Scientist Jobs in Savage, MN

Lead Scientist, Cell Line Development About Us: We are a rapidly growing biotech company specializing in mammalian cell culture solutions. As we expand our capabilities, we are launching a new Cell Line Development Division and seeking a Lead Scientist to build and drive this effort. If you have a strong background in commercial cell line development, hands-on industry experience at a CRO or CDMO, and a passion for building something impactful, we want to hear from you! Key Responsibilities: Establish and lead our cell line development division, developing workflows for stable cell line generation. Develop and optimize mammalian cell lines (e.g., CHO, HEK293) for commercial applications outside of pharma and cell/gene therapy. Implement cutting-edge technologies to enhance productivity and efficiency. Author technical reports, SOPs, and regulatory documentation aligned with ISO and cGMP standards. Collaborate with internal teams and represent the company in strategic partnerships and industry events. Qualifications: PhD (preferred) or MS in Molecular Biology, Cell Biology, Biotechnology, or a related field. Minimum 5+ years of industry experience in a CRO or CDMO environment (not just academic research). Proven expertise in commercial cell line development, including transfection, clone screening, and high-productivity optimization. Familiarity with cGMP, 21 CFR Part 820, and ISO quality standards. Entrepreneurial mindset with the ability to build and scale a new program. Why Join Us? This is a rare opportunity to create and lead a new division in a fast-growing biotech company. We offer: Competitive salary & benefits High-impact leadership role without large-team management requirements A dynamic environment focused on commercial innovation in cell culture Ready to shape the future of commercial cell line development? Apply today!

Element has a current opening for a Bioaerosol Scientist to join our growing team in Eagan, MN. Responsibilities: Responsible for ensuring successful progression of Bioaerosol projects through method and protocol development, design of research and development projects and implementing or validating new methods or adapting current methods. Understanding of HVAC and engineering operations of laboratory, with ability to troubleshoot and improve lab mechanical operation. Responsible for serving as technical and regulatory leadership resource to customers, potential clients and the entire Element Eagan Labs team. Develops/Implements new or revised technical methods and integrates new service offerings. Maintains effective relationships with other management, staff and departments to deliver high quality service to the organization. Utilizes all financial, operational, administrative, and technical resources needed to accomplish the responsibilities of this position. Evaluates and assesses project results, provides recommendations for future improvements. Provides support to the commercial team, attends customer visits, and/or conferences when necessary. Work with the commercial team to prepare quotations, proposals, protocols and sales presentations as needed. Work with members of commercial and operational teams to improve performance and client satisfaction. Communicate effectively with internal personnel, as well as external customers. Build teamwork within department and all other company departments. Represent department and the organization favorably and in accordance with established Company standards and associate attributes at all times. Implements systems and communicates processes intended to prevent recurrence of routine control failures or unplanned deviations in the laboratory. Responds to inquiries from the General Manager and other management regarding test results, special requests, etc. Requirements: Thorough understanding of governing regulations and pertinent scientific literature to ensure overall compliance. Ability to make complex mathematical computations, use statistical techniques in the treatment of data, and interpret and apply findings. Ability to maintain records, and prepare reports and correspondence. Able to give full attention to what other people say, take time to understand the points being made, and ask questions as appropriate. Able to use critical thinking, logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems. Able to communicate effectively verbally and in writing as appropriate for the needs of the audience. Able to identify complex problems and reviewing related information to develop and evaluate options and implement solutions. Able to plan, prioritize, coordinate, and manage own work in a fast-paced environment. Able to work unsupervised, make high level decisions independently, and solve problems effectively and creatively. Able to display high levels of customer service, responding promptly and thoroughly to the inquiries and needs of individuals both internal and external to the organization. Understand and maintain confidential nature of organization, customer and employee information. Show professional knowledge, proficiency and initiative in achieving goals and meeting standards.

Are you an experienced R&D Technician with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced R&D Technician to work at their company in Maple Grove, MN. Works under limited supervision assisting R&D engineers, scientists, and/or teams in the development and analysis of products, materials, processes, or equipment. Primary Responsibilities/Accountabilities: Design and set up of pilot and production equipment. Designing methods for using the equipment. Measurement of the process variables. Analysis of the processing variables. Control of the processing variables. Scale-up of the system for expected capacities. Build quality into all aspects of their work by maintaining compliance with all quality requirements. Qualifications: AA Degree or equivalent work experience in a related discipline and 1 year of related experience. Preferred: Experience with mechanical testing. Hands-on catheter build experience. Experience with nitinol implants.

