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<h3>Job Description</h3>
 Responsibilities 
<ul>
<li>In collaboration with the Medical Laboratory Director, manages the Quality Assurance Program for the department</li>
<li>Develops and maintains a service orientation in performing duties with fellow employees, patients, medical staff and visitors.</li>
<li>Has operational responsibility for the clinical/technical aspects of a section of the laboratory.</li>
<li>Performs job duties of Medical Technologist; performing a variety of chemical, microscopic, and bacteriologic procedures of a moderately and highly complex nature, following established standards and practices to obtain data for use in diagnosis and treatment of disease.</li>
</ul>
 Qualifications 
<ul>
<li>Bachelor's Degree in Medical Technology or related science from an accredited school</li>
<li>Current California CLS license</li>
<li>Current licensure with the American Society for Clinical Pathology (ASCP), or National Credentialing Agency for Laboratory Personnel (NCA) or Clinical Laboratory Scientist (CLS), or equivalent</li>
<li>Minimum of three (3) years laboratory experience in Medical Technology/Clinical Laboratory Science</li>
</ul>
Overview 
As a Lab Supervisor at Mercy Hospital Bakersfield in Bakersfield, California, you'll oversee the day-to-day management of the laboratory for our 194-bed hospital located in the heart of downtown. You will contribute to the development of annual goals, objectives and departmental budget while actively facilitating the achievement of the goals and objectives and the ongoing evaluation of results.&nbsp;
Every interaction is an opportunity to improve your understanding of a patient's needs, the needs of your patient care team, or the needs of your facility.&nbsp; You'll advocate for your team as you support them in reaching their full potential, aligning with our operational goals and objectives.
To thrive in this role, you need to be accountable and confident.&nbsp; You're an excellent communicator in 1:1 interactions and in front of groups.&nbsp; It's also important for you to be comfortable holding tough conversations, as you are responsible for the performance of your people and your laboratory.
About Us:
Founded by the Sisters of Mercy, Mercy Hospitals have a history of caring for our community that goes back more than 100 years. We provide a broad range of medical and surgical services including minimally invasive and outpatient options. Our family of services includes the area's only inpatient oncology unit, the Orthopedic, Spine, and Hand Center, Family Birth Center, the Lactation Support Center and retail store, and many others. Mercy Hospital Downtown is a 194-bed facility located in downtown Bakersfield. Mercy Hospital Southwest is a 78-bed facility and the only hospital located in the rapidly growing area west of Highway 99. Mercy Hospital is a member of Dignity Health and is a trusted community partner, serving residents of Bakersfield and Kern County with quality, compassionate care since 1910. Learn more here at <a href="https://www.dignityhealth.org/central-california/locations/mercy-bakersfield" target="_blank">https://www.dignityhealth.org/central-california/locations/mercy-bakers…</a>. #bakersfieldRN
One Community. One Mission. One California&nbsp;
 Pay Range $46.96 - $68.10 /hour

Supervisor Laboratory Services

<h3>Job Description</h3>
Summary:
 The main function of a chemist is to conduct qualitative and quantitative chemical analyses in laboratories for quality, process control or to develop new products or knowledge. A typical chemist is responsible for creating new products and processes or improving existing ones for clients.

 Job Responsibilities:
 • Analyze organic and inorganic compounds to determine chemical and physical properties, composition, structure, relationships and reactions.
 • Improve and customize products, equipment, formulas, processes and analytical methods.
 • Compile and analyze test information to determine process or equipment operating efficiency and to diagnose malfunctions.
 • Adhere to production flow model. 
 • Prepare test solutions, compounds and reagents for laboratory personnel to conduct tests.
 • Confer with scientists and engineers to conduct analyses of research projects and assist in the interpretation of test results.
 Skills:
 • Verbal and written communication skills, attention to detail, and problem solving skills.
 • Basic ability to work independently and manage one’s time.
 • Previous manufacturing experience or knowledge of product flow principles. 
 • Basic ability to analyze data and accurately document and record results.

