Chemist Jobs in Edina, MN

6 month contract Must be able to work on a W2 On-site in St. Paul, MN We are seeking an Associate Scientist with 2-5 years of experience to join our Science and Technology Materials Group lab in Little Canada, Minnesota (Woodridge location). The scientist will be responsible for acquiring and processing data for materials assessments and supporting medical device project teams with both development and operational activities. The ideal candidate will bring technical expertise in materials assessment techniques and thrive in a collaborative, fast-paced environment. Familiarity with medical devices and regulated documentation practices is preferred. Job Responsibilities Perform materials assessments using techniques such as thermal analysis, microscopy, metallurgy, and failure analysis. Support scientists and engineers on project teams to meet technical and operational goals. Document experiments and analyses in compliance with regulatory standards. Apply knowledge of technical concepts and principles underlying Materials Science techniques. Utilize surface analysis tools including microscopy, SEM/EDS, FIB, and laser confocal microscopy. Conduct vibrational spectroscopy techniques such as FTIR and Raman. Perform thermal analysis methods including DSC, TGA, TMA, and rheological techniques. Job Qualifications Bachelor's degree in Material Science, Polymer Science, or a related field; or equivalent work experience. 2-5+ years of relevant experience in Materials Science and Engineering. Hands-on experience with materials characterization techniques and laboratory instrumentation. Strong verbal, written, and organizational skills. Proven ability to work both independently and collaboratively within a team. Experience in a regulated environment and knowledge of medical devices is a plus.

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.

Collabera Inc (Staffing Firm). We are based out of Morristown, NJ and we have been providing contingent labor to our clients for last 25 years. In 2015 we placed more than 6,000 contractors across select 100+ clients that we service. End client for this project is a large legal organization with operations in more than 100 countries and has more than 50,000 employees around the world. For eight consecutive years, Fortune has named this company as World's ‘Most Admired Companies to work for'. Job Description Top 3 must haves: Chromatography experience analytical lavatory experience Seasoned HPLC chemist. Duties o 3 months contract position performing method development on GPC methodology o Perform and document laboratory work o Review and approve test records o Participate in the validation of the new GPC test method Qualifications o Education - Minimum BS in Chemistry or related scientific degrees o 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 o Documenting work accurately and completely o Ability to use common software including MS Word, MS Excel, Powerpoint o Self-motivated, able to plan/execute work tasks independently o Critical thinking skills o Safely handle chemical and hazardous materials Preferred Skills and Experience o Prior experience and knowledge of materials properties and GPC testing o Experience working with laboratory data management system o Experience working with Empower chromatography software o Experience working with electronic laboratory notebooks Additional Information To set up an Interview, please contact: Sagar Rathore Technical Recruiter ************ *******************************

Job Title Senior Analytical Chemist 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 Senior Analytical Chemist in 3M Corporate Research Analytical Laboratory, 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: * Providing analytical chemistry measurements for 3M corporate research laboratories and divisions * Conducting analytical testing of 3M materials and products using chromatography techniques * Preparing samples, operating analytical instruments, and documenting test results * Leveraging and developing new and existing analytical techniques and methods to drive 3M advancements in science through GC analysis. * Collaborating with a cross-functional team to develop innovative solutions. * Applying knowledge of chemistry or chemical engineering to solve complex problems. * Strengthening 3M's proprietary position through development of intellectual property. * Collaborating with global, multi-disciplinary teams to identify and implement new solutions toward customer applications. Your Skills and Expertise To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: * Possess a PhD degree (completed and verified prior to start) in chemistry, organic chemistry, chemical engineering, or Microbiology from an accredited university plus two (2) years of experience in laboratory research in a private, public, government or military environment. This can include experience earned through a PhD program. OR * Masters degree with at least 4 years laboratory experience OR * Bachelors degree (completed and verified prior to start) with at least 6 years of laboratory experience. AND * Experience with Gas Chromatography and Mass Spectroscopy, especially in method development. Additional qualifications that could help you succeed even further in this role include: * Experience either direct or through collaborations utilizing or developing data analytics tools * Experience either direct or through collaborations utilizing laboratory automation tools * Experience / proficiency in Python, Databricks, SQL, etc.. * Experience with routine preventative maintenance tasks for GC instruments. Not afraid to be "hands on" with the hardware. Work location: * On site at 3M Campus in Maplewood, MN, Building 201 Travel: May include up to 10% [domestic/international] Relocation Assistance: Not 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 $122,292 - $149,468, 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: *************************************************************** Good Faith Posting Date Range 04/01/2025 To 05/01/2025 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. Pay & Benefits Overview: https://**********/3M/en_US/careers-us/working-at-3m/benefits/ 3M is an equal opportunity employer. 3M will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, pregnancy, gender identity, national origin, age, disability, or veteran status. 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.

