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<h3>Job Description</h3>
We’re seeking a hands-on Scientist I / Formulation Technician to support a preclinical formulation team preparing dosing formulations for nonclinical studies. This is an execution-focused lab role ideal for someone who enjoys wet-lab work, structured processes, and working in a regulated environment.
What You’ll Do
<ul>
<li>Prepare oral and parenteral dosing formulations for preclinical and toxicology studies</li>
<li>Execute formulation prep for in-house studies and support early-stage programs</li>
<li>Maintain batch records, formulation documentation, and study records</li>
<li>Handle pharmaceutical materials, excipients, and test compounds per SOPs</li>
<li>Support test item logistics, including inventory management and domestic/international shipments to CROs</li>
<li>Coordinate with internal teams and external partners to meet study timelines</li>
<li>Assist with GLP documentation, archiving, and lab compliance</li>
<li>Support routine lab organization, inspections, and EHS compliance</li>
</ul>
What We’re Looking For
<ul>
<li>Hands-on lab experience with formulation, chemistry, or pharmaceutical materials</li>
<li>Comfortable working in a wet-lab environment</li>
<li>Strong organization, documentation, and time-management skills</li>
<li>Proficiency with MS Office (Excel, Word, PowerPoint, Teams)</li>
<li>Team-oriented, proactive, and detail-focused</li>
</ul>
Nice to Have
<ul>
<li>Experience in a GLP or regulated lab environment (trainable)</li>
<li>Exposure to preclinical or early-stage formulation</li>
<li>Experience with LIMS systems (e.g., Pristima or similar)</li>
<li>Prior CRO coordination or shipment logistics experience</li>
</ul>
Education
<ul>
<li>Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Biology, or related field</li>
<li>(Master’s a plus)</li>
</ul>

Scientist I - Preclinical Formulation

<h3>Job Description</h3>
Senior Wetlands Biologist
 
Location(s): Southern California (OC, LA, SD, Riverside)
Practice/Department: Biological
Work Environment: Hybrid
Compensation: $100,000-150,000/annually*
 
Dudek’s journey began in 1980 with a vision to serve Southern California’s water and wastewater agencies.
Today, we are a 100% employee-owned firm supporting clients nationwide and delivering projects that improve and protect the built and natural environments of communities throughout the United States. Our work has been recognized by leading industry organizations, and we’ve been honored with multiple national Top Workplace Awards.
Our employee-owners are unified by a singular commitment to supporting projects that address key societal issues, such as the transition to renewable energy, infrastructure hardening and repair, environmental protection, and community resilience.
Learn more about our award-winning culture, the benefits and perks of being a Dudekian, and the projects you will have the opportunity to shape.
 
Who You Are
As an employee-owner, you embrace accountability, working safely, and collaboration while thinking resourcefully and independently.
Like all Dudekians, you are curious and solution-oriented, with the ability to adapt quickly to changes and approach challenges with a spirit of innovation.
 
How You’ll Make an Impact
Dudek is currently seeking a full-time senior-level Biologist to join our biological resources team. The successful candidate will help grow Dudek’s biological resources practice; with a focus on aquatic resource/wetland delineations and permitting; and work collaboratively with other Dudek staff based throughout our California offices. This position will necessitate both in-office and field-based work and can be located out of any of our California offices.
 
Duties and Responsibilities
<ul>
<li>Plan and lead aquatic resource wetland delineations;</li>
<li>Plan and lead collection of detailed field data, work in remote field locations, hike steep slopes over uneven terrain, and work full days in all types of weather</li>
<li>Prepare and oversee preparation of reports summarizing methodology, field survey results and recommendations;</li>
<li>Prepare and oversee preparation of Aquatic Resources wetland Delineation Reports;</li>
<li>Prepare and oversee preparation of documents supporting environmental permit applications and CEQA/NEPA aquatic resources evaluations;</li>
<li>Prepare scopes of work and cost estimates for aquatic resources wetland delineation work;</li>
<li>Manage technical projects from inception to completion, ensuring timely and efficient delivery;</li>
<li>Lead, mentor, and support project teams with the goal of maximizing performance and efficiency in the field and with report writing;</li>
<li>Mentor and train junior staff in collaboration with other senior staff;</li>
<li>Participate in the development of guides and training materials;</li>
<li>Represent Dudek and clients in agency meetings and public hearings as a subject matter expert for aquatic resource delineations and permitting;</li>
<li>Track and keep abreast of regulatory and delineation protocol changes to ensure compliance with the latest requirements.</li>
</ul>
 
