Research and development technician jobs in Saint Louis, MO

16Consultancy is a dynamic and forward-thinking business consulting company based in Singapore, specializing in gathering and analyzing industry insights. We guide clients towards informed decisions with expertise in sourcing, purchasing trends, and product development across various sectors, primarily focusing on actionable intelligence. Visit us at our website. Job Overview We are seeking skilled Food Industry Consultants specializing in Supply Chain Procurement for a part-time, remote, freelance, or hybrid position with 16Consultancy. This role requires at least 2 year of professional experience. The ideal candidate will have a passion for the food industry, with a particular focus on the freeze-dried fruit sector. Qualifications and Skills Proven experience in supply chain management within the food industry, particularly in the freeze-dried fruit sector. Strong background in global sourcing strategies to efficiently manage and optimize supply chain operations. Comprehensive knowledge and experience in procurement contracts, ensuring favorable terms for the business. Demonstrated ability to identify and select suitable suppliers that match business needs and quality standards. Experience working as a category buyer, focusing on product lines and market trends to enhance procurement strategy. Exceptional analytical skills to assess market trends and identify opportunities for cost-saving in supply chain activities. Strong communication skills to effectively negotiate with suppliers and liaise across different stakeholders internally. Proven capacity to work independently in a flexible, remote, or hybrid setting without compromising productivity. Roles and Responsibilities Analyze and enhance supply chain processes within the food industry, specifically targeting the freeze-dried fruit sector. Identify potential suppliers and establish procurement contracts that align with the strategic goals of the business. Conduct in-depth market research to track purchasing trends and provide insights for product development and sourcing strategies. Ensure compliance with industry standards and regulations related to food supply chain operations and procurement practices. Collaborate with cross-functional teams to support the design and implementation of supply chain improvement initiatives. Maintain and expand professional relationships with suppliers and industry stakeholders to foster long-term partnerships. Deliver actionable recommendations to improve sourcing efficiency while reducing costs and maintaining quality standards. Prepare detailed reports and presentations to convey analysis results and project outcomes to clients and management.

Formulation R&D Technician- Oral Product Development Humanwell Pharmaceuticals US, St Louis, MO Interested candidate, please submit resumes to email: ******************** Summary Humanwell Pharmaceutical US, Inc., based in St Louis, MO, is committed to advancing pharmaceutical research and development, with a particular emphasis on novel therapeutics that address unmet medical needs. The organization strives to enhance the quality of life for patients and shape a healthier future. Humanwell seeks individuals motivated by a desire to make a meaningful impact and is currently recruiting a dedicated Formulation R&D Technician. The individual will collaborate closely with senior scientists and management to execute hands-on pharmaceutical development activities. Primary Duties and Responsibilities Maintain compliance, cleanliness, and organization within the operational areas of the pilot plant. Set up, operate, maintain, and sanitize a broad array of formulation equipment and testing instruments, including but not limited to scales, high shear and fluid bed granulators, blenders, tablet press, film coater, homogenizer, density tester, and hardness tester. Document laboratory activities in accordance with Good Documentation Practices. Summarize study outcomes and assist in the preparation of technical reports and presentations. Independently plan and accomplish assigned responsibilities within established timelines as directed by supervisory personnel. Conduct physical inventory for both controlled and non-controlled substances. Contribute to the development, revision, and delivery of training on manufacturing Standard Operating Procedures (SOPs). Comply with current Good Manufacturing Practices (cGMP) and all applicable regulatory guidelines. Work extended hours occasionally, as necessitated by project requirements. Be available to travel up to 10% of the time. Perform additional duties and assignments as required. Required Qualifications and Skills: Bachelor's or Master's degree in Pharmaceutical Science, Chemical Engineering, Chemistry, or a closely related discipline. Preferably possesses relevant experience within the pharmaceutical industry. Preferably possesses hands-on experience in pharmaceutical research and development as well as GMP manufacturing environments. Demonstrates willingness and capability to comply with FDA, OSHA, and DEA regulations. Exhibits a proven ability to collaborate effectively as part of a cross-functional team. Displays excellent oral and written communication skills. Job Type: Full-time Job Location: Ballwin, MO

Target Level: Consultant / Senior Consultant This is a hybrid role based out of our St. Louis, Missouri office. Individuals must reside near the office location and have the ability to travel to the office or client site as needed for training, meetings, office events, and other purposes. Who You'll Work With At Slalom, our Delivery capability is the engine that powers transformation. We are the connective tissue across all capabilities-bringing strategy to life through execution that is rigorous, adaptive, and outcome-driven. You'll join a community of delivery professionals who thrive in complexity and are passionate about making things happen. Our teams lead high-impact initiatives across industries, partnering with clients to navigate ambiguity, align stakeholders, and deliver results that matter. Whether it's a multi-workstream transformation or a product launch, we bring clarity, structure, and momentum to every engagement. We work shoulder-to-shoulder with clients, tailoring delivery approaches to meet them where they are-whether Agile, Waterfall, or hybrid. Our focus is on enabling predictable, repeatable outcomes that help organizations dream bigger, move faster, and build better tomorrows. What You'll Do * Lead the delivery of business and technology projects, ensuring alignment with client goals and Slalom's delivery standards. * Apply agile methodologies to drive iterative progress, foster collaboration, and adapt quickly to evolving needs. * Define project scope, timelines, and success metrics in partnership with clients and internal teams, with particular emphasis on enabling smooth migration efforts and transformation initiatives. * Oversee project execution through effective resource coordination, risk mitigation, and stakeholder communication, while guiding teams through agile ceremonies to ensure the successful delivery of migration and modernization projects. * Leverage AI tools and techniques-such as generative AI for documentation, predictive analytics for