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<h3>Job Description</h3>
Job Title : Research Associate ( Research Assistant )
Location : South San Francisco - 94080
Duration : 12 Months 
Job Description : 
<ul>
<li>B.S. in Biology, Biochemistry, Molecular Biology, or a related discipline, with 1+ years of industry experience in pharmaceutical or biotechnology settings.</li>
<li>Hands-on experience performing quantitative assays (e.g. ELISA), for the characterization of proteins, nucleic acids, viruses or other biological products.</li>
<li>Strong hands-on experience with sterile technique and mammalian cell culture, including cell maintenance, expansion, characterization, and banking.</li>
<li>Working knowledge of core molecular biology techniques (DNA/RNA/protein isolation, cDNA synthesis, RT-PCR, qPCR, digital PCR).</li>
</ul>
Experience working with Adeno-Associated Virus (AAV) is a plus

Research Assistant

<h3>Job Description</h3>
Job DescriptionJob Title: Production ChemistJob Description
We are seeking a skilled Production Chemist to join our team and contribute to our chemical manufacturing processes. You will be responsible for handling raw materials, operating manufacturing equipment, and ensuring that all chemical operations are performed according to specific formulas to create new chemical compounds.
Responsibilities
<ul>
<li>Handle and manage all raw materials for chemical operations.</li>
<li>Operate chemical manufacturing equipment and follow specific chemical formulas.</li>
<li>Collaborate with engineers, production personnel, and the analytical team to ensure product specifications are met.</li>
<li>Work closely with chemical engineers and R&amp;D personnel to scale up processes.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Chemistry or related scientific field.</li>
<li>Experience in chemical processing and manufacturing.</li>
<li>Ability to work with R&amp;D personnel, scale-up and process teams, operations, and laboratory settings.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in chemical synthesis.</li>
<li>Strong laboratory skills.</li>
</ul>
Work Environment
The role involves working in a chemical manufacturing setting. Initial training occurs Monday through Friday on first shift hours (6 am to 2:30/3:30 pm). After training, the schedule shifts to a weekend day shift from 6:00 am to 6:00 pm on Friday, Saturday, and Sunday.
Job Type &amp; Location
This is a Contract to Hire position based out of Milwaukee, WI.
Pay and Benefits
The pay range for this position is $29.50 - $29.50/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 Milwaukee,WI.
Application Deadline
This position is anticipated to close on Jan 21, 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.

Production Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Cleanroom AssemblerJob Description
Join a dedicated and high-performing team at our new Grand Rapids, MI site, where you will play a crucial role in the production and packaging of components for medical devices. Your work will be instrumental in our mission to alleviate pain, restore health, and extend life for millions of people worldwide. This role involves working in a cleanroom environment with personal protective equipment including eyewear, ear plugs, hair net, and protective gowning.
Responsibilities
<ul>
<li>Perform a variety of tasks ranging from repetitive to non-repetitive production assembly operations following Good Manufacturing Practices and Standard Operating Procedures.</li>
<li>Work from visual aids, method layouts, diagrams, schematics, process flow sheets, and written or verbal assembly instructions.</li>
<li>Set initial layouts and use a variety of tools to prepare products.</li>
<li>Conduct continuity checks on work in process and completed items.</li>
<li>Conduct quality inspections on processing line in accordance with quality specifications.</li>
<li>Operate packaging machines and handle boxing and labeling materials.</li>
</ul>
Essential Skills
<ul>
<li>General labor skills in a cleanroom environment</li>
<li>Ability to follow assembly and production procedures</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in a cleanroom manufacturing environment is a plus</li>
<li>Experience using measuring devices and hand tools</li>
</ul>
Why Work Here?
Be part of a nationwide company that is committed to improving healthcare and saving lives. Enjoy an air-conditioned, sit-down job that offers a supportive and innovative work culture.
Work Environment
This position involves working in a cleanroom with required personal protective equipment. The role is scheduled for the 2nd shift, Monday through Friday, from 2:30 PM to 10:30 PM.
Job Type &amp; Location
This is a Contract to Hire position based out of Grand Rapids, MI.
Pay and Benefits
The pay range for this position is $20.00 - $20.00/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 Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Jan 21, 2026.

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.