Interplastic Corporation is seeking a Chemist. This position is responsible for developing new products, evaluating competitive products, assisting in product problem resolution, and presiding over product scale up and field trials. A person in this position will succeed by obtaining, analyzing, and presenting data efficiently. They are responsible for adding to the company knowledge and driving development forward. Responsibilities: Perform all required activities in a manner deemed to be safe and with minimal risk to self and co-workers. Participate in laboratory work activities involving polymer development, quality control, materials evaluation, and matching competitive products. Respond properly and quickly to inquiries, either directly to the customer, to sales, or to the supervisor, regarding technical problems or matters. Make appropriate recommendations to the Director of Research and Development or other appropriate personnel. Maintain laboratory facilities in neat and orderly condition to permit maximum employee efficiency and productivity. Accurate and timely record-keeping, with recommendations for further laboratory efforts. Required: BS/BA Degree in chemistry, polymer or material science, or chemical engineering; 3-5 years of Industrial experience Exceptional interpersonal and communication skills. Knowledge and practical experience in project management, experimental design and other problem-solving methodologies. Must be able to lift 50 pounds and must be able to pass a Respirator Test. Ideal Candidate will have: Experience with polymer synthesis, polymer characterization techniques and knowledge of surface science. Product development experience in the manufacturing industry. Experience in polymer characterization by physical and chemical methods. Knowledge of thermoset polyesters or vinyl esters. Knowledge of fillers and additives used in the formulation of composite materials. Competitive Benefit package that includes: competitive salary, Medical Benefit Plan Options, Dental Plan, Vision Plan, Flexible Benefit Plan, Short Term and Long Term Disability Plans, 401K Plan that includes matching. #LI-IPCORP

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: *************************************************************************************** continues to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Job Description: Product Development Scientist, Hybrid, Maplewood, MN 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you. The Impact You'll Make in this Role As a Product Development Scientist, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Leads programs of major importance to the organization's interests and portfolios. Develops mechanistic understanding of technologies Cultures adherent mammalian cells and establishes 3D cultures Cultures and maintains medically relevant bacterial strains Leads preclinical studies and analyzes data Develops novel experimental techniques around cellular metabolism and inflammation Communicates and contextualizes results to management and project teams Your Skills and Expertise PhD in biological science preferably cell biology, physiology, microbiology or other appropriate discipline AND 5 years industry experience in mammalian cell culturing and monitoring and specific experience with 3D cell culturing of adherent cells OR Master's degree and 9 years industry experience in mammalian cell culturing and monitoring and specific experience with 3D cell culturing of adherent cells AND In addition to the above requirements, the following are also required: Expertise in development of novel experimental procedures and metabolic test methods including both 2D and 3D cell models Expertise in sterile technique and microbial procedures as well as experience in work with medically relevant microbial strains including bacterial cell culturing, proliferation and maintenance of cell lines Expertise in immunoassays including multiplexed immunoassays Expertise in testing antimicrobial technologies. Experience with preclinical models and studies Good understanding of experimental design, data analysis and technical writing and communication Additional qualifications that could help you succeed even further in this role include: Experience with basic statistical methods Experience with design control Work location: · Hybrid - 60% onsite Travel: May include up to 10 % domestic/international Relocation Assistance: AuthorizedMust be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).Supporting Your Well-being Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.Applicable to US Applicants Only:The expected compensation range for this position is $137,439 - $167,981, 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: *************************************************************************************** of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers. Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain *****************. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains. Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. 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. Solventum 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 Solventum 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.

