Research and development technician jobs in Shakopee, MN

Responsibilitiesarrow_right * Assist in the development and maintenance of the engineering bill of material (BOM) * Assist in development and implementation of new processes, technologies or tooling needed to build products. * Assist in identifying/developing/qualifying fixture for manufacturing processes. * Assist in the creation and maintenance of tool files. * Support engineering studies and data analysis. * Fabricate or assist in fabrication of units for prototypes and engineering builds. * Assist in setup and performing design verification and process validation. * Assist with drafting and executing protocols within all areas of Product Development such as Design, Process Development and Design Assurance. * Work with engineers to specify, procure and commission equipment and procure material. * Manage product development materials to help maintain traceability and quantities. * Execute inspections of components and devices. Qualificationsarrow_right * Associate Degree in a technical area is preferred * Years of experience required depends on level of seniority * Demonstrated mechanical aptitude * Experience performing tedious processes, building prototypes and working with small parts * Basic statistical skills * Basic SolidWorks skills is a plus * Demonstrated ability in Microsoft Word and Excel * Continue to learn and utilize new skills related to typical product development capabilities * Ability to utilize metrology equipment such as calipers, micrometers etc..

The R&D Technician will support the formulation and development of cosmetic and OTC personal care products, with a focus on skincare and suncare. This role involves preparing and modifying formulations under the guidance of R&D Chemists, performing lab tests, documenting processes, and supporting scale-up activities. The technician must adhere to lab protocols, ensure compliance with regulatory guidelines, and maintain a clean and safe laboratory environment. This position reports directly to the VP of R & D and plays a key role in bringing innovative, high-quality products from concept to launch. Key Responsibilities: * Prepare lab batches based on new or modified formulations according to directions from R&D Chemists and Management. * Assist in formulation adjustments to meet product performance, stability, and regulatory requirements. * Conduct routine testing of lab batches, including pH, viscosity, specific gravity, appearance, texture, and odor. * Maintain accurate and organized records of all formulation work, testing data, and observations. * Ensure all samples and documentation meet internal standards and are archived appropriately. * Gain familiarity with regulations related to OTC and cosmetic products, including FDA monograph requirements. * Support scale-up and pilot batching processes, and assist in the transfer of formulas to the production floor as requested by the chemists and R & D management * Learn and follow proper procedures for weighing, mixing, and batching raw materials in accordance with Good Manufacturing Practices (cGMP). * Identify and communicate any issues during batching, testing, or stability evaluations to the chemists * Maintain cleanliness, safety, and organization in the lab environment, including routine maintenance of lab equipment. * Work on multiple development projects simultaneously and manage shifting priorities as needed. Requirements Required Skills/Abilities * Hands-on experience with laboratory equipment and processes * Knowledge of safe chemical handling procedures. * Ability to accurately perform calculations for batching and scaling. * Strong attention to detail, organizational skills, and commitment to documentation accuracy. * Effective written and verbal communication skills. * High level of initiative and problem-solving ability in a fast-paced environment. * Ability to work both independently and collaboratively as part of a cross-functional team. * Proficient in Microsoft Office (Excel, Word, Outlook). * Willingness to learn and adapt quickly to new methods, regulations, and technologies. Required Education and Experience * Bachelor's degree in Chemistry, Chemical Engineering, Cosmetic Science, or a related scientific discipline. Preferred Education and Experience * Experience working within cosmetic or OTC product environment under FDA regulations (e.g., sunscreens, acne treatments, antiperspirants). * Familiarity with GMP documentation practices and regulatory compliance requirements. * Bachelor's degree in Chemistry or Cosmetic Science or advanced training in formulation chemistry.

Contract Duration: 12 Months About the Role: We are seeking a detail-oriented Medical Device Test Technician to join our team for a 12-month, on-site contract. This role involves performing a variety of mechanical, electrical, and visual tests on medical devices, specifically heart catheters. You'll work closely with engineers, following established test methods and protocols to ensure the highest quality standards are met. This position is ideal for someone with prior experience in a medical device or R&D setting, who enjoys hands-on work and can stay focused in a lab environment. Key Responsibilities: Perform mechanical, electrical, conditioning, length, OD (outer diameter), and visual tests on heart catheters. Conduct both simple and complex testing following written procedures and verbal instructions. Work primarily in a lab environment (85% lab / 15% desk work). Maintain accurate and clear documentation of test results using data sheets and Microsoft Office tools. Communicate effectively with engineers, providing feedback on test results, potential issues, and process improvements. Manage time efficiently and prioritize tasks based on project deadlines. Adhere strictly to safety guidelines and use appropriate safety devices while performing all tasks. Preferred Qualifications: Prior experience in a medical device testing or R&D environment. Familiarity with test methods and good documentation practices (GDP). Comfortable using lab tools and equipment such as: Calipers MTS systems Multimeters Digital thermometers Force gages Cognex systems LabView software Basic hand tools Strong attention to detail and the ability to follow both verbal and written instructions. Some experience drafting documents is a plus. Proactive communicator with the ability to work effectively within a team.

