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<h3>Job Description</h3>
Dynamic start-up medical device firm seeks individual to join its r&amp;d organization. Responsibilities will be broad based, sharing responsibilities with the VP of R&amp;D. This may include overseeing early feasibility study submission and submissions for the European Union. 
This is a hands-on technical management role. The technology consists of implants and catheter delivery systems to treat mitral valve regurgitation. This firm has about 20 employees and is currently conducting clinical trials OUS.

Research And Development Manager

<h3>Job Description</h3>
Job Description
Hygiena provides rapid microbiology diagnostic tests and solutions for mission-critical, time-sensitive processes around the world. Hygiena’s proprietary diagnostic technologies enable customers to; prevent illness and save lives, comply with regulations, protect products and brands, run businesses more effectively. Solutions are sold in a wide range of industries globally, but the core focus is food safety. Headquartered in Camarillo, California and with offices around the world, we are actively looking for talented individuals to help grow the business! 
At Hygiena we believe:
<ul>
<li>In providing the highest quality products &amp; service </li>
<li>Being a leader in innovation </li>
<li>Having a compelling desire to improve and win in the marketplace </li>
<li>In contributing positively not only in the workplace, but in our community and environment! </li>
</ul>
With rapid growth comes opportunity. We are looking for a Laboratory Associate I for our Reagent team to join our team in Camarillo!
The Laboratory Associate – Molecular Diagnostics Reagent position is responsible for reagent solution manufacturing, in-process testing, reagent sample collection for in-process testing, product issue investigation, assisting other departments upon request and collaborating with Research and Development (R&amp;D) and Production to ensure all products meet product specifications. This is a full-time, non-exempt/hourly, position.
Responsibilities:
<ul>
<li>Assist Engineering, Quality and Production during filling process as required. Prepare and deliver reagent solutions to filling rooms in the morning and throughout the day as needed.</li>
<li>Prepare and protect reagent Solutions as required to ensure product integrity and quality from start to finish of the manufacturing process including filling process. Continually checks chemical availability ahead of scheduled manufacturing including availability of other supplies and equipment. Prepare and coordinate the preparation and handling of special equipment required for special medias. Maintain all documentation in order, ensures written information is legible and recorded as part of the manufacturing process as required and required forms are completed as part of the SOP.</li>
<li>Maintain an organized and clean work environment in the working Laboratory and other work areas required for product manufacturing, including the sterilization and cleaning of all equipment. Perform pre-inspection of equipment to ensure equipment is properly clean and has been sterilized, correctly by careful review of sterilization print out. Maintain required equipment in good working order and verifies equipment is calibrated.</li>
<li>Ensure compliance with and/or follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seek guidance as necessary.</li>
<li>Actively support and participate in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Safety Manual and Injury Illness Prevention Program (IIPP).</li>
<li>Carry out all responsibilities in an honest, ethical and professional manner.</li>
<li>Must be able to fulfill essential job function in a consistent state of alertness and safe manner.</li>
<li>Handle various other duties as delegated by the Supervisor or Manager</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry or related field, or equivalent education and work experience in a laboratory or manufacturing environment, required.</li>
<li>Recent graduate and/or a minimum of 0-2 years of experience working in a laboratory or manufacturing environment required that includes the following: knowledge of cGMP; aseptic technique</li>
<li>Intermediate knowledge of Microsoft Office (Outlook, Word, Excel, Visio, PowerPoint) and Adobe Acrobat required.</li>
</ul>
Salary Range (applicable to California):
$26.00/ hr. 
Skills/Abilities:
<ul>
<li>Excellent verbal and written communication.</li>
<li>Must be able to use discretion and independent judgement.</li>
<li> Must be able to work in a team environment.</li>
<li>Must be able to pay close attention to details.</li>
<li>Must be able to adapt and adjust to a constant changing environment.</li>
</ul>

Why you’ll want to join our team:
Teamwork as a core value.
At Hygiena, our emphasis on teamwork and cross-functional communication enables us to build stronger bonds within our business.
Be a part of something big.
Hygiena plays a critical role in helping to prevent global health crisis such as foodborne illness, healthcare-associated infections, and other outbreaks.