 Education/Experience:
 • Bachelor’s degree in chemistry or a related discipline required or 3+ years of manufacturing and production experience. 
 • Previous work experience required.

Chemist

<h3>Job Description</h3>
Job Title: Scientist
Location: North Chicago, IL
6 months contract with possible extension
 
What are the top 3-5 skills, experience or education required for this position:
 1 . Significant cell culture expertise: maintenance, freezing, thawing, and passaging BS degree or master’s degree in biological sciences, molecular biology, neuroscience, or biochemistry and significant 2-3 years tissue culture experience are a must. (Or a master’s degree with at least one year of experience).
 The applicant should already be trained in proper wet lab procedures and should be familiar with using basic lab equipment. Having strong communication, organizational and documentation skills is a must.
 2. Biochemistry such as: Western blot, Immunofluorescence, flow cytometry
 3. molecular biology such as: RNA extraction, cDNA synthesis, RT-qPCR
 4 Gene editing using CRISPR technology
 5 lentivirus production and lentiviral transduction
 What is a nice to have (but not required) regarding skills, experience, education, or certification: Having experience in stem reprogramming, maintenance and differentiation is highly preferred.
 1. Job description and title: A research technician position is available at Genomic Research Center (GRC) . We are looking for a highly motivated research technician to work independently and in collaboration with other scientists in projects involving human induced pluripotent stem cells reprogramming, cell differentiation, CRISPR editing, and high throughput functional screenings. The successful candidate will be involved in critically timed experiments and long differentiation protocols that require daily attention. The applicant is expected to:
 a. Conduct routine wet lab experimental protocols and procedures.
 b. Maintain cultured stem cells and stem cell-derived cells
 c. Keep an accurate record of experimental setup, SOP protocols, and data quality control notes.
 d. Maintain efficient and continuous communication with team members and managers.
 e. Support team members with basic routine cell culture procedures including media preparation and reagents aliquoting.
 3. What hours and days will this person be working?
 Monday to Friday, with expectations to work on weekends and some holidays.
 4. What are the top 5 skills/requirements this person is required have?
 a. Required Skill 1: significant cell culture expertise: maintenance, freezing, thawing, and passaging.
 b. Required Skill 2: Biochemistry such as: Western blot, Immunofluorescence, flow cytometry
 c. Required Skill 3: molecular biology such as: RNA extraction, cDNA synthesis, RT-QPCR
 d. Optional Skill 4: Gene editing using CRISPR technology
 5. What years of experience, education, and/or certification are required?
 BS degree or master’s degree in biological sciences, molecular biology, neuroscience, or biochemistry and significant 2-3 years tissue culture experience are a must. (Or a master’s degree with at least one year of experience).
 The applicant should already be trained in proper wet lab procedures and should be familiar with using basic lab equipment. Having strong communication, organizational and documentation skills is a must.
 6. What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification?
 Having experience in stem reprogramming, maintenance and differentiation is highly preferred.
 7. What is the environment that this person will be working in (i.e., group setting vs individual role)?
 The candidate will be involved in a highly enthusiastic, motivated, supportive, and diverse team. The candidate will be involved in multidisciplinary projects across different teams in GRC and is expected to work independently and support the team.
 10. Other notable details about the environment from the hiring manager about this role
 Ability to participate in manuscripts preparation and authorship. The working schedule is flexible in agreement with the manager.
 11. What positions/background experience do you feel are successful in this role?
 Research technicians, lab managers, research technologists, a master’s student with significant cell culture expertise.
EEO:
 
“Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

Scientist

<h3>Job Description</h3>
Job Description:
 
