field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<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:
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 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 Descriptionjob summary: 
Step into a vital role at a state-of-the-art biopharma research facility in Worcester, MA, where innovation fuels the development of life-changing therapies. As a Research and Development Laboratory Technician, you'll be at the heart of scientific discovery-managing and processing critical biological and chemical samples that support early-stage drug development.
This is a hands-on opportunity to work alongside a collaborative team of scientists in a fast-paced lab environment. You'll leverage your biology background and attention to detail to maintain sample inventory, operate specialized lab equipment, and contribute directly to research that makes a real-world impact. If you're motivated, organized, and ready to be part of something meaningful, this role offers challenge, growth, and purpose.
 location: Worcester, Massachusetts job type: Contract salary: $30.00 - 34.23 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Coordinate and manage the shipment of materials from Company to other sites and collaborators, ensuring compliance with all applicable regulations and guidelines.</li>
<li>Prepare and review shipping documents, including bills of lading, shipping labels, and customs documentation, to ensure accuracy and completeness.</li>
<li>Collaborate with internal teams to ensure proper coordination and execution of shipments.</li>
<li>Communicate with internal and external partners, including freight forwarders and carriers, to schedule and track shipments, ensuring on-time delivery.</li>
<li>Maintain accurate records of all shipments, including tracking numbers, delivery confirmations, and any relevant documentation.</li>
<li>Monitor and manage inventory levels of shipping supplies, such as boxes, labels, and packing materials, ensuring adequate stock is maintained.</li>
<li>Identify and resolve any issues or delays in the shipping process, working closely with internal and external stakeholders to find timely solutions.</li>
<li>Stay up-to-date with relevant shipping regulations, guidelines, and industry best practices, ensuring compliance and continuous improvement.</li>
<li>Assist in the development and implementation of shipping-related policies, procedures, and standard operating protocols.</li>
<li>Provide regular reports and updates to management on shipping activities, including metrics, performance, and any potential risks or opportunities.</li>
</ul>
 qualifications: 
<ul>
<li>Proven experience as a Shipping Coordinator or similar role, preferably in a pharmaceutical or biotechnology industry.</li>
<li>Accustomed to spending extended periods of time working in a bio-hood</li>
<li>Strong knowledge of shipping regulations, including domestic and international requirements, customs procedures, and hazardous materials handling.</li>
<li>Proficient in using shipping software and systems, such as FedEx, UPS, or DHL, to schedule and track shipments.</li>
<li>Excellent organizational and time management skills, with the ability to prioritize tasks and meet deadlines in a fast-paced environment.</li>
<li>Attention to detail and accuracy, ensuring all shipping documents and records are complete and error-free.</li>
<li>Effective communication and interpersonal skills, with the ability to collaborate and build relationships with internal and external stakeholders.</li>
<li>Problem-solving and decision-making abilities, with a proactive approach to identifying and resolving shipping-related issues.</li>
<li>Proficient in using Microsoft Office Suite (Word, Excel, Outlook) and other relevant software applications.</li>
<li>Ability to lift and move heavy packages, as required. </li>
<li>Independent, take leadership, well organized, juggle or manager</li>
</ul>
 #LI-ST1? 
 skills: GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay 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. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Research and Development Laboratory Technician

<h3>Job Description</h3>
Job DescriptionRipple Effect Consulting is looking for an Staff Level Geotechnical Engineer who can work in a leadership role within our client’s Geotechnical division in Colorado. Description: 
<ul>
<li>Perform geotechnical investigations and analyses to assess subsurface and site conditions.</li>
<li>Plan and conduct geotechnical exploration programs effectively.</li>
<li>Perform field and laboratory investigations for geotechnical engineering and geological study projects.</li>
<li>Analyze geotechnical findings, perform appropriate calculations, and prepare technical reports for review by senior geotechnical engineers.</li>
<li>Provide direction to technical team during field inspection activities.</li>
<li>Interact with customers and team members to complete the assigned projects on-time.</li>
<li>Evaluate team performance and determine training needs to meet performance objectives.</li>
<li>Perform basic office administration tasks when needed.</li>
</ul>
Required Skills: 
<ul>
<li>Bachelors of Science in Geotechnical, Geologic, or Civil Engineering or related field.</li>
<li>1-2 years of related work experience within the State of Utah.</li>
<li>Proficient in soil mechanics.</li>
<li>Able to creatively apply engineering principals to solve new problems.</li>
<li>Good written and verbal communication skills.</li>
<li>Able to work effectively in teams.</li>
</ul>

Geotechnical Staff Engineer (EIT)