Minimum Qualifications
<ul>
<li>Bachelor’s degree in biology, ecology, botany, environmental science or related natural resources field;</li>
<li>A minimum of 12 years’ of experience preparing and focusing solely on aquatic wetland delineations and identifying wetland mapping boundaries using the 1987 US Army Corps of Engineers Wetland Delineation Manual and Regional Supplements.</li>
<li>Expert-level knowledge of state and federal statutes, regulations, and permitting requirements relating to the Federal Clean Water Act, California Porter-Cologne Water Quality Control Act, and California Fish and Game Code;</li>
<li>Expert-level knowledge of California aquatic resource types and systems; including disturbed and difficult sites in diverse environments (deserts, coasts, mountains, etc.)</li>
<li>Knowledge and applied experience with soil science;</li>
<li>Demonstrated experience with management of projects involving complex biological/aquatic resource impact analyses and mitigation planning;</li>
<li>Strong written and oral communication skills;</li>
<li>Expert-level experience with GPS technologies (e.g, ESRI FieldMaps) for mapping aquatic resources;</li>
<li>Willingness to travel throughout California for work, including over-night stays in hotels;</li>
<li>Must possess a valid driver’s license and have active personal automobile liability insurance by first day of employment.</li>
</ul>
 
Preferred Qualifications
<ul>
<li>Master’s degree in biology, ecology, botany, environmental science or related natural resources field;</li>
<li>Leadership and strong ability to work in a collaborative environment;</li>
<li>Regarded as an expert in the field and sought out as an instructor and presenter by outside parties;</li>
<li>Understanding of delineation process for two-parameter wetlands per California Coastal Commission;</li>
<li>Strong customer service emphasis and solution-oriented project delivery approach;</li>
<li>Conscientious and detail-oriented with demonstrated accuracy and attention to detail;</li>
<li>Exercises good judgment and demonstrates sound decision-making skills.</li>
</ul>
 
Compensation: $100,000-150,000/annually*
*Dudek considers multiple factors in determining final compensation for a position, including, but not limited to, an individual’s relevant work experience, skills, education, certifications and competencies that align to the specified role, and geographic location. Successful candidates must pass a pre-employment drug test and background check prior to beginning employment.
 
Working Conditions:
Environment
<ul>
<li>This job operates in a remote or office-based environment and this role routinely uses standard office equipment such as computers, phones, printers, etc.</li>
<li>This job may also require occasional project site visits, based outdoors which can include excessive noise, uneven walking surfaces, extreme weather, and moving vehicles and equipment.</li>
</ul>
 
Physical Requirements
The physical demands described here are representative of those that must be met to successfully perform the essential functions of the job. This job requires the following:
<ul>
<li>Working on a computer, sitting, or standing for long periods of time in an office or remote office setting.</li>
<li>Employees must be capable of bending, squatting, climbing ladders, and lifting up to 35 lbs. unassisted; 50lbs in a team lift (two or more employees).</li>
<li>Attending meetings, both in person and virtually, and speaking on the phone with peers, clients, etc.</li>
<li>Specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.</li>
</ul>
 
Dudek is committed to creating a workplace where all employees, regardless of their background, feel valued, respected, and have equal opportunities to succeed. We believe that a diverse and inclusive workforce is essential to our business success, and we are dedicated to fostering a culture where everyone can thrive. We are committed to fair and equitable processes, based on merit, free from any discrimination.
 
