Chemist jobs in Minnesota

**Why Mayo Clinic** Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans (************************************** - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. **Benefits Highlights** + Medical: Multiple plan options. + Dental: Delta Dental or reimbursement account for flexible coverage. + Vision: Affordable plan with national network. + Pre-Tax Savings: HSA and FSAs for eligible expenses. + Retirement: Competitive retirement package to secure your future. **Responsibilities** The PET Radiochemist is responsible for the daily production and quality control of routine PET drugs. The PET RC assists in the synthesis of PET radiopharmaceuticals for clinical and research studies. The PET Radiochemist will also be responsible for completing and maintaining the appropriate documentation required by federal and state agencies associated with the production and distribution of the PET drug product/radioisotopes. The PET Radiochemist will help in set up and maintain automated chemistry modules and other laboratory equipment and the development of synthesis procedures in the production of PET radiopharmaceuticals/radioisotopes and will provide instruction and training to other radiochemistry staff as needed. PET Radiochemist - quality control: - Responsible for daily quality control of routine PET drug products - Responsible for setup and use of analytical chemistry equipment - Responsible for assessing suitability of incoming materials - Responsible for determining acceptability of productions for release - Responsible for retrospective testing on productions post-release - Responsible for quality control method validation and post repair instrument verification. PET Radiochemist - quality assurance: - Responsible for qualification and monitoring of all vendors and suppliers. - Responsible for the accuracy and upkeep of documentation used in all aspects of the facility - Responsible for ensuring adequate training of all PET Radiochemists - Responsible for conducting regular internal audits and self-inspections - Involved in deviation/OOS and CAPA investigations - Reviews and approves change control events and processes. **This vacancy is not eligible for sponsorship/we will not sponsor or transfer visas for this position. Also, Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program.** **Qualifications** + Bachelor's degree in chemistry or nuclear medicine technology certification, or pharmacy certification. + Must have a strong background in analytical chemistry, preferably organic chemistry. + Experience working with radioactivity such as in a PET radiochemistry laboratory, nuclear medicine environment, or commercial nuclear pharmacy specializing in PET drug production. + Strong word processing and database skills specifically with Microsoft Word and Excel. **Additional Qualifications:** + Two years' experience in production, manufacturing and handling PET drug products is preferred. + Experience assisting in the development of PET drug synthesis procedures is preferred. + Prior experience teaching, training, group interaction and presentations. **Exemption Status** Nonexempt **Compensation Detail** $41.48 - $62.25 / hour **Benefits Eligible** Yes **Schedule** Full Time **Hours/Pay Period** 80 **Schedule Details** Monday to Friday shift. Details TBD. **Weekend Schedule** No. **International Assignment** No **Site Description** Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is. (***************************************** **Equal Opportunity** All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the "EOE is the Law" (**************************** . Mayo Clinic participates in E-Verify (******************************************************************************************** and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. **Recruiter** Stephanie Brackey **Equal opportunity** As an Affirmative Action and Equal Opportunity Employer Mayo Clinic is committed to creating an inclusive environment that values the diversity of its employees and does not discriminate against any employee or candidate. Women, minorities, veterans, people from the LGBTQ communities and people with disabilities are strongly encouraged to apply to join our teams. Reasonable accommodations to access job openings or to apply for a job are available.

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. Salary Description $90k/yr - $110k/yr

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 ************ *******************************

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Employee Responsibilities: * Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, aerosols, liquids, creams, and gels) * Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus * Preparing samples for analysis and running some instrumentation with minimum supervision * Set up and validate new analytical or related processes used by the department * Prepare standards and samples for analysis * Execute method transfer protocols * Document work as required for GMP compliance * Perform monthly maintenance of laboratory equipment Qualifications EDUCATION and/or EXPERIENCE: * Bachelor's degree in chemistry or other related degree concentration, or equivalent directly-related experience * Authorization to work in the United States indefinitely without restriction or sponsorship * Must be able to speak well to technical lab skills Additional Information Position is full time, Monday to Friday, 3PM - 11PM. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

We are looking to fill a **Scientist II or III - Metrology Specialist** position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer sponsorship.** **Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment** . This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement **Qualifications -** B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline + **Scientist II** - B.S. with 1-2 years of relevant experience or M.S. with 0-1 years of relevant experience + **Scientist III** - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience **Responsibilities** + Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation + Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships + Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or perform maintenance or calibration activities + Participate in computer system validation activities associated with new or upgraded equipment or software packages + Support the purchase, installation, and equipment qualification of new laboratory equipment + Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support + Originate and progress Notice of Event (NOE) and Change Management (CM) records + Perform and document investigations and assist in developing/implementing CAPA plans + Represent the laboratory on all aspects of laboratory equipment during audits + Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures **Required Skills and Experience** + Experience working within a regulated (GMP) laboratory + **Experience maintaining or operating laboratory equipment including HPLCs, GCs, UVs, dissolution systems, or other specialized computerized systems** + Familiarity with standalone computer system validation requirements + Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks + Capable of working independently under moderate supervision + Strong verbal and written communication skills + Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators **Desired Skills and Experience** + Experience with maintenance of analytical instrumentation such as HPLC, UPLC, GC, UV, IR, Karl Fischer, and dissolution with ability to troubleshoot them. + Experience with computerized standalone systems GMP validation requirements + Familiarity with authoring relevant instrument standard operating procedures (SOPs) **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Responsible for the performance of tasks associated with preparing, testing, packing and inspecting all chemical wastes in accordance with Company policies and procedures while at the client site. What does it take to work for Clean Harbors? * High School diploma * Valid driver's license * Prior chemical handling experience or chemistry knowledge preferred * BS/BA in Chemistry, Biology, or Environmental Science a plus; * Willingness to complete a background check, drug test, and physical. To learn more about Clean Harbors, and to view and apply online for exciting opportunities in our company, visit us at ********************************* Clean Harbors is the leading provider of environmental, energy, and industrial services throughout the United States, Canada, Mexico, and Puerto Rico. Our mission is to create a safer, cleaner environment through the treatment, recycling, and disposal of hazardous materials. Come help us save the world! Clean Harbors is an equal opportunity employer. Clean Harbors is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation, contact ******************** or **************. Clean Harbors is a Military & Veteran friendly company. Clean Harbors is committed to complying with applicable pay transparency laws and ensuring fair and equitable compensation. The posted salary range reflects the minimum and maximum target for this role. Final compensation may vary based on factors such as location, experience, skills, and business needs. In addition to the base salary, some roles may be eligible for bonus or incentive compensation and a comprehensive benefits package. * CH InSite Chemists perform a wide range of tasks, including: * Making waste pickups at labs as needed * Packaging and labeling waste products and other materials * Identifying unknown chemicals when they are encountered * Performing inspections of staging, accumulating, and storage areas to ensure proper housekeeping procedures and compliance * Collect, segregate, and properly package waste chemicals for efficient and compliant disposal * Overall quality control of waste materials being stored and shipped * Completing required manifests and tracking paperwork * Utilizing CHOICE waste management software to efficiently and accurately manage waste programs. This position is an entry level role, but many of our leaders started in this job! With safety as our top priority, you'll get the training and support to not only succeed at your job but advance your career.

