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Job Description Salary Range: $20.00 per hour Benefit Eligible: Yes Location: Onsite in Mesa, AZ Classification: Non-exempt, full time Reports to: Production Manager About the Company Paleovalley and Wild Pastures were born from a simple but radical idea: real food can heal — people, animals, and the planet. When Paleovalley co-founders Autumn and Chas Smith saw how industrialized food was affecting human health and the health of the land, they refused to play along. Autumn’s own journey of healing through nutrient-dense foods lit a fire that became Paleovalley. From there, the mission grew roots, sprouted wings, and eventually expanded into Wild Pastures to bring regeneratively raised meats directly to families nationwide. Today, Paleovalley crafts deeply nourishing snacks and supplements made with organic ingredients and honorable sourcing. Wild Pastures connects small American farmers practicing regenerative agriculture with customers who believe better food is worth fighting for. Every product, every partnership, and every decision is guided by a commitment to real ingredients, regenerative practices, and the belief that health is built from the soil up. We’re a team of grounded doers, curious thinkers, bold builders, and warm humans who like to laugh while doing meaningful work. We're growing quickly, fueled by purpose and a shared desire to repair the food system one thoughtful choice at a time. If you feel energized by impact, drawn to mission, and ready to join a company rewriting the future of food, we’d love to meet you! About the Opportunity The Machine Operator plays a critical role in ensuring our production processes run safely, efficiently, and in full compliance with food safety standards. By operating and maintaining key processing equipment such as kettles, dehydrators, and packaging systems, this role directly supports the consistent production of high-quality products our customers trust. Through attention to detail, sanitation excellence, and operational reliability, the Machine Operator helps protect product integrity and keep our production goals on track. What You’ll Do • Operate and monitor food-grade processing and packaging equipment including kettles, dehydrators, separators, mills, labelers, and date coders to ensure efficient and consistent production., • Execute machine setups and changeovers accurately and efficiently to support production schedules and minimize downtime., • Perform Clean-in-Place (CIP) and sanitation procedures to maintain food safety standards and ensure equipment is audit-ready at all times., • Maintain proper production flow by monitoring materials, removing finished goods, and adjusting machine settings as needed., • Inspect finished products for correct labels, seals, net weights, and date codes to ensure compliance with specification sheets., • Document batch, LOT, and production data accurately to maintain full traceability and regulatory compliance., • Troubleshoot minor equipment issues and escalate mechanical concerns promptly to reduce downtime and protect product quality., • Collaborate with QA, Production Leads, and Maintenance teams to ensure smooth operations and adherence to GMP, FDA, and USDA standards., • Identify opportunities for process improvement and proactively communicate recommendations that enhance efficiency and quality., • Maintain a clean, organized, and safe work environment by consistently following PPE requirements and safety protocols.What You’ll Need to Succeed, • 1+ year of experience in a food, beverage, supplement, or pharmaceutical manufacturing environment., • Experience operating production or processing equipment in a regulated manufacturing setting., • Ability to follow Good Manufacturing Practices (GMP), SOPs, and food safety regulations (FDA/USDA)., • Ability to perform equipment cleaning and sanitation procedures, including adherence to safety protocols., • Basic mechanical aptitude and ability to troubleshoot minor equipment issues., • Ability to lift up to 50 pounds and stand/walk for the duration of a shift in a manufacturing environment., • Flexibility to work assigned shifts, including evenings or overtime as needed., • Legally authorized to work in the United StatesBonus Points, • Experience operating kettles, dehydrators, milling equipment, or other food-grade processing systems., • Familiarity with Clean-in-Place (CIP) systems and advanced sanitation procedures., • Experience performing equipment changeovers, labeler/date coder adjustments, and production line setups., • Bilingual (English/Spanish) communication skills., • Experience in CPG, nutraceutical, or regulated food manufacturing environments with batch/LOT traceability systems.Our Commitment to You, • Medical, dental, and vision coverage with 100% employer-paid dental/vision and a small monthly medical premium for employees; dependents may be added at employee cost, • Generous Paid time off to support balance and rest, • Paid sick time for when you need it, • Six (6) paid holidays each year, • Paid parental leave for growing families, • 100% company-paid Short-Term Disability, Long-Term Disability, and Life Insurance, • 401(k) with up to a 4% company match after one year of service This role takes place in a manufacturing/warehouse environment and may involve exposure to varying temperatures, noise, and airborne particles. Employees must follow all safety guidelines and use required Personal Protective Equipment (PPE). The position requires regular standing, walking, bending, reaching, and