – ability to proactively engage and collaboration with colleagues and mentor more junior staff</li>
</ul>
Preferred skills and experience 
<ul>
<li>Experience bringing programs through in vivo proof of concept and into the clinic</li>
<li>Experience working with primary cells, ex vivo disease models, or in vivo species is a plus</li>
<li>Evaluation, analysis, and interpretation of multi-omics and complex data sets</li>
<li>Experience with biomarker development (pharmacodynamic, predictive, and safety) to inform clinical translation and patient selection strategies</li>
<li>Previous work leading a program in therapeutic discovery/development</li>
<li>Experience mentoring more junior scientists, leading cross-functional project teams, and a track record of successful managing external teams or CROs</li>
</ul>
The anticipated salary range for candidates who will work in South San Francisco, CA is $150,000 - $180,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions.
We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Staff Scientist/ Sr. Staff Scientist, In Vivo Pharmacology (industry experience required)

<h3>Job Description</h3>
Job DescriptionResearch Associate III - General and Research Associate III - Assay Transfer (see job descriptions attached) On-site position Nesco Resource provides 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.Company DescriptionNESCO Resource Company Overview Established in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers. Nesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities. 
<h3>Company Description</h3>
NESCO Resource Company Overview\r\nEstablished in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers.\r\n\r\nNesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.

Research Associate III

<h3>Job Description</h3>
Job DescriptionNight Shift Construction Laborers Needed - 60+ HRS/Week - $25/HR
Job Description
6PM - 6AM, Mon-Saturday, optional overtime on Sundays
You and your team will be responsible for construction cleanup within a 100k sqft area of the Panasonic building in De Soto, KS. You will be primarily pushing a broom/operating a sweeper scrubber/picking up trash/wiping down materials. This is not a glamorous job - if you expect to perform a trade while performing this job, this isn't for you.
Responsibilities
<ul>
<li>Clean and sanitize all surfaces in a cleanroom environment, including walls, floors, and windows.</li>
<li>Maintain cleanliness and order while adhering to strict cleanroom protocols and procedures.</li>
<li>Complete the cleaning of two rooms per week within a 5 million square feet job site.</li>
<li>Adhere to gowning requirements, including wearing a gown and booties.</li>
</ul>
Essential Skills
<ul>
<li>3+ years of recent, relevant experience in industrial janitorial services.</li>
<li>Proficiency in cleanroom cleaning and sanitation procedures.</li>
<li>Ability to walk 15,000 steps and climb 10 flights of stairs daily.</li>
<li>Capability to wear cleanroom attire and perform housekeeping tasks effectively.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with hazmat protocols.</li>
<li>Familiarity with using state-of-the-art cleaning equipment.</li>
</ul>
Why Work Here?
Join a team where you can enhance your skills using state-of-the-art equipment, with the opportunity for overtime and competitive pay. Enjoy a supportive work environment that values your expertise and dedication.
Work Environment
Work in a climate-controlled, indoor cleanroom setting, requiring the wearing of gowns and booties. The role involves wiping down floors and manufacturing equipment, ensuring a high standard of cleanliness and sanitation.
Pay and Benefits
The pay range for this position is $25.00 - $27.00/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 De Soto,KS.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Cleanroom Technician

<h3>Job Description</h3>
Job DescriptionContract/hourly position, pay rate $30/hr for qualified/experienced candidates. Working in a laboratory environment supporting manufacturing operations, this individual will be responsible for executing release testing and data analysis for release of product. The individual will run, maintain, and troubleshoot Vitros 350, FS 5,1, 3400XT, and 4600 blood/specimen analyzers. This position works in partnership with manufacturing Operations, Product Support, and other technical support groups to ensure Quality and customer expectations are met prior to final release of the product. The individual will routinely interact with Document Management Systems (Windchill). Candidate must be willing to learn to operate, maintain, and troubleshoot Vitros 350, FS 5,1, 3400XT, and 4600 analyzers. Careful attention to detail and accuracy of work are required. As an FDA-regulated facility, documentation is key to this position in order to meet regulatory requirements; therefore, the candidate must have experience in or an understanding of cGMPs and documentation in a regulated industry. Candidate must have a proven track record of planning and organization of daily workload, high affinity toward teamwork, and demonstrated problem-solving using innovative solutions. Having a working knowledge of computers and Windows software is desired. A full understanding of quality control is expected. This position requires an individual who can multi-task, adapt to changes in daily workload and priorities, and operate in a cross-functional team setting. This position requires working in a lab environment which includes standing for long periods of time, wearing personal protective equipment (PPE), and handling human samples. Qualifications: A BA/BS degree or equivalent is required; a degree with a science concentration is preferred. Previous laboratory or similar experience is preferred. This position requires flexibility between A-shift (~7:00am -3:30pm) and B-shift (1:30pm -10:00pm) Monday-Friday. Nesco Resource provides 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.Company DescriptionNESCO Resource Company Overview Established in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers. Nesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities. 
<h3>Company Description</h3>
NESCO Resource Company Overview\r\nEstablished in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers.\r\n\r\nNesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.