Local Candidates only INTERPLASTIC CORPORATION is the leading manufacturer of unsaturated polyester, vinyl ester and specialty resins, gel coats, colorants and putties under the CoREZYN and Silmar brand names for the composites, cast polymer, and solid surface industries. As a pioneer of cutting-edge technology, we grow to meet the needs of the composites industry. In addition, all of our manufacturing facilities and research and development laboratories are ISO 9001:2015 and ISO 14001:2015 certified. Position Summary: 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. What you can expect to do in this role as a Chemist: 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 product 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 conditions to permit maximum employee efficiency and productivity. Accurate and timely record-keeping, with recommendations for further What we're looking for in a Chemist: BS/BA Degree in chemistry, polymer or material science, or chemical engineering; an advanced degree is preferred. Exceptional interpersonal and communication skills. Knowledge and practical experience in project management, experimental design and other problem-solving methodologies. Industrial experience. Must be able to lift 50 pounds and must be able to pass a Respirator Test. Experience with polymer synthesis, characterization of coatings, and knowledge of surface science is preferred Product development experience in the manufacturing industry. Experience in polymer characterization by physical and chemical methods. Knowledge of gel coats, colorants, and thermoset polyesters or vinyl esters. Knowledge of fillers and additives used in the formulation of composite materials. Knowledge of the cured in place pipe process or trenchless technology. Why IP Corporation? Positive, challenging and supportive work environment. Competitive benefits, including dental, vision, generous PTO, 401(k)with company match and more. Freedom to innovate and make a difference in a vibrant, values-driven company that cares about its people. IP Corporation is an equal opportunity employer and encourages diversity in the workplace. If you are an experienced Chemist with a strong background in manufacturing, we encourage you to apply and join our team!

If you are a Chemical Engineer looking for an exciting opportunity, join Emerson's Liquid Analysis team! Based at our Shakopee, MN location, you will join a global leader in the development and manufacturing of process analytical equipment for liquid analysis as a Chemist. This is a laboratory-based role that works within a cross-functional engineering teams to support new technology development, new product development and sustaining engineering efforts. In This Role, Your Responsibilities Will Be: Support testing activities for new technology research, new product development and sustaining engineering. Work and collaborate within cross-functional engineering team to formulate test goals and plans. Execute laboratory testing, analyse data, document and communicate test results. Maintain laboratory safety by safely handling chemicals and developing safe testing procedures. Participate in product development reviews, quality reviews, design reviews and peer reviews. Initiates routine engineering change authorizations. Who You Are: You make new connections and build relationships in other areas and teams. You adjust communication to fit the audience and the message. You break down objectives into appropriate initiatives and actions. For This Role, You Will Need: Bachelor's degree in Chemistry or related fields Zero (0) years of related experience Legal authorization to work in the United States Preferred Qualifications That Set You Apart: Hands-on laboratory experiences Knowledge of analytical chemistry and electrochemical sensors Experience of working and communicating in cross-functional teams Attention to detail Our Culture & Commitment to You: At Emerson, we prioritize a workplace where every employee is valued, respected, and empowered to grow. We foster an environment that encourages innovation, collaboration, and diverse perspectives-because we know that great ideas come from great teams. Our commitment to ongoing career development and growing an inclusive culture ensures you have the support to thrive. Whether through mentorship, training, or leadership opportunities, we invest in your success so you can make a lasting impact. We believe diverse teams, working together are key to driving growth and delivering business results. We recognize the importance of employee wellbeing and know that to do your best you must have flexible, competitive benefits plans to meet you and your family's physical, mental, financial, and social needs. We provide, a variety of medical insurance plans, with dental and vision coverage, Employee Assistance Program, profit sharing retirement, tuition reimbursement, employee resource groups, recognition, and much more. Our culture prioritizes work-life balance and offers flexible time off plans, including paid parental leave (maternal and paternal), vacation and holiday leave. Our training programs and initiatives focus on end-to-end development, from onboarding through senior leadership. We provide a wide range of development opportunities, including face-to-face and virtual training, mentorship and coaching, project management, and on-the-job training. Our compensation philosophy is simple: we pay a competitive base salary, within the local market in which we operate, and reward performance during our annual merit review process. The starting salary for this role is $70,000-$74,000 annually, commensurate with the skills, talent, capabilities and experience each candidate brings to a role. Learn more about our Culture & Values. #LI-MS11