Cleanroom Assembler

<h3>Job Description</h3>
Job Description
Job Description
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As an Associate Research Coordinator, one will assist the research coordinator (CRC/CCRC) in conducting clinical trials. The associate research coordinator is responsible for collecting, processing, storing and handling clinical specimens (as needed), scheduling study subjects for study visits, and collecting, recording, and filing clinical research data. Additionally, the associate research coordinator conducts study visits under the supervision of a study coordinator or senior coordinator.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II – IV Clinical Research services. The QPS location in Miami, Florida is a multi-specialty research center employing clinical research professionals, including board-certified physicians, in a 32,000 square foot space. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (<a href="http://www.qps.com" target="_blank">www.qps.com</a>) for more information and to see all current openings.
The Job
<ul>
<li>Ensuring GCP is followed throughout the entire study conduct.</li>
<li>Ensuring subject confidentiality.</li>
<li>Ensuring the subject or subject’s legal representative is provided with a copy of the signed and dated informed consent form.</li>
<li>Possess a sound and in-depth understanding of each protocol that has been assigned</li>
<li>Source document creation per Protocol requirements (if applicable) or as needed</li>
<li>Ensuring compliance with applicable MRA SOP’s/MRA Clinical Research SOP’s, Good Clinical Practice guidelines and regulations</li>
<li>Timely communication of study issues to the study coordinator</li>
<li>Screening, Enrollment, and Ongoing Study Procedures
<ol>
<li>Establish good rapport with potential study subjects</li>
<li>Conduct telephone screening process</li>
<li>Conduct Informed Consent Process (must complete Consenting Process module and quiz prior to consenting)</li>
<li>Clinical data collection such as vital signs, ECG recording, subject height and weight, etc.</li>
<li>Medical records retrieval and review</li>
<li>Laboratory specimen collection, processing and shipment (as needed)</li>
<li>Transporting clinical specimens to the laboratory</li>
<li>Study visits scheduling </li>
</ol>
</li>
</ul>
Requirements
<ul>
<li>Combination of relevant education &amp; experience that provides sufficient knowledge &amp; skills to ensure incumbent’s success in this role, such as: </li>
<li>High School Diploma, and/or </li>
<li>Experience in a similar role </li>
<li>Prior experience as a medical assistant or in an ancillary or allied health specialty a plus</li>
</ul>
Why You Should Apply
<ul>
<li>Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li>
<li>Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li>
<li>Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&amp;D and Short and Long-term Disability Insurance</li>
</ul>

QPS is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Associate Research Coordinator

<h3>Job Description</h3>
Job Description Location(s): New Mexico Practice/Department: Emerging Regions Internal Title: As-Needed Field Technician Work Environment: Field Work Compensation: $25-45/hourly * 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 We are seeking entry- and mid-level professionals to conduct stormwater inspections and environmental construction compliance monitoring in NM. Positions will be based at project sites located throughout New Mexico. Candidates will have some experience with environmental survey techniques, a background in environmental, a willingness to perform strenuous physical activity in harsh desert climates with uneven and sometimes difficult terrain, problem-solving capabilities, and a desire to learn and work as part of a team. Preference will be given to candidates that have experience with stormwater inspections. These candidates have participated in or led/helped lead inspections. Any candidate must possess the ability and willingness to continually hike in desert climates for days or weeks at a time, use GIS and data collection applications, navigate terrain and drive off road. Having a 4wd and/or high clearance vehicle is a plus. Duties and Responsibilities 
<ul>
<li>May be involved with all or a selection of the following, individually or as part of a team:</li>
<li>Compiling available research data and evaluating applicability to specific project sites</li>
<li>Vegetation mapping and habitat characterization</li>
<li>General environmental inspections for compliance with applicable rules and regulations</li>
<li>Construction monitoring</li>
<li>Work as a member of our team in the preparation of technical reports and studies including biological constraints analyses, wetland delineation reports, wetland permit applications, focused survey reports, threatened and endangered species permitting documentation, and biological resources technical reports.&nbsp; This includes working individually and as part of a team on the following:</li>
<li>Assembly and synthesis of data related to biological issues and impact assessment</li>
<li>Coordination with internal staff and sub-consultants preparing technical reports</li>
<li>Coordination with technical staff in document preparation, map and exhibit preparation, editing and production and distribution tasks</li>
</ul>
Minimum Qualifications
<ul>
<li>Bachelor’s degree in biology, ecology, botany, or related natural resources field, or equivalent experience</li>
<li>Experience in performing environmental inspections, or a willingness to learn.</li>
<li>Background and/or coursework in environmental field methods or biological science</li>
<li>Ability to hike in harsh desert conditions for many days at a time</li>
<li>Must possess a valid driver’s license and have active personal automobile liability insurance by the first day of employment</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience in performing stormwater inspections</li>
<li>Background and/or coursework in environmental field</li>
<li>Stormwater inspection experience in&nbsp;NM</li>
<li>Must demonstrate solid written and verbal communication skills.</li>
<li>Highly organized with the ability to multi-task in a fast-paced environment.</li>
<li>Self-motivated with an interest to learn and grow as a project team.</li>
</ul>
 Compensation: $25-45/hourly* *Final agreed-upon compensation will be based on a variety of factors including, but not limited to, an individual’s related experience, education, certifications, skills, and work 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>This job requires attending meetings, both in person and virtually as well as speaking on the phone with government agency representatives, members of the public, and others. Speaking, hearing and listening are required.</li>
<li>Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.</li>
<li>Outdoor activity may involve walking/trekking in uneven terrain over long distances in extreme weather conditions for extended periods of time.</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.
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As-Needed Biologist / Biological Monitor - NM