The candidate will join the group focusing on the development of topical ophthalmic formulations and help solve manufacturing and stability challenges in new solution and emulsion formulations, evaluate the properties of new formulations and materials, characterize new manufacturing processes.
The candidate is expected to
• be able to carry out experiments under the limited supervision, following GxP guidelines. Capable of taking initiative, self-driven, capable of focusing on objectives, and strong ability for prioritization. Detail oriented and hand-on is a must.
• contribute to DOE development in collaboration with supervising scientists
• analyze, summarize, and present the data.
• have in depth experience in polymer chemistry, surface chemistry, colloid chemistry, or similar, with strong formulation and characterization skills.
generate, review and approve documents such as batch records, study protocols, reports, and standard operational procedures
• Have strong ability to work independently with little direction and tight timeline;
 
Minimum requirements:
BS degree in chemistry, polymer science, surface science, colloid chemistry, or similar. Chemical lab experience. Ability to work following SOPs and instructions.
 
Desired:
• MS or PhD degree with experience in polymer science, surface science, colloid chemistry, or similar.
• Experience working with polymer solutions and / or with emulsions, familiarity with rheology, microscopy, and particle size characterization methods.
• Experience developing ophthalmic products
• Understanding of formulations development principles.
• Experience working in regulated industry such as pharmaceutical or medical devices.
• Strong oral and written communication skills, excellent presentation skills
• Experience in GxP

Clinical Research Scientist

<h3>Job Description</h3>
We are one of the world’s most dynamic central reference laboratories, specializing in the field of anti-infectives. We serve the pharmaceutical, diagnostic, and biotech industries. We depend on our talented professionals to provide exceptional customized products and services to clients engaged in the fight against infectious disease.
 
The Microbiologist I is responsible for conducting those aspects of studies undertaken by IHMA that require general and clinical microbiology.&nbsp;These responsibilities include culturing of bacteria, routine identification and antimicrobial susceptibility testing, testing for evaluation of new compounds, specialty studies and global surveillance studies.
 
Starting pay range:&nbsp;$23.00 - $26.00 per hour
 
Benefits include:&nbsp;Medical, Dental, Vision, Life Insurance, AD&amp;D, Paid Time Off, Paid Parental Leave, 401(k)
 
IHMA offers a friendly, welcoming culture and work-life balance!
 
Specific Duties:
 
<ul>
<li>Identify organisms (aerobes and anaerobes) to genus and species by colony morphology and MALDI-TOF mass spectrometry</li>
<li>Perform antimicrobial susceptibility testing methods including broth microdilution panels, E-test, disk diffusion, and agar dilution</li>
<li>Perform accurate and precise testing according to established IHMA protocols; document all deviations from standard protocols</li>
<li>Report results legibly or by computer conforming precisely to documentation procedures</li>
<li>Perform necessary quality control procedures, properly evaluate control data, and implement and document corrective action as needed</li>
<li>Operate, calibrate, maintain, and troubleshoot instrumentation and equipment used in performance of job duties</li>
<li>Perform sample archiving and retrieval</li>
<li>Organize work according to laboratory priorities and complete assigned responsibilities with little supervision</li>
<li>Assist other department employees as necessary</li>
</ul>
 
Background Requirements:
 
<ul>
<li>MT(ASCP) or M(ASCP) or MLS(ASCP) with &lt;5 years of experience in clinical microbiology or the equivalent&nbsp;</li>
<li>OR</li>
<li>Bachelor’s degree from an accredited institution with &lt;5 years of experience in clinical microbiology or the equivalent</li>
<li>OR</li>
<li>MLT (ASCP)with &lt;10 years of experience in clinical microbiology or the equivalent</li>
<li>Experience is a clinical microbiology laboratory a plus</li>
<li>Experience in Microsoft Word, Excel and Access preferred</li>
</ul>

Microbiologist I

<h3>Job Description</h3>
Primary role is to perform chemical analysis of pharmaceutical products and routine laboratory operations in a cGMP environment.
 
Reports to the Quality Control Manager. Internal relationships include Manufacturing, Research &amp; Development, Analytical Development and Quality Assurance.
 
