Invivoscribe jobs - 24 jobs

Invivoscribe is an industry pioneer, dedicated to Improving Lives with Precision Diagnostics . Invivoscribe has been the global leader in driving international standardization of testing and accelerating patient access to the newest and best cancer treatments for over 30 years.

A life sciences technology company is seeking a Field Service Engineer to provide technical support for revolutionary protein analysis equipment. The position is remote with potential travel across the Greater San Francisco Bay area and North America. Candidates should have a relevant engineering or science degree along with field service experience. The company offers competitive insurance benefits, 401k plans, and career development opportunities. #J-18808-Ljbffr

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: $21.20 - $29.15 **Key Responsibilities:** + Assist in the setup and running of automated liquid filling, labeling and packaging equipment. + Assist in the setup and running of manual liquid and powder portable filling equipment. + Perform daily filling, labeling, kitting duties according to the production schedule. + Comply with Good Manufacturing Practices (GMP's) and Quality Systems Regulations (QSR). + General organization of filling, labeling and packaging tasks. + Inspect all materials being issued to and returning from shop orders. + Accurately count and return all materials. + Maintain supplies for the CER, and packaging areas. + Read, follow and sign off on filling, labeling and packaging Standard Operating Procedures (SOP's). + Maintain and clean Controlled Environment Rooms, dry rooms and filling equipment. + Clean all equipment, parts and facilities following project completion. + Assist in aseptically aliquoting materials for production or shipment as needed. + Perform other tasks and duties as directed by management and supervisory personnel. + Must be able to lift, move, and operate heavy machinery. **Education & Experience:** + HS Diploma or GED Equivalent. 1-2 years' experience directly related to the duties and responsibilities specified preferred. + Prior experience working in a packaging environment, dry room and / or clean room beneficial. **Knowledge, Skills and Abilities:** + Follows departmental policies, procedures and objectives, and safety standards. + Ability to wear a half face respirator for extended periods of time. + Must have good English communication skills to understand and follow verbal and written instructions. Must have basic math skills. + Must be computer literate. + Ability to work well as part of a team. + Ability to meet packaging and filling requirements on schedule. + An orientation to detail and accuracy. + Excellent organizational skills. Must be able to handle multiple tasks. + Must be adaptable to quickly changing processes or environments. + Ability to setup, troubleshoot and understand basics of department machinery. **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: $132,400.00 - $217,600.00 **Position Summary:** The EHS Manager is responsible for developing, planning, coordinating, and directing environment, health and safety activities at Bio-Techne and its sites, while ensuring compliance and providing guidance to the company's California sites (San Jose, Newark, and San Marcos). This position focuses on achieving the highest levels of EHS performance through behavior-based initiatives, auditing, mentoring, and rapidly implementing change. The role requires understanding and implementing Federal, state, and local regulatory requirements, and supporting Cal/OSHA compliance programs at all California locations. **Key Responsibilities:** + Serve as the primary liaison for EHS activities in California (San Jose, Newark, San Marcos (remotely)). + Develop, implement, and maintain EHS policies, procedures, and training programs to meet federal (OSHA, EPA) and California (Cal/OSHA, CalEPA, DTSC, SCAQMD/Bay Area AQMD) regulatory requirements. + Ensure California site compliance with: + Cal/OSHA Injury and Illness Prevention Program (IIPP) + Cal/OSHA Heat Illness Prevention Standard (CCR Title 8 §3395) for indoor and outdoor work + Cal/OSHA Emergency Action and Fire Prevention Plans + Hazard Communication (HazCom) and GHS labeling per Cal/OSHA Title 8 §5194 + Ergonomic standards (CCR Title 8 §5110) for repetitive motion injuries + Oversee hazardous materials management, including: + Compliance with California Hazardous Waste Control Law and DTSC cradle-to-grave requirements + Submittal of Hazardous Materials Business Plans (HMBP) to local CUPAs + Management of Tiered Permitting or RCRA waste as required + Coordinate environmental compliance activities for California sites including: + Stormwater Pollution Prevention Plans (SWPPP) + Air permit compliance (SCAQMD/BAAQMD) + Hazardous Materials Release Response Plans and spill reporting requirements + Oversee recordkeeping including: + OSHA 300A/301 logs for all sites + California Log 300 posting and retention requirements + Participate in detailed incident investigations and root cause analyses for all sites and ensure corrective actions are completed and verified. + Conduct internal audits and compliance at all sites. + Lead EHS-related training programs, including Bloodborne Pathogens, Chemical Hygiene, Hazard Communication, and California-specific required training modules. + Provide mentoring, coaching, and cultural leadership to enhance safety culture across all supported sites. **QUALIFICATIONS** **Education and Experience:** + This position requires a B.A./B.S. degree and 5+ years of EHS / Hazardous materials professional experience or a combination of education, experience, managerial skills and training which provides the necessary background for performing the work. + A Certified Safety Professional (CSP), Certified Industrial Hygienist (CIH), or other safety management certificate is preferred + Prior experience with the FDA's Good Manufacturing Practices is preferred + Experience with Large Facilities EHS operations **Knowledge, Skills, and Abilities:** + Working knowledge of OSHA, EPA, ISO14001, ISO9001/ISO13485 and other regulatory requirements applicable to the company's operations + Knowledgeable in biosafety, ergonomics, materials management, and other programs outside regulatory oversight + Ability to influence key business decisions that involve operational EH&S functions + Proven ability to collaborate and lead a group of people in dramatically improving their culture of safety + Excellent interpersonal and communication skills. + Strong organizational skills + Computer skills including Microsoft Word, Excel and PowerPoint + Skills in problem solving; including the ability to identify and appropriately evaluate a course of action. + Skills in trouble shooting and critical thinking. + Ability to be flexible. + Ability to act independently on routine assignments or projects. + Ability to plan, organize and multi-task to complete assignments in an efficient manner. + Ability to communicate professionally, both oral and written. + Ability to pay attention to details and perform at a high-level accuracy. + Ability to work independently and with a team. **Working Conditions:** + On-site presence required. + Occasional travel may be necessary + May require extended hours, including evenings, weekends, and holidays. + Ability to work hours that conform to standard business operations (8:00 A.M. to 5:00 P.M.). **Physical Requirements:** + Must be able to walk facilities, conduct inspections, and respond to emergencies. + Ability to lift up to 25 pounds. + Prolonged periods sitting at a desk and working on a computer. **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