<h3>Job Description</h3>
Job Description
Environmental Laboratory Analyst
Location: 3226 Commander Dr, Carrollton, TX 75006 Reports To: Lab Manager Office Hours: 8:00 AM – 5:00 PM (Overtime required as needed) Pay Range: $19.00 - $22.00 per hour, depending on experience
At Alliance Technical Group, we’re dedicated to providing exceptional environmental testing services in a collaborative and innovative work environment. Our Dallas Lab specializes in air sample analysis, offering critical data to support pollution control, hazardous waste management, and regulatory compliance.
About Alliance Technical Group
Alliance Technical Group, LLC (Alliance), headquartered in Decatur, AL, is a leading environmental services and solutions provider dedicated to helping clients meet their environmental goals and adapt to evolving regulations. With over 1,700 employees across 50+ offices in the U.S. and Canada, Alliance offers expertise in Environmental Compliance, On-site Testing and Monitoring, and Laboratory Testing and Analysis.
Our team is driven by innovation, committed to exceptional service, and focused on ensuring client success. At Alliance, we pride ourselves on delivering reliability, results, and responsiveness in every aspect of our work.
Required Qualifications
<ul>
<li>Education: Bachelor’s degree in Chemistry or related field, or equivalent experience.</li>
<li>Experience: 1-2 years in an analytical or environmental laboratory.</li>
<li>Technical Skills:</li>
<ul>
<li>Experience with ion chromatography (Chromeleon software), gas chromatography (PeakSimple software), ISE (Fluoride), and pH meters preferred.</li>
<li>Knowledge of NELAC/NELAP standards is a plus.</li>
<li>Some MS Excel experience required</li>
</ul>
</ul>
Key Responsibilities
<ul>
<li>Sample Management and Analysis:</li>
<ul>
<li>Approve, log, and process air samples, including PM samples, M26/M26A, M6/8, M18, and M13B (in development).</li>
<li>Perform analyses using ICS 1100 systems, SRI GC, Orion fluoride meter, and Oakton pH meter.</li>
<li>Maintain proper documentation and chain of custody (COC) for all samples.</li>
</ul>
<li>Data Integrity and Reporting:</li>
<ul>
<li>Maintain detailed records of all analyses, reagents, and preparations to ensure data accuracy.</li>
<li>Document all QC data directly on forms, as the Dallas Lab does not use a LIMS system.</li>
<li>Compile and report results in line with EPA and NELAC standards.</li>
</ul>
<li>Instrument Maintenance and Calibration:</li>
<ul>
<li>Perform routine maintenance and calibration of lab instruments.</li>
<li>While not required, candidates with troubleshooting skills are highly valued.</li>
</ul>
<li>Independent Workflow with Collaborative Updates:</li>
<ul>
<li>Work independently to manage daily tasks and project progress.</li>
<li>Provide regular updates to the Lab Manager for seamless tag-out/tag-in transitions.</li>
</ul>
<li>Other Duties:</li>
<ul>
<li>Prepare reagents and media for lab and field use.</li>
<li>Ensure compliance with lab safety standards and protocols.</li>
<li>Perform other job-related tasks as assigned.</li>
</ul>
</ul>
Key Competencies and Skills
<ul>
<li>Attention to Detail: Ensures accuracy in all analyses and maintains data integrity.</li>
<li>Independent Work Ethic: Manages daily tasks with minimal supervision while keeping the Lab Manager informed.</li>
<li>Teamwork: Works within a small two-person team, focusing on efficient handoffs rather than direct collaboration.</li>
<li>Communication: Primary communication involves lab updates to the Lab Manager, including supply needs and sample anomalies.</li>
</ul>
Daily Workflow and Sample Types
<ul>
<li>Sample Types: Primarily air samples from stack tests, including PM, M26/M26A, M6/8, and M18.</li>
<li>Volume: Current daily volume ranges from 0-5 samples, with potential growth to 10-15 samples.</li>
<li>Quality Control: Built directly into lab forms to ensure thorough documentation and compliance.</li>
</ul>
Growth and Development Opportunities
<ul>
<li>Training: Extensive training on all lab methods, with opportunities for cross-site training.</li>
<li>Career Path: Growth potential includes promotion to Analyst II, Assistant Manager, or roles in QC/QA or Tech Services.</li>
<li>Professional Development: Encouragement to pursue certifications and advanced training.</li>
</ul>
Work Environment
<ul>
<li>Physical Requirements: Standing for extended periods, with anti-fatigue mats provided. Heavy lifting is not required.</li>
<li>Safety Equipment: Lab coats, safety glasses, gloves, fume hoods, face shields, and spill kits provided. Weekly safety shower tests ensure a safe work environment.</li>
<li>Team Structure: This role is part of a two-person team, reporting directly to the Lab Manager.</li>
</ul>
Why Work with Us?
<ul>
<li>Impact the Environment: Help protect the environment by analyzing samples that influence key decisions in pollution control and regulatory compliance.</li>
<li>Professional Growth: Access training, development programs, and promotion opportunities.</li>
<li>Comprehensive Benefits: Enjoy excellent benefits, including healthcare, profit-sharing, tuition reimbursement, and performance bonuses.</li>
<li>Positive Work Environment: Thrive in a culture of teamwork, integrity, and professionalism where your contributions are valued.</li>
</ul>
EEO Commitment: We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, national origin, ethnicity, sex, pregnancy, sexual orientation, gender identity/expression, including transgender identity, religion, disability, age, genetics, active military or veteran status and any other characteristics protected under applicable federal or state law.
KEY BENEFITS INCLUDE:
<ol>
<li>Medical, Dental, and Vision Insurance </li>
<li>Flexible Spending Accounts </li>
<li>401(K) Plan with Competitive Match </li>
<li>Continuing Education and Tuition Assistance </li>
<li>Employer-Sponsored Disability Benefits </li>
<li>Life Insurance </li>
<li>Employee Assistance Program (EAP) </li>
<li>Paid Time Off (PTO), Paid Holidays, &amp; Bonus Floating Holiday (if hired after July 1st)</li>
<li>Profit Sharing or Individual Bonus Programs </li>
<li>Referral Program</li>
<li>Per Diem &amp; Paid Travel</li>
<li>Employee Discount Hub</li>
</ol>
#LABS

