field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionSalary: 
At Argenta, were more than a company were a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it. 
 
Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.
 
Were in a unique position. We are the worlds only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health.
Our uniqueness means:
 
We are ambitious, growing and building a one team culture, guided by our values.
<ul>
<li>
<ul>
<li>We are team players;</li>
<li>We are doers;</li>
<li>We are customer-centric;</li>
<li>We are innovators.</li>
</ul>
</li>
</ul>
We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best paw forward we will make the lives of the animals we care for, better.
 
With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Lets Make It Happen, Together.
 
TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply.
 
Argenta is currently looking to fill the role of Microbiologist Iat our Shawnee, KS location. Incumbents in this position are responsible for testing of raw materials, intermediates and finished products according to cGMP's in order to ensure satisfactory levels of microbial quality are met. Fundamental microbiological principles are applied in order to interpret test results. Responsibilities also include monitoring of controlled environments to ensure that manufacturing and testing processes occur under appropriate conditions. The incumbent maintains, compiles and reviews laboratory worksheets to assure accuracy of test data.

On a daily basis, the incumbent must plan for and respond to the analytical needs of a laboratory involved in fast turnaround of pharmaceutical analyses to meet manufacturing deadlines. This planning requires good communication, attention to detail, organization skills and the use of the various analytical instrumentation systems and procedures. All incumbents are responsible for following applicable Division &amp; Company policies and procedures.
 
Key Accountabilities
<ul>
<li>Performs testing of raw material, in-process and finished product samples according to approved procedures.</li>
<li>Perform Environmental monitoring of the manufacturing and laboratory facilities including cleanroom environments, personnel, water systems, compressed gases, and laminar flow hoods.</li>
<li>Identify microbial isolates using manual or automated techniques per written procedures in a timeframe that supports customer requirements.</li>
<li>Prepares media, solutions, materials and equipment to support sampling and testing.</li>
<li>Performs growth promotion and quality testing on media used for microbiological testing, and environmental monitoring in the Microbiology QC Department as needed.</li>
<li>Maintain the record storage systems in a manner that ensures quick and reliable retrieval of the data as needed.</li>
<li>Provide support to laboratory projects and assist other team members as needed.</li>
<li>Adhere to the pertinent aspects of compliance and plant safety programs.</li>
<li>Critical understanding of proper and thorough laboratory investigations</li>
<li>Support QA Operations as required for laboratory investigations</li>
<li>Continuous improvement and assessment of laboratory practices to eliminate over-processing of data</li>
<li>Adhere to GMP and/or GLP standards as required for daily operations</li>
<li>Safety first in the laboratories</li>
</ul>
 
Qualifications
<ul>
<li>BA / BS in a related scientific field such as biology, chemistry, microbiology, or biochemistry.</li>
<li>1+ year laboratory experience, which can include academic experience or microbiology laboratory.</li>
<li>The incumbent should have basic background for the understanding, planning, and execution of laboratory Standard Operating Procedures relating to instrument use, sample analysis, document generation and control, personal safety, and environmental safety.</li>
<li>Knowledge of FDA regulations (or similar regulated environment) to include Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP)</li>
<li>Basic computer skills are required.</li>
<li>The incumbent must be able to pass a DEA background check.</li>
<li>Proven, effective written and verbal communication skills.</li>
<li>Demonstrated skills in the use of a wide range of microbiology test methods and instrumentation, including the following:
<ul>
<li>Bioburden testing</li>
<li>Endotoxin testing</li>
<li>Aseptic technique</li>
</ul>
</li>
<li>Water quality sampling and testing</li>
<li>Standing and/or moving &gt;50% of the time</li>
</ul>
 
Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through strong culture, great benefits, and opportunity for growth. Argenta is an equal opportunity employer

