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job_organization_name

city

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<h3>Job Description</h3>
Job Description
Help us change lives
At Exact Sciences, we’re helping&nbsp;change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.
Position Overview
The Clinical Lab Associate I, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department including, but not limited to, lab productivity and process line support, such as:&nbsp; accessioning, processing, automation usage, sample racking, lab maintenance, and lab cleaning, as well as other lab support tasks.
The Clinical Lab Associate I, Specimen Processing follows all Laboratory policies and procedures and maintains accurate data reporting practices to ensure consistent and diligent execution of Specimen Processing. This role supports the mission and vision of Exact Sciences Laboratories and shares the responsibility of ensuring the Specimen Processing department operates effectively. The function of this position is performed under the guided direction of the Specimen Processing Supervisor or designee.
Shift: Saturday - Monday 6:00am - 6:30pm
Essential Duties
include but are not limited to the following:
<ul>
<li>Perform primary responsibilities listed below completely, timely and accurately:
<ul>
<li>Support and comply with the company’s Quality Management System policies and procedures.</li>
<li>Maintain documentation of problems and problem resolutions following Good Documentation Practices (GDP).</li>
<li>Support department goals that align with organizational priorities.</li>
<li>Work with leadership to identify and progress on individual development goals that align with organizational priorities.</li>
<li>Support operational initiatives including, but not limited to, quality and process improvements, SOP development, department inspections and audits.</li>
<li>Complete all mandatory training assignments and annual competencies within &nbsp;established timelines.</li>
<li>Handle and dispose of all specimens following standard precautions and applicable safety policies.</li>
<li>Understand and comply with all lab and safety regulations.</li>
<li>Support employee engagement initiatives and activities to maintain and improve team morale.</li>
</ul>
</li>
</ul>
<ul>
<li>Meet performance and behavior expectations listed below:
<ul>
<li>Exemplify the core values of Integrity, Teamwork, Accountability, Quality, and Innovation at all times.</li>
<li>Self-motivation with a results-driven approach.</li>
<li>Maintain a high level of professionalism in written and verbal communications.</li>
<li>Act with an inclusion mindset and model these behaviors for the organization.</li>
<li>Maintain regular and reliable attendance.</li>
</ul>
</li>
</ul>
<ul>
<li>Demonstrate the necessary skills and abilities:
<ul>
<li>Ability to work in a fast-paced team environment, adapt to changing workload and circumstances effectively and respond to new information quickly.</li>
<li>Strong critical thinking skills with the ability to make decisions in a fast-paced environment.</li>
<li>Ability to communicate effectively with all levels of the organization through both verbal and written communication.</li>
<li>High level of listening skills and attention to detail with strong organizational and prioritization skills.</li>
<li>Ability to flex hours and work nights and/or weekends as needed to support the success of ES Labs.</li>
<li>Ability to work overtime, as needed.</li>
<li>Ability to lift and move up to 40 pounds for approximately 25% of a typical working day.</li>
<li>Ability to work seated for approximately 50% of a typical working day.</li>
<li>Ability to work standing for approximately 50% of a typical working day.</li>
<li>Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 75% of a typical working day.</li>
<li>Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.</li>
<li>Ability to comply with any applicable personal protective equipment requirements.</li>
<li>Ability to perform repetitive motions.</li>
<li>Understand potential exposure to hazardous materials, tissue specimens and instruments with moving parts, heating and freezing elements.</li>
<li>Tolerate the handling of bodily fluids and solids (e.g., blood, urine and feces).</li>
<li>Ability and means to travel to and work at all other sites within the same city, as needed.</li>
</ul>
</li>
</ul>
Minimum Qualifications
<ul>
<li>High School Degree/General Education Diploma.</li>
<li>Must be 18 years of age or older.</li>
<li>Experience using computers to include Internet navigation, email, Microsoft Office Suite.</li>
<li>Demonstrated ability to perform the Essential Duties of the position with or without accommodation.</li>
<li>Authorization to work in the United States without sponsorship.</li>
</ul>
Preferred Qualifications
<ul>
<li>Associate degree or Bachelor’s degree in Life Sciences, Physical Sciences, or field related to the essential duties of the job.</li>
<li>Experience in a laboratory or similar environment with maintaining sample integrity, following procedures and protocols, and sample collecting/handling.</li>
<li>Knowledge and understanding of CAP, GLP, GDP, CLIA, New York State Department of Health (NYSDOH), and HIPAA.</li>
<li>Experience in troubleshooting automation and performing instrument maintenance.</li>
<li>Lean experience (Kaizen, Kanban, root cause analysis, countermeasure implementation, etc.).</li>
</ul>
#LI-JL2
Salary Range:
$31,000.00 - $52,000.00