risk and timeline forecasting, and automation for reporting-to accelerate delivery and enhance quality. * Support business development through scoping, estimation, and proposal contributions, while also mentoring junior consultants and contributing to internal capability growth. What You'll Bring * Experience in product ownership, product management, or agile delivery, ideally in consulting or enterprise environments, in the financial services industry. * Proven success in delivering business or technology solutions. * Strong understanding of agile delivery methodologies and project governance. * Experience applying AI-enabled tools to streamline delivery workflows and enhance team productivity. * Excellent communication, facilitation, and stakeholder management skills. * Pragmatic Institute, Scrum.org, Scrum Alliance, Scaled Agile, or other relevant certifications are a plus. About Us Slalom is a fiercely human business and technology consulting company that leads with outcomes to bring more value, in all ways, always. From strategy through delivery, our agile teams across 52 offices in 12 countries collaborate with clients to bring powerful customer experiences, innovative ways of working, and new products and services to life. We are trusted by leaders across the Global 1000, many successful enterprise and mid-market companies, and 500+ public sector organizations to improve operations, drive growth, and create value. At Slalom, we believe that together, we can move faster, dream bigger, and build better tomorrows for all. Compensation and Benefits Slalom prides itself on helping team members thrive in their work and life. As a result, Slalom is proud to invest in benefits that include meaningful time off and paid holidays, parental leave, 401(k) with a match, a range of choices for highly subsidized health, dental, & vision coverage, adoption and fertility assistance, and short/long-term disability. We also offer yearly $350 reimbursement account for any well-being-related expenses, as well as discounted home, auto, and pet insurance. Slalom is committed to fair and equitable compensation practices. For this position, the base salary pay range for a Consultant is $109,000 to $130,000, and for a Senior Consultant $125,000 to $150,000. In addition, individuals may be eligible for an annual discretionary bonus. Actual compensation will depend upon an individual's skills, experience, qualifications, location, and other relevant factors. The salary pay range is subject to change and may be modified at any time. EEO and Accommodations Slalom is an equal opportunity employer and is committed to attracting, developing and retaining highly qualified talent who empower our innovative teams through unique perspectives and experiences. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veterans' status, or any other characteristic protected by federal, state, or local laws. Slalom will also consider qualified applications with criminal histories, consistent with legal requirements. Slalom welcomes and encourages applications from individuals with disabilities. Reasonable accommodations are available for candidates during all aspects of the selection process. Please advise the talent acquisition team if you require accommodations during the interview process. #li-bs1

What Research and Development Engineering contributes to Cardinal Health Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. Job Summary This position is responsible for providing technical support at an intermediary level to new product development projects and post product release projects. This individual is expected to be proficient in the various competencies relevant to their job. Requires limited supervision; limited instruction on routine work, and general instructions are given on new work or special assignments. First Shift position (Monday - Friday) in Hazelwood, MO Responsibilities Product Testing * Under general supervision, follows testing protocols, selects appropriate test fixtures and set-ups. * Assists in test method development. * Coordinates with project Engineer(s) to setup, execute, and report out results for each test project. Protocol/Report Writing * Under direction, writes protocols. * Writes reports including data, analysis, and observations from testing performed according to protocols. Laboratory Management * Maintains laboratory supplies. * Aids in maintaining calibration and repair of equipment. Qualifications * High School Diploma or GED required * 2 or more years related work experience preferred * Verification, Validation, and Evaluation testing for medical devices, preferred * Tensile Test Equipment (i.e. MTS, Instron, or similar), preferred * Optical Measurement Equipment (i.e. OGP, Keyonce, or similar), preferred What is expected of you and others at this level * Applies acquired knowledge and skills to complete standard tasks * Readily learns and applies new information and methods to work in assigned area * Utilization of time management and organizational skills to coordinate projects, as needed, in parallel. * Leverage critical thinking skill on a daily basis, as it related to product testing, to understand and communicate test findings to the Engineering team. * Maintains appropriate licenses, training and certifications * Works on routine assignments that require some problem resolution * Works within clearly defined standard operating procedures and/or scientific methods * Adheres to all quality guidelines * Works under moderate degree of supervision * Work typically involves regular review of output by work lead or supervisor * Refers complex unusual problems to supervisor Anticipated hourly range: $22.00 per hour - $31.60 per hour Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. * Medical, dental and vision coverage * Paid time off plan * Health savings account (HSA) * 401k savings plan * Access to wages before pay day with my FlexPay * Flexible spending accounts (FSAs) * Short- and long-term disability coverage * Work-Life resources * Paid parental leave * Healthy lifestyle programs Application window anticipated to close: 11/28/2025 *if interested in opportunity, please submit application as soon as possible. The hourly range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. #LI-MP1 Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: Join our St. Louis Cherokee facility at MilliporeSigma, a leading contract development and manufacturing organization (CDMO) and a recognized Center of Excellence for antibody-drug conjugate (ADC) manufacturing. We are seeking passionate and enthusiastic professionals to contribute to our innovative bioconjugate production, leveraging over 35 years of expertise in the field. As a vital part of our dedicated team, you will play a key role in delivering high-quality ADCs that improve the quality of life for patients suffering from cancer and other debilitating diseases. With our state-of-the-art technologies and commitment to excellence, you will ensure the highest standards of quality and compliance in our ADC manufacturing processes. As an Associate Production Scientist - Rotating Shift you will manufacture products according to established protocols under ICH Q7 pharmaceutical regulations, provide technical support to others and perform operations in support