LGC Biosearch Technologies locations Petaluma and Novato, CA, as well as our sister site in Denmark, represent a focused, collaborative culture of producing mission-critical genomics components, primarily oligonucleotides and supporting reagents, for our diverse customer base. We believe in Science for a Safer World and have embodied our mission by supporting first responders during the COVID-19 pandemic where our Biosearch Technologies portfolio has been and continues to be enabling millions of PCR tests worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organization. Job Description We are seeking a strategic and results-driven Procurement Category Manager to join our Procurement team supporting the LGC Diagnostics and Genomics Business Unit. This role will responsible for managing key product categories and strategic vendor relationships, supporting purchasing activities within our sites while also leading initiatives to improve processes and optimize spend. The ideal candidate will bring a blend of category expertise, supplier management skills, negotiation and have demonstrated results within the Procurement function in an operational environment. Key Responsibilities Category Management Develop and execute category strategies aligned with business goals. Conduct market analysis and benchmarking to identify sourcing opportunities. Manage end-to-end procurement activities for assigned categories, including RFx processes, negotiations, and contracting. Monitor category performance and implement cost-saving initiatives. Supplier & Vendor Management Build and maintain strong relationships with strategic suppliers. Lead supplier performance reviews and implement corrective actions when needed. Collaborate with internal stakeholders to ensure supplier alignment with business needs. Negotiate commercial terms and manage supplier risk. Process Improvement & Team Collaboration Identify and implement improvements to procurement processes, tools, and policies. Support the development of standardized ways of working across the procurement team. Collaborate cross-functionally to drive procurement excellence and operational efficiency. Contribute to procurement transformation initiatives and change management efforts. Direct and indirect team management General Procurement Support Ensure compliance with procurement policies and procedures. Support internal stakeholders with purchasing needs and guidance. Maintain accurate records and documentation in procurement systems. Provide mentorship and support to junior team members as needed. Qualifications Bachelor's degree in Business, Supply Chain, or other related field. 5+ years of experience in procurement, category management, or strategic sourcing. Strong analytical, negotiation, and project management skills. Proven experience in process improvement and change management. Excellent communication and stakeholder engagement abilities. Team management skills and experience Proficiency in procurement systems and tools (e.g., ERP, e-sourcing platforms). Experience with MS Office suite (Word, Excel, PowerPoint, etc). Competencies & Behaviours: Resonate and operate in line with LGC's core value behaviors: Passion, Curiosity, Integrity, Brilliance, and Respect Self-motivated to uncover issues and drive improvement. Passion for continuous improvement, process and metric driven. Proven ability to deliver results. Work well in a team environment and communicate with all levels of the organization. Ability to influence others across a matrixed organization, as well as externally (e.g. suppliers) Additional Information Pay range for this role is: Minimum: USD$87,500/ per year Maximum: USD$145,000/ per year The salary range provided covers the minimum and maximum amounts projected for this role. The base salary will be influenced by factors like experience, skills, and location. What we offer (US based-employees): Competitive compensation with strong bonus program Comprehensive medical, dental, and vision benefits for employees and dependents FSA/HSA Pre-tax savings plans for health care, childcare, and elder care Deductible Buffer Insurance and Critical Illness Insurance 401(k) retirement plan with matching employer contribution Company-paid short- and long- term disability, life insurance, and employee assistance program Flexible work options Pet Insurance for our furry friends Enhanced Parental leave of 8 additional weeks PTO that begins immediately Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Company wide social events, frequent catered lunches and much more! LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership. All your information will be kept confidential according to EEO guidelines. For more information about LGC, please visit our website **************** #scienceforasaferworld

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: $56,700.00 - $93,300.00 **Position Summary:** The Research and Development (R&D Science) group at ProteinSimple, a Bio-Techne brand, is seeking an inquisitive and motivated Advanced Research Associate to join our growing team on our mission to develop game-changing analytical instrumentation. As a part of the Product Development Team, you will work among innovative and supportive scientists and engineers that have a passion for product development and a knack for disrupting the way people typically characterize their samples. Our team works on exciting technologies for analysis of biomolecules and cells, including capillary electrophoresis, automated immunoassays, microfluidics, and cell sorting. In this role, you will be involved in product development from early concept to commercialization for ProteinSimple products through assay optimization and validation, with the goal of delivering cutting edge technologies to our global customer base. If you have experience with analytical instruments, assay development, or capillary electrophoresis - this might be the role for you. If you want to make better analytical tools to enable our customers to make better medicines, apply today. **Key Responsibilities:** + Work closely with scientists from diverse backgrounds to learn and develop new analytical assays and reagents + Design, execute, and optimize experimental plans and protocols + Analyze, interpret, and troubleshoot results + Document and present experimental results to project and department team members + Participate in technical discussions and team meetings + Technical ownership for various study types (e.g., stability, verification, and validation) + Collaborate with hardware and software engineers during development + Participate in technical transfer of products from Product Development to Manufacturing + Help train new employees as needed **Education and Experience:** + BS (with 5-8 years industry experience) or MS (with 2-5 years industry experience) in analytical chemistry, biotechnology, biochemistry, molecular biology, or related field + Experience working in a biotechnology, pharmaceutical, CRO, or CDMO company is preferred **Knowledge, Skills, and Abilities:** + Hands-on experience with biomolecule characterization technique is required (e.g., LC, Octet, cIEF, CE-SDS, DLS, etc.) + Experience running capillary electrophoresis is strongly preferred + Experience running Maurice instrument is strongly preferred + Experience with biotechnology assay development is a plus + Eagerness to learn innovative analytical platforms