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Job Description Job Title: QC Chemist II Job Description We are seeking a QC Chemist I or II who will ensure the quality and compliance of raw materials and products by performing analytical testing on samples relative to the release of materials and products according to cGMP requirements. Responsibilities • Test purchased materials and/or manufactured products per cGMP requirements., • Document all test data and related information., • Operate laboratory equipment., • Participate in training and development., • Maintain personal laboratory work area and assist with general laboratory cleaning., • Participate in continuous improvement projects as well as internal and external quality audits., • Proficiency in chemistry and laboratory operations., • Experience with wet chemistry techniques., • 1-3 years of hands-on in-lab experience., • Knowledge of HPLC., • Bachelor's degree in chemistry, biochemistry, or related field., • 1-3 years of industry experience within a chemistry lab. The QC Chemist II will be part of Team B within the QC Chemist department, which includes three teams. The role involves 70% laboratory work and 30% desk work. This position offers shift flexibility with a focus on first shift hours, and holiday pay is provided. Team members will have the opportunity to be trained on analytical equipment, particularly HPLC, even without previous experience. Job Type & Location This is a Contract position based out of Minneapolis, MN. Pay and Benefits The pay range for this position is $27.00 - $32.00/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 Feb 25, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionHPLC Chemist (Multiple Levels Available) Job Description The Chemist will primarily work with HPLC in a regulated environment. This includes sample preparation, instrument operation, and data analysis. Additional Skills & Qualifications • Hands-on experience with HPLC operation and troubleshooting., • Bachelor's degree required. Access to the company's internal benefits, PTO structure, 401k, etc. Workplace Type This is a fully onsite position in St Paul,MN. Application Deadline This position is anticipated to close on Mar 3, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description Job Title: QC Chemist II Job Description We are seeking a QC Chemist I or II who will ensure the quality and compliance of raw materials and products by performing analytical testing on samples relative to the release of materials and products according to cGMP requirements. Responsibilities • Test purchased materials and/or manufactured products per cGMP requirements., • Document all test data and related information., • Operate laboratory equipment., • Participate in training and development., • Maintain personal laboratory work area and assist with general laboratory cleaning., • Participate in continuous improvement projects as well as internal and external quality audits., • Proficiency in chemistry and laboratory operations., • Experience with wet chemistry techniques., • 1-3 years of hands-on in-lab experience., • Knowledge of HPLC., • Bachelor's degree in chemistry, biochemistry, or related field., • 1-3 years of industry experience within a chemistry lab. The QC Chemist II will be part of Team B within the QC Chemist department, which includes three teams. The role involves 70% laboratory work and 30% desk work. This position offers shift flexibility with a focus on first shift hours, and holiday pay is provided. Team members will have the opportunity to be trained on analytical equipment, particularly HPLC, even without previous experience. Job Type & Location This is a Contract position based out of Minneapolis, MN. Pay and Benefits The pay range for this position is $27.00 - $32.00/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 Feb 25, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description About LTS: LTS Lohmann is a premier, global Contract Development and Manufacturing Organization (CDMO) and partner the pharma industry trusts most to deliver innovative oral, transdermal, and intradermal drug delivery systems. From concept to market, launch to lifecycle management, we deliver single source oral and transdermal drug delivery solutions that power partners’ market advantage. Every one of our 2,000 plus members of the LTS family, across three continents, is focused on utilizing our collective strength and innovation to explore new therapeutic opportunities, maximize partner value and improve patient outcomes. We Care. We Create. We Deliver. Job Summary: As an R&D Chemist at LTS Lohmann, you will play a crucial role in supporting product development and ensuring analytical compliance within our cGMP/cGLP laboratory environment. This is a full time, role located in West St. Paul, MN. What You Will Do: • Conduct analytical testing and analysis to support product development and revenue growth., • Ensure adherence to QbD standards and regulatory requirements., • Provide analytical support for key performance indicators (KPIs) and scale-up activities., • Develop, optimize, and scale up analytical methods for various dosage forms., • Create and review technical documentation, including analytical method development reports and standard operating procedures., • Bachelor's degree in a relevant science field with 1-3 years of experience., • Experience in a cGMP or cGLP laboratory environment., • Knowledge of analytical techniques, including HPLC (GC, dissolution & stability testing experience preferred)., • Proficiency in chromatographic software (Empower 3 strongly preferred)., • Excellent analytical, technical writing, communication, and data management skills., • Ability to design and execute experimental studies, analyze data, and author/review protocols and reports., • Strong problem-solving and troubleshooting skills for analytical instrumentation., • Understanding of cGMP, cGLP, USP, and regulatory requirements for pharmaceuticals. Preferred Skills: • 2-3 years’ experience in the FDA drug/pharmaceutical industry, • Demonstrated in-depth scientific knowledge & experience in analytical method development, & validation, • Experience in the development of pharmaceutical dosage forms and polymeric drug delivery systems with emphasis in transdermals., • Experience in statistical data analysis and QbD principles, • Competitive compensation and benefits package, • Opportunities for professional growth and development, • A collaborative and supportive work environment, • The chance to contribute to improving patient lives If this sounds like you, we want to hear from you! LTS is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Job Description What is IP Corporation: At IP Corporation, we empower you to make a difference, learn new skills, and achieve your goals. We’re committed to providing rewarding career opportunities, and we’re always looking for talented individuals to join our team. IP Corporation has been a supplier to the composites industry for over four decades. With our four subsidiaries (Interplastic, North American Composites, Molding Products and HK Research), we are uniquely positioned to meet the needs of our diverse customers. More than ever, our commitment to becoming the finest supplier and distributor of resins, gel coats and composite materials in our industry still stands. What you'll do at IP Corporation as a Sr. Chemist: This position is responsible for developing unsaturated polyester and vinyl ester resins for use in fiber reinforced plastics. This position also plays a key role in the development and improvement of polyester and vinyl ester processing and has responsibility for projects that lead to product qualification by the customer and implementation of technology transfer to manufacturing. What you’ll bring to IP Corporation: • BS/BA Degree in chemistry, polymer, or material science., • 5 + years of industrial R&D experience within a manufacturing setting., • Knowledge and practical experience in project management, experimental design, and other problem-solving methodologies., • Ability to travel 10%, • Experience with polymer synthesis, characterization of polymers and composites, and knowledge of surface science., • Experience in polymer characterization by physical and chemical methods., • Knowledge of unsaturated polyesters and vinyl esters or other similar thermoset resins and coatings., • Knowledge of fillers and additives used in the formulation of composite materials., • 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 of 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 neat and orderly to maximize employee efficiency and productivity., • Accurate and timely record-keeping, with recommendations for further laboratory efforts. Join our team and make a lasting impact on our business by empowering our teams through technology. If you’re ready to bring your expertise to a collaborative and energized environment, we’d love to hear from you! 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 as well as profit sharing, #LI-IPCORP

