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<h3>Job Description</h3>
Job Description
Job Title: Laboratory Analyst Associate 3262706 (Biotechnology)
Location: Easr of Puerto Rico - 100% Onsite on Administrative Shift
Duration: Approximately 5 months
Open to Residents of Puerto Rico Only
 
ProQuality Network is seeking two highly skilled professionals for the position of Process Development Sr. Associate Scientist to join our client, a leading biotechnology organization. Selected candidates will represent ProQuality Network with professionalism and excellence, contributing to vital scientific work that directly impacts the quality and safety of medical products.
 
Summary of Role
The selected individuals will be responsible for developing and executing studies related to primary packaging defects (vials and syringes) for research, equipment characterization, training, and setup of commercial systems. This is a hands-on laboratory-based role requiring technical proficiency, innovation, and collaboration across departments.
 
Preferred Qualifications
<ul>
<li>Proven experience in preparing syringes/vials with cosmetic, particulate, or solution defects for development purposes.</li>
<li>Skilled in using laboratory equipment such as:</li>
<li>Micrometer</li>
<li>Caliper</li>
<li>Microscope</li>
<li>Analytical balance</li>
<li>Creative mindset and strong manual dexterity to develop and replicate defects on glass and polymer surfaces.</li>
<li>Ability to:</li>
<li>Introduce or improve defect creation methods in the laboratory.</li>
<li>Evaluate and classify primary container defects.</li>
<li>Create documentation based on technical assessments and reports.</li>
<li>Solid understanding of:</li>
<li>Aseptic techniques</li>
<li>Visual Manual Inspection techniques</li>
<li>5S and Lean Manufacturing concepts</li>
<li>Excellent communication and interpersonal skills to support and motivate team activities.</li>
<li>Demonstrated capability to prioritize multiple tasks in a fast-paced environment.</li>
<li>Innovative, analytical, and results-driven mindset with a strong team orientation.</li>
</ul>
 
Essential Responsibilities
<ul>
<li>Design, plan, and perform experiments with minimal supervision.</li>
<li>Record, organize, and analyze data to support packaging defect-related studies.</li>
<li>Participate in developing new methods and improve existing lab protocols.</li>
<li>Evaluate and interpret experimental results to provide clear recommendations.</li>
<li>Serve as a resource and technical expert in the development of cosmetic defects.</li>
<li>Collaborate across departments to ensure timely project execution.</li>
<li>Maintain compliance with cGMPs, internal protocols, and regulatory requirements.</li>
<li>Author technical reports, regulatory documents, and related publications.</li>
<li>Represent the department in cross-functional teams and contribute to safety and quality initiatives.</li>
</ul>
 
Educational / Software Requirements
<ul>
<li>Masters Degree in Engineering or related scientific discipline with 3+ years of directly related experience</li>
<li>OR</li>
<li>Bachelors Degree in Engineering or related scientific discipline with 5+ years of directly related experience</li>
</ul>
 
Competencies &amp; Skills
<ul>
<li>Advanced scientific analysis and troubleshooting</li>
<li>Laboratory expertise in scientific experimentation and data interpretation</li>
<li>Strong technical writing, verbal communication, and problem-solving skills</li>
<li>Proficiency in project management, negotiation, and conflict resolution</li>
<li>Adaptability to manage change and multitask across priorities</li>
<li>Fully bilingual in English and Spanish</li>
<li>Strong knowledge of current Good Manufacturing Practices (cGMPs)</li>
</ul>
 
If you are passionate about science and innovation and would like to be a key contributor representing ProQuality Network in a dynamic biotechnology setting, we invite you to apply at the link below with your most updated resume.

Laboratory Analyst Associate 3262706 (Biotechnology)

<h3>Job Description</h3>
Job DescriptionDescription:
 An excellent opportunity exists to work for a government contractor with competitive compensation and work-life balance. Posterity Group is seeking experienced Therapeutic Medical Physicist with the West Palm Beach VA Medical Center. 
 
