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<h3>Job Description</h3>
Job Description
Title: Scientist – Night Shift
Location: San Jose CA 95134
Duration: 09/29/2025 to 12/31/2025
We are seeking a Microbiologist with experience in Research and Development to work evenings (2:30pm to 11:00pm) Wednesday, Thursday and Friday and AM shift (10:00am to 7:00pm) Saturday and Sunday. You will be a key contributor and critical to the success of the company.
Position Summary:
· As part of the Microbiology team, you will be responsible for designing, documenting, and testing both instruments and consumables to support the company’s product lines. You will be responsible for executing protocols and writing reports.
· As part of the Microbiology team, you will help build up toward the commercial readiness of our products and will execute laboratory functions.
Primary Duties 
· Perform microbiological testing to support ongoing study protocols as well as testing of new instruments, AST panels, and consumables.
· Daily data analysis for completed assays.
· Perform initial inspection of incoming consumables.
· Process biological specimen samples using aseptic techniques and lab safety protocols.
· Coordinating with other teams and departments
· Create and present reports on conducted experiments, and failure investigations.
· Participation in regular lab operations included running experiments, maintenance, cleaning, and routine tests.
· Perform other duties and projects related to lab and department operations as requested by management.
Experience:
· Minimum time and type experience required for this position.
· A Bachelor’s Degree is required.
· Perform microbiological testing to support ongoing study protocols as well as testing of new instruments, AST panels, and consumables.
· Daily data analysis for completed assays.
· Perform initial inspection of incoming consumables.
· Process biological specimen samples using aseptic techniques and lab safety protocols.
· Coordinating with other teams and departments
· Create and present reports on conducted experiments, and failure investigations.
· Participation in regular lab operations included running experiments, maintenance, cleaning, and routine tests.
· Perform other duties and projects related to lab and department operations as requested by management.
Knowledge, Skills, and Abilities:
· Knowledge, special skills, and/or abilities required to perform the job functions (e.g., negotiation, technical writing, statistical evaluation).
· Knowledge of aseptic techniques, good documentation practices (GDP), and good laboratory practices (GLP).
· Proficiency using Microsoft Office applications (Word, Excel, PowerPoint).
· Strong focus and attention to detail, with the ability to prioritize accuracy while following best practices in a fast-paced industrial laboratory environment.
· Must be flexible and able to adapt to changes in task priority and able to work under time constraints.
· Good organizational skills, communication, teamwork, and troubleshooting skills.
· Excellent communication skills and ability to work independently (after training) to complete assigned tasks
· Knowledge of ISO 9001 and FDA Quality System Regulations is advantageous.
Working Conditions and Physical Requirements:
· Ability to remain in stationary position, often standing, for prolonged periods.
· Ability to ascend/descend stairs, ladders, ramps, and the like.
· Ability to wear PPE correctly most of the day.
· Ability to operate heavy machinery.
· Ability to adjust or move objects up to 50 pounds in all directions.
Lifting (up to 50 lbs) laboratory equipment and supplies and moving containers of various materials.
· Work involves performing computer applications and standing for extended periods of time.
· May be exposed to and require the handling of antibiotics and other hazardous materials.
· May be exposed and require the handling of body fluids and potentially infectious biohazardous materials.
· May be exposed to odors incurred during media preparation and frozen panel production.
· Lab work is performed wearing safety glasses and lab coat and following standard BSL2 safety guidelines. Excellent personal hygiene required.
Reasonable, reliable attendance and punctuality is an essential job function required for this position.
Company DescriptionWe believe in service that helps you solve a problem, move forward with a project, manage a difficult situation, or simply check something off your list. 
<h3>Company Description</h3>
We believe in service that helps you solve a problem, move forward with a project, manage a difficult situation, or simply check something off your list.

Microbiologist

<h3>Job Description</h3>
About the Company
Unnatural Products (UNP) is a growing discovery-stage biotech company pioneering macrocyclic peptide drug discovery. Our goal is to unlock the full therapeutic potential of macrocycles by bringing small molecule-like behavior to molecules with high target affinity - unlocking undruggable targets and enabling oral delivery to targets traditionally only addressable with injectable modalities.
 
Based in Santa Cruz, CA, we are a passionate team of scientists and operators doing high-quality science in a beautiful setting—where innovation and work-life balance go hand in hand. Come shape the future of UNP with us!
 