Dudek is genuinely committed to equal employment opportunities within our company and on our project teams. Dudek is also committed to compliance with all applicable laws providing equal employment opportunities. This commitment applies to all persons involved in Dudek’s operations and prohibits unlawful discrimination by any employee of Dudek, including supervisors and coworkers. Equal employment opportunities will be extended to all persons (including those with disability and veteran status) in all aspects of the employment relationship, including recruitment, hiring, training, promotion, transfer, compensation, benefits, discipline, layoff, recall, and termination. Any employee who violates this policy and Dudek’s commitment to equal employment opportunities will be subject to disciplinary action.
 
Dudek is a U.S.-based employer. All positions are based in the United States and require U.S. work authorization.

Senior Biologist

<h3>Job Description</h3>
In Vivo Research Associate II/III, Large Animals (Contract to Hire) Looking to hone your animal surgery skills? One of San Diego’s leading biotech companies is looking for a competent, reliable Research Associate to add to their dynamic team. This role offers the opportunity to build upon the foundation you’ve already laid in your industry experience and refine your in-vivo surgical skills. Don’t miss this rare opportunity to learn from top professionals, grow into a more senior role, and excel in a challenging and supportive environment. What you will do: 
<ul>
<li>Administer test substances by various dosing methods, perform catheter placements, and prepare study activities.</li>
<li>Manage and observe animals pre/post-surgery for general health and well-being.</li>
<li>Collection of biological specimens including but not limited to skin, tissue, and blood from all animal species onsite. </li>
</ul>
Who you are: 
<ul>
<li>AS OR BS with at least 4 years of experience with medical device studies or similar.</li>
<li>Must have experience handling large animals (pigs, sheep, goats, rabbits, etc)</li>
<li>Experience with dosing/injections (IM, SubQ, IV, IP, oral)</li>
<li>Experience in a surgical environment is preferred. </li>
</ul>
What does this position pay? 
<ul>
<li>Compensation is determined by several factors which may include skillset, experience level, and geographic location. The expected range for this role is $28.00 to $35.00 per hour. Please note this range is an estimate and actual pay may vary based on qualifications and experience. </li>
</ul>
Please email your resume to <a href="mailto:sshields@provenrecruiting.com" target="_blank">sshields@provenrecruiting.com</a> if you’d like to work alongside some of the finest professionals in the Life Sciences industry! Note: We actively support and promote people of various backgrounds, from race, religion, gender to geographical area, university, lifestyle, and personality type. Proven Recruiting is minority-owned, majority women, and is a strong advocate for diversity and inclusion in the broader community. Apply today!

In Vivo Research Associate II - Large Animal

<h3>Job Description</h3>
Job Description
Job Title: Quality Control Chemist
Job Description
The Quality Control Chemist is responsible for conducting wet analyses and physical testing of in-process chemical samples, ranging from raw materials to finished DEET products. The chemist will confidently utilize instruments such as HPLC, GC, Flame AA, KF, and perform titrations. The role involves interpreting, computing, recording, and reporting all test data to production and other relevant personnel using LabWorks. Promptly alerting production and quality management of any suspect test data or deviations is crucial.
Responsibilities
<ul>
<li>Perform wet analyses and physical testing of in-process chemical samples using standard techniques.</li>
<li>Utilize instruments including HPLC, GC, Flame AA, KF, and conduct titrations.</li>
<li>Interpret, compute, record, and report test data using LabWorks.</li>
<li>Alert production and quality management of suspect test data or deviations.</li>
<li>Calibrate and maintain analytical equipment as instructed by lab management.</li>
<li>Prepare laboratory reagents, standards, and mobile phases as instructed by lab management.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in GMP, analytical chemistry, and quality control processes.</li>
<li>Experience with GC, HPLC, and titrations (manual and automated).</li>
<li>Strong analytical and problem-solving skills.</li>
<li>Ability to work independently with minimal supervision.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in wet chemistry within a chemical manufacturing facility.</li>
<li>Proficiency with Microsoft Office.</li>
<li>Associate degree in Chemistry or another science-related field preferred.</li>
</ul>
Work Environment
The position is based in an older but updated lab, focused on in-process product testing directly from chemical operators. The environment is fast-paced, performing 120 tests per shift with over 300 methods. The lab follows standardized procedures aligned with regulatory agencies, and no R&amp;D is conducted. The shift is 12 hours, from 7pm to 7am, with initial training on the first shift for 2-3 weeks. Long-term opportunities are contingent on the product line's sales performance.
Job Type &amp; Location
This is a Contract to Hire position based out of Greensboro, NC.
Pay and Benefits
The pay range for this position is $24.00 - $27.00/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 Greensboro,NC.
Application Deadline
This position is anticipated to close on Jan 16, 2026.
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.

