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<h3>Job Description</h3>
Job Description
Essential Duties and Responsibilities of the Position:
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Planning, scheduling, conducting, tracking, or coordinating detailed phases of work for projects with moderate to high level scope and complexity.
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; May attend on and off-site client meetings.
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Material sampling and testing, which may include soil, water, air, or construction materials as needed.
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Evaluate laboratory and field data and assemble into written reports.
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Draft written reports to comply with state and federal regulations.
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; General project management activities relating to construction and regulatory compliance activities
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Assist with and perform required monitoring activities
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Perform sampling activities to address design or permit requirements per scheduled dates and frequencies, if necessary;
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; General project oversight
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Prepare reports of work accomplished and project status. &nbsp;
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Conduct construction inspections, evaluate construction/design change orders.
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Assist as needed in activities related to project construction, site development, compliance monitoring and reporting, or company development.
•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Other environmental tasks as needed.
Work from home 60%, field work 40%.

Field Geologist

<h3>Job Description</h3>
Job Description
Part-Time Swine Nursery Research Assistant
 As Kalmbach Feeds continues to grow, we are looking for passionate, hard-working team members that live our values and help us develop new ideas, serve customers, improve our processes, build teams, and realize our growth. The Team Member in this role will be responsible for providing and helping with daily animal care at our swine research nursery facility. The selected individual(s) will work directly with our research nursery manager, veterinarian, and nutrition and research teams to assist in research trials related to nutrition and production management.
About the Role:
<ul>
<li>Hours consist of 15-25+ hours per week, including weekend hours</li>
<li>Provide support for research measurement days and between research studies</li>
<li>Assist with daily pig care including feeding, watering, weighing, medicating, and moving animals </li>
<li>Assist with cleaning and power washing facilities </li>
<li>Carry out and understand the importance of all biosecurity procedures </li>
<li>Conduct accurate record keeping for weight, health occurrences, and feed intake of pigs</li>
<li>Perform other job duties assigned that are found to be necessary by the barn manager</li>
<li>Located in the Sycamore, OH area</li>
</ul>
Who You Are:
<ul>
<li>GED or high school diploma required</li>
<li>Willingness and ability to work a flexible schedule that includes some weekends and holidays</li>
<li>Able to stand for long periods of time</li>
<li>Must be able to lift up to 50 pounds consecutively </li>
<li>Farm experience preferred, but not required</li>
<li>Have a passion for agriculture </li>
<li>Able to handle multiple assignments and tasks around the barn</li>
<li>Self-motivated, detail-oriented, and punctual</li>
<li>Do not own or work with pigs and/or chickens</li>
</ul>

About the Company:
Kalmbach Feeds offers the highest quality nutritional products for livestock, poultry, and companion animals. The company was founded in 1963 by Milton and Ruth Kalmbach with a vision to develop the finest products, providing customers with the best possible nutritional value. The Kalmbach family’s traditional core values have served as the compass for consistent success for over five decades, and the company has become the regional leader within the animal nutrition industry. Kalmbach Feeds enjoys an excellent reputation for quality and integrity within the animal nutrition industry and is comprised of smart self-starters who are driven to serve customers. Our experienced, talented team utilizes cutting-edge technology and proprietary processes to deliver safe, innovative products. Our stringent ingredient testing, computer automated systems, patented technologies, dedicated manufacturing facilities, and in-house nutrition specialists guarantee it. Additional information regarding our exciting company can be found at <a href="https://bit.ly/kalmbachfeedsculturevalues" target="_blank">https://bit.ly/kalmbachfeedsculturevalues</a> and <a href="http://www.kalmbachfeeds.com/" target="_blank">www.kalmbachfeeds.com/</a>.
Kalmbach Feeds Offers: 
<ul>
<li>Competitive Compensation</li>
<li>On Staff Life Coach</li>
</ul>
Kalmbach Feeds is an Equal Opportunity Employer. Each applicant for employment is considered solely based on job qualifications, without regard to race, color, religion, sex, age, disability, national origin, veteran status, or any other classification protected by law. The information contained within your resume and application, including employment history, educational history, and references, are subject to verification. Pre-employment drug screen (hair and urine), physical, and criminal background check required.
Only qualified candidates will be contacted.

