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city

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<h3>Job Description</h3>
Job Description
Located at our North American research hub, you will be at the heart of where pet health and nutrition are revolutionized. Your work in our microbiological and analytical laboratory directly supports the development of future product innovations. By ensuring every sample meets our uncompromising standards for quality and safety, you help provide pets with the nutrition they need to live longer, happier lives.
salary: $19.99 - $20 per hour shift: First work hours: 8 AM - 4 PM education: Bachelors 
Responsibilities
What You’ll Do:
<ul>
<li>Plan and conduct laboratory experiments to verify the physical and biological specifications of various substances and pet nutrition materials.</li>
<li>Assisting senior scientists in a high-tech lab environment by collecting samples and performing detailed biological or chemical analyses.</li>
<li>Record precise observations and prepare comprehensive reports that include conclude findings and offer actionable recommendations for the R&amp;D team.</li>
<li>Maintain the integrity of our world-class facility by performing routine maintenance and safety checks on advanced laboratory equipment to ensure it remains in top working order.</li>
</ul>
What You’ll Bring:
<ul>
<li>Vocational or technical education in Microbiology, Biology, Chemistry, or a related scientific field.</li>
<li>Hands-on knowledge of routine laboratory procedures, aseptic techniques, and tool management obtained through work or academic experience.</li>
<li>Previous experience in an R&amp;D or quality testing environment, particularly within the food or pet care sectors. (preferred)</li>
</ul>
What's in it for you?
<ul>
<li>Pay: $20.00 per hour.</li>
<li>Schedule: Tuesday to Saturday, 8am to 4:30pm CST </li>
<li>Work on a pet-friendly, eco-conscious campus featuring outdoor green spaces, walking trails, and a unique "pet-first" culture.</li>
<li>Gain exposure to global R&amp;D standards and learn from industry-leading experts in microbiology and nutrition.</li>
</ul>
For a faster response, please email your resume to <a href="mailto:michael.wilson@randstadusa.com" target="_blank">michael.wilson@randstadusa.com</a>
 Skills
<ul>
<li>Laboratory/Sciences</li>
<li>Sampling</li>
<li>Analysis</li>
<li>Nutrition</li>
</ul>
 Qualifications
<ul>
<li>Years of experience: 1 year</li>
<li>Experience level: Entry Level</li>
</ul>
 Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.

Laboratory Associate

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical EngineerJob Description
We are seeking a skilled Chemical Engineer to perform all chemical process functions related to chemical batching. This role involves conducting root cause analysis (RCA) to troubleshoot batching issues and implementing corrective and preventive actions (CAPAs) for both internal and external challenges. You will be responsible for scaling up and commercializing new formulas, adjusting existing formulas, and validating all manufacturing and quality processes and specifications. Additionally, you will perform in-process batch adjustments, support production scaling to meet product specifications, and analyze production and laboratory data to optimize processes and reduce costs.
Responsibilities
<ul>
<li>Conduct root cause analysis for customer complaints and internal production issues.</li>
<li>Ensure all batch adjustments are executed accurately when raw materials or formulas change.</li>
<li>Scale up and commercialize new formulas and products, ensuring correct implementation.</li>
<li>Analyze production data and quality data to identify optimization and cost reduction opportunities.</li>
<li>Participate in the disposition of non-conforming materials and support deviation management.</li>
<li>Mentor and coach fellow engineers and quality and production personnel in continuous improvement activities.</li>
</ul>
Essential Skills
<ul>
<li>1-5 years of experience in chemical engineering or chemical process engineering.</li>
<li>Ability to diagnose and resolve customer complaints and internal production issues.</li>
<li>Experience with root cause analysis and implementation of CAPA.</li>
<li>Expertise in chemical manufacturing, quality control, and process engineering.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Degree in Chemical Engineering or a related field.</li>
<li>Experience in scale-up and commercialization processes.</li>
<li>Familiarity with chemical equipment and laboratory practices.</li>
<li>Knowledge of new product development and chemical processing.</li>
</ul>
Work Environment
This position operates in a chemical manufacturing environment, working across offices, laboratories, production areas, and production labs. The role follows a first shift schedule from Monday through Friday, with flexible working hours typically ranging from 40 to 45 hours per week, extending to 50 hours during major projects or issues. You will collaborate with various organizational levels, including R&amp;D, Quality, Production, Maintenance, Customers, Sales, and leadership roles.
Job Type &amp; Location
This is a Permanent position based out of Germantown, WI.
Pay and Benefits
The pay range for this position is $90000.00 - $110000.00/yr.
This company offers health insurance, dental insurance, vision insurance, 401k match, bonuses, etc. They also provide paid vacation and paid holiday.
Workplace Type
This is a fully onsite position in Germantown,WI.
Application Deadline
This position is anticipated to close on Jan 26, 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.