We are seeking an experienced and innovative R&D Scientist with deep expertise in the Tile & Stone product segment to join our R&D team in the Consumer Product Goods (CPG) sector. This role focuses on developing and optimizing both interior and exterior tile, stone, and masonry sealers and treatments, ensuring they meet the highest standards of performance, safety, and regulatory compliance. The ideal candidate will possess a strong background in chemistry, particularly in the formulation and application of tile & stone products. Rust-Oleum Corporation is a worldwide leader in protective paints and coatings for both home and industry. We offer a wide range of products including decorative fashion paints, durable industrial roof repair coatings and, of course, our famous rust-fighting formula that started it all. Technology Competency: The R&D Scientist candidate will demonstrate and apply the following skills to their work. * Strong understanding of Scientific Methodology. Hypothesis driven research and problem-solving capability using experimental design, data analysis and documentation. * Coating Chemistries: Primary expertise in SB and WB acrylics and sil(ox)anes formulas for use in sealers and protectants on both interior and exterior tile, stone, masonry and concrete surfaces. Expertise in epoxy, urethane, polyaspartics etc. valuable * Coating Formulation Science: Lead the design, development, and optimization of Tile & Stone sealers, treatments and specialty products for countertops, flooring and other related surfaces. * Utilize in-depth knowledge of Tile & Stone sealer market, specifications (TCNA, ANSI, ASTM etc..), and professional end user requirements to develop high-performance products tailored to specific market needs. * Apply expert knowledge of organic chemistry and material science to troubleshoot complex formulation issues, enhance product performance, and ensure product stability and safety. Technical Leadership: * Ability to develop and implement project plans and timelines while managing multiple high level projects. Measuring progress and providing updates in alignment with marketing * Demonstrated capability of becoming a vocal and influential voice in project planning and deliverables together in collaboration with a cross functional team * Ability to make strategic decisions (technical and staff utilization) and influence leaders and scientist to execute those initiative while managing business strategy and value creation * Outstanding technical skills, interpersonal communication, and presentation skills. * Drive product innovation by researching and integrating new raw materials, technologies, and methodologies into aerosol formulations to enhance performance, durability, and user experience. * Proven track record of identifying, researching and prototyping innovative ideas. * Address and resolve complex formulation and application challenges, including issues related to stability, compatibility, and application efficacy * Continuous learning and intimate awareness of open literature and competitive landscape * The R&D Scientist works to assist in the allocation of resources towards initiatives by working with the leadership team to identify long term platform strategies * The R&D Scientist demonstrates the ability to have influence in decision making and a demonstrated ability to communicate with project stakeholders and cross-functional teams, leadership and the external scientific community Organization Leadership: The R&D Scientist should exhibit the following attributes: * Agility to respond to emerging business needs with strong management of change skills * Builds strong partnerships internally within R&D, internal functions (marketing, manufacturing, sourcing, etc.) and externally (vendors, customers, etc.) * Manage high stakes and challenging situations with all levels of the organization * Assess the organizational processes and develop new processes to improve efficiency and quality * Demonstrate strong career ambition - potential to become a top leader * Strong business acumen Education Guidelines * BS in Chemistry, Chemical Engineering, Materials, or other equivalent scientific field required * MS or PhD is preferred Salary Range: up to $100,000 annually, with bonus eligibility From big benefits to small, we take care of our associates! After 30 days of employment, you will be eligible for a benefits package. We also offer a 401(k) plan after three months of employment. Associates are vested in the RPM Pension plan after completing five years of service. Rust-Oleum offers 10.5 paid holidays and one floating holiday per year. You are also eligible to earn three weeks of vacation on an annualized basis. Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

Science Led, Enterprise Driven - Accelerating Quantum Computing Quantinuum is the world's largest integrated quantum company, pioneering powerful quantum computers and advanced software solutions. Quantinuum's technology drives breakthroughs in materials discovery, cybersecurity, and next-gen quantum AI. With approximately 500 employees, including 370+ scientists and engineers, Quantinuum leads the quantum computing revolution across continents. We unite best-in-class software with high-fidelity hardware to accelerate quantum computing. With integrated full-stack technology, our world-class team is rapidly scaling quantum computing. Quantinuum recently secured $300M in funding, visit our news pages to learn more about this and other Quantinuum scientific breakthroughs and achievements: ******************************* We are seeking a Quantum Hardware Scientist in our Golden Valley, MN location to work on the integration and verification of our Helios line of next-generation quantum computers, targeting 96 physical qubits and 10^(-3) error rates with a QCCD architecture. You will work with scientists and engineers to receive subsystem deliveries, integrate into fully functional QPUs, and demonstrate the system level performance and robustness before handing off to deployment teams. Key Responsibilities: * You will work to develop, integrate, and verify quantum computers using trapped ions as qubits. * You will collaborate with teams of scientists and engineers to translate system requirements and designs into functional hardware. * You will be responsible for working in a research lab environment to collect data on system performance and characterizing device characteristics. * You will communicate scientific and technical results via trade studies, presentations, or publications. YOU MUST HAVE: * PhD completed prior to starting * Minimum 4+ years' experience (PhD inclusive) involving one or more of the following areas: quantum information, qubits, atomic physics, precision spectroscopy, optics, vacuum systems, electronics, cryogenics, or laser * Due to Contractual requirements, must be a U.S. Person. defined as, U.S. citizen permanent resident or green card holder, workers granted asylum or refugee status * Due to national security requirements imposed by the U.S. Government, candidates for this position must not be a People's Republic of China national or Russian national unless the candidate is also a U.S. citizen. WE VALUE: * A previous history of work specifically tied to the QCCD architecture and/or general scaling of trapped ion quantum computers * Extensive and demonstrable hardware skills related to integral subsystems of trapped ion quantum computers including lasers, optics, radio frequency and microwave analog electronics, digital control electronics, ultrahigh vacuum, cryogenics, etc. * Experience with design or operation of a device for quantum information processing * Experience with laser cooling and trapping of ions or neutral atoms * Experience performing simulation and modeling to inform experiments * Experience programming experimental control systems for data collection, signal processing, and data analysis * Excellent written and oral communication skills, with published results within their field of research. * Experience in post-doctoral research positions or other mentorship positions * Demonstrated organizational and leadership skills $123,000 - $153,000 a year Compensation & Benefits: Non-Incentive Eligible Estimated Salary Wage: $123,000 - $153,000 Annually What is in it for you? * A competitive salary and innovative, game-changing work * Flexible work schedule * Employer subsidized health, dental, and vision insurance * 401(k) match for student loan repayment benefit * Equity, 401k retirement savings plan + 12 Paid holidays and generous vacation + sick time * Paid parental leave * Employee discounts Quantinuum is an equal opportunity employer. You will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status.