<h3>Job Description</h3>
Job DescriptionCompany Overview
Before we opened Strive Pharmacy we were unsatisfied with the current state of the pharmaceutical industry. Most of the current pharmaceuticals only offer a one size fits all approach and often come with unwanted and potentially dangerous side effects. We found that through compounding we can offer a much more personalized solution to medicine.
Through this we have been able to help patients get the results they are seeking for their personal needs. After years of working for corporate chains we took the risk and opened Strive Pharmacy. We are dedicated to providing a better experience for each customer and clinic that we work with. Come see the Strive difference.
Our Mission
We're flipping the script with personal medicine. We strive to interrupt an industry that has been closed to personalized care, accessibility, and nuance for too long. We strive to shift a reactive view of self-care and ignite a proactive baseline-shifting approach to health for all. 'The human element' is our crux and catalyst, driving all that we do, whether we're interacting with patients, providers, or practices. We're here to partner with those ready for a change. More than a compounding pharmacy, we're on a mission to positively disrupt healthcare as we know it. Strive is about more than medicine. Strive is about striving for the personal side of healthcare.
Position Type: Full-Time
Department: Product Development
Location: Remote but must be located near Tampa, FL, Phoenix, AZ, or St. Louis, MO.
Pay Range: $105,000 - $120,000 + 10% bonus
Position Overview:
The Chemist will support both 503A and 503B efforts of compounding pharmacy operations by leading R&amp;D initiatives, overseeing sterile and non-sterile third-party testing programs, and supporting site standardization and compliance activities. This role is responsible for developing scalable, compliant compounded drug products while ensuring alignment with USP, FDA, and cGMP requirements.
In addition to hands-on development and testing oversight, this position will play a key role in establishing and building the company's internal analytical laboratory. The Chemist will help define analytical capabilities, develop testing methods, and implement systems and workflows to support ongoing product release, stability, and investigative testing. This role will also contribute to building and mentoring an internal R&amp;D and analytical team as the organization grows.
Primary Responsibilities:
<ul>
<li>Manage all sterile and non-sterile third-party testing communication activities, including method selection, sample coordination, data review, and vendor qualification</li>
<li>Leading/developing our in-house analytical lab upon site-readiness</li>
<li>Design and execute R&amp;D studies, including formulation feasibility, stability, compatibility, and process development and manage R&amp;D direct reports</li>
<li>Establish analytical workflows, SOPs, and best practices to support long-term business growth</li>
<li>Adjusting MFR methods of preparation to reflect formula/quality optimization</li>
<li>Verifying stability and compatibility of ingredients</li>
<li>Reviewing and developing compound formulations</li>
<li>Supporting staff training on best practices</li>
<li>Ensuring adherence to USP guidelines</li>
<li>Acts as a key resource for maintaining product efficacy and aligning with compliance and regulatory standards for customized medication preparations</li>
<li>Willingness to travel to site locations up to 25%</li>
<li>Working cross functionally with all departments within the enterprise</li>
</ul>
Qualifications:
<ul>
<li>Advanced degree in Pharmacy, Medicine, Life Sciences, or related field (PharmD, MD, PhD).</li>
<li>Ability to work independently, prioritize tasks, and adapt to changing priorities in a fast-paced environment.</li>
<li>Excellent communication, presentation, and interpersonal skills with the ability to effectively engage with diverse audiences.</li>
<li>Experience within the analytical lab setting.</li>
</ul>
Join Us in Making an Impact:
Are you ready to make a genuine impact on patient care and contribute to better healthcare outcomes with every interaction? Embrace this integral role and be a part of the Strive Pharmacies team today. Your journey towards healthcare excellence starts here! Apply now.
Benefits/ Perks
Strive Pharmacy provides a comprehensive benefits package that encompasses various perks such as employer paid healthcare coverage available after 30 days of employment, the choice of an FSA/HSA, a voucher for new hire scrubs (if applicable), parental leave, a 401(k) plan with matching contributions, and the benefit of weekends and holidays off. FREE COMPOUNDED MEDS to employees and immediate family members.
Culture 
At Strive, culture plays a fundamental role in shaping our workplace atmosphere. Beyond our exceptional benefits package, we foster a sense of community. Throughout the year, we arrange various holiday potlucks and festive celebrations. Strive is committed to promoting both personal and professional development, striving for our employees to excel and grow in every aspect of their lives, both within and outside of the workplace. 
EEO
Strive Pharmacy is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristics as outlined by federal, state or local laws.
Disclaimer*** Please do not call the pharmacy location with questions about your application or interview. A talent acquisition partner will reach out to you.

