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job_organization_name

city

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<h3>Job Description</h3>
Job DescriptionJob Description The future is what you make it. Honeywell is hiring an Advanced R&amp;D Engineer/Scientist - Navigation Analysis located in Plymouth, MN. As an Advanced R&amp;D Engineer/Scientist - Navigation Analysis, you will be responsible for providing technical expertise on a variety of projects and programs for exciting new technologies in the field of Alternative Position, Navigation, and Timing Systems. You will use your expert knowledge of navigation systems, engineering discipline and standards, and processes and tools to complete and ensure compliance of various new product introduction projects. Additionally, you will be the point of contact for external customers, and you may participate in the development of new business opportunities and product lines. Are you ready to help make the future with us? BENEFITS: In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. Benefits provided may differ by role and location. Learn more at benefits.honeywell.com. • Unlimited Vacation Plan with No Preset Maximums • Flexible Hybrid Work Schedule • Medical/Rx Health Savings Account (HSA) • Dental/Vision • Life Insurance • Short/Long-Term Disability • Employee Assistance Program (EAP) • 401(k) Match • Education Assistance • Flexible Spending Accounts • Parental Leave • 12 Paid Holidays Responsibilities • New Product Design &amp; Development: Develop new navigation algorithms, perform analysis and test campaigns, engaging with systems engineering throughout the process to ensure the product meets customer needs. • Innovation &amp; Growth: Spearhead ideation efforts with the goal of developing technologies and features that will contribute to new and existing products. • Technical Expertise: Become the technical expert for an Integrated Product Team of engineers, providing technical direction, reporting to management, and becoming an advocate of Navigation Alternative Technologies. • Standardization &amp; Process Development: Support the development and improvement of team internal processes, cooperating with other Aerospace Technologies departments in broader standardization efforts • Ability to analyze and solve complex and challenging problems • Track record of successful contribution to products &amp; projects Qualifications YOU MUST HAVE: • Bachelor's degree from an accredited institution in a technical discipline such as the sciences, technology, engineering or mathematics • 3+ years of Research &amp; Development Experience with Navigation Systems as an Analyst. U.S. PERSON REQUIREMENT: Due to U.S. export control laws, candidates must be U.S. citizen, U.S. permanent resident, or have protected status under asylum or refugee. WE VALUE: • Masters degree in engineering (Aerospace engineering, Computer Science, Electrical Engineering or similar). • Knowledge of Inertial, GPS, or Alternative PNT sensors. • Navigation algorithm development. • Understanding of industry standards and security practices. • Highly skilled in C/C++, MATLAB, ROS. • Experience with OpenCV, Ubuntu, Python, GDAL, CUDA. • Ability to lead, motivate, develop and mentor others • Experience with new product and technology development in a highly regulated environment In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. For more information visit: Benefits at Honeywell The annual base salary or/ hourly pay range for this position is $114,000 - $145,000. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations. The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Job Posted: 10/21/2025 About Us Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments - powered by our Honeywell Forge software - that help make the world smarter, safer and more sustainable.