Part-Time Swine Nursery Research Assistant

<h3>Job Description</h3>
Job Description
Chemical Operator (Night Shift: 7 PM – 7 AM)
Capital Resin Corporation (CRC) is passionate about innovation and pushing the boundaries of customer service. Our focus is helping companies create new and innovative organic chemistries, improving upon current chemistries, and delivering greater consistency and process stability. 
We manufacture and sell engineered chemistries as well as design and build chemical processes for a variety of Fortune 500 companies. 
Who we are.
Capital Resin Corp. is a 24/7 production environment dedicated to quality &amp; customer responsiveness. We’ve had significant growth in the past few years and are continuing to build upon that growth. Our company is seeking individuals who are adaptive, creative, responsive, logical, and able to make quick decisions to join our team. Chemical operators, supervisors, chemists, engineers, and salespersons are just to name a few positions that we seek.
We have an immediate opening for “Chemical Operator” positions.
Summary:
The Chemical Operator position will assist in meeting the schedule by completing assignments. The position will participate in daily ‘huddles’ to discuss continuous improvement opportunities and filling out visual production boards.
The Chemical Operator position will typically work 12-hour shifts. The schedule for “Night Shift” is 7:00 PM to 7:00 AM. Over a 2-week period, associates are typically scheduled to work three (3) 12-hours days one week, followed by four (4) 12-hour days the following week, or vice versa. Candidates must be willing to work additional days as required. Initial training may be on Day Shift (7:00 AM to 7:00 PM) until sufficiently trained to work night shift. 
Responsibilities:
<ul>
<li>Monitors batch while in process and make any adjustments as required. Properly communicates to supervisor when it appears that a goal or deadline will not be met.</li>
</ul>
<ul>
<li>Measure and mix chemicals according to specified formulas.</li>
<li>Monitor and adjust process variables such as temperature, pressure, and flow rates.</li>
<li>Follows all provisions of operating instructions. Responsible for the completion and accuracy of all batch ticket data entry. Responsible for meeting standard batch ticket cycle times while maintaining safety and quality.</li>
</ul>
<ul>
<li>Perform quality control checks on finished products. Monitors quality of output and takes appropriate action, including shutdown of process, to prevent or limit production. Follows all quality policies and production procedures to ensure quality product is produced.</li>
<li>Operates and monitors chemical processing equipment - Follow standard operating procedures to ensure safe and efficient production.</li>
<li>Stages raw materials and puts away finished product. Responsible for raw material and finished goods location integrity. Package and label finished products for shipment.</li>
</ul>
<ul>
<li>Maintain a clean and organized work area. Follow all safety protocols and wear appropriate personal protective equipment (PPE). Report any equipment malfunctions or safety hazards to the supervisor.</li>
<li>Other duties as assigned.</li>
</ul>
Requirements:
<ul>
<li>High School Diploma or GED</li>
<li>Technical manufacturing experience in a chemical facility a bonus.</li>
<li>Standing for extended periods of time, ability to lift, push and pull up to 55 pounds frequently, exposure to outside conditions and ability to work any shift.</li>
<li>Previous experience in chemical manufacturing or related field preferred.</li>
<li>Familiarity with machining, packaging, warehouse, or materials handling is a plus.</li>
<li>Ability to read and interpret technical documents and instructions.</li>
<li>Strong attention to detail and ability to follow precise instructions.</li>
<li>Good communication skills and ability to work well in a team environment.</li>
<li>Basic computer skills for data entry and equipment monitoring.</li>
</ul>
If you are a motivated individual with a strong attention to detail and a passion for chemical manufacturing, we encourage you to apply for the position of Chemical Operator. 
We offer competitive pay, benefits, and opportunities for career growth within our organization.
 