Job Description Principal Formulation Chemist Duke Cannon Supply Co. is a growth-oriented CPG company that operates with an entrepreneurial mindset - and has become one of the fastest-growing brands in the men's grooming category. Our mission is to better the day of hard-working men, and we fulfill this mission through both the products we build and the conversations we create. We have ambitions to become a household brand by taking share from large national players while having fun and giving back to veterans (our cause). We're looking to hire smart, fun, and wildly talented folks to join us on our journey. We are currently seeking applicants for the role of Principal Formulation Chemist. This position will be responsible for all lab operations, new formula creation and associated testing, line extensions, formula and new ingredient research, documentation, and commercialization with internal and external partners. This role will lead products from ideation through launch and beyond, with heavy involvement in formulation, research, and scale-up activities. Successful candidates will have a proven track record of in-market formulations, formulation technical acumen across multiple product forms (surfactant experience required), the ability to work independently, plan strategically, pivot quickly, and build strong partnerships. PRIMARY RESPONSIBILITIES: Formulation & Development: Formulate in-house fragrance line extensions, innovation projects, reformulations, second source ingredient qualifications (cost-op), and assist in smooth technology transfers to meet critical deadlines, cost targets, and established product aesthetics/performance parameters. Partner closely with TPMs to ensure seamless launches. Research & Innovation Pipeline: Drive brand growth through regular research and evaluation of new product and ingredient technologies within the competitive, raw material, and technological landscape. Attend conferences, seminars, etc., as opportunities arise. Leverage available resources (analytics, internal SMEs, consumer panels, etc.) to deepen Duke Cannon's understanding of competitive landscape and innovate our BIGGEST bets yet. Product Evaluation: Evaluate formulas through various sensory or consumer testing methods to determine aesthetic and performance fitness versus established product pillars and benchmarks. Testing & Scale-Up: Coordinate and execute product testing, ensuring products meet minimum testing requirements (PET, stability, HRIPT, heavy metals & 1, 4-Dioxane levels, etc.). Facilitate smooth transition of products from lab to production scale with manufacturing partners. Attend pilot and first production batches at TPMs to ensure they are executed with excellence and positioned to sustain brand growth. Laboratory Operations: Responsible for lab equipment maintenance and calibration, ingredient management, lab SOP management, workflow, and daily lab functionality. Document Management: Ensure product documentation is accurate and complete in advance of each launch. Partner with Quality/Regulatory to ensure all requirements and deadlines (eg: WERCS listing) are met. QUALIFICATIONS: Bachelor's degree in chemistry, biology, engineering, or related field. 10+ years of experience in a dynamic CPG formulation role, specifically in the personal care industry. Experience formulating across multiple product forms, including surfactants (deep surfactant knowledge a MUST), emulsions, hot pours, hydroalcoholics, OTCs. Color matching experience preferred, but not essential. Technical expertise to solve complex formulation issues. Proven experience commercializing multiple consumer product goods. Collaborative communication and interpersonal skills. Creative thinker with a strategic approach to decision-making. Ability to manage multiple projects simultaneously and meet tight deadlines. Experience with controlled document systems. COMPANY CULTURE Duke Cannon Supply Co. offers a fast-paced environment where decisions are vetted quickly, and opportunities are relentlessly pursued. We work hard, but we value flexibility as well. We have an informal culture with an emphasis on having fun (we sell soap, after all), though we have the most fun when we exceed our goals. The company's leaders are dedicated to the growth and development of the team; as such, we want to ensure that our people have a rich and rewarding experience with unique opportunities to grow. Duke Cannon Supply Co.'s Main Lodge (aka the office) is in Minneapolis' North Loop, one of the city's most vibrant and walkable neighborhoods, with award-winning restaurants, fashionable boutiques, live music and Major League Baseball just steps away. SALARY AND BENEFITS Duke Cannon offers a competitive market salary and bonus based on role and professional experience. The salary range for this role is $100,000 - $125,000. Our benefits are top-notch and include health & dental insurance, HSA and 401k programs supported by regular company contributions, a tuition reimbursement program, and monthly parking stipend. We also host monthly moments of Team camaraderie ranging from community service events to social hours in the Main Lodge (aka the office) to Lunch & Learns covering business, team, and industry topics. Duke Cannon provides equal access to and opportunity in employment without regard to race, color, creed, religion, national origin, gender, age, marital status, disability, public assistance status, veteran status, sexual orientation, gender identity, or gender expression. Powered by JazzHR zijd ZbISFq

Rovensa Next is the Rovensa Group's global business unit, specialising in biosolutions for agriculture. It is made up of twelve pioneering Rovensa Group companies: Agrichembio, Agro-K, Agrotecnología, Cosmocel, Idai Nature, Microquimica, MIP Agro, Oro Agri, OGT, Rodel, SDP and Tradecorp, with a consolidated background in sustainable crop nutrition and biocontrol management. Rovensa Next combines local technical knowledge, innovation and teams that work alongside farmers and distributors in the field to solve their sustainability challenges, backed by the global expertise and leadership of the Rovensa Group. It is aimed to shape a sustainable future for agriculture and drive its biotransformation. When you join Rovensa Next you are not just joining a dynamic team of people gearing up to create a sustainable future - you are joining a team that is intent on making it a reality. Let's grow greener! ******************** Responsibilities Formulations & Process Development Lead the development of new formulations and product improvements from concept through commercialization, aligned with company strategy. Conduct process development and stability studies, ensuring scalability and successful pilot trials before commercial launch. Support manufacturing launches of new products, including the preparation of experimental samples for external research partners. Partner with Operations and Industrialization teams to drive process improvements and prepare technical documentation for quality and safety. Validate raw materials and adjust formulations to ensure compliance and optimize performance. Provide technical expertise to R&D, Quality, Regulatory, Manufacturing, and Commercial teams. Operate a variety of processing equipment (e.g., mixers, mills, weighing systems). Laboratory Management & Safety Oversee laboratory operations, ensuring proper equipment maintenance and compliance with good laboratory practices. Ensure safe chemical handling and PPE usage, developing SOPs in collaboration with the Safety Officer. Maintain adequate inventory of raw materials, chemicals, and active ingredients, working closely with Procurement. Occasionally handle larger product quantities (e.g., 50 lb bags). Documentation & Reporting Maintain accurate formulation records in line with global R&D requirements. Prepare reports and present findings regularly to international teams and management through written updates, presentations, and virtual meetings. Requirements Master's degree in Chemistry or related field (PhD a plus). Minimum 10 years' experience in agricultural product formulation and development. Strong knowledge of plant nutrition, biostimulant, and/or biological formulations. Familiarity with agrochemical applications and general agricultural practices. Hands-on experience with FTIR, ICP, LC/LCMS, GC, and CHN/S analyses preferred. Excellent written and verbal communication in English; Spanish or Portuguese is an advantage. Proven ability to deliver results within a matrix organization and collaborate effectively with international teams. Proficiency in Microsoft Office and SharePoint. Strong analytical, organizational, and time-management skills, with high attention to detail. Resilient, proactive, and collaborative mindset. Willingness to travel locally and occasionally internationally. Please note that Rovensa Group does not assume responsibility for the legalization process of employees applying for positions in countries outside their current workplace. Employees interested in applying for international positions must ensure that they meet all the legal and immigration requirements for the country in question. If local support is available for the relocation process, the recruitment team will provide specific details to candidates during the hiring process.