Quality Control Chemist

<h3>Job Description</h3>
Job Description

Water Treatment Chemical Service Technician (Data Center)— Fort Wayne, IN

A Water treatment Chemical Technician will be responsible for working at a customer's data center in the Fort Wayne area. The Chemical Technician will solve customer water treatment concerns, perform extensive water treatment lab work, and troubleshoot water treatment and control equipment at a customer's massive data center.

As a Service Technician, you will receive an industry competitive salary, expenses, and benefits. In addition, ample technical support is provided along with continuous training. Compensation is based upon experience and the ability to succeed. $55,000 to $75,000 first year base for a qualified candidate. Plus a year end bonus!

We hire with a focus that favors the committed employee both in terms of overall compensation and growth opportunities. We have designed our compensation package accordingly. Benefits include a corporate 401k, health, dental, vision, and life insurance.
Garratt-Callahan (wwwgarrattcallahan.com) is family friendly, profitable, stable, and fiercely private. No layoffs in 120+ years. No ownership change in 120+ years. 75+ straight years of profitability. We have operations from Asia, to the Caribbean, and in every state in the USA. Let's talk.
Job Responsibilities:
<ul>
<li>Solve customers' water problems.</li>
<li>Treat industrial cooling towers to keep them energy efficient and environmentally friendly.</li>
<li>Perform detailed water testing &amp; analyses at a data center.</li>
<li>Help deliver on customer KPIs and promote Garratt-Callahan solutions including proprietary chemical blends, equipment, &amp; monitoring technology.</li>
<li>Reports directly to the Site Manager.</li>
<li>Keep our existing customers happy and safe.</li>
</ul>
About Garratt-Callahan:
Garratt-Callahan is a US based private 120+ year old, nationwide water treatment chemical company. Garratt-Callahan <a href="http://www.garrattcallahan.com" target="_blank">www.garrattcallahan.com</a> treats industrial boilers and cooling towers to keep them energy efficient and environmentally friendly with one of the most advanced product lines in the industry. We are registered to ISO 9001:2015 and sell an industry leading line of “green" solutions, G-C GreenTech. We are headquartered in Burlingame, California.
G-C is family owned, profitable, and expanding. We have five chemical plants in the USA, sales people in every state, and operations in Asia, the Pacific, and the Caribbean.
Benefits:
<ul>
<li>We offer a competitive benefit package which includes medical, dental, vision, AD&amp;D, LT, and 401k. </li>
<li>First year compensation $55,000 to $75,000 plus bonus, depending on experience.</li>
<li>Advanced training, and a clear career path.</li>
<li>Family friendly, flexible hours.</li>
<li>A huge benefit of working for Garratt-Callahan is our stability and low turnover. </li>
<li>No Layoffs in our 119 year history.</li>
<li>G-C is a profitable company. The last year that G-C did not turn a profit was during World War 2.</li>
</ul>

To Apply, please log on to: 
 
<a href="https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=16ed56fa-3af7-47fc-878a-c4d47df49e2f&amp;ccId=19000101_000001&amp;jobId=558913&amp;source=CC2&amp;lang=en_US" target="_blank">https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment…</a>
 Thank you for considering Garratt-Callahan Company. Garratt-Callahan is an EEO/AAE employer. Minorities, women, veterans and individuals with disabilities are encouraged to apply.
 Requirements:

You will be a successful applicant if you have a technical degree such as Chemistry, Chemical Engineering, Biology, Mechanical Engineering, Paper Science, or Water Resources. You must have a 4 year technical degree in the sciences to qualify for this position.
 