Meta Platforms, Inc. (Meta), formerly known as Facebook Inc., builds technologies that help people connect, find communities, and grow businesses. When Facebook launched in 2004, it changed the way people connect. Apps and services like Messenger, Instagram, and WhatsApp further empowered billions around the world. Now, Meta is moving beyond 2D screens toward immersive experiences like augmented and virtual reality to help build the next evolution in social technology. To apply, click "Apply to Job" online on this web page. **Required Skills:** Research Scientist Responsibilities: 1. Perform research and develop solutions to computer software and computer hardware problems. 2. Research, design, and develop new optimization algorithms and techniques to improve the efficiency and performance of Meta's platforms. 3. Design and implement large-scale distributed software systems to serve large numbers of complex requests simultaneously and without failure. 4. Utilize technical research background, train new ranking models, and run experiments. 5. Create tools for migrating large bodies of user data across systems for new products, scalability efforts, and development of new core infrastructure. 6. Use machine learning, statistics, or other data techniques to build algorithms. 7. Suggest, collect, and synthesize system requirements from stakeholders and create effective feature roadmaps. 8. Analyze and resolve computer challenges from a system engineering standpoint. 9. Work on problems of diverse scope where analysis of data requires evaluation of identifiable factors. 10. Demonstrate good judgment in selecting methods and techniques for obtaining solutions. 11. Telecommuting is permitted from anywhere in the U.S. **Minimum Qualifications:** Minimum Qualifications: 12. PhD in Computer Science, Engineering, Analytics, Statistics, Mathematics, or a related field. Foreign degree equivalent accepted. 13. Requires Completion of a university-level course, research project, or internship involving the following: 14. 1. Algorithms, data structures, or systems software 15. 2. Solving analytical problems using quantitative approaches 16. 3. Gathering, manipulating, or analyzing complex, high-volume, high-dimensionality data from varying sources 17. 4. Communicating complex research in a clear, precise, and actionable manner 18. 5. Research in topics closely related to machine learning, NLP, recommendation systems, pattern recognition, signal processing, data mining, artificial intelligence, information retrieval, or computer vision 19. 6. Developing highly scalable classifiers and tools leveraging machine learning, statistics, regression, rules-based models, or mathematical models and 20. 7. Java, C++, Perl, PHP, or Python. **Public Compensation:** $214,032/year to $240,240/year + bonus + equity + benefits **Industry:** Internet **Equal Opportunity:** Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $78,100.00 - $128,500.00 POSITION SUMMARY The responsibilities of this position are to lead improvements for current products as well as developments for new products. You will evaluate these new technologies to improve processes and the identification of novel applications for the department. This position requires the ability to work on extremely complex problems, where analysis of situations or data requires an evaluation of intangible variables. Perform additional duties as assigned. ESSENTIAL FUNCTIONS Design and perform complex experiments to improve existing products and/or develop new products Investigate and identify new research areas and technologies to support further product development Follow literature and commercial trends to remain current in areas related to production of recombinant protein in cell culture Plan and conduct experiments with the purpose of improving recombinant protein yields, quality, and process efficiency, while implementing these process improvements. Suggest new product targets. Participate in processes to identify and prioritize products. Identify and propose new product specifications and new projects or products needed in the field Train and mentor others in the lab Gather and analyze data to draw conclusions and determine next steps for future experimentation Create and write work instructions and standard operating procedures Collaborate cross-functionally to lead multi-department projects and further product development across Bio-Techne Troubleshoot issues of high complexity Ability to lead projects of large scope while delegating responsibilities to those within the group Follow guidelines and comply with all company safety, quality, and training procedures and regulations Draft and revise standard operating procedures (SOPs) Share lab duties with team, which includes stocking solutions, buffers and media preparation, cleaning and ongoing instrument maintenance Demonstrate EPIC Values in daily work Perform additional duties as assigned Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job. Performs additional duties as assigned. JOB SPECIFICATIONS Education and Experience: Ph.D. in a related field and up to 5 years of relevant experience is required Or, Master's degree in a related field (or equivalent experience) and 8+ years of experience is required Knowledge, Skills, and Abilities: Possess a high level of understanding and expertise of underlying principles of cell biology, microbiology, cell culture, biochemistry, and related areas. Must have demonstrated ability to create new products Must have the ability to analyze complex data and results to draw conclusions, which includes presentation of data Must demonstrate leadership in training other lab members and leading projects cross-functionally Must have exceptional verbal and written communication skills Must have the ability to identify and define process improvement procedures Must have demonstrated ability to work independently on complex projects and determine priorities for self and others Ability to act independently on routine assignments or projects. Ability to plan, organize and multi-task to complete assignments in an efficient manner. Ability to communicate professionally, both oral and written. Ability to pay attention to details and perform at a high-level accuracy. Ability to work independently and with a team. Ability to work hours that conform to standard business operations. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