The PET Radiochemist is responsible for the daily production and quality control of routine PET drugs. The PET RC assists in the synthesis of PET radiopharmaceuticals for clinical and research studies. The PET Radiochemist will also be responsible for completing and maintaining the appropriate documentation required by federal and state agencies associated with the production and distribution of the PET drug product/radioisotopes. The PET Radiochemist will help in set up and maintain automated chemistry modules and other laboratory equipment and the development of synthesis procedures in the production of PET radiopharmaceuticals/radioisotopes and will provide instruction and training to other radiochemistry staff as needed. PET Radiochemist - quality control: • Responsible for daily quality control of routine PET drug products • Responsible for setup and use of analytical chemistry equipment • Responsible for assessing suitability of incoming materials • Responsible for determining acceptability of productions for release • Responsible for retrospective testing on productions post-release • Responsible for quality control method validation and post repair instrument verification. PET Radiochemist - quality assurance: • Responsible for qualification and monitoring of all vendors and suppliers. • Responsible for the accuracy and upkeep of documentation used in all aspects of the facility • Responsible for ensuring adequate training of all PET Radiochemists • Responsible for conducting regular internal audits and self-inspections • Involved in deviation/OOS and CAPA investigations • Reviews and approves change control events and processes. This vacancy is not eligible for sponsorship/we will not sponsor or transfer visas for this position. Also, Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program. Bachelor's degree in chemistry or nuclear medicine technology certification, or pharmacy certification. Must have a strong background in analytical chemistry, preferably organic chemistry. Experience working with radioactivity such as in a PET radiochemistry laboratory, nuclear medicine environment, or commercial nuclear pharmacy specializing in PET drug production. Strong word processing and database skills specifically with Microsoft Word and Excel. Additional Qualifications: Two years' experience in production, manufacturing and handling PET drug products is preferred. Experience assisting in the development of PET drug synthesis procedures is preferred. Prior experience teaching, training, group interaction and presentations.

Food Scientist - Kenny's Candy & Confections *Onsite in Perham, MN - officed out of Building 1* Compensation: Total Compensation Range: $75,000 to $105,000 Base Pay: $65,000 to $85,000 Year 1 Bonus Guarantee: $10,000 to $20,000 Profit Sharing Eligibility: Begins after completing 1 year of employment ($7.5 Million in Profits Paid to Profit Sharing Pool in 2024) Our Coolest Benefit - Profit Sharing! In our most recent fiscal year, KLN Family Brands contributed over $7.5 million into our employee profit sharing pool!!! Our Story KLN Family Brands is a 3rd generation family-owned business that started in 1964 with its corporate headquarters located in Perham, MN, in the heart of MN lakes country. Together, our companies manufacture a diverse and expanding range of high-quality human and pet food products. At KLN Family Brands, our vision is that “We are a proud people-first company. We are successful because of trust-based relationships and first-rate products for our families and friends. We better the world by caring for others. We challenge. We grow. We inspire.” Some companies have to “fudge the story” a little. Some need the extra “spin” to shine a positive light on themselves. That's not who we are at KLN Family Brands, and that's not what we do. We tell the story of our brand - our people, the quality of our products, our spirit & moxie, our tradition, and the way we treat our community & beyond. We do it in a genuine way because we genuinely believe we're a pretty amazing company. The Opportunity The Food Scientist plays a critical role in driving innovation and ensuring product excellence at KLN Family Brands. This position is responsible for developing new product formulations that align with market trends and consumer expectations, while also supporting the research and development (R&D) process from concept to commercialization. The Food Scientist will collaborate cross-functionally to maintain and enhance product quality, consistency, and safety across all stages of production. Additionally, this role involves building and nurturing relationships with both customers and suppliers to support product development, sourcing, and continuous improvement initiatives. Responsibilities: Prepare for and represent Kenny's Candy & Confections with customers, trade organizations, and trade meetings and conventions including: Work with customers to meet their needs regarding flavor, nutritional, and label claims. Develop new products that follow regulatory and market trends. Maintain relationships with suppliers and utilize their insight to develop new products and troubleshoot existing issues. Maintain relationships with industry associations and regulatory trends. Prepare all necessary reports as required by customers Develop and maintain formulation strategies for existing and new product development including Understanding the synergy between/among functional ingredients. Understand processing parameters and effects on ingredients. Understand scale up process from benchtop to production. Utilize consistent formulation calculations/tools. Support and complete benchtop samples including Support analytical equipment and data collection tools. Providing and updating R&D laboratory tools, utensils, supplies, etc Work with purchasing department/suppliers to ensure necessary materials/ingredients are in house for benchtop samples Request necessary paperwork, logistical information and pricing to determine applicability of material for project needs. Organize and retain benchtop and trial samples for further review and shelf life analysis Coordinate, manage, monitor, and document plant trials Understand the transfer of formulas from benchtop to line trial Provide paperwork & instructions to production team to run production line trials Collect data, samples, and attend to detail during production line trials and first production runs Organize and file collected data for future reference Work on current formulations to make any changes as directed by management teams Support nutritional and labeling strategy and proof labeling information Determine appropriate nutritional database and maintain administrative relationship. Work side by side & when necessary provide assistance as needed to other Food Techs and R&D Application Specialist. Create first draft tentative nutritional labels when necessary Maintain proofing standards according to the FDA's Code of Federal Regulations. Proof and review nutritional panels for packaging Communicate with other department and other R&D team members to work strategically through projects Prepare all necessary reports required by department heads Communicate with sales team on project timelines and updates Utilize change process management project tools to update projects & manage timelines. Additional Responsibilities: Assist Food Technologist & R&D Application Specialist on projects as time allows Continue additional ingredient education and model current processing systems Assist in sourcing and trialing new ingredients as needed Set up and operate equipment needed for sample production Use ingredients knowledge, processing experience, and project goals to define processing specifications in conjunction with the quality department Assist with product issues (processing, formulation, quality, etc.) with the understanding of scientific principles to prove root cause and provide processing or formulation solutions Qualifications A BS degree, or higher, in Food Science 2 years of hands-on experience in Food Science within the food industry, contributing to product development Understanding multi-ingredient functionality Experience in new product development and formulations Self-Motivated Excellent computer skills Excellent communication and organizational skills Ability to work well with others Benefits Health, Dental, & Vision Wellness program discounts - up to $150 discounted towards health insurance monthly 80 Hours of PTO Accrued in First Year of Employment 7 Paid Holidays KLN Clinic - Free doctor visits & more than 300 free prescriptions 401k Match Opportunity Opportunity to meet with our onsite financial advisors $10,000 Forgivable Home Grant Program Tuition Assistance Situational Relocation *This opportunity is contingent upon successful completion of a drug test and background check.*