Duties include but are not limited to:
<ul>
<li>Performs the clinical practice of therapeutic medical physics in its entirety with considerable discretion and independent judgment.</li>
<li>Oversees the chain of events from image acquisitions to treatment verification and delivery to assure consistent geometry and optimal treatment delivery.</li>
<li>Provides assessments and monitoring of image quality throughout this chain of events.</li>
<li>Acquires and stores data for treatment plans such that the information is secure and retrievable</li>
<li>Designs and/or oversees the design, and fabrication of treatment aids and beam modifies as needed.</li>
<li>Calculates and/or supervises the calculation of dose distributions and machine settings for patient treatments.</li>
<li>Establishes protocols to ensure high quality patient dosimetry and determination of actual delivered dose.</li>
</ul>
Requirements:
Education. Master's degree or higher in a physics, science, or engineering discipline recognized by an accredited college or university with at least 30 semester hours in medical physics, health physics, radiological science, physics, engineering, chemistry, or biology; or an equivalent foreign degree and coursework substantiated by the National Association of Credential Evaluation Services. 
Board Certification. Persons hired or reassigned to TMP positions in the VHA must be board certified in the field of therapeutic medical physics by an approved certifying body. The board certificate must be current and the applicant must abide by the certifying body's requirements for continuing education. 
Approved Certifying Bodies(a) The American Board of Radiology (ABR) in any of the following field titles:
<ul>
<li>1. Therapeutic Medical Physics</li>
<li>2. Therapeutic Radiologic or Therapeutic Radiological Physics</li>
<li>3. Radiologic Physics or Radiological Physics</li>
</ul>

Therapeutic Medical Physicist

<h3>Job Description</h3>
Job DescriptionDescription:
The National WWII Museum is currently seeking a WWII Military Historian. The Military Historian position offers a unique opportunity for a scholar to be a part of the intellectual life of the Jenny Craig Institute for the Study of War and Democracy at The National WWII Museum, providing particular expertise on how and why the war was fought. The World War II Military Historian will engage fully in Museum and Institute scholarly activities, actively participate in the Museum’s higher education programs, perform research and writing functions for the Institute’s Historical Research Services, take part in public programs and presentations, and represent the Museum to the scholarly community at professional and academic conferences.
 
This position reports to the Executive Director of the Jenny Craig Institute for the Study of War and Democracy.
Requirements:
<ul>
<li> Participate in and teach graduate-level courses as part of MA and continuing education programs.</li>
<li>Regularly contribute and peer-review written content to the Museum and the Institute’s website.</li>
<li>Regularly attend and participate in seminars, lectures, and public presentations.</li>
<li>Participate in Institute Public Programming by interviewing guest speakers, taking part in panels and discussions, and providing talks on WWII leadership and other relevant aspects of the war.</li>
<li>Assist the Institute’s WWII Research Service team in the research and writing of monographs detailing individual WWII veterans’ stories.</li>
<li>Support and play an active role in the production and promotion of Museum content and projects.</li>
<li>Perform other duties and special projects as assigned by the Executive Director of the Institute for the Study of War and Democracy.</li>
</ul>
Qualifications
<ul>
<li>Applicants must demonstrate a strong knowledge of WWII, the US role in the war, and a commitment to research and professional goals that support the mission of the Jenny Craig Institute for the Study of War and Democracy, and, more broadly, The National WWII Museum.</li>
<li>A PhD is highly preferred. Applicants must hold either a doctorate degree (PhD) in U.S. Military History (or a related specialty) or possess a relevant Master’s Degree and significant professional experience. Expertise in areas such as World War II operational history and campaign analysis, American military leadership and warfighting, or naval history are considered a plus.</li>
<li>Excellent communications and interpersonal skills and abilities – verbal, written, and digital.</li>
<li>Ability to travel to attend conferences, to meetings sponsored by associations or industries, to meet clients or representatives of potential clients, and to participate in overseas programs. </li>
<li>Willingness to work a flexible schedule that goes beyond a 40-hour week, including some weekends and evenings. </li>
</ul>
In addition to offering competitive wages, the Museum’s benefits package includes: 
<ul>
<li>Medical insurance – 2 plan options; Museum pays 75% of premium </li>
<li>Dental and vision insurance </li>
<li>Flexible spending account </li>
<li>401(k) – Museum matches 50% of employee contribution up to 6%; employer contribution full vested after 3 years of employment </li>
<li>Life insurance and AD&amp;D - $15,000 policy employer paid; additional life and AD&amp;D available </li>
<li>Long term disability insurance </li>
<li>Paid vacation and sick leave, 10 paid holidays per year </li>
<li>Free parking </li>
<li>Tuition assistance and professional development </li>
<li>Employee assistance program </li>
</ul>
The National WWII Museum is an Equal Opportunity Employer and seeks diversity in its workforce. We are dedicated to a policy of non-discrimination in employment on any basis including age, sex, race, religion, national origin, sexual orientation, or disability. Consistent with the Americans with Disabilities Act, applicants may request accommodations needed to participate in the application process.