Chemical Engineer

<h3>Job Description</h3>
Job Description
Quality Control Chemist - 2nd shift (Monday-Thursday, 2pm-1am)
Job Description
The Quality Control Chemist plays a crucial role in supporting manufacturing by conducting laboratory analysis of raw materials, intermediate blends, and finished products. This analysis is performed using wet chemistry techniques such as pH measurement, UV-Vis spectroscopy, FTIR, and titration, along with advanced instrumentation including HPLC and GC.
Responsibilities
<ul>
<li>Follow standard operating procedures to ensure quality control.</li>
<li>Conduct quality testing and document results accurately.</li>
<li>Maintain and calibrate laboratory instruments regularly.</li>
<li>Assist with the transfer of test methods.</li>
<li>Train personnel on equipment usage and testing methods.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's Degree in Chemistry</li>
<li>Minimum of 3 years of laboratory experience</li>
<li>Proficiency in HPLC, GC, pH measurement, UV-Vis spectroscopy, FTIR, and other wet chemistry techniques</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in HPLC, GC, and analytical test method development and transfer</li>
<li>Familiarity with microbial testing and procedures</li>
<li>Experience in contract manufacturing and testing</li>
</ul>
Work Environment
The position is based in a laboratory environment requiring adherence to safety protocols. Proper PPE including safety glasses, gloves, lab coat, and ear plugs will be provided and must be worn at all times. The role involves 75% standing, 25% sitting, and occasional lifting of up to 25 lbs. The work schedule is 2nd shift, Monday to Thursday, from 2pm to 1am, consisting of four 10-hour shifts. Occasional weekend work or overtime may be required. Initial training will require some first shift hours.
Job Type &amp; Location
This is a Permanent position based out of Edgerton, WI.
Pay and Benefits
The pay range for this position is $62400.00 - $62400.00/yr.
Medical, dental, vision, 401K
Workplace Type
This is a fully onsite position in Edgerton,WI.
Application Deadline
This position is anticipated to close on Jan 26, 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
Molecular Biologist
Job Description
The biologist in this role will utilize molecular cloning, transient plant transformation, DNA extraction, DNA sample cleanup, and basic sequence analysis to test recombinase variants for activity and specificity. Candidates should possess hands-on experience in a molecular biology laboratory environment and preferably with plant tissue culture.
Responsibilities
<ul>
<li>Perform molecular cloning using techniques such as restriction/ligation and assembly.</li>
<li>Conduct DNA extraction and purification.</li>
<li>Execute PCR and qPCR procedures.</li>
<li>Analyze sequences using basic bioinformatics tools like BLAST, SnapGene, and Geneious.</li>
<li>Carry out transient plant transformation, for example, Agrobacterium-mediated methods.</li>
<li>Engage in plant tissue culture, if preferred.</li>
<li>Understand site-specific recombination systems including Cre/lox and FLP/FRT.</li>
<li>Evaluate the activity and specificity of recombinase variants.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in molecular cloning techniques.</li>
<li>Experience in DNA extraction and purification.</li>
<li>Ability to perform PCR and qPCR.</li>
<li>Competence in sequence analysis with bioinformatics tools.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Microbiology, Molecular Biology, Plant Biology, or a related field.</li>
<li>Hands-on experience in a molecular biology lab, either academic or industry.</li>
<li>Familiarity with plant systems is a strong advantage.</li>
<li>Experience with DNA cleanup kits and protocol troubleshooting.</li>
</ul>
Work Environment
The role involves working in a molecular biology laboratory setting, requiring attention to detail in experimental design and data recording. The candidate must be able to work independently as well as collaboratively within a team. The work environment supports strong problem-solving and troubleshooting skills, fostering a culture of continuous learning and scientific exploration.
Job Type &amp; Location
This is a Contract position based out of Chesterfield, MO.
Pay and Benefits
The pay range for this position is $28.00 - $35.00/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 Chesterfield,MO.
Application Deadline
This position is anticipated to close on Jan 27, 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.