the ability to lift and move items up to 50 pounds. Work may involve operating or working near machinery and other equipment. These physical demands are representative of those necessary to perform the essential functions of the job, with or without reasonable accommodation. Compliance & Employment Practices Paleovalley and Wild Pastures are proud to be equal opportunity employers. All employment decisions — including hiring, promotion, discipline, and termination — are made based on qualifications, merit, and business needs. We do not discriminate on the basis of race, color, religion, national origin, ancestry, age, sex, gender identity or expression, sexual orientation, disability, medical condition, pregnancy, genetic information, marital status, veteran status, or any other status protected by applicable federal, state, or local law. We are committed to providing reasonable accommodations to qualified individuals with disabilities. If you need assistance or an accommodation during the application or hiring process, please reach out to to let us know. Reasonable accommodations are considered on a case-by-case basis in accordance with the Americans with Disabilities Act (ADA) and applicable laws. Applicants must be authorized to work in the United States for any employer. At this time, Paleovalley and Wild Pastures are unable to sponsor or assume sponsorship of employment visas, including but not limited to H-1B, TN, or OPT. This role is open until filled. EEO Statement: Paleovalley and Wild Pastures are equal opportunity employers. Employment and processes, including decisions to hire, promote, discipline, or discharge, are based on merit, competence, performance, and business needs. We do not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. E-Verify: Paleovalley and Wild Pastures participate in E-Verify, the federal program for electronic verification of employment eligibility. Powered by JazzHR 9HUROCTyzv

Job DescriptionCelerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you a Bioanalytical Quality Professional with experience in quality assurance and team management looking to make an impact in a dynamic clinical research environment? At Celerion, we're transforming clinical research through translational medicine. We're seeking a talented Manager/Senior Manager, Quality Assurance, Bioanalytical for our Global QA department to drive quality and compliance of our studies, processes and systems which is key to our mission of accelerating medicine for patients. Ideally this role would be locally based at our Lincoln, Nebraska US location or alternatively at our Tempe, Arizona US location. Hybrid working and willingness to travel from other locations in the United States would also be considered. What You’ll Do: • QA Bioanalytical Team Direction and Management, • Driving QMS and Process Improvement Initiatives, • Oversight of Study Audits, System/Process Audits and Vendor Audits, • Hosting Sponsor Audits and Regulatory Inspections, • Actively contributing to Global QA StrategyWhat You’ll Bring:, • Ability to communicate and interact at all levels within multicultural environment, • Ability to organize and manage multiple priorities, • Strong problem solving, comprehension and analytical skills, • Collaborative team player, open minded, ethical and culturally sensitive, • Ability to manage and resolve conflict, • Good, well-developed leadership skills, • Excellent written and oral communication skills, • Attention to detail, tactful and diplomatic, • Advanced Computer skills and literacyWhat is Required:, • Bachelor’s degree in Business, Science, or related field or equivalent experience, • Minimum of 8 to 10 years experience in Quality Assurance, • Minimum of 4 to 5 years team management experience, • Proficient knowledge of GXP (specifically GLP and/or GCP) and FDA 21 CFR Part 11 regulations, • Robust knowledge of Bioanalytical techniques, regulations and industry guidelines

Job Description About Gummi World Gummi World is not a slow-moving, corporate environment — we are a fast-paced, highly structured, innovation-driven nutraceutical manufacturer and the most certified gummy manufacturer in the industry. Our standards are high, our expectations are clear, and our team operates with a gold-standard mentality every day. We move quickly, we stay organized, and we hold ourselves accountable to the highest level of quality and compliance in the market. Based in Chandler, Arizona, Gummi World partners closely with leading brands to produce consistent, trusted, and innovative vitamin and supplement products. Every batch we manufacture reflects precision, discipline, and a commitment to excellence. We are looking for someone who can hit the ground running, thrive in a structured environment, and lead with urgency, ownership, and attention to detail. Position Summary The Quality Manager is a hands-on leader responsible for ensuring that Gummi World’s products meet or exceed all quality and regulatory standards. This role requires being present on the production floor the majority of the day to monitor processes, perform inspections, and resolve issues in real time. The Quality Manager oversees daily QA/QC operations, leads root cause analysis for deviations, and ensures rapid, effective corrective actions. This position requires the ability to work with speed, precision, and organization while managing multiple priorities in a fast-paced manufacturing environment. Key ResponsibilitiesOn-the-Floor Quality Leadership • Be physically present on the production