In this critical role, the Clinical Development Scientist will support and be accountable for clinical evidence strategy development, delivery, and dissemination throughout the product life cycle. This role involves executing clinical and economic evidence activities for Heart Rhythm Management/Structural Heart products, from ideation through post-market. The Clinical Development Scientist will ensure clinical data is generated to support product claims, reimbursement, health economic outcomes, and market access strategies. Key Responsibilities: Execute clinical evidence activities across the product development life cycle, focusing on Heart Rhythm Management products. Develop and author clinical trial designs, including scientific justification and analysis plan guidance. Ensure clinical data supports business objectives, product claims, and market strategies. Contribute to clinical study reports, evaluation reports, abstracts, presentations, and peer-reviewed publications. Collaborate closely with key opinion leaders, investigators, and external stakeholders. Support clinical evidence discussions with regulatory bodies, notified bodies, and physician advisory boards. Develop rapport across organizational levels to influence decision-making and facilitate change. Foster a collaborative team environment and adapt to changing priorities. Requirements Requirements: PhD or MD in science, engineering, or a medical field, with a background in medical device design and/or Structural Heart procedures preferred. 5+ years of experience in clinical research, including methodology, statistics, and trial design. Strong medical writing and verbal communication skills, with experience in technical/clinical presentations. Proficiency in conducting literature searches relevant to clinical and medical research. Knowledge of clinical research, medical device development processes, regulatory requirements, and good clinical practices. Ability to meet physical, cognitive, and environmental job demands with or without accommodation. Willingness to travel up to 25% of the time.

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, apply with us today! Job Description Seeking a scientist to perform analytical testing for biologic product release and characterization in a cGMP/GLP environment. Responsibilities include routine testing, documentation, troubleshooting HPLC/UPLC/CE methods, and ensuring compliance. Responsibilities Include: * Contributes as part of a team of AD scientists towards execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment. * Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE, iCE, cIEF, CE-SDS, Titer, Peptide, and Glycan mapping - using established Test Methods, including associated protocol/report documentation and presentations. * Conducts work in compliance with cGMP/GLP, safety, and regulatory requirements. * Responsible for working on other non-lab-based tasks from time to time if assigned. * Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives. * Demonstrate HPLC, UPLC, and/or CE troubleshooting capabilities. Qualifications The Ideal Candidate will Have: * Experience with ELISA techniques * Ability to quickly learn new techniques * Strong multitasking and organizational skills * Attention to detail with accurate record-keeping * Ability to follow instructions and adhere to company policies Minimum Qualifications: * Bachelor's or Master's in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other science-related degree concentration * Equivalent directly related work/internship experience with HPLC/UPLC required. * Knowledge of principles of HPLC/UPLC/CE and theories of relevant techniques and a basic understanding of industry practices and standards required * Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information What to Expect in the Hiring Process: * 10-15 Minute Phone Interview with the Region Recruiter * 45-60 Minute Virtual Interview with the Manager and/or Group Leader * 30 Minute Virtual Meeting with the Site Director Additional Details: The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply. * Excellent full-time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holiday Eurofins Lancaster Laboratories Professional Scientific Services (PSS) is a global, award-winning insourcing solution that places our people at our clients' sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries. We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client's quality systems and equipment. To learn more about Eurofins Lancaster Laboratories, please explore our website ******************* Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description MBGT Associate Scientist I is dedicated to supporting select activities within the Agrigenomics Lab. Activities focus on sample preparation, DNA extraction, PCR set up, array genotyping, Next Generation Sequencing (NGS) and data analysis for both plant, animal, and human specimens. Responsibilities and Duties General: Knowledge and ability to conduct specific processes related to testing in Agrigenomics lab that may include work in any of the following areas: Preparation of paperwork Sample preparation (leaf, seed, and animal samples) DNA Extraction General Lab cleaning Genotyping PCR Microarray technology NGS Data analysis Customer communication Assist in training of staff Internal communication about processes Other duties as needed Specific: Assists in equipment maintenance and calibration Support and maintain ISO quality system Support and maintain EBDI Safety program Others as required by workflows Qualifications A Bachelor of Science in a field related to Agriculture or Laboratory Science is required. Relevant work experience may replace some education. Good attention to detail, ability to effectively work in a team environment and good communication skills are required for this position. An Associate Scientist must also have a working knowledge of Microsoft Office and the ability to learn to use lab specific hardware and software as needed. Knowledge of DNA extraction and PCR set up and interpretation will be preferred. Additional Information Schedule: Monday-Friday 6:30am-2:30pm or 10:30am-6:30 pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Genomic Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description MBGT Associate Scientist I is dedicated to supporting select activities within the Agrigenomics Lab. Activities focus on sample preparation, DNA extraction, PCR set up, array genotyping, Next Generation Sequencing (NGS) and data analysis for both plant, animal, and human specimens. Responsibilities and Duties General: Knowledge and ability to conduct specific processes related to testing in Agrigenomics lab that may include work in any of the following areas: Preparation of paperwork Sample preparation (leaf, seed, and animal samples) DNA Extraction General Lab cleaning Genotyping PCR Microarray technology NGS Data analysis Customer communication Assist in training of staff Internal communication about processes Other duties as needed Specific: Assists in equipment maintenance and calibration Support and maintain ISO quality system Support and maintain EBDI Safety program Others as required by workflows Qualifications A Bachelor of Science in a field related to Agriculture or Laboratory Science is required. Relevant work experience may replace some education. Good attention to detail, ability to effectively work in a team environment and good communication skills are required for this position. An Associate Scientist must also have a working knowledge of Microsoft Office and the ability to learn to use lab specific hardware and software as needed. Knowledge of DNA extraction and PCR set up and interpretation will be preferred. Additional Information Schedule: Monday-Friday 6:30am-2:30pm or 10:30am-6:30 pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Genomic Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