and contribute to their advancement + Creative and critical thinker with careful execution of experiments + Ability to quickly learn and thoughtfully apply new skills and procedures + Desire to grow with a fast-paced and highly collaborative team + Must have strong organizational skills with high attention to detail + Must have good verbal and written communication skills + Strong team player and self-starter with the ability to work independently and collaboratively + Ability to prioritize own work and manage time efficiently for project deadlines, with flexibility to changing priorities + Experience performing verification and validation studies is a plus + Must be proficient in MS Office (Excel, Powerpoint, Word). Experience with JMP statistical software and/or a programming language (Python, MATLAB, R etc.) is preferred. **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $79,800.00 - $131,100.00 Job Purpose This role will report directly to the Supervisor, Planning & Procurement and will be responsible for developing, managing, and executing the master production schedule for a rapidly growing life sciences reagent manufacturing facility. Primary activities will be inventory planning of finished goods from start to finish, coordinating and printing manufacturing jobs, and leading other production planning activities such as managing scrap, conducting cycle counts, and deductions. Responsibilities * Set master production schedule for finished goods consisting of bulks, intermediate bulks, fills, kits, and any internal customer forecast needs. * Collaborate with Supervisor to lock the schedule for production launches weekly by monitoring inventory levels daily. Ensure due diligence on raw material availability, lot size requirements, and any other exceptions prior to locking schedule. * Provide finalized schedule to manufacturing and QC. * Prepare, print, and provide work orders and job/batch record packets to manufacturing and QC team for production and testing. * Monitor work orders throughout the production and QC process - checking for delays / issues and escalating appropriately. * Lead cross functional daily status meetings with manufacturing and quality control teams. * Collaborate with buyers to ensure alignment between the schedule and raw material allocation. * Minimize material scrap by managing expiration date of product, starting jobs on time, and optimizing job quantity. * Conduct all material transactions needed in ERP system including but not limited to backflushing, job creation, adjustments, cycle counting, and variances. * Lead cycle count quarterly for all production bulks, fills, and finished good kits. * Lead Bill of Material, Part Number creation, and Cost Roll for all NPIs and production requirements. * Support all change orders and NCPs as needed related to production and planning Qualifications Education: * Bachelor's degree in Supply Chain, Operations Management, Business, Engineering, or a related field required, or equivalent experience in production planning, scheduling, or manufacturing operations may be considered in lieu of a degree. Experience: * 3+ years of production planning or scheduling experience in a manufacturing environment, preferably in life sciences, biotech, or regulated industries (ISO 13485 a plus). * Demonstrated experience managing master production schedules and coordinating cross functional execution. * Strong working knowledge of ERP systems; experience with advanced planning/scheduling modules preferred. * Experience supporting NPIs, BOM creation, and cost structures. * Experience with a regular cycle count program * Experience working in a build to stock business within planning or buying * Experience working in an Assay / reagent manufacturing facility a plus Skills: * Advanced knowledge of production planning, scheduling, and material flow principles. * Strong analytical and problem-solving skills with the ability to resolve scheduling conflicts and production constraints. * High proficiency in ERP systems and Microsoft Excel. * Excellent communication and facilitation skills to lead cross-functional discussions and drive alignment. * Strong attention to detail, accuracy, and data integrity. * Ability to work in a fast-paced environment, manage competing priorities, and meet deadlines. * Knowledge of lean manufacturing, MRP, and inventory management best practices. Physical Requirements: * Occasionally lifting 25lbs * Working at a computer station for long periods * Ability to enter warehouse, production labs Why Join Bio-Techne: * We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. * We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. * We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. * We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. * We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. * We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: $89,300.00 - $146,900.00 As the Inventory, Planning, and Logistics Manager, you will ensure optimal inventory levels through strategic planning, forecasting, and collaboration with supply chain partners. By continuously improving accuracy, minimizing stockouts, balancing costs, and ensuring on-time deliveries we aim to support Bio-Techne's operational goals and enhance customer satisfaction. **Duties and Responsibilities:** + Ensures an accurate and timely accounting of all inventory stored on and off site, including rejected (MRB) and returned material oversight/disposition. + Provides actionable insights based on inventory data and support data driven strategies. + Process Improvement: + Identify and implement opportunities to streamline inventory management processes. + Leverage inventory management systems and technology to enhance tracking and reporting. + Oversee and manage daily warehouse operations, ensuring efficiency and compliance with company policies. + Supervise warehouse staff, providing leadership, training, and performance evaluations. + Proactively maintain a clean, organized, and safe warehouse environment. + Develop and implement process improvements to optimize warehouse efficiency. **Required Qualifications/Skills:** + Experience operating in a lean warehouse environment. + Ability to lead, motivate, and develop high-performing planning team. + Skills in developing and executing inventory control strategies. + Strong knowledge of shipping, receiving, and inventory control processes. + Proficiency in warehouse management systems and shipping software. + Experience implementing warehouse management or barcoding systems. **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: **Position Summary:** We are seeking an exceptional Field Applications Scientist (FAS) - Biologics Specialist based in the San Francisco Bay Area to provide advanced technical expertise and customer support for our cutting-edge biologics workflows and instrumentation. This role is pivotal in delivering pre- and post-sales application support, driving adoption of Bio-Techne's biologics solutions, and serving as a subject matter expert (SME) for complex biologics applications, including protein therapeutics, CGT, and downstream processing. **Key Responsibilities: ** + Provide expert-level technical supportfor Bio-techne's suite of biologicsinstrumentation;including method development, fractionation, and downstream applications. + Partner with Sales and Business Development Managers to deliver pre-sales consultations, technical presentations, and product demonstrations. + Conduct on-site and virtual training for customers on instrument