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: *************************************************************************************** continues to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Job Description: Product Development Scientist, Hybrid, Maplewood, MN 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you. The Impact You'll Make in this Role As a Product Development Scientist, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Leads programs of major importance to the organization's interests and portfolios. Develops mechanistic understanding of technologies Cultures adherent mammalian cells and establishes 3D cultures Cultures and maintains medically relevant bacterial strains Leads preclinical studies and analyzes data Develops novel experimental techniques around cellular metabolism and inflammation Communicates and contextualizes results to management and project teams Your Skills and Expertise PhD in biological science preferably cell biology, physiology, microbiology or other appropriate discipline AND 5 years industry experience in mammalian cell culturing and monitoring and specific experience with 3D cell culturing of adherent cells OR Master's degree and 9 years industry experience in mammalian cell culturing and monitoring and specific experience with 3D cell culturing of adherent cells AND In addition to the above requirements, the following are also required: Expertise in development of novel experimental procedures and metabolic test methods including both 2D and 3D cell models Expertise in sterile technique and microbial procedures as well as experience in work with medically relevant microbial strains including bacterial cell culturing, proliferation and maintenance of cell lines Expertise in immunoassays including multiplexed immunoassays Expertise in testing antimicrobial technologies. Experience with preclinical models and studies Good understanding of experimental design, data analysis and technical writing and communication Additional qualifications that could help you succeed even further in this role include: Experience with basic statistical methods Experience with design control Work location: · Hybrid - 60% onsite Travel: May include up to 10 % domestic/international Relocation Assistance: AuthorizedMust be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).Supporting Your Well-being Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.Applicable to US Applicants Only:The expected compensation range for this position is $137,439 - $167,981, 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: *************************************************************************************** of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers. Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain *****************. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains. Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. 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. Solventum 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 Solventum 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.

Who We Are Quality Work. Quality Results. Bay West stands at the forefront of the environmental consulting and remediation sector. Our dedication to safety, innovation, and our skilled team has driven us for over fifty years, delivering top-tier environmental consulting, industrial, and emergency response services. At Bay West, you'll be driven to innovate and make a real impact on environmental issues, all while advancing your career in a dynamic and supportive environment. This Opportunity Bay West is seeking a Transportation and Disposal (T&D) Chemist to support our hazardous and non-hazardous waste operations. This role involves waste profiling, lab packing, manifest preparation, and assisting with industrial services and emergency response projects. The ideal candidate will have strong knowledge of waste regulations and hands-on experience in the field. Your Key Responsibilities Perform waste profiling, manifest creation, lab packing and transportation services for hazardous and non-hazardous materials at customer sites. Create and prints manifests, labels, Land Disposal Restrictions, waste profiles, etc. for T&D projects using web-based Waste Management program. Accurately segregate and package hazardous and non-hazardous waste containers according to DOT and EPA regulations Perform waste sampling and waste characterization in the field. Track and store T&D related information in the electronic internal document management system Assist in the management of the 10-day hazardous waste storage trailer. Assists T&D Coordinator daily in developing and documenting transportation and disposal procedures. Assist with Industrial Services (IS) projects including tank cleanings and facility decontaminations/cleanings. When not traveling, be available for one week every six to nine weeks to be part of an on-call Emergency Response (ER) team to clean-up hazardous and non-hazardous material spills, loading, unloading, and decontaminating ER equipment in an efficient and accurate manner. On-call requires that staff stay within one hour of the Bay West office and be prepared to respond 24-7. Communicate effectively with internal and external customers in a courteous and professional manner. Provide open communication with Team Leader on ways to improve Bay West techniques, operations, and functions. Up to 25% out-of-town travel mainly in the Midwest region (ND, SD, IA, WI, MN) Who You Are Required Qualifications High school diploma or equivalent required; bachelor's degree in a science related field preferred Minimum 1-3 years of related field experience including waste transportation and packaging. Valid US driver's license with acceptable driving record required; Class A or B CDL with Hazmat endorsement Comprehensive knowledge of DOT and RCRA Hazardous waste rules and regulations preferred Proficiency using Word and Excel applications Currently have or willing to obtain a 40 Hour HAZWOPER certification Reliable means of transportation on a 24-hour basis Strong interpersonal and communication skills both written and verbal Experience supporting multiple projects on deadline while providing excellent customer service Superb problem-solving skills, time-management, and organizational skills Ability to work independently Willingness to champion changes and improvements Preferred Qualifications Experience with field equipment such as box trucks, lift gates, forklifts, drum carts and pallet jacks. Knowledge of state and federal environmental regulations and laws, including, but not limited to, Minnesota Pollution Control Agency (MPCA) cleanup guidance and United States Environmental Protection Agency (USEPA) Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), and Resource Conservation and Recovery Act (RCRA) Physical Requirements Repetitive motions: frequent standing, walking, lifting, carrying, bending, and grasping Frequently lift 25 lbs. over an 8-hour period, and occasionally up to 50 lbs. for less than one hour Frequent exposure to non-hazardous and hazardous work environments including contaminated air, soil, dust, fumes, smoke and other toxins Ability to work outside in varying conditions, such as high heat, high humidity and extreme cold in remote locations. Ability to read and interpret general documents, safety rules, and Standard Operating Procedures Benefits Bay West offers a comprehensive benefits package available to eligible employees, including but not limited to paid time off, health insurance options, ancillary benefits to support life at all stages, 401(k), employee assistance programs, and subsidies. Bay West is an Equal Opportunity Employer.

