Key Responsibilities

Leadership & Team Development

• Recruit, develop and retain a high-performing team to meet the business needs.
• Lead, coach, and inspire associates to exceed performance expectations and uphold a positive team culture.
• Conduct regular performance evaluations, provide feedback, and create development plans to support individual and team growth.

Customer Experience & Brand Representation

• Represent Sur La Table’s brand and culture by creating memorable, educational experiences that inspire repeat visits and customer loyalty.
• Maintain expertise by staying current on products, actively engaging in available training, and independently seeking out additional resources.
• Ensure exceptional customer experience by leading a customer-focused, Guest Obsessed culture.
• Address customer concerns and resolve issues in a timely manner to maintain satisfaction and loyalty.

Sales & Business Performance

• Develop and implement strategies, including effective merchandising, marketing, and customer engagement, to exceed sales and financial goals across retail operations.
• Monitor and analyze key performance metrics daily to identify opportunities and optimize store performance.
• Consistently meet or exceed culinary and retail goals by delivering exceptional classes and customer experiences that drive engagement and sales.

Operations & Compliance

• Oversee daily store operations, ensuring compliance with company policies and procedures.
• Maintain accurate inventory levels, minimize shrink, and ensure proper product merchandising.
• Ensure store safety and cleanliness, addressing any maintenance needs promptly.

Physical Requirements

• Ability to communicate verbally and work cooperatively with associates and customers.
• Ability to remain standing for up to 5 hours at a time.
• Ability to move about the store coaching and directing associates; selling to customers and retrieving merchandise from stockroom or sales floor.
• Ability to grab, reach, push, pull, bend, stoop, kneel, and crouch to retrieve and replenish merchandise from stockroom or sales floor.
• Ability to lift and/or move merchandise weighing up to 50 lbs.
• Ability to ascend/descend ladders to retrieve and/or move merchandise.
• Ability to operate a computer, POS system, keyboards, merchandise scanners and mouse to accomplish work.
• Workweeks are expected to be between 46 and 48 hours with the ability to have a flexible schedule, including nights, weekends, and holidays.
• Regular and predictable attendance.

Qualifications & Experience

• Must be 21 years of age or older at the time of employment.
• 3+ years of retail management experience, preferably in a specialty or culinary retail environment.
• Proven track record of achieving sales and motivating high performing sales teams while meeting operational goals.
• Strong leadership skills with the ability to inspire, develop, and retain a high performing team.
• Excellent communication, problem-solving, and decision-making abilities.
• Passion for community engagement and providing exceptional customer experiences.
• Proficiency in Microsoft Office and retail management systems preferred.

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Join our team as a QC Analyst, where you will play a crucial role in conducting chemical and physical analyses in our production site laboratory. Your responsibilities will include performing product release and in-process control tests, conducting stability tests, maintaining and calibrating analytical equipment, managing sample administration in SAP/LIMS, and performing root cause analyses for nonconformities.

Additionally, you will support GMP operations through computer system validation, method validation, raw data control and archiving, and the creation of GMP documents and regulations. This position supports the quality control testing of cell therapy, commercial rFVIII, and CCTC products.

Your Tasks and Responsibilities:

• Perform GMP analytical testing of cell therapy products, focusing on methods using flow cytometers, microscopic technologies, and ddPCR;
• Conduct testing of raw materials, starting materials, process intermediates, and final cell therapy products such as CAR-T cells and iPSCs;
• Provide technical scientific support for QC functional areas, maintaining subject matter expertise for USP/NF, EP, and JP compendia;
• Follow SOPs accurately, perform activities in accordance with cGMP requirements, and report abnormalities;
• Execute method validations and transfers, manage discrepancies, and implement corrective and preventative actions;
• Keep accurate documentation to ensure completeness and accuracy per cGMPs, compile and review data in LIMS or other databases;
• Demonstrate knowledge of operation, maintenance, and troubleshooting skills for analytical instruments;
• Independently design and conduct experiments, assays, or operational procedures of considerable complexity;
• Communicate complex scientific findings and recommendations effectively in various settings;
• Interact with multiple departments such as Quality Control, Quality Assurance, Supply Chain, Operations, Engineering, Maintenance, and Safety.