Job Description Job Title: Chemist Type: Contract - 12 Months Pay: $27.00-$32.00/hr Location: Minneapolis, MN We are looking for a Chemist I - Exempt for a very important client. Responsibilities may include the following and other duties may be assigned. Entry level role with responsibility for performing a variety of routine and non-routine tasks in a regulated laboratory environment in order to support, as well as help develop, pharmaceutical platforms. The chemist I will work in conformance with company policies and current Good Lab Practices (GLP), regulatory requirements and standards to meet quality and accuracy requirements. Individuals will perform procedures for process / analysis, and assist their manager and peers with routine and non-routine Quality Control and Research procedures. A Day in the Life Complies with all quality system requirements Performs preparation, collection, measurement and recordkeeping of samples Documents test and data analysis results Participates on cross-functional teams for continuous improvement activities Communicates with team members to ensure schedule requirements are met Applies knowledge of performed tasks to elucidate test method failures Analyzes and deduces data and collates test results Communicates priority and timeliness for completion of customer requests Helps drive the team to meet business goals Supports development area as needed / commercial QC release Learns and understands the manufacturing organization that the lab supports Responsibilities may include the following and other duties may be assigned. Conducts exploratory research to produce new knowledge and potential products; conceives, organizes, promotes, and executes ideas and plans to increase chemistry's role in and contribution to the discovery and chemical approaches to meet exploratory objectives in product discovery. Develops research proposals to provide a technically and economically sound basis for developing and evaluating new or improved products, synthetic methods, processes, and analytical and physical testing techniques. Recommends utilization of the results or changes in the scope of work or termination of projects. SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University). DIFFERENTIATING FACTORS Autonomy: Entrylevel individual contributor on a project or work team. Works with close supervision. Organizational Impact: Delivers work of limited scope, typically smaller, less complex projects or related activities. Innovation and Complexity: Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex. Makes minor changes in systems and processes to solve problems . Communication and Influence: Communicates primarily with internal contacts within immediate group. Contacts others to gather, confirm and convey information. Leadership and Talent Management: N / A job at this level is focused on selfdevelopment The ideal candidate will possess the following: Minimum requirements: Bachelor’s Degree in Chemistry, Biology or related technical discipline with a 0 years of laboratory experience. The employee must be able to stand/sit/walk up to 8 hrs/day, perform experiments at bench height, perform light lifting / bending or stretching to support test apparatus setup or teardown, and use computer and phones to participate in meetings. Nice to have: General wet chemistry laboratory techniques and/or experience with liquid chromatography (UPLC/HPLC), gas chromatography (GC), dissolution (Apparatus 2, Apparatus 7), Karl Fischer, and FT-IR, UV-Vis. Experience with chromatography software (Empower). Microsoft Word and Excel skills. The ability to work in a laboratory with solvents and pharmaceutical substances. Solid technical ability, experience with equipment set up, and troubleshooting skills. Required Knowledge and Experience: Requires broad theoretical job knowledge typically obtained through advanced education. Requires a University Degree, 0 years of experience required. HM's Top 3: General wet chemistry Experience with GMP/cGMP Chromatography (HPLC/UPLC/GC) Education Required: Bachelor’s degree in chemistry, biology, or related technical discipline

