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Description Introduction 7 ON/7 OFF SCHEDULE Do you have the career opportunities as a(an) Medical Lab Scientist ASCP you want with your current employer? We have an exciting opportunity for you to join Lakeview Hospital which is part of the nation's leading provider of healthcare services, HCA Healthcare. Benefits Lakeview Hospital offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include: • Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation., • Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more., • Free counseling services and resources for emotional, physical and financial wellbeing, • 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service), • Employee Stock Purchase Plan with 10% off HCA Healthcare stock, • Family support through fertility and family building benefits with Progyny and adoption assistance., • Referral services for child, elder and pet care, home and auto repair, event planning and more, • Consumer discounts through Abenity and Consumer Discounts, • Retirement readiness, rollover assistance services and preferred banking partnerships, • Education assistance (tuition, student loan, certification support, dependent scholarships), • Colleague recognition program, • Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence), • Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income. Note: Eligibility for benefits may vary by location. Our teams are a committed, caring group of colleagues. Do you want to work as a(an) Medical Lab Scientist ASCP where your passion for creating positive patient interactions is valued? If you are dedicated to caring for the well-being of others, this could be your next opportunity. We want your knowledge and expertise! Job Summary and Qualifications THIS IS A 7 ON/7 OFF SCHEDULE As a Medical Laboratory Scientist at our facility you will be an integral part of our Laboratory team. We are a highly functioning team that supports many different departments and has a passion for providing the best patient care through compassionate, professional interactions and reliable testing. In this role: * You will be responsible for receiving blood specimens, performing blood tests, and studying the morphology of the components of blood. * You will perform various routine or special clinical laboratory tests in one or more sections of the Laboratory using automated equipment, manual testing, and microscopic analysis to obtain data for use in diagnosis and treatment of disease. * You will be responsible for maintaining and using various equipment in the Laboratory including automated, chemistry analyzers, ion-specific electrodes, osmometers, and other analyzers. * You will perform antibody screening, antibody identification, and cross-matching procedures required in the administration of blood/blood components and identify antibodies in donors or patient’s blood that could react adversely during transfusion. * You will notify nursing units and/or physicians of critical lab values. * You will implement new testing methods, products, and instrumentation as appropriate to keep department current with technology. Qualifications: * Graduate of an accredited Medical Technology program (Associate’s degree acceptable) and/or a Bachelor of Science degree in Medical Technology, Chemistry, or Biology with appropriate certification (may be hired prior to graduation upon completion of required course work for graduation). * Nationally recognized certification as a Medical Technologist (MT/MLS or MLT) from the American Society for Clinical Pathologists (ASCP) or equivalent. * This licensure must be completed within 1 year of hire. * One year of experience working in a hospital or other clinical laboratory setting is preferred; new graduates will be considered. * American Red Cross or American Heart Association Basic Life Support Course (BLS or BCLS) and Certification. Lakeview Hospital: Where Compassion Meets Excellence ___ is a 125+ bed community hospital located in Bountiful, Utah, just north of Salt Lake City. We are proud to be nationally recognized as one of the nation’s 100 Top Hospitals for fourteen years and honored as one of Modern Healthcare’s Best Places to Work. Our mission is simple: to care for and improve human life. Every day, our caregivers deliver high-quality, compassionate care to the people who matter most—our families, friends, and neighbors. This commitment to caring is the foundation of everything we do. Bountiful offers a unique blend of small-town charm and year-round recreation. From skiing and snowboarding in the winter to boating, hiking, and golf in the summer, our location provides an exceptional lifestyle for our colleagues and their families. As part of HCA Healthcare, Lakeview Hospital is connected to a nationwide network of over 300 affiliated facilities. This means greater opportunities for career growth, professional development, and relocation across the country. We’re more than a hospital—we’re a community of caregivers united by purpose and passion. Join us at Lakeview Hospital and discover a career where your dedication is valued, your growth is supported, and your work truly makes a difference. HCA Healthcare has been recognized as one of the World’s Most Ethical Companies® by the Ethisphere Institute more than ten times. In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses. "Bricks and mortar do not make a hospital. People do."- Dr. Thomas Frist, Sr. HCA Healthcare Co-Founder If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Medical Lab Scientist ASCP opening. We promptly review all applications. Highly qualified candidates will be contacted for interviews. Unlock the possibilities and apply today! We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Quality Manager/Engineer Status: Full Time Reports To: Vice President of Operations Apex Biologix - We are a regenerative medicine company, providing high-quality biologic medical supplies and equipment to physicians and clinics nationwide. We are a fast-growing company in an evolving industry with projections to substantially increase our operations and sales this year. We’re looking for either an engineer with strong quality management experience or a quality leader with a solid engineering toolkit. We need someone to take over the role of Management Representative and own all the typical Quality Manager responsibilities in regards to the QMS (CAPAs, Complaints, NCMRs, Internal Audits, Management Reviews, etc.). But we also need some additional support in what an engineering role would typically be: DHFs, ECOs, managing testing and writing test reports, managing supplier and component approvals/specifications, etc. We have strong consultant and internal support/expertise in all areas but simply cannot handle the workload. We do not expect any given candidate to satisfy all requirements. We are looking for someone who can take the lead on the following initiatives, with significant support provided, and ensure proper execution of all deliverables. RESPONSIBILITIES AND DUTIES: Quality System/Leadership · Assume the role of Management Representative: Own and maintain a lean, pre-existing, audit- ready QMS aligned to ISO 13485 and the FDA QMSR transition (from 21 CFR Part 820); maintain/update SOPs, forms, and training. · Lead internal audits, supplier audits, management reviews, quality objectives, and KPIs (e.g., yield, complaints/1,000 units, OTD, NCMR/ECO/CAPA cycle time). · Oversee document control, training effectiveness, and change control (ECOs/Deviations), ensuring risk-based decisions and full traceability. · Mentor and develop quality techs. · Qualify and monitor CMs, sterilizers, and packaging suppliers (SCARs, QBRs, performance scorecards). · Partner with Operations and R&D on DHF, verification/validation test plans, and cost-of-quality reductions without compromising safety or compliance. · Partner with Operations to ensure efficient production, training, compliance, and documentation (Work Instruction development, record keeping, etc.). Product Engineering · Lead phase-gated design controls, properly document in the DHFs, plan/execute/document design verification testing. · Manage/maintain/update the Risk Management Files and FMEAs. Maintain product risk management to ISO 14971 across design/process/post-market; link hazards ↔ controls ↔ verification. · Manage change control/ECOs with risk-based regulatory impact assessments. · Develop statistically sound sampling plans (ANSI/ASQ Z1.4 / ISO 2859-1); drive root cause analysis (5-Why, Ishikawa, DOE) and corrections. · Review and release DHRs/lot records; define acceptance criteria, trending, and lot-release dashboards. · Own sterilization lifecycle with partners: ISO 11135/37 validations, quarterly/annual requalification, bioburden/BI oversight, and SAL justification. · Own packaging system lifecycle under ISO 11607-1/-2: seal strength (ASTM F88), dye/bubble leak (ASTM F1929/F2096), distribution integrity (ASTM D4169 / ISTA 3A), aging studies, label/IFU durability, and shelf-life claims. Ensure complaint-driven re-assessment of worst-case packaging and sterile barrier systems. · Ensure compliant UDI/labeling (21 CFR 801), IFUs, and claims; partner with Regulatory on submissions and change assessments. REQUIREMENTS: · 7+ years in medical devices with increasing responsibility across Quality and/or Manufacturing/Process/Packaging Engineering (small-company experience a plus). · Hands-on ownership of: ISO 13485, ISO 14971, ISO 11135/37, ISO 11607, and distribution testing. · Comfortable reviewing DHRs/batch records, various trending dashboards; strong writing for procedures, reports, and investigations. · Audit experience (internal, supplier, and at least one external: Notified Body or FDA/Health Canada). · Working knowledge of biocompatibility basics (ISO 10993), label controls/UDI, and complaint/MDR pathways. • Clear understanding of EtO and Gamma sterilization processes and their impacts to product design and packaging selection. ADDITIONAL SKILLS: · Sterile kit experience; contract manufacturing and sterilization management. · Specific engineering background (mechanical design, packaging tooling and pouch/tray/label specs, process engineering). · Qualification of cleanroom environments and environmental monitoring programs. · Knowledge of importing and FDA customs importing/exporting. · Some understanding of MDSAP compliance and implementation over an existing ISO 13485 foundation. · OUS device listing/registration experience. • CAD experience such as SolidWorks, Inventor or even SketchUp., • Statistical analysis, • Scientific method, human cell biology and chemistry., • Worked on any studies relate to medical devices or drug PAY AND BENEFITS: · Salary-W2 Position (80,000-100,000) per year • Health, dental, vision and life benefits available, • 401K matching, • 120 hours of Paid time off