WWII Military Historian

<h3>Job Description</h3>
Job Description
SGI Global is seeking Senior Intelligence Analysts to support FBI's Insider Threat Office (InTO). The Senior Analyst supports InTO operations by leading analytical tasks and mentoring junior staff. This position focuses on synthesizing large volumes of data into actionable intelligence and managing the development of technical and analytical outputs that support investigations into insider threats.
*Contingent on contract award*
Responsibilities
<ul>
<li>Provide intelligence and threat analysis of information that is tailored to InTO requirements.</li>
<li>Review and evaluate incoming reports and information, collection plans, and programs. </li>
<li>Write clear, concise, and timely reports that identify, interpret, and collate disparate pieces of information.</li>
<li>Develop information and technical support documents, summaries, reports, presentations, and other designated products in support of program information and technical support requirements.</li>
<li>Present briefings to personnel designated by program management. </li>
<li>Conduct analytical and critical thinking (i.e., understand problem set, review facts, make accurate observations and judgments, and provide recommendations to management). </li>
<li>Identify relevant data sources to clarify or corroborate investigative or operational program initiatives. </li>
<li>Access information from classified and open-source databases. </li>
<li>Access, analyze, and interpret as well as perform research on designated systems and databases for the purpose of identifying information of interest to the requestor, organizing and reporting the identified information to an appropriate medium, and editing the information into format(s) specified by the InTO SOP.</li>
<li>Evaluate information using good judgment and decision making. </li>
<li>Analyze data, develop information, and assess available solutions or alternative methods of proceeding. </li>
<li>Develop and project data, draw conclusions, estimate probabilities based upon knowledge of current and past program situations, and understand the significance of conditions and trends. </li>
<li>Oversee and manage projects, programs, and/or tasks. </li>
<li>Provide leadership to junior team members. </li>
<li>Identify impacts and effects of study findings and make recommendations. </li>
<li>Ability to prioritize multiple projects simultaneously. </li>
<li>Ability to assist in the preparation of presentations. </li>
<li>Conduct massive data analysis to include development of query techniques, prototype programs, and algorithms. </li>
<li>Prepares finished studies of factual data. </li>
<li>Prepare, review, and submit required reports and communicate policies, purpose, and goals of the organization to junior staff. </li>
<li>Responsible for presenting briefings to personnel designated by program management.</li>
</ul>
Qualifications
<ul>
<li>US Citizen.</li>
<li>Active Top Secret/SCI with Counterintelligence (CI) Polygraph</li>
<li>Bachelor's degree </li>
<li>Minimum 8 years of analytical experience, including project or team leadership.</li>
<li>Experience in national security or security-related analysis preferred.</li>
<li>Proficient in Microsoft Office tools and analytical software.</li>
<li>Excellent written and verbal communication skills.</li>
</ul>
Preferred Qualifications
<ul>
<li>Work experience in national security or security-related matters is preferred.</li>
<li>Preferred work experience in national security or security-related matters with an emphasis on information analysis.</li>
<li>Proficiency in understanding security risk management concepts; a security related certification; and experience with intelligence-focused operation environment.</li>
</ul>
SGI Global provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws.
 Job Posted by ApplicantPro

Senior Intelligence Analyst - Insider Threat Program

<h3>Job Description</h3>
Job Description
Pest Control Technician - Wildlife
Arrow Exterminators is looking to hire a full-time Wildlife Technician to provide uncompromised service to Arrow's residential and commercial wildlife control customers through exclusion, trapping, and removal of wildlife. Exclusion includes sealing, caulking, or installation of sheet metal to soffits, gutter lines, roof ridges, vents, and voids etc. This work is often done from rooftops or ladders and may require basic carpentry
Our technicians enjoy a company vehicle and other benefits including:
<ul>
<li>generous time off, </li>
<li>11 paid holidays, </li>
<li>401(k) with company match, Roth IRA, </li>
<li>medical, dental and vision insurance, </li>
<li>high deductible HSA, </li>
<li>telemedicine, </li>
<li>disability, cancer, and accident insurance. </li>
<li>health &amp; wellness suite </li>
<li>company-paid + additional, optional, life insurance. </li>
</ul>
 