A successful applicant must have experience or interest in learning advanced water treatment technologies. A successful applicant must be detail-oriented, adhere to safety protocols, and be able to lift 50 pounds wearing PPE in all weather conditions. One year technical sales, or an internship related to water treatment chemicals is preferred, but we are willing to train and mentor. Outside industrial sales experience is a plus. You must live in or near the Fort Wayne area and be familiar with the industrial marketplace of the area.

Additional Preferred Qualifications:
• Familiarity With Industrial Cooling Towers
• Knowledge and Proficiency with Lab Procedures, Water Equipment, &amp; Water Chemistry
• Ability to Provide Virtual Presentations to Group 
• Experience Working in a Team Setting as a Collaborative Partner


If you have a disability, and need assistance during the application and selection process as a result, please contact the Garratt-Callahan Human Resources department at 650.697.5811. Arrangements can be made to provide an accommodation in order to assist you in applying for an open position using our on-line system, completing any other related paperwork, interviewing, or any other portion of the employment process. This phone number is only for disability assistance.
When requesting an accommodation, please provide your name, phone, email address, or any other means of contacting you. Provide a brief description of the nature of the requested accommodation. A member of the Human Resources team will then contact you to discuss your request. A request for an accommodation will not affect your opportunities for employment with Garratt-Callahan.
Garratt-Callahan values differing experiences, backgrounds and perspectives among our employees, and see them as a competitive advantage. Garratt-Callahan is committed to the fair and equal treatment of all associates and applicants.
Garratt-Callahan is an equal opportunity employer that evaluates qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.
<ul>
<li>The “Equal Employment Opportunity is the Law” poster is available at: <a href="http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf" target="_blank">http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf</a></li>
<li>Garratt-Callahan Company’s reaffirmation of Equal Employment/Affirmative Action Statement <a href="http://www.g-c.com/documents/human_resources/EEO_Letter_Jeff_Garratt.pdf" target="_blank">http://www.g-c.com/documents/human_resources/EEO_Letter_Jeff_Garratt.pdf</a></li>
</ul>

Key Words: Chemistry, chemicals, scientific, science, salesperson, salesman, saleswoman, outside sales, technical sales, account representative, account executive, territory sales, territory manager, district sales, district manager, field engineer, field service, AE, sales engineer, data center, chemical engineer, chemist, mechanical engineer, biologist, biology, microbiology, nalco, ecolab, us water, Suez, ge water, chemtreat, drew industrial, solenis, chem-aqua, kurita, evoqua, fremont, water treatment, boilers, cooling towers, waste water, pumps, equipment, chillers, polymers, biocides, data center, Fort Wayne, Indiana.

Water Treatment Chemical Service Technician at a Data Center

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Associate Manufacturing Scientist I (third shift) supports the production of drug substances and drug products. Their responsibility will focus on the preparation of solutions and reagents by following standard protocols. This technically focused position supports lab work, helps solve problems, and effectively communicates with colleagues.
3rd shift work hours are 10 pm – 8:30 am and includes a 15% shift differential.
Responsibilities
<ul>
<li>Follow batch records, SOPs, and work instructions to detail</li>
<li>Document all operations in batch records and notebooks</li>
<li>Comply with GMP protocols</li>
<li>Assist other chemists within the CMC group during synthesis and chromatography of oligonucleotides including:
<ul>
<li>Reagent solution preparation</li>
<li>Column Packing</li>
<li>Mobile phase preparation</li>
<li>Fraction collection</li>
</ul>
</li>
<li>Operate TFF to desalt purified RNA solutions</li>
<li>Operate a lyophilizer and package solid drug substance</li>
<li>Execute processes as part of a team to ensure production timelines are kept and quality product is produced</li>
<li>Maintain a clean work space</li>
<li>Maintain safety by wearing required personal protective equipment</li>
</ul>
Requirements
<ul>
<li>BS or MS in chemistry, biochemistry, engineering, or related scientific field</li>
<li>Entry level to 3 years experience in a similar position</li>
<li>Good verbal and written communication skills</li>
<li>Ability to work in a team environment</li>
<li>Ability to pay attention to detail</li>
</ul>
Preferred
<ul>
<li>Experience working in a GMP setting with controlled documentation</li>
</ul>
Wisconsin pay range $63,000—$73,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Associate Manufacturing Scientist I (3rd Shift)