Job Description Certerra is a growing national provider of testing, inspection, and certification services that support innovation in new product development, quality assurance, for project delivery, and engineered solutions for asset management. We are passionate about contributing to the sustainable development of the communities we serve. We are a national firm with a global reach serving national and international clients from 30+ offices located in 10 states and are ranked on ENR’s Top 500 list alongside the nation’s top firms. With a 60-year history, Certerra has a passion for high-end services, constant innovation, and investment in the development of world-class laboratory facilities, and interactive management technologies. Each member of our staff is committed to service, innovation, and the success of our clients. This Opportunity Certerra has immediate opportunities for a Group Leader of Environmental Services in Tucson, Arizona. You will manage projects, mentor staff, and expand business activity. We are looking for a candidate with a broad range of experience spanning due diligence, NEPA environmental reviews, building science evaluations, remedial investigations and corrective actions, underground storage tank management, indoor air quality, asbestos and lead-based paint services, and industrial hygiene consulting. Experience in the construction industry is a plus. This role will be working out of our Western Technology division in the Albuquerque, NM location. Your Impact Your responsibilities will consist of supervising personnel and projects, directing and leading field activities, reviewing and interpreting data, and developing recommendations consistent with industry standards and regulatory guidelines. You will review technical reports for accuracy, completeness and conformity to scopes and specifications. As a mentor, you will coach staff on project-related tasks and provide encouragement, advice, and direction on overall task performance. The Group Leader will offer guidance for the advancement of professional, academic, workplace and technical competencies. Through daily interactions, you will assist junior staff with identifying career path interests and encouraging training and development to achieve their objectives. You will participate in the interview and candidate selection process for staff additions to the group. Your business development activities will manage existing client relationships, influence business development, and promote growth. The Group Leader designs scopes of services to meet clients’ needs and develops competitive pricing and budgets that are competitive in the marketplace and achieve the firm’s profitability goals. You will collaborate with technical experts and marketing personnel to prepare and submit winning proposals for long-term, competitively bid government contracts. Key Responsibilities · In conjunction with senior level peers, promote and expand service-sector capabilities in one or more disciplines including asbestos, lead-based paint, indoor air quality, industrial hygiene, occupational safety, environmental exposures, construction/infrastructure management, and building sciences. · Participate in collaborative efforts on cross-discipline projects both within your assigned office, and regionally across the company’s business footprint. · Manage budgets, schedules, deliverables, and consultation to meet established project and business metrics for overall project performance. · You will coach and mentor junior staff on job performance, data quality objectives, and reporting. · Provide consultation and guidance regarding local, state, and federal regulations as they impact work practices, strategies, and project outcomes. · Requirements: · Bachelor of Science in chemistry, biology, geology, engineering, or industrial hygiene. · OSHA 40-Hour HAZWOPER Training with current updates. · Professional registration as an engineer or geologist, or as a Certified Industrial Hygienist or Certified Safety Professional, preferred, but not required · AHERA accreditations for asbestos inspector, management planner, contractor supervisor, site monitor, and abatement designer. · EPA or State certifications for lead-based paint risk assessor. · Minimum 5 years’ experience with environmental, building sciences and industrial hygiene. · Valid driver’s license acceptable per our insurance policy · Clear pre-hire drug screen · Excellent written and verbal communication skills. We are an Equal Opportunity Employer. This Company is dedicated to both the letter and the spirit of the equal opportunity employment laws. All applicants and all employees will be evaluated on the basis of their ability, competence, and performance of the essential functions of their positions. There will be no discrimination on the basis of race, sex, national origin, religion, age 40 and over, disability, sexual orientation, marital status, or any other classification which may be protected by federal, state, or local laws. In compliance with the Americans with Disabilities Act, we specifically offer equal opportunity for all employees or job applicants who may have a physical or mental disability. Such persons will be hired on the basis of their ability to perform the essential functions of the job in question. Likewise, their work will be evaluated on their performance of these essential functions. We will offer reasonable accommodation to individuals with disabilities, to the extent that Company resources allow without undue hardship. As part of our equal employment policy, there will be no wage differentials based on gender, between men and women employed in the same establishment, on jobs that require equal skill, effort, and responsibility, and which are performed under similar working condition

