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<h3>Job Description</h3>
Job Description
Job Title: Associate Scientist II
Work Site: St. Paul, MN 55117 – 100% Onsite
Duration: 12 Months Contract with possible extension
Shift/Schedule: Mon – Friday 8:00am to 4:30pm
Pay Rate/Range: $40.00/hr on W-2 through Select Source International
&nbsp;
Job Description:
The scientist has a focus in polymer materials characterization with experience working with various techniques such as DSC, TGA, FTIR, and SEM. Additionally, scientist will work in a fast-paced laboratory environment, possessing strong attention to detail and excellent problem-solving skills.
&nbsp;
Essential Functions:
<ul>
<li>Perform material characterization and assessment using a variety of techniques including DSC, TGA, FTIR to support medical device project teams with various Materials Science needs.</li>
<li>Thermal analysis experience (DSC/TGA)</li>
<li>Partner with other scientists and project teams to define test plans.</li>
<li>Work in a dynamic team environment and have strong interpersonal skills.</li>
<li>Conduct hands-on laboratory analysis and testing.</li>
<li>Document experiments in a highly regulated environment in an electronic notebook system.</li>
<li>Knowledge of technical concepts and principles underlying Materials Science techniques.</li>
<li>Analyze test results and draft technical reports.</li>
</ul>
&nbsp;
Accountability/Supervision:
<ul>
<li>Possess ability to apply chemistry/materials education and experience in fast-moving laboratory.</li>
<li>Willingness to be hands on in a science laboratory.</li>
<li>Will receive work direction and prioritization from supervisor and/or other S&amp;T scientists.</li>
<li>Possess strong attention to detail and excellent problem-solving skills.</li>
<li>Strong technical writing skills</li>
</ul>
&nbsp;
Working Conditions:
<ul>
<li>Working in lab environment with proper safety equipment.</li>
<li>Working with common laboratory chemicals and biological tissue.</li>
<li>Working while sitting and /or standing.</li>
</ul>
&nbsp;
Minimum Qualifications:
<ul>
<li>Ability to work in fast-moving environment where priorities frequently change.</li>
<li>Experience with common materials characterization techniques.</li>
<li>Ability to perform multiple assignments concurrently and meet required deadlines.</li>
<li>Bachelor’s degree in materials science, chemistry or closely related degree with 1-3 years demonstrated experience</li>
<li>Ability to operate analytical instrumentation through relevant industry experience</li>
<li>Experience documenting laboratory work in electronic/paper notebook system according to GMP guidelines.</li>
</ul>
&nbsp;
Preferred Qualifications:
<ul>
<li>Experience with polymer characterization and understanding of structure/property relationships.</li>
<li>Working knowledge of Trios, Omnic software system and Labvantage ELN documentation system.</li>
</ul>
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Associate Scientist II