Product Formulation Chemist

<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>Bonus based on performance</li>
<li>Company parties</li>
<li>Flexible schedule</li>
<li>Free food &amp; snacks</li>
<li>Free uniforms</li>
<li>Opportunity for advancement</li>
<li>Paid time off</li>
<li>Training &amp; development</li>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Vision insurance</li>
</ul>
 Position Title: Window Cleaning Technician Position Type: Part-time Hours: Flexible / Custom Pay: $17~$25 per hour Are you looking for an opportunity to be a part of a growing dynamic company? Do you wish you could be a part of a growth minded team to support you in your personal and professional goals? Do you find fulfillment with results driven tasks? Here at Fish Window Cleaning we are a mission focused company that believe that our employees are our greatest asset and tool in brightening our community one window at a time. This job is a great fit for you if an office is the last place youd enjoy working in. Our team of cleaning technicians enjoy working outside within the community interacting with our commercial and residential customers. The cleaning technician is responsible for managing daily work order completion, jobsite quality control, and fulling the needs of our customers to the best of their capabilities. It is our mission to become the best and most respected window cleaning company in the world. Description of duties: Provide excellent customer service to our clients Manage and execute daily assigned work orders Able to demonstrate importance of safety in the workplace, set and follow safety standards, and report unsafe conditions to appropriate Supervisor Maintain weekly completed production standards and expectations Acts as the liaison/ambassador for Fish Window Cleaning while interacting with customers Qualifications: Strong Communication skills Willingness to learn Ability to contribute to a high-functioning team as well as working independently Strong time management skills Perks and Benefits: Compensation- Hourly and Commission based pay structure Flexible Schedule- No Nights or Weekends Potential for merit increase/bonus Paid Holidays Paid Vacation Insurance Options Application: If this sounds like a position you would be happy in, APPLY now and lets get connected. If you like this position so much you want to skip to the front of the line TEXT us at (636-584-9190)

Part time Window Cleaning Technician

<h3>Job Description</h3>
Powerwell is a leading recruitment firm helping our clients discover top talent. We’re recruiting for a Lead Food Scientist I. 
 
About Our Client:
Our client’s purpose is unlocking the potential of people, nature, and science to nourish the world. We consistently incorporate social and environmental impact into decision making given its importance to the success and profitability to our business. Our client is committed to creating a diverse and inclusive environment by embracing the wisdom and strengths that diversity brings.
 
Job Summary:
Our client’s Taste and Sensory Innovation team is the foundation and driving force of our client’s business through developing new food concepts and flavor formulations to gain new businesses. As a core team member, you will focus on the development and optimization of savory flavors, including reactions, top notes and EU compliant flavors to ensure that our client remains a leader in delivering high-quality and customized flavor solutions. The successful candidate support both product innovation and customer-specific projects.
 