We are seeking an experienced and innovative R&D Scientist with deep expertise in the Tile & Stone product segment to join our R&D team in the Consumer Product Goods (CPG) sector. This role focuses on developing and optimizing both interior and exterior tile, stone, and masonry sealers and treatments, ensuring they meet the highest standards of performance, safety, and regulatory compliance. The ideal candidate will possess a strong background in chemistry, particularly in the formulation and application of tile & stone products. Rust-Oleum Corporation is a worldwide leader in protective paints and coatings for both home and industry. We offer a wide range of products including decorative fashion paints, durable industrial roof repair coatings and, of course, our famous rust-fighting formula that started it all. Technology Competency: The R&D Scientist candidate will demonstrate and apply the following skills to their work. Strong understanding of Scientific Methodology. Hypothesis driven research and problem-solving capability using experimental design, data analysis and documentation. Coating Chemistries: Primary expertise in SB and WB acrylics and sil(ox)anes formulas for use in sealers and protectants on both interior and exterior tile, stone, masonry and concrete surfaces. Expertise in epoxy, urethane, polyaspartics etc. valuable Coating Formulation Science: Lead the design, development, and optimization of Tile & Stone sealers, treatments and specialty products for countertops, flooring and other related surfaces. Utilize in-depth knowledge of Tile & Stone sealer market, specifications (TCNA, ANSI, ASTM etc..), and professional end user requirements to develop high-performance products tailored to specific market needs. Apply expert knowledge of organic chemistry and material science to troubleshoot complex formulation issues, enhance product performance, and ensure product stability and safety. Technical Leadership: Ability to develop and implement project plans and timelines while managing multiple high level projects. Measuring progress and providing updates in alignment with marketing Demonstrated capability of becoming a vocal and influential voice in project planning and deliverables together in collaboration with a cross functional team Ability to make strategic decisions (technical and staff utilization) and influence leaders and scientist to execute those initiative while managing business strategy and value creation Outstanding technical skills, interpersonal communication, and presentation skills. Drive product innovation by researching and integrating new raw materials, technologies, and methodologies into aerosol formulations to enhance performance, durability, and user experience. Proven track record of identifying, researching and prototyping innovative ideas. Address and resolve complex formulation and application challenges, including issues related to stability, compatibility, and application efficacy Continuous learning and intimate awareness of open literature and competitive landscape The R&D Scientist works to assist in the allocation of resources towards initiatives by working with the leadership team to identify long term platform strategies The R&D Scientist demonstrates the ability to have influence in decision making and a demonstrated ability to communicate with project stakeholders and cross-functional teams, leadership and the external scientific community Organization Leadership: The R&D Scientist should exhibit the following attributes: Agility to respond to emerging business needs with strong management of change skills Builds strong partnerships internally within R&D, internal functions (marketing, manufacturing, sourcing, etc.) and externally (vendors, customers, etc.) Manage high stakes and challenging situations with all levels of the organization Assess the organizational processes and develop new processes to improve efficiency and quality Demonstrate strong career ambition - potential to become a top leader Strong business acumen Education Guidelines BS in Chemistry, Chemical Engineering, Materials, or other equivalent scientific field required MS or PhD is preferred Salary Range: up to $100,000 annually, with bonus eligibility From big benefits to small, we take care of our associates! After 30 days of employment, you will be eligible for a benefits package. We also offer a 401(k) plan after three months of employment. Associates are vested in the RPM Pension plan after completing five years of service. Rust-Oleum offers 10.5 paid holidays and one floating holiday per year. You are also eligible to earn three weeks of vacation on an annualized basis. Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

MGK has 100+ years' of experience focusing on sustainable & environmentally conscious ways to protect families and crops from pests around the world, using our synthetic and certified organic, botanically based pesticide products. General Description: The purpose of the R&D Scientist position is to support MGK's research and new product development efforts focusing on vector control through the coordination and management of biological efficacy studies. This position requires an individual with the ability to effectively manage multiple projects simultaneously while providing creative input in the areas of discovery and exploration, technology platform construction, and new product development. A successful Scientist candidate must also work effectively within teams and be able to collaborate with others from different departments. Principal Responsibilities: Work closely with R&D personnel, Marketing, Chemistry, Regulatory and project teams to design laboratory and field-based bio-efficacy trials that support