Giving back to our communities.
Hygiena believes in giving back by supporting local organizations committed to improving the lives of children and youth in our communities.
Benefits and Perks:
<ul>
<li>15 days of PTO &amp; 9 paid company holidays</li>
<li>Medical with HSA employer contribution, Dental, Vision available 1st of the month after start date</li>
<li>Company paid Life Insurance, Short* and Long-Term Disability and an Employee Assistance Program</li>
<li>401(k) with Safe Harbor and Profit-Sharing employer contributions</li>
<li>Tuition Reimbursement program</li>
<li>Charitable Contribution matching</li>
<li>Employee Referral bonus opportunities</li>
</ul>
*State paid short-term disability for California based employees
We are an equal opportunity employer and value diversity. All employment is decided on the basis of qualifications, merit and business need. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Hygiena participates in E-Verify.

Laboratory Associate I

<h3>Job Description</h3>
Job DescriptionSalary: $110,000 - $120,000/year 
Job Overview
BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, and recombinant cell lines for drug discovery. We are seeking an exceptional scientist, with a strong background in enzymology, enzyme kinetics, protein/protein interactions, and fluorescence and luminescence-based assays.
 
We are seeking a highly skilled Senior Scientist I with deep expertise in antibody generation to join our Molecular and Cellular Biology team. This position plays a critical role in driving research and development efforts, with a primary focus on the design, expression, engineering for multiple targets, purification, and optimization of antibodies, including phage display, single B cell isolation, humanization, and stable cell line generation. The ideal candidate will have strong industry experience and be adept at independently designing and executing experiments at a high standard.
 
Responsibilities:
<ul>
<li>Lead and execute projects related to antibody generation, including: 
<ul>
<li>Antibody design and engineering (e.g., humanization, affinity maturation, bispecific antibody)</li>
<li>Molecular cloning and vector design</li>
<li>Transient and stable expression in mammalian system</li>
<li>Antibody purification using affinity chromatography and other techniques</li>
</ul>
</li>
<li>Develop and optimize stable cell lines for antibody production</li>
<li>Utilize fermentation systems for antibody expression (small- to mid-scale)</li>
<li>Evaluate and integrate new technologies to enhance R&amp;D capabilities</li>
<li>Participate in team meetings, project planning, and cross-functional collaborations</li>
</ul>
<ul>
<li>Design and perform cell-based functional assays to characterize antibody activity</li>
<li>Present research findings internally and externally, including at scientific conferences</li>
<li>Maintain rigorous documentation and ensure high standards of data integrity</li>
<li>Maintaining excellent working relationships with partners throughout the company.</li>
<li>Maintaining updated and well-organized lab notebooks.</li>
<li>Other tasks and duties as assigned.</li>
</ul>
Requirements: 
<ul>
<li>A Ph.D. degree in Molecular Biology, Cell Biology required.</li>
<li>Minimum 3 - 5 years industry experience focused on antibody generation required</li>
<li>The candidate must have proven experience performing enzyme kinetics and assay optimization.</li>
<li>Proven track record in antibody discovery and development, including engineering and functional validation</li>
<li>Extensive experience with phage display, mammalian cell culture, sterile technique, and molecular biology methods</li>
<li>Proficiency in downstream processing including protein purification and analytical characterization</li>
<li>Strong problem-solving skills and ability to manage multiple projects in parallel</li>
<li>Excellent written and verbal communication skills</li>
<li>Team-oriented with a collaborative mindset and attention to detail</li>
</ul>
Benefits!
<ul>
<li>401k with 4% company match</li>
<li>Medical/Dental/Vision health insurance plans</li>
<li>Vacation and paid holidays</li>
<li>Companywide lunches provided quarterly</li>
</ul>
 
BPS Bioscience is an equal opportunity employer, without regard to race, color, religion, age, gender, sexual orientation, disability, or any other characteristic protected by applicable law.

