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Job Description Responsibilities: • Catalogues, records, and organizes materials received at the warehouse; Arrange materials for order assembly, • Fulfills worksheets or tickets for customers by reading production schedules, order forms and requisitions, • Locates and gathers products for to move and distribute to production workers, assembly line, or to shipping areas, • Assembles, builds, wraps, sorts, and transports customer orders, • Operates hand truck, cart, doilies, forklift, order-picker, and walkie to transport items, • Maintain a clean and safe work area Required Experience: • Ability to speak, read, and write English with proficiency. Ability to read and comprehend simple instructions, short correspondence and memos. Basic keypunch skills, • Ability to bend, twist, reach, push, lift for extended periods daily, • Ability to lift 50 lbs, • Must be able to stand for 8 hours per day for up to 6 days a week, • Must have high sense of urgency, • Flexibility to work mandatory overtime based on business needs Preferred Qualifications: • High school diploma or General Education Degree (GED), • 1-3 months related experience and/or training Company DescriptionMedline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.

Job Description Whether you are working in a Pharmacy looking for additional income, a seasoned healthcare sales expert, or aspiring to break into the Medical Sales industry, Healthcare Marketing Group, LLC provides an excellent opportunity for you. As a Pharmacy Relationship Manager, you will help drive the growth of our company through building and retaining customer relationships. You can even change the way healthcare is delivered to Americans. Our Pharmacy Savings Card works like GoodRx and SingleCare. With savings of up to 80% off prescriptions, we provide the highest discounts in the industry! We are now seeking Pharmacy Relationship Managers in your area!* What does a Pharmacy Relationship Manager do? • Educate Pharmacy Staff about how their customers can save up to 80% on prescriptions, • Provide Savings Cards by engaging with medical offices and educating Office Staff about how their patients can save up to 80% on medications What you need to qualify: • Pharmaceutical/medical sales experience is preferred but not required, • Sales skills with a proven track record, • Exceptional interpersonal skills (building strong relationships), • Excellent verbal and written communication skills, • Ability to work independently to oversee accounts and increase revenue, • Reliable transportation (this position is partially remote and you will be visiting medical professionals in your area) *We are currently hiring Pharmacy Relationship Managers in the San Antonio metropolitan area. Please only apply to one city; your desired territories will be discussed during the interview. Benefits Training and compensation: • We include comprehensive training and ongoing coaching, • Monthly Bonuses, • Great Commission!

Job DescriptionAre you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn. This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: • Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs), • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical documents, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity, • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data, • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents, • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports), • Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC, • Demonstrated ability to lead others to complete complex projects, • Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines, • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment, • Organizational expert within the nonclinical subject area, • Excellent written/oral communication and strong time and project management skills, • Ability to attend regular team meetings, lead client meeting and CRMs, • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars, • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP)Requirements:, • BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control, • Knowledge of GLP, ICH guidelines, and applicable regulatory requirements, • 2+ years of pharmaceutical regulatory nonclinical writing experience, • Strong writing and analytical skills, • Proficiency with MS Office applications., • Hands-on experience with clinical trial and pharmaceutical development preferred iYpUppICQ8

Job Description Leading and innovative plaintiff’s trial law firm offering nationwide legal services is looking for an experienced senior partner level attorney to take charge of their Scottsdale, AZ office. The ideal candidate will have personal injury litigation experience at both the state and federal level and a comprehensive understanding of product liability law, preferably in the areas of medical device and pharmaceutical. The successful candidate will also have the desire to take on responsibility quickly, and grow as a leader in the role, have the capability of running a high volume docket of cases from start to trial, be willing to lead, mentor and train new lawyers at the firm and develop processes and systems with KPIs for the staff. This is a full time position allowing for a hybrid work schedule and based at the firm’s Scottsdale, AZ office. Qualifications and Experience: • Must have 7+ years of personal injury litigation experience with a comprehensive understanding of product liability law, preferably in the areas of medical device and pharmaceutical at both the state and federal level, • Must be licensed to practice law in AZ, with bar membership in good standing, • Must have the ability to take cases from start to trial, including working up experts in Federal court cases., • Must have an understanding of all aspects of personal injury matters from intake to trial., • Must have the capability of running a volume docket of cases., • Must have experience working with mediators in high value cases., • Must have basic knowledge of ESI and working with opposing counsel to get documents produced., • Must have excellent legal research, writing, and communication skills. The right person for this job will Must be able to provide excellent, reliable, persuasive, work product with little to no editing and or supervision., • Must embrace the unpredictable nature of litigations and appreciate the time demands of an active litigation practice, • Must be able to manage multiple deadlines and projects at once, while working both independently and on a team., • Must have the desire to serve on leadership in MDLs., • Must have the desire to take on responsibility quickly and grow as a leader in this role., • Must be able to lead, mentor and train new lawyers at the firm as well as Arizona staff., • Must have the ability to develop processes and systems with KPIs for the staff., • Must have the ability to utilize technology and case management software and adhere to data integrity standards., • Must be able to maintain positive relationships with colleagues, staff, clients, opposing attorneys, and court personnel. Benefits: • Salary is commensurate with experience plus performance-based bonuses which are an important component of the overall compensation plan, • Hybrid Work Schedule, • Firm Paid Professional Development, • Bonus Incentives for Business Generation, • Paid Time Off, • Health And Dental Insurance. #promote