research and development objectives Coordinate and manage in-house and commissioned biological efficacy trials conducted through contract research organizations (CROs), universities and commercial development partners Develop strong working relationships with cooperators and external influencers, especially with mosquito abatement districts Report study outcomes via timely written reports and presentations at project management and team meetings; provide routine updates via monthly R&D activity reports Provide technical support for existing products and support Sales and Marketing initiatives Provide technical field support and interface with technical services team to support customer needs Assist with writing product labels, official trial reports and other registration support as requested Collaborate with SCC group companies and other development partners Qualifications: Master's degree in Entomology or related field required Ph.D. in Entomology desired 5+ years' experience working with experimental design and statistical procedures. Experience with JMP-SAS beneficial Experience working with or researching vector arthropods, especially mosquitoes, required Proficiency in project management and ability to analyze biological data & present trial results in a clear, meaningful manner Strong team and interpersonal skills Proficiency with MS Office (Word, Excel, PowerPoint, & Outlook) Additional Requirements: Position is full-time, onsite in Brooklyn Park, MN. Annual Salary Range: $80,000 - $95,000 (commensurate with experience and qualifications). This role offers a competitive benefits package, including health insurance, 401(k) matching, and paid time off. Physical Demands and Work Environment (OFFICE Position): The physical demands and work environment characteristics described below are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Physical Demands include constant sitting, walking, standing, simple grasping and fine manipulation with hands; frequent bending at the neck and waist; and occasional squatting, climbing, kneeling, crawling, twisting at the neck and waist, power grasping, pushing and pulling with hands, reaching above shoulder level, lifting and carrying up to 25 lbs. Work Environment includes exposure to or working in or around equipment and machinery including a computer keyboard and mouse. Domestic and international travel required occasionally.

Zepto Life Technology, Inc. (“Zepto”) is devoted to improving people's quality of life through the development of point-of-care molecular diagnostics that benefit healthcare providers, patients, and their families by quickly diagnosing diseases. Zepto has improved the accuracy of molecular diagnostics through using giant magnetic resistance as the sensing technology instead of fluorescence. Summary Zepto Life Technology is seeking a highly skilled and motivated Research Scientist with significant industry R&D experience to join our assay development team. This position requires a Ph.D.-level scientist capable of designing, troubleshooting, and executing advanced molecular diagnostic assays independently and collaboratively across cross-functional teams. The ideal candidate will bring deep expertise in assay development, at least two years of hands-on industry experience with PCR and qRT-PCR, strong problem-solving skills, and a commitment to maintaining rigorous aseptic techniques. This individual will play a key role in driving innovative assay designs and mentoring team members to achieve operational excellence. Essential Duties Design, develop, optimize, and execute molecular diagnostic assays, with a primary focus on PCR, qRT-PCR, and next-generation sequencing (NGS). Independently design and execute hypothesis-driven experiments for assay development, advancing molecular diagnostic technologies. Lead and support the development and validation of innovative assay platforms in collaboration with the Assay, Engineering, and Software teams. Maintain and enforce aseptic techniques to ensure the integrity and reliability of experimental results. Perform material and chemistry analysis, including nucleic acid extraction and purification, using methods such as PCR, qRT-PCR, NGS, and other molecular diagnostic tools. Conduct testing on virology, fungology, mycology, and bacteriology specimens, ensuring compliance with laboratory guidelines and regulatory standards. Collect and store specimens, and develop procedures and quality control manuals to ensure accurate and reliable testing protocols. Prepare detailed technical reports, analyze data, and deliver presentations to internal stakeholders and external partners. Mentor and train team members, fostering a culture of high performance and continuous learning. Demonstrate self-motivation, taking ownership of responsibilities, and contributing to the overall success of the team and company. Utilize strong technical writing skills to accurately document research findings and protocols. Perform other duties as assigned. Required Education and Experience Ph.D. in Biochemistry, Molecular Biology, or a related field. Minimum of 3 years of industry R&D experience in molecular diagnostics or assay development. At least 2 years of hands-on experience with DNA/RNA extraction, PCR, qRT-PCR, and related molecular biology techniques. Proven ability to troubleshoot complex assay and laboratory challenges. Strong knowledge of aseptic techniques and regulatory requirements in R&D environments. Excellent critical thinking, problem-solving, and project management skills. Exceptional verbal and written communication skills, with a focus on technical documentation. Preferred Education and Experience 5+ years of hands-on experience in microbiology and molecular biology. Experience with biomarker applications, including ELISA, flow cytometry, gene expression analysis, and microarrays. Familiarity with industrial R&D processes or postdoctoral experience in a related field. Proficiency in data analytics and visualization tools for interpreting and presenting scientific findings. Competencies Expertise in PCR techniques, including assay design, optimization, troubleshooting, and data interpretation. Strong understanding of qRT-PCR methodologies, including primer/probe design, reaction efficiency, and quantification strategies. Experience with nucleic acid extraction, purification, and quality assessment to ensure reliable assay performance. Strong understanding of next-generation sequencing (NGS) methodologies and their application in molecular diagnostics. Proficiency in bioinformatics tools for analyzing sequencing data, interpreting results, and troubleshooting complex molecular assays. Proven ability to