of the group and department. Job duties include: * 12 hour rotating Day (6:00am - 6:30pm)/ Night (6:00pm - 6:30am) shifts with a 20% shift differential * Evaluate products per established protocols, providing technical support and performing operations to meet departmental goals. * Safely conduct routine processes and unit operations, including cleaning equipment and work areas, while ensuring quality expectations. * Maintain required training and qualifications, train team members, and act as a technical consultant. * Support facility functions by maintaining equipment, preparing reagents, restocking supplies, and managing waste disposal. * Maintain accurate records and logbooks according to quality guidelines, communicating operational status and concerns to supervision. * Collaborate with other departments, participate in quality audits and customer interactions, and perform procedures independently or in a team. * Improve processes using scientific knowledge and principles, ensuring compliance with change control. * Address unsafe conditions promptly and troubleshoot challenges related to biological processes and GMP compliance. Physical Attributes: * Ability to lift to 50lbs. * Ability to wear personal protective equipment, such as respirator or chemical protective clothing, for extended periods. * Expected on-floor time: (70%) Who you are: Minimum Qualifications: * Bachelor's Degree in a scientific discipline (e.g., Chemistry, Biochemistry, Biology, etc.) OR * Associate Degree in Chemistry, Biochemistry Biology or any other Life Science discipline * 2+ years industry Production/Laboratory experience Preferred Qualifications: * Experience with Antibody Drug Conjugates (ADCs), including knowledge of their formulation and manufacturing processes. * Experience with Automated Tangential Flow and Automated Chromatography systems. * Familiar with laboratory instruments and production equipment * Familiarity with process techniques, unit operations, and safe chemical handling methods. * Experience with Microsoft Office (Word, Outlook, Excel, etc.). * Mechanical and troubleshooting skills. * Knowledge of cGMP and ICH Regulatory and Quality standards. * Knowledge of Operational Excellence. * Clean room experience * Ability to interact professionally in customer-facing meetings, including challenging discussions on process planning and process execution RSREMD Pay Range for this position: $25.00 - $45.00 The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Job Description About Confluence Genetics Confluence Genetics develops soybean technologies and varieties that create value from farm-gate to feed, food and fuel end-markets by unlocking the natural genetic diversity of plants. The Company leverages their proprietary CropOS™ machine learning platform with proprietary germplasm data and speed breeding technologies in our Crop Accelerator facility to drastically accelerate and simplify the product development process. This platform allows for cost-effective and more efficient ways to analyze and make improvements in plant genetics. Confluence Genetics brings a unique and holistic approach to our product and platform development, as we span a broader workflow involving trait and seed development, genome editing, and breeding all the way to creating better ingredients and varieties that tap a strong customer demand. More information can be found online at *********************** Our Purpose and Core Values Our Core Values are a set of common principles we share that are fundamental to our company's identity. Real. Inspired! Real. We show up with honesty, accountability, and purpose. We lead with integrity and speak with candor, knowing that trust and transparency drive performance. We challenge each other respectfully and stay grounded in what matters-our shared mission and one another. Inspired! We're driven by possibility and energized by progress. With open minds and a bold spirit, we embrace change, take smart risks, and push boundaries. We stay curious, creative, and connected-to each other, our partners, and the future we're building together Department Overview The Crop Accelerator is a state-of-the-art, controlled environment research facility that allows Confluence Genetics to accelerate biology, enabling the rapid development of feed and food ingredients. Our innovative facility has dynamically adaptive growth chambers providing 365 days of optimal growing conditions. Furthermore, Confluence Genetics CropOS technology coupled with the Crop Accelerator's world-leading high-throughput phenotyping and automation capabilities enables predictive outcomes allowing Confluence Genetics to develop varieties significantly faster than traditional cropping methods; essentially moving us beyond the speed of biology. Position Summary The Research Associate I will be responsible for providing support to the Indoor Operations and Controlled environment through coordination and execution of production nursery grow-outs and additional research projects while exercising independent judgment and ensuring clear communication with team members. The RA will analyze and record data and communicate research progress with internal stakeholders. You Will: Maintain, organize, and summarize results of experiments, detailing issues, while problem solving. Coordinate the logistics of plant grow-outs within the TI workflow, as well support any needs from other Indoor Operations workflows. Perform tasks related with general operations of nurseries grow-outs including planting, tissue sampling, transplanting, tying, pollinating, and harvesting. Input data into the corporate database and collect experimental notes. Ensure data integrity and transparency for plant and seed records within the Crop Accelerator. Scout for plant disease symptoms, insect pressure, and other IPM considerations and communicate issues to appropriate support staff. Partner with CEI, GE and Speed Breeding teams within the Crop Accelerator to align best practices in plant care. Participate in weekend plant cross-pollination rotation as needed Perform other duties as assigned You Have: (Competencies and Qualifications) Education Bachelor's degree in Plant Biology or other relevant degree Experience +1 years relevant experience, preferably within an indoor growing facility and/or greenhouse Experience in soybean cross-pollination is a plus Software/Skillset Proficient at Microsoft suite of products Experience working in protected Ag, controlled environments, or a seed company preferred Other Process improvement mindset with a strong drive to simplify complex operations. Courage to promote ideas within an organization. Team player who gives support when able and asks for it when needed. Ability to communicate results to peers and leaders through written and verbal communications. We have a Total Rewards Package at Confluence Genetics that consists of more than just your paycheck. Total Rewards at Confluence Genetics covers Pay (salary and bonus), Health (employer benefit contributions) and Wealth (investments). Some of the perks include: A Collaborative Environment A flexible PTO program with a focus on work/life balance Competitive medical, dental and vision benefits Retirement savings plan with a company match Education reimbursement PAID parental leave And more….