EOE M/F/D/V

Chemical Operator - Night Shift

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate IIJob Description
The Research Associate II will work in the Flow Cytometry and Immune Monitoring Core, providing full-service support for research studies that involve routine PBMC processing, cryopreservation, T cell ELISPOT analysis, multiplexing, or immunophenotyping. This centralized core laboratory offers immune monitoring services for rAAV development and Phase I Trials, cell-based therapy studies, and other projects upon request. While services adhere to academic research standards, they do not meet criteria for 21 CRF 58 definition of GLP for non-clinical studies, OECD Test Guidelines, or CAP/CLIA accreditation.
Responsibilities
<ul>
<li>Collaborate in determining schedule and project timelines/capabilities.</li>
<li>Support GMP resources and supply chain, including maintaining materials inventory control to meet production goals.</li>
<li>Operate and perform calibration, validation, cleaning, and maintenance of facility equipment and systems as specified in SOPs.</li>
<li>Conduct testing using PCR, Flow cytometry, aseptic techniques, uv-vis, pipetting, sorters, ELISPOT, ELISA, dilutions, peptides, cell staining, and more.</li>
<li>Perform daily operational activities related to biological products, ensuring availability of materials and proper documentation for GLP activities and product quality.</li>
<li>Assist in process documentation review, revision, remediation, and process change controls.</li>
<li>Handle specimens of blood, urine, tissue, and fecal matter.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in biology, cell culture, aseptic technique, PCR, flow cytometry, and pipetting.</li>
<li>Strong history in immunology research, tissue culture, GMP, and cGMP.</li>
<li>Bachelor's degree in Life Science Field with 2+ years of industry experience or a Master's with strong research experience from schooling.</li>
<li>Minimum of 2+ years of experience in the scientific industry outside of school or strong research experience from school.</li>
<li>Comfortable using Microsoft Office.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with purification techniques.</li>
<li>Experience in tissue culture.</li>
<li>GMP experience.</li>
<li>Biochemical experience.</li>
</ul>
Work Environment
The work environment is team-oriented, comprising a diverse group of individuals that is continually expanding. The current team consists of 23 members and aims to grow significantly by the end of the year. Collaboration is essential as work and testing are not conducted alone. The position operates on a 1st shift schedule from Monday to Friday, 8:00 AM to 4:30 PM, with occasional overtime.
Pay and Benefits
The pay range for this position is $26.00 - $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 Columbus,OH.
Application Deadline
This position is anticipated to close on Aug 15, 2025.
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.

Research Associate II

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate IIJob Description
The Research Associate II will work in the Flow Cytometry and Immune Monitoring Core, providing full-service support for research studies that involve routine PBMC processing, cryopreservation, T cell ELISPOT analysis, multiplexing, or immunophenotyping. This centralized core laboratory offers immune monitoring services for rAAV development and Phase I Trials, cell-based therapy studies, and other projects upon request. While services adhere to academic research standards, they do not meet criteria for 21 CRF 58 definition of GLP for non-clinical studies, OECD Test Guidelines, or CAP/CLIA accreditation.
Responsibilities
<ul>
<li>Collaborate in determining schedule and project timelines/capabilities.</li>
<li>Support GMP resources and supply chain, including maintaining materials inventory control to meet production goals.</li>
<li>Operate and perform calibration, validation, cleaning, and maintenance of facility equipment and systems as specified in SOPs.</li>
<li>Conduct testing using PCR, Flow cytometry, aseptic techniques, uv-vis, pipetting, sorters, ELISPOT, ELISA, dilutions, peptides, cell staining, and more.</li>
<li>Perform daily operational activities related to biological products, ensuring availability of materials and proper documentation for GLP activities and product quality.</li>
<li>Assist in process documentation review, revision, remediation, and process change controls.</li>
<li>Handle specimens of blood, urine, tissue, and fecal matter.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in biology, cell culture, aseptic technique, PCR, flow cytometry, and pipetting.</li>
<li>Strong history in immunology research, tissue culture, GMP, and cGMP.</li>
<li>Bachelor's degree in Life Science Field with 2+ years of industry experience or a Master's with strong research experience from schooling.</li>
<li>Minimum of 2+ years of experience in the scientific industry outside of school or strong research experience from school.</li>
<li>Comfortable using Microsoft Office.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with purification techniques.</li>
<li>Experience in tissue culture.</li>
<li>GMP experience.</li>
<li>Biochemical experience.</li>
</ul>
Work Environment
The work environment is team-oriented, comprising a diverse group of individuals that is continually expanding. The current team consists of 23 members and aims to grow significantly by the end of the year. Collaboration is essential as work and testing are not conducted alone. The position operates on a 1st shift schedule from Monday to Friday, 8:00 AM to 4:30 PM, with occasional overtime.
Pay and Benefits
The pay range for this position is $26.00 - $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 Columbus,OH.
Application Deadline
This position is anticipated to close on Aug 22, 2025.
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.