Job Title Product Development Adv Specialist - Tape Technology Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. This position provides an opportunity to transition from other private, public, government or military experience to a 3M career. The Impact You'll Make in this Role As a Product Development Adv Specialist for Tape Technology, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by: Leveraging expertise to advance technologies, develop product designs, and commercialize new products aligned to customer needs around the world. Formulating, developing, and commercializing new tapes, adhesives, and materials used in home improvement by DIYers and professionals. Supporting a group of product developers focused on improving current painter's tapes, duct tapes, and specialty tapes through encouraging technical exploration, developing people and lab capabilities, ideating and delivering on a product pipeline that differentiates, achieves delivered cost expectations, and delights customers and makes their projects easier. Collaborating with teams from the corporate research labs and our global lab peers on developing new product capabilities and applications to meet the global evolving home trends. Successfully scale products from lab to pilot line and to manufacturing, working with product engineers, business supply chain, third party manufacturing and quality. Your Skills and Expertise To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: Bachelor's degree or higher in chemistry, chemical engineering, material science or a science discipline (completed and verified prior to start) Seven (7) years of research and development in a private, public, government or military environment Additional qualifications that could help you succeed even further in this role include: Master's degree or higher in Chemistry, Chemical Engineering, Material Science, and/or Polymer Chemistry or related discipline from an accredited institution Ten (10) years of Research and Development experience in a private, public, government or military environment Experience in research and development of new tape products Hands-on experience with adhesives and tape development and/or process understanding Demonstrated expertise and success in exploration of new products/platform work and scaling from bench to pilot line and then to manufacturing Experience compounding, coating, polymer processing, curing, aging studies & weathering, adhesives, and analytical testing. Experience in test method development and fundamental understanding of adhesive properties, interfaces, and systems Demonstrated ability to collaborate with cross functional global team members in manufacturing, regulatory, application engineering, and business Work location: 3M Campus, Maplewood, MN Travel: May include up to 10% Relocation Assistance: May be authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Supporting Your Well-being 3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope. Chat with Max For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers. Applicable to US Applicants Only:The expected compensation range for this position is $164,612 - $201,193, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: ******************************************************************* Faith Posting Date Range 09/10/2025 To 10/10/2025 Or until filled All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M.Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M.Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement.Pay & Benefits Overview: https://**********/3M/en_US/careers-us/working-at-3m/benefits/3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law. Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly. 3M Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.

**_The future is what you make it._** When you join Honeywell, you become a member of our global team of thinkers, innovators, dreamers and doers who make the things that make the future. That means changing the way we fly, fueling jets in an eco-friendly way, keeping buildings smart and safe and even making it possible to breathe on Mars. Working at Honeywell isn't just about developing cool things. That's why all of our employees enjoy access to dynamic career opportunities across different fields and industries. **_Are you ready to help us make the future?_** **Honeywell's Advanced and Applied Technology** organization is seeking an exceptional Photonics Research Scientist to join our Advanced Sensing Technology group. In this role, you'll have the unique opportunity to explore new paradigm-changing technologies that could shape future products for the Aerospace industry. In this position you will develop resonant Fiber Optic Gyroscopes, and support a wide variety of other projects and programs which evolve and grow to meet the evolving needs of our customers and sponsors As an Integrated Photonics Scientist here at Honeywell, you will be at the forefront of innovation, driving the advancement of cutting-edge technologies and solutions, ensuring that Honeywell remains a leader in technological advancements. In this role, you will impact the future of Aerospace technologies by contributing to the ideation, conceptualization, research, and development of innovative new solutions. + Work as part of our team of scientists and engineers to develop advanced Sensor technologies and then demonstrate them for mission critical systems. + Engage with customers and partners to define their needs and requirements, then apply your skills to find creative solutions through rigorous analysis, engineering, and experimentation. + Effectively communicate your ideas and results to research sponsors, scientific peers, and business leadership, through effective presentations, publications, and the writing of proposals. + Develop new concepts, write proposals, and create and test hardware prototypes. **YOU MUST HAVE** + Master's Degree + R&D experience or academic research experience in one of the following areas: + Optics + Atomic physics + Inertial sensors + Precision measurement **WE VALUE** + Ph.D. degree in Electrical Engineering, Physics, Applied Physics, Optical Engineering, or equivalent + Demonstrated expertise in 2 or more of the fields below and/or skills within the last 4 years: + Optical Sensing + Fiber and guided wave optics + Signal processing and feedback + Data Collection and analysis + Enthusiasm for learning about new technologies and engaging difficult technical problems + Excellent written and communication skills + Track record of innovation and ability to solve complex problems through analysis and innovation + Ability to manage and understand complex customer requirements and manage stakeholders **U.S. PERSON REQUIREMENTS** Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. Person, which is defined as, a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status or have the ability to obtain an export authorization. **BENEFITS OF WORKING FOR HONEYWELL** In addition to a competitive, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays .For more Honeywell Benefits information visit: ******************************* _The annual base salary range for this position is $134,000 - $167,000. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations._ _The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Job Posting Date: Oct 28th, 2025_ Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments - powered by our Honeywell Forge software - that help make the world smarter, safer and more sustainable. Honeywell is an equal opportunity employer. Qualified applicants 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, religion, or veteran status.