collaborate effectively in a multidisciplinary team, leveraging diverse expertise to achieve common goals. Demonstrated self-motivation and strong accountability, taking ownership of responsibilities and driving them to successful completion. Work Environment This position is based in a research and development biosafety level 2 laboratory, where strict adherence to corporate policies and regulations is required. Reasonable accommodations may be provided to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is typical for a laboratory setting. Minimal exposure to blood-borne pathogens and infectious diseases, mitigated by appropriate PPE. The work environment may involve handling cleaning and sanitizing products, as well as various laboratory solutions. Requires occasional travel for conferences, collaborations, or stakeholder meetings. Visa Support Zepto Life Technology supports OPT, CPT, and H1B visa sponsorships for qualified candidates. Job Type Full-time, exempt, 40 hours per week, Monday-Friday 9:00am - 5:30pm (half-hour unpaid lunch), onsite. Salary Range: $60,000.00-$80,000.00 The expected US base salary range for this position is $60k - $80k plus benefits. Actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skillset, years & depth of experience, certifications & relevant education, geography. Eligible for benefits including holiday time off, paid time off (PTO), sick time off, health insurance (medical, dental, and vision), health savings account (HSA), 401(k), and life insurance. This role is not open to recruitment agency submissions or partnerships. E-Verify Zepto Life Technology participates in the U.S. Department of Homeland Security E-Verify program in all facilities located in the United States and certain U.S. territories. The E-Verify program is an Internet-based employment eligibility verification system operated by the U.S. Citizenship and Immigration Services.

: Claros Technologies is a venture backed, deep-tech company solving the worldwide challenge of destroying PFAS in the environment. PFAS remediation is rapidly becoming a multi-billion-dollar, global market and is at the center of regulatory action in the US, Europe and Asia that requires the removal of this carcinogen from drinking water, industrial processes and waste sites. Claros has developed a patented, scalable destruction technology proven to fully destroy 99.99% of PFAS in customers' samples. We are a diverse team of scientists, business-builders, and impact leaders committed to solving problems without creating new ones. The company closed a $20M financing round in the beginning of 2024 with leading environment venture capital firms, which provides the credibility and resources required to convert current pilot users into full scale commercial customers as well as to sell easy-to-identify prospects across the globe. If you are a mission driven, highly motivated Research Scientist, join us as we solve one of the greatest environmental challenges of our time. Position Overview: Claros Technologies' Functional Materials team is primarily focused on using sustainable chemistries to enable advanced materials in textiles and selective filtration application areas. We are seeking a collaborative, driven individual to join our team as a Research Scientist. The Research Scientist will be tasked with partnering the technical team to execute application-driven, fundamental research. Reporting to the Director of Functional Materials, this individual will require technical know-how, and will be responsible for day-to-day, hands-on laboratory activities. Essential Job Functions: Designing and executing laboratory experiments Collecting and analyzing data Reading, understanding, and interpreting scientific publications Writing and presenting reports to internal team stakeholders Maintaining a clean and safe workspace; Safety first mindset General laboratory maintenance and upkeep Competencies & Skills: Strong communication skills, both written and verbal Independent thinker; strong problem solving skills; ability to troubleshoot technical issues Ability to analyze data and make recommendations Inquisitive mindset; curiosity-driven Strong organizational skills Understanding of basic chemistry principles, preferably exposure to materials science (emphasis on organic chemistry) Design of experiments Formulation chemistry; basic material characterization techniques such as FTIR, DSC, and TGA Comfortable working in a fast past environment in a growing lab Preferred Experience: Bachelor's degree or higher in chemistry related field (preference for materials science or chemistry); Masters degree a plus 3-5 years experience in a research environment for private, commercial, or governmental work Job Specifications Compensation: $70,000 - $80,000 Location: In person at the Claros Headquarters in Minneapolis, Minnesota. Travel: May be required periodically for purposes such as client site visits; not required on a regular or frequent basis. Claros Technologies offers attractive salary and benefits including health, vision, and dental insurance, PTO as well as 401k plans and options. For more information, please visit ****************** The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Wondering what's within Beckman Coulter Diagnostics? Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Staff Manufacturing Scientist for Beckman Coulter Diagnostics is responsible for supporting the daily production needs of the Reagent manufacturing cell culture work cell. This position is part of Reagent Operations located in Chaska, MN and will be a full-time on-site position. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Technical Operations Team and report to the Manager of Manufacturing Science responsible for supporting daily production needs and process improvement in our cell culture manufacturing area. If you thrive in a fast-paced, data-driven role and want to work to build a world-class supply chain organization-read on. In this role, you will have the opportunity to: Provide technical expertise and direction in cell culture manufacturing and address issues as they arise. Lead multi-department teams to resolve non-conforming issues for products, processes, and manufacturability. Assess and improve manufacturing processes and systems for performance, quality, and cost. Communicate investigation status and proposals via oral and written reports; update documentation promptly. Ensure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO requirements. The essential requirements of the job include: Degree in Cellular Biology, Biochemistry, Chemistry, or Biology preferred, with relevant experience: Bachelor's (9+ years), Master's (7+ years), or Doctoral (4 years) including aseptic techniques and/or mammalian cell culture. Understanding of in vivo and in vitro antibody/antigen production Analytical methods (example: HPLC, Octet) Experience with stable cell generation along with clonal selection It would be a plus if you also possess previous experience in: Project Management experience Validation/verification experience and Process transfer Experience in a regulated industry preferred (e.g. FDA, ISO) with advanced knowledge of cell culture production Familiarity with large-scale bioreactor systems The salary range for this role is $127K-$147K. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope This position is responsible for material processing, reagent formulation, technical manufacturing, in-process and final quality control of reagents, critical raw materials, and components for in-vitro diagnostic products. Key Duties and Responsibilities Perform in-process testing and final Quality Control for Serum Proteins products per established procedures. Assist with cell culture and ascites production tasks on an as needed basis. Perform second-checking to ensure accurate records. Utilize Good laboratory practices - maintain clean workspace in Serum Proteins and Reagent Preparation labs. Contribute to group Reagent Preparation and Serum Proteins duties, including lab and equipment maintenance. Utilize SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting, and flow through facility. Participate in inventory accountability - Production area cycle counts, accurate charging of materials to work orders, etc. Follow regulatory requirements - follow document instructions and maintain reasonable documentation error rates. Ensure proper documentation by correcting errors noted in procedures and forms (ECO) with assistance. Perform tasks assigned in NCR/ Deviations, Validations or CAPAs as needed. Ensure safety of self and others by complying with all company safety policies, including use of PPE. Participate in team meetings and attend group training sessions. Education, Experience, and Qualifications Bachelor's or Master's degree in Chemistry, Biology, Medical Technology or related science field or a 2 year degree (i.e. MLT) with equivalent experience 1+ years of related laboratory experience and/or demonstrated competence within the in-vitro diagnostic industry Basic understanding of immunology and immunoassay techniques Ability to work in a regulated environment Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.) Working knowledge of MS Excel Basic understanding of statistical analysis Advanced skills in: Math and calculations Writing and documentation Grasping complex concepts and solutions Problem-solving and analytical skills What we offer Salary Range The salary range for this position is $ $61,000 - $70,000 Annually. The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.

I work as our Leading Scientific Hiring Recruiter for the state of Minnesota and Western Wisconsin. I hire for the following job positions: * Lab Technician * Lab Assistant * Microbiologist * Biologist * Associate Scientist * Clinical Lab Technician * Biochemist * Chemist - Formulations or Analytical * Data Analyst * Bioinformatics * Medical Sales * Animal Scientist * Lab Managers * Study Coordinators * Study Directors * Etc I hire for candidates who are entry level or who have extensive industry experience. Please apply to this positing if you are looking for any positions in this field and I would be happy discuss all of our current openings with you. You can also email me at *****************************, directly, if you prefer. Pay and Benefits Since this is a general posting, the pay ranges for this role can vary greatly depending on job title and your experience level but we typically see positions paying $20.00 - $35.00/hr, or more depending on experience level. Pay and Benefits The pay range for this position is $27.00 - $29.00/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 & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&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 Minneapolis,MN. Application Deadline This position is anticipated to close on Apr 14, 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. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

ATTN: Position requires a minimum 8 years of experience AFTER POST-DOC, please do not apply if you are counting education in your years' experience. Optimal candidate will have research & commercial experience working with CROs & CDMOs. Company Description We are a rapidly growing biotech company located just outside Minneapolis. We're expanding our capabilities with a new Cell Line Development Division and are seeking a visionary Lead Scientist to spearhead this effort. If you are an entrepreneurial-minded scientist with a strong background in cell line development and a passion for building something impactful, we want to hear from you! Role Description This is a full-time on-site role for a Lead Scientist in Cell Line Development at Cell Culture Company in Minneapolis, MN. The Lead Scientist will need to be a forward thinker driven towards new innovation and growth! They will be responsible for overseeing the development and optimization of cell lines, designing experiments, analyzing data, and collaborating with cross-functional teams to drive innovation and product development in biotechnology. Key Responsibilities: • Establish and lead our cell line development division, creating workflows for stable cell line generation. • Develop and optimize mammalian cell lines (e.g., CHO, HEK293) for customers. • Stay ahead of industry trends by evaluating and implementing cutting-edge technologies. • Author technical reports, SOPs, and regulatory documentation. • Represent the company at occasional external events and build strategic partnerships. Qualifications: DO NOT APPLY WITHOUT 8 YEARS EXP AFTER POST DOC. EDUCATION IS NOT COUNTED TOWARDS EXP. • PhD Molecular Biology, Cell Biology, Biotechnology, or related field. **8 years' experience (preferably commercial & research) • Strong experience in cell line development, with a proven track record of success. • Proficiency in transfection techniques, clone screening, and high-productivity cell line optimization. • Familiarity with cGMP, 21 CFR Part 820, and ISO quality standards. • Entrepreneurial mindset with excellent leadership and strategic planning skills. • Strong communication skills to interact with stakeholders at all levels. Why Join Us? This is a rare opportunity to shape and lead a new division in a growing biotech company. We offer a competitive salary, benefits, and the chance to make a lasting impact in the industry.