<h3>Job Description</h3>
Pay Rate Low: 28.00 | Pay Rate High: 35.00 Microbiologist Microbiologist I (Contract) Exciting Microbiologist I development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care Location: Johns Creek, GA Duration: 2-Year Contract Schedule: Monday–Friday, 8:00 AM–5:00 PM EST Pay: 28.00-35.00 DOE Benefits: Medical, Dental, Holiday, PTO 401K matching Support routine laboratory operations. The ideal candidate will have 1–2 years of hands-on microbiology lab experience and a strong understanding of standard laboratory practices. Responsibilities 
<ul>
<li>Culture, isolate, and identify microorganisms using standard microbiological techniques</li>
<li>Perform environmental, water, and product testing for microbial contamination</li>
<li>Operate laboratory equipment and microscopes to analyze samples</li>
<li>Document test results and prepare technical reports in accordance with SOPs</li>
<li>Follow GMP, safety, and quality guidelines</li>
<li>Collaborate with lab technicians, scientists, and cross-functional teams </li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Biology, Microbiology, or related field</li>
<li>1–2 years of general laboratory or microbiology experience</li>
<li>Familiarity with GMP or regulated laboratory environments preferred</li>
<li>Strong attention to detail and documentation skills </li>
</ul>
Additional Information 
<ul>
<li>Long-term contract with potential for extension or conversion</li>
<li>No sponsorship available</li>
<li>Candidates must be authorized to work in the U.S. </li>
</ul>
This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH

Microbiologist I

<h3>Job Description</h3>
Sr Associate with Chemistry/Biochemistry background (Onsite Job in Thousand Oaks, CA)
Location: Thousand Oaks, CA
Terms: Contract W2
Duration : 12 Months Contract (Will Get Extended for Long)
 
Description:
Fully Onsite
Standard Working Hours
 
Nice to have:
Biotech Industry experience
 
Client in Thousand Oaks, CA, this role in Pivotal Drug Product Technologies will be to provide support of drug product formulation and process development of biologics. The candidate will work closely with a team of engineers and scientists responsible for the technical aspects of client’s drug product commercialization and lifecycle management.
 
Responsibilities will include:
• Participate in the planning, design, execution, and documentation of studies related to drug product formulation and process development in support of commercialization and life cycle management of biologics.
o Support and conduct related studies, e.g. UF/DF, filtration, freeze/thaw and fill/finish, for products in various formulations and formats (liquid, lyophilized, etc.).
o Evaluate process and product performance through analytical testing via measurement of pH, conductivity, osmolality, protein concentration, HPLC and CE methodologies, solid state characterization, particle quantitation/characterization, physical properties, etc.
• Data analysis and documentation/review in electronic notebooks.
• Author, review, and data verify technical documents such as protocols, reports, regulatory documents, etc.
 
Skill Sets:
• 2+ years of relevant lab experience.