The future is what you make it. When you join Honeywell, you become a member of our global team of thinkers, innovators, dreamers and doers who make the things that make the future. That means changing the way we fly, fueling jets in an eco-friendly way, keeping buildings smart and safe and even making it possible to breathe on Mars. Working at Honeywell isn't just about developing cool things. That's why all of our employees enjoy access to dynamic career opportunities across different fields and industries. Are you ready to help us make the future? Honeywell's Advanced and Applied Technology organization is seeking an exceptional Atomic, Molecular, and Optical (AMO) experimentalist to join our Advanced Sensing Technology group located in Plymouth, Minnesota. We are a team of scientists and engineers translating today's research into tomorrow's sensors for air and space applications. We are currently developing and deploying such cutting-edge technology as: ultra-stable inertial sensors based on atom interferometry, precision timing references based on laser cooled atoms, compact magnetometers based on NV diamond, and ultra-wideband electromagnetic sensors based on Rydberg atoms, among a wide variety of other projects and programs which evolves and grows to meet the evolving needs of our customers and sponsors. YOU MUST HAVE Ph.D. in physics, applied physics Research experience in one or more of the following areas: Experimental Atomic, Molecular, and Optical (AMO) Physics Atomic Sensors Atomic Clocks Precision Measurement Atom Interferometry Track record of solving difficult, complex problems through innovation, analysis, engineering, and experimentation. Excellent written and oral communication skills reflected in a record of published results and public presentations in your field of research. WE VALUE Hardware experience with some of the following is of value: Laser systems including diode lasers and ultra-stable optical cavities. Microwave frequency (>6 GHZ) test and measurement equipment. UHV ( Fiber optic components Analog and digital circuitry Integrated photonics Software experience with any of the following is of value: COMSOL or other multiphysics simulation software LabView or other experimental control software BENEFITS OF WORKING FOR HONEYWELL In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. For more information visit: Benefits at Honeywell The annual base salary range for this position is $115,000 - $144,000. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations. The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Job Posting Date: Oct 10, 2025. Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. Person, which is defined as, a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status or have the ability to obtain an export authorization. Work as part of our team of scientists and engineers to develop new atomic sensor technology concepts, and then demonstrate them in practical devices. Engage with customers and partners to define their needs and requirements, then apply your skills to find creative solutions through rigorous analysis, engineering, and experimentation. Effectively communicate your ideas and results to research sponsors, scientific peers, and business leadership, through effective presentations, publications, and the writing of proposals. Use your expertise to spur the growth of our technology portfolio in new directions, shaping the future of sensing technology. As an Advanced R&D Quantum & Optical Scientist here at Honeywell, you will be at the forefront of innovation, driving the advancement of cutting-edge technologies and solutions, ensuring that Honeywell remains a leader in technological advancements. In this role, you will impact the future of Honeywell Sensing technologies by contributing to the ideation, conceptualization, research, and development of innovative new solutions.

Job Title: Lab TechnicianJob Description Perform laboratory tests and other laboratory work using both conventional and computerized machines and work aids. Conduct tests in accordance with prescribed standards to determine chemical and physical characteristics or composition. Set up, readjust, and operate laboratory equipment and instruments. Responsibilities + Enter a variety of data to maintain records, update information, and track results. + Respond to basic or standard customer questions regarding formulas and the mixture process. + Clean, maintain, and calibrate standard equipment while ensuring a clean and safe working environment. + Perform other duties as assigned. Essential Skills + Proficiency in laboratory work, chemistry, research, and testing. + Experience with R&D, formulation, mixing, measuring, and experimentation. + Knowledge in synthesis, quality control, and batch processing. + Experience with liquids, coatings, paint, and color matching. Additional Skills & Qualifications + High School Diploma or GED is required; Associates degree or non-degree is preferred. + 1 year of chemical lab experience is preferred. + Basic math skills are required. + Experience in color differentiation is necessary. + Proven good organization and documentation skills, verified with references. + Proven ability to take direction, verified with references. Work Environment This role is situated in an industrial lab environment, not a clean room or biological lab. The position offers flexible 1st shift hours, Monday through Friday, typically working an 8-hour shift from 7/8 AM to 4/5 PM, with core hours from 8 AM to 4 PM. The dress code is business casual, and a lab coat is required. The organization is known for promoting from within, though candidates should be aware that the expectation is to be in this role for 9 months, with potential conversion not guaranteed. Job Type & Location This is a Contract position based out of Minneapolis, MN. Pay and Benefits The pay range for this position is $21.00 - $21.00/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 Dec 19, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

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 Conduct, analyze and document experiments for the development and validation of automated immunodiagnostic assays as part of a project team under direction of a Project Leader. Key Duties and Responsibilities * Support new and current diagnostic product lines. * Successfully complete complex research work in one or more of the following: technology development, product design and development, test of materials or products, preparation of specifications, process studies, research investigations, and report preparation. * Summarize, analyze and draw conclusions from complex test results * Conduct experiments for the development of immunodiagnostic assays * Contribute to multiple product development projects * Maintain accurate and complete records through computer systems and laboratory notebooks according to QSR/ISO requirements * Conduct work according to Good Manufacturing Practices and Safety Procedures * Provide analysis and reporting of data and results using Microsoft Excel, Word and PowerPoint. * Maintain laboratory equipment. Education, Experience, and Qualifications * Bachelor's degree in Biology, Chemistry, Biochemistry, Chemical Engineering or related discipline. * 1 year of Experience working in an academic, government or industrial life sciences laboratory setting * Experience in the development of immunodiagnostic assays preferred * Experience working in the medical device/diagnostics industry preferred * Understanding of immunology, gastroenterology, infectious disease, endocrinology, protein chemistry, laboratory automation, or ELISA-based assays * Ability to execute experiments related to the development of immunodiagnostic products * Self-motivation with a passion for solving problems. What we offer Receive a competitive salary and benefits package as you grow your career at Diasorin. Join our team and discover how your work can impact the lives of people all over the world. This position is $60,000 - $70,000 . 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.