operation, assay development, and data interpretation. + Act as a tiered technical resource for complex escalations prior to Applications Support teams. + Present at scientific meetings, user groups, and conferences toshowcase Bio-Techne'sbiologicscapabilities. + Collaborate with internal teams to provide customer feedback for product development and marketing initiatives. + Maintain competitive and business knowledge within assigned accounts and share insights with the broader team. + Support new product introductions (NPIs) and serve as a technical consultant for challenging applications. + Provide technical support and training for customers using Empower and Chromeleonchromatography data systems (CDS) inbiologicsworkflows. + Assistwith method setup, data acquisition, processing, and reporting within these platforms. + Troubleshoot software-related issues and ensure seamless integration with laboratory instruments. + Travel within the assigned territory (up to 50-75%) to provide on-site support and training. **Education and Experience:** + Requires a minimum of a BS/BA degree in Biochemistry, Pharmaceutical Sciences, or a related scientific field; MS/PhD preferred + 5+ years of hands-on experience in biologics and Cell & Gene Therapy workflows, including protein purification, characterization, and downstream processing + Previous experience as a Field Applications Scientist or technical support specialist is highly desirable **Knowledge, Skills, and Abilities:** + Deep understanding ofbiologicsdevelopment principles, including CGT andproteintherapeuticsworkflows. + Strong familiarity with capillary electrophoresis (CE) applications, chromatography and mass spec of proteins, virus particles, and LNP's. + Ability to troubleshoot,optimize, andvalidatecomplexbiologicsmethods independently. + Strong presentation and training skills for diverse scientific audiences. + Excellent time management, organizational, and communication skills. + Ability to travel extensively and work independently while collaborating effectively with cross-functional teams. + Strong working knowledge of Empower and ChromeleonCDS for chromatographic data management. + Ability to configure,validate, and maintain CDS systems in compliance with regulatory requirements (e.g., 21 CFR Part 11). + Skilled in interpreting chromatographic data and generatingaccuratereports using these platforms. + Familiarity with integration of CDS with LIMS and other laboratory software systems. + Excellent troubleshooting skills for software and data integrity issues. + Must have the ability to travel 50-75% of the time within the assigned territory Base Salary Range: $89,400 - $146,850 In addition, this position is eligible to receive a commission plan, in accordance with company policy. **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $25.20 - $34.65 Job Purpose The Quality Control Technician receives raw materials and performs product inspection and/or audits in accordance with established quality control program. This role involves sampling and testing of incoming raw materials to ensure that they, along with in-process and finished products meet the company's quality standards Responsibilities * Receive and perform inspection of incoming raw material/components to ensure compliance with company quality standards * Perform visual inspections on sub-assemblies and finished good products to identify defects and non-conformances * Maintain product quality by adhering to data management protocols * Support efficient supply chain operations by complying with and maintaining inventory control procedures * Ensure compliance with internal quality control standards and external regulations, and continuously improve quality control processes * Assist in the development and implementation of quality control procedures. * Collaborate with production teams to address quality issues and recommend corrective actions Qualifications Education: * High School Diploma * A.A Degree a plus Skills and Experience: * Life Sciences industry experience preferred. * Experience working in a Quality Control environment is strongly desired. * Previous experience performing incoming inspections is strongly desired. * Detail-oriented, efficient, and excellent organization skills. * Excellent verbal and written communication skills * Strong team player with the ability to work independently. * Able to multi-task and prioritize. * Proficiency in Microsoft Office and other relevant software * ISO and GMP experience preferred Working Conditions: * Significant amount of time on the production floor, in a laboratory setting * Some time in an office setting documenting inspection result, analyzing data, and communicating with team members Physical Requirements: * Standing and walking * Lifting and moving materials up to 50 pounds * Use of hands for precises tasks such as handling samples and testing equipment Why Join Bio-Techne: * We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. * We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. * We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. * We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. * We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. * We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: $89,300.00 - $146,900.00 **Position Summary:** As a **Senior Data Analyst - Operations & Supply Chain** , you will be a key contributor in driving supply chain agility, operational excellence, and cost efficiency through data. This role sits at the intersection of analytics, business operations, and strategy, supporting teams across **manufacturing, planning, inventory management, and fulfillment.** You will develop scalable analytics tools and provide actionable insights that directly influence decision-making, with a focus on areas such as **inventory optimization, demand forecasting, MRP alignment, and** **capacity** **planning.** You will work cross-functionally with business leaders, stakeholders, and technical teams to build scalable analytics solutions that optimize our supply chain and operational processes. **Key Responsibilities:** + **Develop Advanced Analytics Solutions:** Build and maintain dashboards and tools using Power BI, SQL, and Excel to deliver end-to-end visibility across supply chain KPIs including inventory turns, forecast accuracy, OTD, and production throughput. + **Supply Chain & Manufacturing Analysis:** Analyze complex datasets from ERP/MRP systems, demand plans, and production schedules to uncoverinefficiencies, delays, and root causes. Drive continuous improvement in areas such as order flow, raw material availability, safety stock, and build plans. + **Inventory Planning & Forecasting:** Support demand and supply planning by building models that improve inventory health, predict shortages or overages, and align stock levels with customer demand and production constraints. + **MRP System Integration:** Partner with planning and operations teams to ensure data models and recommendations align with MRP logic and master data structures. Help shape BOM, lead time, and lot size assumptions to improve planning accuracy. + **Strategic Insights & Decision Support:** Translate data into strategic recommendations for operations and supply chain leaders. Focus on balancing service levels, working capital, and operational cost through better planning and scenario modeling. + **Automation & Scalability:** Design and implement automated pipelines, workflows, and reporting processes that reduce manual work, increase visibility, and enable proactive