We are seeking a motivated and knowledgeable Food Product Development Specialist with a B.S. degree in Food Science, Food Technology, Culinary Arts, or a related field. This role involves managing the entire product development cycle, from concept to market launch with a focus on innovation, quality, and cost efficiency. This is a dynamic, hands-on role for a professional passionate about Asian food innovation and quality. Education: B.S degree in food science, food technology, culinary arts, or a related field is required Physical demands: Able to lift 30-40 lbs, with or without assistance Travel: Estimated up to 20% Requirements: · Knowledge of food industry standards, including quality and food safety requirements, GMPs, HACCP, food labeling and FDA/USDA regulations · Good understanding of food science principles, food microbiology, technology, and lab test practices and procedures · Proficient in MS Office · Able to communicate effectively verbal and written in English. · Experience in Asian food product development and process flow design · Self-motivated, with the ability to work independently and collaboratively in cross-functional teams. Job responsibilities. Responsibilities may include, but are not limited to: · Manage the full product development cycle of creating new products, from initial concept through commercialization, ensuring successful market launch. · Own and maintain product lifecycle documentation including formulations, specifications, technical data sheets, and shelf-life protocols. · Develop and refine product prototypes for multiple concurrent projects. · Ensure products are developed within established cost parameters. · Manage the customer sampling program, including sample preparation, shipping, and coordination to support sales and product development needs. · Design, coordinate, and execute pilot and plant trials, including product scale-up and performance testing · Research and source new or alternative ingredients and suppliers for both new and existing products. · New technology and equipment research. Summarize findings and present recommendations to the leadership team. · Create and verify product nutrition labels and ingredient statement · Conduct product shelf life, sensory and microbiological testing to ensure product quality and compliance · Lead product process improvement, formula renovation for better quality, or cost reduction. · Support diagnosis and resolution of formulation, processing, and manufacturing challenges by applying food science principles and developing creative solutions to improve product stability, stability, self-life, quality, sensory attributes, scalability, and overall product and process performance · Provide regular progress updates and status reports on project milestones for all projects · Continuously monitor global food technology trends to identify and introduce new ideas, ingredients, technology, or products aligned with the company's innovation strategy · Organize and manage product tastings and cutting for internal and customer evaluation · Participate in customer visits and support sales events with technical insights and product presentations · Support special project and cross department initiatives as needed

**Our Purpose** _Mastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we're helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation, partnerships and networks combine to deliver a unique set of products and services that help people, businesses and governments realize their greatest potential._ **Title and Summary** Specialist, Product Development Job Overview: Provides designs specifications for and develops new products and services or their components. Defines functional and technical requirements. Researches new technologies and competitive products to develop additional product ideas and enhancements. Performs launch-related activities associated with new or highly customized product implementations, including marketing/communication and collateral. Defines business and technical requirements and manages the relationships of technical resources and the Global Technology Organization to maintain and build out platforms. Major Accountabilities: - Participate in the development of new products and product enhancement by performing assigned tasks in the product development life cycle - Compile information regarding market trends, the competitive landscape, and new product opportunities - Participate in defining product requirements and specifications - Support product launches and implementations - Contribute to the execution of product marketing programs - Prepare reports and presentations as directed Education: - Bachelor's degree or equivalent work experience desirable Knowledge / Experience: - Experience of payments industry and/or financial services experience - Broad knowledge of product development functions Skills/ Abilities: - Some understanding of general product development concepts and practices - Demonstrated ability to multi-task, establish priorities and work independently - Solid organization and project management skills - Solid verbal and written communications skills - Ability to understand and analyze financial information - Ability to interact effectively with colleagues and work collaboratively with internal and external business partners Work Conditions: - 5% domestic/international travel required Mastercard is a merit-based, inclusive, equal opportunity employer that considers applicants without regard to gender, gender identity, sexual orientation, race, ethnicity, disabled or veteran status, or any other characteristic protected by law. We hire the most qualified candidate for the role. In the US or Canada, if you require accommodations or assistance to complete the online application process or during the recruitment process, please contact reasonable_accommodation@mastercard.com and identify the type of accommodation or assistance you are requesting. Do not include any medical or health information in this email. The Reasonable Accommodations team will respond to your email promptly. **Corporate Security Responsibility** All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must: + Abide by Mastercard's security policies and practices; + Ensure the confidentiality and integrity of the information being accessed; + Report any suspected information security violation or breach, and + Complete all periodic mandatory security trainings in accordance with Mastercard's guidelines. In line with Mastercard's total compensation philosophy and assuming that the job will be performed in the US, the successful candidate will be offered a competitive base salary and may be eligible for an annual bonus or commissions depending on the role. The base salary offered may vary depending on multiple factors, including but not limited to location, job-related knowledge, skills, and experience. Mastercard benefits for full time (and certain part time) employees generally include: insurance (including medical, prescription drug, dental, vision, disability, life insurance); flexible spending account and health savings account; paid leaves (including 16 weeks of new parent leave and up to 20 days of bereavement leave); 80 hours of Paid Sick and Safe Time, 25 days of vacation time and 5 personal days, pro-rated based on date of hire; 10 annual paid U.S. observed holidays; 401k with a best-in-class company match; deferred compensation for eligible roles; fitness reimbursement or on-site fitness facilities; eligibility for tuition reimbursement; and many more. Mastercard benefits for interns generally include: 56 hours of Paid Sick and Safe Time; jury duty leave; and on-site fitness facilities in some locations. **Pay Ranges** O'Fallon, Missouri: $83,000 - $137,000 USD

QC Scientist - Weekend Shift Department: Quality Control - Analytical Team Schedule: Friday to Monday | 4x10 Hour Shifts | Flexible Start Times (7 AM-5 PM or 8 AM-6 PM) Why Join Us? Be part of a growing, innovative team at the forefront of pharmaceutical quality control. As a QC Scientist, you'll play a vital role in ensuring the safety and efficacy of life-changing biologic products. This is a unique opportunity