The Role 
We are looking for a Senior Scientist, Peptide Chemistry that can apply contemporary medicinal chemistry strategies and new methodologies to advance our macrocyclic peptide pipeline and discovery platform as we define and create next generation bRo5 drugs. This will require deep medicinal chemistry experience to navigate the lead optimization process and expedite development of preclinical candidates. Ideal candidates will be able to work cross functionally within our organization – they will interact daily with our data science and computational group for interpretation and design, our biology and pharmacology group to develop assay workflows for in vivo translation, and our chemistry group to push the boundaries of what is possible with parallel chemistry and library syntheses.
 
What You’ll Do 
<ul>
<li>Lead major projects in the lab with significant scientific impact</li>
<li>Work closely with program leadership to spearhead projects driving drug discovery for one of our pipeline programs</li>
<li>Propose research plans, identify issues, and overcome scientific challenges to advance project goals within specified timelines</li>
<li>Collaborate with other medicinal chemists to interpret SAR, develop hypotheses, generate, and design molecules to deliver high quality chemical matter</li>
<li>Directly manage external CRO work and priorities while providing regular progress updates to internal team members</li>
<li>Mentor junior colleagues in medicinal chemistry principles and best practices, synthetic activity prioritization, and time management</li>
<li>Lead synthetic route development both from a theoretical and practical standpoint and troubleshoot issues when necessary</li>
<li>Work closely with the biology, software, and de-novo teams to coordinate research activities and execute against project goals</li>
<li>Communicate results to internal teams and managers in the form of presentations, reports, and ad-hoc meetings/calls</li>
<li>Contribute to and guide further development of UNP’s proprietary parallel synthetic platform</li>
</ul>
 
Required Knowledge, Skills and Abilities
<ul>
<li>Ph.D. in Chemistry or related field, with 6+ years of relevant industry experience</li>
<li>Proven industry track record and expertise in peptide synthesis and medicinal chemistry as evinced by publications, patents, and/or case studies from prior work</li>
<li>Experience with peptide design, including SAR studies and scaffold optimization</li>
<li>Experience with analytical methods, including HPLC/LC-MS</li>
<li>Demonstrated experience with the drug discovery process including hit identification, hit-to-lead, and lead optimization</li>
<li>Significant experience with structure based drug design and all medicinal chemistry principles</li>
<li>Strong oral and written communication skills and ability to deliver clear and concise presentations of data and interpretations</li>
<li>Highly self-motivated and proactive when it comes to identifying and solving problems and helping team members</li>
<li>Accountable, meticulous with attention to detail, and able to multitask</li>
<li>Must be willing to work onsite 5 days per week</li>
</ul>
 
Additional experience preferred: 
<ul>
<li>Experience managing or mentoring junior colleagues</li>
<li>Previous CRO management experience</li>
<li>Prior experience with bRo5 drug design (macrocycles, PROTACs, large small molecules, etc)</li>
</ul>
 
 
Why Join Us?
You will have to have an opportunity to help shape the future of a company on the rise. As a Senior Scientist, Peptide Medicinal Chemistry you will have the ability to help define and shape the next generation of peptide drugs. We value integrity, transparency, curiosity, and a collaborative spirit. If you are passionate about peptide medchem and are highly self-motivated, we’d love to talk.
 
The salary range for the Senior Scientist, Peptide Medicinal Chemistry position is $150,000 to $188,000. Title and compensation will be competitive and commensurate with the candidate's career experience, qualifications, and the responsibilities of the position.
 
We are proud to be an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees and applicants and welcome individuals of all backgrounds, experiences, and perspectives. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability status, or any other status protected by law.

Senior Scientist, Peptide Medicinal Chemistry

<h3>Job Description</h3>
Scientist I, Protein Chemistry
W2 Contract-to-Hire
Salary Range: $124,800 - $145,600 per year
Location: Redwood City, CA - Onsite Role
Job Summary:
We are seeking an experienced and creative protein biochemist to support our in-house protein chemistry team within the Structural Biology group. They will be responsible for purifying and characterizing small-molecule protein targets to support screening pipelines, biophysical studies, and structural biology. The ideal candidate will have a strong track record of leveraging internal and external resources to produce high-quality proteins of therapeutic interest to support downstream in vitro assays and structural biology efforts. This role will report to the principal scientist leading protein chemistry and will have responsibility and visibility across the early discovery pipeline. This is an excellent opportunity for an experienced individual looking to work in a fast-paced, dynamic biotech environment. The candidate will have a range of responsibilities detailed below.
 