<h3>Job Description</h3>
Job Description
Enjoy what you do while contributing to a company that makes a difference in people’s lives. IVF Florida, one of the premier fertility centers in the United States, seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward.
We have an immediate opening for an Embryology Research Scientist to join our team in Margate, Florida. The schedule is Monday through Friday, from 9:00 AM to 5:00 PM, with weekends and holidays as needed.
This position is responsible for collaborating with the research team to keep the practice at the cutting edge of current technology and on the forefront in developing new technology. The Embryology Research Scientist is responsible for carrying out scientific research (40%) within the IVF laboratory under the direction of the Laboratory Management Team. In addition, this position is responsible for collaborating with the Scientific Director (45%) and the Research Coordinator (10%) in compliance with procedural processes associated with clinical and scientific research trials. The position may require occasional coverage in the clinical embryology laboratory (5%).
How You'll Contribute: 
We always do whatever it takes, even if it isn't specifically our "job." In general, the Embryology Research Scientist is responsible for:
<ul>
<li>Designs, plans and Implements projects that have the possibility of improving patient outcomes</li>
<li>Demonstrates proficiency in laboratory services and procedures: Identification, assessment and culture of oocytes; Sperm preparation and insemination of oocytes; Embryo culture; Assessment and selection of embryos for transfer; Embryo freezing, storage, and thawing; Media preparation; Instrumentation involved in research; Recording and reporting laboratory results; Semen analysis</li>
<li>Undertakes research and/or coordinates research in human embryo biology as agreed upon by the Scientific and Laboratory Director, and Physician Chair of the Research Committee</li>
<li>Lead and confirm all projects are monitored and completed in the desired time frames and that the outcomes of such projects are effectively communicated, as appropriate</li>
<li>Lead and confirm projects remain productive and achieve desired, agreed upon milestones</li>
<li>Lead all data analysis and writing of research articles for publication in peer-reviewed scientific journals on the clinical research and development at the Company/practice</li>
<li>Lead and presents oral and poster presentations of laboratory research results for scientific meetings</li>
<li>Oversee the preparation and submission of applications for Institutional Review Board approval of study protocols and patient consent forms for prospective studies</li>
<li>Fully complies with US Fertility quality management policies and OH&amp;S policies and guidelines</li>
<li>Must develop competency in more complex reproductive technologies as required by research studies/projects</li>
<li>Execute laboratory policies, practices and procedures to ensure that laboratory accreditation is maintained in good standing under OSHA and CLIA, and that laboratory practices conform to all other applicable Federal, State and local regulatory laws and guidelines</li>
<li>Ensure that the laboratory is operated in such a manner that it is in continuous readiness for inspection and review by the appropriate regulatory agencies and the Corporate Standards Review</li>
<li>Assist the Laboratory Director/Supervisor with laboratory quality assurance and quality control programs to ensure they satisfy Company requirements and meet industry standards as established by qualified outside agencies</li>
<li>Identify and anticipate safety and health concerns and hazards by surveying environmental, operational, and occupational conditions; rendering opinions on new equipment and procedures; recommending preventative programs as needed</li>
<li>Participates as required in appropriate proficiency testing programs to monitor laboratory practice outcomes, and to measure on a regular basis that such outcomes meet or exceed industry and practice standards</li>
<li>Ensure operation of equipment by completing preventative maintenance requirements; following manufacturer’s instructions; troubleshooting malfunctions; calling for repairs; maintaining equipment inventories; evaluating new equipment and techniques</li>
<li>Maintain supply inventory by checking stock to determine inventory level; anticipating needed supplies; placing and expediting orders for supplies</li>
<li>Interface with clinical embryologists to integrate research projects into the laboratory</li>
<li>Work cooperatively with a multidisciplinary team to provide good patient care and achieve the objectives and goals of the practice</li>
<li>Work weekends and holidays as scheduled, inclusive of on-call responsibilities</li>
<li>Attend Company/Practice and department meetings as required</li>
<li>Works with physicians, laboratory personnel, nurses and other team members contributing to research projects</li>
<li>Contributes to research projects in relevant project development, data collection, literature review, presentation preparation, manuscript writing, and related research activities</li>
<li>Participates in monthly journal club and clinical meetings; communicates issues where appropriate</li>
<li>Cooperates, interfaces and works independently to assure the program goals are achieved</li>
</ul>
What You'll Bring:
The skills and education we need are:
<ul>
<li>Graduate Degree (MSc), preferably in Reproductive Biology or other relevant field required</li>
<li>Minimum of 2 years research experience in Reproductive Biology, Infertility or related field</li>
<li>Minimum of 2-3 years of embryologist experience</li>
<li>Ability to access, input, and retrieve information from a computer</li>
<li>Proficiency with computing software including Word, PowerPoint, Excel, and statistical analysis software</li>
<li>Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.)</li>
<li>Ability to work independently and demonstrate good judgment</li>
<li>Excellent interpersonal skills and ability to work as part of a multi-disciplinary team and build and maintain effective working relationships</li>
<li>Excellent verbal &amp; written communication skills</li>
<li>Proficiency in medical/scientific writing</li>
<li>Proven ability to meet deadlines and follow-through on projects</li>
<li>Ability to maintain the highest level of confidentiality</li>
</ul>
More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful.
What We Offer:
We are proud to provide a comprehensive and competitive benefits package tailored to support the needs of our team members across all employment types:
<ul>
<li>Full-Time Employees (30+ hours/week): Medical, dental, and vision insurance, 401(k) with company match, tuition assistance, performance-based bonus opportunities, generous paid time off, and paid holidays</li>
<li>Part-Time Employees: 401(k) with company match and performance-based bonus opportunities</li>
<li>Per Diem Employees: 401(k) with company match</li>
</ul>
<ul></ul>
At IVF Florida, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We’re committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team!
To learn more about our company and culture, visit here.