The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible.
Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits.
Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here.
Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences.
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law.
To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub. The documents summarize important details of the law and provide key points that you have a right to know.
PandoLogic. Keywords: Medical Laboratory Technician (MLT), Location: Madison, WI - 53725 , PL: 600368317

Lab Processing Associate - Weekend AM

<h3>Job Description</h3>
Innova Solutions has a client that is immediately hiring a Bench Scientist. &nbsp;&nbsp; Position type: &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Full Time - Contract Duration: &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 6 Months Location: &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Cambridge, MA &nbsp; As a Bench Scientist, you will: &nbsp; Description We are seeking a scientist to join the Molecular Profiling &amp; Bioconjugation group in BioMedicine Design. The candidate will work with a talented team of scientists to develop innovative protein biotherapeutics to bring curative treatments to patients.&nbsp; The candidate will be a key member of the conjugation chemistry team, responsible for the hands-on execution of bioconjugation experiments. &nbsp; Responsibilities will include the generation, purification, and characterization of bioconjugates. 
<ul>
<li>Hands-on experience with standard lab techniques and basic protein handling.</li>
<li>Familiarity with bioconjugation reactions and associated analytical and purification methods such as chromatography and mass spectrometry</li>
<li>Able to clearly communicate experiment results; experienced with using Microsoft PowerPoint and Excel for data presenting and reporting</li>
</ul>
&nbsp; Qualified candidates should&nbsp;APPLY NOW&nbsp;for immediate consideration!&nbsp; Please hit APPLY to provide the required information, and we will be back in touch as soon as possible. &nbsp; We are currently interviewing to fill this and other similar positions. If this role is not a fit for you, we do offer a referral bonus program for referrals that we successfully place with our clients, subject to program guidelines. ASK ME HOW. &nbsp; Thank you! Pradip Joshi Phone: 213-401-2633 Email - <a href="mailto:Pradip.Joshi@innovasolutions.com" target="_blank">Pradip.Joshi@innovasolutions.com</a> &nbsp; PAY RANGE AND BENEFITS: Pay Range*: &nbsp;$30-$35/hr *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. &nbsp; Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical &amp; pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident &amp; Critical illness coverage, Pre-paid legal &amp; ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). &nbsp; About Innova Solutions: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. &nbsp; Recent Recognitions: Named One of America’s Best Employers for New Grads by Forbes (2024 Named One of the Best Companies to Work for by U.S. News &amp; World Report (Private Companies List, 2024-2025) One of the Largest IT Staffing Firms in the US – Ranked #3 by Staffing Industry Analysts (SIA, 2024) One of the Largest Staffing Firms in the US – Ranked #13 by Staffing Industry Analysts (SIA, 2024; includes Innova Solutions, Volt, &amp; HireGenics) Named One of the Top Ten Private Companies in Atlanta by the Atlanta Business Chronicle (2023) One of the Largest Certified Minority Business Enterprises (MBEs) in the United States (NMSDC, 2024) AWS Advanced Tier Services Partner with 100+ certifications &nbsp; Website: <a href="https://www.innovasolutions.com/" target="_blank">https://www.innovasolutions.com/</a> &nbsp; Innova Solutions offers a referral bonus for qualified Ambassadors who refer eligible referrals. Submit referrals at <a href="https://innovasolutions.workllama.com/atsuser/anonreferafriend&amp;nbsp" target="_blank">https://innovasolutions.workllama.com/atsuser/anonreferafriend&amp;nbsp</a>; and earn $250-$1,000 per referral. Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates.&nbsp; If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at <a href="mailto:hr@innovasolutions.com" target="_blank">hr@innovasolutions.com</a> or (770) 493-5588. Please indicate the specifics of the assistance needed.&nbsp; Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities.&nbsp;&nbsp; Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

Bench Scientist

<h3>Job Description</h3>
Senior Scientist – Assay Development &amp; Quality Control
&nbsp;Location: Pittsburgh, PA |&nbsp; Full Time | Reports to Director of Life Science
 
BioForge’s mission is to accelerate innovations and breakthroughs in both the development and manufacturing of precision medicines to speed their delivery, use, and impact.
 