floor most of the day, monitoring operations and ensuring compliance with quality standards., • Proactively identify potential quality concerns and intervene before they become issues., • Oversee daily quality control activities for raw materials, in-process goods, and finished products., • Maintain compliance with cGMP, HACCP, FSMA, CFR 111, and all applicable regulatory requirements., • Lead and document thorough root cause investigations for non-conformances, OOS results, and customer complaints., • Develop and implement timely and effective CAPAs to prevent recurrence., • Conduct internal audits and support external regulatory and customer audits., • Maintain accurate and complete quality documentation, including batch records and test results., • Work cross-functionally to improve processes, reduce defects, and increase efficiency., • Support new product development and validation with strong quality integration., • Supervise, mentor, and develop QA/QC staff., • Train production personnel on quality standards, GMP, and compliance procedures., • Bachelor’s degree in Food Science, Microbiology, Chemistry, Engineering, or related field (preferred)., • 4–7 years of experience in a Quality role within food, nutraceutical, or dietary supplement manufacturing., • Strong knowledge of cGMP, HACCP, FSMA, and CFR 111., • Proven experience with root cause analysis and corrective action programs., • Ability to work with urgency, stay highly organized, and manage multiple priorities., • Experience with FDA, NSF, SQF, or third-party audits preferred., • Proficiency with Microsoft Office, quality systems, and ERP software (NetSuite preferred)., • 100% company-paid medical, dental, and vision insurance for employees (dependent coverage available at cost)., • 4 weeks PTO annually, with potential for additional accrual over time., • Paid company holidays. Powered by JazzHR hYdtScw10n

Job DescriptionDescription:Warehouse Associate LeadAbout Us At Gifthealth, we're revolutionizing the way people experience healthcare by simplifying the process of managing prescriptions and health services. Our mission is to provide a seamless, personalized, and efficient healthcare experience for all our customers. We're a dynamic, innovative, and customer-centric company dedicated to making a positive impact on people's lives. Position Summary The Warehouse Associate Lead is responsible for performing a variety of tasks to ensure the smooth and efficient operation of the warehouse. This includes managing inventory, maintaining warehouse cleanliness, completing the closing checklists and supporting various logistical tasks. This role involves leading the warehouse team with packouts of product, managing inventory accuracy, managing inbound deliveries, maintaining warehouse organization, and handling product shipments and deliveries. In addition, this role is responsible for ensuring a clean and safe working environment. The role is critical to supporting daily warehouse operations and ensuring timely and accurate order fulfillment. The ideal candidate will have strong leadership skills with the ability to work with a sense of urgency. Key Responsibilities • Lead and motivate a team of warehouse associates to achieve operational goals and ensure efficient workflows., • Train, mentor, and provide guidance to new and existing team members, ensuring high levels of productivity and accuracy., • Monitor and support all functions of the warehouse, including but not limited to, inventory audits, receiving, inspecting, and storing products, preparing orders for shipment and closing checklist., • Ensure compliance with regulatory and safety requirements such as OSHA, local fire code, FDA, DEA, and Pharmacy board., • Collaborate with warehouse leadership to ensure inventory stock is sufficient for forecasted orders., • Collaborate with other departments to resolve issues and improve overall operations., • Ensuring the warehouse is clean and organized daily by managing trash bins, bailing discarded cardboard, organizing stock and ensuring workspaces are free of hazards., • Lead by example in all areas including the code of conduct, safety and cleanliness of the warehouse, reliability and productivity., • Willingness to perform other related duties as assigned., • Work a schedule to close the day from 12:00pm to 8:00pm daily but flexibility to change as needed.Qualifications, • High school diploma or equivalent., • Previous warehouse or logistics experience is preferred with at least 1 year in a lead or supervisory role., • Strong attention to detail to ensure the accuracy of inventory counts and usage., • Ability to perform basic math calculations for inventory counts, order preparation, and shipping., • Experience with warehouse equipment such as pallet jacks, forklifts, hand trucks., • Ability to work well within a team environment and take direction from managers., • Ability to manage time efficiently, prioritize tasks, and meet deadlines in a fast-paced environment., • Knowledge of warehouse safety protocols and a commitment to maintaining a safe working environment., • Experience using warehouse management systems (WMS) or basic inventory software is preferred.Desired Attributes, • Dependable, safety-oriented, and well-organized., • Ability to develop and lead employees in an employee-friendly and respectful environment., • Team player who thrives in fast-paced environments., • Committed to operational excellence and continuous improvement., • Proactive problem solver with strong accountability.Work Environment, • Location: On-site, • Schedule: Full-time, • Full-time; flexibility may be required for project coordination., • Meetings: Regular coordination with warehouse and other leadership teams.Key Essential Functions [example below key provision - you may require others], • Ability to lift, carry, and move products up to 50 lbs., • Ability to stand or walk for extended periods., • Physical ability to operate equipment and machinery such as pallet jack, hand trucks, cardboard bailer, and forklift (upon training and certification) We celebrate diversity and are committed to creating an inclusive environment for all employees. If you do not meet every requirement but still feel you would be a great fit for this role, we encourage you to apply! Disclaimer This job description is intended to describe the general nature and level of work being performed. It is not intended to be an exhaustive list of all responsibilities, duties, or skills required of personnel. Gifthealth reserves the right to modify job duties or descriptions at any time. Requirements:

Job Description Job Summary: The role of a Bilingual Clinical Pharmacist is to provide exceptional care for patients with specialized pharmacy requirements. This includes gathering and assessing clinical data from patients, creating and supervising care plans, communicating with prescribers to obtain orders, reporting outcomes, making therapeutic suggestions, and overseeing the activities of therapy care specialists in compliance with all state and federal laws, accrediting bodies, and policies and procedures set forth by Anovo Specialty Pharmacy. The below is intended to describe the general content of and requirements for the performance of this job and is not to be construed as an exhaustive statement of essential functions, responsibilities, or requirements. Primary Duties and Responsibilities • Has oversight of dispensing, pharmacy operations, and pharmacy personnel (technicians, and other pharmacy associates.), • Complies with FDA mandates and self-imposed manufacturer restrictions., • Evaluates medication orders for appropriateness of drug, dosage, route of administration, potential drug interactions, and special high-risk patient considerations, warnings/precautions associated with prescribed medication, potential adverse reactions, and stability., • Suggest therapeutic intervention where appropriate/needed, and ensure availability for consultation to residents, prescribers, nursing staff, and/or designated health care representatives., • Maintains patient/resident medication profile including current and past medications-both prescription and non-prescription, pertinent medical history, clinical/laboratory data, and relevant clinical notes., • Procures and maintains all required documentation in accordance with federal and state regulations as well as ‘AnovoRx’ policy., • Dispenses pharmaceuticals including biotech drugs and other related items for patients with rare diseases., • Provides drug information, counsels patients, adheres to state/federal licensure requirements/regulations, and maintains required paperwork as directed., • Participates in Continuing Quality/Improvement program and ensures that pharmacies are in compliance with all standards., • When AnovoRx has written agreements with manufacturers for pharmacovigilance services, then as to such services: participates in training as required, receives reporters’ call concerning adverse events, product complaints and medical inquiries, completes the submission to the manufacturer and manufacturer designated partners, assists with follow-up as required. Always maintain patient confidentiality. * Maintains regulatory requirements, including all federal, state, local regulations, and accrediting organization standards. * Wears identification while on duty. * Represents the organization in a positive and professional manner. * Regular and reliable attendance expected. * Other work-related duties as assigned by supervisor/manager. Minimum Knowledge, Abilities, and Skills Required • Bachelor’s degree in Pharmacy or Graduate degree from an accredited school of pharmacy and 1+ years of pharmacy experience preferred., • Must possess a current unrestricted license or registration/certification in the required state(s) of practice, as required by law, and must be evidenced., • Must be willing and able to work any dedicated 8-hour AnovoRx shift between the hours of 7am-7pm., • Fluent in Spanish/English both written and oral; effective communication skills. Must be able to articulate thoughts well and communicate them clearly., • Must be willing and able to work onsite on your regularly scheduled shift Monday-Friday, if applicable., • Must be willing and able to cover on-call rotation as needed., • Must present professionally on the phone and in person., • Must articulate thoughts well and communicate them clearly, both verbally and in writing., • Comfortable with repetitive motions in answering phones and using computer keyboard., • Adept at handling sensitive and confidential situations