response to supply/demand variability. + **Stakeholder Engagement:** Act as a thought partner to manufacturing, logistics, and finance stakeholders. Communicate findings clearly and tailor insights to operational, technical, and executive audiences. + **Mentorship & Collaboration:** Provide guidance to junior analysts and support a culture of data fluency across the supply chain team. + **Project Leadership:** Lead and manage high-impact analytics initiatives, ensuring timely delivery and alignment with organizational goals. **Required Qualifications:** + Bachelor's degree in Supply Chain, Finance, Accounting, Operations, Business Analytics, Industrial Engineering, or related field + 6-8 years of experience in data analytics with a strong focus on supply chain, operations, or manufacturing + Advanced proficiency in **Power BI, SQL, and Excel** , with experience in automation and scripting + Proven experience with **inventory planning, demand forecasting, M** **RP,** **ERP systems** + Experience with **predictive modeling, regression analysis, and correlation techniques** + Ability to distinguish signal from noise in complex datasets, providing clear insights for leadership + Proven track record of **developing scalable, long-term analytical solutions** + Strong **project management skills** with the ability to lead and execute initiatives + Strong **business acumen** and understanding of how supply chain data impacts cost, service, and capacity + Strong understanding of financial and operational metrics and how they influence business performance + Clear and confident communication skills, including stakeholder-facing presentations **Preferred Qualifications:** + Experience working with **Salesforce, Smartsheet, or other business intelligence tools** is a plus + Experience building dashboards and tools that drive operational execution and planning decisions + Experience in a **warehouse** , **manufacturing** **or production environment** + Familiarity with **production scheduling,** **capacity** **planning, and BOM structures** + Statistical or ML modeling experience for forecast or simulation + Knowledge of Lean, Six Sigma, or process improvement methodologies + Experience working with cross-functional data (e.g., sales, finance, operations) to enable full-picture decision-making **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: **Target Base Salary: $187,750** **Position Description:** Software Support Engineer for ProteinSimple, located in San Jose, CA: ● Use advanced troubleshooting and software debugging techniques, including log analysis, and error code diagnostics, to identify software defects and provide root cause analysis of the defects. Utilize Software Development Life Cycle (SDLC), Agile methodologies, Fishbone diagram, 5 Why analysis, Failure Mode and Effect Analysis (FMEA), and root cause analysis. Provide recommendations and course of action for defect resolutions. ● Lead the management of software patch releases, ensuring seamless deployment, testing, and documentation across all impacted systems through document management software like Arena. ● Analyze and solve complex technical problems related to software functionality, performance, and usability, leveraging sound technical knowledge and judgement of Software problem solving and analytical techniques. ● Collaborate with internal teams to perform end-to-end solution testing and validate software before deployment. ● Serve as a Subject Matter Expert (SME) for all software-related inquiries which requires debugging customer environments, triaging issues and reproducing defects for further analysis of its impact on applications' operations. Understand software architecture and data structure modeling, Windows & Linux Operating Systems. Debug and develop applications with backend & frontend software stack tools including Python, Flask, Java, or Pycharm. ● Work closely with software development, product management, and quality assurance teams to assess criticality of reported/existing issues and ensure appropriate escalations are tracked and resolutions are delivered as per defined Service Level Agreements using Jira & Salesforce. ● Participate in bug reporting, root cause analysis, and code debugging in collaboration with functional developers by utilizing tools including Microsoft Visual Studio Code, Oracle Virtual box, Git, Jenkins, Jira, Zephyr; offering insights from customer experience. ● Proactively identify and suggest improvements to software support workflows where feasible to increase efficiency. ● Track, analyze, and report key performance metrics related to software support, including response times, issue resolution rates, and customer satisfaction scores. ● Create and maintain comprehensive documentation for software releases, technical specifications, and user guides. ● Participate in cross functional tasks such as new product development projects, support readiness teams, knowledge base improvement, and help improve internal processes and tools. **Requirements:** Master's degree in Computer Science or closely related field with a minimum of 6 months of experience as a software customer support engineer or related occupation; or Bachelor's degree in Computer Science or closely related field with a minimum of 2 years of experience as a software customer support engineer or related occupation. Must possess a minimum of 6 months with a Master's degree or 2 years with a Bachelor's of experience with each of the following: software problem solving and analytical techniques; software architecture and data structure modeling; SDLC, Agile methodologies, Fishbone diagram, 5 Why analysis, FMEA, and root cause analysis; Windows & Linux Operating Systems; reporting, analysis, and software management tools including Oracle Virtual box, Jira, Salesforce, Git, Jenkins, Zephyr, or Microsoft Visual Studio; and debugging and developing applications with both backend & frontend software stack tools, including Python, Flask, Java, or Pycharm. \#LI-DNI **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $152,300.00 - $250,400.00 Do you dream about reinventing the Human Resources function by focusing on deepening the employee experience and emboldening a purpose-centered culture? Do you aspire to transform talent through mission centered guiding principles? Do you want to contribute to a company that improves lives through innovative health science? Do you deserve a career where you are empowered and trusted? If yes, come to Bio-Techne. As the Director, People Business Partner you will serve as the strategic HR partner for Bio-Techne's Diagnostic and Spatial Division and hold responsibility for overseeing all People initiatives within the division. As such, you will: partner with business leaders to drive organizational effectiveness, talent strategy, culture transformation, and change management capabilities; and partner globally within a OneHR team to support the business in achieving these goals. This position is based in the San Francisco Bay Area, reporting into the Vice President of Human Resources. Function Overview * Organization Effectiveness: Create and align processes and methods for efficiency that are modern and sustainable; deliver nimble execution of plans and strategies; utilize talent systems; practice collaboration across all HR centers of excellence. * Talent Management: Lead with a global mindset and assist with assessing, hiring, engaging, and retaining for talent succession. Partner with the business leaders to proactively build talent forecasting strategies and