Sr. Scientist I, Molecular and Cellular Biology

<h3>Job Description</h3>
Job Description
We are currently seeking a Research Associate III, Cell Line Development for a prominent Pharmaceutical client of ours. This position is in Oceanside, CA. Details for the position are as follows:
Job Description:
<ul>
<li>Pay: 53.00-56.00/hr.</li>
<li>Length of Assignment: 1 year to start with potential for extension.</li>
<li>Working hours: Mon-Fri, 8:30am-5pm or 8:00am-5pm type of business hours; occasional weekend hours (will have notice).</li>
<li>Seeking a highly motivated, team-oriented individual to design and execute experiments to support cell culture and clone development for our rapidly growing biologics pipeline.</li>
<li>Must have cell line development experience.</li>
<li>Participate in end-to-end Cell Line Development pipeline projects, including activities from vector design and construction to clonal cell lines ready for Master Cell Bank generation.</li>
<li>Support CLD activities including clone selection, technology development, media development, process optimization, and process characterization studies.</li>
<li>Support process improvements for increased speed and efficiency to generate highly productive, high quality, robust cell lines that meet all regulatory requirements with high quality documentation.</li>
<li>Hands-on laboratory operations such as molecular biology, shake flask, bench scale bioreactor and Client culture platforms.</li>
<li>Experience with mammalian cell culture (CHO) and automation/high-throughput technologies for mammalian cell line generation and process optimization preferred.</li>
</ul>
Company DescriptionThe Fountain Group is a nationwide staffing firm with over 80 Fortune 100-500 clients. Since 2001, TFG has maintained a consistent standard of excellence, and our work is broadly recognized every year through numerous industry performance awards. Our success is a team effort. Browse our website below for additional information on our company. The Fountain Group “We work in Life Sciences, Clinical, Engineering, IT, and more. Above all, we specialize in people.” 
<h3>Company Description</h3>
The Fountain Group is a nationwide staffing firm with over 80 Fortune 100-500 clients. Since 2001, TFG has maintained a consistent standard of excellence, and our work is broadly recognized every year through numerous industry performance awards. Our success is a team effort.\r\n\r\nBrowse our website below for additional information on our company.\r\n\r\nThe Fountain Group\r\n\r\n“We work in Life Sciences, Clinical, Engineering, IT, and more. Above all, we specialize in people.”