to join a newly formed weekend team, receive comprehensive training, and contribute to meaningful work in a collaborative, fast-paced environment. What You'll Do As a QC Scientist, you'll work hands-on in a state-of-the-art laboratory, performing advanced analytical testing to support GMP manufacturing. Your responsibilities will include: * Conducting analytical tests using HPLC, UPLC, CGE, iCE, Cell-Based Assays, and Compendial Testing (pH, UV, Osmolality, Appearance). * Supporting commercial product testing, stability studies, and client-driven projects. * Reviewing laboratory data packets and authoring investigations. * Collaborating with cross-functional teams including Quality Assurance and Data Review. * Ensuring compliance with GMP standards, SOPs, and safety protocols. * Participating in lab operations such as safety inspections and inventory management. What You Bring * Education: Bachelor's degree in Chemical Pharmaceutical, Biology, Chemistry, Biotechnology, or a related field. * Experience: 1-5 years in a GMP-regulated environment, preferably in pharmaceuticals. * Hands-on experience with analytical instruments and techniques: HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, Cell-Based Bioassays. * Familiarity with EMPOWER, MS Office, and laboratory software. * Strong organizational skills, attention to detail, and a collaborative mindset. Training & Team Environment You'll be part of a tight-knit team of 6 Scientists and 1 Supervisor, supported by a larger QC Analytical group of 80+ professionals. Expect 3-6 months of structured training, with hands-on testing and mentorship before transitioning to weekend operations # Job Type & Location This is a Contract to Hire position based out of St. Louis, MO. Pay and Benefits The pay range for this position is $28.00 - $38.00/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 St. Louis,MO. Application Deadline This position is anticipated to close on Dec 9, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? * Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves. * Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges. * Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, Always. * Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded. Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Field Chemist As a Field Chemist you will be responsible for sorting and transporting hazardous and non-hazardous materials and waste, always ensuring compatibility and safety in all processes for each service provided to customers. Essential Functions & Requirements: * Prioritizes health and safety by adhering to policies, processes, and maintaining safe practices at all times * Assists in the segregation of chemicals by hazard class and packs compatible materials in appropriate containers and prepares for transportation; completes necessary paperwork for each job * Determines and loads supplies needed for job completion and travels to various industry, laboratory, and educational sites to perform lab pack services * Assists in characterizing materials at field project sites * Adheres to proper placarding and load segregation requirements when transporting hazardous materials * Develops good customer relations by effectively communicating with site points of contact and others at customer location / site * Appropriately directs Field Technicians / Drivers who are assisting with waste collection * Maintains an introductory knowledge of high-hazard materials management / assessment and cylinder handling * Maintains the ability to travel to support outside locations as needed * Takes on additional duties as assigned to support the team and organization Education: * Bachelor's degree (required), with a focus in environmental science or science (preferred) Experience: * In lieu of degree 2+ years of related experience (required), previous experience in lab packing or environmental waste (preferred) * Valid Driver's License and ability to obtain a Class B CDL with Hazmat endorsement within 6 months of hire date (required) * Ability to pass a Motor Vehicle Record search to Company standards (required) Competencies: * Ability to work in a constant state of alertness and in a safe manner * Ability to develop a working knowledge of all Federal, State, and local laws and regulations pertaining to the Environmental Services industry * Excellent interpersonal skills to effectively communicate with internal and external customers * Regular and predictable attendance to perform the functions and requirements of this role Additional Requirements: * Due to the potential exposure to atmospheres/waste/materials this position requires individuals to be clean shaven at all times in order to don a respirator for protection. Benefits, Compensation, & Workforce Diversity: Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran or status as a qualified individual with a disability. A post-offer drug screen will be required.

Are you ready to embark on a career where innovation meets excellence? At Jost Chemical Company, we're on a mission to push the boundaries of chemical manufacturing, delivering high-quality products that make a positive impact on global industries. If you're passionate about chemistry, dedicated to precision, and eager to contribute to a company that values both innovation and integrity, explore our exciting job opportunities. Join us in shaping the future of chemical manufacturing at Jost Chemical Company, where your career is more than just a job - it's a journey of growth and achievement. Then, this position is right for you! Founded in 1985, Jost Chemical is a global leader in the manufacture of high purity mineral salts for the nutritional, pharmaceutical and specialty markets. Expansion, growth of capabilities, and investment in people, lab and production equipment have been a part of Jost's company culture for 35 years. To learn more about Jost Chemical please visit ******************** Our offer: * Shift Differential * Medical/Dental/Vision Plan Insurance, Short and Long-Term Disability and Life Insurance first of the month following 60 days. * 401k plan which includes safe-harbor contribution and discretionary match. * Paid Time Off (PTO) Employees eligible first day of employment. * 9 Company Paid Holidays (72 hours) each year. * Uniforms Provided * Foot Protection- annual allowance for all laboratory, maintenance and production employees. * 24-hour access to our free, on-site fitness center. * We provide Individual development, on-the-job training, and development programs designed to enhance your professional growth and development while ensuring you feel valued, inspired and appreciated at work. Jost Chemical is an equal opportunity employer and affirmatively seeks diversity in its workforce. We consider applicants, and make all employment decisions, without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, or any other legally protected status. We are committed to recruiting and retaining the best talent in the chemical manufacturing industry. Background * Works under general direction of the Quality Control Manager in a c-GMP regulated manufacturing environment operating under Q7A standards. * Employees in positions at this level of the series exercise a considerable degree of independence in conducting a wide range of experiments requiring expertise in the application and adaptation of numerous research techniques and produce desired results. Tasks * Perform analytical testing using wet chemistry techniques and instrumentation on c-GMP regulated products following compendial methods (USP/NF, EP, FCC, JP etc). * Perform microbiological testing on c-GMP regulated products using compendial methods. * Perform routine and non-routine testing using basic and advanced laboratory instrumentation and adhere to a strict calibration / preventative maintenance program. * Interpret analytical data and assist chemical operators and chemical engineers with applying this data to the manufacturing process. * Write research methods, results, and conclusions for publication; may present at professional conferences. * Review scientific literature, abstracts, and applicable method papers; identify appropriate