Sr R&D Engineer Scientist - Navigation Analysis

<h3>Job Description</h3>
Job DescriptionEmpirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines is seeking a chemist with an interest in solid-phase oligonucleotide synthesis and analytics. This is an excellent opportunity for a highly motivated, creative scientist to be a vital member of our team.Responsibilities:
<ul>
<li>You will be responsible for supporting the synthesis, purification, and characterization of oligonucleotides and their conjugates, and optimizing methodologies to support the development of siRNA medicines. The ideal candidate will have experience in organic and analytical chemistry and both upstream and downstream oligonucleotide manufacturing processes. A key focus of this role will be developing scalable processes suitable for technology transfer to CDMOs. You will be expected to –</li>
<li>Perform solid-phase synthesis, purification, and characterization of oligonucleotides</li>
<li>Develop and optimize scalable upstream (synthesis) and downstream (purification, formulation) manufacturing processes</li>
<li>Support process development activities to enable successful technology transfer to CDMOs</li>
<li>Analyze, interpret, and clearly communicate synthetic and analytical data</li>
<li>Present findings to senior staff and cross-functional teams</li>
<li>Troubleshoot and refine synthesis and purification protocols</li>
<li>Manage multiple projects simultaneously in a fast paced environment</li>
<li>Support GLP related activities and IND-enabling process development efforts</li>
</ul>
Requirements:
<ul>
<li>This position requires a BS in Chemistry with at least 12 years of relevant industry experience, or an MS in Organic Chemistry, Biochemistry, or Chemical Engineering with at least 7 years of relevant experience, or a PhD with at least 3 years of relevant experience.</li>
<li>Industry experience in solid-phase oligonucleotide synthesis is preferred, as well as familiarity with both upstream and downstream oligonucleotide manufacturing processes</li>
<li>Minimum 1 year of experience working in a cGMP environment with demonstrated understanding of cGMP principles</li>
<li>Hands-on proficiency with analytical instrumentation such as NMR, LC-MS, and RP-HPLC</li>
<li>Demonstrated ability in analytical and purification method development using RPIP-HPLC, AEX-HPLC, UV, MALDI, and HRMS</li>
<li>Background in process development and technology transfer to CDMOs, including development of scalable purification and formulation methodologies</li>
<li>Working knowledge of tangential flow filtration (TFF) method development</li>
<li>Experience supporting GLP studies and familiarity with regulatory expectations for IND-enabling work</li>
<li>Experience with lyophilization and aseptic fill/finish operations</li>
<li>Applicants must have authorization to work in the U.S.</li>
</ul>
The estimated annual base salary range for this role is $110,000 to $160,000. Individual compensation decisions will be based on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills.&nbsp; We offer a wide range of benefits including a retirement savings plan (with company match), paid vacation, holidays, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans. About Empirico: Empirico is a clinical-stage biotechnology company that discovers and develops siRNA medicines designed to mimic naturally-occurring genetic variants that confer beneficial effects on health and disease. Empirico’s two foundational and proprietary technology platforms - the Precision Insights Platform™ for genetically-validated target discovery, and the siRCH™ platform for the discovery and development of siRNA medicines - enable Empirico and its collaborators to rapidly advance programs from the discovery and validation of novel targets to clinically-viable therapeutics. Empirico’s exceptional internal capabilities, augmented by those of its partners, are driving the advancement of a growing and differentiated pipeline of wholly-owned and partnered programs for a broad range of common diseases with unmet medical need. Empirico is headquartered in San Diego, CA with a major second R&amp;D site in Madison, WI. We’re striving to build a strong culture of inclusivity, transparency and collaboration at Empirico, where our diverse and equitable workforce is empowered to contribute to our mission. We always seek the best candidate for the position and encourage you to apply even if your experience or qualifications don’t match up exactly with the job description. Empirico is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. To All Agencies: Please do not contact any employee of Empirico about this position. All resumes submitted by agencies to any employee of Empirico via-email or in any form and by any method will be deemed the sole property of Empirico, unless such agencies were engaged by Empirico for this position and a valid agreement is in place.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Senior Scientist - CMC