Job Description Welcome to DiscGenics, a pioneering, late-clinical stage biopharmaceutical company dedicated to advancing regenerative cell-based therapies for patients suffering from degenerative diseases of the spine. Privately held and passionately driven, our mission is to enhance lives by alleviating pain and restoring function through innovative treatment. At DiscGenics, we are committed to improving the quality of life for individuals debilitated by degenerative diseases of the spine. Our focus lies in developing cutting-edge therapies that offer hope and tangible results, fostering a future where patients can regain mobility and comfort. Our team is characterized by a relentless pursuit of excellence and a nimble approach to addressing challenges. Our core values of Integrity, Innovation, Accuracy, Teamwork, and Stewardship guide everything we do. Join us at DiscGenics and be part of a transformative journey where your contributions have the potential to impact the lives of millions. Together we innovate with purpose and compassion, striving towards a future where pain and limitations of degenerative spine diseases are a thing of the past. Discover more about us at discgenics.com and see how you can contribute to revolutionizing patient care through regenerative therapies. Job Summary: The Senior Scientist, Analytical Sciences is responsible to develop and qualify cell-based analytical methods and evaluate new analytical technologies. Also responsible to author and review method development reports, test methods, SOPs, protocols, supporting the technical review of CMC sections and supporting documents for regulatory filings. Must have industry experience in the development, qualification, and validation of cell bioassays (ELISA, Flow Cytometry, etc.) including experience with scale-up of methods to commercialization. Leads the collection and interpretation of data for biomarker and biological characterization assays including cell-based, multiplexed protein assays, and flow cytometry methods. Will work with manufacturing and quality control to develop tests, as well as analyze and author reports. Prepares technical reports, summaries, protocols and quantitative analyses. This role interacts with all levels of the organization in a collaborative and positive way with colleagues to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. Essential Duties and Responsibilities: • Manage strategic, SME, technical, and scientific development related to biological assays and other critical analytical methods., • Advance and implement cell-based bioassay/potency and immunophenotyping by multi-parametric flow cytometry methods from conception through optimization, qualification, and method transfer to Quality Control and external partners as part of an analytical control strategy and to support Process Development., • Employ quality by design (QbD) and design of experiment (DOE) approaches to method development to quickly identify operating regions within phase-appropriate pre-defined acceptance criteria aimed to meet ICH guidelines., • Work with Process Development, implementing and documenting analytical methods as part of experimental study plans to progress and characterize novel engineered cell therapy platforms., • Work with Quality partners to draft study protocols, qualification reports, change controls, and occasionally perform routine assays as QC personnel for drug product release and characterization., • Write, review, and edit accurate technical and development reports, CMC sections for regulatory submissions, and SOP/maintenance/user requirements for relevant equipment platforms., • Provide technical guidance to junior staff, assign tasks, review data, and strengthen regulatory concepts (cGMP)., • Participate in group and department meetings, present scientific data, and provide expertise in areas of responsibility., • Maintain, calibrate, and operate analytical equipment and instrumentation that is used in the execution of assays., • Author quality records (change controls, deviations, investigations) to implement method changes and/or to investigate non-conformances, OOS/OOT, and CAPA., • Author/contribute to other technical reports, including but not limited to comparability protocols/reports, risk assessments, and justification of specification, etc., • Others duties as required. Job Requirements: • Demonstrated knowledge of Process Development or cellular therapy products and Analytical Method Development within a regulated environment., • Experience with bioassay analytical science methods., • Strong interpersonal, communication (verbal and written), and organizational skills., • Independence and creative problem-solving abilities., • Ability to handle highly confidential business information., • Exceptional time management and multi-tasking skills., • Team leadership skills and team player., • Adheres to and leads with the Company Values of Integrity, Innovation, Accuracy, Teamwork and Stewardship., • Regular and predictable attendance., • Ability to report to work responsive, free from sedatives, and in a non-sedative state., • Advanced degree in biological, biochemical, chemistry, cell-biology, or related field., • 10+ years of relevant industry experience, preferable prior GMP roles for CMC., • Experience with commercial development of pharmaceutical, biological or cell therapy product., • First-hand experience in development and qualification of immunoassays, multi-parameter flow cytometry, and cell-based potency methods for release in a QC/regulated environment., • Must have experience with scale-up to commercialization. Working Conditions: Position requires qualified individuals to see, hear and speak (verbally and audibly). Required to ascend and descend stairs; sit, stand, lift, bend, stoop, crawl and kneel. The employee must also use hands to finger, handle or feel. Occasionally reaching with hands and arms, climbing or balancing are required. May be asked to drive or travel by car, air, or other transportation for business purposes. Must be able to lift and carry up to 20 pounds. Must be able to function effectively with noise in a lab environment. Natural and regular stressors occur on the job. Disclaimer: Please note: DiscGenics reserves the right to change, modify, suspend, interpret, or cancel in whole, or in part, any of the duties outlined above, at any time, and without advance notice to the employee.