Research Associate III, Cell Line Development

<h3>Job Description</h3>
Job Description
About the Company
We envision a world where we continuously, sustainably, and affordably improve human life with synthetic biology. Our proprietary set of enzymes and our manufacturing approach enables the production of thousands of amino acids that were previously too difficult and expensive to make. These "noncanonical" amino acids that we make are already catalyzing the creation of revolutionary and innovative products that are good for people and the planet. 
Our technology outperforms traditional manufacturing approaches by 10–100x across the board. We already sell products to Big 10 Pharmaceutical companies, and our product family includes the key components of multi-billion dollar blockbuster drugs such as Ozempic and Mounjaro.
We are a diverse, passionate, interdisciplinary team that finds joy in building something new that leaves the world better than we found it. We strive to always learn and improve and have a deep desire to capitalize on our creativity and be exceptional at what we do.
About the role
Aralez Bio is seeking an experienced problem-solver in fermentation and protein purification to join the enzyme production team. This team makes the enzymes used to manufacture our innovative line of noncanonical amino acids (ncAAs), which are produced for peptide R&amp;D pipeline drug discovery and commercial scale peptide manufacturing. As a startup we are constantly developing and improving our processes. Successful candidates will have:
<ul>
<li>Expertise in process development to improve enzyme expression/activity and the know-how to fulfill production at both bench and large scales to meet project demands.</li>
<li>A track record of working with cross-functional teams to ensure that fermentation process development keeps pace with ongoing projects.</li>
<li>The ability to balance best practice and expediency to ensure the delivery of high-quality enzymes while meeting what is optimal for our aggressive timelines to develop new products that are currently being sold into the drug development industry.</li>
</ul>
What You'll Do
<ul>
<li>Drive upstream enzyme production efforts, including hands-on execution of fermentation and expression optimization in bioreactors ranging from bench-scale to 100L.</li>
<li>Conduct downstream processing, including cell lysis, enzyme purification, and quantification for characterization and lot release.</li>
<li>Troubleshoot complex expression challenges and develop strategies for difficult or novel proteins.</li>
<li>Model technical excellence and data integrity across all stages of process development and scale-up.</li>
</ul>
What You'll Bring
Must have experience with:
<ul>
<li>Optimizing fermentation processes, including feeding and induction strategies to enhance enzyme expression.</li>
<li>Refining SOPs, as well as generating and maintaining equipment and quality records.</li>
<li>Producing enzymes at pilot/commercial scale, tech transfer, and working with CDMOs when necessary.</li>
<li>Maintaining databases and records of unit operations, production data, and enzyme stocks.</li>
</ul>
Nice to have experience with:
<ul>
<li>Bioreactor construction and maintenance.</li>
<li>Vector design and construction. </li>
<li>Fermentation factors that affect enzyme solubility and activity. </li>
<li>Purification conditions, enzymatic by-products, cofactors that will improve expression and solubility. </li>
<li>Enzyme activity screening.</li>
<li>Project management and scheduling.</li>
<li>Media formulations. </li>
</ul>
Essential traits:
<ul>
<li>You are reliable, proactive, and a go-getter willing to jump right in.</li>
<li>You have an ownership mindset and are a strategic thinker. Setting goals and priorities when appropriate, creating and executing plans, measuring KPIs and metrics, and aligning tactics with key results all come naturally to you.</li>
<li>You're incredibly nimble, scrappy, and a leader in ambiguous situations. You create solutions to problems and keep a positive attitude even when times are tough.</li>
</ul>
Qualifications:
<ul>
<li>PhD in biochemical engineering, biomedical engineering, microbiology, or a related field with 5+ years industry experience.</li>
<li>Master's with 8+ years industry experience.</li>
<li>BS with 10+ years industry experience.</li>
</ul>
Compensation 
Aralez Bio's salary range for this position is $90,000-$130,000 per year, based on your performance and experience. In addition, your total rewards package will include equity and benefits.
Benefits at Aralez Bio
<ul>
<li>Medical / dental / vision insurance coverage</li>
<li>401k</li>
<li>Flexible Spending Account</li>
<li>Unlimited time off policy</li>
<li>Weekly catered lunch</li>
<li>Professional Development opportunities</li>
<li>Annual company retreat</li>
</ul>
Equal Employment Opportunity
Aralez Bio is an equal opportunity employer and does not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical conditions, veteran status, sexual orientation, gender, sex, and any other group protected under federal, state, or local laws. 
We celebrate diversity and are committed to creating an inclusive environment for all employees. Please reach out if an accommodation is needed. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

Senior Scientist, Fermentation (Individual Contributor)