Molecular Biologist

<h3>Job Description</h3>
Job Description1st shift Assembler $19-20/HR
*If interested, please apply. Then text: Jack @ 513-229-2006+
Job Description
Join a leading company in the commercial van industry, specializing in leasing refrigerated vans for the last mile of distribution. Our clients include well-known companies in various sectors such as edible arrangements, brewing, and hospital equipment.
Responsibilities
<ul>
<li>Assemble and install components in commercial vans using hand and power tools.</li>
<li>Conduct mechanical assembly tasks efficiently and accurately.</li>
<li>Maintain a clean and organized work area.</li>
<li>Collaborate with the team to manage inventory and support shipping activities.</li>
</ul>
Essential Skills
<ul>
<li>Experience in the automotive industry.</li>
<li>Proficiency with hand and power tools.</li>
<li>Mechanical assembly knowledge.</li>
<li>Ability to lift and bend to handle up to 50 lbs.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Mechanical aptitude is essential.</li>
</ul>
Why Work Here?
Be part of a growing company that offers significant opportunities for career advancement.
Work Environment
Work in a non-temperature controlled warehouse setting, where teamwork and productivity are key.
Job Type &amp; Location
This is a Contract to Hire position based out of Sharonville, OH.
Pay and Benefits
The pay range for this position is $19.00 - $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 Sharonville,OH.
Application Deadline
This position is anticipated to close on Jan 26, 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.

Clean Room Assembler

<h3>Job Description</h3>
Job Description
Our client is seeking a Geotechnical Department Manager to lead its geotechnical engineering operations, manage a growing team, and oversee a diverse portfolio of industrial, commercial, and residential site development projects. This role combines technical leadership, project oversight, business development, and departmental management within a hybrid work environment.
No Visa Sponsorship | Relocation Assistance: Limited 
Work Model &amp; Schedule:
<ul>
<li>Hybrid: 2–3 days in office per week, remaining days remote</li>
<li>Hours: Monday–Friday, 8AM–5PM, with overtime as needed</li>
<li>Travel: Local travel to job sites required</li>
</ul>
Responsibilities:
Department Leadership &amp; Team Management
<ul>
<li>Lead and manage the geotechnical department, including staffing, workload planning, and performance management.</li>
<li>Mentor and develop junior and mid‑level engineers, fostering professional growth and technical excellence.</li>
<li>Conduct team meetings, oversee day‑to‑day operations, and maintain a positive, productive work environment.</li>
</ul>
Technical &amp; Project Oversight
<ul>
<li>Review and approve geotechnical reports, proposals, and design recommendations.</li>
<li>Ensure adherence to QA/QC standards, Michigan codes, and regulatory requirements.</li>
<li>Provide technical leadership on geotechnical investigations, soil mechanics, foundation design, slope stability, retaining structures, and site development.</li>
<li>Coordinate with civil, structural, architectural, and construction teams to ensure integrated project delivery.</li>
</ul>
Business Development &amp; Client Relations
<ul>
<li>Support proposal development, scope definition, and fee estimates.</li>
<li>Participate in networking, client meetings, and revenue‑generating initiatives.</li>
<li>Build and maintain strong client relationships through regular communication and project updates.</li>
</ul>
Financial &amp; Strategic Management
<ul>
<li>Contribute to long‑term strategic planning and annual business planning.</li>
<li>Manage departmental budgets, project profitability, invoices, and collections.</li>
<li>Identify opportunities for operational improvements, revenue growth, and process optimization.</li>
</ul>
Policy, Compliance &amp; Cross‑Department Collaboration
<ul>
<li>Support internal and external audits as required.</li>
<li>Develop and enforce departmental policies, procedures, and best practices.</li>
<li>Collaborate with HR, IT, and other department managers on staffing, technology, and resource allocation.</li>
</ul>
Additional Responsibilities
<ul>
<li>Participate in special projects supporting corporate goals.</li>
<li>Perform other duties as needed to support departmental and organizational success.</li>
</ul>
Qualifications/Must Haves:
<ul>
<li>Michigan P.E. license (or ability to obtain)</li>
<li>Bachelor's Degree in Civil Engineering (or equivalent)</li>
<li>Proficiency with geotechnical engineering software and Microsoft Office.</li>
<li>10+ years of geotechnical engineering experience with progressive responsibility.</li>
<li>Proven leadership experience managing teams, budgets, and multidisciplinary projects.</li>
<li>Strong knowledge of Michigan geotechnical codes, regulations, and site development standards.</li>
</ul>
Nice‑to‑Haves:
<ul>
<li>Experience mentoring and developing engineering staff.</li>
<li>Business development experience (proposals, networking, revenue growth)</li>
<li>Strong financial management skills (budgeting, profitability analysis, collections)</li>
<li>Familiarity with PLAXIS, GeoStudio, Rocscience, ArcGIS/QGIS, MS Project, or Primavera P6.</li>
<li>Board Certification in Geotechnical Engineering (ASCE) or relevant environmental certifications.</li>
</ul>
Benefits &amp; Perks:
<ul>
<li>Life Insurance</li>
<li>Tuition Assistance</li>
<li>Fitness Reimbursement</li>
<li>401(k) + Profit Sharing</li>
<li>Medical, Dental, Vision</li>
<li>Maternity &amp; Paternity Leave</li>
<li>Paid Volunteer Time Off</li>
<li>Short‑Term &amp; Long‑Term Disability</li>
<li>Health benefits begin the first of the month after 30 days</li>
</ul>