Job Description Overview Amerita is a leading provider of Specialty Infusion services focused on providing complex pharmaceutical products and clinical services to patients outside of the hospital. As one of the most respected Specialty Infusion providers in America, we service thousands of patients nationwide through our growing network of branches and healthcare professionals. The Registered Dietitian (RD/RDN) is responsible for implementing an individualized nutritional care plan for each patient. This role is also responsible for developing or obtaining patient nutrition educations materials. The Registered Dietitian counsels the patient, family, significant other or caregiver on prescribed diet, parenteral nutrition, and/or enteral nutrition and monitors adherence and response to therapy. This is a hybrid position, based out of your home office but travels to 3 branches working with clients receiving parenteral nutrition. Schedule: Monday - Friday, 8:30am - 5:30 pm We are looking for a Registered Dietitian with a minimum of 2 years of clinical experience, including experience in Nutrition Support Must be Registered in accordance with the Commission on Dietetics Must be Licensed in AZ Certified Nutrition Support Clinician, preferred We Offer • Medical, Dental & Vision Benefits plus, HSA & FSA Savings Accounts, • Supplemental Coverage – Accident, Critical Illness and Hospital Indemnity Insurance, • 401(k) Retirement Plan with Employer Match, • Company paid Life and AD&D Insurance, Short-Term and Long-Term Disability, • Employee Discounts, • Tuition Reimbursement, • Paid Time Off & Holidays Responsibilities • Co Develops, implements and monitors the clinical management of parenteral and enteral patients as part of the Nutrition Support Team, • Makes recommendations for nutrition intervention when necessary, • Reviews patient medical history, anthropometrics and pertinent lab values to assess home nutrition support protocols and insurance payer requirements, • Counsel patients and caregivers on home enteral and parenteral nutrition therapy. Assesses patients’ understanding of and compliance with prescribed diet principles, • Ensure continuity of care with patient’s physician, nurses and nutrition support teams to provide high quality patient centered care, • Participate in Performance Improvement Program and ACHC accreditation, • Identifies and promotes nutrition program services to clinical and professional referral base and performs necessary in-service education, • Supervisory Responsibility: No Qualifications • Bachelor of Science in Nutrition or related field, • Registered Dietitian with license to practice in assigned state(s); Certified Nutrition Support Clinician preferred, • Minimum of two (2) years of clinical experience required., • Must have strong communication skills and organizational skills