Who You Are: Bayer seeks an incumbent who possesses the following:

Required Qualifications:

• B.S. in Biological Sciences, Biochemistry, Molecular Biology, Chemistry, or related field;
• Demonstrated expertise and hands-on experience in flow cytometric assays for characterization of cell therapy products;
• Thorough knowledge of GLP/GMP guidelines as applied to the testing of biologics molecules;
• Excellent verbal and written communication skills including writing of scientific and technical reports.

Preferred Qualifications:

• A minimum of 6 years relevant experience in biopharma, healthcare, or manufacturing environment;
• M.S. in Biological Sciences, Molecular Biology, Biochemistry, Chemistry, or related field with a minimum of 2 years relevant experience in biopharma, healthcare, or manufacturing environment;
• Experience in other analytical methods for cell therapy products, e.g., cell-based functional assays, quantitative PCR/ddPCR assays, quantitative imaging assays, virology;
• Hands-on experience in handling human cells/cell lines including PBMC, CAR-T cells, iPSC;
• Thorough knowledge of compendial requirements (USP, EP, JP), ACS, and FCC requirements.

Shift Hours: 8:00 AM – 4:30 PM, Monday through Friday. Candidates must be flexible to support business needs, including occasional weekend work when required to meet operational timelines.

Salary: $93,840.00 - $125,000.00

Benefits: Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.

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The Senior Regulatory CMC Strategist (Senior Director) leads innovative global CMC strategies for product development and approval and provides regulatory CMC leadership and guidance to CMC teams developing cell and gene therapy products.

Key Responsibilities:

• Represent Regulatory CMC and lead matrix teams for cell therapy programs, including participation in development and global regulatory teams across therapeutic areas;
• Develop and implement robust, innovative CMC strategies for cell and gene therapy programs, providing guidance on regulatory requirements for clinical trial and marketing applications;
• Lead CMC-related Health Authority interactions, including briefing documents, responses to questions, submissions, and resolution of regulatory issues;
• Partner closely with CMC, Analytical Development, Quality, Nonclinical, Clinical, Regulatory Strategy, and Quality Assurance teams to support compliant development and submissions;
• Identify, assess, escalate, and propose solutions for major, routine, and complex regulatory risks, deficiencies, change controls, and strategic issues.

Requirements:

• Advanced scientific degree (e.g., PhD, MSc, PharmD);
• Biotech or pharmaceutical industry experience including relevant regulatory CMC experience with development of biologics (cell therapy required, gene therapy a plus), and US and global submissions;
• Strong background in Regulatory Affairs CMC in a global pharmaceutical and/or biotechnology company with expertise in biologics, deep experience in product development and understanding of US, international regulations, and ICH guidelines related to biologics and cell therapy development;
• Extensive experience in preparing quality sections of regulatory filings including global Health Authority briefing documents, IND/CTA/IMPDs, and BLA/MAAs following eCTD format.

Preferred Qualifications:

• 15 years biotech or pharmaceutical industry experience including at least 10 years of relevant regulatory CMC experience with development of biologics (cell therapy required, gene therapy a plus), and US and global submissions;
• Experience with combination products and device filing also preferred.

Salary Range: $218,800 to $328,300

Benefits: Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.

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The QC Potency Analyst I plays a pivotal role in ensuring the potency, quality, and reliability of biologic products through chemical and physical analyses performed in a GMP-regulated production site laboratory.

Responsibilities

The primary responsibilities of this role, QC Potency Analyst I, are to:

• Perform routine potency and related analytical testing in accordance with approved methods, specifications, SOPs, and cGMP requirements to support in-process, release, stability, and special testing during graveyard-shift operations;
• Prepare samples, reagents, standards, controls, and laboratory equipment required for assigned testing, and maintain laboratory readiness through cleaning, inventory checks, reagent and supply preparation, and organization of assigned work areas;
• Operate laboratory instruments and automated systems after completion of required training and qualification, performing routine checks, cleaning, and basic troubleshooting to ensure reliable performance and data integrity;
• Document activities and results contemporaneously, accurately, and legibly in controlled records and approved electronic systems, including LIMS or other laboratory databases, and review test data for completeness while promptly reporting deviations, atypical observations, instrument issues, or other abnormalities to appropriate colleagues;
• Initiate or support laboratory discrepancy and investigation records as assigned, including collection of relevant data and completion of required documentation within established timelines in alignment with GMP and inspection-readiness expectations;
• Follow laboratory safety requirements, including appropriate handling of biological materials, chemicals, sharps, and laboratory waste, and uphold quality, safety, and data-integrity standards in all aspects of daily work;
• Manage multiple assignments and changing priorities while maintaining data integrity, quality, and schedule commitments, completing required training and progressively qualifying on QC Potency methods, systems, and supporting laboratory processes;
• Provide clear shift handoffs and communicate testing status, issues, and follow-up needs to graveyard and day-shift colleagues, participating in continuous-improvement, inspection-readiness, and team activities that enhance QC Potency performance and support the broader site quality goals.