A fundamental shift is occurring in how medicines and therapeutics are delivered to people.&nbsp; Treatments are increasingly moving from an era of chemicals and drugs towards gene and cell therapies for multiple and diverse conditions such as cancer, blindness and degenerative neural diseases. Furthermore, precision biologic medicines – by their very nature – need manufacturing solutions capable of rapid, efficient and cost-effective switching between therapy productions without switching production tools or processes. How do we deliver a billion therapies, a hundred, ten thousand, or a hundred thousand at a time?
 
Such a shift requires fundamentally new approaches and innovations in the manufacturing of such gene and cell therapies. These approaches will bring to bear new and emerging technologies such as artificial intelligence/machine learning, continuous-flow fluidic processing, in-line sensing and control and closed-system automated design to develop next-generation manufacturing tools. With innovation comes the need for quality—demanding robust QC and QA tools that ensure standards are upheld throughout the R&amp;D pipeline.
 
We are seeking a Senior Scientist with expertise in analytical method development, assay design, and quality control. This role is central to developing, optimizing, and executing assays that characterize critical quality attributes (CQAs) across a range of biologic platforms. The ideal candidate has a deep command of assay technologies and is equally comfortable executing validated protocols and developing novel methods from scratch.
 
About the Role
 
You will work as a key member of our R&amp;D team, leading the development and execution of both routine and innovative assay platforms to support the characterization of complex biologics. This role offers the opportunity to shape and implement critical quality control strategies, contribute to cross-functional platform development, and design custom analytical workflows that support scalable, high-quality biomanufacturing. It is ideal for a technically advanced scientist passionate about continued assay development, building quality systems, and enabling the future of biologics through analytical science.
 
Responsibilities:
 
<ul>
<li>Design, develop, and optimize analytical assays to support quality control and product characterization</li>
<li>Independently lead method development efforts across biochemical, molecular, and cell-based techniques</li>
<li>Evaluate and measure product quality attributes and create CoAs</li>
<li>Create standard operating procedures (SOPs) and qualification reports</li>
<li>Perform assay qualification and validation in alignment with regulatory expectations (e.g., precision, accuracy, linearity, specificity)</li>
<li>Collaborate with R&amp;D, manufacturing, and regulatory teams to ensure analytical strategies meet program goals</li>
<li>Investigate assay failures, troubleshoot technical issues, and drive continuous improvement</li>
<li>Maintain rigorous documentation and ensure compliance with internal and external quality standards</li>
</ul>
 
Qualifications:
 
<ul>
<li>PhD or MS in Biology, Biochemistry, Bioengineering, Analytical Chemistry, or related field&nbsp;</li>
<li>5-8 years of laboratory experience in a QC, assay development, or analytical environment</li>
<li>Proven hands-on expertise with multiple assay formats, such as:</li>
<li>HPLC/RP/SEC/IE</li>
<li>Spectroscopy (UV-Vis, fluorescence, absorbance)</li>
<li>Electrophoresis (gel, capillary)</li>
<li>PCR/ddPCR/qPCR</li>
<li>ELISA or immunoassays</li>
<li>Cell-based assays</li>
<li>Chromatography or particle sizing</li>
<li>Microscopy</li>
<li>Demonstrated ability to develop and qualify custom assays</li>
<li>Strong documentation and technical writing skills</li>
<li>Experience working in regulated environments (GMP, GLP, ISO)</li>
</ul>
Desirable:
<ul>
<li>Strong interpersonal skills and the ability to work as part of a team</li>
<li>Familiarity with statistical tools for method validation (e.g., DOE, regression, precision studies)</li>
<li>Experience transferring methods between teams or to external partners</li>
<li>Strong project ownership and ability to work independently in a fast-paced setting</li>
<li>Strong interpersonal skills and the ability to work as part of a team for company wide goals</li>
</ul>
 