Job Description About Scientia Vascular: Our mission is to save lives. Scientia Vascular is a leading innovator and manufacturer of endovascular medical devices. We use micromachining and microfabrication processes to manufacture products that provide physicians with enhanced performance for optimal outcomes for their patients. Job Position Summary: The Senior Regulatory Affairs Specialist (hereafter: “the specialist”) who thrives in a fast paced, cross-functional environment. They will be responsible for establishing regulatory strategies and provide input to management and cross functional team for future product pipeline. They will be performing activities necessary to comply with global regulation, primarily in the United States and the European Union. Specifically, the specialist will work to help establish systems and obtain regulatory approvals for new devices in development and will work to maintain approvals for Scientia Vascular’s portfolio of marketed devices. The specialist will also offer guidance generally on regulatory matters. Primary Responsibilities: The senior regulatory affairs specialist will be responsible for the following: • Supporting New Product Development, • Develop and execute regulatory strategies for obtaining approval for new products in development, • Lead and prepare and submit regulatory filings, • Maintain necessary FDA product databases, facility registrations and small business registrations, • Maintain international technical documentation, • Review product and quality system changes for compliance to regulatory requirements, • Review labelling and marketing materials for compliance to regulatory requirements, • Document post-market device changes, • Monitors compliance with existing regulations and upcoming or changing regulations, • Assist with impact analysis of regulatory changes and produces status reports, • Participates in processes to report, investigate, and addresses any issues of non-compliance, • Mentor team members on regulation review and application, • Offer guidance on regulatory matters, • Correspond and interface with regulatory authorities Required • BA/BS degree in Biology, Science, Engineering, Math or related field of study or equivalent, • Minimum of 4 years of experience in a medical device regulatory affairs role, • Computer proficiency, Microsoft Word and Excel in particular, • Work individually and self-starter, • Excellent analysis, writing, and communication skills, • Ability to communicate with cross-functional teams, • Ability to appropriately manage time and prioritize tasks, • Demonstrate knowledge of a regulated environment, • Some history of authoring or contributing to successful 510(k), PMA, and/or CE Mark submissions, • Pre-submission preparation and/or FDA interactions, • Ability to understand technical documents and drawings Key benefits we provide: • Medical, Dental, Vision insurance, • Generous Paid Time Off (PTO), • Paid Parental Leave, • Paid Holidays, • 401k Plan (with a generous employer match), • Life Insurance (company paid), • Short-Term & Long-Term Disability Insurance (company paid), • Subscription to Calmhealth.com, • Employee Assistance Program, • An environment of belonging where everyone can thrive