Job Description Title: Quality Engineer Location: Phoenix, AZ Our client, a leading global company specializing in custom packaging solutions for the medical device and pharmaceutical industries, is seeking a Quality Engineer for its Phoenix, AZ, location. The company focuses on designing and manufacturing high-quality packaging using advanced plastic manufacturing technology and stringent quality control measures. Position Overview Role: As the Quality Engineer, you would be responsible for collaborating with design and manufacturing to establish project quality standards, specifications, and inspection methods. Key duties include maintaining and analyzing customer prints, requirements, and specifications to ensure customer requirements will be consistently met and supporting new product development and changes to customer specifications by writing protocols and analyzing results from 1st article and Process validations (IQ-OQ-PQ) studies during product launch and subsequent changes to tooling or specifications and developing new inspection methods and product specifications for use during production. Training workers engaged in measuring and testing products and tabulating data concerning materials, product, or process quality and reliability. Responsibilities and Functions: * Work with manufacturing and quality inspectors to contain and dispose of non-conforming products. Troubleshoots and participates in solving quality-related production problems. Recommends design and processing revisions to reduce actual or potential quality costs. Takes a lead role in facilitating and aiding in scrap reduction initiatives * Assist in the development process, such as process improvement, problem-solving, AQL Levels, FMEA, validations (IQ/OQ/PQ), DOE, and metrics. * Provide guidance/leadership/decision-making to the QA Department * Assist in the development process, such as process improvement, pack out, AQL levels, control plan for inspection, validations, and Metrics. * Participates and facilitates internal /external corrective action activities and ensures activities are properly tracked and documented. * Ability to read and interpret engineering drawings and technical specifications. * 1st article process includes measurement, analysis, and reporting data. Qualifications: Education: * BS, AS in Engineering or equivalent is preferred Experience: * Required:5-7 years of Quality Engineering experience in a Manufacturing environment, including validation and measurement analysis, or a combination of education and experience. * ASQ Certified Quality Engineer (CQE) or other certification preferred * Good math and PC skills. Working knowledge of statistical software (Minitab preferred) * Excellent organizational and oral / written communication skills are required * Formal training in procedures, ISO 13485 standard, and inspection methods and techniques * Thermoforming and/or medical packaging experience is a plus. Benefits: * 401(k) match program * Annual bonus * Dental, health, and vision insurance * Paid time off Location: Phoenix, AZ If you are interested in this position, please apply here or send your resume to . Equal Opportunity Employer Disclaimer This organization is an Equal Opportunity Employer and is committed to creating an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability status, genetic information, protected veteran status, or any other characteristic protected by applicable law. Employment decisions are based solely on qualifications, merit, and business needs.

Job Description Doctor of Pharmacy (PharmD) degree, active Pharmacist license, and minimum 1+ years Pharmacist experience required. Applicants who do not meet these qualifications will not be considered. A contract opportunity is available for a Staff Pharmacist skilled in pharmacy operations and prescription management. This role requires expertise in dispensing medications, counseling patients on proper medication usage, and ensuring pliance with pharmacy laws and standards. The position is located in San Carlos, AZ, offering an engaging environment to apply your pharmacy knowledge within a supportive team. Key Responsibilities: • Accurately dispense prescription medications to patients in accordance with prescribed instructions, • Provide patient counseling on medication usage, potential side effects, and storage requirements, • Collaborate with healthcare providers to resolve prescription issues and optimize patient outes, • Maintain meticulous records of prescriptions, inventories, and regulatory documentation, • Monitor inventory levels and assist with ordering and restocking of pharmaceutical supplies, • Current pharmacist licensure and registration required, • Proven experience as a Staff Pharmacist or in a similar role within a retail or hospital pharmacy setting, • Strong knowledge of drug classifications, interactions, and proper dispensing procedures, • Excellent munication skills, both verbal and written, with a patient-centered approach, • Ability to work independently and as part of a multidisciplinary healthcare team Take the next step in your pharmacy career by submitting your application today!

Job Description Overview PharMerica is hiring a non-exempt Pharmacy Order Entry Technician in Phoenix, AZ! Join our closed-door pharmacy team where you’ll work in a non-retail environment, dedicated to meeting the pharmaceutical needs of long-term care and senior living clients. If you’re passionate about delivering exceptional service and high-quality care, we want to hear from you. Apply today and become part of a team committed to making a difference! Schedule: Mon-Fri 8:00am-3:30pm (with occasional variation) Weekend/Holiday Rotation Benefits and perks for you! • Medical, Dental, Vision insurance, • Health Savings & Flexible Spending Accounts (up to $5,000 for childcare), • Tuition discounts & reimbursement, • 401(k), • Company Paid Time Off, • Shift Differential, • DailyPay, • Pet Insurance Responsibilities How YOU will benefit: • Supportive team with room to work independently, • Ongoing training and career growth, • Advancement opportunities in a growing company, • Referral bonuses, • We cover Pharmacy Technician license fees (new hires & current staff eligible) As a Pharmacy Order Entry Technician you will: • Enter and verify medication orders in a computerized system with a high level of accuracy and efficiency., • Conduct basic drug calculations, including dosage and conversion tasks., • Investigate and resolve pharmacy claim denials; perform follow-up actions in POS systems., • Stay current with Medicaid claim regulations and ensure compliance in processing., • Track unpaid or delayed claims; generate reports for management., • Provide excellent customer service in line with company values and policies., • Assist with medication preparation and dispensing under Pharmacist supervision., • Support additional pharmacy tasks and operations as directed by management. Qualifications Qualifications Required: • High School diploma or equivalent., • Pharmacy Technician license as required by state, • Experience in a pharmacy setting and medical terminology., • Ability to operate a computer; recognize and identify medications.