As an Associate Decision Scientist for the Strategic Analytics team, you will be responsible for conducting ad-hoc analyses to support strategic decisions and address key business questions related to customer growth across digital commerce channels, including the Best Buy App. This role will be focused on tackling open-ended business problems with a strategic lens, offering creative, data-driven solutions. This includes participating in scoping sessions, assisting in defining project requirements, executing data analysis, visualizing findings, and communicating insights to support business decisions. You will partner with business stakeholders and data science, delivering actionable insights that inform decisions across the organization. This role is hybrid, which means you will be required to work some days on-site at the Best Buy location listed on this posting and some days virtually from home or other non-Best Buy location. The specific work arrangements vary by role and team. The recruiter or hiring manager will provide more details during the hiring process. Unfortunately there is no sponsorship for this role. What you'll do Complete open-ended business problems with a strategic lens, offering creative, data-driven solutions. Participate in scoping sessions and delivery meetings with business clients, documenting requirements, objectives, and specifications. Perform analytics using scientific methods that rely upon mathematics, statistics and hypothesis testing. Create and package insights to business stakeholders in a non-technical, easy to understand manner. Querying structured data and reports using SQL, Python or R. Perform data validation to ensure the accuracy of analytical results. Answer questions on dataset types and their limitations. Basic qualifications 2 years of experience in a professional business environment 2 years of experience in business, analytics, or related area 2 years with analytics, reporting and/or database knowledge and experience (using tools, applications and platforms such as SQL, Python or R) 1 year of work experience working with digital/clickstream data 1 year of working experience with analytics tools such as Adobe Analytics, Google Analytics, or equivalent technologies Ability to clearly present and articulate complex ideas Experience collaborating cross functionally with various business teams Preferred qualifications A bachelor's degree in a quantitative or business field (e.g., statistics, mathematics, engineering, economics, management, supply chain, marketing) Proficiency in writing SQL queries to extract, analyze, and manipulate data Experience presenting to various levels within an organization Knowledge of AB Testing methods What you'll do Complete open-ended business problems with a strategic lens, offering creative, data-driven solutions. Participate in scoping sessions and delivery meetings with business clients, documenting requirements, objectives, and specifications. Perform analytics using scientific methods that rely upon mathematics, statistics and hypothesis testing. Create and package insights to business stakeholders in a non-technical, easy to understand manner. Querying structured data and reports using SQL, Python or R. Perform data validation to ensure the accuracy of analytical results. Answer questions on dataset types and their limitations. Basic qualifications 2 years of experience in business, analytics, or related area 2 years with analytics, reporting and/or database knowledge and experience (using tools, applications and platforms such as SQL, Python or R) Ability to clearly present and articulate complex ideas Experience collaborating cross functionally with various business teams Preferred qualifications A bachelor's degree in a quantitative or business field (e.g., statistics, mathematics, engineering, economics, management, supply chain, marketing) Proficiency in writing SQL queries to extract, analyze, and manipulate data Experience with digital clickstream data or marketing measurement data (Marketing Mix models) Experience with tools such as Adobe Analytics, Google Analytics, or similar digital analytics platforms Ability to story tell through data and translate complex information into clear and actionable insights What's in it for you We're committed to helping our people thrive at work and at home. We offer generous benefits that address your total well-being and provide support as you need it, especially key moments in your life. Our benefits include: Competitive pay Generous employee discount Physical and mental well-being support About us As part of the Best Buy team, you'll help us fulfill our purpose to enrich lives through technology. We bring that to life every day by humanizing and personalizing tech solutions for every stage of life - in our stores, online and in customers' homes. Our culture is built on deeply supporting and valuing our amazing employees who make it all possible. We're committed to being a great place to work, where you can unlock unique career possibilities. Above all, we aim to provide a place where you can bring your full, authentic self to work now and into the future. Tomorrow works here.™ Best Buy is an equal opportunity employer.

Quality Control Chemist Responsibilities + Conduct routine and non-routine analysis of raw materials, in-process samples, and finished products to ensure compliance with established specifications. + Perform laboratory tests using analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy. + Validate existing methods and develop new analytical methods as needed. + Document and report test results accurately and promptly. + Investigate and troubleshoot any quality issues that arise during the manufacturing process. + Collaborate with cross-functional teams to ensure quality standards are met. + Maintain laboratory equipment and ensure calibration and validation are up to date. Additional Skills & Qualifications + Bachelor's degree in Chemistry or a related field. + 3-8+ years of industry experience within a FDA regulated environment. + Experience in method development within HPLC or GC. + Experience mentoring or training employees. + Working knowledge of 21 CFR Parts 210 & 211 regulations. + Technical writing skills (SOPs, documents, reports, etc.). Pay and Benefits The pay range for this position is $32.00 - $48.00/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 Chanhassen,MN. Application Deadline This position is anticipated to close on Apr 25, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.