Embryology Research Scientist

<h3>Job Description</h3>
Job Description
Reports to: Curatorial Department Employment Status: Full-time, Non-exempt
Hillwood Estate, Museum &amp; Gardens welcomes over 100,000 visitors annually to experience the beauty of our gardens, the richness of our decorative arts collection, and the lasting legacy of Marjorie Merriweather Post. Our mission is to share our founder’s vision and foster a greater understanding of the arts and cultures that shaped her world.
The Research Assistant supports Hillwood’s Curatorial Department through research, cataloging, writing, and project coordination across exhibitions, publications, and long-term collection initiatives. This role plays a key part in maintaining accurate and up-to-date collection information in TMS and object files; producing scholarly and interpretive research; contributing to exhibition and publication development; and supporting curators in meeting project deadlines.
Working collaboratively across Collections, Curatorial, Exhibitions, Archives, and other departments, the Research Assistant ensures that Hillwood’s curators have the research materials, documentation, and organizational support necessary to advance exhibitions, interpretive content, acquisition research, and thematic scholarship
About the Role:
Research &amp; Writing
<ul>
<li>Conduct primary and secondary research on Hillwood’s collections, including textiles, decorative arts, and related subject areas.</li>
<li>Compile research for exhibitions, publications, interpretive labels, and internal files.</li>
<li>Prepare research summaries, annotated bibliographies, timelines, object histories, and reference packets.</li>
<li>Assist in drafting interpretive and didactic content in collaboration with curators.</li>
<li>Support research needed for grant narratives, proposals, and scholarly contributions.</li>
</ul>
Collection Cataloging &amp; Documentation
<ul>
<li>Update and maintain TMS object records and associated paper files.</li>
<li>Support long-term cataloging initiatives, provenance research, and documentation projects.</li>
<li>Verify object information through on-site review, including occasional object handling under supervision.</li>
<li>Ensure documentation follows museum standards and departmental procedures.</li>
</ul>
Project Coordination
<ul>
<li>Track project timelines and assist curators in meeting deadlines for exhibitions, publications, and grants.</li>
<li>Organize research materials and manage research-related communications.</li>
<li>Coordinate workflow across departments as projects require.</li>
<li>Support the scheduling and organization of research priorities for curators.</li>
</ul>
Exhibition &amp; Publication Support
<ul>
<li>Gather research materials for upcoming exhibitions.</li>
<li>Organize and maintain research files, interpretive drafts, and supporting documents.</li>
<li>Contribute to publication preparation, including research verification and fact-checking.</li>
<li>Assist with reference images, copyright information, and background research.</li>
</ul>
General Administrative Support
<ul>
<li>Organize digital and physical research files.</li>
<li>Maintain bibliographic and archival research logs.</li>
<li>Assist curators with administrative tasks requiring research, writing, or organization.</li>
</ul>
About You:
<ul>
<li>Bachelor’s degree in Art History, History, Museum Studies, Material Culture, or related field required.</li>
<li>Demonstrated research, writing, and source-citation experience.</li>
<li>Experience with museum cataloging systems; familiarity with TMS strongly preferred.</li>
<li>Prior museum, library, archives, or academic research experience desirable.</li>
<li>Experience handling historical or art objects (through coursework or museum practice).</li>
<li>Strong proficiency in Microsoft Office; familiarity with SharePoint.</li>
<li>Experience with library and archival research systems; Adobe Acrobat or Adobe Suite helpful.</li>
</ul>
Skills and Abilities
<ul>
<li>Excellent written communication skills and ability to synthesize information clearly and accurately.</li>
<li>High attention to detail, accuracy, and consistency in research and data entry.</li>
<li>Strong organizational and project-management skills.</li>
<li>Intellectual curiosity and a collaborative, team-oriented approach.</li>
<li>Ability to work independently while meeting deadlines.</li>
</ul>
About Us:
Hillwood Estate, Museum &amp; Gardens is deeply committed to fostering a positive, inclusive, and engaging workplace where all voices are valued, and where staff and visitors of all backgrounds can be inspired by the life and legacy of our founder, Marjorie Merriweather Post.
We Offer:
<ul>
<li>A fabulous work culture that inspires your best work.</li>
<li>Casual Monday.</li>
<li>Support for career development with internal and external opportunities to learn and grow.</li>
<li>Retirement Savings Plan</li>
<li>Metro commuter benefits of up to $50 per month or free on-site parking.</li>
<li>Mental wellness support.</li>
<li>Discounts in the shop and Merriweather Café.</li>
<li>Free admission to the museum and festival days for employees, families, and friends.</li>
</ul>
Hillwood is seeking applicants from all backgrounds and educational levels to ensure we get the best, most creative talent on our team. We are an equal opportunity employer, and we encourage people who identify as Black, Indigenous, people of color and people with marginalized identities to apply for open positions. We strive to make the hiring process as accessible as possible. Please do not hesitate to share what will make the process best for you. We cannot guarantee all accommodations; our team will make accommodations where possible with sufficient notice. 
The compensation for the Research Assistant position is $55,000 annually. This is a full-time salaried role lasting through December 31, 2026, with the potential to become a permanent position in 2027.