<h3>Job Description</h3>
About the Job: The Research Coordinator’s role is to help the research practice operate more efficiently. They do this by handling the logistics to make research run smoothly so that researchers can focus on what they do best – conduct research. Research Coordinator duties may include project and client management, creating and managing materials for research, participant recruitment and session scheduling, incentive management, tool and data management, etc. 
What You’ll Do:
<ul>
<li>Coordinate research participant recruitment</li>
<li>o Identify and recruit research participants per researcher specifications</li>
<li>o Coordinate schedules of research participants, researchers, and stakeholders</li>
<li>o Manage incentives</li>
<li>o Manage lists of past and future research participants</li>
<li>Manage software systems used for data collection and analysis</li>
<li>Coordinate with Design Program Managers, Design Leads, and other stakeholders</li>
<li>Work as part of the larger Design Operations team and may be called upon to do operational work for the broader design organization.</li>
<li>If capacity allows, manage projects across the research organization. Including</li>
<li>o Prepare study materials and data collection tools for research sessions</li>
<li>o Schedule planning, research, and report-out sessions for researchers</li>
<li>o Prepare data for analysis</li>
<li>o Create and manage data repositories and handle records retention</li>
</ul>
Skills You Have:
<ul>
<li>Bachelor’s degree, or equivalent</li>
<li>Experience providing operational support to fast-paced research teams.</li>
<li>Experience with research participant recruitment</li>
<li>Demonstrated skills in increasing team efficiency.</li>
<li>Strong communication and organizational skills with attention to the right details to ensure operations run smoothly</li>
<li>An ability to anticipate and proactively solve logistical issues so your team knows they’ll never miss a beat when you’re coordinating their work</li>
</ul>
Additional Qualifications We’d Love:
<ul>
<li>2 years’ experience collaborating with live research teams.</li>
<li>Experience working in a highly regulated environment like healthcare or financial services.</li>
<li>Professional association with the Research Ops community.</li>
</ul>

#LI-Hybrid 


Compensation Range:

Pay Range - Start:
$60,340.00

Pay Range - End:
$112,060.00

Geographic Specific Pay Structure:

Structure 110:
$66,360.00 USD - $123,240.00 USD
Structure 115:
$69,370.00 USD - $128,830.00 USD

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<ul>
<li>Flexible work schedules</li>
<li>Concierge service</li>
<li>Comprehensive benefits</li>
<li>Employee resource groups</li>
</ul>
PandoLogic. Keywords: Research Coordinator, Location: Milwaukee, WI - 53205

UX Research Coordinator

<h3>Job Description</h3>
ProMed Staffing Resources B is seeking a travel Physicist for a travel job in Boise, Idaho.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Duration: 13 weeks</li>
<li>36 hours per week</li>
<li>Shift: 12 hours, days</li>
<li>Employment Type: Travel</li>
</ul>

Shift 7a-7p, Experience with EPIC, ARIA RadOnc, SHARE DRIVE CTC-RadOnc preferred. Certification by ABR.
Shift 7a-7p, Experience with EPIC, ARIA RadOnc, SHARE DRIVE CTC-RadOnc preferred. Certification by ABR REQUIRED
About ProMed Staffing Resources B
ProMed Staffing Resources has been a trusted leader in healthcare staffing for over three decades, delivering top-tier workforce solutions with a commitment to excellence. Located in the heart of Midtown Manhattan, we serve clients and candidates across the United States.
Our extensive network connects Registered Nurses and allied clinicians with premium local and travel contract opportunities at leading healthcare organizations, including renowned hospitals, medical centers, healthcare systems, and schools.&nbsp;
We pride ourselves on offering a seamless hiring process, supported by a one-on-one dedicated recruiter who serves as your guide and advocate every step of the way. Our concierge-level service ensures you feel supported and valued throughout your hiring journey and beyond.
Recognized for our unwavering dedication to quality, we are proud to hold the Joint Commission's prestigious Certified Gold Seal of Approval, a testament to the superior standards we uphold for both our clients and personnel.
At ProMed Staffing Resources, "Your Trusted Healthcare Partner" isn’t just a slogan—it’s a promise. Experience our expertise, reliability, and personalized approach. Join the countless nurses and allied clinicians who have chosen ProMed Staffing Resources for outstanding solutions tailored to their unique needs.

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