Lab Analyst I

<h3>Job Description</h3>
Job Description
Position Summary:
The Senior Research Associate&nbsp;is a member of the Platform Group and will support laboratory research activities towards development of novel technologies enabling next generation genomic medicines. The successful candidate will have a strong understanding of the technical and equipment needs in a lab as well as significant hands-on experience with standard and cell culturing and in vitro cell biology techniques. They will work independently and as part of a collaborative team.

Key Responsibilities:
Performing laboratory assays and tasks including flow cytometry, mammalian cell culture, animal sample processing, cell isolation, plate-based reporter assays, cell killing assays, transfection, and protein binding assays.
Developing new assays or optimizing existing ones based on in-depth knowledge of laboratory techniques
Analyzing and accurately documenting assay results in an electronic lab notebook or other technical reporting formats

Basic Qualifications:
<ul>
<li>M.S. or B.S. in Biology, Biochemistry, Molecular Biology, or related field with 3-5+ years of relevant experience</li>
<li>Previous experience with immune cell isolation and flow cytometry characterization is required.</li>
<li>Strong primary and cell line culture experience, including experience executing protocols, troubleshooting assays, and carrying out literature searches for method evaluation and refinement</li>
<li>Knowledge of immunology and experience with BLI on octet instruments is a plus</li>
<li>Prior experience working with lipid nanoparticles is a plus</li>
<li>Proven ability to work independently and cross-functionally with highly skilled teams in a fast-paced, entrepreneurial, and technical environment</li>
<li>Strong organizational and problem-solving skills.</li>
<li>Motivated, curious, and comfortable working with highly technical projects and personnel</li>
<li>Excellent communication and presentation skills, capable of conveying technical information in a clear and thorough manner</li>
<li>Comfortable delivering against challenging commitments</li>
</ul>
Company DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities. 
<h3>Company Description</h3>
Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Sr. Research Associate

<h3>Job Description</h3>
Job Description
As a member of the Analytics/Gene Therapy group, this position will be responsible for performing analytical assays supporting the evaluation of early-stage production processes for the AAV vector research pipeline and supporting AAV product testing. The individual may collaborate with Process Development and additional internal and external stakeholders to ensure the development and transfer of robust analytical methods.
The Opportunity to Make a Difference
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Perform analytical assays to support production, purification, and comparability of AAV gene therapy products using qPCR, ddPCR, BLI, DLS, ELISA, and other general laboratory techniques
<ul>
<li>Work seamlessly with cross functional stakeholders to help advance the AAV vector production portfolios</li>
<li>Participate in project related teams and other internal/external collaborations</li>
<li>Ensure that scientific and technical challenges are resolved in a timely manner</li>
<li>Maintain all appropriate laboratory records</li>
<li>Perform routine data analysis for use in presentations, publications, and internal reports</li>
<li>Contribute to a safe, efficient, and effective environment with personal accountability</li>
<li>Perform other related duties as required</li>
</ul>