<h3>Job Description</h3>
Job Description
INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW! 
Job Description
Job Summary
The Micro Lab Technician is responsible for performing microbiological testing in compliance with internal Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role ensures the maintenance of the microbiology laboratory, its equipment, and testing methodologies.
Essential Functions &amp; Key Responsibilities
Conduct aseptic microbiological testing of raw materials, in-process materials, and finished products using USP agar methods in accordance with SOPs and GMP regulations.
Handle live microbiological agents and cultures; perform growth promotion testing per USP and SOP requirements.
Maintain cleanliness and compliance of the Micro Lab per SOP standards.
Collect and analyze environmental monitoring samples, including USP Purified Water, soft water, air, and equipment surfaces.
Evaluate data for trends and contribute to the development and revision of SOPs and microbiological test methods.
Complete administrative documentation and support lab investigations as needed.
Review and approve laboratory data for accuracy and compliance.
Calibrate, operate, and maintain laboratory instrumentation used in product testing.
Assist with inventory management and ensure adequate lab supplies are maintained.
Provide support to other QC personnel as needed.
Participate in Out-of-Specification (OOS) investigations, deviations, and Corrective and Preventive Actions (CAPAs).
Communicate effectively with other shifts regarding special testing requirements and relevant issues.
Perform other duties and special projects as assigned.
Additional Skills &amp; Qualifications
Education &amp; Experience
Bachelor of Science in Microbiology, Biology,Biochemistry, or related field
Knowledge, Skills &amp; Abilities
Strong understanding of scientific principles and logical problem-solving.
Ability to read, interpret, and follow technical data and SOPs.
Excellent math and reasoning skills; detail-oriented and highly organized.
Effective verbal and written communication skills.
Familiarity with various microbiological testing apparatus.
Proficiency in relevant computer software and laboratory systems.
Self-motivated with the ability to work independently.
Pay and Benefits
The pay range for this position is $23.00 - $23.00/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 Aug 21, 2025.
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.