ABOUT OUR FAMILY OF BRANDS 
We have been a family owned and operated business since our start in 1964. Over the years, we have grown rapidly, and we now have the privilege of servicing 12 states. To ensure the quality and satisfaction of our customers, we have several offices in each state we are in to offer a more personalized approach to our communities. Ranked by revenue, Atlanta-based Arrow Exterminators is the sixth largest pest and termite control company in the United States! We instill family values in the company culture to create a welcoming work environment and a successful company. We attribute our success to passionate, highly trained team members who are committed to protecting everyone's quality of life.
As Arrow grows and continues to exceed industry expectations, we are always looking for new talent to bring on board. We know our team has a lot of options and we are humbled that they choose to work with us. That's why we offer competitive compensation, a robust benefits package, and a family-oriented company culture.
 
A DAY IN THE LIFE AS A WILDLIFE TECHNICIAN
Your primary focus will be to identify, remove, prevent, or repair anything damaged by wildlife. Your first course of action will be to ask questions on the issue your customer is experiencing. Problem solving will help you form an in-depth inspection of the customer's home to find the source of the issue. Your wealth of knowledge about wildlife will help you determine the best solution and explain to the customer your next steps. Upon the completion of your service whether it be exclusion, trapping, or removal, you will be responsible for collecting payment due and proposing additional services that would benefit them. Your independence and accountability will help you as you run and schedule your own services. 
 
Minimum Qualifications:
<ul>
<li>Ability to pass and maintain any state regulatory agency required licensing/certification exams</li>
<li>Able to pass internal technical exams</li>
<li>Possess current Driver's License </li>
<li>High school diploma or equivalent</li>
<li>Present a professional appearance including wearing an approved Arrow uniform</li>
<li>Able to work a 40-hour (minimum) work week</li>
<li>Willing to work evenings and weekends as needed</li>
</ul>
ARE YOU READY TO JOIN OUR TEAM?
 
If you feel that you would be right for this position, please fill out our initial 3-minute, mobile-friendly application so that we can review your information. We look forward to meeting you! #ArrowExterminators
 
We are an Equal Opportunity Employer
(The job description is not an exhaustive statement of all the duties, responsibilities, or qualifications of the job, nor is it intended to limit opportunities for necessary modifications).
Arrow Exterminators as a PestVets Company is committed to hiring and participating in acts of service for Veterans and active-duty members of the U.S. Military.
 
Arrow Exterminators is a Drug-Free Workplace and performs Pre-employment Drug Screens and Background Checks on all employees. 
 Job Posted by ApplicantPro

Pest Control Technician - Wildlife

<h3>Job Description</h3>
Job DescriptionDescription:
We are seeking a skilled and ambitious R&amp;D Associate to contribute to our growing, fast-paced Research &amp; Development team. If you thrive in a collaborative environment where science meets real-world impact, this is your chance to make a difference. 
<ul>
<li>Lead &amp; Execute Experiments – Perform tests and analyze results to drive innovation and product improvements.</li>
<li>Hands-On Lab Work – Operate lab equipment, perform sample testing, and contribute to research publications or technical documentation.</li>
<li>Data Analysis &amp; Reporting – Define, enter, track, and trend data using tools like Excel, ClickUp, and PowerBI to support data-driven decision-making.</li>
<li>Innovate &amp; Problem Solve – Assist in the design control process from concept to commercialization, contributing to protocol development, risk assessments, and validation studies.</li>
</ul>
Responsibilities You Will Own:
As an R&amp;D Associate, you will play a critical role in product development, testing, and driving research that shapes the future of dental safety.
<ul>
<li>Extended periods of time in a laboratory configuring test methods and running experiments.</li>
<li>Work autonomously under pressure and effectively communicate with peers.</li>
<li>Contribute to technical presentations, protocol writing, and drafting reports.</li>
<li>Comply with all safety guidelines (laboratory, equipment, and material handling).</li>
</ul>
Requirements:
<ul>
<li>Bachelor’s degree in a STEM field (Biology, Chemistry, Biomedical Engineering, or related) or 5 years of applicable hands-on experience.</li>
<li>2-5 years of applicable experience.</li>
<li>Experience in laboratory testing, data analysis, and documentation.</li>
<li>Strong analytical skills with the ability to interpret results and identify trends.</li>
<li>Comfortability working with BSL-2 level organisms and following safety protocols.</li>
<li>Proficient in Microsoft Office Suite (Excel, Word, Teams, PowerPoint, Outlook).</li>
<li>Excellent communication and problem-solving skills with a proactive mindset.</li>
<li>Ability to work independently under pressure and collaborate in cross-functional teams.</li>
<li>Capable of lifting 50 lbs (equipment and supplies).</li>
</ul>
Desired:
<ul>
<li>Experience with FDA medical device regulations, design control, and ISO 13485.</li>
<li>Knowledge of water testing techniques (Flow Cytometry, HPC, etc.).</li>
<li>Experience in product development, verification &amp; validation, and regulatory submissions.</li>
</ul>
 