<h3>Job Description</h3>
Job DescriptionYU &amp; Associates is seeking a Geotechnical Project Manager in our Elmwood Park, New Jersey Office. You will be responsible for planning, scheduling and execute common to complex projects establishing techniques and standards for analysis and design, coordinating with senior level management, performing mathematical calculations, and training subordinates. The candidate will be managing within an integrated multidiscipline environment and be further responsible for reviewing and certifying the work of staff, performance, managing billings, and maintain strong billability. Duties &amp; Responsibilities:
<ul>
<li>Perform and oversee engineering calculations and design drawings related to geotechnical work.</li>
<li>Focus on public/private development with regulatory permitting expertise in NJ and PA.</li>
<li>Demonstrated ability to supervise and review others work.</li>
<li>Prepare proposals for professional services.</li>
<li>Perform and direct others with geotechnical inspections, site reconnaissance, soil borings, and field investigations.</li>
<li>Review proposed contracts to determine significant parameters, time schedules and mileposts and define the major task areas.</li>
<li>Resolve problems and coordinate the final turnover of the project to the client, as the primary contact with the client throughout the entire project.</li>
<li>Direct the planning and development of the project scope, procedures, and budget.</li>
<li>Ensure contractual commitments are met and the work is being performed according to the client's instructions.</li>
<li>Maintain effective relationships with members of all divisions and departments responsible for performing services in connection with the project.</li>
<li>Control and/or review all project forecasts, schedules, cost estimates and reports. Responsible for quality control over the complete project; maintain project files.</li>
<li>Monitor fees and budgets; report problems to the appropriate department and division managers.</li>
<li>Review and address health &amp; safety concerns on projects assigned.</li>
<li>Work with the accounting department to keep billings and receipts current and accurate.</li>
<li>Perform other duties as assigned.</li>
</ul>
Requirements:
<ul>
<li>B.S. degree in Civil Engineering and M.S. degree with geotechnical specialty (preferred).</li>
<li>Registered Professional Engineer in New Jersey and/or New York.</li>
<li>Possess 10+ years of geotechnical related regional experience.</li>
<li>Demonstrated ability to develop diverse clients and grow a business.</li>
<li>Proven ability to identify, develop and mentor talent.</li>
<li>Effectively manage projects from concept through completion.</li>
<li>Proven leadership and decision-making skills.</li>
<li>Strong attention to detail with excellent analytical and judgment capabilities.</li>
<li>Excellent communication, interpersonal, report writing, and project management skills.</li>
<li>Excellent listening, written and oral communication skills.</li>
<li>Working knowledge of computers and related geotechnical design software.</li>
<li>Possess a valid driver’s license in good standing.</li>
<li>Ability to establish a vision and create an environment for excellence.</li>
<li>Demonstrated record of ethics and high standards.</li>
</ul>
We offer employees competitive compensation packages, medical/dental/vision, life insurance, short, and long-term disability, paid holidays, paid time off, and&nbsp;401k retirement plan with company match. YU &amp; Associates' is an Equal Employment Opportunity employer fully committed to providing equal opportunity in all areas of employment practices.&nbsp;No employee or applicant for employment is discriminated against because of race, creed, color, religion, gender, gender identity or expression, sexual or affectional preference, sexual orientation, sex, ancestry or national origin, citizenship status, age, disability, marital or domestic status, veteran status, atypical hereditary cellular or blood trait, genetic information or testing, or any other legally protected category in all employment decisions. We foster a work environment that’s inclusive as well as diverse, where our employees can be themselves.&nbsp; Every idea and perspective are valued to meet our common goals. YU &amp; Associates is committed to supporting our employees’ well-being by providing benefits that are a valuable part of the compensation package. We partner with our employees to foster a healthy, safe and rewarding lifestyle both at work and at home. The Y&amp;A benefits program for full-time employees include: ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Benefits:&nbsp;&nbsp;
<ul>
<li>Medical-National plan with low out of pocket costs to members.</li>
<li>Dental-National plan.</li>
<li>Vision-National plan with the largest vision network.</li>
<li>Life/AD&amp;D-Benefit available should an employee pass away while employed.</li>
<li>Short-Term Disability-Benefit in the event an employee is unable to work for a short period of time.</li>
<li>Long Term Disability-Benefit in the event an employee&nbsp;is unable to work for an extended period.</li>
<li>Employee Assistance Program-Employee 3rd&nbsp;party support available when needed.</li>
<li>ADP Retirement Plan with company match.</li>
<li>Bonus Program – based on individual and company performance.</li>
<li>Yearly review – based on individual and company performance.</li>
</ul>
Tax Savings Tools:&nbsp;&nbsp;
<ul>
<li>&nbsp; &nbsp; &nbsp; Healthcare Reimbursement Accounts-Tax Free benefit to employees.</li>
<li>&nbsp; &nbsp; &nbsp; Flexible Spending Accounts-Tax Deductible benefit for employees.</li>
<li>&nbsp; &nbsp; &nbsp; Dependent Care and Commuter Program-Tax Deductible benefit for employees.</li>
</ul>
Value Adds:&nbsp;&nbsp;
<ul>
<li>&nbsp; &nbsp; &nbsp; Will Preparation</li>
<li>&nbsp; &nbsp; &nbsp; Beneficiary Grief Support</li>
</ul>
 SALARY RANGE:&nbsp; $118,000 TO $150,000 &nbsp; &nbsp;
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Geotechnical Project Manager

<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>401(k) matching</li>
<li>Free uniforms</li>
<li>Health insurance</li>
<li>Opportunity for advancement</li>
</ul>
 Looking for job security, a safe work environment, advancement opportunities and to fill that gap in your resume? Are you a student looking for work in the summer. Our offices work Monday Friday managing accounts with business and residential clients. Our team enjoys the friendly atmosphere and the job flexibility. We work no evening hours, weekends or holidays! Working alone or in pairs, we spend more than 50% of our time outside in the fresh air! The more efficient you get at this position, the more of the day you will have for your leisure. If this sounds like a good fit for you, apply to join our window cleaning team today! Typical Schedule: Mon-Fri, 7:30am 4:00pm Pay: $15.00 - $22.00+ per hour Fish offers: 
<ul>
<li>Paid training, no experience necessary</li>
<li>No nights or weekends</li>
<li>Flexible hours</li>
<li>Full or Part time available year-round</li>
<li>Tips and additional commission opportunities</li>
<li>Inside and outside work</li>
<li>Equipment and uniforms furnished</li>
<li>No high rise or skyscraper work</li>
</ul>
Other Qualifications: 
<ul>
<li>Valid drivers license</li>
<li>Reliable transportation</li>
<li>Valid car insurance</li>
<li>Provide excellent customer service</li>
<li>Self-motivated</li>
<li>Tips, and bonus opportunities!</li>
</ul>
This is a general labor position and a perfect opportunity for anyone currently working as a construction or warehouse worker, laborers, restaurant and hospitality workers, cashiers, servers, line cooks and retail/customer service workers.