Microbiology Lab Technician

<h3>Job Description</h3>
Job Description
Ideal Candidate will have experience with:
<ul>
<li>Sample Analysis: Perform sample preparation, chemical analysis, and quantification of chemicals in accordance with EPA methods including 5, 18, 29, 202, 308, 323, NCASI 98.01, and fuel analysis.</li>
<li>Equipment Operation: Utilize advanced laboratory equipment such as Gas Chromatography (GC - FID, NPD, TCD, FPD), ICP, ICP-MS, CVAAS, HPLC, GC-MS, UV-VIS analyses, FTIR (gas-phase), balances, ovens, and more.</li>
<li>Data Documentation: Maintain detailed records including laboratory notebooks, software data, standard preparations, and equipment logs.</li>
<li>Equipment Maintenance: Conduct routine and in-depth maintenance, including troubleshooting and electronic board replacement for laboratory equipment.</li>
<li>Accreditation Support: Perform tasks required to maintain laboratory accreditation, such as running and reporting audit samples, completing MDL studies bi-annually, and updating documentation (e.g., SOPs, DOC forms).</li>
<li>Quality Control: Perform and document standardizations, calibrations, and performance verifications daily.</li>
<li>Safety &amp; Compliance: Ensure proper sample custody, control, and hazardous waste disposal in compliance with safety protocols.</li>
<li>Additional Duties: Assist with editing and reviewing SOPs, guidance documents, and other tasks as assigned. </li>
</ul>
Essential Functions:
<ul>
<li>Performs laboratory operations, including preparation, analysis, quantification of chemicals; prepares standards and samples for analysis, including quality control samples, and reports final results; analyses include: microbiology, chemical oxygen demand, chlorophyll-A, specific conductivity, chlorine, solids, turbidity, Method 5, Method 17, Method 18, Method 201A, etc.</li>
<li>Documents work performed; maintains laboratory notebooks, recordings, software data, etc. for raw data, standard preparations, and equipment</li>
<li>Performs routine daily, weekly, and monthly maintenance of equipment; conducts in-depth maintenance, such as electronic board replacement and troubleshooting of equipment by diagnostic methods, such as Voltage-Ohm-Meter (VOM) and Internal computer diagnostics</li>
<li>Places orders for stack, lab, water sampling and office needs; keeps track of arrival of packages and completion of orders</li>
<li>Performs actions required to maintain accreditation; runs, reports, and passes audit samples bi-annually; completes MDL studies for each required method bi-annually, creates DOC forms for each quarter, and ensures all methods are run according to the requirements in each SOP</li>
<li>Edits and reviews documents; reviews SOPs and guidance documents to ensure all procedures accurately reflect laboratory practices and meet NELAC and/or EPA requirements</li>
<li>Maintains sample custody, control, and hazardous waste disposal</li>
<li>Performs other job-related duties as assigned</li>
</ul>
Supervisor Responsibilities - No supervisor responsibilities
Required Qualifications:
<ul>
<li>EDUCATION REQUIREMENT – Bachelor’s degree in chemistry or science-related field</li>
<li>Some experience in a laboratory setting</li>
<li>Experience working with hazardous chemicals</li>
<li>Able to obtain OSHA certification and H2S Safety Awareness</li>
<li>Able to obtain First aid + CPR + AED certification</li>
<li>Familiarity with various sample methods</li>
</ul>
Knowledge, Skills &amp; Abilities:
<ul>
<li>General knowledge of chemistry and lab analysis operations and lab safety</li>
<li>Proficiency in Microsoft Office programs, including MS Word and Excel</li>
<li>Strong verbal and written communication skills</li>
<li>Ability to lead a team and provide training and guidance to subordinates</li>
<li>Professional demeanor and appearance; ability to serve as a representative of the company</li>
<li>Ability to prioritize and multi-task</li>
<li>Strong organizational skills and attention to detail</li>
</ul>
<ul>
<li>Ability to read, count, and write to accurately complete all documentation</li>
</ul>
Work Environment - While performing the duties of this job, the employee regularly works in a laboratory setting. 
Physical Demands
<ul>
<li>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</li>
<li>Sitting or standing for extended periods and the use of hands to finger is common. Hearing and vision within normal ranges is helpful for normal conversations, to receive ordinary information and to prepare or inspect documents. Duties frequently involve repetitive motions and eye/hand/foot coordination. Testing priorities and timelines may serve as a source of emotional stress.</li>
<li>Occasional heavy lifting is expected. Exertion of up to 30 lbs. of force may occasionally be required. While performing the duties of this job, good manual dexterity for the use of laboratory equipment is needed. The employee is occasionally required to walk, lift, carry, push, pull, climb, stoop, kneel, crouch, reach, handle, grasp, and feel.</li>
<li>Use of applicable Personal Protective Equipment is mandatory.</li>
</ul>
Travel - Not applicable
Other Duties
Please note this job description is intended to describe the general nature and level of work performed by employees assigned to this position. It is not designed to contain or be interpreted as a comprehensive list of all duties, responsibilities, and qualifications. Additional job-related duties may be assigned. Alliance reserves the right to amend and change responsibilities to meet business and organizational needs as necessary with or without notice.
KEY BENEFITS INCLUDE:
<ol>
<li>Medical, Dental, and Vision Insurance </li>
<li>Flexible Spending Accounts </li>
<li>401(K) Plan with Competitive Match </li>
<li>Continuing Education and Tuition Assistance </li>
<li>Employer-Sponsored Disability Benefits </li>
<li>Life Insurance </li>
<li>Employee Assistance Program (EAP) </li>
<li>Paid Time Off (PTO), Paid Holidays, &amp; Bonus Floating Holiday (if hired after July 1st)</li>
<li>Profit Sharing or Individual Bonus Programs </li>
<li>Referral Program</li>
<li>Per Diem &amp; Paid Travel</li>
<li>Employee Discount Hub</li>
</ol>
EEO Commitment
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, national origin, ethnicity, sex, pregnancy, sexual orientation, gender identity/expression, religion, disability, age, genetics, active military or veteran status, and any other characteristics protected under applicable federal or state law.

Lab Analyst I

<h3>Job Description</h3>
Job Description
As a member of the Analytics/Gene Therapy group, this position will be responsible for performing analytical assays supporting the evaluation of early-stage production processes for the AAV vector research pipeline and supporting AAV product testing. The individual may collaborate with Process Development and additional internal and external stakeholders to ensure the development and transfer of robust analytical methods.
The Opportunity to Make a Difference
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Perform analytical assays to support production, purification, and comparability of AAV gene therapy products using qPCR, ddPCR, BLI, DLS, ELISA, and other general laboratory techniques
<ul>
<li>Work seamlessly with cross functional stakeholders to help advance the AAV vector production portfolios</li>
<li>Participate in project related teams and other internal/external collaborations</li>
<li>Ensure that scientific and technical challenges are resolved in a timely manner</li>
<li>Maintain all appropriate laboratory records</li>
<li>Perform routine data analysis for use in presentations, publications, and internal reports</li>
<li>Contribute to a safe, efficient, and effective environment with personal accountability</li>
<li>Perform other related duties as required</li>
</ul>