Job DescriptionSalary: $27 DOE Research Associate I or II Position Summary This position is part of a team that supports the analytical studies for regulatory submissions ofin vitro diagnostic (IVD) products developed by BioFire Defense. The primary responsibility is to execute and report on performance studies that demonstrate products and devices are functioning in accordance with design and regulatory requirements and specifications. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisors. Other key skills required: • Knowledge of microbiology and molecular biology principles, tools, and techniques, • Knowledge of basic laboratory practices including pipetting, handling of biological and chemical materials, sterile techniques, and contamination control, • Knowledge of basic statistical and concentration calculations, • Attention to detail, critical thinking, trouble shooting, and problem solving skills, • Ability to collaborate in a fast-paced environment, • Proficiency with Microsoft Office Suite, • May be required to obtain and maintain a DoD Personnel Security Clearance. Education Minimum of a bachelors degree with emphasis in a science, or related field. Experience • Research Associate I Six months experience in an academic, industry, or healthcare laboratory, • Research Associate II Two years experience in an academic, industry, or healthcare laboratory in addition to experience with real-time PCR and/or sequence analysis and familiarity with Biosafety Level 2 practices Benefits: • Medical, • Dental, • Vision, • 401k - company match of 5% regardless of participation and up to a total of 9.5% company match if contributing, • 4 Weeks of PTO, • 9 Paid Holidays, • Paid Winter Break from the work week between December 24 thru December 31, • Participation in Company's Wellness Program (discounted medical premiums), • Multiple Company Sponsored Events Each Year (catered breakfast/lunch, holiday parties, snacks), • Stimulating work environment, • Convenient location near I-15 and Trax Station, • Free Parking Our EEO Policy BioFire Defense is an equal opportunity employer (M/F/D/V). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law. BioFire Defense complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