Seasonal Window Technician

<h3>Job Description</h3>
Job Description
Palermo Villa Inc. is looking for a high-energy, poised, and confident individual to assist in the development of concepts, products, and optimization projects through Palermo's vigorous consumer-driven R&amp;D process.
Associate Food Scientist Fulltime Milwaukee, WI $55,000-$60,000 Annually 
Who you’ll work for…
While most companies that sell Pizza have no real connection to Italy, Palermo’s passion for food and family reaches all the way back to the country where Pizza was born. “Papa Palermo” carried the cherished recipes to America from Sicily!
Innovation is at the heart of who we are. We use an entrepreneurial, forward-thinking approach resulting in high quality products that are consistently recognized by both the industry and consumers.
Our commitment to quality has made Palermo’s a leader in private label frozen Pizza and contract manufacturing!
Perks…
<ul>
<li>20 free Pizzas per month</li>
<li>Opportunity for training and career advancement</li>
<li>Paid Time Off and Floating Holiday of your choice</li>
<li>401k &amp; Roth with company match and fully vested on the 1st of the Month after Hire</li>
<li>Fantastic benefit offering starting on the 1st of the Month after Hire</li>
</ul>
Where you’ll work…
<ul>
<li>Located in Milwaukee’s Menomonee River Valley, Villa Palermo is a state-of-the industry manufacturing facility that adjoins our company headquarters.</li>
<li>Our high-tech pizza manufacturing operations include an on-site bakery to produce best-in-class crusts, robotic packaging equipment, and a 24-hour shipping and receiving facility.</li>
</ul>
When you’ll work…
<ul>
<li>The Associate Food Scientist role works predominantly day shift hours with occasional nights/weekends to complete projects.</li>
</ul>
What you’ll do…
<ul>
<li>Execute Product Development and/or improvement projects including formulating finished product and sub-assembly for pizzas.</li>
<li>Prepare small-scale samples for testing, document study results according to company procedures, and maintain a clean and organized environment with accurate recordkeeping.</li>
<li>Demonstrate strong knowledge of food science best practices to test materials, develop formulas improvements and/or new formulas, and prepare lab sheets.</li>
<li>Assist with PR events, food shows, food presentations and production presentations.</li>
</ul>
Why you’ll be successful…
<ul>
<li>Proven ability to provide support to the organization in the areas of food technology, product design, food manufacturing, and food safety.</li>
<li>Utilizing knowledge from your Bachelor’s Degree in Food Science, Biology, Chemistry, Culinary and any experience with food manufacturing, major food companies or restaurant industry.</li>
<li>Organized and methodical approach to problem solving – often in a time-sensitive, tight-deadline situation where accuracy is critical.</li>
<li>Passionate lifelong learner with a strong interest in mastering new techniques in the culinary arts and food science.</li>
<li>Team player with excellent communication skills ready to work hard to ensure the whole Palermo’s team succeeds.</li>
</ul>
How to join our team…
Let us learn a little more about how you'll fit on our team <a href="https://take.surveys.ci/s/PALEF7E657/79266" target="_blank">https://take.surveys.ci/s/PALEF7E657/79266</a>