Who You Are You're a strategic, driven leader with a strong technical foundation and a passion for building high-performing teams. You thrive in environments that give you the freedom to set direction and execute bold ideas. With a strong analytical mindset and a deep understanding of FDA-regulated environments, you focus on the big picture, yet you know when to dig into the details to drive results. You're decisive, confident, and future-focused. You lead through systems, not micromanagement, and bring an entrepreneurial approach to problem solving, improvement, and innovation. What You'll Do Lead, mentor, and develop a dynamic team of QC Analytical Chemists. Set the strategic direction for the QC Laboratory, aligning with internal goals and customer expectations Oversee all laboratory operations related to raw materials, in-process testing, and finished goods Act as the subject matter expert for analytical techniques including HPLC, GC, ICP, wet chemistry, and more Develop, validate, and maintain test methods, quality systems, and compliance procedures Ensure adherence to FDA regulations (21 CFR Parts 210 & 211), GLPs, USP, and environmental safety protocols Implement internal audit programs and create training plans to support continuous improvement Own quality data integrity, ERP system integration, and real-time reporting Collaborate cross-functionally with Production, R&D, Regulatory, and Executive Leadership Manage laboratory budgets, equipment investments, and resource planning Cultivate a culture of quality, accountability, and innovation across the organization What You Bring Bachelor's degree in Chemistry or a related scientific field 10+ years of experience in a regulated testing lab environment (cosmetic, OTC, or pharmaceutical preferred. Strong command of analytical instrumentation and method development (HPLC, GC, ICP, pH, etc.) Experience implementing quality systems and compliance with FDA, GLP, and USP standards Excellent communication skills-able to simplify complex technical issues for varied audiences Direct, solutions-oriented leadership style with a clear sense of ownership and urgency Proven ability to develop systems, delegate effectively, and manage shifting priorities Skilled in documentation, audit preparation, and process improvement ERP experience and strong documentation/reporting proficiency Why Federal Package? As we continue to grow, we're actively investing in our people, our technology, and our future. That means this is the perfect time to join our team and make your mark. You'll have the opportunity to contribute meaningfully, take ownership of your work, and help shape the direction of our organization. Whether you're passionate about innovation, leadership, or operational excellence, there's room to grow here. At Federal Package we believe that you work your best when you feel your best. Here is what you can expect from us: Comprehensive Benefits Package : Medical, dental, vision, life insurance, and disability coverage Retirement Support : 401(k) with company contributions to help you plan for your future Generous PTO & Leave : Paid time off, volunteer time, bereavement leave, and new parent paid leave Flexible Scheduling : Flex time and support for work-life balance Education Reimbursement Program : We invest in your continued personal and professional development A Culture That Values You : Your energy, ideas, and ambition will be recognized and rewarded.

Who You Are You're a strategic, driven leader with a strong technical foundation and a passion for building high-performing teams. You thrive in environments that give you the freedom to set direction and execute bold ideas. With a strong analytical mindset and a deep understanding of FDA-regulated environments, you focus on the big picture, yet you know when to dig into the details to drive results. You're decisive, confident, and future-focused. You lead through systems, not micromanagement, and bring an entrepreneurial approach to problem solving, improvement, and innovation. What You'll Do Lead, mentor, and develop a dynamic team of QC Analytical Chemists. Set the strategic direction for the QC Laboratory, aligning with internal goals and customer expectations Oversee all laboratory operations related to raw materials, in-process testing, and finished goods Act as the subject matter expert for analytical techniques including HPLC, GC, ICP, wet chemistry, and more Develop, validate, and maintain test methods, quality systems, and compliance procedures Ensure adherence to FDA regulations (21 CFR Parts 210 & 211), GLPs, USP, and environmental safety protocols Implement internal audit programs and create training plans to support continuous improvement Own quality data integrity, ERP system integration, and real-time reporting Collaborate cross-functionally with Production, R&D, Regulatory, and Executive Leadership Manage laboratory budgets, equipment investments, and resource planning Cultivate a culture of quality, accountability, and innovation across the organization What You Bring Bachelor's degree in Chemistry or a related scientific field 10+ years of experience in a regulated testing lab environment (cosmetic, OTC, or pharmaceutical preferred. Strong command of analytical instrumentation and method development (HPLC, GC, ICP, pH, etc.) Experience implementing quality systems and compliance with FDA, GLP, and USP standards Excellent communication skills-able to simplify complex technical issues for varied audiences Direct, solutions-oriented leadership style with a clear sense of ownership and urgency Proven ability to develop systems, delegate effectively, and manage shifting priorities Skilled in documentation, audit preparation, and process improvement ERP experience and strong documentation/reporting proficiency Why Federal Package? As we continue to grow, we're actively investing in our people, our technology, and our future. That means this is the perfect time to join our team and make your mark. You'll have the opportunity to contribute meaningfully, take ownership of your work, and help shape the direction of our organization. Whether you're passionate about innovation, leadership, or operational excellence, there's room to grow here. At Federal Package we believe that you work your best when you feel your best. Here is what you can expect from us: Comprehensive Benefits Package: Medical, dental, vision, life insurance, and disability coverage Retirement Support: 401(k) with company contributions to help you plan for your future Generous PTO & Leave: Paid time off, volunteer time, bereavement leave, and new parent paid leave Flexible Scheduling: Flex time and support for work-life balance Education Reimbursement Program: We invest in your continued personal and professional development A Culture That Values You: Your energy, ideas, and ambition will be recognized and rewarded.