New York, New York; Salt Lake City, Utah.Recursion is at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics.We are seeking a highly motivated and skilled Senior Clinical Project Manager wi

Senior Clinical Project Manager.Be among the first 25 applicants.Senior Clinical Project Manager.Get AI-powered advice on this job and more exclusive features.Recursion is at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse d

Job DescriptionThe Company and the Opportunity: Expanscience Laboratoires is a 100% family-owned French pharmaceutical company that has been perfecting its expertise in skincare and well-being for the last 70 years. The Company has three global business activities: dermo-cosmetics, natural active ingredients and positive ageing. Our commitment to being a sustainable company was recognized with the B Corp certification in 2018. Expanscience Laboratoires was the first ever pharmaceutical company to be awarded this accolade. Our Active Ingredients Division has built a strong reputation in the cosmetics industry for developing plant-based active ingredients with proven efficacy for skin health and well-being. Building on this expertise, we have just launched our nutraceutical division, with the same dedication to scientific excellence, responsible sourcing, and delivering effective solutions to support overall well-being. We are now looking for a dynamic Nutraceutical Ingredients Sales Account Manager to join this exciting new adventure dedicated exclusively to the nutraceutical business. More information can be found on Position Summary: Join us as we launch and develop a new line of natural nutraceutical ingredients targeted to the dietary supplements industry in your territory. You will be responsible for building and growing the nutraceutical client portfolio and associated sales, actively promoting our ingredients through customer meetings, calls, and industry trade shows. This is a fully remote role, ideally based out of California or Utah. You will work closely with our local U.S. team based in New York City, and occasionally with the French headquarters team. This role is expected to start in October 2025. Note: the title of the job is subject to change based on the final candidate’s job-specific knowledge, education, skills and depth of professional experience. Job Responsibilities (include but are not limited to): • Product & market knowledge, • Develop in-depth knowledge of our natural ingredient portfolio and its scientific positioning., • Understand market trends, customer needs, and product performance to effectively promote our ingredients to nutraceutical companies.2. Customer relationships & lead generation, • Build and maintain a strong base of dietary supplement and nutrition customers through regular customer visits, calls, networking, and participation in trade shows., • Proactively identify new business opportunities within the assigned territory and drive lead generation efforts., • Sales support & project follow-up, • Act as the primary point of contact for customers, ensuring smooth communication and coordination across internal teams, • Support customers throughout their development projects with regular follow-up, • Lead price updates and commercial negotiations as needed., • Internal reporting & forecasting, • Prepare and manage accurate sales forecasts and budgets., • Minimum 3–5 years of experience in B2B sales within the dietary supplement or nutrition industry., • Solid understanding of the dietary supplement market and its players, • Comfortable with frequent travel across the assigned territory to meet customers and attend industry events., • Technical background is strongly appreciated, or at least a good grasp of human biology, physiological targets, and product mechanisms of action., • Salary range of $90,000-$110,000 based on location, job-specific knowledge, education, skills and depth of professional experience., • Discretionary annual bonus, • Fully remote work arrangement, • Comprehensive medical, dental and vision insurance with a company contribution well above the national average., • Short-term and Long-term disability insurance (company paid), • Flexible spending accounts (health care and dependent care), • Maternity and paternity leave (company paid), • 401K with a Company match of 100% of the first 6%, • Employee assistance program, • Annual paid time off (PTO):, • 15 days per year, • 12 holidays (10 company holidays and 2 floating holidays), • 5 sick days, • Summer Fridays, • $175 bi-monthly Mustela and Babo Botanicals product allowance, • $100 monthly wellness reimbursement, • $85 monthly cell phone reimbursement, • Paid volunteer days, • Professional development training and learning opportunities, • Internal and international mobility, • Annual corporate offsite, • Various initiatives throughout the year in line with our B-Corp commitments including Health Week and Sustainable Development Week Why Join Us? You’ll be part of a B-Corp certified company that is committed to using business as a force for good and values sustainability, natural ingredients, and making a positive impact to the lives of families worldwide. Ready to take part in something new? Join us at the very start of an exciting new business activity! Expanscience is an Equal Opportunity Employer and does not discriminate on the basis of race, color, gender identity, religion, sex, age, national origin, disability, veteran status, sexual orientation, genetic information or any other classification protected by Federal, State or Local laws. Powered by JazzHR 9tlQrep2kZ