Essential Job Responsibilities:
<ol>
<li>Utilize knowledge of flavor science to create complex and authentic savory flavors to meet customer and market demands.</li>
<li>Conduct research to explore and understand the functionalities of raw materials and processes that allow the creation of natural flavors for the US, EU and APAC.</li>
<li>Stay abreast of the latest trends and innovations in the flavor world, bringing concepts from ideation to commercialization.</li>
<li>Ensure compliance with regulatory requirements, customer specifications, and food safety standards during the development of flavor products.</li>
<li>Manage innovation projects by collaborating with cross functional teams such as Regulatory, Marketing, Sales, and the Business Unit Leadership teams, and to plan, prioritize, communicate, and execute multiple tasks efficiently.</li>
</ol>
 
Required Education/Experience:
<ul>
<li>Must be a certified Flavorist or in process of obtaining.</li>
<li>Master’s Degree in Food Science or Chemistry or related field.</li>
<li>Experience in developing and enhancing top note profiles for savory applications.</li>
<li>Experience in designing and optimizing reaction flavor systems, including ingredient interactions, thermal processing, and yield efficiency improvements.</li>
<li>Experience in balancing top notes with reaction flavors to achieve complex, authentic flavor profiles.</li>
<li>Ability to analyze and interpret data, communicate, and provide recommendations for research projects.</li>
<li>Excellent communication skills</li>
<li>Excellent project management skills with strong attention to detail.</li>
</ul>
 
Equipment Operation:
<ul>
<li>Standard and Advanced laboratory equipment and instrumentation</li>
<li>Lab scale grinding and extraction equipment</li>
</ul>
This job description is not intended to cover every detail or every aspect of the job identified. Other duties may and will be assigned based upon the workload and needs of the department. Our client is committed to providing safe food to its customers. This position requires completing annual food safety training. Food safety training is conducted through our client’s electronic training program and on-the-job training in each department.
 
Benefit Information:
<ul>
<li>Benefits are effective Day 1 of employment.</li>
<li>Blue Cross Blue Sheild of MI, Delta Dental &amp; VSP Vision</li>
<li>5% direct contribution to 401(k) by our client.</li>
<li>128 hours of PTO/10 Federal Holidays/4 hours volunteer time.</li>
<li>Eligible for 10% Administrative Bonus based on company performance annually.</li>
<li>Paid weekly.</li>
</ul>

Lead Food Scientist I

<h3>Job Description</h3>
Job Description
M-F, 8 am to 5 pm 
 
Summary
The Research Coordinator will support and oversee the execution of multiple clinical research studies across inpatient and outpatient units at The Menninger Clinic. This position may contribute to clinic-wide outcomes research as well as focused research projects examining topics such as mental health, predictors of treatment response, resilience, recovery and relapse, and emerging and innovative interventions.
The role involves direct interaction with patients and clinical staff, coordination with academic and institutional partners, and administrative responsibilities related to regulatory compliance, data quality, and reporting. Depending on the study, the Research Coordinator may also accompany participants to off-site locations (e.g., academic medical centers) for study procedures such as neuroimaging.
This position offers a unique opportunity for meaningful patient-facing research experience within a nationally recognized psychiatric hospital and is particularly well-suited for individuals seeking advanced training in medicine, psychology, social work, public health, or related fields.
Key Functions
Study Coordination &amp; Operations
<ul>
<li>Oversee day-to-day execution of multiple research protocols across Menninger Clinic units (inpatient and/or outpatient).</li>
<li>Serve as a primary point of contact between research teams and Principal Investigator(s).</li>
<li>Track study progress and communicate recruitment, retention, and milestone updates to investigators.</li>
<li>Coordinate research workflows and, when applicable, supervise research assistants or trainees.</li>
<li>Prepare and maintain study-related documentation, including protocols, manuals of procedures, consent forms, and correspondence.</li>
</ul>
Regulatory &amp; Compliance
<ul>
<li>Prepare, submit, and manage Institutional Review Board (IRB) applications, amendments, continuing reviews, and related correspondence.</li>
<li>Ensure adherence to institutional policies and federal and sponsor regulations.</li>
<li>Maintain accurate and up-to-date regulatory binders and study records.</li>
</ul>
Participant Interaction &amp; Clinical Research Activities
<ul>
<li>Recruit, screen, consent, and enroll patients across inpatient and outpatient programs into research studies.</li>
<li>Communicate with participants via face-to-face interactions, phone calls, and email throughout their participation.</li>
<li>Conduct standardized assessments and clinically complex research or diagnostic interviews, as appropriate to training and protocol requirements.</li>
<li>Schedule and coordinate research-related appointments, tests, and procedures (e.g., laboratory tests, imaging, behavioral tasks).</li>
<li>Coordinate and attend off-site study visits when required (e.g., MRI scans at Baylor College of Medicine or other partner institutions).</li>
<li>Communicate relevant study participation information to clinical teams to support coordinated and safe patient care.</li>
</ul>
Data Management &amp; Outcomes Research
<ul>
<li>Ensure timely and accurate data collection across studies.</li>
<li>Perform data cleaning and quality assurance checks, to ensure data are analysis-ready.</li>
<li>Generate and distribute research and outcomes reports for participants, clinicians, investigators, and other stakeholders in a timely manner as appropriate given the study.</li>
<li>Support longitudinal follow-up and retention efforts for outcomes research.</li>
</ul>
Research Dissemination &amp; Professional Development
<ul>
<li>Work closely with clinician-scientists and interdisciplinary research teams and receive mentorship in clinical research methods and scientific communication.</li>
<li>Participate, as appropriate and based on interest and performance, in data analysis, abstract preparation, conference presentations, and manuscript development.</li>
<li>Participate, as appropriate and based on interest and performance, in research meetings and contribute to discussions related to study design, interpretation, and dissemination.</li>
</ul>
Administrative &amp; Resource Management
<ul>
<li>Coordinate acquisition and management of research supplies and equipment.</li>
<li>Assist with budget tracking and financial oversight for research projects.</li>
<li>Perform other research-related duties as assigned.</li>
</ul>
Education
Required: Bachelor’ degree.
Preferred: Bachelor’s degree in psychiatry, psychology, social work, neuroscience, public health, or other degrees translational mental health research.This position is ideal for highly motivated early-career professionals seeking hands-on clinical research experience prior to applying to medical school, graduate programs (PhD, PsyD, MPH), or other health-related training programs. 