Food Scientist - Kenny's Candy & Confections *Onsite in Perham, MN - officed out of Building 1* Compensation: Total Compensation Range: $75,000 to $105,000 Base Pay: $65,000 to $85,000 Year 1 Bonus Guarantee: $10,000 to $20,000 Profit Sharing Eligibility: Begins after completing 1 year of employment ($7.5 Million in Profits Paid to Profit Sharing Pool in 2024) Our Coolest Benefit - Profit Sharing! In our most recent fiscal year, KLN Family Brands contributed over $7.5 million into our employee profit sharing pool!!! Our Story KLN Family Brands is a 3rd generation family-owned business that started in 1964 with its corporate headquarters located in Perham, MN, in the heart of MN lakes country. Together, our companies manufacture a diverse and expanding range of high-quality human and pet food products. At KLN Family Brands, our vision is that “We are a proud people-first company. We are successful because of trust-based relationships and first-rate products for our families and friends. We better the world by caring for others. We challenge. We grow. We inspire.” Some companies have to “fudge the story” a little. Some need the extra “spin” to shine a positive light on themselves. That's not who we are at KLN Family Brands, and that's not what we do. We tell the story of our brand - our people, the quality of our products, our spirit & moxie, our tradition, and the way we treat our community & beyond. We do it in a genuine way because we genuinely believe we're a pretty amazing company. The Opportunity The Food Scientist plays a critical role in driving innovation and ensuring product excellence at KLN Family Brands. This position is responsible for developing new product formulations that align with market trends and consumer expectations, while also supporting the research and development (R&D) process from concept to commercialization. The Food Scientist will collaborate cross-functionally to maintain and enhance product quality, consistency, and safety across all stages of production. Additionally, this role involves building and nurturing relationships with both customers and suppliers to support product development, sourcing, and continuous improvement initiatives. Responsibilities: Prepare for and represent Kenny's Candy & Confections with customers, trade organizations, and trade meetings and conventions including: Work with customers to meet their needs regarding flavor, nutritional, and label claims. Develop new products that follow regulatory and market trends. Maintain relationships with suppliers and utilize their insight to develop new products and troubleshoot existing issues. Maintain relationships with industry associations and regulatory trends. Prepare all necessary reports as required by customers Develop and maintain formulation strategies for existing and new product development including Understanding the synergy between/among functional ingredients. Understand processing parameters and effects on ingredients. Understand scale up process from benchtop to production. Utilize consistent formulation calculations/tools. Support and complete benchtop samples including Support analytical equipment and data collection tools. Providing and updating R&D laboratory tools, utensils, supplies, etc Work with purchasing department/suppliers to ensure necessary materials/ingredients are in house for benchtop samples Request necessary paperwork, logistical information and pricing to determine applicability of material for project needs. Organize and retain benchtop and trial samples for further review and shelf life analysis Coordinate, manage, monitor, and document plant trials Understand the transfer of formulas from benchtop to line trial Provide paperwork & instructions to production team to run production line trials Collect data, samples, and attend to detail during production line trials and first production runs Organize and file collected data for future reference Work on current formulations to make any changes as directed by management teams Support nutritional and labeling strategy and proof labeling information Determine appropriate nutritional database and maintain administrative relationship. Work side by side & when necessary provide assistance as needed to other Food Techs and R&D Application Specialist. Create first draft tentative nutritional labels when necessary Maintain proofing standards according to the FDA's Code of Federal Regulations. Proof and review nutritional panels for packaging Communicate with other department and other R&D team members to work strategically through projects Prepare all necessary reports required by department heads Communicate with sales team on project timelines and updates Utilize change process management project tools to update projects & manage timelines. Additional Responsibilities: Assist Food Technologist & R&D Application Specialist on projects as time allows Continue additional ingredient education and model current processing systems Assist in sourcing and trialing new ingredients as needed Set up and operate equipment needed for sample production Use ingredients knowledge, processing experience, and project goals to define processing specifications in conjunction with the quality department Assist with product issues (processing, formulation, quality, etc.) with the understanding of scientific principles to prove root cause and provide processing or formulation solutions Qualifications A BS degree, or higher, in Food Science Experience formulating Candy 2 years of hands-on experience in Food Science within the food industry, contributing to product development Understanding multi-ingredient functionality Experience in new product development and formulations Self-Motivated Excellent computer skills Excellent communication and organizational skills Ability to work well with others Benefits Health, Dental, & Vision Wellness program discounts - up to $150 discounted towards health insurance monthly 80 Hours of PTO Accrued in First Year of Employment 7 Paid Holidays KLN Clinic - Free doctor visits & more than 300 free prescriptions 401k Match Opportunity Opportunity to meet with our onsite financial advisors $10,000 Forgivable Home Grant Program Tuition Assistance Situational Relocation *This opportunity is contingent upon successful completion of a drug test and background check.*

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

Job Title: New Product Development Scientist Location: Owatonna, MN Summary This position will be based out of Owatonna, MN manufacturing plant reporting to the Technical Director. NPD Scientist is responsible for overseeing and executing product development activities and providing technical support to internal and external stakeholders related to the Duraco Specialty Tapes & Liners business. This includes recommending, planning, prioritizing, and conducting experimental lab work, product prototyping and optimization, product testing, literature research, as well as data gathering, processing, and reporting. NPD Scientist will also be responsible for maintaining relationships with key suppliers, new raw material qualifications, supporting secondary raw material qualifications, cost savings efforts, and working closely with other functional teams on NPD trial, scale-up, and new product commercialization activities. Responsibilities Oversee and execute development and technical support for Duraco Specialty Tapes & Liners New Product Development (NPD) pipeline, with ability to deliver minimum 5 product launches per year Conduct required laboratory experimentation and testing, provide leadership in Silicone release coating formulation development, new release liner prototyping, materials design, process optimization, and product testing that aligns with Duraco Specialty Tapes & Liners site capabilities and strategic initiatives Provide technical assistance in related regulatory compliance matters related to Silicone release coatings and liner products Engage and collaborate with customers as well as Marketing and Sales Teams to identify key development opportunities and appropriately prioritize projects and initiatives Strong collaboration with Production, Quality, and other functional teams to ensure efficient product development, scale-up, performance optimization, consistent quality, and successful commercialization Establishing and cultivating relationships with suppliers of key raw materials Provide technical leadership in support of cost-savings initiatives including, but not limited to, alternate raw material identification, insource/outsource decisions, and Silicone release coating formulation enhancements for increased throughput and efficiencies Provide timely data processing, organizing, and reporting to superiors and functional teams, including generating and sharing ideas for NPD projects and opportunities Proactively identify and implement best safety practices in both laboratory and manufacturing settings Enhance NPD and Project Management processes and establishing improved IP protection practices Other duties as assigned Personal Attributes: Results driven and able to focus on, prioritize, and execute individual activities Curious and eager to learn - enjoys leveraging new knowledge to enhance current Silicone release coating chemistries, release liner constructions, and products Excellent written and verbal communication skills Excellent laboratory and analytical skills including FTIR, XRF, and basic Release Liner testing Comfortable working in a high-pace manufacturing and laboratory environments, and navigating changing priorities Effective in engaging and collaborating with cross-functional teams, including production floor supervisors, operators and QC technicians Outstanding personal integrity and ethics Understands and easily connects products, technologies, and capabilities across a diverse portfolio of customers and markets Demonstrated ability to work across different systems and adapt to new processes Strong planning and organizational skills and high degree of comfort working in and around production / manufacturing settings Qualifications: Required Skills, Education, and Experience BS or MS in a Technical field; preferably Chemistry, Polymer Science, Chemical Engineering, Material Science, or Plastics Engineering with excellent hands-on lab experience 3-5 Years of proven track record of developing new Silicone release coating formulations and paper and film release liner products Understanding and experience with PSAs and PSTC testing methods is desired to help complement release liner and Silicone coating formulation development Experience with development methodologies including project management, stage-gate, ideation, Design of Experiments (DOE), IP management, and literature and patent research Good knowledge of additives, formulation processing, applications, and analytical test methods as they relate to the development of Si release coating formulations Experience in Silicone release coating and web handling processes is highly desirable Knowledge of Microsoft Office products with advanced experience in Excel and analytics programs (e.g., Minitab, JMP, etc.) Travel Must be able to travel within the US 10-15% Domestic Travel The job description is not an exhaustive listing of all responsibilities and may be revised at any time.