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Executive Director, Translational Biology. Recursion is looking for a highly collaborative, strategic, and experienced translational biology leader to guide a future-driven, technology-oriented approach to robust preclinical data packages. Oncology experience is a must, with a deep understanding of

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Being a Construction Project Manager at Momentum means you play a critical role in bringing our gyms to life.From site selection through lease negotiation, design, and construction, you will coordinate with architects, contractors, and our climbing wall builder, Walltopia, to make sure projects are

Be a part of the nationwide law enforcement initiative that removes the tools of crime from criminal organizations, depriving wrongdoers of proceeds from their crime and impacting the infrastructure of criminal enterprises.FSA Federal (FSA) is focused on delivering unsurpassed services in support of

Administrative Assistant Senior Living Community.Do you thrive in an organized environment and enjoy supporting both people and processes? Bridgewater - A Legacy Retirement Community is looking for a dedicated Administrative Assistant to join our growing team.This position is a great fit for someon

The Project Manager provides the overall leadership for the execution of successful outcomes on commercial/light industrial projects.The Project Manager leads the project team with a focus on the customer, utilizing open communication, setting clear direction, and establishing high levels of expecta

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Bachelor's degree in Business Management, Project Management, Medical Laboratory Science, Biology, Chemistry or equivalent degree OR Associate's degree and PMP Certification.

The Department of Pediatrics has an immediate opening for an experienced, highly motivated Administrative Assistant to support its division of Pediatric Nephrology as well as other subspecialty divisions as department needs dictate.The University of Utah offers a wellness program, great benefits pac

This role will provide essential administrative support to the Evidence Generation and Biostatistics & Data Management teams within Global Medical Affairs (approximately 25 team members).You will work in an international, matrixed environment, with regular interactions with the Global Medical Affair

Gpac and a well-established company in the commercial construction industry are partnered to hire an experienced Assistant Project Manager.This is an excellent and exciting opportunity for the right candidate looking for new challenges, opportunity for growth and a change in their career.The Assista

The Customer Services Functional Area of the Utah State Tax Commission is looking for individuals who are highly motivated, with strong work ethic and exceptional interpersonal skills to fill an administrative assistant entry level position.This individual will accompany staff to take notes in meeti

University Of Utah Health Administrative Support.As a patient-focused organization, University of Utah Health exists to enhance the health and well-being of people through patient care, research and education.Success in this mission requires a culture of collaboration, excellence, leadership, and re

CCI Mechanical is a wholly owned subsidiary of EMCOR Group, Inc.EMCOR is the world's leading provider of mechanical and electrical construction and facilities services, including planning, consulting, and operations and maintenance.CCI Mechanical is a HVAC design build mechanical services company th

Project Manager, Enterprise Facilities Management - West Region.Ferguson is actively hiring a Project Manager, Enterprise Facilities Management - West Region.This is a great opportunity to lead in the management and oversight of facilities project management across Ferguson's entire portfolio.We are

L3Harris Technologies is the Trusted Disruptor in the defense industry.With customers' mission-critical needs always in mind, our employees deliver end-to-end technology solutions connecting the space, air, land, sea and cyber domains in the interest of national security.Job Location: Salt Lake City

Executive Administrative Assistant - Remote.We help people get the medicine they need to feel better and live well.It fuels our passion and drives every decision we make.The Executive Administrative Assistant provides dedicated administrative support to one or more of Prime's Executive Leadership Te

At Regions, the Home Improvement Financing Administrative Assistant provides administrative and clerical services related to the activities of a division, department, section, or unit.Regions Home Improvement Financing, a division of Regions Bank, engages in strategic partnerships with home-improvem

Secret Unspecified Business - Support.Salt Lake City, UT (On-Site/Office).We've determined which skillsets are most beneficial for this role.These skills are listed first below as the Must Haves and Nice to Haves our hiring team highly prefers.Below that you'll find the standard job description for