Job DescriptionDescription: Job Type: Full-time Pay: $50,000.00 - $65,000.00 per year, new client sign-on bonus, plus commission Schedule: 8 am - 5 pm, Monday - Friday Location: Phoenix Metropolitan Area A2Z Workforce Solutions is looking for self-driven talent who are willing to take charge of the marketing of our pharmacy. We are searching for potential team members with some past experience in marketing in the healthcare field. Our pharmacy aims to create a direct bond between us and other medical offices so that we can directly partner to service newer clients. This position will be a direct link the pharmacy and other providers. Our pharmacy is located in Mesa, AZ and team members will be traveling around the metropolitan area to focus on marketing within Arizona. Responsibilities: • Foster new relationships with medical offices and other healthcare facilities through person-to-person interaction, • Understand and create solutions to cater towards the needs of clients, • Develop focused plans for strategic approach to marketing and catering towards the need of the clients, • Educate medical office staff on how we can save their valuable time and increase their patient satisfaction with our services while also working to save money for patients out-of-pocket, • Establishes, develops and maintains successful business partnerships with targeted health care providers (HCPs) and staffs within assigned geographical territory, • Identifies and investigates client concerns and communicates with appropriate staff, • Analyzes sales data to determine potential and then executes an action plan in the territory to ensure appropriate calls, reach, frequency, lunch and learns, etc Must haves: • Prior experience in sales/marketing in the healthcare field, • Excellent verbal, written, and presentation skills, • Experience interacting with other medical providers, • Ability to quickly analyze, understand, and come up with solutions to cater to provider needs, • Catering presentation and services to specific medical offices, • Aim, track, and exceed sales targets, • Valid US driver’s license and vehicle Benefits: • Dental insurance, • Health insurance, • Vision insurance

Job Description The Job: The Quality Assurance Specialist ensures that all manufacturing, testing, documentation, and operational processes comply with cGMP, FDA 21 CFR Part 111, internal quality standards, and customer requirements. This role is responsible for developing and maintaining quality systems, managing change control and deviations, supporting batch release, and ensuring the accuracy and integrity of product and process documentation. Responsibilities: • Create, revise, and maintain MMRs, MBRs, specification sheets, COA templates, and other controlled documents, • Ensure all procedures comply with cGMP, regulatory, and company standards, • Initiate, assess, and manage change control requests impacting formulations, suppliers, equipment, processes, or documents, • Ensure timely closure and proper documentation of all quality events, • Review QC lab results, data sheets, and testing documentation for completeness and accuracy., • Support ingredient and finished-product sampling as needed, • Review batch records for accuracy, completeness, and compliance with the “right-first-time” standard, • Ensuring all production and warehouse personnel are in compliance with cGMPs, • Conducting visual inspections on processes and products on the production floor, • Conduct production line clearances for start-up, cleaning verification, and changeover., • Conducting product inspections and ensuring all finished goods meet company quality and industry standards, • Recommending corrective actions for potential problems, • Verifying that all equipment are calibrated, • Ensure all products meant for disposal are isolated and dispositioned correctly, • Conduct periodic audits, including glass and brittle material, and equipment inspection to ensure compliance, • Collaborate closely with production, QC, R&D, procurement, and warehouse teams to resolve quality issues, • Bachelor’s degree in Life Sciences, Chemistry, Biology, Food Science, or related field (or equivalent experience), • One to five years or more in Quality Assurance within dietary supplements, nutraceuticals, food, or pharmaceutical manufacturing, • Strong knowledge of cGMP, FDA 21 CFR Part 111, HACCP, and quality systems, • Experience with deviation/CAPA, document control, and change management, • Good written and verbal communication skills, • Basic computer and mathematical skills, • Excellent problem-solving skills, • Detail-oriented with excellent documentation and analytical skills, • Ability to work cross-functionally and communicate clearly, • Good understanding of company standards and expectations, • PTO (Paid Time Off), • 9% 401k Match, • Company paid Medical, Life, Dental insurance, • Wellness Credit, • Employee Store Credit, • Annual Bonus, • Company Sponsored Events