application for current or anticipated research projects. * Maintain data integrity in both written and digital form. * Prepare laboratory test solutions and perform standardizations of volumetric solutions. * May be required to inventory and order laboratory supplies, instruments, and reagents. * Maintain a clean and organized work area. * Maintain and enhance site safety. * Instruct other personnel in specific areas of quality control laboratory testing. * Data mining and trending; Process Validation support; Root Cause Analyses; Problem Solving Tools use; Statistical Data trending; Support for Non-conformance Investigations; Production support activities. Specifications * A.S or B.S. Chemistry or related technical field that included instrumentation, or industry experience. * 0-2 years professional level chemist experience. Knowledge of: * Theories, principles, and methods of instrumental and wet chemistry * Method development and method validation * Mathematics and statistics * Basic analytical laboratory equipment * MS Office software package Skill in: * Working effectively and efficiently on multiple projects at once * Working effectively in a team environment * Responding to rapidly changing demands Ability to: * Lead and/or train others in assigned activities * Follow compendia and other test methods * Develop creative solutions to more varied research procedural problems * Design and manage projects * Identify, gather, process, and record data accurately * Maintain quality, safety, and/or infection control standards * Operate and maintain laboratory equipment * Communicate effectively, orally and in writing (including documenting research methods, results, and conclusions) * Exercise independent judgment

At the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight 21st century listed technology companies in the world to cross $1bn in Net Profit, $6bn in Revenue and $15bn in Market Capitalization. Job Description • Molecular biologist to aid in characterization of recombinant mammalian cell lines. Requires BS/MS in molecular biology or related field and at least one year of laboratory experience. • Must be familiar with general cell culture techniques (ex. aseptic passaging of cell lines), RNA, cDNA and genomic DNA preparation, DNA/RNA electrophoresis, and Northern and Southern analyses. • Experience with molecular cloning techniques such as plasmid construction, preparation and analysis, DNA sequencing technologies and analysis of DNA sequencing data multiple sequence alignments, identification of mutant sequences, in silico protein translation, etc. would be a definite plus MOST CRITICAL SKILLS: gDNA/RNA preparation; northern/southern blot analysis. Additional Skills:REQUIRED PERSONALITY TRAITS: team oriented, fast learner, good attention. MOST CRITICAL SKILLS: gDNA/RNA preparation; northern/southern blot analysis. Additional Information Best Regards, Anuj Mehta ************

**_What Research and Development Engineering contributes to Cardinal Health_** Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. **_Job Summary_** This position is responsible for providing technical support at an intermediary level to new product development projects and post product release projects. This individual is expected to be proficient in the various competencies relevant to their job. Requires limited supervision; limited instruction on routine work, and general instructions are given on new work or special assignments. **_First Shift position (Monday - Friday) in Hazelwood, MO_** **_Responsibilities_** Product Testing + Under general supervision, follows testing protocols, selects appropriate test fixtures and set-ups. + Assists in test method development. + Coordinates with project Engineer(s) to setup, execute, and report out results for each test project. Protocol/Report Writing + Under direction, writes protocols. + Writes reports including data, analysis, and observations from testing performed according to protocols. Laboratory Management + Maintains laboratory supplies. + Aids in maintaining calibration and repair of equipment. **_Qualifications_** + High School Diploma or GED required + 2 or more years related work experience preferred + Verification, Validation, and Evaluation testing for medical devices, preferred + Tensile Test Equipment (i.e. MTS, Instron, or similar), preferred + Optical Measurement Equipment (i.e. OGP, Keyonce, or similar), preferred **_What is expected of you and others at this level_** + Applies acquired knowledge and skills to complete standard tasks + Readily learns and applies new information and methods to work in assigned area + Utilization of time management and organizational skills to coordinate projects, as needed, in parallel. + Leverage critical thinking skill on a daily basis, as it related to product testing, to understand and communicate test findings to the Engineering team. + Maintains appropriate licenses, training and certifications + Works on routine assignments that require some problem resolution + Works within clearly defined standard operating procedures and/or scientific methods + Adheres to all quality guidelines + Works under moderate degree of supervision + Work typically involves regular review of output by work lead or supervisor + Refers complex unusual problems to supervisor **Anticipated hourly range:** $22.00 per hour - $31.60 per hour **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 11/28/2025 *if interested in opportunity, please submit application as soon as possible. The hourly range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. \#LI-MP1 _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: In this role you will provide leading functional genomics technologies including RNA interference (sh RNA) for gene silencing and cutting-edge systems for gene editing and gene knockout (CRISPR/Cas9, ZFN's). Responsibilities include but are not limited to: * Manufacture made to order products in Bacteria, DNA, RNA, and Lentiviral formats for Academic, Pharma and Research centers. * Work closely with R&D, Marketing, Sales, and Bioinformatics teams on development, transfer and manufacturing of existing and new products. * Responsible for all Manufacturing, QC, Packaging and Shipping. Perform production operations. * Set-up and prepare products according to current manufacturing procedures. Ensure quality and quantity of product throughout production process. * Clean-up equipment and working areas after production operations. * Coordinate appropriate disposal of waste and complete compliance documentation. * Communicate and document status of processes, products, and equipment. Communicate the status of production operations and bring deviations to the attention of supervisor. * Provide a complete and accurate batch record at the conclusion of production operations consistent with quality guidelines including Non-Conformance Reports (NCR) if applicable. * Enter hours worked and raw materials used into SAP. * Ensure all applicable logbooks have been filled out completely as required by current procedures. Write and modify production procedures consistent with quality guidelines. Physical Attributes: * Wear appropriate Personal Protective Equipment. Who You Are: Minimum Qualifications: * Bachelor's Degree in Biology, Biochemistry or other Life Science discipline. * 1+ years laboratory and/or production experience. Preferred Qualifications: * Experience with laboratory instruments, molecular biology and cell culture procedures, and production equipment. * Experience with process techniques and unit operations. * Experience with problem solving and analytical techniques. RSREMD Pay Range for this position: $25/hr-$44/hr The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Our Purpose Mastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we're helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation, partnerships and networks combine to deliver a unique set of products and services that help people, businesses and governments realize their greatest potential. Title and Summary Specialist, Product DevelopmentJob Overview: Provides designs specifications for and develops new products and services or