Job DescriptionICP - Chemist 1st Shift: Monday - Friday | DIRECT PLACEMENT | Offers Benefits Job Description The Chemist will primarily work with ICP-MS, ICP, Mercury Analyzers, and Atomic Absorption instruments. This role requires a high level of proficiency in operating and troubleshooting ICP-MS. The Chemist will conduct analyses in compliance with EPA 200.7/6010 and/or EPA 200.8/6020 standards, adhering to TNI regulations. Responsibilities include managing sample processing and scheduling tests to maintain holding times and company-defined turnaround times within the metals department. Responsibilities • Perform and document daily standardization, calibration, and performance verifications on ICP and ICP/MS., • Complete daily run data by batch, including supporting data packets., • Utilize computer software to prioritize work, track samples, acquire data, perform calculations and statistical analysis, and store data to meet established deadlines., • Conduct review of analytical sample preparation data, checking for completeness, calculation accuracy, and data quality coherence., • Perform and interpret required QA/QC procedures; recommend, perform, and document corrective actions and possible impacts to data quality., • Troubleshoot instrument problems, perform routine maintenance, and consult with vendor technicians when necessary., • Demonstrate proactive commitment and adherence to industry and company safety regulations and procedures., • Manage completion of regular training and demonstration of capabilities for staff according to quality policies under the direction of the QA department., • Ensure investigation reports and internal/external audit findings are completed on time., • Manage inventory needs, assist in ordering supplies, and maintain stock of necessary components, supplies, standards, and reagents., • Train coworkers in sample preparation and analysis, instrument operation and maintenance, troubleshooting techniques, and data quality objective adherence., • Provide feedback to the Lab Manager, Quality Assurance Manager, and/or Project Managers about analysis, data, or other issues., • Ensure department-specific Standard Operating Procedures are reviewed and updated on time., • Process electronic data using procedures that ensure data integrity and security., • Hands-on experience in ICP-MS/ICP operation and troubleshooting., • 3+ years of ICP-MS experience., • Bachelor's degree required. The work environment is a high throughput lab, not R&D based, with the metals lab being the fastest growing department currently. The facility is newly remodeled, spanning 20,000 square feet, and is known for its cleanliness and beauty. The company has quadrupled in size in the last three years and is family-owned, valuing its employees and fostering a great work culture. Job Type & Location This is a Permanent position based out of Minneapolis, MN. Pay and Benefits The pay range for this position is $45000.00 - $70000.00/yr. Access to the company's internal benefits, PTO structure, 401k, etc. Workplace Type This is a fully onsite position in Minneapolis,MN. Application Deadline This position is anticipated to close on Feb 28, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionDescription: A Senior Research and Development Chemist is an experienced researcher/formulator who combines technical knowledge and innovation when formulating a variety of personal care products, cosmetics and OTC (lip balms and sunscreens) from concept to finished product based on customers’ requests. Shows the ability to look at different brands’ gaps and develop products based on those gaps or customer specification. The Senior R&D Chemist II demonstrates strong leadership and communication skills that are utilized within the organization and with external customers. Requirements: Responsibilities • Responsible for initiating project concepts, developing objectives, planning and assigning priorities, and completing multiple projects under minimal supervision., • Independently investigate/resolve research problems/scale up issues., • Ability to communicate with customers on technical aspects as well as regulatory and performance., • Utilize and follow relevant legal requirements, regulations and product development standards., • Determine and perform appropriate cost reductions (raw materials)., • Scale-up of approved formulations, to include identification of critical process variables., • Ability to troubleshoot production issues and address batch variations., • Set product specifications and write compounding procedures., • Supervise and coordinate pilot batches., • Provide paperwork for new formula and new raw materials to operations., • Provide specifications and other information to QC to receive and test new ingredients and finished goods., • Test stabilities and monitor testing statuses., • Research product formulations and properties and interactions of raw materials., • Vendor research for raw materials., • Compose and check ingredient lists, QQs and artwork, • Interpret results of laboratory findings and assess risks involved in new products and communicate findings to sales and upper management., • Remain up to date and current on trends in the retail market and trends on formulations materials, ingredients, etc., • Training and supervising lab staff (permanent and temporary)., • Notebook documentation, • Other duties as assigned. Required Skills/Abilities • Working knowledge of laboratory equipment set-up and operation, common laboratory techniques and safe chemical handling, • Advanced formulation skills and technical knowledge, • Thorough understanding of FDA regulations and cGMP’s, • Excellent written, verbal and interpersonal communication skills, • High level of initiative, innovation, critical thinking and problem-solving skills, • Ability to work cross-functionally & at all levels within the organization including senior leadership, • Ability to prioritize multiple responsibilities and manage deadlines accordingly., • Communicate effectively and professionally with clients and vendors, • Exceptional attention to detail and high level of accuracy & organization, • Ability to work as part of a team and excel independently in fast-paced environment, • Ability to adapt quickly to changing policies and procedures, • Demonstrated leadership skills, • Proficient with Microsoft Office Required Education and Experience • BS in Chemistry, Cosmetic Science, Physical Chemistry, Chemical Engineering or related sciences with 8+ years of formulating personal care products, • -OR- advanced degree in cosmetic chemistry and more than 6 years’ experience. Preferred Education and Experience • Master’s Degree in Chemistry, Cosmetic Science, Chemical Engineering or related field, • 10+ years of experience in formulation of personal care products 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.