Requirements

Bayer seeks an incumbent who possesses the following:

• Entry-level professional mindset with up to two years of laboratory experience in an academic, biotechnology, pharmaceutical, or cGMP environment, or equivalent hands-on laboratory training that demonstrates readiness to contribute in a regulated QC setting;
• Bachelor's degree in biology, biochemistry, chemistry, medical laboratory science, pharmaceutical science, or a related scientific discipline, or an equivalent combination of education and relevant laboratory training;
• Foundational knowledge of core laboratory practices, including calculations, solution preparation, pipetting, and safe handling of laboratory materials, along with the ability to follow detailed written procedures and accurately document laboratory activities and results in controlled records;
• Comfort using standard computer applications and learning validated laboratory software and automated instrumentation, with the ability to work within electronic systems such as LIMS and SAP in alignment with cGMP and data-integrity principles;
• Attention to detail and a consistent commitment to quality, safety, and data integrity, coupled with the ability to learn technical procedures, accept feedback, and apply training independently after qualification;
• Clear verbal and written communication skills, including timely escalation of questions and unexpected observations, and the ability to organize work, manage multiple priorities, and perform effectively in a team-based graveyard-shift environment;
• Reliability, adaptability, and willingness to support changing laboratory priorities and scheduled testing needs, including the regular graveyard schedule of 12:00 a.m. to 8:30 a.m. and occasional additional coverage, including weekends or holidays, when required by laboratory operations and consistent with applicable policies.

Benefits

Employees can expect to be paid a salary between $66,560.00 - $99,840.00. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.

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As a Production Specialist III – Cell Culture Technology Center (CCTC), you'll be responsible for manufacturing monoclonal antibody (mAb) drug substance within the CCTC and Manufacturing Biologics cluster.

Your Tasks and Responsibilities:

• Execute end-to-end manufacturing operations for mAb drug substance across Cell Expansion, Cell Culture, Purification, Solution Preparation, and Weigh/Dispense, acting as a subject matter expert (SME) for at least one area.
• Manufacture products across multiple life-cycle phases, from clinical through launch, managing differences in documentation, sample handling, automation, and cGMP expectations.
• Handle and troubleshoot single-use technology (SUT) throughout the manufacturing process, ensuring reliable and compliant operation of equipment and systems.
• Monitor and control processes using data trending and statistical process control, working cross-functionally to maintain a controlled state and escalate and investigate issues as needed.
• Author, redline, and review controlled documents for equipment and processes, ensuring alignment with CCTC platform philosophy.
• Create, own, and drive business processes of moderate complexity within CCTC to ensure operational readiness and efficient manufacturing.
• Participate in regulatory and internal audits, including leading internal audit walkthroughs, and support commissioning, qualification (IOPQ), and execution of C&Q documentation for CCTC equipment.
• Support development of training curricula and materials, deliver training as an SME, and ensure your own training remains compliant and up to date.
• Identify and drive continuous improvement opportunities, challenge the status quo, and promote safe behaviors.
• Act as a delegate to the Sr. Production Specialist and CCTC Production Manager to support business continuity and leadership coverage.

Who You Are:

• Bachelor's degree with 4+ years of industry experience, or a Master's or PhD with no prior industry experience, preferably in a science-related discipline.
• Demonstrated ability to work with flexibility, adapt to last-minute production schedule changes, and provide off-hour coverage.
• Strong independent thinking and decision-making skills, with the ability to make logical decisions for multiple process workstreams.
• Proven ability to understand and troubleshoot equipment, resolve issues independently, and experience with single-use technologies.
• Experience with data integrity, regulatory, and cGMP requirements for pharmaceutical manufacturing.
• Proficiency with business IT systems and Microsoft Office.