What You’ll Gain:
<ul>
<li>A collaborative, forward-thinking environment with cutting-edge projects</li>
<li>Hands-on access to state-of-the-art analytical tools</li>
<li>Competitive compensation and benefits</li>
</ul>
 
How to Apply
 
To apply, please apply through Linkedin or submit the following materials to <a href="mailto:info@pittbioforge.org" target="_blank">info@pittbioforge.org</a> with the subject line: “QC”
<ol>
<li>Resume/CV</li>
<li>Brief statement of interest (1–2 paragraphs) outlining your relevant experience</li>
</ol>
 
Application Deadline: December 15, 2025
Start Date: January 2026

Senior Scientist - Assay Development & Quality Control

<h3>Job Description</h3>
Job Description
Position Purpose:
The primary purpose of this position is to prepare samples and perform data collection activities using physics and X-ray based instrumentation at the Transportation Security Laboratory (TSL).
Essential Duties &amp; Responsibilities:
<ul>
<li>Performs material characterization (e.g. microscope imaging, density measurements, rheological and mechanical properties).</li>
<li>Prepares test samples for analyses</li>
<li>Operates explosive detection systems (EDS) as well as analytical physics instrumentation (computed tomography, x-ray fluorescence, x-ray diffraction, etc.) for data collection.</li>
<li>Performs troubleshooting, maintenance, and method development on EDS and analytical instrumentation.</li>
<li>Safely handles explosive and other hazardous materials.</li>
<li>Assembles test articles and bags per test specifications.</li>
<li>Develops and uses code (MATLAB, Python, R) for data analysis.</li>
<li>Analyzes, compiles, and reports data collection results for research and development and quality control testing events.</li>
<li>Composes and reviews technical reports and standard operating procedures.</li>
<li>Composes, reviews, and executes test plans.</li>
<li>Performs literature reviews.</li>
<li>Other duties as assigned.</li>
</ul>
Required Knowledge, Skills and Abilities:
<ul>
<li>Good interpersonal, verbal, and written communication skills.</li>
<li>Good listening skills.</li>
<li>Good working knowledge of scientific and analytical techniques.</li>
<li>Good working skills of software and tools necessary for job functions including Microsoft Office suite, MATLAB, Python.</li>
</ul>
Education/Experience:
Incumbent should have a minimum of a bachelor's degree in chemistry, engineering, physics, or other core science and up to five years of experience.
Clearance: 
The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position.
Supervisory Responsibilities: 
The incumbent professional has little to no supervisory responsibilities.
Working Conditions/Experience:
The incumbent is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%.
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor.
 Powered by ExactHire:160579