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

This role entails assisting in executing SunOpta's commercial growth plans through the development of new products and adaptation/optimization of existing products to meet the requirements of current and new SunOpta customers. The successful candidate will collaborate with Business Management, FSQ, Sales, Operations, and Supply Chain teams to support business needs for innovation, cost improvement and business essential projects. They will ensure delivery of product development and product improvement projects to meet customer and company needs and specifications and provide R&D/Product development subject matter expertise to the cross functional team. Essential Functions of the Job: * Communicate, collaborate and provide technical support to Business Management, Sales, FSQ, and Manufacturing. * Develop products from concept to production to meet customer specifications and needs. * Responsibilities include product formulation, ingredient sourcing & validation (in cooperation with Procurement), bench top work, and scale up trials across the SunOpta portfolio (plant-based and value-added beverages, barista products, plant- and animal-based broths, BFY fruit snacks). * Ability to manage and complete multiple product development efforts within specified timelines. * Develop products within cost parameters as required. * Execute sensory and shelf-life evaluation as needed on new ingredients and finished products. * Establish finished product specifications (formula, ingredients, nutrition, allergen labeling) on new products and update as needed. * Provide product information and technical support to customers. Supervisory Responsibilities: * None. Minimum Qualifications: * Bachelor's degree in Food Science (preferred), Chemistry, Biology, or related field. * 2 years of industry experience in product development with relevant experience in non-dairy or aseptic beverages, highly desirable. * Knowledge of regulatory, organic, non-GMO and kosher requirements. * Computer proficiency in Windows based programs including MS Word, Outlook and MS Excel. Preferred Qualifications: * Master's degree in Food Science (preferred), Chemistry, Biology, or related field. * Some manufacturing Experience preferred. * Knowledge of Genesis Nutritional programs a plus. Knowledge and Skills: * Candidate must possess a strong working knowledge of Food preparation. * Knowledge of Lean Manufacturing practices is beneficial. * Outstanding verbal, written, multi-tasking and presentation skills. * Ability to create momentum and drive excellence. Featured benefits * Medical insurance * Dental insurance * Vision insurance * Paid Family leave * Paid maternity leave * 401(k) with Match * Voluntary Life, Accident, Critical Illness and Hospital indemnity * Paid Holidays * Tuition assistance * Short-term and Long-term Disability insurance Additional Considerations: * Travel Expectation: Up to 25%. * This position will be at the SunOpta Corporate Office in Eden Prairie, MN. * Relocation or international remote working arrangements (outside of the US) will not be considered. Work Environment/Physical Demands: Approximately; 75% of the work is performed in an office environment. 25% of work may involve being in the agricultural or manufacturing environment. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time, with or without notice.

It's not what we make. It's what we make possible and the possibilities at Lifecore are endless! This full time position offers incredible benefits, a four day work week, and a company culture focused on development and growth which include promotion opportunities. As a Formulation Technician, you will work in an aseptic (cleanroom) environment to operate formulation and filtration equipment. During the course of your shift you will be trained to perform the following: Maintain records and cleanroom environment to comply with regulatory requirements, good manufacturing practices and standard operating procedures Demonstrate proficiency in Clean in Place (CIP)/Steam in Place (SIP) of process vessels and all related processing equipment Follow the process flow work instructions and communicate all processing variations to the supervisor Understand and adhere to the assigned standard operating procedures in the Aseptic area Operate the Water for Injection heat exchangers Qualify to gown for cleanroom entrance Utilize aseptic technique good manufacturing practices Complete batch records as processing steps occurring utilizing good documentation practice To qualify as a Formulation Technician, you'll need the following: High school diploma or equivalent Minimum of 1 year of manufacturing experience preferably in the medical device, pharmaceutical or similarly regulated industry Strong attention to detail and ability to follow processes at all times Willingness to be flexible with a work schedule that may require overtime Have a strong mechanical ability Able to stand for the majority of your shift In addition, it's preferred that you have some post-secondary science and/or technical training, along with previous cleanroom experience Schedule: 1st Shift: Monday - Thursday, 5:00am - 3:30pm Starting Pay: $24.50/hour Lifecore is a growing company and offers a highly competitive total rewards package, including: Opportunities to learn and grow with a well-respected company Competitive compensation with annual reviews and a company-wide incentive bonus Benefits that start the first of the month after you join Lifecore as a full time employee: 3 medical insurance plans to fit your needs and budget including an HSA Plan with a generous company contribution Low cost dental and vision insurance Short term disability, long term disability and life insurance all 100% company paid 3 weeks of PTO in the first year (increases to 4 weeks after just 2 years!) 9 paid company holidays plus 2 personal holidays 4 weeks of paid family leave after 1 year of employment Tuition reimbursement 401k plan with company matching contribution Annual bonus based on company performance Meet Lifecore Biomedical, LLC: Lifecore Biomedical, Inc. (Nasdaq: LFCR) is a fully integrated contract development and manufacturing organization (CDMO) that offers highly differentiated capabilities in the development, fill and finish of sterile injectable pharmaceutical products in syringes, vials, and cartridges, including complex formulations. As a leading manufacturer of premium, injectable-grade hyaluronic acid, Lifecore brings more than 40 years of expertise as a partner for global and emerging biopharmaceutical and biotechnology companies across multiple therapeutic categories.