What we offer Starting pay at $29.43 per hour Benefits begin 30 days after hire INSERT BONUS HERE Ask about our Hourly Bonus Program Fully customizable medical plans (HRA, HSA, FSA), 5 different carrier choices + Prescription (Rx) card Full suite of additional plans: vision, dental, life, disability, adoption/family planning reimbursement, childcare, parental leave LiveWell lifestyle/well-being discount and rewards program (for example, $50 subsidy for fitness tracker) 401(k) matching + extra 3% freebie company contribution Employee Perks include FREE Product & Swag Business Resource Groups (BRGs) Award-winning Ownerversity learning & development resource library Employee Assistance Program (EAP) for mental health support Location New Ulm, Minnesota - Home of VELVEETA Work Schedule Monday - Friday work week, 2nd shift/Afternoons Essential Functions & Responsibilities The Senior Rotating Analyst is responsible for all finished product testing. Occasionally may also be responsible for blender testing, blender standardization, problem solving and in process testing. Works from brief verbal and complex written instructions and is expected to exercise individual judgment and resolve questions independently in a timely manner. When 1 to 2 lines are running, Analysts work alone - therefore they must exercise good judgment with all aspects of in process and finished product testing when issues arise. Rotating Analysts are expected to work between areas and help out when needed. Must have good written and oral communications skills. Work requires mathematical skills including fractions, decimals and knowledge of personal computers. Work is expected to meet the high standards of Kraft Heinz, AOAC and legal parameters. Must be able to perform sensitive adjustments of complex controls requiring skill in fine tuning of the process variables. Job Responsibilities: Regular Moisture/Finished Product Testing: Performs five-hour vacuum moisture tests or NIR moisture test on every hourly sample for every product run daily. Responsible for all accurate recording of data and documenting out of standard results. Performs recheck testing on all samples out of standard and special samples. Calculates all results by use of personal computers and makes decisions accordingly. Performs moisture and fat tests on raw material cheese as requested by supervisor. Responsible for cleaning, labeling and preparation utensils and equipment. Responsible for cleaning and maintaining work area at all times. Responsible for performing pH tests on hourly samples, as specifications require. Accountable for all retests and monitoring of equipment. Responsible for performing extraneous tests as required on finished product and raw materials. Projects as requested by supervisors. Fat Testing: Performed tests, requires safety awareness at all times due to the chemicals being worked with. Safety eye wear, apron and gloves are mandatory in this area. Performs fat tests on samples as required by specifications. Performs fat tests on blender samples on an as needed basis. Responsible for all special fat testing required on natural cheese samples. Performs fat testing on ingredients and liquid loads as specifications require. Accountable for all data entry, calculating and recording of fat results. Accountable for any data that is out of standard and must be retested and/or special samples received. Responsible for knowledge of all fat testing procedures, techniques and methods as prescribed by Kraft Heinz, AOAC and legal standards. Salt and Lactose Testing: Preforms tests on samples as required by specifications. Accountable for all data entry, calculating and recording of all Salt and Lactose results. Accountable for any data that is out of standard and must be retested and /or special samples received. Responsible for knowledge of the procedures, techniques and methods as prescribed by Kraft Heinz, AOAC and legal standards. Responsible for all critical control point checks performed in areas. Responsible for cleaning and maintaining work area and equipment at all times. Rapids Area: When required, responsible for accurate testing of blend samples for moisture and fat on a timely basis. Methods used include NIR, vacuum oven and Roccal Method. Concise and quick decisions must be made based on these results. Responsible for solving blender errors/problems using G40 personal computer. Responsible for activating, adding and deleting liquid load data in the G40 for proper blender standardization. Responsible for maintaining and operating the G40 back up and special standardization programs on the personal computer. Prepares in process testing tools for each blender standardization. Maintains an ample supply of folded, numbered and weighed foils daily. Responsible for knowledge of all methods, techniques and procedures according to Kraft Heinz, AOAC and legal standards. Responsible for maintaining and cleaning work area at all times. Hot Tests/In-Process Testing: When required, performs in-process testing on certain blenders on a timely basis. Accountable for all decisions made for corrections at the cooker to adhere to 100% compliance for every product. Timely decision making skills are utilized. Utilizes various methods for testing including a vacuum oven and NIR units. Performs in process testing on wet mix and liquid loads. Responsible for additions and data reporting. Personal computers and mathematical skills are used to compute data. Utilizes a personal computer for computing calculations on all vacuum tests. Responsible for an in-process test on certain blenders of standardized product. Communicates correction/additions to the cook room cooks. Responsible for checking all corrections. Responsible for knowledge of proper methods, techniques and procedures according to Kraft Heinz, AOAC and legal standards. Accountable for maintaining and cleaning of work area at all times. Responsible for all critical control point checks performed in areas. Responsibilities: Work on programs and other requests. Record cooker steam out results and grade the steam out pads. Test standardized cream, cream whey and WPC as required by the specifications and record results. When needed, performs blender checks as required. Involves retesting blender samples for moisture and fat. Responsible for the salvage of blender, moisture, fat, NIR, naturals and raw material samples. Miscellaneous testing required on ingredients as to adhere to the specifications. Preparation of solutions for miscellaneous testing (pepsin, acid pH). Responsible for cleaning five-hour ovens centrifuge, grading room buckets, fat bottles, beakers, moisture pans and all other lab dishes and glassware. Prepares fat (Roccal) solution and fills acid bottles. Monitoring and cleaning of water bath and acid dispensers. Monitor the hazardous waste that is produced by some of the testing and dispose of it properly. Responsible for air exposures and swabs for start-up, qualifications and regular production. Responsible for entering COA results into SAP for incoming ingredients. Responsible for net content scale and weight verifications. Maintenance: Responsible for all thermometer checks in the Laboratory. (Primary, secondary and calibration thermometers) for start-up. Responsible for all balance and scale calibrations in Laboratory for start-up. General Requirements: Computer skills, operating knowledge of SAP, Quality Suites, Excel, demonstrated math skills (including decimals, fractions, divisions) and decision-making skills. Person must be willing to train in other areas of the Lab (Special Testing, Bacti, etc.) or take upgrading when offered. Safety: Follow all OSHA and safety procedures. Working with acids, heat and glassware are a safety hazard. Knowledge of proper treatment, response, and care and preventative measures required. Equipment Operated: Primarily responsible for the safe and efficient operation of NIR units, G40, 6500, personal computers, vacuum ovens, centrifuges, water baths and scales. Value of Material: Lack of responsible decision making skills and inattention to required duties may result in substantial monetary losses, delays or inconveniences. The results not are readily detectable until 10-20 hours later. Lifting Requirements: Moderate - Lifting requires handling materials up to 20 lbs. frequently or less and up to 45 lbs. infrequently. Working Conditions: Fair - Standing throughout the shift required of several job areas. Hazards are present when working with Laboratory testing reagents and disposals. Work may be a fast pace and hectic; therefore, cautions and common sense must be exercise. Exposure to noise and unfavorable working conditions (such as wet slippery floors) at times. Training: The Senior Rotating Analyst will have a three phase training period; 30 days, 3 months and 6 months. An evaluation will be done after each phase. The successful Senior Lab Analyst will be able to demonstrate the following competencies throughout each phase of training: 30 days Decision making skills Technical aptitude Math and computer skills 3 months Effective communications skills Dependability Analytical skills 6 months Self-confidence Team working skills Versatility This job description is not designed to cover or contain all duties or responsibilities that are required of the role. Duties or responsibilities may change or be added with or without notice. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. #INDMFGH Benefits: Coverage for employees (and their eligible dependents) through affordable access to healthcare, protection, and saving for the future, we offer plans tailored to meet you and your family's needs. Coverage for benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. Wellbeing: We offer events, resources, and learning opportunities that inspire a physical, social, emotional, and financial well-being lifestyle for our employees and their families. You'll be able to participate in a variety of benefits and wellbeing programs that may vary by role, country, region, union status, and other employment status factors, for example: Physical - Medical, Prescription Drug, Dental, Vision, Screenings/Assessments Social - Paid Time Off, Company Holidays, Leave of Absence, Recognition, Training Emotional - Employee Assistance Program , Wellbeing Programs, Family Support Programs Financial - 401k, Life, Accidental Death & Dismemberment, Disability Location(s) New Ulm Plant Kraft Heinz is an Equal Opportunity Employer that prohibits discrimination or harassment of any type. All qualified applicants are considered for employment without regard to race, color, national origin, age, sex, sexual orientation, gender, gender identity or expression, disability status, protected veteran status, or any other characteristic protected by law. Applicants who require an accommodation to participate in the job application or hiring process should contact ***********************.