their components. Defines functional and technical requirements. Researches new technologies and competitive products to develop additional product ideas and enhancements. Performs launch-related activities associated with new or highly customized product implementations, including marketing/communication and collateral. Defines business and technical requirements and manages the relationships of technical resources and the Global Technology Organization to maintain and build out platforms. Major Accountabilities: • Participate in the development of new products and product enhancement by performing assigned tasks in the product development life cycle • Compile information regarding market trends, the competitive landscape, and new product opportunities • Participate in defining product requirements and specifications • Support product launches and implementations • Contribute to the execution of product marketing programs • Prepare reports and presentations as directed Education: • Bachelor's degree or equivalent work experience desirable Knowledge / Experience: • Experience of payments industry and/or financial services experience • Broad knowledge of product development functions Skills/ Abilities: • Some understanding of general product development concepts and practices • Demonstrated ability to multi-task, establish priorities and work independently • Solid organization and project management skills • Solid verbal and written communications skills • Ability to understand and analyze financial information • Ability to interact effectively with colleagues and work collaboratively with internal and external business partners Work Conditions: • 5% domestic/international travel required Mastercard is a merit-based, inclusive, equal opportunity employer that considers applicants without regard to gender, gender identity, sexual orientation, race, ethnicity, disabled or veteran status, or any other characteristic protected by law. We hire the most qualified candidate for the role. In the US or Canada, if you require accommodations or assistance to complete the online application process or during the recruitment process, please contact reasonable_accommodation@mastercard.com and identify the type of accommodation or assistance you are requesting. Do not include any medical or health information in this email. The Reasonable Accommodations team will respond to your email promptly. Corporate Security Responsibility All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must: Abide by Mastercard's security policies and practices; Ensure the confidentiality and integrity of the information being accessed; Report any suspected information security violation or breach, and Complete all periodic mandatory security trainings in accordance with Mastercard's guidelines. In line with Mastercard's total compensation philosophy and assuming that the job will be performed in the US, the successful candidate will be offered a competitive base salary and may be eligible for an annual bonus or commissions depending on the role. The base salary offered may vary depending on multiple factors, including but not limited to location, job-related knowledge, skills, and experience. Mastercard benefits for full time (and certain part time) employees generally include: insurance (including medical, prescription drug, dental, vision, disability, life insurance); flexible spending account and health savings account; paid leaves (including 16 weeks of new parent leave and up to 20 days of bereavement leave); 80 hours of Paid Sick and Safe Time, 25 days of vacation time and 5 personal days, pro-rated based on date of hire; 10 annual paid U.S. observed holidays; 401k with a best-in-class company match; deferred compensation for eligible roles; fitness reimbursement or on-site fitness facilities; eligibility for tuition reimbursement; and many more. Mastercard benefits for interns generally include: 56 hours of Paid Sick and Safe Time; jury duty leave; and on-site fitness facilities in some locations. Pay Ranges O'Fallon, Missouri: $83,000 - $137,000 USD

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Candidate must be proficient with wet chemistry and analytical instrumentation (emphasis on proteins desired). Primary roles include routine analytical testing (HPLC, colorimetric assays) and GMP testing (qualification and validation) for a high throughput protein analytics laboratory. Responsible for general laboratory and operational support, including assisting scientific staff with lab maintenance activities. Strong interpersonal skills are required to communicate effectively with our partner lines. Basic laboratory skills including use of balances and adjustable pipets , ability to work with Excel spreadsheets and laboratory notebook software. Qualifications Minimum of BS degree is required. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

QC Scientist - Weekend Shift Department: Quality Control - Analytical Team Schedule: Friday to Monday | 4x10 Hour Shifts | Flexible Start Times (7 AM-5 PM or 8 AM-6 PM) Job Title: QC Scientist Job Description Join our team as a QC Scientist where you will leverage numerous analytical tools for large molecule analysis including HPLC, UPLC, CGE, iCE, and Cell Based Analyses. This role supports GMP manufacturing for commercial product and stability testing. Prior experience in a cGMP environment is required. Pay:$28-$38 Responsibilities * Perform HPLC, UPLC, CGE, iCE, Cell Based Analyses, and Compendial Testing on In-Process, DS release, and stability samples, ensuring timely project delivery. * Review laboratory data packets and author laboratory investigations as assigned. * Conduct GMP testing using HPLC and UPLC test methods such as Reverse Phase, SEC, and CEX. * Compile data for documentation of test procedures and prepare reports. * Collaborate with team members and departments like quality assurance and data reviewers. * Contribute to the development of new concepts, techniques, and standards. * Recognize and report invalid, lab incident, out-of-specification, or out-of-trend results; recommend solutions. * Perform all duties in compliance with SOPs, GMP, and safety guidelines. * Participate in laboratory activities, perform safety inspections, and order supplies. Essential Skills * 0-5 years of proven experience in a GMP regulated environment, preferably pharmaceuticals. * Experience with analytical techniques and required instrumentation such as HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, and cell-based bioassays. * Knowledge of GMP regulations in a cGMP manufacturing environment. * Working knowledge of scientific principles for a wide range of analytical techniques. * Proficiency with EMPOWER, MS Office, and laboratory computer programs. Additional Skills & Qualifications * Bachelor's degree in chemical pharmaceutical, biology, chemistry, biotechnology, or related field. * Prior use of EMPOWER is preferred. * Good organization and planning skills. * Attention to detail and a positive, collaborative demeanor. Work Environment You will be part of a newly formed team of 6 Scientists and 1 Supervisor supporting the weekend shift within a QC Analytical team of over 80 members. The role involves 3-6 months of training and testing on each test before progressing. Work in a pharmaceutical lab setting doing bench work. Shifts are 4-10 hour days from Friday to Monday, with flexible hours between 7am-5pm or 8am-6pm. Job Type & Location This is a Contract to Hire position based out of Berkeley, Missouri. Job Type & Location This is a Contract to Hire position based out of Berkeley, MO. Pay and Benefits The pay range for this position is $28.00 - $38.00/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 Berkeley,MO. Application Deadline This position is anticipated to close on Dec 8, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