Job Description Job Summary: The role of a Clinical Pharmacist is to provide exceptional care for patients with specialized pharmacy requirements. This includes gathering and assessing clinical data from patients, creating and supervising care plans, communicating with prescribers to obtain orders, reporting outcomes, making therapeutic suggestions, and overseeing the activities of therapy care specialists in compliance with all state and federal laws, accrediting bodies, and policies and procedures set forth by Anovo Specialty Pharmacy. The below is intended to describe the general content of and requirements for the performance of this job and is not to be construed as an exhaustive statement of essential functions, responsibilities, or requirements. Primary Duties and Responsibilities • Has oversight of dispensing, pharmacy operations, and pharmacy personnel (technicians, and other pharmacy associates.), • Complies with FDA mandates and self-imposed manufacturer restrictions., • Evaluates medication orders for appropriateness of drug, dosage, route of administration, potential drug interactions, and special high-risk patient considerations, warnings/precautions associated with prescribed medication, potential adverse reactions, and stability., • Suggest therapeutic intervention where appropriate/needed, and ensure availability for consultation to residents, prescribers, nursing staff, and/or designated health care representatives., • Maintains patient/resident medication profile including current and past medications-both prescription and non-prescription, pertinent medical history, clinical/laboratory data, and relevant clinical notes., • Procures and maintains all required documentation in accordance with federal and state regulations as well as ‘AnovoRx’ policy., • Dispenses pharmaceuticals including biotech drugs and other related items for patients with rare diseases., • Provides drug information, counsels patients, adheres to state/federal licensure requirements/regulations, and maintains required paperwork as directed., • Participates in Continuing Quality/Improvement program and ensures that pharmacies are in compliance with all standards., • When AnovoRx has written agreements with manufacturers for pharmacovigilance services, then as to such services: participates in training as required, receives reporters’ call concerning adverse events, product complaints and medical inquiries, completes the submission to the manufacturer and manufacturer designated partners, assists with follow-up as required., • Always maintain patient confidentiality., • Maintains regulatory requirements, including all federal, state, local regulations, and accrediting organization standards., • Wears identification while on duty., • Represents the organization in a positive and professional manner., • Regular and reliable attendance expected., • Bachelor’s degree in Pharmacy or Graduate degree from an accredited school of pharmacy and 1+ years of pharmacy experience preferred., • Must possess a current unrestricted license or registration/certification in the required state(s) of practice, as required by law, and must be evidenced., • Must be willing and able to work any dedicated 8-hour AnovoRx shift between the hours of 7am-7pm., • Must be willing and able to work onsite on your regularly scheduled shift Monday-Friday, if applicable., • Must be willing and able to cover on-call rotation as needed., • Must present professionally on the phone and in person., • Must articulate thoughts well and communicate them clearly, both verbally and in writing., • Comfortable with repetitive motions in answering phones and using computer keyboard., • Adept at handling sensitive and confidential situations This description is intended to be only a general outline of major activities. It is expected that the employee performs these and any other activities which may be assigned, or which may occur in the normal course of work. This description is not a contract or guarantee of employment. AnovoRx is an Equal Opportunity Employer.

Job DescriptionDescription: The Pharmacist in Charge (PIC) is responsible for the overall operation, compliance, and clinical integrity of the specialty pharmacy. This role ensures adherence to all state and federal regulations, accreditation standards (e.g., URAC), and internal policies, while leading pharmacy operations, managing staff, and supporting high-quality patient care. The PIC plays a critical leadership role in optimizing specialty medication workflows, ensuring safe dispensing practices, and supporting growth initiatives across targeted disease states. Job Responsiblities • Serve as the designated Pharmacist in Charge per state Board of Pharmacy requirements, • Ensure full compliance with federal and state pharmacy laws (DEA, HIPAA, FDA, Board of Pharmacy regulations), • Maintain pharmacy licensure, controlled substance records, and inspection readiness, • Oversee adherence to URAC and other specialty pharmacy accreditation standards, • Develop, implement, and enforce policies and procedures, • Oversee daily pharmacy operations including prescription processing, verification, and dispensing, • Ensure accuracy, safety, and efficiency of all pharmacy workflows, • Monitor inventory management, procurement, and storage of specialty medications, • Implement and maintain quality assurance and performance improvement programs, • Oversee cold chain management and specialty drug handling requirements, • Provide clinical oversight for specialty therapies (e.g., SUD LAIs, oncology, Hep C, inflammatory conditions), • Support medication therapy management, patient education, and adherence programs, • Review and approve clinical protocols and therapy guidelines, • Collaborate with providers and care teams to optimize patient outcomes, • Supervise pharmacists, technicians, and support staff, • Recruit, train, and evaluate pharmacy personnel, • Foster a culture of accountability, compliance, and patient-centered care, • Ensure staff competency with specialty workflows and regulatory requirements, • Lead efforts for URAC or ACHC accreditation and ongoing compliance, • Monitor key performance indicators (KPIs) related to quality, turnaround times, and patient outcomes, • Conduct internal audits and implement corrective action plans, • Partner with leadership on pharmacy expansion and service line growth, • Support integration with care management, provider networks, and specialty programs, • Participate in payer relationships, audits, and contract requirementsRequirements:, • Active Registered Pharmacist license (Arizona), • Retail pharmacy experience required, • Prior managerial or leadership experience, • Strong problem-solving and decision-making skills, • Ability to work independently in a fast-paced retail environment, • Registered Pharmacist acceptable/ PharmD preferred, • Knowledge of 340B programs