Job DescriptionAnalytical Chemist (3+ ICP-MS Experience Needed, ideally in water/soil/metals testing environment) Job Description We are seeking a highly skilled ICP-Chemist who will primarily work with ICP-MS, ICP, Mercury Analyzers, and Atomic Absorption equipment. The ideal candidate will be proficient in operating and troubleshooting ICP-MS instruments. Responsibilities • Perform and document daily standardization, calibration, and performance verifications on ICP and ICP/MS instruments., • Complete daily run data by batch, including supporting data packets., • Utilize computer software to prioritize work, track samples, acquire data, perform calculations and statistical analysis, and store data to meet established deadlines., • Ensure investigation reports and internal/external audit findings are completed on time., • 3+ years of experience with ICP-MS, including operating and troubleshooting. Access to the company's internal benefits, PTO structure, 401k, etc. Workplace Type This is a fully onsite position in St Paul,MN. Application Deadline This position is anticipated to close on Feb 26, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

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We provide science-driven, independent testing, inspection, certification, and advisory services and develop the very standards that drive the food, water, and life sciences industries worldwide. With a legacy spanning more than 80 years, NSF leverages science and innovation to improve human and pla

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Bachelor's degree or higher in social science, environmental studies, or related fields with relevant coursework in social science research methods. The Evaluation and Social Science Researcher will apply their research expertise to gauge the effectiveness of our market transformation initiatives an

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Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. The Medical Science Liaison (MSL) is a member of a field-based team of scientists who function as an extension

The ideal candidate should have 8-10+ years in Data Science, experience in deploying high-impact solutions, and proficiency in Python and Snowflake.

Role Overview** Mercor is partnering with a leading AI lab to engage independent Data Science Experts for diverse research and development initiatives. Ideal Qualifications** - 3+ years of experience in data science, machine learning, or a related analytical field. Proficiency in Python and key

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