workforce plans, staying attuned to market trends within the life sciences industry. * Leadership Development: Work closely with senior leaders and managers to build organizational capability by utilizing a range of strategic people-related processes and programs including talent management, performance management and resource planning. Support the leadership capability development to create a qualified internal candidate pool to support growth. * Leader Partner: Facilitate and drive strategic discussions with the business leaders on organization design and structure to sustain growth across the Division(s). Support the leadership by building associated change management strategies and playbooks. * People Optimization: Provide a leadership role across the segment in enhancing the people experience through strategic partnership, global practices and streamlined processes. Accountabilities * Steward Bio-Techne's culture values. * Lead People Talent imperatives and advance the strategic roadmap. * Build talent * Co-create always on recruiting * Deepen employee experience * Fortify Belonging * Integrate learning & development * Optimize talent systems * Invest in the growth and development of broader People business partners. * Apply depth and breadth of human resources expertise to solve problems proactively and reactively. * Drive organizational effectiveness by supporting and implementing Bio-Teche's culture framework and tools for: recruiting, learning & development, Belonging, talent management, workforce planning, performance management, organizational development, internal communication, operational excellence and total rewards health. * Collaborate with People COEs to implement and drive adoption of practices and processes across all facets of People. * Utilize talent systems and people data for progressive effectiveness and efficiency. * Contribute to continuous improvement by setting growth standards, committing to quality experiences and leading an internal service model to assure market leadership. * Challenge with composure and professionalism. * Proactively partner to solve problems with creativity and a growth mindset. * Address employee relations issues to create an engaging environment, drive compliance and resolve performance/behavioral issues. * Lead large-scale organizational change with a track record of successful change management. * Lead talent architect and leadership development. * Work successfully within a global, highly matrixed organization. Education and Experience * Bachelor's degree required. Master's and/or MBA preferred. * 10+ years of progressive People leadership experience including organizational design experience and working across a matrix organization, leadership partnership and influence, and global exposure. * 5+ years of management experience preferred. * Developing direct reports to meet organizational growth goals and objectives and personal career aspirations. * Strategic business partner and advisor to leaders at all levels. * Leveraging people metrics and technology as a strategic asset to guide effectiveness and efficiency. * Domestic travel may be required. * Newark, California location preferred Why Join Bio-Techne: * We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. * We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. * We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. * We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. * We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. * We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Job Description Senior Director, Business Development Invivoscribe - Improving Lives with Precision Diagnostics Invivoscribe is an industry pioneer and global leader in precision oncology diagnostics. For more than 30 years, we have driven international standardization of molecular and flow cytometry testing and expanded access to advanced cancer therapies worldwide. Our mission is simple and unwavering: Improving Lives with Precision Diagnostics . We are seeking a strategic, entrepreneurial, and relationship-focused Director, Business Development to expand Invivoscribe's global footprint across the pharmaceutical, biotechnology, and diagnostics sectors. This is a high-impact leadership role for a true dealmaker-someone who excels at the intersection of science, strategy, and commercialization. You will architect and execute partnerships that accelerate adoption of our assays, services, and emerging offerings, helping shape the future of precision oncology. Headquartered in San Diego, with operations across North America, Europe, and Asia, Invivoscribe develops and manufactures a comprehensive portfolio of molecular and flow cytometry assays, reagents, controls, and bioinformatics tools under ISO 13485 design control. Our products and services support more than 700 clinical laboratories in over 160 countries. Core Responsibilities Strategic Partnership Development Identify, cultivate, and manage high-value partnerships across pharma, biotech, clinical laboratories, and diagnostic technology companies. Develop strategic frameworks that align partner needs with Invivoscribe solutions, including CDx co-development, clinical trial support, and global testing programs. Negotiation & Deal Execution Lead the full deal lifecycle, including opportunity evaluation, structuring, negotiation, contracting, and operational transition. Drive strategic collaborations, licensing agreements, technology access deals, and companion diagnostic partnerships. Market & Competitive Insight Deliver actionable insights on market trends, competitive dynamics, customer needs, and emerging scientific advancements. Inform portfolio strategy, new product opportunities, and geographic market expansion. Commercial & Scientific Growth Enablement Translate complex scientific capabilities into compelling commercial opportunities and business cases. Partner cross-functionally with R&D, Product Management, Regulatory, Finance, and Commercial teams to operationalize and scale partnerships. Core Requirements Established network and strong relationships across pharma, biotech, and/or diagnostics to accelerate partnership development. Proven success navigating and closing complex deal structures, including CDx, licensing, co-development, and international collaborations. Solid understanding of drug development, flow cytometry, molecular diagnostics, clinical research, or advanced biotechnology platforms. Bachelor's degree in Life Sciences, Biotechnology, Business, or a related field; 10+ years of business development experience in biotech, pharma, or life sciences with a strong record of closing high-impact partnerships. Advanced degree (MBA, MS, PhD, MPH) preferred; equivalent experience considered. Resilient and driven. Dealmaker mentality: able to open doors to new opportunities, negotiate, and close high-value, complex deals. Adept at influencing stakeholders both direct and indirect, internal and external. Why Join Us At Invivoscribe, you will join a mission-driven global organization advancing the future of precision oncology. You will have the opportunity to shape major scientific and commercial partnerships that impact patients around the world. We offer: Competitive compensation and performance incentives Comprehensive global benefits A collaborative, innovation-driven culture The opportunity to make a significant global impact in precision medicine If you are strategic, relationship-driven, and energized by high-impact dealmaking in the life sciences, we look forward to speaking with you.