Entry Level Physical Scientist

<h3>Job Description</h3>
Yoh presents an excellent long-term&nbsp;Internal Laboratory Testing Coordinator&nbsp;opportunity with a trusted, long-term client located in Waltham, MA. Scientist/Sr. Research Associate -ESI&nbsp;Multiplex assays/Flow Cytometry Scientist/Sr. Research Associate The Yoh resource is expected to apply expertise across several areas in support of Sanofi Vaccines R&amp;D Global Immunology function developing innovative vaccine solutions for infectious diseases. Key Responsibilities:
<ul>
<li>Design and execute complex immunological experiments to evaluate vaccine candidates</li>
<li>Analyze immune responses using state-of-the-art techniques including multiparameter flow cytometry, ligand-binding, and cell-based assays</li>
<li>Support optimization of the automation of protocols and testing of the samples in automated immune assays as needed</li>
<li>Develop novel immunological assays to support vaccine development programs</li>
<li>Generate, analyze, visualize, and interpret scientific data sets, record experimental procedures and raw and analyzed data in electronic laboratory notebook</li>
<li>Author technical reports, SOPs, and contribute to regulatory submissions as required</li>
<li>Prepare and present findings to internal stakeholders</li>
<li>Provide technical guidance to junior team members as required</li>
<li>Collaborate within immunology and cross-functional teams across R&amp;D</li>
<li>Comply with the company HSE policies and minimize risk to self, others, and the environment, consistent with the community and industry standards.</li>
</ul>
Required Responsibilities:
<ul>
<li>Expertise in cellular and molecular immunology techniques</li>
<li>Proven experience with:</li>
<li>Spectral flow cytometry or flow cytometry with primary mammalian cells</li>
<li>Primary cells isolation and culture</li>
<li>Immunological assays development and implementation (ligand binding, multiplex (Luminex, MSD), cell-based)</li>
<li>Data visualization and analysis</li>
<li>Strong analytical and problem-solving skills</li>
<li>Excellent documentation and record-keeping abilities</li>
<li>Proficiency in standard laboratory software and data analysis tools</li>
<li>Strong written and verbal communication skills</li>
</ul>
Preferred Responsibilities:
<ul>
<li>Experience with vaccine development or infectious disease research</li>
<li>Working knowledge of Good Research Practices (GRP) and electronic note booking</li>
<li>Proficiency in advanced data analysis tools (FlowJo, OMIQ, GraphPad Prism, &amp; other)</li>
<li>Experience with automated/semi-automated platforms/ liquid handlers</li>
</ul>
Education Experience:
<ul>
<li>Data Review</li>
<li>Training</li>
<li>Scheduling</li>
<li>GDP</li>
<li>GRP, compliance requirements for clinical trial samples</li>
<li>Master's degree in Immunology, Microbiology, or related field with 2+ years of relevant industry or academia experience</li>
<li>Bachelor's degree with 4+ years of relevant experience</li>
<li>Experience in pharmaceutical or biotechnology industry preferred. </li>
</ul>
 Estimated Min Rate: $31.50 Estimated Max Rate: $45.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: 
<ul>
<li>Medical, Prescription, Dental &amp; Vision Benefits (for employees working 20+ hours per week)</li>
<li>Health Savings Account (HSA) (for employees working 20+ hours per week)</li>
<li>Life &amp; Disability Insurance (for employees working 20+ hours per week)</li>
<li>MetLife Voluntary Benefits</li>
<li>Employee Assistance Program (EAP)</li>
<li>401K Retirement Savings Plan</li>
<li>Direct Deposit &amp; weekly epayroll</li>
<li>Referral Bonus Programs</li>
<li>Certification and training opportunities </li>
</ul>
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day &amp; Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit <a href="https://www.yoh.com/applicants-with-disabilities" target="_blank">https://www.yoh.com/applicants-with-disabilities</a> to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:&nbsp;<a href="https://www.yoh.com/privacy-notice" target="_blank">https://www.yoh.com/privacy-notice</a>

Scientist/Sr. Research Associate-ESI Multiplex assays/Flow Cytometry

<h3>Job Description</h3>
Job Description
NOW HIRING WEEKEND SHIFT ENTRY LEVEL ASSEMBLERS!
Location – Mira Mesa, CA 
Shift – Weekend Shift (5:00AM – 5:30PM Friday - Sunday)
Pay Rate - $17.40/HR
Responsibilities
· Will be assembling insulin pumps
 · Will be working on a manufacturing line in work stations, working with a team to complete assemblies
 · Perform manual assembly- electro mechanical assembly duties 
 · Use some small tools 
 · Use a computer to log data
 · Perform testing and troubleshooting
 · Reviewing batch records and monitor documentation for accuracy
<ul>
<li>Ensure a clean and safe work environment</li>
</ul>
Essential Skills
<ul>
<li>Strong attention to detail to monitor machine operations effectively.</li>
<li>Ability to work in a fast-paced environment</li>
<li>Reliable work ethic with punctual attendance.</li>
<li>Team-oriented attitude and adaptability to changing tasks.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in machine operating, mechanical assembly, and medical device packaging.</li>
<li>Familiarity with GMP (Good Manufacturing Practice) standards.</li>
</ul>
If you are interested and qualified, please apply directly with your updated resume!
Job Type &amp; Location
This is a Contract to Hire position based out of San Diego, CA.
Pay and Benefits
The pay range for this position is $17.40 - $17.40/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 San Diego,CA.
Application Deadline
This position is anticipated to close on Nov 14, 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.

Weekend Shift Clean Room Assembler

<h3>Job Description</h3>
Medical Physics Consulting (MPC), an ONE Physics Partner, is seeking a full time Therapy Medical Physicist based in St. Louis, Missouri to join our growing team located in the Midwest. MPC is a new ONE Physics Partner and is an innovative and growing medical physics consulting practice servicing clients throughout Oklahoma, Kansas, Missouri and Illinois.
 