Benefits:

• Salary between $97,000.00 to $125,000.00
• Additional compensation may include a bonus or commission
• Health care, vision, dental, retirement, PTO, sick leave, etc.

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In this role, you will lead the mechanical design and integration of hardware that enables RF signal delivery and silicon device packaging within dilution refrigerators. These systems form the critical interface between room-temperature control electronics and ultra-low-temperature environments where superconducting qubits operate.

Key Responsibilities: System Design & Development

• Lead the mechanical design of complex hardware subsystems including cryostat internal architecture, custom components for signal chain and metal enclosures
• Develop and maintain detailed 3D CAD models, drawings, and Bills of Materials (BOMs)
• Drive end-to-end design of mechanical interfaces from room temperature down to the millikelvin regime
• Design thermal anchoring and shielding systems optimized for mechanical stability and quantum coherence
• Perform thermal, vibrational, and structural simulations using FEA tools to ensure performance and robustness
• Build and validate mechanical/cryogenic prototypes in lab
• Collaborate with quantum physics teams to ensure system-level functionality in live quantum experiments
• Work closely with hardware, cryo, RF, and systems teams to deliver integrated, scalable quantum hardware platforms
• Develop specifications for outsourced components and manage supplier relationships for critical assemblies such as vacuum flanges, cryo fixtures, and RF housings
• Author assembly documentation, and maintain design traceability in PLM system

Required Qualifications

• M.S. degree or higher in Mechanical Engineering or equivalent field
• 7+ years of industry experience in mechanical design and systems engineering
• Proficiency with 3D CAD software (SolidWorks preferred)
• Strong background in tolerance analysis and GD&T principles
• Experience in thermal and structural modeling and simulation
• Familiarity with documentation control, revision management, and PLM tools
• Excellent cross-disciplinary communication and project collaboration skills
• Demonstrated ability to develop and document assembly processes

Preferred Qualifications

• Familiarity with thermal-mechanical effects in cryogenic materials and multi-physics system design
• Experience with RF packaging and electronic device integration in cryogenic or vacuum environments
• Quality assurance experience including inspection methodologies and non-conformance resolution
• Hands-on machining or fabrication experience to support rapid prototyping and design iteration

Additional Information

As engineering leaders, we value diversity and are committed to building a culture of inclusion to attract and engage innovative thinkers. Our technology, meant to serve all of humanity, cannot succeed if those who built it do not mirror the diversity of the communities we serve. Applications from women, minorities, and other under-represented groups are encouraged.

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The successful candidate will work closely with physicists, engineers, and technicians to operate, maintain, and troubleshoot advanced RF and cryogenic systems that enable next-generation quantum processors.

Responsibilities:

• Test, validate, and debug custom RF control systems using advanced electronic test equipment
• Operate, monitor, and debug dilution refrigerators, including cooldowns, steady-state operation, and fault diagnosis
• Operate, troubleshoot and service cryogenic and vacuum systems
• Perform helium leak detection, pump rebuilds, and thermal system management
• Assemble, validate, and install complex electro-mechanical, cryogenic, vacuum, and RF assemblies
• Contribute to test plan development and execute validation testing for next-generation RF hardware
• Participate in an on-call rotation to support system uptime in a customer-facing environment
• Prepare, inspect, and package quantum chip assemblies for testing
• Follow established procedures and contribute to the creation and improvement of standard operating procedures and best practices
• Read and interpret CAD drawings, schematics, and engineering specifications
• Work directly with customer teams across different regions to support system operation, issue resolution, and ongoing optimization
• Navigate logistics of international travel, including customs/import considerations for tools and equipment, visas, and site-specific access requirements

Requirements:

• Technical background in Physics, Engineering, or a related field
• Strong proficiency with general-purpose electronic test equipment
• Direct, hands-on experience operating and troubleshooting dilution refrigerators
• Substantial hands-on experience working with sub-Kelvin cryogenic systems
• Experience operating and maintaining high-availability laboratory or industrial equipment
• Experience assembling, servicing, and maintaining scientific instruments or complex electro-mechanical systems
• Familiarity with vacuum systems, vacuum plumbing, P&IDs, and standard fittings and practices
• Working knowledge of statistical methods for test and validation
• Attention to detail in documentation and excellent written and verbal communication skills
• Experience working with external vendors, partners, or customers across different regions and cultural contexts
• Willingness and ability to travel internationally on short notice