DUTIES AND RESPONSIBILITIES
Analytical Testing &amp; Review
<ul>
<li>Conduct and review routine and non-routine analysis of raw materials, in-process materials, APIs, and finished products in compliance with SOPs, cGMPs, and cGLPs.</li>
<li>Perform testing using HPLC, GC, GC-MS, ICP-MS, FTIR, UV-Vis, and wet chemistry methods.</li>
<li>Participate in method validation and method transfer activities.</li>
</ul>
 
Equipment &amp; Instrumentation
<ul>
<li>Calibrate, maintain, and troubleshoot laboratory equipment to ensure operational readiness.</li>
<li>Proactively prevent production delays through scheduled maintenance.</li>
<li>Maintain expert knowledge of instrument components and functionality.</li>
</ul>
 
Documentation &amp; Compliance
<ul>
<li>Compile and interpret data, document test procedures, and prepare reports.</li>
<li>Administer quality control systems in compliance with FDA guidelines.</li>
<li>Write and revise Standard Operating Procedures (SOPs).</li>
<li>Ensure thorough cGMP/cGLP documentation and maintenance of quality records.</li>
</ul>
 
Leadership &amp; Team Development
<ul>
<li>Provide clear direction, coaching, and mentoring to team members to enhance skills and performance.</li>
<li>Foster a culture of accountability, integrity, and continuous improvement.</li>
<li>Demonstrate strong decision-making skills in prioritizing work under changing deadlines.</li>
<li>Lead by example in quality, safety, and compliance standards.</li>
<li>Encourage cross-functional collaboration to resolve technical challenges.</li>
<li>Take ownership of special analytical projects, including authoring protocols and reports.</li>
</ul>
 
QUALIFICATIONS
<ul>
<li>Bachelor’s degree in a science discipline (Chemistry or pharmaceutical preferred) with a minimum 3-4 years hands-on laboratory experience in FDA regulated industry or associate degree with 7-10 years of hands-on laboratory experience in GMP environment, or equivalent.</li>
<li>Strong background in principles of separation using analytical instrumentation such as HPLC, GC, UV/VIS in a GMP environment.</li>
<li>Expert knowledge of ICH and FDA guidelines.</li>
<li>Expertise in Chromatographic Data Acquisition and LIMS Systems experience such as ChemStation (OpenLab), Chromeleon, or Empower 3. </li>
<li>Attention to details in collecting data and accurately maintaining laboratory notebooks required.</li>
<li>Drug Screen and DEA Background check required.</li>
</ul>
 
WORKING CONDITIONS/PHYSICAL REQIUREMENTS
<ul>
<li>Must be able to conduct visual inspections of incoming materials to verify appearance and printed content (e.g. product labels) meet product specifications. </li>
<li>Must accurately distinguish different colors for reporting of appearance and colorimetric tests.</li>
<li>Occasional lifting of up to 50 lbs.</li>
<li>Annual occupational medical assessment required to ensure ability to meet position requirements and based on site requirements.</li>
</ul>
 
WORKING HOURS
<ul>
<li>Monday - Friday</li>
</ul>
 
LOCATION
This position is located in Round Rock, Texas. Rock Round is located 15 miles north of Austin, TX.
 
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Quality Control Chemist III

<h3>Job Description</h3>
Performs qualitative and quantitative chemical analyses on raw materials, intermediates, final products, and water to ensure quality compliance. Operates and maintains lab equipment, including troubleshooting, calibration, and preventative maintenance. Ensures adherence to internal systems and external certification requirements. Disposes of expired samples/chemicals per safety standards. Develops/validates analytical methods (HPLC-MS, GC-MS) to ensure accuracy and reliability. Conducts inspections, data audits, and capability studies to maintain process integrity.
Responsibilities:
<ul>
<li>Prepare and test samples using approved protocols.</li>
<li>Perform SDS testing (flash point, corrosivity).</li>
<li>Maintain chemical inventory and lab cleanliness.</li>
<li>Document and report results in compliance with SOPs.</li>
<li>Apply advanced analytical chemistry techniques to problem-solving.</li>
</ul>
Qualifications:
Bachelor’s in chemistry, Biology, or Biotech preferred. 0–5 years’ professional or academic lab experience. Knowledge of GC, GC/MS, MS, and HPLC methods. Understanding of organic/inorganic chemistry relevant to beverage products. Strong attention to detail, safety adherence, and data integrity.