The Role
We are searching for a highly skilled, compassionate Therapy Medical Physicist to join our dedicated team of experts. Our candidates must be well-trained in Radiation Oncology and be able to work in a collaborative team environment. 
 
Clinic Information:
<ul>
<li>This position is located in St. Louis, Missouri but will be also supporting surrounding areas. </li>
<li>This clinics you will support have both Varian and Elekta </li>
<li>Treatment planning systems include Mosaiq, Monaco, Aria &amp; Eclipse.</li>
<li>This role will join a great team of several physicists, dosimetrist (onsite and remote), and physicians. </li>
</ul>
 
What You’ll Do
<ul>
<li>Perform weekly and monthly radiation measurements, as well as yearly calibration on all treatment units.</li>
<li>Monitor equipment in the Radiation Oncology Department to ensure that it is functioning correctly and safely.</li>
<li>Maintain regulatory agency records and reports.</li>
<li>Analyze alternative treatment plans and supervise dosimetry treatment planning functions.</li>
<li>Implement assessment/treatment and care based on the developmental stages of the patient.</li>
<li>Perform additional duties, as needed.</li>
</ul>
 
What You’ll Need
<ul>
<li>Master’s Degree and/or PhD in Medical Physics.</li>
<li>A board certification by the American Board of Radiology in Therapeutic Medical Physics, or board eligibility as demonstrated by graduation from a CAMPEP accredited residency in therapy physics. </li>
<li>2+ years of clinical Therapy Medical Physics experience preferred.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to interpret regulations.</li>
<li>A willingness to go “above and beyond” for clients and fellow colleagues.</li>
<li>Demonstrate initiative, organization, and ownership of daily tasks and projects.</li>
<li>Ability to problem solve by seeking, developing, and implementing viable solutions.</li>
</ul>
 
Physical Requirements
<ul>
<li>Requires ability to use and move equipment.</li>
<li>Requires a variety of physical activities including sitting, standing, walking, stopping, lifting, carrying.</li>
<li>Exposure to radiation, communicable diseases, and other conditions common to radiation therapy setting.</li>
<li>Occasional evening or weekend work.</li>
</ul>
 
Benefits 
<ul>
<li>Competitive compensation.</li>
<li>PTO plan with paid company holidays.</li>
<li>Health Insurance (Medical, Dental, Vision and Prescription).</li>
<li>401(k) Plan with company match after 1 year of employment.</li>
<li>Group Life &amp; Voluntary Life Insurance.</li>
<li>Short Term &amp; Long Term Disability.</li>
<li>Flexible Spending Account (FSA).</li>
<li>Health Spending Account (HSA).</li>
</ul>
 
Final offer amounts are determined by multiple factors, including geographic location, as well as candidate experience, education level and expertise. If you have questions on compensation, please ask your recruiter. Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.
 
We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class.