Geotechnical Department Manager | Michigan | Hybrid

<h3>Job Description</h3>
Summary:
Entry-level Lab Scientist role within an Immunology team, ideal for recent graduates with a background in biology, immunology, or biotechnology. The position supports hands-on experimental work involving immune cell isolation, sterile cell culture, differentiation, flow cytometry, and functional immune assays.
 
Key responsibilities include isolating primary immune cells, maintaining and differentiating cell cultures, preparing and analyzing flow cytometry samples, and conducting immune cell–based functional and cytotoxicity assays. The role requires strong attention to detail, adherence to SOPs and biosafety practices, and effective collaboration within a research team.
 
Preferred candidates have exposure to immune assays, flow cytometry data analysis, and are eager to learn advanced immunology techniques in a collaborative research environment.

Biologist

<h3>Job Description</h3>
Position Overview: Lead Chemist 
 
We are seeking an experienced Lead Chemist to join our laboratory team. This position is critical within our cGMP manufacturing facility, where you will play a key role in ensuring the quality and reliability of our pharmaceutical products. The Lead Chemist will not only conduct advanced analytical testing but will also lead method development and validation efforts, as well as oversee laboratory operations to maintain compliance with regulatory standards.
In this role, you will have the opportunity to implement and uphold best practices in analytical chemistry, contribute to continuous improvement initiatives, and mentor junior laboratory staff. As a leader within the laboratory, you will be expected to collaborate closely with other departments, including production and quality assurance, to forecast analytical needs and ensure timely delivery of results that meet both production schedules and regulatory requirements.
 
Qualifications: 
● Minimum of a Bachelor’s Degree in Chemistry or a closely related discipline.
● 5+ years of experience in a cGMP/cGLP environment.
 