Research Assistant

<h3>Job Description</h3>
Job Description
GeoSoils, Inc., a well-established geotechnical and engineering geology consulting firm (serving Southern California since 1974) GeoSoils, Inc., is seeking a highly qualified Certified Engineering Geologist (CEG) to join our growing team in Carlsbad, CA. This is a senior-level opportunity for a licensed professional to lead geotechnical and engineering-geology projects that support development, infrastructure, grading, coastal, and environmental clients across the region.
Key Responsibilities
<ul>
<li>
Serve as Geologist-of-Record on geotechnical and engineering geology assignments
</li>
<li>
Oversee and conduct subsurface investigations (soil borings, test pits, rock/soil sampling, geologic mapping) for foundation design, grading, slope stability, and site development GeoSoils, Inc.
</li>
<li>
Perform geologic hazard assessments (landslides, faulting, subsidence), seismic hazard and fault-zone studies, hydrogeological investigations, seismic refraction / remote-sensing surveys, and soil/rock rippability assessments when required GeoSoils, Inc.
</li>
<li>
Provide geologic and geotechnical engineering reports, recommendations for foundations, earthworks, slope stability, retaining structures, and ground improvement or stabilization strategies GeoSoils, Inc.
</li>
<li>
Provide construction observation and geologic oversight during grading, excavation, and foundation installation, including quality-control testing and compliance monitoring (soil/rock mechanics, compaction, settlement evaluations, etc.) GeoSoils, Inc.
</li>
<li>
Coordinate with civil/structural engineers, project managers, clients, regulatory agencies, and other stakeholders throughout project lifecycle
</li>
</ul>
Required Qualifications
<ul>
<li>
Active California Certified Engineering Geologist (CEG) license – REQUIRED
</li>
<li>
B.S. or M.S. in Geology, Engineering Geology, or a closely related discipline
</li>
<li>
7+ years of professional experience in geotechnical engineering and/or engineering geology
</li>
<li>
Demonstrated experience with subsurface investigations, soil/rock mechanics, foundation and earthwork design support, slope stability, seismic hazard analysis, and geologic hazard assessments
</li>
<li>
Strong technical writing, analysis, communication, and leadership skills
</li>
<li>
Valid California driver’s license with acceptable driving record
</li>
</ul>
Preferred Experience
<ul>
<li>
Expertise in hazard-zone evaluations: landslide risk, fault-rupture, liquefaction, subsidence, and seismic hazard assessments
</li>
<li>
Experience with coastal and waterfront geotechnical / coastal engineering projects (shoreline/bluff analysis, erosion control, pile / pier / waterfront structure support) — reflecting GeoSoils’ coastal-engineering capabilities GeoSoils, Inc.
</li>
<li>
Familiarity with field-exploration methods, remote-sensing, seismic refraction, hydrogeological studies, and on-site laboratory testing for soils/rock materials GeoSoils, Inc.
</li>
<li>
Experience preparing geologic hazard reports, consulting, or expert services for clients including private developers, municipalities, and public-works projects
</li>
</ul>
Compensation &amp; Benefits
<ul>
<li>
Competitive salary commensurate with experience and credentials
</li>
<li>
Incentive/performance bonuses
</li>
<li>
Medical, dental, and vision insurance
</li>
<li>
Paid time off and holidays
</li>
<li>
Ongoing professional development and license-maintenance support
</li>
<li>
Long-term growth potential within a respected and established firm
</li>
</ul>
Why Join GeoSoils?
<ul>
<li>
Be part of a leading Southern California geotechnical-engineering firm with a reputation for excellence and over 50 years of operational history GeoSoils, Inc.+1
</li>
<li>
Work on a wide variety of challenging, high-impact projects ranging from grading and foundations to seismic hazard assessments, coastal engineering, and environmental/geologic investigations
</li>
<li>
Collaborate with seasoned geologists, engineers, and technical experts — and build a long-term career in engineering geology and geotechnical consulting
</li>
<li>
Contribute to projects that shape safe, reliable infrastructure and community development in California
</li>
</ul>

Staff or Senior Staff Certified Engineering Geologist (CEG)

<h3>Job Description</h3>
Job Description
Quality Control Chemist - 2nd shift (Monday-Thursday, 2pm-1am)
Job Description
The Quality Control Chemist plays a crucial role in supporting manufacturing by conducting laboratory analysis of raw materials, intermediate blends, and finished products. This analysis is performed using wet chemistry techniques such as pH measurement, UV-Vis spectroscopy, FTIR, and titration, along with advanced instrumentation including HPLC and GC.
Responsibilities
<ul>
<li>Follow standard operating procedures to ensure quality control.</li>
<li>Conduct quality testing and document results accurately.</li>
<li>Maintain and calibrate laboratory instruments regularly.</li>
<li>Assist with the transfer of test methods.</li>
<li>Train personnel on equipment usage and testing methods.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's Degree in Chemistry</li>
<li>Minimum of 3 years of laboratory experience</li>
<li>Proficiency in HPLC, GC, pH measurement, UV-Vis spectroscopy, FTIR, and other wet chemistry techniques</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in HPLC, GC, and analytical test method development and transfer</li>
<li>Familiarity with microbial testing and procedures</li>
<li>Experience in contract manufacturing and testing</li>
</ul>
Work Environment
The position is based in a laboratory environment requiring adherence to safety protocols. Proper PPE including safety glasses, gloves, lab coat, and ear plugs will be provided and must be worn at all times. The role involves 75% standing, 25% sitting, and occasional lifting of up to 25 lbs. The work schedule is 2nd shift, Monday to Thursday, from 2pm to 1am, consisting of four 10-hour shifts. Occasional weekend work or overtime may be required. Initial training will require some first shift hours.
Job Type &amp; Location
This is a Permanent position based out of Edgerton, WI.
Pay and Benefits
The pay range for this position is $62400.00 - $62400.00/yr.
Medical, dental, vision, 401K
Workplace Type
This is a fully onsite position in Edgerton,WI.
Application Deadline
This position is anticipated to close on Jan 16, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job DescriptionSalary: $60K-&amp;70K, DOE 
Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation.
 
Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values:
 
<ul>
<li>Client Focused: We only succeed when our clients succeed.</li>
<li>Outstanding: We deliver meticulous results through outstanding performance.</li>
<li>Good: We act ethically and morally.</li>
<li>Employee-Centric: We honor and support our employees.</li>
<li>Nimble: We are prepared to adapt in an ever-changing industry.</li>
<li>Team-Oriented: We collaborate with each other and with our clients.</li>
</ul>
 
We currently have a role available for a Pharma Cell Biologist to join our San Diego based team.
 
Job duties include, but are not limited to, the following:
 Maintain and culture mammalian cells, including both adherent and suspension cell lines. Prepare, optimize, and maintain various cell culture media, supplements, and reagents. Perform routine cell passaging, counting, viability assessment, and cryopreservation.
<ul>
<li>Hands-on experience with mammalian cell culture, including adherent and suspension cells is a must.</li>
<li>Experience preparing and handling multiple types of cell culture media is required.</li>
</ul>
 Lyse cells and extract genomic DNA for downstream molecular biology applications.
<ul>
<li>Working knowledge of molecular biology techniques such as cell lysis, genomic DNA extraction, and PCR is required.</li>
</ul>
 Perform PCR and related molecular biology assays for genotyping or construct verification. Scale up plasmid DNA preparations for transfection and experimental use.
<ul>
<li> Experience with plasmid DNA preparation, including mid- to large-scale plasmid production is highly desirable.</li>
</ul>
 Support transfection and cell-based assays as needed.
<ul>
<li>Prior transfection experience is highly desirable.</li>
</ul>
 Prepare and maintain laboratory reagents, buffers, and consumables. Accurately document experimental procedures and results in lab notebooks or electronic systems. Work collaboratively with team members to support project timelines and experimental goals. Ensure compliance with laboratory safety, biosafety, and regulatory requirements. This position is a hands-on, lab-based role. 
Job requirements include, but are not limited to:
<ul>
<li>BS/MS degree in Cell/Molecular Biology (or related field) and at least 1 year laboratory experience in industry is required.</li>
<li>Team player mentality with strong written and verbal communication skills. Will be required to work collaboratively with cross-functional teams including structural biology, molecular biology, biochemistry, and biophysics.</li>
<li>The ideal candidate will be organized, comfortable with multi-tasking, enthusiastic, self-motivated and details oriented, with the skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery.</li>
</ul>
 This job posting will close by March 31st 2026 or when candidates are identified, whichever comes first.

Pharma Cell Biologist

<h3>Job Description</h3>
Job Description
Job Title: Associate Research Scientist - Stability
Job Description
The Associate Research Scientist - Stability will provide scientific and technical support in the research and development of plasma-derived or recombinant proteins. This role supports the Stability Group by managing the stability program, ensuring compliance with regulatory standards, overseeing stability chambers, and maintaining product safety and quality for both licensed products and developmental projects.
Responsibilities
<ul>
<li>Maintain product inventory for active stability studies, ensuring accountability and compliance with all requirements.</li>
<li>Coordinate with Packaging to acquire samples for stability evaluation and ensure the accuracy of sample labeling and documentation.</li>
<li>Facilitate the delivery of stability samples for laboratory testing and resolve discrepancies in collaboration with QC Sample Specialists and stability supervisors.</li>
<li>Monitor and maintain label printers, ensuring they are in good working order for stability requests.</li>
<li>Track requests for additional samples and generate monthly pull schedules for stability testing.</li>
<li>Generate and manage work orders for maintenance and repairs of stability equipment to prevent product loss.</li>
<li>Ensure compliance with test request sheets and conduct investigations to resolve GMP discrepancies.</li>
<li>Enter test data into stability databases and assist with filing stability records.</li>
<li>Remove samples from inventory upon completion of stability studies and initiate purchase and work orders for the Stability Group.</li>
<li>Train staff on sample handling and inventory procedures, and perform daily assessments of stability incubators and freezers.</li>
<li>Investigate excursions outside validated temperature ranges and analyze chamber temperature and humidity trends.</li>
<li>Conduct reviews to ensure equipment compliance and address chamber concerns proactively.</li>
</ul>
Essential Skills
<ul>
<li>Understanding of ICH guidelines and GMP requirements for Stability product storage.</li>
<li>Excellent communication skills for generating clear, accurate reports and interacting with cross-functional teams.</li>
<li>Working knowledge of equipment and storage facility operations.</li>
<li>Ability to resolve chamber-related issues quickly and assess the impact of deviations.</li>
<li>Proficiency in ScienTek Stability System, labeling solutions software, Intermec printers, SAP, DeltaV Monitoring System, LabWatch, Maximo Management System, and TempTale Monitoring Devices.</li>
<li>Experience in visual inspection and vial integrity testing, as well as biological sample shipment.</li>
<li>Basic calculation skills, attention to detail, and effective verbal and written communication skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>MS Degree or BS with 1-2 years of experience, or no degree with 5 years of experience relevant to the role.</li>
<li>Education in a scientific field or experience in the regulated pharmaceutical industry.</li>
<li>Technical expertise in separations-based analytical techniques such as HPLC, Capillary Electrophoresis, and SDS-PAGE.</li>
<li>Working knowledge of Waters Empower and proficiency in method development and qualification based on ICH guidelines.</li>
</ul>
Work Environment
The work environment includes clinical and laboratory settings with exposure to biological fluids, potential infectious organisms, and chemicals. Personal protective equipment such as protective eyewear, garments, and gloves is required. The position involves frequent sitting and neck bending, occasional standing and waist twisting, and hand movements. Moderate lifting of 15-30 lbs. is required. The role demands precise coordinated movements and the ability to communicate complex information effectively. The work involves collaborating with diverse groups to address complex issues and performing tasks with variable demands.
Job Type &amp; Location
This is a Contract position based out of Durham, NC.
Pay and Benefits
The pay range for this position is $37.50 - $43.00/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 Durham,NC.
Application Deadline
This position is anticipated to close on Jan 20, 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.