Associate Food Scientist

<h3>Job Description</h3>
Job Description
Job Title: Preclinical Research Assistant
Job Description
We are seeking a dedicated Preclinical Research Assistant to support the Study Director and Preclinical Sponsor Representatives in the preparation and conduct of preclinical research studies. These studies aim to develop products or procedures utilizing in-vivo, ex-vivo, and in-vitro models.
Responsibilities
<ul>
<li>Setup study binders as per local procedures.</li>
<li>Develop study-specific data sheets.</li>
<li>Support the study director in addressing QAU audit findings.</li>
<li>Quality check all study-related documentation throughout the study lifecycle.</li>
<li>Document study data as required by protocol and SOP.</li>
<li>Archive study files according to SOP.</li>
<li>Interface with principal investigators and contributing scientists for studies conducted on-site and at contract laboratories.</li>
<li>Support the study director with the preparation of draft study protocols and reports.</li>
<li>Coordinate project/study logistics.</li>
<li>Request study-specific equipment and instrumentation.</li>
<li>Collaborate with study coordinator to request and schedule studies to meet project timelines.</li>
<li>Place animal orders in accordance with protocol and study schedule.</li>
<li>Request ordering of appropriate animal-related drugs to meet protocol and SOP requirements.</li>
<li>Coordinate receipt, submission, and transfer of test and/or control articles.</li>
<li>Support the conduct of histopathology work tasks, including management, transfer, and receipt of histology specimens to an external laboratory.</li>
</ul>
Essential Skills
<ul>
<li>Experience with preclinical animal research, including comfort with large animals such as dogs, sheep, and pigs.</li>
<li>Willingness to learn and strong record-keeping experience.</li>
<li>Proficiency in Microsoft Suite.</li>
<li>Experience in a GLP-regulated environment.</li>
<li>Knowledge of both human and animal anatomy/physiology.</li>
<li>Surgical support experience, comfortable assisting during surgical procedures.</li>
<li>Ability to understand and precisely follow Standard Operating Procedures.</li>
<li>Meticulous attention to detail to identify and correct discrepancies/errors.</li>
<li>Strong background in data collection, data management, and data integrity.</li>
<li>Ability to set priorities and manage time effectively to meet deadlines.</li>
<li>Demonstrated ability to work both independently and as part of a team.</li>
<li>Strong organizational and project management skills.</li>
<li>Safety-minded in workspace organization and conduct.</li>
<li>Accountability for one's own actions and work.</li>
<li>Basic computer proficiency in Outlook, Word, Excel, and PowerPoint.</li>
<li>Excellent verbal, written, and interpersonal communication skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Biology, Zoology, Animal Science, Engineering, Mathematics, or a closely related STEM field preferred. Equivalent education and experience may be substituted.</li>
<li>Leadership and public speaking skills are preferred but not required.</li>
<li>Surgical Research Specialist (SRS) certification is preferred but not required.</li>
<li>Associates may be asked to bring their own device (BYOD) for this role, unless other arrangements have been made to provide a laptop.</li>
</ul>
Work Environment
This Actalent Services LLC position requires working onsite. 
Job Type &amp; Location
This is a Contract position based out of Cincinnati, OH.
Pay and Benefits
The pay range for this position is $28.00 - $32.00/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 Cincinnati,OH.
Application Deadline
This position is anticipated to close on Jan 22, 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.

Preclinical Research Assistant

<h3>Job Description</h3>
Job Description
Job Title: Microbiologist
Job Description
We are seeking a dedicated and detail-oriented Microbiologist to join our team. The successful candidate will perform microbiological and cleaning validation sampling, while ensuring compliance with GMP and data integrity standards. This is an excellent opportunity for an entry-level professional with a strong experience in microbiology, looking to contribute to a dynamic and collaborative environment.
Responsibilities
<ul>
<li>Perform microbiological and cleaning validation sampling, including swab and rinse samples.</li>
<li>Create and execute protocols for routine cleaning verification and TOC sampling.</li>
<li>Apply proper aseptic and low-bioburden handling techniques during sampling activities.</li>
<li>Develop and execute TOC-based cleaning validation, including sample handling, data review, and coordination with QC or external laboratories.</li>
<li>Assist with microbial and chemical cleanliness risk assessments for equipment and processes.</li>
<li>Document sampling activities and results in compliance with GMP and data integrity (ALCOA+) requirements.</li>
<li>Support validation, PPQ, and process verification activities during new product introductions and equipment changes.</li>
<li>Participate in deviations, investigations, and CAPA support related to cleaning or microbiological events.</li>
<li>Collaborate cross-functionally with MS&amp;T, QA, QC, Engineering, and Manufacturing teams.</li>
</ul>
Essential Skills
<ul>
<li>Microbiology principles and contamination control</li>
<li>Environmental monitoring</li>
<li>Aseptic and low-bioburden handling practices</li>
<li>Quality control and documentation</li>
<li>Plating and sterilization techniques</li>
<li>Knowledge of FDA and cGMP regulations</li>
<li>Strong data integrity mindset</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Master’s degree in Microbiology, Biology, or Biotechnology.</li>
<li>Internships, academic research, or co-op experience in microbiology or GMP environments preferred.</li>
<li>Exposure to pharmaceutical manufacturing, quality, validation, or laboratory operations is a plus.</li>
<li>Digital literacy with exposure to basic AI/ML and its use in day-to-day work.</li>
</ul>
Work Environment
The role is based in a cleanroom environment, with working hours from Monday to Friday, 8 AM to 5 PM. The position involves working collaboratively with various departments to ensure the highest standards of quality and safety are met.
Job Type &amp; Location
This is a Contract position based out of Davie, FL.
Pay and Benefits
The pay range for this position is $35.00 - $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 Davie,FL.
Application Deadline
This position is anticipated to close on Jan 22, 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.

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