Duties and Responsibilities:
<ul>
<li>Expertise in all steps of the gene-to-protein process. Experienced in the generation of high-quality recombinant proteins that are well characterized using biophysical and biochemical techniques.</li>
<li>Perform expression, purification (with and without affinity tags), and characterization of challenging targets to establish robust protocols that can be used internally or transferred to external (CRO) resources as needed. Ability to evaluate and establish protocols transferred in from external resources.</li>
<li>Develop robust and reproducible biochemical and biophysical assays to characterize enzymatic activity, protein stability, protein-protein interaction, etc.</li>
<li>Support protein chemistry by exploring new technologies, contributing to long-term activity planning and budgets, and maintaining modern instrumentation in the laboratory.</li>
<li>Communicate experimental design, results, and timelines to cross-functional teams.</li>
<li>Generate high-quality, reproducible data. Analyze and interpret data, keep organized and detailed records. Communicate findings to cross functional team members.</li>
<li>Partner and integrate with multidisciplinary, highly collaborative discovery teams to design, optimize, and produce reagents that play a critical role in structure-based drug design and screening</li>
</ul>
 
Requirements and Qualifications:
<ul>
<li>Ph.D. degree, MS +5, BS +7 years experience (or equivalent) in biochemistry, structural biology, or related discipline, and biopharmaceutical experience are a plus.</li>
<li>Expertise with the expression of proteins and protein complexes using multiple host systems (e.g., mammalian, insect, bacterial).</li>
<li>Expert in designing and optimizing DNA constructs for the expression and purification of challenging targets.</li>
<li>Expert in protein purification using AKTA and multiple chromatography techniques (e.g., affinity, IEX, SEC, HIC).</li>
<li>Extensive protein biochemistry experience working with challenging proteins and multi-protein complexes.</li>
<li>Knowledge of protein structure and experience in the preparation of high-quality protein samples for assay (e.g., BLI, SPR, DEL, TR-FRET), biophysical (e.g., ITC, DSF, MALS, SLS, DLS, CD, anSEC, thermal melt, LC-MS), and structural studies (e.g., NMR, X-ray crystallography, Cryo-EM).</li>
<li>Creative and capable of developing new techniques and methods to drive science forward.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to develop and optimize written protocols and document research progress.</li>
<li>Conscientious team player interested in a fast-paced biotech environment.</li>
<li>Demonstrated willingness to learn and improve processes.</li>
</ul>
 
Preferred Qualifications:
<ul>
<li>Experience with mass spectrometry and sample preparation is desired.</li>
<li>Experience balancing CRO and internal resources to solve problems and drive progress is beneficial.</li>
<li>Clear examples of establishing new technologies to increase throughput in protein expression/purification.</li>
<li>Demonstrated collaborations with Structural Biology and/or Assay groups through publications and/or patents.</li>
<li>Experience with protein-protein complexes, including antibodies/Fabs, molecular glues, PROTACs, etc., is highly desirable.</li>
</ul>
 
Desired Skills and Experience
protein biochemistry, protein purification, recombinant protein expression, protein characterization, biophysical techniques, biochemical techniques, gene-to-protein process, mammalian expression systems, insect cell expression, bacterial expression systems, DNA construct design, AKTA chromatography, affinity chromatography, ion exchange chromatography, size exclusion chromatography, hydrophobic interaction chromatography, protein complexes, multi-protein complexes, enzymatic activity assays, protein stability assays, protein-protein interaction assays, BLI, SPR, DEL screening, TR-FRET, ITC, DSF, MALS, static light scattering, dynamic light scattering, circular dichroism, analytical SEC, thermal melt analysis, LC-MS, mass spectrometry, sample preparation, NMR, X-ray crystallography, Cryo-EM, structural biology, structure-based drug design, high-throughput screening, protocol development, protocol optimization, CRO management, technology implementation, laboratory instrumentation, data analysis, experimental design, cross-functional collaboration, antibody purification, Fab fragments, molecular glues, PROTACs, therapeutic protein targets, biopharmaceutical experience
 
 
Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate.
 
Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at <a href="http://www.baysidesolutions.com" target="_blank">www.baysidesolutions.com</a>.