Important Skills and Competencies: 
● Analytical Proficiency
- Extensive experience with chromatographic techniques such as High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC).
- Strong understanding of spectroscopic techniques, including Ultraviolet (UV) and Infrared (IR) spectroscopy.
- Ability to perform Total Organic Carbon (TOC) analysis, particularly in the context of cleaning validation.
● Method Development and Validation
- Expertise in developing robust analytical methods tailored to specific product requirements.
- Proven experience in validating analytical methods in accordance with regulatory guidelines to ensure accuracy, precision, and reproducibility.
- Knowledge of statistical analysis tools for data interpretation and method optimization.
● Instrumentation Skills
- Familiarity with a range of laboratory instrumentation, including troubleshooting, calibration, and routine maintenance.
- Ability to assess and improve instrument performance, ensuring adherence to operational standards.
● Regulatory Knowledge
- In-depth understanding of cGMP and cGLP regulations as they pertain to laboratory operations.
- Experience with regulatory audits and the ability to maintain compliance documentation.
● Problem Solving and Critical Thinking
- Strong analytical and problem-solving skills to identify root causes of issues, particularly during Out Of Specification (OOS) and Non-Conforming Material Reports (NCMR).
- Capability to devise and implement corrective and preventive actions based on investigation outcomes.
● Leadership and Team Collaboration
- Proven leadership skills to effectively manage and mentor laboratory personnel, fostering a culture of continuous learning and improvement. - Ability to communicate clearly and effectively across departments to ensure alignment on analytical needs and priorities.
● Project Management
- Strong organizational skills to prioritize multiple laboratory analyses, balancing production demands with regulatory requirements.
- Experience in project management principles to oversee method validation and laboratory initiatives.
● Interpersonal Skills:
- Excellent communication skills to convey complex scientific information to both technical and non-technical stakeholders.
- Ability to foster a collaborative team environment that emphasizes mutual respect and accountability.
● Continuous Improvement Mindset:
- A proactive approach to identifying areas for improvement within laboratory processes and methodologies.
- Commitment to staying current with advancements in analytical chemistry techniques and regulatory changes.
 
Full-Time Benefits: 
● Comprehensive Dental, Health, and Vision Insurance.
● Paid Time Off and Holidays.
● 401(k) Plan with limited matching.

Lead Chemist

<h3>Job Description</h3>
Job DescriptionWho We Are We are a community built on care. Our caregivers and supporting staff extend compassion to those in need, helping to improve the health and well-being of those we serve, and provide comfort and healing. Your community is our community. Our Story We started out as a small operation in California. In May 1969, we acquired four hospitals, some additional care facilities and real estate for the future development of hospitals. Over the years, we've grown tremendously in size, scope and capability, building a home in new markets over time, and curating those homes to provide a compassionate environment for those entrusting us with their care. We have a rich history at Tenet. There are so many stories of compassionate care; so many "firsts" in terms of medical innovation; so many examples of enhancing healthcare delivery and shaping a business that is truly centered around patients and community need. Tenet and our predecessors have enabled us to touch many different elements of healthcare and make a difference in the lives of others. Our Impact Today Today, we are leading health system and services platform that continues to evolve in lockstep with community need. Tenet's operations include three businesses - our hospitals and physicians, USPI and Conifer Health Solutions. Our impact spreads far and deep with 65 hospitals and approximately 510 outpatient centers and additional sites of care. We are differentiated by our top notch medical specialists and service lines that are tailored within each community we serve. The work Conifer is doing will help provide the foundation for better health for clients across the country, through the delivery of healthcare-focused revenue cycle management and value-based care solutions. Together as an enterprise, we work to save lives and can accept nothing less than excellence from ourselves in service of our patients and their families, every day.
Lab Supervisor - Hematology Full Time Evenings 
 Up to $10,000 Sign-On bonus based on experience 
Position Summary
The Laboratory Supervisor provides laboratory services to meet the needs of patients performed in compliance with all applicable regulation, standards and practices. Directs, supervises and coordinates functions and activities in any or all areas assigned and in which a professional license is held. Plans, organizes and supervises the activities of all employees in areas of supervision to assure the prompt efficient, accurate and cost effective delivery of clinical laboratory information, test results, and services. Ensures the delivery of quality laboratory services which meets the standards of practice, established policies and procedures, and applicable laws and regulations at West Boca Medical Center. Assists in the administration of the laboratory department. Coordinates a wide variety of administrative, fiscal and technical activities to ensure efficient operation of all clinical laboratories. A Supervisor adheres to the legal responsibilities and scope of practice as written by the Board of Clinical Laboratory Personnel, State of Florida. The Laboratory Supervisor's role subsumes all aspects of the Medical Technologist's role.
Minimum: &nbsp;Bachelor degree, Florida Clinical Laboratory Supervisor license in specific area(s) supervised and/or Florida Clinical Laboratory Technologist license in other areas.
Preferred: &nbsp; &nbsp; Minimum of three (3) to five (5) years of clinical laboratory supervisor experience in multiple technical areas in an acute care hospital laboratory. Florida Clinical Laboratory Supervisor license in an all five areas.
Must successfully pass a color blindness test prior to employment.
&nbsp;
#LI-RS1
Tenet complies with federal, state, and/or local laws regarding mandatory vaccination of its workforce. If you are offered this position and must be vaccinated under any applicable law, you will be required to show proof of full vaccination or obtain an approval of a religious or medical exemption prior to your start date. If you receive an exemption from the vaccination requirement, you will be required to submit to regular testing in accordance with the law.&nbsp;
Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status.Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship. Tenet participates in the E-Verify program. Follow the link below for additional information. E-Verify: <a href="http://www.uscis.gov/e-verify" target="_blank">http://www.uscis.gov/e-verify</a> The employment practices of Tenet Healthcare and its companies comply with all applicable laws and regulations.
2503018660 
 