<h3>Job Description</h3>
Job Description
L3Harris is dedicated to recruiting and developing high-performing talent who are passionate about what they do. Our employees are unified in a shared dedication to our customers’ mission and quest for professional growth. L3Harris provides an inclusive, engaging environment designed to empower employees and promote work-life success. Fundamental to our culture is an unwavering focus on values, dedication to our communities, and commitment to excellence in everything we do.
L3Harris Technologies is the Trusted Disruptor in the defense industry. With customers’ mission-critical needs always in mind, our employees deliver end-to-end technology solutions connecting the space, air, land, sea and cyber domains in the interest of national security.
Job Title: Specialist, Quality Process Engineer - Metrology
Job Code: 24454
Job Location: Canoga Park, CA
Job Schedule: 9/80&nbsp;Employees work 9 out of every 14 days – totaling 80 hours worked – and have every other Friday off
Job Description:
Aerojet Rocketdyne segment of L3Harris, is seeking a skilled Metrology Engineer to join our team at our Canoga Park, CA facility. The ideal candidate will have knowledge in the field of metrology, with a strong background in precision measurement, calibration, and quality assurance. The Metrology Engineer will be responsible for ensuring the accuracy and reliability of measurement systems and instruments used in our manufacturing and quality control processes. 
Essential Functions:
<ul>
<li>Maintain metrology processes and systems to ensure the accuracy and reliability of measurements.</li>
<li>Perform calibration and validation of measurement instruments and systems and maintain procedures for others to follow.</li>
<li>Analyze measurement data and provide technical reports and recommendations.</li>
<li>Collaborate with cross-functional teams to support manufacturing processes.</li>
<li>Troubleshoot and resolve measurement-related issues in a timely manner.</li>
<li>Ensure compliance with industry standards and regulatory requirements, with knowledge on ISO 17025.</li>
<li>Maintain detailed records of calibration, validation, and maintenance activities.</li>
<li>Continuously improve metrology processes and systems through research and implementation of new technologies and methodologies.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's degree and a minimum of 4 years of prior related experience in precision measurement and/or metrology processes. Graduate Degree and a minimum of 2 years of prior related metrology experience. In lieu of a degree, minimum of 8 years of prior related metrology experience.</li>
</ul>
Preferred Additional Skills:
<ul>
<li>Knowledge and understanding of ISO 17025 requirements.</li>
<li>Certification in metrology or related disciplines (e.g., ASQ Certified Calibration Technician).</li>
<li>Experience operating in a laboratory to ISO 17025 requirements.</li>
<li>Knowledge of industry standards and regulatory requirements related to metrology.</li>
<li>Experience in a manufacturing or quality assurance environment.</li>
<li>Understanding of measurement principles, techniques, and equipment.</li>
<li>Proficiency in using metrology software and tools (GAGEtrak).</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Strong attention to detail and precision.</li>
<li>Effective communication and interpersonal skills.</li>
<li>Ability to work independently and as part of a team.</li>
</ul>
In compliance with pay transparency requirements, the salary range for this role is $76,500 - $142,500. This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. L3Harris also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on date of hire, schedule type, and the applicability of collective bargaining agreements.
#LI-HJ1
L3Harris Technologies is proud to be an Equal Opportunity Employer. L3Harris is committed to treating all employees and applicants for employment with respect and dignity and maintaining a workplace that is free from unlawful discrimination. All applicants will be considered for employment without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender (including pregnancy, childbirth, breastfeeding or other related medical conditions), gender identity, gender expression, sexual orientation, marital status, veteran status, disability, genetic information, citizenship status, characteristic or membership in any other group protected by federal, state or local laws. L3Harris maintains a drug-free workplace and performs pre-employment substance abuse testing and background checks, where permitted by law.
Please be aware many of our positions require the ability to obtain a security clearance. Security clearances may only be granted to U.S. citizens. In addition, applicants who accept a conditional offer of employment may be subject to government security investigation(s) and must meet eligibility requirements for access to classified information. 
By submitting your resume for this position, you understand and agree that L3Harris Technologies may share your resume, as well as any other related personal information or documentation you provide, with its subsidiaries and affiliated companies for the purpose of considering you for other available positions.
L3Harris Technologies is an E-Verify Employer. Please click here for the E-Verify Poster in English or Spanish. For information regarding your Right To Work, please click here for English or Spanish.
PandoLogic. Keywords: Quality Control / Quality Assurance Engineer, Location: West Hills, CA - 91307 , PL: 599664777