Scientist I, Protein Chemistry

<h3>Job Description</h3>
Job DescriptionJob Title:&nbsp;Research scientist (Robotics, AI) Position Type: Full time Location: Santa Clara, CA, USA Salary Range:&nbsp;$150,000 - $230, 000 (USD) Job ID#: 158284​​​​​​​ Job Description:
We are looking for a creative, skilled, and motivated research scientists to join our team in advancing robot manipulation capabilities. We are looking for people with proven expertise in machine learning and/or robotics. You will collaborate with a team of talented researchers and engineers, and drive ongoing innovation and technological advancements within the company. This is a full-time on-site role in Santa Clara, CA.
Responsibilities
<ul>
<li>
Develop new algorithms and methods for training AI models for enhancing the robot dexterity.
</li>
<li>
Conduct cutting edge research across multiple disciplines (Robotics, RL/IL, control, perception, LLM, VLM, etc.).
</li>
<li>
Work with large-scale ML systems and large-scale model training/fine-tuning.
</li>
<li>
Design and implement state-of-the-art learning-based manipulation/navigation/control algorithms on real robots.
</li>
<li>
Work with other teams to develop a diverse set of robust manipulation skills for robots.
</li>
</ul>
Requirements:
<ul>
<li>
Ph.D. degree in Robotics, Computer Science/Engineering, Electrical Engineering, Mechanical Engineering, etc., or equivalent research experience.
</li>
<li>
Passionate about working with robots and building robot products.
</li>
<li>
Excellent analytical, problem-solving, and communication skills.
</li>
<li>
At least 3 years of experience conducting independent research.
</li>
<li>
Deep understanding of the SOTA robot learning techniques (reinforcement learning, imitation learning, etc.)
</li>
<li>
A track record of research excellence with your work published in top conferences and journals such as Science Robotics, IJRR, RSS, CoRL, ICRA, NeurIPS, ICML, ICLR, CVPR, etc.
</li>
<li>
Proficient with Python.
</li>
<li>
Proficient with deep learning libraries such as PyTorch/TensorFlow/Jax.
</li>
<li>
Experience with real robot experiments.
</li>
<li>
Experienced with robot simulators such as Isaac Gym/ Isaac Sim/ SAPIEN/ MuJoCo/Drake, etc.
</li>
</ul>
About Us: Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU. IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at <a href="https://intelliprogroup.com/" target="_blank">https://intelliprogroup.com/</a>. Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.
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Research scientist (Robotics, AI)

<h3>Job Description</h3>
QC Associate Scientist
 
We are seeking a motivated and detail-oriented professional with experience in cell and molecular biology, including iPSC-related research. This hands-on role offers broad exposure to diverse products and testing methods within personalized medicine, regenerative medicine, and cell and gene therapy. It’s an excellent opportunity for someone who thrives in a dynamic, client-focused environment.
 
Responsibilities:
<ul>
<li>Perform QC testing for products according to established quality control procedures</li>
<li>Conduct QC testing on deliverables arising from pre-clinical services as specified in Statements of Work (SOWs)</li>
<li>Perform QC testing of in-licensed products and OEM product evaluations as needed</li>
<li>Ensure all test data is accurate, complete, and compliant with GLP, applicable standards, and project timelines</li>
<li>Prepare and maintain laboratory documentation including test records, notebooks, equipment logs, and certificates of analysis (COAs)</li>
<li>Collaborate with cross-functional teams (QA, Manufacturing, Service, Sales) to ensure timely testing, batch release, and issue resolution</li>
<li>Support post-sale activities and transfer activities in collaboration with manufacturing or service teams</li>
<li>Perform other duties as necessary to meet the evolving needs of the organization</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor’s degree with 4+ years, or Master’s degree with 2+ years of experience in Cell Biology, Biochemistry, Microbiology, or a related scientific field</li>
<li>Hands-on experience culturing primary cells, iPSCs, and iPSC-derived cell types</li>
<li>Expertise in immunostaining, flow cytometry, mycoplasma testing, and luminescence-based assays for cell characterization and quality control</li>
<li>2+ years of QC laboratory experience in a GLP environment (preferred)</li>
<li>Excellent documentation, organizational, and problem-solving skills</li>
<li>Ability to manage multiple priorities and client expectations in a fast-paced setting</li>
<li>Comfortable working in a lean team with broad responsibilities and a proactive mindset</li>
</ul>
 
Pay Rate:
<ul>
<li>$33-40/hr</li>
</ul>

QC Associate Scientist

<h3>Job Description</h3>
We are working with a team at the forefront of reproductive biology, developing human eggs from stem cells (iPSCs) to transform fertility, reproductive health, and genetic diversity—powered by expertise in stem cell, developmental, and synthetic biology.
 
The Role
We’re looking for a scientist with deep expertise in transcription factor and gene network–guided cell fate engineering to lead a critical new initiative.
 