Microbiologist I

<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>401(k)</li>
<li>Competitive salary</li>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Opportunity for advancement</li>
<li>Paid time off</li>
<li>Vision insurance</li>
</ul>
 Reports To: President of R&amp;D Position Summary: We are seeking an inventive and highly strategic Director of R&amp;D Color Cosmetics to lead our formulation lab in the development of high-performance, clean, and on-trend color products. This role requires a rare blend of scientific depth and creative experimentation to deliver the next generation of beauty innovations for our clients. Key Responsibilities: 
<ul>
<li>Lead the formulation and technical development of color cosmetics (lip, eye, face, and complexion).</li>
<li>Manage a team of chemists and technicians in a collaborative, innovation-first culture.</li>
<li>Translate trend insights, client briefs, and consumer needs into innovative, scalable formulas.</li>
<li>Partner cross-functionally to ensure smooth handoff from concept to commercialization.</li>
<li>Drive a strong innovation pipeline using new raw materials, textures, and technologies.</li>
<li>Ensure products meet all regulatory, safety, and quality standards globally.</li>
<li>Contribute to IP development, technical claims, and prototype presentation.</li>
<li>Foster a culture of curiosity, exploration, and excellence in formulation science.</li>
</ul>
Qualifications: 
<ul>
<li>810 years of formulation experience in the color cosmetics industry.</li>
<li>Expertise in emulsion, anhydrous, pigment dispersion, and pressed powder technologies.</li>
<li>Strong understanding of ingredient trends (e.g. clean, vegan, long-wear, multifunctional).</li>
<li>Proven leadership of R&amp;D teams and complex product portfolios.</li>
<li>Passion for innovation, formulation science, and working at the cutting edge of beauty.</li>
</ul>

Director of Research & Development- Color Cosmetics

<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 DescriptionJob Title: Chemist Operator LeadJob Description
The Chemist Operator Lead will be responsible for producing Active Pharmaceutical Ingredients (APIs) using chemical reactors. This role involves following specific batch records to ensure consistent product quality.
Responsibilities
<ul>
<li>Handle various unit operations, including reactions, filtration, distillation, drying, and milling, on raw materials and during various stages of chemical processing according to written manufacturing procedures and SOPs.</li>
<li>Follow and document per batch sheet instructions to produce products in compliance with all cGMP guidelines.</li>
<li>Set up equipment such as vessels, tanks, centrifuges, and dryers for proper processing.</li>
<li>Clean and verify equipment and vessels to maintain operational integrity.</li>
<li>Record observations of operating conditions to ensure optimal performance.</li>
<li>Drive and operate a forklift truck safely and efficiently.</li>
<li>Make work prioritization or timing decisions with supervisory oversight.</li>
<li>Adjust utilities to maintain reaction parameters.</li>
<li>Maintain process flow through the plant while adhering to all safety, GMP, and environmental regulations and standards.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in operating chemical reactors and handling various unit operations.</li>
<li>Strong understanding of cGMP guidelines and ability to follow batch records.</li>
<li>Experience in setting up and cleaning chemical processing equipment.</li>
<li>Ability to record and analyze operating conditions effectively.</li>
<li>Forklift operation skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>AS Degree in Sciences, with a preference for Chemical Technology or Chemistry.</li>
<li>5-7 years of experience in pharmaceutical chemical operating.</li>
<li>Knowledge of analytical chemistry and experience with GC (Gas Chromatography).</li>
</ul>
Work Environment
The role is based in a clean laboratory and production environment. The work schedule follows a 2-2-3 shift pattern from 6:00 a.m. to 6:30 p.m., including work on alternate weekends. The position offers opportunities for growth into leadership roles as the innovation hub expands.
Job Type &amp; Location
This is a Contract to Hire position based out of Grafton, WI.
Pay and Benefits
The pay range for this position is $32.00 - $37.00/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 Grafton,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.