Benefits:
<ul>
<li>Starting salary is $60,000-$80,000 depending on experience</li>
<li>ProEdge covers the monthly premiums for medical, dental and vision insurance for eligible Full-time Employees</li>
<li>Provides a 125 Plan for those eligible Full-time Employees the ability to cover any dependents through pre-tax deductions</li>
<li>Eligible Full-time Employees may receive a discretionary annual bonus based on the performance of the individual Employee and profits of the Company</li>
<li>May lead to additional opportunities; based solely on the performance and cultural fit of the Employee</li>
<li>Outstanding team and work environment</li>
</ul>
 
Our purpose: Protecting dental patients as well as those involved in their care from infectious diseases
This Team Member will possess integrity with solid values that fall in line with the company’s culture; respect toward one another, our products, and our services
About the Company: ProEdge Dental Water Labs is a high growth, dynamic company, located in Centennial, Colorado. Our company specializes in maintaining the safety of dental offices and patients alike through cutting edge dental products and services within a niche market. ProEdge has been leading the market with our products and individualized services for dental offices across the country. As a financially solid and thriving company, this is truly an exciting time to come on board.
About Us: ProEdge Dental Water Labs fosters initiative, self-directed work and teamwork in order to help one another accomplish our business objectives. We welcome your ideas and value you as a part of our Team. Employees are well provided for and in return our employees deliver the highest level of service for our Team and our customers. We acknowledge that our employees are our most valuable asset!

R&D Associate

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Essential Duties and Responsibilities:
<ul>
<li>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Applies the highest quality standard in all areas of responsibility</li>
<li>Demonstrates and promotes the company vision</li>
<li>Demonstrates strong client service skills, teamwork, and collaboration</li>
<li>Proactively plans and multitasks to maximize productivity</li>
<li>Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration</li>
<li>Regular attendance and punctuality</li>
<li>Applies 17025 compliance standards in all areas of responsibility, as appropriate</li>
<li>Performs complex analyses and non-routine testing in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g. ICP, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.)</li>
<li>Operates and maintains job related equipment as required</li>
<li>Performs advanced troubleshooting of laboratory equipment</li>
<li>Performs supporting verification, calibration, and maintenance tasks (e.g., balance calibration and pipet verifications)</li>
<li>Performs laboratory tasks as assigned following supervisor direction, SOPs, WI and other documentation</li>
<li>Assists other staff in the edits and updates of SOPs, WI and other documentation</li>
<li>Follows all Good Documentation Practices appropriately, including digital platforms</li>
<li>Maintains working areas appropriately (cleaning, disinfecting, etc…)</li>
<li>Possesses strong organizational skills</li>
<li>Provides clear feedback</li>
<li>Keeps accurate records, follows instructions, and complies with company policies</li>
<li>Proactively checks and stays current with all training across multiple learning platforms</li>
<li>Provides instruction/training to new staff</li>
<li>Recognizes errors, identifies root causes, and applies process improvements</li>
<li>Provides analyses support for method validation as needed</li>
<li>Evaluates, reviews, and approves data by other analysts</li>
<li>Independently drafts, edits and updates SOPs, WI and other documentation</li>
<li>Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision</li>
<li>Makes recommendations for technical improvements, as needed</li>
<li>Communicates effectively with client staff members</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li>
<li>4 – 7 years of related experience</li>
<li>GMP experience a plus; experience in the tobacco industry a plus</li>
</ul>
 Additional Information 
<ul>
<li>Position is Monday- Friday 8:00 AM- 5:00PM.&nbsp;Overtime as needed.&nbsp; Candidates currently living within a commutable distance of&nbsp;Winston-Salem, NC&nbsp;are encouraged to apply.&nbsp;</li>
</ul>
<ul>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>#LI-EB1</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Senior Chemist - Metals