You’ll be responsible for designing and executing RNA- and TF-based strategies to accelerate iPSC differentiation into germline fates. This means driving transcription factor–guided differentiation projects, developing RNA-based gene perturbation approaches, and shaping the strategy that defines this program.
 
This is a high-impact leadership role: you’ll begin hands-on in the lab with a small team, then quickly expand into managing direct reports and building a broader program. We want someone who thrives in a fast-moving, startup-like environment, is comfortable taking ownership, and is motivated to deliver rigorous results that make a real-world impact.
 
Responsibilities
<ul>
<li>Design and lead transcription factor and gene perturbation projects, with emphasis on RNA-based, non-integrative strategies.</li>
<li>Develop a company strategy for applying a clinically viable gene perturbation approach to speed up differentiation across multiple areas of our existing pipeline.</li>
<li>Build, manage, and mentor a small team of scientists and research associates.</li>
<li>Drive innovation in non-integrative gene expression systems (mRNA, circRNA, CRISPRa/dCas9), especially adapting these technologies to high-throughput screens.</li>
<li>Develop and apply high-throughput pooled TF/gene screening approaches (e.g., TFome, ORF libraries) as implicated by scientific strategy.</li>
<li>Integrate machine learning–guided or computational pipelines (e.g., ATAC-seq, DNase-seq, RNA-seq–driven predictions) with experimental design.</li>
</ul>
 
Qualifications
Required:
<ul>
<li>PhD in Synthetic Biology, Developmental Biology, Stem Cell Biology, RNA Biology, or related field.</li>
<li>Strong publication record demonstrating impact in cell fate engineering, stem cell or developmental biology, transcription factor biology, or RNA biology.</li>
<li>Hands-on expertise with transcription factor–guided differentiation and gene perturbation approaches.</li>
<li>Experience designing and executing high-throughput genetic, ideally RNA-based screens.</li>
<li>Expertise with non-integrative gene modulation tools (mRNA, circRNA, dCAS/CRISPRa systems).</li>
<li>Familiarity with computational and/or machine learning approaches for TF or target discovery (via direct work or collaborations). Ideal if you have spearheaded initiatives to mine data yourself for target overexpression candidates or developed new computational tools to do so.</li>
<li>Demonstrated leadership in academia (e.g., leading large collaborations) or biotech (e.g., managing small teams).</li>
<li>Desire to thrive in a fast-paced, high-ownership startup environment.</li>
</ul>
 
Preferred:
<ul>
<li>Experience with pooled ORF/TFome libraries, combinatorial TF perturbation, or barcoded screening workflows.</li>
<li>Experience integrating chromatin accessibility data (ATAC-seq, DNase-seq) or transcriptomics into TF discovery.</li>
<li>Prior management of small teams in academia or industry.</li>
</ul>