<h3>Job Description</h3>
Role: Senior or Lead Clinical AI Research Scientist
Location: Hybrid in Palo Alto, CA.
Company Stage: Seed ($50 Million)
Compensation: 200k-225k salary range, bonus, equity
 
About the Company
Our client is an AI-first healthcare technology company transforming how hyper-personalized care is delivered. Their precision care platform empowers clinicians to provide whole-person care by combining generative AI with predictive analytics. Backed by extensive proprietary data assets covering hundreds of millions of patients and healthcare providers, the company is led by a team of experts spanning healthcare, technology, and clinical research. Their mission is to bridge cutting-edge AI innovation with practical, real-world healthcare applications that improve patient outcomes.
 
About the Role
We are seeking a Senior Data Scientist with deep expertise in Large Language Models (LLMs) and their application in healthcare. In this role, you will design, build, and deploy advanced AI solutions that seamlessly integrate into existing clinical and operational systems, driving measurable impact for providers and patients.
 
Key Responsibilities
<ul>
<li>End-to-End Development: Lead the design and implementation of LLM-powered healthcare applications that are secure, scalable, and production-ready.</li>
<li>Model Specialization: Fine-tune and adapt LLMs such as LLaMA 2, Mistral, and other cutting-edge open-source models for healthcare-specific use cases.</li>
<li>Tool Application: Leverage frameworks like LangChain, LlamaIndex, and related tools to create innovative AI-driven healthcare workflows.</li>
<li>Problem-Solving: Address complex challenges in healthcare using creative, data-driven approaches that transform AI capabilities into real-world patient outcomes.</li>
<li>Cross-Functional Collaboration: Partner with clinicians, engineers, and business stakeholders, translating technical concepts into clear, actionable insights.</li>
<li>Continuous Innovation: Stay ahead of emerging trends in AI and healthcare technology, integrating new methodologies and tools where beneficial.</li>
</ul>
 
Qualifications
<ul>
<li>Advanced degree in Computer Science, Data Science, Artificial Intelligence, or a related discipline.</li>
<li>Proven experience developing and deploying LLM applications in a healthcare context.</li>
<li>Experience with SFT, RLHF, RAG, Agents, etc.</li>
<li>Proficiency with LLaMA 2, Mistral, LangChain, LlamaIndex, and comparable technologies.</li>
<li>Strong analytical, problem-solving, and critical-thinking skills.</li>
<li>Excellent written and verbal communication abilities, with a collaborative mindset.</li>
</ul>

Lead Clinical AI Research Scientist

<h3>Job Description</h3>
Scientist 2
$35.50-$44.25/hr
Onsite: San Diego, CA 92122
6 month assignment
 
 
JOB DESCRIPTION
We are seeking a motivated, skilled Scientist 2 to join our interdisciplinary Analytical Core Laboratory team. In this role, you will support reagent and consumables development with innovative and agile characterization, leveraging our portfolio of chromatography, mass spectrometry, and spectroscopic instrumentation. A strong technical background in analytical chemistry is required, paired with the forward-facing collaborative skills needed to support a Core facility. The successful candidate will be detail-oriented, self-motivated, and eager to grow the laboratory’s capabilities alongside their own.
 