Nice to Have:

• Experience in field deployment or on-site support roles at customer or partner facilities
• Familiarity with import/export logistics for scientific or electronic equipment
• Programming or scripting experience in Python or related languages
• Additional language proficiency relevant to target deployment regions

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You will reach new consumers, excite university students, increase sales, and drive visibility of the Red Bull brand. This includes direct contact with consumers and customers, inviting product trials, and working at Red Bull events to ensure an unforgettable brand experience for consumers.

Responsibilities

• Be a brand and product ambassador:
• Live and breathe the brand personality traits and company values, representing the brand in a premium way through everyday interactions with consumers or customers.
• Build and execute a tailored and innovative campus plan that engages students and brings the brand to life at your university.
• Create a strong network on and around your campus, establishing and maintaining relationships with key local individuals.
• Identify local collegiate content creators in relevant Red Bull scenes and work with your FMS to bring them into the World of Red Bull.
• Grow the user base by inviting positive trial and awareness of Red Bull through product sampling to consumers at the right place and right time - answering any questions and concerns from consumers.
• Work at Red Bull events, collegiate activations, and supported events to help ensure an unforgettable brand experience for consumers.
• Build awareness and encourage participation in the World of Red Bull, including collegiate events and activations.
• Increase brand engagement on your Social Media handles through authentic content.

• Be a sales expert:
• Build relationships with local sales account managers and ensure Red Bull is available and visible in outlets, on your campus and in your region.
• Collaborate with sales to open new distribution points for Red Bull within your university campus and beyond.
• Leverage relevant assets from the world of Red Bull in order to keep us top of mind in sales accounts.
• Ensure perfect execution of defined store standards.

• Executional excellence:
• Deliver executional excellence and show love for the details in all areas of your role.
• Share ideas and collaborate with your team through regular face-to-face and online interaction.
• Plan & report your activities in the dedicated online platform in a timely manner and with accuracy.
• Contribute to business development by providing local insights, trends and overall opportunities.

Requirements

• Must be at least 18 years of age
• Must have a valid US driver’s license
• University or college enrollment required
• Must be fluent in English, additional languages an advantage
• Able to work flexible part-time hours, including some evenings and weekends for a minimum of 15 hours per week
• Immersed in student life with an understanding of the collegiate landscape and local city, including behind-the-scenes activities & hot-spots
• Connected with a diverse range of influential groups and individuals on campus
• Affinity for project management, working 'behind the scenes’, and winning sales
• A team player, willing to represent Red Bull with branded outfits and onboard the Red Bull Mini
• Employees may be required to lift and/or move items weighing 25 pounds or more, as needed.

Hourly Rate: $21.00/hour

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We are seeking a Senior Mechanical/Cryogenic Engineer to own the mechanical architecture of our quantum hardware systems, from room-temperature infrastructure down to the millikelvin core of our dilution refrigerators.

You will lead the design of the cryogenic signal chain, define mechanical interfaces across thermal stages, and work directly alongside quantum physicists, RF engineers, and systems teams.

This is a high-ownership role: you will drive design decisions end-to-end, from concept through qualification, on some of the most technically demanding hardware in the industry.

Key Responsibilities

Cryogenic Hardware Design

• Own the mechanical design of cryogenic hardware from 300 K to millikelvin , thermal anchoring, RF wiring, flex interconnects, coaxial routing, filter housings, and connector packaging across all temperature stages.
• Lead the full design lifecycle: concept, CAD, GD&T drawings, BOMs, tolerance analysis, prototype builds, qualification testing, and manufacturing release.
• Define cryogenic mechanical interfaces and thermal conduction budgets; drive design-for-manufacturability with external machine shops and precision vendors.

Simulation & Analysis

• Perform mechanical, thermal, and vibration analyses independently using COMSOL, ANSYS, or equivalent; use simulation results to drive design decisions and iteration.
• Conduct tolerance stack-up analyses for multi-component assemblies in constrained cryostat environments.