Syngenta Seeds is one of the world's largest developers and producers of seed for farmers, commercial growers, retailers and small seed companies. Syngenta seeds improve the quality and yields of crops. High-quality seeds ensure better and more productive crops, which is why farmers invest in them. Advanced seeds help mitigate risks such as disease and drought and allow farmers to grow food using less land, less water and fewer inputs. Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions. Syngenta Seeds is headquartered in the United States. Job Description We are seeking a detail-oriented Research Associate to lead complex activities and projects, ensuring the successful execution and management of end-to-end process in seed production across multiple crops. Duties: Functioning as an integral member of a team leading all aspects of small plot seed production activities including packaging, treating, planting, harvesting, inventory, and shipping. Manage and train up to 15 part-time staff. Coordinate weekly labor needs based on current and future workload. Deliver projects on time and within budget. Ensure compliance with safety and stewardship policies. Qualifications PLEASE NOTE -- Candidates must be already located in the United States and not require visa sponsorship Required: B.S. in Agriculture, Logistics, Operations Management, or related field . Experience with seed production quality, quantity, and timelines and knowledge of international shipping logistics for research seed. Demonstrated collaboration and problem solving skills. Ability to lift 70 pounds and work in an outdoor field environment. Ability and willingness to work extended hours and Saturdays' during peak season. Valid driver's license and ability to travel to off-site field locations as required. Excellent communication and team management skills. Bilingual in Spanish and English (a plus). Proficiency in MS Office, especially Excel and Word. Preferred: Familiarity with seed technology industry and plant breeding methodologies. Experience with basic lab equipment (seed counters, scales, scanners). Additional Information What We Offer: A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs. Full Benefit Package (Medical, Dental & Vision) that starts your first day. 401k plan with company match, Profit Sharing & Retirement Savings Contribution. Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits. Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: ******************************************* Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. WL2A #LI-KR1 #LI-ONSITE

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Title: Method Development Chemist Location: Minneapolis, MN Duration: 3+ months (Possibility of extension) local candidate needed - Minneapolis, MN. REQUIRED: Top 3 must haves: Chromatography experience analytical lavatory experience Seasoned HPLC chemist. Job Roles & Responsibilities 3 months contract position performing method development on GPC methodology. Perform and document laboratory work. Review and approve test records. Participate in the validation of the new GPC test method Basic Qualifications and Experience EDUCATION - Minimum BS in Chemistry or related scientific degrees EXPERIENCE - Minimum 1 year in a regulated industry environment with a Bachelor's Degree in Chemistry. Minimum 3 years of hands on experience operating HPLC Performing chemistry and/or material properties testing in a high throughput laboratory Documenting work accurately and completely Ability to use common software including MS Word, MS Excel, Powerpoint Self-motivated, able to plan/execute work tasks independently Critical thinking skills Safely handle chemical and hazardous materials Preferred Skills and Experience Prior experience and knowledge of materials properties and GPC testing Experience working with laboratory data management system Experience working with Empower chromatography software Additional Information · We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job. Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732-844-8724 Email id - seema @irionline.com| www.irionline.com LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance. Job Description The Senior R&D Development Engineer will perform design and development activities on medical device/equipment products and improvements of ClosureFast products through frequent interaction with Manufacturing and Quality Engineering, Marketing, and other functions. Key responsibilities include conducting product testing and analysis on existing electrical products. You will work in a Sustaining Engineering role, improving existing endovenous products which include a generator and catheter components. Qualifications Bachelor's degree in Electrical Engineering, Mechanical Engineering scientific, or related technical field • 5+ years of Engineering experience • 3+ years of Medical device experience • Thorough understanding of medical device industry and competitor products. • Proficient in electrical medical device requirements, such as IEC 60601-1, IEC 60601-2 • Thorough understanding of clinical and regulatory pathways, IP and internal processes. • In depth knowledge and wide application of technical principles, theories, and concepts in related field of expertise to develop innovative approaches to work. • Effectively communicates and works cooperatively with others as part of a team. Shares information, status, needs, and issues with others in order to inform, gain input, and support decision-making. • Knowledge of and ability to design reliable and innovative mechanical systems and mechanisms for consumer products. • Knowledge of manufacturing processes. • Proficient in Design FMECA and Design Verification and Validation activities. • Application of statistical and analytical methods such as DOE and capability analysis. Additional Information If you are interested, please send your updated resume to ****************************** or call directly at ************. Sagar Rathore ************