Job Description Location: Tempe, AZ Department: Quality Reports To: Site Leadership / Operations Director Position Type: Full-Time | Contract (Temporary – Through October 2026- Exempt) Position Summary Aptyx is seeking a Senior Quality Engineer (Contract) to lead the Quality function at our Tempe site during a transitional period. This individual will serve as the senior on-site quality authority, overseeing quality operations, ensuring regulatory compliance, supporting production and transfer activities, and guiding the quality team to maintain operational excellence. This is a high-impact leadership role responsible for stabilizing and strengthening the Quality Management System (QMS), supporting production output, managing facility transfer activities, and ensuring compliance with FDA and ISO requirements within a medical device manufacturing environment. Key Responsibilities Quality Leadership & Department Oversight • Serve as the on-site Quality lead and Management Representative, providing daily direction to Quality Inspectors, QE's and Technicians., • Oversee production quality activities including in-process inspection, final release, and lot history record review., • Lead Material Review Board (MRB) activities and disposition of nonconforming product., • Ensure timely release of product to meet customer delivery commitments., • Ensure compliance with ISO 13485, and FDA 21 CFR Part 820 requirements., • Maintain site readiness for internal, customer, and regulatory audits., • Lead and/or support internal audits and corrective action initiatives., • Drive CAPA and Complaint investigations, root cause analysis, and implementation of effective corrective actions., • Lead and support quality oversight of product and process transfers from one building/facility to another, ensuring regulatory compliance and process integrity., • Partner with Operations, Engineering, and Validation teams to support equipment moves, process re-qualification, and documentation updates., • Ensure proper execution of IQ/OQ/PQ or revalidation activities associated with facility transfers., • Update risk assessments, control plans, inspection methods, and quality documentation as required due to transfer activities., • Provide hands-on quality engineering support across production and new product transfer activities., • Review and optimize inspection methods, sampling plans, and quality documentation., • Monitor and analyze quality metrics; provide trend reporting to site leadership., • Oversee supplier quality performance, including corrective action management and material disposition., • Support PPAP reviews and supplier qualification activities as needed., • Evaluate customer complaints and returned product investigations. Qualifications • Bachelor's Degree in Engineering, Life Sciences, or related technical discipline or equivalent work experience (10 years)., • 5+ years of experience in medical device manufacturing quality., • 3+ years in a senior or lead quality role., • Direct experience supporting facility transfers, line moves, or manufacturing site transitions strongly preferred., • Strong working knowledge of ISO 13485, FDA 21 CFR Part 820, and risk management principles., • Demonstrated experience leading CAPA, root cause investigations, and audit readiness initiatives., • Experience supporting production environments with urgency and operational accountability., • ASQ Certification (CQE, CQA, or CQM) preferred. Skills & Competencies • Strong leadership presence with ability to guide teams during transition., • Advanced problem-solving and analytical skills., • Experience with SPC, MSA, and statistical tools (Minitab preferred)., • High sense of urgency and accountability., • Excellent written and verbal communication skills., • Ability to balance strategic quality oversight with hands-on floor engagement., • Strong cross-functional collaboration skills during operational transitions. Regulatory Requirements • Maintain compliance with FDA, ISO 13485, and applicable regulatory standards., • Ensure adherence to company Quality Management System procedures., • Support continued certification and site registration requirements. Physical & Work Environment • Combination of office and cleanroom/manufacturing floor environment., • Regular standing, walking production floor, and reviewing documentation., • Occasional lifting up to 25 lbs., • Use of inspection equipment and computer systems. Contract Duration This is a temporary contract position expected to run through October , 2026- with potential for extension based on business needs.

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Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

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