(Sr Sci) Principal Scientist, Gene Perturbation & Cell Fate

<h3>Job Description</h3>
Job Description
Job Summary
The company. is a geotechnical services company with over 60 years of combined engineering experience in residential and commercial projects. We are located in San Jose and Walnut creek, California and proudly serve theentire Bay Area.
We are seeking a skilled and detail-oriented Geotechnical Engineer to join our team. The ideal candidate will be responsible for analyzing data, and providing recommendations for residential projects.
Conduct geotechnical investigations and assessments for residential projects.
Analyze soil samples and test results to determine material properties and suitability.
Prepare detailed reports that include recomendationsfor foundation design, slope stability, earthwork, and site preprationsand technical documentation outlining findings and recommendations.
Recommend a foundation appropriate for the site conditions,
Identify potential geotechnicalhazars such assoil setlements, landslides or liquifaction.
Requirements
Bachelor's degree in Geotechnical Engineering; Master's degree preferred.
Proven experience in geotechnical engineering or a similar role.
Strong report writing and communication.
Ability to work independently as well as part of a multidisciplinary team.
Job Type: Full-time
Benefits:
Health insurance
Paid time off
Work Location: In person
Company DescriptionW3Global was established in 2006 in Fremont, CA with a vision: simplify the recruiting process and develop an industry-disrupting platform to connect candidates with clients. Our cutting-edge Applicant Tracking System enables us to find the right person for the right job, creating value for job seekers and employers. While W3Global initially focused on IT staffing, we have expanded the business to serve many other industries, including accounting and finance, legal, engineering, human resources, government and more. We’re proud of the investments we’ve made in our team, having grown from four to 1000 employees and evolving into one of the leading recruitment and staffing solution providers in the industry. Our recruiters and account managers are passionate about connecting qualified professionals with the right positions in small, medium, and large companies. Our Services W3Global understands the natural ups and downs of an organization’s staffing needs. We are continuously adapting to industry and economic changes to find the right candidates. We specialize in placing permanent, direct, contract, and temporary positions for companies of any size. Our recruiting services include sourcing, recruiting, screening, interview management, salary negotiations, training, and onboarding. We are committed to helping organizations redefine their recruitment process by delivering our SaaS-based proprietary application tracking system software. Our Expertise W3Global has been delivering staffing solutions for nearly two decades; we know which recruiting strategies work best. Our expert team is committed to developing a customized solution to fit your company’s unique needs. As a W3Global client, you’ll also receive personalized assistance from a seasoned team of staffing specialists. We are committed to providing both technical support and industry expertise to simplify the hiring process. We know that your time matters. W3Global will help you streamline the hiring process, getting it done and getting it right. 
<h3>Company Description</h3>
W3Global was established in 2006 in Fremont, CA with a vision: simplify the recruiting process and develop an industry-disrupting platform to connect candidates with clients. Our cutting-edge Applicant Tracking System enables us to find the right person for the right job, creating value for job seekers and employers. While W3Global initially focused on IT staffing, we have expanded the business to serve many other industries, including accounting and finance, legal, engineering, human resources, government and more.\r\n\r\nWe’re proud of the investments we’ve made in our team, having grown from four to 1000 employees and evolving into one of the leading recruitment and staffing solution providers in the industry. Our recruiters and account managers are passionate about connecting qualified professionals with the right positions in small, medium, and large companies.\r\n\r\nOur Services\r\nW3Global understands the natural ups and downs of an organization’s staffing needs. We are continuously adapting to industry and economic changes to find the right candidates.\r\n\r\nWe specialize in placing permanent, direct, contract, and temporary positions for companies of any size. Our recruiting services include sourcing, recruiting, screening, interview management, salary negotiations, training, and onboarding.\r\n\r\nWe are committed to helping organizations redefine their recruitment process by delivering our SaaS-based proprietary application tracking system software.\r\n\r\nOur Expertise\r\nW3Global has been delivering staffing solutions for nearly two decades; we know which recruiting strategies work best. Our expert team is committed to developing a customized solution to fit your company’s unique needs.\r\n\r\nAs a W3Global client, you’ll also receive personalized assistance from a seasoned team of staffing specialists. We are committed to providing both technical support and industry expertise to simplify the hiring process. We know that your time matters. W3Global will help you streamline the hiring process, getting it done and getting it right.

Geotechnical Engineer

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate
Job Description
We are seeking a dedicated Research Associate to join a dynamic team, working primarily on bench-based molecular biology techniques. This role involves performing DNA extractions from blood, conducting PCR and sequencing (including n-point PCR or r-PCR), and applying aseptic techniques. The ideal candidate will follow standard operating procedures meticulously and document their work with precision. This position offers opportunities to learn and apply molecular techniques in an automated process and to work collaboratively within a specialized biotech team.
Responsibilities
<ul>
<li>Perform DNA extractions from blood samples using aseptic techniques.</li>
<li>Conduct PCR and sequencing procedures, including n-point PCR or r-PCR.</li>
<li>Follow and document standard operating procedures (SOPs) accurately.</li>
<li>Create and manage bench controls, performing tasks that may vary in time commitment from half a day to two weeks.</li>
<li>Collaborate with the platform integration team and cross-functional teams during different project stages.</li>
<li>Solve problems effectively and communicate efficiently within the team.</li>
<li>Adapt to repetitive tasks while maintaining high performance and delivering quality bench controls.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in GLP, PCR, DNA extraction, and aseptic techniques.</li>
<li>Experience with nucleic acid techniques, including purification and quantification.</li>
<li>Familiarity with molecular biology, including sample preparation using magnetic particles.</li>
<li>Competency in data interpretation and analysis.</li>
<li>Experience with standard laboratory techniques in a BSL-2 environment is a plus.</li>
<li>Ability to work with human blood samples.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Molecular Biology, Biochemistry, Microbiology, Chemistry, or Immunology with 1.5 to 3 years of relevant experience.</li>
<li>Proficiency in Microsoft Office Suite (MS Word, Excel, PowerPoint).</li>
<li>Ability to contribute to a team-oriented environment with strong interpersonal skills.</li>
</ul>
Work Environment
This position is part of a seven-member integration team within a larger group of 17 professionals. The role is predominantly lab-based, requiring 90% of work time on bench tasks. The work schedule is flexible with an 8am-5pm timeframe, with a preference for earlier starts. The company culture is supportive, fostering a kind and personable atmosphere, and accommodating flexible work needs.
Pay and Benefits
The pay range for this position is $26.00 - $33.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in CARLSBAD,CA.
Application Deadline
This position is anticipated to close on Oct 3, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Research Associate