More about You
<ul>
<li>Degree in Biology, Biotechnology, Molecular Biology, Virology, or a related field</li>
<li>BS degree (or equivalent) with at least 1-2 years of relevant experience preferred</li>
<li>Working experience in gene therapy and/or viral vector biology is preferred</li>
<li>Experience with at least 2 techniques – qPCR, ddPCR, BLI, DLS, and ELISA is desirable</li>
<li>Attention to details is a must</li>
<li>Strong organizational skills</li>
</ul>
Company DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities. 
<h3>Company Description</h3>
Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Research Associate I, Analytics, Gene Therapy

<h3>Job Description</h3>
Job Description
INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW!
Description
The Micro Lab Technician is responsible for performing microbiological testing in compliance with internal Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role ensures the maintenance of the microbiology laboratory, its equipment, and testing methodologies.
Essential Functions &amp; Key Responsibilities
Conduct aseptic microbiological testing of raw materials, in-process materials, and finished products using USP agar methods in accordance with SOPs and GMP regulations.
Handle live microbiological agents and cultures; perform growth promotion testing per USP and SOP requirements.
Maintain cleanliness and compliance of the Micro Lab per SOP standards.
Collect and analyze environmental monitoring samples, including USP Purified Water, soft water, air, and equipment surfaces.
Evaluate data for trends and contribute to the development and revision of SOPs and microbiological test methods.
Complete administrative documentation and support lab investigations as needed.
Review and approve laboratory data for accuracy and compliance.
Calibrate, operate, and maintain laboratory instrumentation used in product testing.
Assist with inventory management and ensure adequate lab supplies are maintained.
Provide support to other QC personnel as needed.
Participate in Out-of-Specification (OOS) investigations, deviations, and Corrective and Preventive Actions (CAPAs).
Communicate effectively with other shifts regarding special testing requirements and relevant issues.
Perform other duties and special projects as assigned.
Additional Skills &amp; Qualifications
Education &amp; Experience
Bachelor of Science in Microbiology, Biology,Biochemistry, or related field
Knowledge, Skills &amp; Abilities
Strong understanding of scientific principles and logical problem-solving.
Ability to read, interpret, and follow technical data and SOPs.
Excellent math and reasoning skills; detail-oriented and highly organized.
Effective verbal and written communication skills.
Familiarity with various microbiological testing apparatus.
Proficiency in relevant computer software and laboratory systems.
Self-motivated with the ability to work independently.
Pay and Benefits
The pay range for this position is $23.00 - $23.00/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 Aug 19, 2025.
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.

<h3>Job Description</h3>
Job DescriptionJob Title: Lab Technician
INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO mamcdonough @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW! 
Job Description
We are seeking a dedicated Lab Technician to join our team and contribute to various laboratory tasks and projects. The role involves setting up and running laboratory experiments, analyzing test specimens, and working on materials selection, corrosion testing, and analysis. This position offers the opportunity to work under supervision, assisting more experienced team members while developing the capability to work independently.
Responsibilities
<ul>
<li>Set up and run laboratory experiments.</li>
<li>Analyze test specimens.</li>
<li>Perform tasks related to materials selection and corrosion testing and analysis, including experimental setup, data collection, and data reporting.</li>
<li>Inspect, test, repair, and install equipment.</li>
<li>Develop the capability to work independently on project activities while performing work under supervision.</li>
<li>Assist more experienced technicians, technologists, and professionals on technical assignments.</li>
<li>Follow the Safety, Health, Environmental, and Quality Assurance program on projects.</li>
<li>Record research activities performed in the lab book.</li>
<li>Prepare solutions, clean test cells, move items throughout the lab, and calibrate equipment following prescribed procedures.</li>
<li>Perform other duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>Experience or knowledge in chemistry, obtained through a degree or work experience.</li>
<li>Strong mechanical aptitude, including troubleshooting and tool utilization.</li>
<li>Ability to work in a lab environment.</li>
<li>Understanding of chemical engineering and chemical testing.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in materials testing.</li>
<li>MUST HAVE: Mechanical aptitude.</li>
</ul>
Work Environment
The Lab Technician will work in a lab setting alongside 12 other technicians. The standard working hours are from 8 AM to 5 PM, with occasional overtime expected. There is flexibility in start times between 7 AM and 9 AM. This position is a 6-12 month contract, with the possibility of conversion to direct employment.
Pay and Benefits
The pay range for this position is $22.00 - $22.00/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 Dublin,OH.
Application Deadline
This position is anticipated to close on Aug 17, 2025.
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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