Integration, Leadership & Collaboration

• Lead prototype builds, system integration, and cryogenic bring-up; diagnose integration failures and drive root cause analysis.
• Serve as the mechanical lead in cross-functional programs alongside quantum physicists, RF engineers, and systems teams, mentor junior engineers and lead design reviews.
• Maintain rigorous documentation , CAD models, drawings, BOMs, and revision-controlled design records , within the company PLM system.

Required Qualifications

• B.S. or M.S. in Mechanical Engineering or related field (M.S. preferred).
• 7+ years designing complex mechanical or electromechanical systems with end-to-end hardware ownership.
• Expert-level SolidWorks , large assemblies, GD&T-compliant drawing packages, and DFM workflows.
• Independent proficiency in SolidWorks, COMSOL or ANSYS for thermal and structural analysis.
• Experience with hardware operating in cryogenic, vacuum, or extreme thermal environments.
• Strong ME fundamentals: stress analysis, tolerance stack-ups, materials selection, and failure mode analysis.
• Proven ability to lead technical efforts and collaborate across multidisciplinary teams.

Preferred Qualifications

• Direct experience with dilution refrigerators, cryostats, or sub-Kelvin systems in quantum computing or precision instrumentation.
• Knowledge of superconducting quantum hardware architecture and millikelvin design constraints.
• RF/microwave packaging experience: connector specification, hermetic sealing, and cable routing in cryostats.
• Familiarity with cleanroom protocols, vacuum-compatible assembly, and contamination-sensitive environments.

Additional Information

As engineering leaders, we value diversity and are committed to building a culture of inclusion to attract and engage innovative thinkers. Our technology, meant to serve all of humanity, cannot succeed if those who built it do not mirror the diversity of the communities we serve. Applications from women, minorities, and other under-represented groups are encouraged.

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We are seeking a Senior Software Engineering Manager to head the team responsible for software systems that enable the creation, delivery and maintenance of Rigetti's quantum computers. This includes systems for device design, chip fabrication workflows, physics-informed data analysis, quantum gate-design, and quantum mitigation and error correction technologies.

As a Senior Software Engineering Manager, you will lead the team responsible for software platforms that enable the design, fabrication, characterization, and measurement of Rigetti's quantum systems – with a strong emphasis on integrating into the engineering process.

Key Responsibilities

Team Leadership & Organizational Development

• Lead and mentor a cross-functional software engineering team spanning scientific tooling, analytics infrastructure, and fabrication-support systems.
• Create stronger operational rigor around prioritization, execution, accountability, and project delivery.
• Provide coaching, growth support, feedback, and career development for engineers across varying levels of seniority.
• Help establish healthy engineering culture, team norms, and stronger collaboration practices.

Technical & Engineering Leadership

• Partner closely with engineers to drive execution across scientific computing, fabrication tooling, analytics systems, and workflow automation.
• Support development of internal tooling and data systems that connect design, fabrication, and device performance workflows.
• Help modernize and operationalize internal tooling that has historically evolved organically through research and prototyping efforts.

Cross-functional Collaboration

• Work closely with quantum engineers, physicists, fabrication engineers, and hardware teams to understand operational pain points and evolving workflow requirements.
• Help balance competing stakeholder requests while improving prioritization discipline and long-term planning.

Operational & Strategic Impact

• Help transition the team from highly reactive support work toward more proactive engineering planning and scalable systems development.
• Improve processes around technical debt management, prototype ownership, platform sustainability, and operational support models.

Qualifications

• BS or equivalent degree in Software Engineering, Electrical Engineering, Physics, Applied Physics, or related field; MS or PhD a plus.
• 7+ years of software engineering experience, including 2+ years in a people leadership role, whether formal management or equivalent tech lead capacity.
• Demonstrated experience building data systems, ideally in scientific computing or physics-informed models.
• Proficiency in Python; familiarity with JavaScript or TypeScript.
• Proficiency with AWS for development and production deployment and distributed computing.

Nice-to-Have

• Knowledge of quantum device physics, such as superconducting qubits, trapped ions, photonics, or quantum information science.
• Familiarity with fabrication processes in semiconductor, quantum, or other hardware/lab-based environments.

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