Specialist, Quality Engineer - Metrology

<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Assembler (Nights)Job Description
Join our team as a Clean Room Assembler, where you will play a crucial role in assembling medical tools. This position involves working in a meticulously maintained clean room, utilizing hand tools, and handling small components to ensure precise assembly.
Responsibilities
<ul>
<li>Inspect hex tips for quality assurance.</li>
<li>Insert hex tips into nose cones using a hydraulic press.</li>
<li>Apply Teflon to clutches with the aid of a hydraulic press.</li>
<li>Assemble torque wrenches with precision.</li>
<li>Install screws to complete the assembly process using a screw-down machine.</li>
<li>Adjust torque on wrenches using a torque tester.</li>
<li>Install caps onto assembled tools.</li>
<li>Perform final cleaning and packaging of completed wrenches.</li>
</ul>
Essential Skills
<ul>
<li>Experience in production and assembly processes.</li>
<li>Knowledge of GMP standards.</li>
<li>Ability to work efficiently in a clean room environment.</li>
<li>Familiarity with medical tool assembly.</li>
<li>No certifications required.</li>
</ul>
Work Environment
You will work in a clean room environment, requiring a head gown and full bunny suit. The dress code prohibits makeup, jewelry, or perfume to maintain cleanliness and safety standards.
Schedule
1st Shift Opportunity: 5:00AM - 1:30PM, up to 2 hours of overtime.
Job Type &amp; Location
This is a Contract to Hire position based out of Newbury Park, California.
Pay and Benefits
The pay range for this position is $20.00 - $22.00/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 Newbury Park,CA.
Application Deadline
This position is anticipated to close on Aug 18, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<h3>Job Description</h3>
Scientist III
$50 - $53/hr medical benefits available at a cost
8 month initial contract
100% onsite in Irvine, CA
Standard first shift
 
Orion Project Services and a leading pharmaceutical company have partnered up to bring you an exciting contract opportunity out of one of their Irvine, CA locations!!! We are seeking candidates experienced with biomaterials and/or biologics related to medical device and drug delivery systems.
 
Don’t pass on this amazing opportunity to work on advancing the field of medical aesthetics and biologics through innovative biomaterials development!!!!!
Position Summary
 The Contractor, Scientist III, Biomaterials –Working under general supervision, the role focuses on the creation of next-generation biomaterials and localized delivery systems for biologics. The responsibilities span the science and engineering of polymers including their design, synthesis, modification, fabrication, and characterization, as well as prototype formulation (injectable hydrogels, particles, implants) and process development.
 Scientist III Key Duties / Responsibilities:
 Role Scientific Execution Oversight: 95%
<ul>
<li>Lead and actively participate in planning experimental studies aimed at developing novel biomaterials and biologics.</li>
<li>Conduct experimental studies related to the synthesis, formulation, fabrication, and characterization of advanced biomaterials and prototypes.</li>
<li>Analyze and interpret experimental data to derive conclusions and propose actionable technical recommendations to propel project progress.</li>
<li>Collaborate with cross-functional R&amp;D teams to achieve shared project goals through joint experimental studies.</li>
</ul>
Scientific Communication Oversight: 5%
<ul>
<li>Engage in and present at project team meetings to discuss project activities, review completed tasks, and assess technical progress.</li>
<li>Contribute to the writing of technical reports, memoranda, and documents for both internal and external dissemination.</li>
</ul>
Qualifications needed to be successful in this role:
<ul>
<li>M.S. or B.S. degree in Biomaterials Science, Biomedical engineering, Polymer Chemistry, Materials Engineering, Bioengineering, Chemical Engineering, or related fields.</li>
<li>3+ (M.S.) or 6+ (B.S.) years of relevant experience, including industrial experience.</li>
<li>Preferred experience with biomaterials and/or biologics related to medical device and drug delivery systems.</li>
<li>Data presentation and collaboration</li>
<li>Proficient in presenting information and responding to inquiries from groups of managers and technical peers.</li>
<li>Skilled in presenting facts and recommendations both orally and in writing.</li>
<li>Possess technical competence and expertise in Biomaterials Science (e.g., polymer synthesis, cross-linked/modified polymers, hydrogels, biomaterial-tissue interfaces, polymer fabrication processes, drug delivery systems)</li>
<li>Possess technical competence and expertise in biologics</li>
</ul>

Senior Scientist

<h3>Job Description</h3>
Job DescriptionThis Jobot Job is hosted by: Brian Perkins Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $80,000 - $150,000 per year 
A bit about us:
 