<h3>Job Description</h3>
Job DescriptionDescription:
*Note: this is an in-person position. The exact level will depend on experience*
 
Company Overview:
 
Vividion is a next generation biotechnology company based in San Diego that is leveraging its proprietary chemical proteomics platform to conduct proteome-wide footprinting of drug-protein interactions with unprecedented breadth and precision. Our technology allows us to screen, identify and optimize novel drugs that selectively bind virtually any protein, including proteins previously considered “undruggable”. Our pipeline and emerging programs reflect a matured and productive platform capable of delivering first in class drugs utilizing novel mechanisms of action (allosteric inhibitors, protein-protein interaction inhibitors, functional activators, degraders etc.) against undruggable targets in the oncology and immunology space.
 
We prize scientific excellence, creativity, team players and we are committed to continued innovation. We have worked hard to create a collaborative and dynamic work culture where your ideas and discoveries are valued and will have an impact. We are growing and there are opportunities for mentorship and career progression.
 
Vividion has been recognized as a Top Workplace by The San Diego Union-Tribune in 2022, 2023, and 2024.
 
Job Summary:
 
The successful candidate will be part of a team devoted to identifying novel drug targets for cancer using our precision oncology platform. This person will play an important role in advancing our discovery platform technology and small molecule pipeline. The candidate will assist in the design and implementation of experiments aimed at identifying and validating drug targets and defining drug or gene mechanism of action. The ideal candidate is a well-rounded molecular biologist with demonstrated experience in cancer drug discovery.
 
This is a unique opportunity to be part of a growing team and make an impact in all aspects of the drug discovery and development process. We are looking for intrinsically motivated people who are driven to make a real difference in the lives of cancer patients.
Requirements:
Essential Duties and Responsibilities:
<ul>
<li>Independently conduct experiments to understand drug mechanism of action</li>
<li>Conduct large-scale mammalian cell culture experiments </li>
<li>Successfully deploy CRISPR/Cas9 techniques to perturb the genome and transcriptome</li>
<li>Conduct large-scale mammalian cell culture genetic perturbation studies using advanced CRISPR/Cas9 techniques</li>
<li>Use molecular biology techniques to support target and hit validation</li>
<li>DNA isolation, library preparation and next-generation sequencing </li>
<li>Cell line engineering</li>
<li>Contribute to experimental design and planning</li>
<li>Perform and optimize cellular assays to support drug discovery efforts</li>
<li>Independently summarize, analyze and regularly present work internally</li>
<li>Maintain exceptional scientific records of projects and experiments</li>
</ul>
Education and Experience Requirements:
<ul>
<li>BS in a relevant scientific field with at least 7 years of hands-on laboratory experience; MS with 5 years; or PhD with 0-2 years of experience; industry experience preferred</li>
<li>Experience working as part of a goal-oriented team</li>
<li>Demonstrated ability to work proficiently, maintain deadlines and think critically</li>
<li>about technical aspects of experiments</li>
<li>Must be detail oriented and demonstrate excellent communication skills</li>
<li>Experience with molecular and cellular biology techniques such as cloning, PCR, qPCR, protein isolation, western blotting, flow cytometry</li>
<li>RNA/DNA isolation and sequencing</li>
<li>Mammalian cell culture experience required</li>
</ul>
The following skills are a plus:
<ul>
<li>CRISPR, shRNA, and/or siRNA experience</li>
<li>Familiarity with genomic sequencing and functional genomic techniques</li>
<li>Experience working with small molecule drug discovery</li>
</ul>
Pay &amp; Benefits:
 
The anticipated base salary for this position ranges from $90,000 to $120,000 depending on relevant skills, competencies, experience, and education. In addition, this position is eligible for target bonus, long-term-incentives, 401k retirement savings plan with company match, and a comprehensive benefits package which includes medical, dental, vision, life, and disability insurance.
 
EEO &amp; Employment Eligibility:
 
Vividion Therapeutics, Inc. is an equal opportunity employer. All applicants will receive consideration for employment without regard to disability or veteran status.
 
Privacy Policy:
 
The protection of your personal information is a commitment we take seriously. For information regarding our Privacy Policy (CA candidates) please visit <a href="https://vividion.com/privacy-notice/" target="_blank">https://vividion.com/privacy-notice/</a>.