Quality Analyst - Medical Device Lab

<h3>Job Description</h3>
Job DescriptionSchedule: 1st shift 8-5 Qualifications: Experience required: 0-3 years Educational qualifications: Associate's degree in Chemistry Job description: - Conduct precise analytical testing on both organic and inorganic samples using standard methods like ASTM. - Perform simple chemical experiments to support ongoing research and operational projects. - Strictly adhere to all Standard Operating Procedures (SOPs) and safety guidelines to ensure a secure work environment. - Record and maintain accurate data from experiments to ensure consistency and reliability of results. - Participate in training sessions to enhance technical skills and stay updated with current industry practices. - Prepare initial reports and assist in the compilation of findings for senior chemists' review. - Collaborate with other team members to address challenges and improve testing methodologies. - Manage and safely dispose of chemicals as per environmental and safety standards. Skills and Competencies: - Basic knowledge of chemical processes and laboratory techniques. - High attention to detail with a commitment to producing accurate and quality work. - Ability to follow complex scientific procedures and protocols. - Efficient organizational skills to balance multiple tasks and priorities. - Experience in using various types of lab equipment and familiarity with computer-based data management. Nesco Resource provides 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.Company DescriptionNESCO Resource Company Overview Established in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers. Nesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities. 
<h3>Company Description</h3>
NESCO Resource Company Overview\r\nEstablished in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers.\r\n\r\nNesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.

Chemist I

<h3>Job Description</h3>
Job DescriptionResponsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities to support Ventana projects. Exercises technical expertise and discretion in the design, execution and interpretation of experiments that contribute to project strategies. Prepares technical reports, summaries, protocols and quantitative analyses. Presents and discusses results of experiments within department and project team. Maintains high level of professional expertise through familiarity with scientific literature and may participate in conferences and professional societies. Follows company policies and procedures for GMP, GLP, Design Control and others as appropriate. Maintains complete and accurate laboratory documentation and electronic files. May act as principal investigator in conducting own experiments. Responsibilities • Executes laboratory experiments; makes detailed observations and analyzes data. • Prepares technical reports, summaries and quantitative analyses. • Maintains complete and accurate records. • Normally receives detailed directions on all work. • Makes suggestions to improve work processes. • Assists in reducing to practice patentable inventions. • Works on projects of moderate scope in which analysis of situation or data requires a review of identifiable factors. • Exercises judgment within defined procedures and practices to determine appropriate action. • May participate in cross functional technical team activities. • Presents and discusses data within group. • Monitors work to ensure quality, and continuously promote Quality First Time. Qualifications: Bachelor's Degree 0-1 years of experience (post education) Nesco Resource provides 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.Company DescriptionNESCO Resource Company Overview Established in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers. Nesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities. 
<h3>Company Description</h3>
NESCO Resource Company Overview\r\nEstablished in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers.\r\n\r\nNesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.

Research Associate I - TPS

<h3>Job Description</h3>
Job Description
Title: Analytical Chemist 1 QC
Location: Whippany, NJ 07981
Duration: 6 Months
Shift: 8 AM to 5 PM
POSITION SUMMARY&nbsp;
The Analytical Chemist will analyze raw material, in-process, finished products and stability samples assuring compliance with standard operating procedures, Compendia sources, Test methods and Protocols.
ESSENTIAL FUNCTIONS
1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; With supervision, conducts Routine and non-routine activities. Performs analytical testing of raw materials, in-process control materials, stability samples, and finished product (Commercial, Clinical and Registration Batches) using different analytical techniques.
2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Diligently follow written laboratory protocols, guidelines, procedures and methods.
3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Expected to utilize established scientific techniques to compile and analyze data.
4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ensure that products are being tested strictly under cGMP conditions and disposition is taken on time as per the committed production plan for every month.
5.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ability to identify creative and innovative solutions of non-routine analytical tasks.
6.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Suggests improvements of laboratory testing procedures, techniques and/or instrumentation
7.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Performs other duties related to the position when required by laboratory management
8.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Proficient in the use of Empower
9.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Exposure to the basic theory and operating principles of HPLC, UV, FTIR, GC, and Malvern particle size analyzers.
10.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Other duties as assigned.