<ul>
<li> Strong Company Culture</li>
<li> Yearly Bonuses</li>
<li> Profit Sharing</li>
<li> Flexible Schedule</li>
<li> Hybrid Schedule</li>
<li> Long Term Growth Potential</li>
</ul>
 
Why join us?
 We provide engineering support services including geotechnical, geological and environmental for clients and projects throughout Northern California. Services include geotechnical investigations &amp; recommendations, geological studies and Environmental Site Assessments (ESA). Our engineering services group work to find solutions and protect the best interest of our clients. 
Job Details
 Participate on teams in the performance of building diagnostics projects that include, but are not limited to, building enclosure assessments, roofing, façade, waterproofing, litigation support, field testing, and distress studies. Perform and/or direct field investigations, including geotechnical drilling, field investigations, identify laboratory testing and develop foundation design requirements. Work with project team design professionals to develop cost effective recommendations and manage the client relationship through to special inspections and materials testing. Participate in development of peer reviews of construction documents, protocols, scopes of work, and other similar documents associated with geotechnical and environmental disciplines. Prepare technical reports, develop technical presentations, and participate in the development of other technical content in conformance with Allerion’s quality and professional standards and policies. Assist with business development including working with new clients, furthering relationships with existing clients, participating in professional organizations, and actively participating in the implementation of marketing strategies. Project management on small-to-mid size projects including establishing project teams, objectives, schedules, project-specific safety plans, and management of project deliverables. Develop scopes of service, establish project budgets, prepare proposals, and participate in client presentations. Experience: Candidate must have a minimum of five years experience performing geotechnical engineering services. Candidate should have at least two years of experience with Environmental Site Assessments. Candidate should have experience work on a variety of construction projects including civil, structures, WWTP, WTP, mid-rise buildings and deep foundations Licenses and Certifications: Registered Professional Engineer in the State of California Registered Geotechnical Engineer in the State of California (Preferred) Certifications related to geotechnical engineering and/or environmental studies A CA Driver’s License is required. Job Requirements: Ability to work in the field and office depending on project requirements Excellent communication skills (both oral and written) Demonstrative experience with project management and meeting deadlines A sound working knowledge of local building codes Perform field inspections during various stages of construction Draft and prepare both foundation investigations reports and environmental assessments Establish and maintain quality working relationships with everyone involved Perform other related duties as required Excellent verbal and written communication skills Education Requirements: Bachelor’s degree in Civil Engineering with an emphasis in soils mechanics Master’s degree in Civil Engineering Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.Company DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

Geotechnical Engineer

<h3>Job Description</h3>
Role: Senior Principal Biological Scientist
Location: South San Francisco , CA
Duration: 12+ Months Contract
 
Candidates should have their PhD (or equivalent) in a quantitative discipline (e.g., Computational Biology, Computer Science, Machine Learning, Mathematics, Statistics, Physics) or in a biological field (e.g., Oncology, Immunology, Molecular Biology) with demonstrated computational fluency.
 
 
We are seeking a visionary Senior Principal Scientist who will lead complex, cross-functional scientific initiatives that bridge cutting-edge AI capabilities and real-world biological applications. This opportunity is ideal for a leader with a record of scientific excellence, cross-disciplinary fluency, and deep translational curiosity.
 
You’ll work in close partnership with: -
BRAID (Biology Research AI Development), our internal AI model development team
- Computational Biology &amp; Medicine (CBM) and therapeutic area scientists
- Experimental and data-generating partners across Genentech R&amp;D (i.e. Research, Translational Medicine, Cellular &amp; Tissue Genomics etc).
 
In this opportunity, you will:
- Lead a small team that focuses on high-impact projects that apply and adapt AI models to translational challenges in disease biology, biomarker discovery, and target exploration.
- Frame biological problems in computational terms and design solutions that are biologically meaningful, interpretable, and experimentally testable.
- Collaborate with BRAID to guide model application, validation, and refinement.
- Partner with experimental and clinical teams to ensure scientific questions are addressed with computational rigor and domain awareness.
- Act as a recognized scientific thought leader and strategic contributor to decisions that shape the direction of Genentech’s discovery and translational pipeline.

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