Associate Scientist / Scientist I, Functional Genomics

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Job Description 
The position will be providing analytical support to biotherapeutic process development teams, specifically focusing on large molecules (proteins, polysaccharides, nucleic acids, etc.).
Candidates will work in a large diverse team, helping with advancing cutting edge pharmaceutical reserarch. Some to the techiques that our future team members will need to be familiar with are:
· Ultraviolet and visual light spectroscopy (UV-Vis)
· Analytical chromatographic separations (HPLC)
· Small-volume multichannel pipetting skills and plate-based assays
Qualifications 
Authorization to work in the United States indefinitely without restriction or sponsorship
<ul>
<li>Experience with&nbsp;UV-VIS and HPLC&nbsp;is required.
<ul>
<li>1-3 years of relevant&nbsp;experience&nbsp;</li>
</ul>
</li>
<li>Bachelors or Masters Degree in Biological or Chemical Science.</li>
<li>Candidates within a commutable distance of Chesterfield, MO&nbsp;are encouraged to apply</li>
</ul>
Preferred experience:&nbsp;
Experience with protein immunoblotting technology&nbsp;and attention to detail.&nbsp; Ability to operate independently after receiving direction
Electronic laboratory notebook systems and/or GMP documentation practice
Empower or OpenLabs Software
 Additional Information 
Position is full-time, Monday to Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of&nbsp;Chesterfield, MO&nbsp;are encouraged to apply.
What we offer:
· Comprehensive medical coverage, with dental and vision options
· Life and disability insurance
· Paid holidays and vacation.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Scientist - Analytical Assay

<h3>Job Description</h3>
Job Description
Located in Redmond WA, SystImmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic bi-specific, and tri-specific antibodies, as well as antibody-drug conjugates (ADC's). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor.
Position Summary:
We are seeking a highly skilled and motivated Upstream Scientist/Senior Scientist to join our team onsite in Redmond, WA. This individual will lead and execute upstream project process development (USP) and technology transfer activities to support the development of clinical manufacturing processes for our protein therapeutics pipeline. The ideal candidate will have hands-on experience with mammalian cell culture, bioreactor operations, and process scale-up for biologics production.&nbsp;
Major Responsibilities:
<ul>
<li>Apply technical knowledge andin upstream process development for CHO cells (bioreactor process design, scale up, media and feed optimization, etc.), draft study protocol, design and execute experiments including in-process tests, characterize and deliver harvest material to downstream team,and author technical reports.</li>
<li>Stay abreast of technical advancements in the CMC area of CHO cell line development and upstream process development and technology transfer aligned with cGMP clinical manufacturing.</li>
<li>Support the transfer, development, and scale-up of CHO cell culture process technology from research into process development and manufacturing, to enable the production of clinical material</li>
<li>Collaborate with teams in downstream process development and analytical development to advance recombinant protein programs</li>
<li>Lead and support various elements of early-stage CMC development activities, including technical support of non-GMP and clinical manufacturing, as well as development and implementation of process improvements, as programs advance through development</li>
<li>Analyze, interpret, present and document complex technical information in statistically meaningful ways. Exhibit and improvein DoE and multi variant analysis.</li>
<li>Work with the team within the project scope, manage timeline in a fast-paced dynamic environment with rigor and agility.</li>
<li>Data analysis, interpretation, and effective communication to management.</li>
</ul>
Qualifications and Experience:
<ul>
<li>PhD. with 3+ years of work experience&nbsp;in upstream bioprocess.</li>
<li>Significant technical bioreactor use, optimization, and scale-up. DasGip or DASware experience is desired. Perfusion experience is a plus.</li>
<li>Ability to work independently to troubleshoot processes and develop new methods in a flat, collaborative matrix.</li>
<li>Experience in scaling up and technology transfer to manufacturing environment and understand GMP well.</li>
<li>Experience and knowledge in other sections of therapeutic protein process development, including downstream, formulation, analytics, are valued.</li>
<li>Exceptional communication and interpersonal skills to&nbsp;positive relationships with stakeholders.</li>
<li>Proactively introduce new methods, provide technical mentorship to colleagues, and identify and execute ways to keep lab running efficiently</li>
<li>Accuracy and attention to detail</li>
<li>Ability to work on multiple projects simultaneously</li>
</ul>
 This job description is intended to present the general content and requirements for this job.&nbsp;The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.
 The hiring pay range for this position is $90,000 - $140,000 per year based on skills, education, and experience relevant to the role.
 SystImmune is a stable, well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
SystImmune is an Equal Opportunity Employer.
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