More about You
<ul>
<li>Degree in Biology, Biotechnology, Molecular Biology, Virology, or a related field</li>
<li>BS degree (or equivalent) with at least 1-2 years of relevant experience preferred</li>
<li>Working experience in gene therapy and/or viral vector biology is preferred</li>
<li>Experience with at least 2 techniques – qPCR, ddPCR, BLI, DLS, and ELISA is desirable</li>
<li>Attention to details is a must</li>
<li>Strong organizational skills</li>
</ul>
Company DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities. 
<h3>Company Description</h3>
Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Research Associate I, Analytics, Gene Therapy

<h3>Job Description</h3>
Job Descriptionjob summary: 
We are seeking an enthusiastic, collaborative Associate Scientist to join our In Vivo Pharmacology Team in the Oncology Therapeutic Area in Thousand Oaks, CA.
 location: Newbury Park, California job type: Contract salary: $29.00 - 33.44 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>In this vital role you will be supporting the group by performing procedures on laboratory rodents such as handling, dosing (via multiple routes), clinical health assessments, and biologic sample collection.</li>
<li>Additional tasks will include assisting with in vivo research models for a variety of programs.</li>
<li>Well-suited applicants will have broad laboratory and rodent training, deep scientific curiosity and a positive approach working in highly dynamic, team-based research environment.</li>
<li>The successful candidate will also be responsible for review and compliance with all applicable SOPs, business practices and company policies.</li>
</ul>
 qualifications: 
Basic Qualifications:
<ul>
<li>Bachelor's degree in related field and 3+ years of laboratory-based research experience in academic or industrial labs.</li>
<li>Experience handling and performing basic manipulations with laboratory rodents.</li>
<li>Highly motivated, collaborative and with excellent attention to detail.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with rodent dosing via multiple routes (oral gavage preferred).</li>
<li>Familiarity with oncology disease models.</li>
<li>Good written and verbal communication skills.</li>
<li>Demonstrated technical aptitude and a strong work ethic.</li>
<li>Organizational and notebook/record keeping skills.</li>
<li>Work effectively in a highly collaborative and dynamic research environment. </li>
<li>Computer literacy, e.g., GraphPad Prism, Excel, PowerPoint and Word.</li>
</ul>
#LI-AO1
 skills: MS-WORD, MS-EXCEL, MS-Powerpoint, GLP (Good Laboratory Practice), Laboratory Information Management Systems (LIMS), LIMS (Laboratory Information Management System 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay 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. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. Qualified applicants in the unincorporated areas of Los Angeles County with criminal histories will be considered for employment in accordance with the Los Angeles County's Fair Chance Ordinance for Employers. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Associate Scientist

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI and San Diego, CA. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
We are seeking a highly skilled computational chemist with Computer-Aided Drug Design (CADD) expertise to join our dynamic team in San Diego, California. In this on-site role, you will apply advanced CADD tools to accelerate the development of targeting ligands and next-generation RNA-based therapeutics. You will work closely with a cross-functional R&amp;D team at the cutting edge of RNA interference (RNAi), where your computational insights will directly impact the development of life-changing therapies.
Responsibilities
<ul>
<li>Perform computational modeling, including molecular dynamics simulations, quantum mechanics calculations, and cheminformatics analyses.</li>
<li>Develop and implement computational workflows to support drug discovery efforts.</li>
<li>Collaborate closely with medicinal chemists, biologists, and multidisciplinary teams to interpret computational results and translate findings into actionable insights.</li>
<li>Design, analyze, and optimize small molecule ligands using structure-based and ligand-based drug design approaches.</li>
<li>Maintain thorough documentation of computational methods, protocols, and results.</li>
<li>Stay updated on emerging computational techniques and apply innovative methods to improve efficiency and accuracy of computational predictions.</li>
</ul>
Requirements:
<ul>
<li>PhD in computational chemistry, Computer-Aided Drug Design, or relevant areas that brings the following set of skills and expertise with 0-5 years of post-graduate experience (industry or post-doctoral experience).</li>
<li>Proficient in structure-/ligand-based drug design, including molecular docking, virtual screening, QSAR, homology modeling, molecular dynamics, and quantum mechanics, etc., and master the relevant tools, including Schrodinger, MOE, Discovery Studio, etc.</li>
<li>A track record of scientific contributions illustrated by publications and/or patents.</li>
<li>Proficient command of at least one programming language (Python, R, C, C++, etc.).</li>
<li>Excellent problem-solving, communication, and collaborative skills.</li>
</ul>
Preferred:
<ul>
<li>Experience with cloud-based computational platforms.</li>
<li>Familiarity with machine learning and AI methods in drug discovery.</li>
<li>Strong publication record in computational chemistry or related fields.</li>
</ul>
California pay range $125,000—$150,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

5,251 Science Jobs