Why Join The Menninger Clinic Research Team?
The Menninger Clinic is a nationally recognized leader in psychiatric care and research. This role offers exceptional exposure to complex mental health populations, innovative research initiatives, and close collaboration with experienced clinician-scientists. The Research Coordinator position provides a strong foundation for future careers in medicine, psychology, neuroscience, public health, and clinical research.

Research Coordinator, Outpatient

<h3>Job Description</h3>
About the Role
We are seeking a detail-oriented Research Programs Specialist to support research funding, investigator support, and research education initiatives within a mission-driven organization. This role plays a key operational and administrative function across grant programs, reporting, financial coordination, and event support.
The ideal candidate is highly organized, comfortable managing multiple deadlines, and enjoys supporting research and professional development initiatives behind the scenes.
 
Key Responsibilities
Grant Administration &amp; Program Support
<ul>
<li>Conduct compliance checks on grant applications prior to review</li>
<li>Maintain submission trackers and reporting databases</li>
<li>Assist with grant review preparation, including reviewer materials</li>
<li>Update application statuses within online grant management systems</li>
<li>Support grant processing, monitoring, and closeout activities</li>
</ul>
Reporting &amp; Program Evaluation
<ul>
<li>Track awardee reports and deliverables</li>
<li>Generate and organize reporting data for internal stakeholders</li>
<li>Follow up with award recipients regarding outstanding reports</li>
<li>Assist with grant outcomes analysis and summary reporting</li>
</ul>
Financial &amp; Administrative Support
<ul>
<li>Prepare payment and travel reimbursement requests, including documentation collection</li>
<li>Submit approved requests for processing</li>
<li>Maintain funded award tracking tools and checklists</li>
<li>Support financial stewardship across research-related programs</li>
</ul>
Meetings, Events &amp; Publications
<ul>
<li>Assist with planning and preparation for professional meetings and educational events</li>
<li>Provide logistical and material support for conferences and workshops</li>
<li>Draft outlines and assist with content preparation for research-related communications</li>
<li>Support internal publication and article development as needed</li>
</ul>
Operations &amp; Clerical Support
<ul>
<li>Maintain shared workspaces and inventory related to program operations</li>
<li>Prepare printed materials, binders, signage, and shipping materials for events</li>
<li>Support general office organization and administrative tasks</li>
</ul>
 
Qualifications
<ul>
<li>Bachelor’s degree preferred (health science, research, or related field a plus)</li>
<li>Experience in research, grants, or program administration strongly preferred</li>
<li>Willingness to attend evening calls (approximately 3–6 per month)</li>
<li>Availability for limited weekend work (3–5 times per year)</li>
</ul>

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