 
Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.
PandoLogic. Keywords: Medical Laboratory Supervisor, Location: Boca Raton, FL - 33431 , PL: 602405212

Lab Supervisor - Hematology

<h3>Job Description</h3>
Job Description
JOB SUMMARY:
<ul>
<li>
Conducting laboratory experiments for development of pharmaceutical products, with focus on sterile liquid dosage forms under supervision and guidance of the group members.
</li>
<li>
Conducting analytical &amp; characterization experiments to generate scientifically sound data supporting the formulation and manufacturing process development efforts of liquid dosage forms.
</li>
<li>
Designing &amp; interpreting experiments independently whenever the situation demands.
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Employing problem-solving and creative scientific skills.
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Working independently to generate accurate, reliable data on time and accurately documenting in electronic laboratory notebooks.
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Practicing good communication (oral and written) and interpersonal skills.
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Plan and execute lab-scale experiments related to sterile liquid formulation and manufacturing process development.
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Prompt and accurate documentation of experiments, results, and conclusions to ensure data integrity and accuracy is critical.
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Analyzes and interprets technical data and utilizes statistical techniques
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Additional responsibilities include proper maintenance of laboratory equipment and instrumentation to ensure laboratory operational capability.
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Eager to contribute to the team through continuous learning, has excellent proactive communication skills, and is willing to work with various team members to achieve team goals.
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Should participate in project and group meetings as requested by presenting and discussing data and future steps.
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Must conduct their work activities in compliance with all company internal requirements and with applicable regulatory requirements.
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Company internal requirements include compliance with ethics, environmental health and safety, financial, human resources and general business policies, requirements, and objectives.
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Qualifications:
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Requires a Bachelor's degree in chemistry, chemical engineering, pharmacy, or other relevant scientific discipline with 3-5 years of relevant industry experience; OR
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Master's degree in chemistry, chemical engineering, pharmacy or other relevant scientific discipline with 2 years of relevant industry experience.
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Strong technical writing and communication skills.
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Must be proficient using Word, Excel, and statistical software.
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Knowledge of fundamental application of statistics is preferred.
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Experience in analyzing data and writing technical reports is desired.
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Demonstrate working knowledge and understanding of formulation and manufacturing process development for sterile liquid drug products, including solutions, emulsions, and suspensions.
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Experience with various sterilization techniques for liquid drug products, such as filtration, and autoclaving, is desired.
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Experience with analytical measurements and characterization techniques such as pH, osmolality, viscosity/rheology, turbidity, particle size, and physical appearance.
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Hands-on experience with HPLC and UPLC (with detectors such as UV, PDA, and RI) is also desired.
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Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

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