Job Title: Lab Assistant Classification: Student Employee (non-exempt) Name and Address of Employer: St. Olaf College, 1520 St. Olaf Ave, Northfield, MN 55057 Department Name: Chemistry Unit Number (5 digits): 11130 See Employment Authorization Contact Person/Supervisor: Instructor for the class Pay Rate (Check One) Standard Hourly Rate X Supervisory/Special Skills Hourly Rate Description of the Position: (Purpose of the Position): As the grader of student lab reports you will generate student scores and likely have access to other scores on websites or in spreadsheets. Duties and Responsibilities: It is the responsibility of lab assistants to do their best to follow grading guidelines, to finish each job in a timely fashion (usually by the next lab session), to ask for clarification when necessary, and to communicate on a regular basis with your faculty member supervisors (lab instructor and/or lab director). The lab director will let you know how/where to record and store the grades. Lab assistants have additional lab safety responsibilities and should always be alert and watchful in the lab. Please do… •help to encourage the proper attention to waste collection and documentation on waste manifests •monitor the proper use of personal protective equipment by the students •help to ensure that all students present are appropriately attired •spend your time circulating in the lab looking for unsafe or incorrect work, answering student questions, inviting student questions, etc. •fill out your online time sheet at the end of your working or grading sessions Your time in the lab is not for grading or sitting on the sidelines observing from afar. Beware of spending more time with some groups than others. You may have friends/acquaintances enrolled in the lab and it is your responsibility to ensure that other students have no reason to be concerned about preferential treatment of some students. Lab assistants are always farther along in the study of chemistry than their students. Nonetheless, lab assistants may not always know the answers to questions asked by students. It is important to admit when you are unsure. It is okay to tell them you don't know the answer. Given the proximity of a lab instructor, it would always be perfectly acceptable to say, “I'm not sure about that, let's go and ask the Professor.” Also, while lab assistants are more advanced in their chemistry studies, it is not a good idea to flaunt this status. Rarely, we have had reports of lab assistants behaving condescendingly toward their students. Use your judgment here. There is a difference between piquing the interest of a younger student by telling them about what is going on in the analytical chemistry lab (for instance) and making that same student feel inadequate with just too much information. If you will have trouble maintaining an unbiased view of student work due to situations such as having close friends in your lab section, please consult with your supervisor. Under no conditions should you be grading lab reports of someone whom you are dating. Please advise your supervisor of the problem immediately. Do not begin a romantic relationship with a student in the lab section for which you assist. If you cannot come to a lab session due to illness or some other commitment, email the other lab assistants for the course to see if anyone can substitute for you. Then email the lab instructor and the lab director to alert them to the problem and ask if there are others that you should email. Then, keep the lab instructor and lab director informed as to whether or not you have found a substitute. Qualifications: (Education/Experience/Skills) 1. Must have taken and completed the lab 2. Knowledge, both theoretical and practical, of the material. 3. Good communication skills. 4. Ability to evaluate student questions and answers. 5. Ability to keep good records. 6. Ability to foster the safety guidelines. Wage Range: $11.75-12.75 This is for general information purposes. It is not intended to list all duties and responsibilities of the position. This job description is subject to change at any time by St. Olaf College, with or without prior notice.