Associate Research Scientist - Stability

<h3>Job Description</h3>
Job DescriptionDescriptionKnowles Valencia is seeking reliable, detail-oriented, multi-area Cleanroom Operators to join our team on third shift.&nbsp; The Cleanroom Operator is responsible for executing manufacturing processes within a semi-automated system, rotating through multiple workstations in a controlled cleanroom environment. The ideal candidate will bring prior cleanroom experience, excellent manual dexterity, and a strong commitment to quality, safety, and precision. Key Responsibilities
<ul>
<li>Operate across various cleanroom workstations to support different stages of the manufacturing process.</li>
<li>Follow established protocols and safety standards to maintain product integrity and a sterile environment.</li>
<li>Monitor equipment and report any irregularities or malfunctions promptly to engineer.</li>
<li>Perform routine cleaning and maintenance of workstations and tools.</li>
<li>Accurately document production data and adhere to quality control procedures</li>
<li>Collaborate with team members to meet production goals and resolve workflow issues</li>
<li>Rotate across multiple workstations within the cleanroom to support various stages of the manufacturing process.</li>
<li>Lift and maneuver metal bars and components weighing up to 15 pounds safely and efficiently.</li>
<li>Read and interpret manufacturing procedures, work instructions, and technical documentation.</li>
<li>Demonstrate reliability by consistently following instructions, meeting deadlines, and taking ownership of assigned tasks.</li>
<li>Maintain cleanliness and organization of workstations in accordance with 5S principles.</li>
<li>Flexibly support multiple areas as required by production demands.</li>
</ul>
 Skills, Knowledge and Expertise
<ul>
<li>High School diploma or general education degree (GED) is required.</li>
<li>Demonstrate knowledge of manufacturing principles practices, and procedures.</li>
<li>Ability to read and comprehend simple instructions</li>
<li>Computer Skills: Basic knowledge in computers, accessing email, training, and documents via company network.</li>
<li>This position will be performed in a clean room production environment which requires certain preparation and gowning practices.</li>
<li>Will and able to work overtime as requested.</li>
<li>Must be able to work in a clean room setting wearing appropriate clean room attires, which includes but is not limited to, jumpsuit, shoe covers, hair covering, and glasses.</li>
<li>To maintain contamination control standards, employees are prohibited from wearing makeup, lotions, or other personal care products while working in the cleanroom. These substances can shed particles or emit vapors that compromise the cleanroom environment and product integrity. All personnel must ensure their face and exposed skin are free of such products prior to gowning and entry.</li>
<li>Complete repetitive movements for extensive periods.</li>
<li>Able to lift, push, pull, or otherwise move objects of up to 15 pounds.</li>
<li>Ability to stand/seat for long periods of time.</li>
</ul>
 BenefitsWhat’s in it for you on Day 1:
<ul>
<li>Medical, dental and vision insurance plans</li>
<li>Prescription Drug Plans</li>
<li>Basic Life Insurance&nbsp;</li>
<li>401k plan with company match</li>
<li>Tuition Reimbursement Program</li>
<li>Employee Referral Program&nbsp;</li>
<li>Vacation and Paid Sick Leave</li>
<li>Paid Holidays</li>
</ul>
Exciting Onsite Perks:&nbsp;
<ul>
<li>Free coffee available at our cafeteria</li>
<li>Employee Appreciation Events</li>
</ul>
&nbsp;Knowles is committed to providing a competitive and fair total compensation package for all employees. One element in our total compensation package is base pay.&nbsp; The pay rate for this role is targeted at $20.00 per hour plus a third shift differential.&nbsp; &nbsp;Individual compensation decisions are based on a number of factors, including but not limited to previous experience and skills acquired prior to joining Knowles, cost of living in the assigned work location, assigned schedule, and salaries of similarly situated peers at the company.&nbsp; It is to be expected that candidates will come to us with different sets of skills and experiences and therefore will be paid at different points in the stated range.&nbsp; We recognize that the person(s) we select for hire may be less experienced or more experienced than the role as posted; if this is the case, any updates to available salary ranges will be communicated with candidates during the recruitment process. &nbsp; &nbsp;Equal Opportunity Statement: Knowles Precision Devices prohibits pay discrimination and discrimination of any kind based on race, color, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation, or other legally protected status. Notice to Staffing Agencies, Search Firms and Recruitment Agencies: The recruitment process at Knowles is managed through the Human Resources department. Knowles does not accept resumes submitted from 3rd party agencies outside of our system. To submit resumes, 3rd party agencies will need to be a pre-approved vendor with a valid contract in place, be actively engaged by Knowles to recruit for a specific position and have agency log in credentials to submit candidates to our careers portal. Please do not submit resumes via e-mail, through our external website or directly to our employees. Any resumes submitted in this way become the property of Knowles and will not be eligible for any placement fee.