<h3>Job Description</h3>
Job Description
Duties:
<ul>
<li>Develop,&nbsp;qualify/validate&nbsp;AAV&nbsp;gene&nbsp;therapy&nbsp;cell-based&nbsp;biological&nbsp;potency&nbsp;assays,&nbsp;protein&nbsp;chemistry&nbsp;assays,&nbsp;and&nbsp;molecular&nbsp;biology&nbsp;assays&nbsp;for&nbsp;process&nbsp;monitoring&nbsp;and&nbsp;drug&nbsp;product&nbsp;release,&nbsp;specifically&nbsp;SDS-PAGE,&nbsp;western&nbsp;blot,&nbsp;droplet&nbsp;digital&nbsp;PCR&nbsp;or&nbsp;qPCR,&nbsp;culture&nbsp;of&nbsp;primary&nbsp;mammalian&nbsp;cells,&nbsp;and&nbsp;cell&nbsp;based&nbsp;potency&nbsp;assays.</li>
<li>Participate&nbsp;in&nbsp;developing&nbsp;timelines,&nbsp;protocols&nbsp;and&nbsp;reports&nbsp;for&nbsp;assay&nbsp;transfers,&nbsp;qualifications&nbsp;/&nbsp;validations.</li>
<li>Contribute&nbsp;to&nbsp;establishing&nbsp;material&nbsp;specifications&nbsp;for&nbsp;drug&nbsp;substance&nbsp;and&nbsp;drug&nbsp;products</li>
<li>Author&nbsp;and&nbsp;review&nbsp;QC&nbsp;analytical&nbsp;SOPs,&nbsp;protocols,&nbsp;and&nbsp;reports&nbsp;as&nbsp;needed</li>
<li>Ensure&nbsp;the&nbsp;timely&nbsp;execution&nbsp;of&nbsp;all&nbsp;routine&nbsp;QC&nbsp;testing,&nbsp;data&nbsp;review,&nbsp;and&nbsp;preparation&nbsp;of&nbsp;summary&nbsp;reports</li>
<li>Perform&nbsp;quality&nbsp;management&nbsp;activities&nbsp;such&nbsp;as&nbsp;deviation,&nbsp;CAPA,&nbsp;change&nbsp;control,&nbsp;investigation&nbsp;of&nbsp;OOS,&nbsp;OOT&nbsp;and&nbsp;anomalous&nbsp;results&nbsp;within&nbsp;the&nbsp;company&nbsp;QMS&nbsp;according&nbsp;to&nbsp;established&nbsp;procedures.</li>
</ul>
Qualifications:
<ul>
<li>BS&nbsp;or&nbsp;equivalent&nbsp;in&nbsp;relevant&nbsp;discipline&nbsp;with&nbsp;a&nbsp;minimum&nbsp;of&nbsp;2-5&nbsp;years&nbsp;of&nbsp;relevant&nbsp;industry&nbsp;experience&nbsp;or&nbsp;Master’s&nbsp;degree&nbsp;in&nbsp;relevant&nbsp;discipline&nbsp;with&nbsp;a&nbsp;minimum&nbsp;of&nbsp;0-1&nbsp;years&nbsp;of&nbsp;relevant&nbsp;industry&nbsp;experience</li>
<li>Experience&nbsp;in&nbsp;pharmaceutical&nbsp;industry&nbsp;with&nbsp;a&nbsp;GMP&nbsp;testing&nbsp;focus,&nbsp;ideally&nbsp;covering&nbsp;the&nbsp;analytical&nbsp;method&nbsp;and&nbsp;testing&nbsp;lifecycle&nbsp;from&nbsp;development&nbsp;through&nbsp;commercial&nbsp;drug&nbsp;product&nbsp;testing,&nbsp;with&nbsp;experience&nbsp;in&nbsp;a&nbsp;GMP&nbsp;QC&nbsp;release&nbsp;testing&nbsp;role</li>
<li>Experience&nbsp;in&nbsp;optimizing&nbsp;methods&nbsp;with&nbsp;particular&nbsp;emphasis&nbsp;on&nbsp;cell-based&nbsp;potency&nbsp;assay,&nbsp;molecular&nbsp;biology&nbsp;assay,&nbsp;and&nbsp;protein&nbsp;chemistry&nbsp;assays</li>
<li>Significant&nbsp;experience&nbsp;in&nbsp;an&nbsp;FDA-regulated&nbsp;environment</li>
</ul>
Why&nbsp;Choose&nbsp;R&amp;D&nbsp;Partners?
As&nbsp;an&nbsp;employee,&nbsp;you&nbsp;have&nbsp;access&nbsp;to&nbsp;a&nbsp;comprehensive&nbsp;benefits&nbsp;package&nbsp;including:
<ul>
<li>Medical&nbsp;insurance&nbsp;–&nbsp;PPO,&nbsp;HMO&nbsp;&amp;&nbsp;HSA</li>
<li>Dental&nbsp;&amp;&nbsp;Vision&nbsp;insurance</li>
<li>401k&nbsp;plan</li>
<li>Employee&nbsp;Assistance&nbsp;Program</li>
<li>Long-term&nbsp;disability</li>
<li>Weekly&nbsp;payroll</li>
<li>Expense&nbsp;reimbursement</li>
<li>Online&nbsp;timecard&nbsp;approval</li>
</ul>
Pay&nbsp;Scale:
$124,000&nbsp;-&nbsp;$144,000&nbsp;(Dependent&nbsp;on&nbsp;Experience)
R&amp;D&nbsp;Partners&nbsp;is&nbsp;a&nbsp;global&nbsp;functional&nbsp;service&nbsp;provider&nbsp;and&nbsp;strategic&nbsp;staffing&nbsp;resource&nbsp;specializing&nbsp;in&nbsp;scientific,&nbsp;clinical&nbsp;research&nbsp;&amp;&nbsp;engineering.&nbsp;We&nbsp;provide&nbsp;job&nbsp;opportunities&nbsp;within&nbsp;major&nbsp;pharmaceutical,&nbsp;biopharmaceutical,&nbsp;biotechnology,&nbsp;and&nbsp;medical&nbsp;device&nbsp;companies.
R&amp;D&nbsp;Partners&nbsp;is&nbsp;an&nbsp;equal-opportunity&nbsp;employer.
Company DescriptionR&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities. 
<h3>Company Description</h3>
R&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