Analytical Technician will ensure the quality and reliability of products thought physical/chemical testing and evaluation against a defined specification range. Assist and aid in company understanding of cGMP quality systems. Use of proper laboratory practices to evaluate samples of: raw material, stability, in-process samples, finished bulk, and finished product. Responsibilities: * Prepare samples for testing raw materials, longitudinal stability, in-process, and finished products. * Physical and chemical testing in accordance with standard procedures, utilizing wet-chemistry and instrumental techniques. * Operation and maintenance of scientific instruments including but not limited to HPLC, GC-FID, GCMS, TOC, EDX, UV-vis, and FTIR. * Write, review, and execute validations of assay methods. * Maintain accurate, up-to-date and concise laboratory notebooks and records. * Work closely as a team to complete all required tasks in a timely manner. * Monitor product quality to ensure compliance to standards and specifications. * Understand and precisely follow Standard Operating Procedures, global methods, local methods and published standard or compendia methods i.e. USP, ISO, ASTM. * Understand and apply basic laboratory safety instructions, reagent handling precautions, and disposal of chemical waste according to local environmental regulations. * Communicate with other departments regarding production, stability, and other business goals. * Participate in/lead OOS investigations and other issues encountered in the analytical lab. * Maintain inventory of required equipment and consumables. * Manage time and assigned projects effectively Requirements Required Skills/Abilities * Knowledge of laboratory equipment set-up and operation, common laboratory techniques and safe chemical handling * Technical writing, verbal and interpersonal communication skills * Robust analytical knowledge, critical thinking and problem-solving skills * Ability to prioritize multiple responsibilities and manage deadlines accordingly. * Communicate effectively with members of organization and levels of management * Ability to work independently in a fast-paced environment * Willingness to grow and adapt to change and structure. * Proficient knowledge of computers and Microsoft Office. Required Education and Experience * BS degree in Chemistry, Biology or related field Preferred Education and Experience * 0-2 years of experience in a manufacturing and/or Quality Control area * Working knowledge of FDA 21 CFR part 210 and 211 requirements. EEO Statement Bell International Laboratories provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

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 Arden Hill, MN. Support R&D engineers and teams to develop and analyze products, materials, processes, or equipment in a testing environment. This role demands a comprehensive knowledge base and a high level of independence. The position is for product testing. Primary Responsibilities/Accountabilities: Build quality into all aspects of their work by maintaining compliance to all quality requirements. Perform various tasks in electrical, mechanical, and optical areas. Follow protocols, test methods, or verbal instructions. Conduct tests, capture data, and create Excel spreadsheets. Maintain detailed documentation throughout all phases of development, testing, and analysis. Primarily conduct mechanical testing (e.g., pull, flex, torque, extension, retraction, insertion, withdrawal) with some high voltage/current testing, all requiring meticulous setup. Assist in technology transfer and participate in cross-functional discussions on device performance issues. Explore and contribute to testing concepts and test method development. Serve as a resource for other employees. Regularly and thoroughly communicate project status to project teams. Qualifications: AA Degree or equivalent work experience in a related field, with 3+ years of R&D technical support or related experience. Proven ability to set up and conduct product testing and collect data according to medical device standards. Experience in operating and maintaining complex test equipment. Proficiency in Microsoft Word, Excel, and file sharing. Ability to work effectively in a team environment, interacting with engineers and technicians. Strong problem-solving skills. Excellent communication skills. Preferred: Experience in medical device testing. Proven ability to interact with highly technical staff in an engineering lab environment. Prior experience in documenting tests through electronic lab notebooks or reports. Experience in developing test methods and training others. Familiarity with equipment such as Instron, MTS, OGP Smartscope, and Keyence. Testing experience including tensile, torque, and RSU. Recent 4-year degree applicants, such as mechanical/electrical engineers, will not be considered.