Full-time Description This position focuses on technical support for R&D, product development, process development, and transfer to manufacturing projects. Essential Functions Work closely with R&D team to design and develop innovative products Develop and refine both R&D and production level manufacturing work instructions Assist in design and construction of developmental components, sub-assemblies and prototype devices Record observations of both assembly processes and assembly (or component) performance Assist in development of test methods, through test method design, construction and execution Perform product testing, record data and perform simple analysis Communicate to teammates about progress and learnings both verbally and in writing, when necessary Train and support operators on new manufacturing projects Drive timelines and assist in product manufacturing when necessary Gather inspection data on new products to refine customer specs Evaluate manufacturing transfer projects and provide line support to ensure a smooth transition Work with project team to build quality product and deliver on time Requirements Education, Experience, Required Skills Experience and/or training in using a microscope in assembly, working with different types of class III implantable devices, working with active medical devices requiring laser welding/soldering. Knowledge of common medical device materials of construction and manufacturing processes 3-5+ years of experience required, with at least 2 years of experience working with active implantable devices. Strong technical ability with focus on quality Ability to work well with teams Motivated with a strong attention to detail Strong written and oral Communication skills Ability to handle and be trusted with confidential and/or sensitive information Able to work in a fast-paced, constantly changing environment Ability to be flexible and to handle multiple projects in an organized, timely manner Able to problem-solve, work under pressure, and to effectively manage stress Support company finance, accounting, human resources, quality, regulatory, and clinical departments as necessary to ensure compliance with requirements. Physical Requirements Prolonged periods sitting at a desk and working on a computer or microscope Prolonged periods of standing Must be able to lift up to 25 pounds at times Possess the manual dexterity to assemble products or machines as directed Must have excellent hand-eye coordination Must wear gown, gloves, ear protection and personal protective equipment when applicable Summary of Benefits Group health & welfare benefits: Options for Medical, Dental and Vision insurance, Health Savings Account (requires participation in eligible medical plan), and Flexible Spending Accounts. Company-paid benefits: Employee Life Insurance & Accidental Death & Dismemberment (AD&D), Long Term Disability (LTD), Kavira (requires participation in medical plan). Voluntary, employee-paid benefits: Employee Supplemental Life & AD&D, Spouse and Dependent Life & AD&D, Short Term Disability (STD), Accident, Critical Illness, and Hospital Indemnity, Employee Assistance Program. Accrued Paid Time Off (PTO) & Floating Holidays Paid Parental Leave Paid Holidays Benefits and incentive compensation may be subject to generally applicable eligibility, waiting period, contribution, and other requirements and conditions. Compensation The typical base pay range for this role is between $30.00-38.00/hour. Compensation may vary based on individual job-related knowledge, skills, expertise, and experience. This position is eligible for a discretionary annual incentive program driven by organization and individual performance. 401(k) Plan: Company-provided Safe Harbor Contribution of 3% of eligible earnings.

**Duration: 12 Months Contract** **Note: Possible temp to hire for right individual and if budget allows** **Someone with:** + Hands on lab experience / test methods + Windchill experience - DCAs (design change analysis) **Day in the life:** + Scheduling Test Activities, focus point for technician work direction and reports to manager. + Scanning returned product to X-ray or CT scan + Possibility to collect sort analyze data + Functional testing + Test methods involving standard equipment procedures + (Instron / MTS, Pressure Gauges, X-Ray Imaging, Photo and Data collection) or Nonstandard test method fixturing for either capital equipment or single use device performance testing. **Job Purpose** + Develops products, materials, processes, or equipment for projects of moderate complexity. + Under limited supervision/guidance, compiles, analyzes, and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials. + This person will be working with other engineers, design assurance team, and PM staff. + About 6-7 on the team **Key Responsibilities** + Fully participates in and successfully contributes to project teams typically including the following activities: product design and development, test of materials, preparation of specifications, process capability studies, research investigations (animal and clinical studies), report preparation, and process/test documentation. + Works independently to plan and schedule own activities necessary to meet timelines. + Designs and coordinates standard engineering tests and experiments. + Designs, procures, and fabricates tooling and fixtures. + Performs troubleshooting on new products/process problems as related to design, material, or process. + Summarizes, analyzes, and draws conclusions from test results. + Prepares standard reports/documentation to communicate results to technical community. + Responsible for engineering documentation. + Invents/ creates concepts and designs for new products/processes and submits idea disclosures. + May train and/or provide work direction to technicians. + Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success. + Demonstrates PDP/TPD system knowledge through delivery of high-quality deliverables. **Quality Systems Duties and Responsibilities:** + Build Quality into all aspects of their work by maintaining compliance to all quality requirements. **Qualifications** + Engineering or physics degree required + 2+ years of experience (internship experience will not be considered for 2 of years of experience) + Hands on lab experience and test methods + MS Office, Operation of equipment & testers **Nice to have (But not required)** + Tooling / Fixturing experience. + 3D printing **About US Tech Solutions:** US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions 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, disability, or status as a protected veteran.