Part-Time Administrative Assistant.Black & McDonald is an integrated, multi-trade service provider that safely delivers high quality construction, facilities management, and technical solutions.We are a family-owned and family-run company that employs thousands of highly skilled and talented profess

Investment Department Administrative Assistant.The Investments Department is responsible for implementing the investment program of the URS Defined Benefit plan.The Investments Team manages investments internally, and selects and monitors external asset managers, with a strong emphasis on alternativ

BD is one of the largest global medical technology companies in the world.Advancing the world of health is our Purpose, and it's no small feat.It takes the imagination and passion of all of usfrom design and engineering to the manufacturing and marketing of our billions of MedTech products per yeart

Big-D Self Perform Concrete is looking for a dynamic Concrete Project Manager with ground-up building experience.This is a great opportunity to continue your career with a company that is on a mission to be the most sought-after company in the business.We seek and employ exceptional, hard-working, l

Build Your Future with a Proven Leader! With over 65 years of excellence, Hughes General Contractors, Inc.General Contractor committed to building more than just structureswe're building a team of talented individuals who share our passion for quality, innovation, and collaboration.We're looking for

Executive Administrative Assistant.We are seeking a highly skilled and professional Executive Administrative Assistant to provide strategic and operational support to senior leaders within the US Medical Affairs and Government Affairs & Market Access (GAMA) teams.This role requires exceptional organ

Gas Fleet Overhaul Project Manager - Salt Lake City, UT.PacifiCorp is seeking customer-centric candidates to grow and sustain our commitment to a culture of customer service excellence, environmental sustainability, and diversity, equity and inclusion.With minimal direction, oversees high-risk proje

Sevan Multi-Site Solutions is a veteran-owned business that provides fully customized, turnkey, program management and construction services at scale.We offer program management, site assessments, design, and engineering services for restaurants, grocery, gas station, retail, and government projects

Sourcing Project Manager is responsible for conducting all sourcing activities and managing suppliers for specific assigned categories in accordance with the prescribed sourcing regulations and procedures.The Sourcing Category Project works in conjunction with Engineering Project Managers, Program M

Retro-Commissioning Project Manager II.The Retro-Commissioning Project Manager II is responsible for delivering the project as efficiently and effectively as possible within the budget, schedule, and quality throughout the life of the project.This position can support a remote candidate, however, pr

Helix Electric was founded in 1985 and is now one of the nation's largest and most successful electrical contracting companies.Our commitment to empowering people and powering projects is realized by our exceptional team of dedicated and highly skilled experts working together and never settling for

Project Manager/Estimator Heavy Civil.Join a proven heavy civil contractor in Arizona delivering large-scale projects in excavation, grading, paving, site concrete, and underground utilities.We take pride in quality, safety, and results and we're looking for a driven Project Manager/Estimator to m

Big-D is looking for a dynamic Sr.This is a great opportunity to start a career with a company that is on a mission to be the most sought-after company in the business.We seek and employ exceptional, hard-working, lifetime learners; we give them the tools to succeed when we find them.We have a cultu

A primary managerial position in a specific project and shares responsibility for project successes.Recognized ability to impact revenue and growth.Manages the firm's resources and assignments with proficiency, fluency and aptitude.Teaches and mentors staff and effectively embodies and expresses the

Bachelor's degree in Business Management, Project Management, Medical Laboratory Science, Biology, Chemistry or equivalent degrees and two years of demonstrated experience managing complex, multi departmental projects OR an Associate's degree with four years of demonstrated experience managing compl

The Senior Program Manager will play a critical role in establishing and leading the Project Control function, which is responsible for monitoring and managing various aspects of data center projects, including cost, schedule, risk, and performance.This position requires a highly organized and detai

Project Manager Masonry / Commercial.Our firm has partnered with a reputable commercial masonry contractor that's actively seeking a Project Manager to oversee multiple projects.This is an excellent opportunity for an experienced construction leader to join a team known for craftsmanship, accountab

Primary managerial position in project-related functions and is ultimately responsible for project successes.Recognized ability to impact revenue and growth for multiple projects.Possesses strong leadership and communication skills, a flexible attitude, ability to solve problems creatively and abili

Working at Breeze Airways is an exciting endeavor and a serious commitment to bring "The World's Nicest Airline" to life.We work cross-functionally with truly awesome Team Members to deliver on our mission: To make the world of travel simple, affordable, and convenient.Improving our guests travel ex