Sr. QC Research Associate

<h3>Job Description</h3>
We are seeking an experienced analytical chemist with expertise in the development and implementation of analytical methods for the identification, quantification, and characterization of small organic molecules and metabolites produced during microbial cell fermentation. This role will require a deep understanding of analytical chemistry method development, validation, and analysis. The analytical team performs routine analyses as well as identification of unknown compounds. This scientist should be able to develop and implement high-throughput screening methods for analyzing large libraries of samples. Experience with precision fermentation sample preparation and product analysis in complex matrices is highly desirable. This position will act as a group leader to manage a small team of scientists to support numerous programs within the company. We want team members with a natural inclination to challenge and work within a culture that is dynamic and self-directed.
NOTE: For all positions posted by Cellibre, education is listed as required but can be overcome with experience. Please do not let education requirements dissuade you from applying for positions for which you think you are qualified on that metric.
Key Responsibilities
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Manage and oversee the analytical chemistry lab and its personnel
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Develop and implement analytical methods as needed for new projects using a wide range of techniques, including but not limited to HPLC, LCMS, GC, GCMS, and NMR
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Maintain equipment and perform repairs as needed for maximum uptime
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Coach and train other scientists at the company in sample preparation and analysis workflows
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Collaborate internally to provide deep insights into analytical results 
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Execute technology transfer to external CMOs and partners as needed in scale-up operations
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Prepare and implement SOPs for QA and QC for chemical products
Additional, but not required skills
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with flash chromatography or small molecule purification, preferably at pilot scale or larger
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with analysis of common fermentation byproducts such as sugars, organic acids, amino acids, FAME analysis, residual solvent, and water content
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with structure elucidation of small molecules using MS, NMR, and other methods
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Familiarity with Agilent hardware and software for HPLC and GC instruments
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with screening large sample libraries (&gt;10,000) with UHPLC techniques
 
Required Experience
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;PhD or MSc with at least 3 years of experience, preferably in pharmaceutical or biotech industries
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Expert in method development using HPLC and GC to separate, quantify, and characterize organic molecules
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;At least 1 year managing direct reports
●&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Complete understanding of HPLC, GC, and MS instrument operation, troubleshooting and maintenance

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