Product Development Specialist - Aerospace Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. This position provides an opportunity to transition from other private, public, government or military experience to a 3M career. The Impact You'll Make in this Role Join our team and make an impact as a Product Development Specialist. In this role, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by: Developing new products and product platforms to maintain and expand 3M's aerospace film portfolio to enable business growth and further our competitive position in the marketplace Commercializing new products aligned to global customer needs in collaboration with customers and cross-functional teams Developing a strong understanding of our customer/market needs especially as it relates to regulatory standards and critical to quality metrics Collaborating with research teams from across 3M, in industry, and in academia to develop new technology, product, and manufacturing capabilities Identifying and leveraging external interactions to identify and anticipate industry trends that will accelerate technology and product development Initiating and contributing to the development of Intellectual Property and IP strategies Your Skills and Expertise To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: Bachelor's degree or higher from an accredited institution (completed and verified prior to start) Five (5) years of product development, process engineering, or laboratory research in a private, public, government or military environment Additional qualifications that could help you succeed even further in this role include: Masters or PhD in Aerospace Engineering, Electrical Engineering, Polymer Science/Engineering, Mechanical Engineering, Chemical Engineering or Materials Science from an accredited institution Experience developing thermoplastic and thermoset film, coating and adhesive products of a variety of compositions including urethane, epoxy, acrylic, etc. Experience in multiple manufacturing processes including extrusion and coating Familiarity, and preferably experience, with aerospace composite manufacturing techniques and modeling/simulation processes Experience in regulated product categories with expertise in product risk assessments, failure mode analysis, and product reliability Proven track record through publications, conference presentations, and/or published IP Collaborative interpersonal style with leadership and networking skills and demonstrated ability to work effectively in a team environment Excellent technical presentation skills and oral communication skills Work location: On site at 3M Center at Maplewood, MN (at least 4 days per week) Travel: May include up to 10% domestic/international travel Relocation Assistance: May be authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Responsibilities of this position may include direct and/or indirect physical or logical access to information, systems, technologies subjected to the regulations/compliance with U.S. Export Control Laws. U.S. Export Control laws and U.S. Government Department of Defense contracts and sub-contracts impose certain restrictions on companies and their ability to share export-controlled and other technology and services with certain "non-U.S. persons" (persons who are not U.S. citizens or nationals, lawful permanent residents of the U.S., refugees, "Temporary Residents" (granted Amnesty or Special Agricultural Worker provisions), or persons granted asylum. To comply with these laws, 3M must help assess candidates' U.S. person status. The questions asked in this application are intended to assess this and will be used for evaluation purposes only. Failure to provide the necessary information in this regard will result in our inability to consider you further for this particular position. Supporting Your Well-being 3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope. Chat with Max For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers. Applicable to US Applicants Only:The expected compensation range for this position is $141,150 - $172,517, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: ******************************************************************* Faith Posting Date Range 09/29/2025 To 10/29/2025 Or until filled All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M.Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M.Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement.Pay & Benefits Overview: https://**********/3M/en_US/careers-us/working-at-3m/benefits/3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law. Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly. 3M Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.

**_The future is what you make it._** When you join Honeywell, you become a member of our global team of thinkers, innovators, dreamers and doers who make the things that make the future. That means changing the way we fly, fueling jets in an eco-friendly way, keeping buildings smart and safe and even making it possible to breathe on Mars. Working at Honeywell isn't just about developing cool things. That's why all of our employees enjoy access to dynamic career opportunities across different fields and industries. **_Are you ready to help us make the future?_** **Honeywell's Advanced and Applied Technology** organization is seeking an exceptional Atomic, Molecular, and Optical (AMO) experimentalist to join our Advanced Sensing Technology group located in Plymouth, Minnesota. We are a team of scientists and engineers translating today's research into tomorrow's sensors for air and space applications. We are currently developing and deploying such cutting-edge technology as: ultra-stable inertial sensors based on atom interferometry, precision timing references based on laser cooled atoms, compact magnetometers based on NV diamond, and ultra-wideband electromagnetic sensors based on Rydberg atoms, among a wide variety of other projects and programs which evolves and grows to meet the evolving needs of our customers and sponsors. + Work as part of our team of scientists and engineers to develop new atomic sensor technology concepts, and then demonstrate them in practical devices. + Engage with customers and partners to define their needs and requirements, then apply your skills to find creative solutions through rigorous analysis, engineering, and experimentation. + Effectively communicate your ideas and results to research sponsors, scientific peers, and business leadership, through effective presentations, publications, and the writing of proposals. + Use your expertise to spur the growth of our technology portfolio in new directions, shaping the future of sensing technology. As an Advanced R&D Quantum & Optical Scientist here at Honeywell, you will be at the forefront of innovation, driving the advancement of cutting-edge technologies and solutions, ensuring that Honeywell remains a leader in technological advancements. In this role, you will impact the future of Honeywell Sensing technologies by contributing to the ideation, conceptualization, research, and development of innovative new solutions. **YOU MUST HAVE** + Ph.D. in physics, applied physics + Research experience in one or more of the following areas: + Experimental Atomic, Molecular, and Optical (AMO) Physics + Atomic Sensors + Atomic Clocks + Precision Measurement + Atom Interferometry + Track record of solving difficult, complex problems through innovation, analysis, engineering, and experimentation. + Excellent written and oral communication skills reflected in a record of published results and public presentations in your field of research. **WE VALUE** + Hardware experience with some of the following is of value: + Laser systems including diode lasers and ultra-stable optical cavities. + Microwave frequency (>6 GHZ) test and measurement equipment. + UHV ( + Fiber optic components + Analog and digital circuitry + Integrated photonics + Software experience with any of the following is of value: + COMSOL or other multiphysics simulation software + LabView or other experimental control software **BENEFITS OF WORKING FOR HONEYWELL** In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. For more information visit: Benefits at Honeywell (******************************** **U.S. PERSON REQUIREMENTS** Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. Person, which is defined as, a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status or have the ability to obtain an export authorization. _The annual base salary range for this position is $125,000 - $144,000. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations._ _The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Job Posting Date: Oct 10, 2025._ Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments - powered by our Honeywell Forge software - that help make the world smarter, safer and more sustainable. Honeywell is an equal opportunity employer. Qualified applicants 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, religion, or veteran status.