Cleanroom Operator - Third Shift 11:30 PM - 7:00 AM

<h3>Job Description</h3>
Job DescriptionThis general submission posting is an opportunity to submit your resume for future consideration only; not for an existing opening. We anticipate this role may be open in the near future. If you wish to be considered for this potential opportunity, please submit your resume. When a position becomes available, you may be contacted by our Talent Acquisition team. The Company will only contact applicants who are selected for further consideration about potential future opportunities.&nbsp; Business Unit: Curated Position: Compositor, Sr Location: New York, NY (Remote) *Pay Range: $59.23 - $88.85 USD hourly POSITION SUMMARY: The Senior Compositor role requires creativity and high technical abilities. They will take direction from the VFX and Compositing Supervisors and will also be expected to work autonomously in a fast paced environment to deliver an extremely high level of work. The Compositor is often given the most complex and demanding shots to complete. They are expected to be comp generalists who can handle a wide range of comp tasks from start to finish including but not limited to compositing live action and CG, blue/green screen keying, camera tracking, photoreal CG integration, set extensions with matte painting projections, complicated removals, beauty work, and paint/rotoscoping. MAIN DUTIES: The Senior Compositor will take instruction and direction from Leads and VFX Supervisors to execute assigned shots in the most efficient and fastest way possible. They will balance&nbsp;the creative and technical aspects of each shot. They will meet&nbsp;task schedules and show deadlines. Other duties include:
<ul>
<li>Have an excellent understanding of the broader VFX pipeline including color space, workflow and industry-standard script layouts.</li>
<li>Ongoing communication with Production and Leads regarding schedules and deadlines.</li>
<li>Taking responsibility for own workload, time management and notes/feedback actions required by Supervisors.</li>
</ul>
 WHAT YOU BRING: The ideal candidate will&nbsp;be an expert in all aspects of compositing in Nuke, integrating 2D, 3D and live-action elements to a high-end visual effects standard. They will be a&nbsp;team player with a great attitude and an independent problem solver. They will take feedback and direction well with ability to understand and apply notes. They&nbsp;will bring experience with sound aesthetic with a good understanding of color, light and photography. The ideal candidate will also bring the following:
<ul>
<li>Clean and efficient script organization / dependable and flexible.</li>
<li>A strong creative eye, artistic and problem-solving skills&nbsp;/ extreme attention for detail.</li>
<li>Thorough understanding of compositing techniques.</li>
<li>Excellent people and communication skills.</li>
<li>Participate in creative and technical discussions.</li>
<li>Experience using Shotgrid.</li>
<li>Ability to work under tight deadlines.</li>
<li>Advanced knowledge of CG rendering and compositing multi-channel EXRs.</li>
<li>Excellent understanding of 2D and 3D tracking.</li>
<li>Highly proficient in using IBK, Primatte or Keylight.</li>
<li>Excellent knowledge of Nuke's 3D system.</li>
<li>Strong understanding of colorspace pipelines.</li>
<li>Experience with mocha, photoshop, other photo editing software is a plus.</li>
<li>Experience with Python scripting preferred.</li>
</ul>
 ABOUT THE COMPANY: Company 3, including its various business units and family of brands, provides a full range of Creative Services for content creators, including conceptual design, pre-vis, look development, ideation and rapid prototyping, 3D animation/CGI, motion graphics/designers, matte painting, compositing, dailies and production services, color grading, post-production finishing, marketing/trailers, live-action production, experiences, and more. Diversity and Inclusion at Company 3: Creativity has diversity at its core. We celebrate the value of each unique experience by being dedicated to fostering the most diverse, equitable, and inclusive culture where every employee feels empowered and safe to show up to work as their full self. It is our policy to provide equal employment opportunities to all applicants and employees. Please inform the Company's HR representative if you need assistance completing any forms or otherwise need any accommodation or support in order to participate in the application process. *The listed pay range represents the lowest to highest range that we in good faith believe we would pay for this role at the time of this posting. This range may be modified in the future. An employee’s pay position within the range may be based on several factors including, but limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, local currency exchange rates, performance, shift, travel requirements, sales or revenue-based metrics, applicable law, and business or organizational needs.&nbsp; The benefits for eligible part-time employees working 25 or more hours per week and full-time employees in the US include a comprehensive package of health, retirement, and insurance benefits and paid time off. The benefits for eligible project hires and part-time employees working less than 25 hours per week in the US include retirement, select insurance benefits, and where required by law, health benefits. For roles filled in Canada and other territories, local benefits plan offerings as adopted and amended from time to time will apply. The above compensation and benefits information is provided in accordance with various state, provincial, and local pay transparency laws. The Company’s recruitment processes will also be conducted in accordance with applicable law as adopted and amended from time to time. Both external and internal candidates can apply for this general submission posting through the Company’s Career Page.
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Compositor, Sr (General Submission)