Key Responsibilities
<ul>
<li>Operate, maintain, troubleshoot, and repair a range of analytical instruments, including but not limited to LC-QTOF, LC-QQQ, HPLC, ICP-MS, FT-IR, and NMR. Expertise</li>
<li>Design, optimize, and execute experimental protocols aligned with internal product development workflows.</li>
<li>Analyze, interpret, and communicate experimental data to diverse internal stakeholders.</li>
<li>Represent the Core team in user meetings, project presentations, and training sessions.</li>
<li>Foster a collaborative and communicative environment within the team, and with Core users.</li>
<li>Adapt responsibilities as needed to meet evolving business needs.</li>
</ul>
 
Required Qualifications:
<ul>
<li>Demonstrated experience in developing analytical methods for complex scientific challenges.</li>
<li>Proficiency in several of the following techniques: HPLC, LC-MS, GC-MS, ICP-MS, NMR.</li>
<li>Strong background in method development and analytical characterization of biomolecules, such as enzymes and oligonucleotides.</li>
<li>Experience with handling complex datasets and data transformations using platforms such as JMP, R, Python, etc.</li>
<li>Excellent multitasking and prioritization skills.</li>
<li>Outstanding verbal and written communication abilities.</li>
<li>Familiarity with next-generation sequencing platforms is a plus.</li>
<li>Experience in a product development setting is highly desirable.</li>
<li>Education &amp; Experience</li>
<li>PhD in a relevant field with 0–2 years of industry experience, or</li>
<li>BS/MS with 3–5 years of industry experience.</li>
</ul>
 
Must Have:
•Ability to nimbly design, optimize, and execute experimental protocols aligned with internal product development workflows.
•Experience with handling complex datasets and data transformations using platforms such as JMP, R, Python, etc.
Expertise in LC-MS is essential.
• Operate, maintain, troubleshoot, and repair a range of analytical instruments, including but not limited to LC-QTOF, LC-QQQ, HPLC, ICP-MS, FT-IR, and NMR.
 
Nice to Have:
FTIR
GC-MS
ICP-MS
JMP
NMR
 
Benefits:(employee contribution)
 Health insurance
 Health savings account
 Dental insurance
 Vision insurance
 Flexible spending accounts
 Life insurance
 Retirement plan
 
 
We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

<h3>Job Description</h3>
Recent PhD graduates highly encouraged to apply!
 
Job Summary:
An ideal candidate will have a strong foundation in modern synthetic organic chemistry and analytical techniques such as NMR, LCMS, UPLC/HPLC (Empower proficiency) and an understanding of early drug development processes and experiments. Experience in small-molecule process development and scale up is highly desired, however not required.
An ideal candidate would have a B.S. or M.S. in Chemistry, or a related field with 3+ years of experience in pharmaceutical research or laboratory setting or, Ph.D. with 0-3 years of experience.
 
<ul>
<li>Responsibilities:Participate in the design, planning and execution of multi-step synthesis, process research and development as a cross-functional team member.</li>
<li>Collaborate with cross-functional teams to ensure successful project outcomes.</li>
<li>Implement process enhancements, scientific approaches and technical improvements to deliver robust chemical processes.</li>
<li>Document and report experimental results and findings.</li>
<li>Draft and review technical documents (development reports, patent applications, tech transfer documents etc.)</li>
<li>Maintain an accurate, timely and compliant laboratory notebook.</li>
<li>Maintain laboratory equipment and ensure compliance with safety regulations.</li>
<li>Qualifications:Strong knowledge of organic chemistry.</li>
<li>Experience with early phase route development and process optimization</li>
</ul>
<ul>
<li>Proficiency in using analytical instruments (HPLC/UPLC, NMR, LCMS) and software.</li>
<li>Strong analytical and problem-solving skills.</li>
<li>Strong written and verbal communication skills.</li>
<li>Ability to work independently and as part of a team.</li>
<li>Strong organizational and time management skills.</li>
<li>Capabilities:Ability to effectively prioritize and manage multiple tasks and compounds</li>
<li>Ability to adapt to change and to work optimally within a variety of situations</li>
<li>Ability to build productive working relationships across functions and highly diverse groups of individuals</li>
<li>Self-motivated and willing to “learn on the job” and ask for assistance when needed</li>
<li>Ability to make a significant impact in a results-driven environment where accountability is key.</li>
<li>A team player, who listens effectively and invites response and discussion</li>
<li>A collaborator who communicates in an open, transparent, complete, timely and consistent manner</li>
</ul>

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