Full-time Description The R&D Regulatory Technician will play a critical role in supporting the Research & Development team with the documentation and compliance aspects of cosmetic and OTC product development. This position is responsible for coordinating regulatory documentation, ensuring formula compliance, verifying ingredient documentation, supporting product claims substantiation, and assisting in the preparation technical files. The ideal candidate will bridge the gap between formulation and regulatory, ensuring all projects meet applicable FDA, INCI, and other regulatory requirements. Reporting directly to the VP of R&D, this role contributes to bringing safe, effective, and compliant skincare and suncare products from concept to commercialization while ensuring best practices and standards are followed throughout the development process. Key Responsibilities: Document Control & Regulatory File Management Maintain and organize all regulatory documentation for R&D projects, including formula worksheets, batch records, ingredient documentation (SDS, COA, TDS, IFRA, allergen statements), and regulatory dossiers. Ensure accurate and complete records are created and maintained for internal and external audits. Formula & Ingredient Compliance Review raw materials and finished product formulations to ensure compliance with applicable FDA, OTC monograph, and other international regulations. Verify that all raw materials used in development have up-to-date documentation and certifications to support product safety, claims, and compliance. Claims Support & Regulatory Substantiation Assist in compiling technical support for product marketing claims (e.g., non-comedogenic, dermatologist tested, reef safe, broad spectrum). Create and maintain claim substantiation files, ensuring all supporting data (clinical, analytical, or third-party testing) is properly documented. Good Face Project Support Act as the regulatory point of contact for the Good Face Project platform, ensuring accurate and timely input of raw material documentation, including SDS, COAs, allergen statements, IFRA certificates, and other required data. Maintain and update ingredient profiles within the platform to enable accurate screening of formulations for regulatory compliance (e.g., EU, US, Sephora clean, Credo, etc.). Support the R&D team in uploading and managing formulations within the Good Face system to evaluate product compliance across multiple regulatory and “clean beauty” standards. Ensure that all data entered into the platform aligns with current FDA guidelines, global cosmetic regulations, and internal best practices. Collaborate with formulators to develop checklists and internal workflows that ensure Good Face Project data remains accurate and up to date on an ongoing basis. Provide regular support and troubleshooting for the platform and stay current on updates or new features released by Good Face to ensure continued optimization Labeling Review Assist in reviewing product labels, ingredient lists (INCI), and Drug Facts (for OTC) to ensure accuracy and compliance Batch & Technical Documentation Support Support R&D Chemists in preparing technical documents for pilot batches, scale-ups, and stability studies. Ensure all documentation associated with lab work (batch sheets, formula revisions, testing results) is reviewed and filed according to SOPs. Cross-Functional Collaboration Collaborate with QA/QC, Project Management, and Production teams to ensure a seamless handoff of compliant formulations and documentation packages as needed Requirements Required Skills & Competencies: Experience in technical writing and managing product-related documentation Excellent organizational skills with strong attention to detail and data accuracy Ability to review and interpret SDS, COAs, IFRA certificates, and other regulatory documents Strong communication and cross-functional collaboration skills Proficiency in Microsoft Office (especially Excel, Word, Outlook) Ability to manage multiple projects and shifting priorities in a deadline-driven environment Required Education & Experience: Bachelor's degree in chemistry, Cosmetic Science, Regulatory Affairs, or a related scientific field Experience with R&D documentation, or compliance support role within the cosmetic, OTC, or personal care industry Preferred Education & Experience: 1-2 years of experience with Good Face Project Experience in regulatory support for OTC products (e.g., sunscreens, acne treatments, antiperspirants) Knowledge of global cosmetic regulations and documentation standards Experience in claim substantiation processes and documentation for personal care products Working knowledge of FDA requirements for labeling, formula review, and product development practices Salary Description $20/hr - $29/hr

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 Product Transfer activities including creation of formulation documentation, implementation of quality control procedures, validation reagent formulation including quality control and support of products post launch within the LIAISON Reagents department. Key Duties and Responsibilities * Work in conjunction with Product Development in creation of all documentation for LIAISON Reagent Manufacturing and Quality Control for new products. Create part numbers for new products in the design cycle. * Create routings for new part numbers created in design cycle. * Aid in creation of part numbers and routings for newer team members. * Manufacture new Internal Controls for product in the design cycle. * Serve on Core Teams for assigned development projects. * Perform material processing and reagent formulation for bulk intermediates and components. * Determine reprocessing need for calibrator, controls and conjugates, with assistance. * Maintain clean work space in QC and Reagent Prep labs, consistent with Good Laboratory Practices (GMP). * Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance. * Utilize basic SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting and flow through facility. * Participate in inventory accountability - PSA count, cycle counts, accurate kitting, etc. * Perform in-process testing and final QC for LIAISON products per established procedures using the LIAISON analyzer family. * Analyze testing results of technical manufacturing, quality control or product performance to determine acceptability of product relative to established requirements. * Assign calibrator values to optimize kit performance, with assistance. * Assign Kit Control ranges per established procedures. * Perform second-checking to ensure accurate records. * Follow regulatory requirements - follow document instructions and maintain reasonable documentation error rates. * Ensure proper documentation by correcting errors noted in procedures and forms. * Ensure proper documentation by creating new documents and making significant revisions to current documentation for process changes, clarity or consistency. * Perform tasks assigned in NCR / Deviations and Validations. * Perform tasks assigned in CAPA. * 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. * Monitor training required in SmartTrain and ensure timely completion of all company training requirements. * Help with basic new employee training such as instrument use, basic software training, etc. * Contribute to business continuity or continuous improvement projects by suggesting improvements and completing assigned tasks. * Complete assigned tasks related to investigations for root cause determination and troubleshoot product or process issues. 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 * 5+ Years of related laboratory experience or demonstrated competence within the in-vitro diagnostic industry * Comprehensive understanding of immunology and immunoassay technology and systems * Ability to work in a regulated industry * Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.) * Knowledge of good manufacturing practices (GMP) * Knowledge of statistical analysis and reporting methods * Ability to train and mentor team members on basic group procedures and tasks * Ability to train and mentor team members in higher level skills * Proven ability to work with minimal supervision * Working knowledge of MS Excel * Familiarity with Google Suite What we offer Salary Range The salary range for this position is $70,000-86,000 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.