Therapy Medical Physicist

<h3>Job Description</h3>
The Pharmaceutical Development Scientist is a hands-on technical role responsible for the formulation, development, optimization, and technology transfer of sterile and non-sterile drug products across STAQ Pharma’s 503B Outsourcing Facilities. Reporting directly to the Chief Pharmaceutical Officer, this position supports product development initiatives from concept through scale-up and commercialization, driving innovation, process improvement, and lifecycle management of compounded drug products.
The scientist collaborates closely with Manufacturing Sciences &amp; Technology (MS&amp;T), Quality, and Production teams to translate laboratory-scale formulations into scalable, validated CGMP manufacturing processes. Responsibilities include conducting pre-formulation and compatibility studies, preparing R&amp;D and pilot-scale batches, and analyzing analytical and stability data to identify optimal formulations that maximize quality, performance, and product expiration dating.
This role requires strong analytical chemistry expertise—including the ability to interpret UPLC chromatograms, assess impurity profiles, and apply ICH and FDA 503B guidance—to guide formulation strategy, product development, and technology transfer activities.
Key Responsibilities:&nbsp;
<ul>
<li>Develop, optimize, and scale formulations for sterile and non-sterile dosage forms in compliance with CGMP, FDA 503B, and ICH guidelines.</li>
<li>Conduct pre-formulation studies, excipient compatibility testing, and stability evaluations to inform formulation design and shelf-life optimization.</li>
<li>Design and execute experiments to assess formulation feasibility, process robustness, and long-term product stability.</li>
<li>Prepare and manufacture laboratory-scale, R&amp;D, and pilot-scale batches for testing and process development.</li>
<li>Lead and support technology transfer activities for new and existing products, ensuring seamless transition from R&amp;D to manufacturing and between STAQ Pharma sites.</li>
<li>Conduct literature reviews and data analysis to identify innovative formulation approaches and support development strategy.</li>
<li>Analyze data from HPLC, GC, dissolution, and stability studies to assess potency, purity, and impurity profiles.</li>
<li>Collaborate with MS&amp;T, Quality, and Production teams to ensure manufacturing processes are robust, validated, and scalable.</li>
<li>Develop and execute stability protocols, trend data, and prepare detailed technical summaries and reports.</li>
<li>Write and maintain technical documentation, including batch records, development protocols, SOPs, and technical reports in accordance with CGMP standards.</li>
<li>Support investigations of out-of-specification (OOS) or out-of-trend (OOT) results and contribute to CAPA development and implementation.</li>
<li>Participate in audits, inspections, and internal quality reviews to ensure regulatory and operational compliance.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s, Master’s, or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline.</li>
<li>Minimum of 3–5 years of hands-on experience in CGMP pharmaceutical formulation or product development (503B, CDMO, or sterile pharma manufacturing preferred).</li>
<li>Demonstrated experience in formulation design, stability testing, and technology transfer.</li>
<li>Proficiency in analytical chemistry techniques, including UPLC, GC, and dissolution testing; ability to interpret chromatograms and impurity profiles.</li>
<li>Strong working knowledge of ICH Q8–Q10, FDA 503B guidance, and applicable USP chapters.</li>
<li>Experience in scale-up and process optimization for aseptic and non-sterile drug products.</li>
<li>Excellent technical writing, communication, and organizational skills.</li>
<li>Ability to work independently, prioritize multiple projects, and collaborate effectively across cross-functional teams and sites.</li>
</ul>

Pharmaceutical Development Scientist

<h3>Job Description</h3>
Job description:
Pride Health is hiring for a Medical Physicist to support our client’s medical facility based in Atlanta, GA. This is a travel contract opportunity and a great way to start working with a top-tier healthcare organization!
 
Job Details:
<ul>
<li>Perform calibration, quality assurance (QA), and performance testing of linear accelerators (LINACs), simulators, brachytherapy units, and radiation measuring instruments.</li>
<li>Conduct patient-specific dose calculations and treatment plan verification for IMRT, VMAT, SBRT, SRS, and 3D conformal treatments.</li>
<li>Participate in treatment planning by reviewing and approving dose distributions and ensuring prescribed dose accuracy.</li>
<li>Oversee brachytherapy planning and source calibration (e.g., HDR, LDR).</li>
<li>Develop and implement radiation safety and quality control programs in compliance with AAPM, NRC, and state regulatory standards.</li>
<li>Perform commissioning, acceptance testing, and annual QA for new radiation therapy and imaging equipment.</li>
<li>Collaborate with radiation oncologists, dosimetrists, and therapists to ensure optimal treatment accuracy and patient safety.</li>
<li>Maintain and document QA records, calibration data, and regulatory compliance reports.</li>
<li>Provide technical guidance and education to residents, technologists, and radiation therapy staff on physics principles and safety protocols.</li>
<li>Participate in research and development projects, process improvement, and implementation of new technologies or techniques.</li>
<li>Act as a liaison with equipment vendors and service engineers for maintenance and upgrades.</li>
<li>Ensure radiation protection for patients, staff, and the public through periodic monitoring and audits.</li>
</ul>
 
Requirement:
<ul>
<li>Minimum of 2 years of experience within the specialty.</li>
<li>AHA BLS</li>
</ul>
 