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: *************************************************************************************** continues to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Job Description: Product Development Scientist, Hybrid, Maplewood, MN 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you. The Impact You'll Make in this Role As a Product Development Scientist, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: * Leads programs of major importance to the organization's interests and portfolios. * Develops mechanistic understanding of technologies * Cultures adherent mammalian cells and establishes 3D cultures * Cultures and maintains medically relevant bacterial strains * Leads preclinical studies and analyzes data * Develops novel experimental techniques around cellular metabolism and inflammation * Communicates and contextualizes results to management and project teams Your Skills and Expertise * PhD in biological science preferably cell biology, physiology, microbiology or other appropriate discipline AND 5 years industry experience in mammalian cell culturing and monitoring and specific experience with 3D cell culturing of adherent cells OR * Master's degree and 9 years industry experience in mammalian cell culturing and monitoring and specific experience with 3D cell culturing of adherent cells AND In addition to the above requirements, the following are also required: * Expertise in development of novel experimental procedures and metabolic test methods including both 2D and 3D cell models * Expertise in sterile technique and microbial procedures as well as experience in work with medically relevant microbial strains including bacterial cell culturing, proliferation and maintenance of cell lines * Expertise in immunoassays including multiplexed immunoassays * Expertise in testing antimicrobial technologies. * Experience with preclinical models and studies * Good understanding of experimental design, data analysis and technical writing and communication Additional qualifications that could help you succeed even further in this role include: * Experience with basic statistical methods * Experience with design control Work location: * Hybrid - 60% onsite Travel: May include up to 10 % domestic/international Relocation Assistance: 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 Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope. Applicable to US Applicants Only:The expected compensation range for this position is $137,439 - $167,981, 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: *********************************************************************** Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers. Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain *****************. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains. Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. 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. Solventum 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 Solventum 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.

Who We Are Quality Work. Quality Results. Bay West stands at the forefront of the environmental consulting and remediation sector. Our dedication to safety, innovation, and our skilled team has driven us for over fifty years, delivering top-tier environmental consulting, industrial, and emergency response services. At Bay West, you'll be driven to innovate and make a real impact on environmental issues, all while advancing your career in a dynamic and supportive environment. This Opportunity Bay West is seeking a Transportation and Disposal (T&D) Chemist to support our hazardous and non-hazardous waste operations. This role involves waste profiling, lab packing, manifest preparation, and assisting with industrial services and emergency response projects. The ideal candidate will have strong knowledge of waste regulations and hands-on experience in the field. Your Key Responsibilities Perform waste profiling, manifest creation, lab packing and transportation services for hazardous and non-hazardous materials at customer sites. Create and prints manifests, labels, Land Disposal Restrictions, waste profiles, etc. for T&D projects using web-based Waste Management program. Accurately segregate and package hazardous and non-hazardous waste containers according to DOT and EPA regulations Perform waste sampling and waste characterization in the field. Track and store T&D related information in the electronic internal document management system Assist in the management of the 10-day hazardous waste storage trailer. Assists T&D Coordinator daily in developing and documenting transportation and disposal procedures. Assist with Industrial Services (IS) projects including tank cleanings and facility decontaminations/cleanings. When not traveling, be available for one week every six to nine weeks to be part of an on-call Emergency Response (ER) team to clean-up hazardous and non-hazardous material spills, loading, unloading, and decontaminating ER equipment in an efficient and accurate manner. On-call requires that staff stay within one hour of the Bay West office and be prepared to respond 24-7. Communicate effectively with internal and external customers in a courteous and professional manner. Provide open communication with Team Leader on ways to improve Bay West techniques, operations, and functions. Up to 25% out-of-town travel mainly in the Midwest region (ND, SD, IA, WI, MN) Who You Are Required Qualifications High school diploma or equivalent required; bachelor's degree in a science related field preferred Minimum 1-3 years of related field experience including waste transportation and packaging. Valid US driver's license with acceptable driving record required; Class A or B CDL with Hazmat endorsement Comprehensive knowledge of DOT and RCRA Hazardous waste rules and regulations preferred Proficiency using Word and Excel applications Currently have or willing to obtain a 40 Hour HAZWOPER certification Reliable means of transportation on a 24-hour basis Strong interpersonal and communication skills both written and verbal Experience supporting multiple projects on deadline while providing excellent customer service Superb problem-solving skills, time-management, and organizational skills Ability to work independently Willingness to champion changes and improvements Preferred Qualifications Experience with field equipment such as box trucks, lift gates, forklifts, drum carts and pallet jacks. Knowledge of state and federal environmental regulations and laws, including, but not limited to, Minnesota Pollution Control Agency (MPCA) cleanup guidance and United States Environmental Protection Agency (USEPA) Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), and Resource Conservation and Recovery Act (RCRA) Physical Requirements Repetitive motions: frequent standing, walking, lifting, carrying, bending, and grasping Frequently lift 25 lbs. over an 8-hour period, and occasionally up to 50 lbs. for less than one hour Frequent exposure to non-hazardous and hazardous work environments including contaminated air, soil, dust, fumes, smoke and other toxins Ability to work outside in varying conditions, such as high heat, high humidity and extreme cold in remote locations. Ability to read and interpret general documents, safety rules, and Standard Operating Procedures Benefits Bay West offers a comprehensive benefits package available to eligible employees, including but not limited to paid time off, health insurance options, ancillary benefits to support life at all stages, 401(k), employee assistance programs, and subsidies. Bay West is an Equal Opportunity Employer.