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: $73,100.00 - $120,200.00 **Position Summary:** Experienced field service engineer to service revolutionary protein analysis instrumentation. The successful candidate will be a key member of a field team responsible for maintaining instruments and supporting customers to a high standard across North America. The position is based in the Greater San Francisco Bay area and will support our customers throughout the Bay Area, the Pacific Northwest and across North America as needed. In addition to salary, this position is eligible to receive a target annual cash bonus based on individual and company performance, in accordance with company policy. **Key Responsibilities:** + Customer and Instrument support - Deliver onsite customer facing and remote support to diagnose and independently repair complex electro-mechanical scientific instruments in a laboratory environment. Maintain daily communications with customers to ensure resolution and proper follow-up. Ability to prepare samples for instrument testing as required, basic laboratory skills are essential. Completion of service protocols, meeting GMP documentation requirements. Field based role with extensive daily travel within North America. + Schedule, Administration and Inventory management - Works independently with minimal direct supervision. Manage and schedule customer appointments until completion and on occasion, the creation of detailed technical paperwork and support documents. Timely submission of service reports to clients, accurate data entry into CRM software, monthly expenses and mileage logs. Management of personal inventory for successful repairs, field support and cost management. + Support of sales, field applications team and technical support team - Work collaboratively to support the sales team with pre and post sales inquiries and tasks. Support the field applications and technical support teams both remotely and onsite to ensure successful resolution of complex customer situations and issues. + The ability to lift and carry tools, parts and instruments weighing up to 50 lbs. **Education and Experience:** + Bachelor's degree, in an engineering / science field and 3 years' field service experience in life science, biotech or medical industry OR minimum of 5 years' field service experience in life science, biotech or medical industry, preferably with laboratory experience + Strong computer skills (Windows, Microsoft Office including Outlook and Salesforce) + Ability to travel as necessary - estimated up to 50% **Skills required/desired:** + Strong brand ambassador with professional demeanor + Excellent written and verbal communication skills with the ability to communicate complex technical issues in an easy to understand manner + Excellent attention to detail, analytical problem solving, time management and interpersonal skills + Resourceful, with the ability to work independently, adapt to frequent changes and do what is required to get the job done + Experience diagnosing and repairing mechanical, electrical, fluidic, pneumatic and/or electronic equipment + Basic laboratory skills, including experience in BSL2 and BSL3 labs + Valid driver's license, good driving record and passport is required **Working Conditions:** + May work remotely from the Silicon Valley or greater San Francisco areas + Some overnight travel in the coverage area, including travel to the Pacific Northwest, Western Canada and occasionally across North America + GMP, Biosafety Level 2 and 3 labs **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $81,900.00 - $134,550.00 We are currently seeking an outstanding Field Applications Scientist, Immunoassay Specialist based in Southern California area to provide exceptional sales and customer support for our revolutionary immunoassay analysis instrumentation and assays. The candidate will be a key member of a team of Field Applications Scientists, responsible for providing pre- and post-sales assay development and technical support for several product families, including the Spear Bio, Ella, and Luminex platforms. A strong background in immunoassays and protein analysis is required, along with the ability to communicate technical information to varied scientific audiences internally and externally. The ideal candidate is an energetic, dependable and enthusiastic team-player, who's savvy about innovative technology. Key Responsibilities: rovide customer assistance on more detailed or complex questions regarding our immunoassay platform, including assay design and planning, correlation and bridging between platforms, and data interpretation. Present scientific seminars to prospects and assist with pre-sales opportunities by carrying out evaluations at prospect sites. Attend, present and interact with customers at scientific meetings, conferences and tradeshows. Provide feedback and updates to other team members (including sales, marketing and PM teams). Provide customer feedback and field visit reports to other team members. Serve as a subject matter expert for immunoassays and stay current on the science and workflows within immunoassay fields with opportunities to present to internal teams on those matters. Collaborate with global FAS teams to help train peers and synergize on resources. Empower scientists by training and supporting them on instrument use, assay development and data analysis for Spear Bio, Luminex & Ella instruments and software. Develop and nurture positive relationships with customers and internal teams in assigned territory Foster increased product usage, support sales efforts through technical presentations, product demonstrations and participation at vendor shows. Accompany Sales Representatives in customer laboratories to provide technical and applications expertise Provide post-sales assay development and troubleshooting support for customers in-person, virtually, and via phone and email Travel to customer laboratories to provide support Contribute customer feedback to marketing, product development and software teams Assist in creation and review of technical literature and training resources Create and maintain customer support information using our CRM (SalesForce) Communicate effectively with customers and team members Education and Experience: Minimum BS/BA degree in biochemistry, bioengineering, pharmaceutical sciences, biology or a related life science field. MS/PhD and Field Applications Scientist experience is preferred Minimum 5 years hands-on experience with immunoassays is required Knowledge, Skills, and Abilities: Display a thorough understanding of the principles of immunoassays and the applicability of these assays in different research fields Independently execute assay and reagent troubleshooting, optimization and validation experiments Excellent oral and written communication skills, to include presentation and training styles. Substantial knowledge of current scientific literature and life science methods and applications Proven record working efficiently both in a team environment and independently is required; previous experience providing Field Applications/Technical support is a plus Ability to multi-task and prioritize is required Excellent time management, organizational, verbal and written communication skills Experience in training and teaching Ability to travel 50-75% of the time Base Salary Range: $89,400 - $146,850 In addition to the base salary, this position is eligible to receive a commission plan, in accordance with company policy. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: $25.20 - $34.65 Job Purpose The Quality Control Technician receives raw materials and performs product inspection and/or audits in accordance with established quality control program. This role involves sampling and testing of incoming raw materials to ensure that they, along with in-process and finished products meet the company's quality standards Responsibilities · Receive and perform inspection of incoming raw material/components to ensure compliance with company quality standards · Perform visual inspections on sub-assemblies and finished good products to identify defects and non-conformances · Maintain product quality by adhering to data management protocols · Support efficient supply chain operations by complying with and maintaining inventory control procedures · Ensure compliance with internal quality control standards and external regulations, and continuously improve quality control processes · Assist in the development and implementation of quality control procedures. · Collaborate with production teams to address quality issues and recommend corrective actions Qualifications Education: · High School Diploma · A.A Degree a plus Skills and Experience: · Life Sciences industry experience preferred. · Experience working in a Quality Control environment is strongly desired. · Previous experience performing incoming inspections is strongly desired. · Detail-oriented, efficient, and excellent organization skills. · Excellent verbal and written communication skills · Strong team player with the ability to work independently. · Able to multi-task and prioritize. · Proficiency in Microsoft Office and other relevant software · ISO and GMP experience preferred Working Conditions: · Significant amount of time on the production floor, in a laboratory setting · Some time in an office setting documenting inspection result, analyzing data, and communicating with team members Physical Requirements: · Standing and walking · Lifting and moving materials up to 50 pounds · Use of hands for precises tasks such as handling samples and testing equipment **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

Job Description Invivoscribe is an industry pioneer, dedicated to Improving Lives with Precision Diagnostics . Invivoscribe has been the global leader in driving international standardization of testing and accelerating patient access to the newest and best cancer treatments for over 30 years. Headquartered in sunny San Diego, California with locations across the world, we offer a comprehensive portfolio of products and services. We work with key collaborators to develop molecular assays, reagents, controls and bioinformatics tools under ISO 13485 design control that are used by over 700 clinical laboratories in over 160 countries. Our global network of laboratories offers internationally standardized next generation molecular and flow cytometry panels to support drug development and accelerate drug approvals worldwide. We work with pharmaceutical partners and international regulatory agencies across the globe to develop companion diagnostics, which are necessary to gain approval of new drugs and treatments for cancer patients. Our harmonized ISO15189 accredited and CLIA/CAP clinical laboratories offer a test menu focused on biomarkers which are clinically actionable to support therapeutic decisions, measurable residual disease (MRD) testing, patient stratification, and trial enrollment, all designed to accelerate approvals of new oncology drugs and treatments. For 30 years, we have been at forefront of precision diagnostics, and we're just getting started! We are looking to add a Desktop Support Technician II to our Information Technology Department. The IT Help Desk is the central point of contact for all IT-related service requests and incidents. The Desktop Support Technician provides internal technical support for the Company's global user and laboratory workstations, applications and related technologies Core Responsibilities Include: Configures, troubleshoots and maintains new, upgrade and replacement end-user desktop/laptop computers and telephones, including software installation and configuration. Provides technical support and user training on IT equipment and systems in a professional, helpful manner. Provides IT on-boarding training to new hires. Installs and configures new IT equipment and maintains installation images for each supported hardware type. Accurately records, tracks and documents user requests utilizing a ticket tracking system. Maintains a complete and accurate inventory of the Company's IT assets. Tracks consumption and inventory levels of computer peripherals and consumables such as printer toner cartridges, headsets, keyboards and mice. Places re-order requests when appropriate. Follows established policies and standard operating procedures for ensuring the security and integrity of the Company's global network and information systems. Maintains a working understanding of the Company's global IT infrastructure. Maintains an updated job knowledge by participating in educational opportunities, reading professional publications, maintaining personal networks and/or participating in professional organizations. You Bring: B.S. in a computer-related field of study and 2+ years desktop support experience in a heterogeneous enterprise network setting. Equivalent combination of education, certifications and work experience will be considered. CompTIA, Microsoft or similar IT certifications are beneficial. Prior experience working with regulated or validated IT systems is beneficial. Experience supporting common Microsoft Windows operating systems (Windows 10 and newer). Experience supporting common business software platforms such as Microsoft Office 365, Microsoft Teams, Microsoft Intune, Adobe Creative Suite, etc. Experience with supporting MacOS is a plus. Experience with TeamViewer or similar remote access tools is desired. We Bring: A beautiful modern facility centrally located in San Diego County, with many jobs conducive to a hybrid work from home arrangement. A diverse and inclusive work environment where you will learn, grow, and make new friends. A well-stocked breakroom with hot and cold beverages, snacks, refrigerator and pantry items to get you through the day. Competitive salaries and discretionary bonus program, incentive stock options, amazing benefit options, a 401k plan with a fully vested employer match, and generous time off benefits that include floating holidays. Invivoscribe is an Equal Opportunity Employer.

**By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** Pay Range: $52,000.00 - $85,600.00 Position Summary: Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to research in a laboratory environment. Duties and Responsibilities: Research Associate + Assist in the development new products or methods, or optimize or refine current product lines. + Create new products using approved procedures and keep detailed and accurate records. + Prepare summary reports for Feasibility, Development, and Transfer as required. + Perform in-process analyses and determine adjustments to bring analytes into specification + Analyze products, stock solutions, and raw materials using automated and manual instrumentation + Evaluate that the analysis instrumentation and procedure is operating correctly, and verify or perform maintenance before use + Measure accurately quantities of material volumetrically and gravimetrically, employing knowledge of chemical and biochemical properties and handling procedures + Continually evaluate and/or create work instructions, QCRs, SOPs and other documents and procedures for effectiveness and modify through formal change process. + Perform processing steps as required in the documentation such as centrifugation, diafiltration, in-process filtration, and column separation + Perform final release testing + Perform aseptic procedures such as, filtration, filling, capping and microbial plating + Assist in training personnel in manufacturing procedures + Assist in the validation testing of equipment and processes + Perform assay testing for Value Assignment as required + Assist in new product transfer and with the development of any new procedures required + Assist in developing ways to increase efficiency and/or reduce costs + Assist with overall maintenance and cleanliness of the laboratory and equipment + Special projects as assigned + Perform additional functions as required Minimum Job Requirements: + Bachelor's degree in Chemistry, Biochemistry, Biological Science, or related field preferred with 1-5 years work experience in In Vitro diagnostics, medical device, pharmaceutical or related industry required. **Why Join Bio-Techne:** **We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.** **We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.** **We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.** **We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.** **We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.** **Bio-Techne is an E-Verify Employer in the United States.** **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.** **To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.** Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.