<h3>Job Description</h3>
Job Description
Position Purpose: 
We are seeking an experienced subject matter expert in molecular biology and/or microbiology to provide technical support to Signature Science’s quality assurance (QA) contracts for national and homeland security programs, with a focus on CBRNe collection and analysis efforts. The successful candidate will also support internal Signature Science quality programs, including the Signature Science ISO 17043 accredited Proficiency Testing Program, through auditing, quality management system document development and QA laboratory support

Essential Duties and Responsibilities:
<ul>
<li>Provide subject matter expertise in the areas of molecular biology and/or microbiology as they pertain to quality assurance of collection or analytical activities</li>
<li>Serve as a Lead Auditor for external audits of client laboratories and/or sample collection teams, providing on-site identification of audit findings, interacting directly with management of auditee organization, delivering an oral out-brief summary of audit findings, and overseeing the development of the written audit report.</li>
<li>Provide feedback on auditee corrective actions</li>
<li>Assist client laboratories in preparing for external ISO 17025 accreditation assessments and attend assessments as an advocate for the client laboratory.</li>
<li>Perform internal audits of Signature Science systems and procedures against relevant internal or external standards, including audits of the Signature Science Proficiency Test Program against the requirements of ISO/IEC 17043 and internal policies and procedures.</li>
<li>Review and summarize quality assurance and/or proficiency test data, provide input and review of technical reports, identify data trends and other issues.</li>
<li>Contribute to the development and revision of project quality documents based on the ISO/IEC 17025, ISO/IEC 17043, ISO 17034, and Clinical Laboratory Improvement Program (CLIP) standards, as applicable.</li>
<li>Provide ISO 17025 (or other quality topics) training to clients</li>
<li>Other activities may include:</li>
<li>Perform proficiency test sample preparation laboratory activities, including sample spiking, microbiological analysis, nucleic acid extraction, PCR analysis, immunoassay analysis, and packaging samples for shipment. o Lead or assist with the validation and/or verification of new methods o Communicate with external laboratory staff to help resolve QA, PT, or other quality-related issues o Serve as a task leader on one or more projects</li>
</ul>
Required Knowledge, Skills &amp; Abilities:
<ul>
<li>Knowledge of PCR, immunoassay, and/or microbiological laboratory methods.</li>
<li>General quality management experience and familiarity with ISO/IEC 17025 and ISO/IEC 17043 standards.</li>
<li>Analytical laboratory auditing experience;</li>
<li>Ability to lead small teams and ensure accurate and timely submission of project deliverables</li>
<li>Proficiency in MS Word, MS Excel, and MS PowerPoint</li>
<li>Strong written and verbal communication skills</li>
<li>Proactive, self-starter</li>
</ul>

Education/Experience:
<ul>
<li>Bachelor degree (or higher) in biology or related field</li>
<li>5-10 years of experience performing molecular biology and/or microbiological laboratory methods and/or providing quality assurance support to molecular biology and/or microbiological analytical programs</li>
</ul>
 

Certificates and Licenses:
Certified Quality Auditor (CQA) certification required. This certification must be obtained within 6 months from date of hire.
 
Clearance:
Candidate must be able to obtain a Secret level security clearance.

Supervisory Responsibilities:
N/A
 
Working Conditions/ Equipment:
<ul>
<li>Ability to work in varying conditions to include: traditional office environments with sedentary extended periods required for voluminous data analysis via office automation;</li>
<li>Climate controlled laboratory environments requiring extended periods of standing when performing laboratory analyses, or during audits and SOP observation;</li>
<li>Mobile laboratories, subject to wide ranges of temperature and humidity requiring extended periods of standing, stooping or kneeling in confined spaces; conference, classrooms or theaters that involve extended periods of standing for training delivery or command briefings; and outdoors in various weather and lighting conditions including heat, humidity, cold, snow, bright sun, and dark night.</li>
<li>Exposure to various chemical and biological materials associated with an analytical lab or facility.</li>
<li>Ability to wear required personal protective equipment (PPE) including gloves, coats or gowns, shoe cover, tyvek coveralls, safety glasses, respirators, and/or PAPRs.</li>
<li>Subject to medical monitoring based on lab functions.</li>
</ul>

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.
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