Job Title: P1 Scientist- Reagent Production OperationsJob Description As a P1 Scientist in Reagent Production Operations, you will be responsible for the transfer and reformatting of Standard Operating Procedures (SOPs) and related documentation, specifically pertaining to immunoassay development. Your role will involve utilizing existing documents and integrating them into current SOP templates. Responsibilities * Transfer and reformat SOPs related to immunoassay development. * Utilize existing documentation to integrate into new SOP templates. * Ensure quality assurance through data entry and document accuracy. * Engage in formulation processes including weighing materials and measuring pH. * Support documentation projects related to site transfer from Karlsbad, CA to Chaska, MN. Essential Skills * Formulation * Laboratory skills * Chemistry * GMP experience * Data entry * Quality assurance expertise Additional Skills & Qualifications * Bachelor's degree in life science (chemistry, biology, biochemistry, microbiology). * 6+ months of experience in a GMP environment. * 6+ months of experience writing SOPs. * Experience in production formulation including weighing materials and using a spectrophotometer. * 3+ months of experience with immunoassay manufacturing. * Knowledge of writing CAPAs, supplier notifications, and change orders. * Familiarity with inventory management systems. Work Environment This position is a full-time, desk-based role, operating Monday through Friday on the first shift with start times between 6 am and 9 am for an 8.5-hour workday. The team has recently undergone reorganization and focuses on new product introduction, site transfer projects, CAPAs, maintenance requests, and supplier notifications. Most team members have a background in biochemistry or chemistry, with a few exceptions in product labeling and inventory management. Job Type & Location This is a Contract position based out of Chaska, MN. Pay and Benefits The pay range for this position is $28.00 - $30.00/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 Chaska,MN. Application Deadline This position is anticipated to close on Dec 31, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Full-time Description The R&D Technician will support the formulation and development of cosmetic and OTC personal care products, with a focus on skincare and suncare. This role involves preparing and modifying formulations under the guidance of R&D Chemists, performing lab tests, documenting processes, and supporting scale-up activities. The technician must adhere to lab protocols, ensure compliance with regulatory guidelines, and maintain a clean and safe laboratory environment. This position reports directly to the VP of R & D and plays a key role in bringing innovative, high-quality products from concept to launch. Key Responsibilities: Prepare lab batches based on new or modified formulations according to directions from R&D Chemists and Management. Assist in formulation adjustments to meet product performance, stability, and regulatory requirements. Conduct routine testing of lab batches, including pH, viscosity, specific gravity, appearance, texture, and odor. Maintain accurate and organized records of all formulation work, testing data, and observations. Ensure all samples and documentation meet internal standards and are archived appropriately. Gain familiarity with regulations related to OTC and cosmetic products, including FDA monograph requirements. Support scale-up and pilot batching processes, and assist in the transfer of formulas to the production floor as requested by the chemists and R & D management Learn and follow proper procedures for weighing, mixing, and batching raw materials in accordance with Good Manufacturing Practices (cGMP). Identify and communicate any issues during batching, testing, or stability evaluations to the chemists Maintain cleanliness, safety, and organization in the lab environment, including routine maintenance of lab equipment. Work on multiple development projects simultaneously and manage shifting priorities as needed. Requirements Required Skills/Abilities Hands-on experience with laboratory equipment and processes Knowledge of safe chemical handling procedures. Ability to accurately perform calculations for batching and scaling. Strong attention to detail, organizational skills, and commitment to documentation accuracy. Effective written and verbal communication skills. High level of initiative and problem-solving ability in a fast-paced environment. Ability to work both independently and collaboratively as part of a cross-functional team. Proficient in Microsoft Office (Excel, Word, Outlook). Willingness to learn and adapt quickly to new methods, regulations, and technologies. Required Education and Experience Bachelor's degree in Chemistry, Chemical Engineering, Cosmetic Science, or a related scientific discipline. Preferred Education and Experience Experience working within cosmetic or OTC product environment under FDA regulations (e.g., sunscreens, acne treatments, antiperspirants). Familiarity with GMP documentation practices and regulatory compliance requirements. Bachelor's degree in Chemistry or Cosmetic Science or advanced training in formulation chemistry. Salary Description $20/hr - $29/hr