Quality Control Chemist Responsibilities * Conduct routine and non-routine analysis of raw materials, in-process samples, and finished products to ensure compliance with established specifications. * Perform laboratory tests using analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy. * Validate existing methods and develop new analytical methods as needed. * Document and report test results accurately and promptly. * Investigate and troubleshoot any quality issues that arise during the manufacturing process. * Collaborate with cross-functional teams to ensure quality standards are met. * Maintain laboratory equipment and ensure calibration and validation are up to date. Additional Skills & Qualifications * Bachelor's degree in Chemistry or a related field. * 3-8+ years of industry experience within a FDA regulated environment. * Experience in method development within HPLC or GC. * Experience mentoring or training employees. * Working knowledge of 21 CFR Parts 210 & 211 regulations. * Technical writing skills (SOPs, documents, reports, etc.). Pay and Benefits The pay range for this position is $32.00 - $48.00/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 Chanhassen,MN. Application Deadline This position is anticipated to close on Apr 25, 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.

Full-time Description Analytical Technician will ensure the quality and reliability of products thought physical/chemical testing and evaluation against a defined specification range. Assist and aid in company understanding of cGMP quality systems. Use of proper laboratory practices to evaluate samples of: raw material, stability, in-process samples, finished bulk, and finished product. Responsibilities: Prepare samples for testing raw materials, longitudinal stability, in-process, and finished products. Physical and chemical testing in accordance with standard procedures, utilizing wet-chemistry and instrumental techniques. Operation and maintenance of scientific instruments including but not limited to HPLC, GC-FID, GCMS, TOC, EDX, UV-vis, and FTIR. Write, review, and execute validations of assay methods. Maintain accurate, up-to-date and concise laboratory notebooks and records. Work closely as a team to complete all required tasks in a timely manner. Monitor product quality to ensure compliance to standards and specifications. Understand and precisely follow Standard Operating Procedures, global methods, local methods and published standard or compendia methods i.e. USP, ISO, ASTM. Understand and apply basic laboratory safety instructions, reagent handling precautions, and disposal of chemical waste according to local environmental regulations. Communicate with other departments regarding production, stability, and other business goals. Participate in/lead OOS investigations and other issues encountered in the analytical lab. Maintain inventory of required equipment and consumables. Manage time and assigned projects effectively Requirements Required Skills/Abilities Knowledge of laboratory equipment set-up and operation, common laboratory techniques and safe chemical handling Technical writing, verbal and interpersonal communication skills Robust analytical knowledge, critical thinking and problem-solving skills Ability to prioritize multiple responsibilities and manage deadlines accordingly. Communicate effectively with members of organization and levels of management Ability to work independently in a fast-paced environment Willingness to grow and adapt to change and structure. Proficient knowledge of computers and Microsoft Office. Required Education and Experience BS degree in Chemistry, Biology or related field Preferred Education and Experience 0-2 years of experience in a manufacturing and/or Quality Control area Working knowledge of FDA 21 CFR part 210 and 211 requirements. EEO Statement Bell International Laboratories provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Salary Description $20/hr - $24/hr