Chemist Operator Lead

<h3>Job Description</h3>
Job Description
Job Title: Chemist
Job Description
We are seeking a dedicated and enthusiastic Chemist to join our team. This role involves general wet chemistry lab testing, including tasks such as pipetting, measuring viscosity, testing pH, and determining boiling points. The successful candidate will work extensively on clear coats involving spray paints, with full PPE provided. Training will be offered on various instruments, including automatic pipetting machines, Gas Chromatography, and IR spectrometers. The overnight team divides work into 60% testing and 40% documentation, with individual work varying by shift.
Responsibilities
<ul>
<li>Conduct routine testing and approval of chemical blends.</li>
<li>Perform incoming, intermediate, and final chemical inspections of raw materials, intermediates, and finished goods.</li>
<li>Document test results, statuses, and chemical non-conformances.</li>
<li>Maintain quality records and verify raw materials, in-process materials, and finished goods against established specifications.</li>
<li>Generate certificates of analysis and conduct USP testing and documentation when applicable.</li>
<li>Inspect USP containers and tankers, gauge, sample, and document incoming ethanol shipments.</li>
<li>Perform quality jobs as required for backup or peak loads.</li>
</ul>
Essential Skills
<ul>
<li>Ability to quickly pick up on chemistry testing and maintain quality at a fast pace.</li>
<li>Capability to learn quickly and work with minimal supervision while following SOPs.</li>
<li>Time management skills and the ability to set an individual agenda for testing after training.</li>
<li>Proficiency in collaborating and communicating with team members and supervisors.</li>
<li>Possession of a BS/BA degree in Chemistry or a related science field.</li>
<li>Proficiency in wet chemistry skills from school or on-the-job experience.</li>
<li>Understanding of modern quality principles and industrial quality practices is preferred.</li>
<li>Strong written and verbal communication skills.</li>
<li>Basic PC skills including typing and filing.</li>
<li>Experience with Windows and Microsoft Office is a plus.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>A degree in Chemistry, Biology, or a related science field.</li>
<li>Experience in quality control and wet chemistry.</li>
</ul>
Work Environment
The position is within a modern and up-to-date lab at a chemical manufacturing facility. The team includes 2 supervisors and 3-5 other chemists. The team enjoy a supportive company culture with opportunities for career advancement, solid training, and a competitive benefits package for permanent employees.
Job Type &amp; Location
This is a Contract to Hire position based out of Waukegan, IL.
Pay and Benefits
The pay range for this position is $21.75 - $21.75/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 Waukegan,IL.
Application Deadline
This position is anticipated to close on Jan 24, 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.

Chemist

<h3>Job Description</h3>
Job Description
Description
Work closely with the Senior Chemist and/or Technical Director to improve the functionality, performance, and application of chemical products. Adjust, refine, or optimize existing product formulations based on feedback from sales engineers, field service personnel, and customers. Replicate specific water qualities and system conditions to conduct testing of new and existing products, ensuring accuracy and relevance to real-world applications. Review, perform, and verify quality control parameters to support consistent production standards. Prepare documentation, technical reports, and presentations as required by the Senior Chemist and/or Technical Director. Maintain accurate laboratory records, test data, and research files in accordance with internal documentation standards. Collaborate with the R&amp;D and QC teams to support product troubleshooting, root-cause analysis, and continuous improvement initiatives. Follow all laboratory safety protocols and maintain clean, organized, and compliant laboratory workspaces. Perform other duties and special projects as assigned.
Additional Skills &amp; Qualifications
The Research &amp; Development Chemist supports the development of new products, enhancement of existing formulations, and testing efforts required for innovation and continuous product improvement. This role also supports Proton Software by providing accurate data, application insights, and testing results that inform internal and external stakeholders.
Experience Level
Entry Level
Job Type &amp; Location
This is a Contract to Hire position based out of Plant City, FL.
Pay and Benefits
The pay range for this position is $24.00 - $26.00/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 Plant City,FL.
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.

R&D Chemist

<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.
</li>
<li>
Employing problem-solving and creative scientific skills.
</li>
<li>
Working independently to generate accurate, reliable data on time and accurately documenting in electronic laboratory notebooks.
</li>
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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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