**Our Purpose** _Mastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we're helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation, partnerships and networks combine to deliver a unique set of products and services that help people, businesses and governments realize their greatest potential._ **Title and Summary** Specialist, Product Development - Business Integration & Excellence Who is Mastercard? Mastercard is a global technology company in the payments industry. Our mission is to connect and power an inclusive, digital economy that benefits everyone, everywhere by making transactions safe, simple, smart, and accessible. Using secure data and networks, partnerships and passion, our innovations and solutions help individuals, financial institutions, governments, and businesses realize their greatest potential. Our decency quotient, or DQ, drives our culture and everything we do inside and outside of our company. With connections across more than 210 countries and territories, we are building a sustainable world that unlocks priceless possibilities for all. Services within Mastercard is responsible for acquiring, engaging, and retaining customers by managing fraud and risk, enhancing cybersecurity, and improving the digital payments experience. We provide value-added services and leverage expertise, data-driven insights, and execution. Overview The Business Integration & Excellence Team in Security Solutions is seeking a Product Development Owner to align business and technology strategies and support product development activities. This role focuses on enabling the creation and implementation of a range of products and services designed to detect fraud, ensure uninterrupted commerce, and maximize transaction value. The ideal candidate thrives in fast-paced environments and excels at transforming business needs into deliverable products. Role As a Product Development Owner, you will: - Manage Program and Intake processes to ensure optimal resource allocation, timeline commitments, external team dependencies, cross synergies, and efficiencies. - Implement the product roadmap by translating business requirements to engineering teams and managing the Epics throughout the software engineering lifecycle. - Collaborate closely with the Product Managers to execute critical tasks for project success. - Ensure development teams deliver high-quality work that aligns with business requirements, removing blockers, and keeping stakeholders informed. - Act as the main point of contact between the business and development teams, ensuring alignment and clear communication. - Evangelize the product goals from the customer perspective with all internal and external stakeholders. - Ensure we are building to meet Program and Product Objectives. All About You The ideal candidate for this position should: - Be a strong communicator, both written and oral. - Have the ability to work autonomously and take ownership of tasks with minimal supervision. - Build partnerships across teams and mediate conflicts effectively. - Possess a proactive mindset with excellent critical thinking and problem-solving capabilities. - Have expert knowledge in the Software Engineering Lifecycle. - Be able to manage priorities and delegate tasks effectively in a fast-paced environment. - Be adaptable to change. Preferable but not required: - Studio experience - AHA expertise - Jira expertise - Product Management experience - Project Management experience/accreditation Education - Bachelor's degree in Information Technology, Computer Science, or Management Information Systems or equivalent combination of relevant experience and education Mastercard is a merit-based, inclusive, equal opportunity employer that considers applicants without regard to gender, gender identity, sexual orientation, race, ethnicity, disabled or veteran status, or any other characteristic protected by law. We hire the most qualified candidate for the role. In the US or Canada, if you require accommodations or assistance to complete the online application process or during the recruitment process, please contact reasonable_accommodation@mastercard.com and identify the type of accommodation or assistance you are requesting. Do not include any medical or health information in this email. The Reasonable Accommodations team will respond to your email promptly. **Corporate Security Responsibility** All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must: + Abide by Mastercard's security policies and practices; + Ensure the confidentiality and integrity of the information being accessed; + Report any suspected information security violation or breach, and + Complete all periodic mandatory security trainings in accordance with Mastercard's guidelines. In line with Mastercard's total compensation philosophy and assuming that the job will be performed in the US, the successful candidate will be offered a competitive base salary and may be eligible for an annual bonus or commissions depending on the role. The base salary offered may vary depending on multiple factors, including but not limited to location, job-related knowledge, skills, and experience. Mastercard benefits for full time (and certain part time) employees generally include: insurance (including medical, prescription drug, dental, vision, disability, life insurance); flexible spending account and health savings account; paid leaves (including 16 weeks of new parent leave and up to 20 days of bereavement leave); 80 hours of Paid Sick and Safe Time, 25 days of vacation time and 5 personal days, pro-rated based on date of hire; 10 annual paid U.S. observed holidays; 401k with a best-in-class company match; deferred compensation for eligible roles; fitness reimbursement or on-site fitness facilities; eligibility for tuition reimbursement; and many more. Mastercard benefits for interns generally include: 56 hours of Paid Sick and Safe Time; jury duty leave; and on-site fitness facilities in some locations. **Pay Ranges** O'Fallon, Missouri: $77,000 - $123,000 USD

What Research and Development Engineering contributes to Cardinal Health Engineering is responsible for performing research and analyses to develop design options for components, products, systems and processes. Specifically, Embedded and laptop software design, development, testing and documentation. Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. This is a hybrid position in the Hazelwood, MO facility. Responsibilities Build and test prototype software of new products in line with regulatory standards and write associated product development reports and supporting documentation. Troubleshoots various issues that arise pertaining to concept designs and production products through testing and computer-based statistical analysis. Assists the research and development process for various mid and long-term projects (1.5 - 3 years) to ensure profitable investment. Interacts with external personnel on significant cross-functional programs The ability to research legacy projects for possible update to end of life parts Qualifications 4-8 years of experience, preferred Bachelor's degree in related field, or equivalent work experience, preferred Strong C language skills Strong RTOS (Real Time Operating System) experience Strong C# language skills for developing and maintaining tools preferred Strong Knowledge of networking and servers is a plus Strong Knowledge of cyber security is a plus What is expected of you and others at this level Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects May contribute to the development of policies and procedures Works on complex projects of large scope Develops technical solutions to a wide range of difficult problems Solutions are innovative and consistent with organization objectives Completes work; independently receives general guidance on new projects Work reviewed for purpose of meeting objectives May act as a mentor to less experienced colleagues Anticipated salary range: $93,500 - $133,600 Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vision coverage Paid time off plan Health savings account (HSA) 401k savings plan Access to wages before pay day with my FlexPay Flexible spending accounts (FSAs) Short- and long-term disability coverage Work-Life resources Paid parental leave Healthy lifestyle programs Application window anticipated to close: 8/29/2025 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. #LI-MP1 #LI-hybrid Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here