Knowledge, Skills &amp; Abilities Required:
Knowledge
<ul>
<li>Comprehensive understanding of radiation physics, dosimetry, and radiobiology.</li>
<li>Expertise in treatment planning systems (e.g., Eclipse, RayStation, Monaco) and record &amp; verify systems (e.g., ARIA, MOSAIQ).</li>
<li>Knowledge of quality assurance procedures and regulatory requirements (AAPM TG reports, NRC, ACR, NCRP).</li>
<li>Familiarity with linear accelerators, brachytherapy, CT simulation, and image-guided radiation therapy (IGRT).</li>
</ul>
Skills
<ul>
<li>Proficient in radiation dose calculation, plan evaluation, and verification.</li>
<li>Strong analytical and problem-solving skills for troubleshooting equipment and plan discrepancies.</li>
<li>Skilled in QA tools, dosimetry software, and data analysis.</li>
<li>Effective communication and documentation skills for clinical collaboration and reporting.</li>
<li>Competent in use of MATLAB, Python, or Excel VBA for data processing and workflow automation (preferred).</li>
</ul>
Abilities
<ul>
<li>Ability to work independently while managing multiple QA and clinical responsibilities.</li>
<li>Ability to train and guide junior staff, residents, and dosimetrists.</li>
<li>Strong commitment to accuracy, precision, and patient safety.</li>
<li>Ability to adapt to new technologies and techniques in radiation oncology.</li>
<li>Maintain composure and sound judgment in high-stakes clinical environments.</li>
</ul>
 
Additional Information:
<ul>
<li>Location: Atlanta, GA</li>
<li>Job Type: 13 weeks- local contract or travel contract</li>
<li>Schedule: 8hr Day Shift - 40 hours per week</li>
<li>Pay Range/Salary Range: $4800/wk to $5000/wk</li>
</ul>
 
Pride Global offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life &amp; disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors.
 
Interested? Apply now!
 
About Pride Health
Pride Health is Pride Global's healthcare staffing branch, providing recruitment solutions for healthcare professionals and the industry at large since 2010.
As a minority-owned business that delivers exceptional service to its clients and candidates by capitalizing on diverse recruiting, account management, and staffing backgrounds, Pride Health's expert team provides tailored and swift sourcing solutions to help connect healthcare talent with their dream jobs. Our personalized approach within the industry shines through as we continue cultivating honest and open relationships with our network of healthcare professionals, creating an unparalleled environment of trust and loyalty.
 
Equal Employment Opportunity Statement
As a certified minority-owned business, Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics.

Medical Physicist

<h3>Job Description</h3>
Job Description
Position Purpose:
The purpose of this position is to provide analytical chemistry subject matter expertise to one or more chemistry-based applied research projects.
Essential Duties and Responsibilities: 
<ul>
<li>Develops and validates analytical methods using thermal desorption (TD), gas chromatography (GC), liquid chromatography (LC), ion chromatography (IC), mass spectrometry (MS), and microscopy.</li>
<li>Performs troubleshooting and non-routine maintenance on TD, GC, LC, IC, MS, and microscopy instrumentation.</li>
<li>Ensures the readiness of TD, GC, LC, IC, MS, and microscopy instrumentation</li>
<li>Facilitates the stand-up of new analytical instrumentation</li>
<li>Leads meetings with company clients by preparing and presenting meeting materials in meetings</li>
<li>Develops innovative solutions to complex problems</li>
<li>Develops improvements to currently used processes and analysis methods</li>
<li>Trains, leads, and mentors junior level scientists to execute analytical chemistry tasks</li>
<li>Performs wet chemistry (dilutions, extractions, etc.)</li>
<li>Composes, reviews, and executes test plans and standard operating procedures</li>
<li>Composes and reviews technical reports</li>
<li>Performs literature reviews</li>
<li>Safely handles explosives and other hazardous materials</li>
<li>Sources materials and submits purchase requests</li>
<li>Other duties as assigned</li>
</ul>
Required Knowledge, Skills &amp; Abilities:
<ul>
<li>Positive attitude with a willingness to learn new things</li>
<li>Previous experience with TD, GC, LC, IC, or MS</li>
<li>Excellent working knowledge of TD, GC, LC, IC, and MS</li>
<li>Technical writing, presentation, verbal communication, and listening skills</li>
</ul>
Education/Experience: 
Incumbent professional should have a minimum of a bachelor's degree in chemistry with five to ten years of analytical chemistry experience or a graduate degree (masters or PhD) chemistry with up to five years of experience.
Certificates and Licenses: 
None

Clearance: 
The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position.
Supervisory Responsibilities:
The incumbent professional has little to no supervisory responsibilities.
Working Conditions/ Equipment: 
The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%.
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor.
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