POSITION QUALIFICATIONS&nbsp;
1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ability to independently prioritize workload.
2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; May work on multiple projects and group to ensure the desired outcome is timely.
3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Consults with supervisor/management on decisions for all the issues.
4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Recognizes problems or compliance issues and reports to management.&nbsp;
5.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Good written and oral communication skills. Proficient in the ability to read/write and comprehend complex instructions, correspondence, and memos.&nbsp;
6.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience in chromatography (e.g. HPLC with Empower data acquisition software, GC, FTIR, UV and wet chemistry)
7.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Knowledge of ICH, FDA, and DEA regulations.
8.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Demonstrate computer literacy with proficiency in Microsoft office software, Trackwise and Empower.
9.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Must be able to move about the facility
10.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Must be able to wear personal protective equipment
11.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Must be able to lift up to 25 lbs
EDUCATION
1. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; A BS in Chemistry degree is required&nbsp;

EXPERIENCE
1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 2 years working in pharmaceutical manufacturing environment.
2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Solid understanding of cGMP practices and concepts.
Company DescriptionWe believe in service that helps you solve a problem, move forward with a project, manage a difficult situation, or simply check something off your list. 
<h3>Company Description</h3>
We believe in service that helps you solve a problem, move forward with a project, manage a difficult situation, or simply check something off your list.

QC Chemist

<h3>Job Description</h3>
Job DescriptionJOB DESCRIPTION • Sample Analysis o Meet dynamic fast paced business demands for analytical measurements in support of R&amp;D/pilot production of materials supplied to customers. o Support analytical measurements for molecular weight characterization, determination of residual monomers and residual solvents, identify unknown components and quantitate overall purity for polymers and small molecules across multiple projects. • Lab and Equipment Operations o Function as an effective and productive member of various project teams. Coordinate analytical measurements within group projects. o Manage and maintain analytical laboratories, including writing SOPs, equipment maintenance and upkeep, and safety documentation. o Maintain electronic lab notebooks and deliver analytical reports. • Safety o Proven safety track record with commitment to ZERO incidents/injuries o Experience working with hazardous chemicals • Proven track record of meeting project goals on aggressive timelines TECHNICAL EXPERIENCE • Proficiency with some analytical techniques below o HPLC, UPLC, LCMS o GC, GCMS o GPC o Karl Fisher titrator, rheometer, UV-vis spectrophotometer • Knowledge of organic chemistry and electronic materials a plus Qualifications: *** Electronics and Industrial (E&amp;I) is seeking to employ an Analytical Chemistry Technical Associate as a contractor. The successful candidate will assist an interdisciplinary process chemistry and engineering team in the Emerging Technologies organization aimed at the scale-up and commercialization of product candidates from the E&amp;I division. The position will provide analytical chemistry support in a team environment for organic synthesis, polymerization and process development. This position is 100% on-site. QUALIFICATIONS • BS/MS Chemistry with a minimum of two years of analytical experience, industrial experience a plus • Excellent organization and communication skills (written and verbal) • Strong multi-tasking skills and ability to contribute to multiple projects simultaneously • Experience in an R&amp;D or Pilot plant environment a plus *THIS IS AN ONSITE ROLE ONLY #EDS014 Nesco Resource provides 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.Company DescriptionNESCO Resource Company Overview Established in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers. Nesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities. 
<h3>Company Description</h3>
NESCO Resource Company Overview\r\nEstablished in 1956, NESCO Resource employs over 10,000 people in 42 states and services a variety of local accounts as well as major accounts. Within NESCO Resource, we have three operating groups with the capability to staff effectively any positions that require Technology, Accounting &amp; Finance, and Clerical &amp; Light Industrial expertise. Rather than the generalist approach most employment agencies pursue, we practice the approach of a specialized staffing firm. We believe our outstanding local growth can be directly attributed to the credibility of our employees and their ability to focus on the specific needs of our customers.\r\n\r\nNesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.

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