Job DescriptionTTF is recruiting a Medical Assistant/Scribe for a healthcare specialty company in Scottsdale, AZ. This is a full-time, Monday-Friday opportunity offering a competitive salary range. Qualified candidates will have previous experience working as a Medical Scribe. Must have strong knowledge in medical terminology, anatomy, and physiology. Please send your resume to Chelle at for consideration. TTF is a search and staffing company that partners with hospitals, physician groups, TPA's, medical management companies, pharmaceutical and pharmacy benefit plan organizations, surgery centers, DME/home health, consulting companies, and all other healthcare fields. The TTF Physician Office Staffing Division places MA’s (Medical Assistants), Medical Front Office, Medical Back Office, Physician Referrals and Authorizations, Schedulers, Nurse Practitioners, Physician Assistants, Medical Billers/Collectors, Coders, and Office Managers/Administrators. We never charge a fee to candidates and all conversations are kept confidential. We would like to be your career consultant and look forward to working with you! #IND2

Job Description Amen Clinics are outpatient health care clinics that have been providing mental wellness strategies to patients of all ages since 1989. We offer patient-first experiences and customized solutions to an array of behavioral and psychiatric conditions. This is an exciting and unique professional opportunity. The psychiatrist provides clinical leadership to ensure treatment is evidence-based and outcome driven. In addition to having the use of master’s level clinical historians, psychological testing, neuropsychological screening tools, functional brain imaging, and emerging treatments such as TMS and neurofeedback, you will be in a healthy and aesthetically pleasing work environment. You will be mentored on a variety of integrative methods that will expand your professional repertoire. You will also have multiple opportunities for writing and speaking, if that appeals to you. Essential Duties and Responsibilities: • Assist in the development, promotion and delivery of the approved Amen Clinics Method to brain health, • Patient evaluations – incorporate clinical history and brain SPECT scan findings during patient evaluation and complete final report on the day of patient evaluations., • Expected to remain current with brain imaging, psychiatric, pharmaceutical and nutraceutical technologies., • Evaluation and treatment of patients with various conditions, including: o Attention deficit/hyperactivity disorders o Mood disorders o Anxiety disorders o OCD o Psychosis o Post-Traumatic Stress Disorder o Traumatic brain injury o Obesity o Medical issues/hormone imbalances o Addictions o Alzheimer’s Disease o Memory and learning issues o Cognitive impairment o Autism spectrum disorders o Brain infections, such as Lyme disease • Commitment to using evidence-based, non-pharmacologic interventions correlated with research findings by Amen Clinics., • Attending Physician and Staff meetings., • Outreach/collaboration with outside professionals in order to build good relationships with referral sources. Qualifications and Requirements: • Board Certified preferred. Double Board Certified – a plus., • Experience working in a private practice setting--being efficient, developing referral relationships, doing outstanding clinical work, and establishing positive therapeutic relationships., • Willingness to learn to use brain imaging in clinical practice. We will train you to use brain SPECT imaging., • Experience dealing with medical issues including hormone imbalance and deficiencies as well as understanding the role they play in contributing to and/or complicating mental illness., • Experience treating patients with interventions other than psychotropic medications, including psychotherapy and evidence-based nutraceuticals. For those with limited experience in nutraceutical and other non-pharmacologic interventions, we will provide training., • Dedication to helping individuals, families and systems (such as schools, businesses, and treatment facilities) reach their full potential by creating and developing “brain healthy” strategies and practices., • Time management, organization and computer skills and ability to work independently and within a team are critical., • Excellent command of spoken and written English., • Empathy, emotional stability, ability to relate well to others, good communications skills, and above all genuine care and regard for the patient. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Sitting for long period of time, • Frequent typing and viewing of computer screen, • Frequent use of hand and fingers with machines, such as computer, copier, fax machine, scanner and telephone, • Frequent hearing, listening and speaking by telephone and in person, • Occasionally required to stand, walk, reach with hands and arms, stoop or bend Work Environment: The work environment described here are representative of those that an employee encounters white performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Work indoors in temperature-controlled environment, • The noise level is usually moderate with occasional outbursts from patients during treatment

Job Description TTF is recruiting a Back Office Medical Assistant for a healthcare specialty company in North Phoenix, AZ. This is a part-time position offering a competitive salary range. Qualified candidates will have at least 2 years of previous experience in back office medical assistant duties; vitals, injections, patient demographics, etc. Experience as a medical scribe is required. Candidates may be asked to travel to North Scottsdale on occasion. Please send your resume to Chelle at for consideration. TTF is a search and staffing company that partners with hospitals, physician groups, TPA's, medical management companies, pharmaceutical and pharmacy benefit plan organizations, surgery centers, DME/home health, consulting companies, and all other healthcare fields. The TTF Physician Office Staffing Division places MA’s (Medical Assistants), Medical Front Office, Medical Back Office, Physician Referrals and Authorizations, Schedulers, Nurse Practitioners, Physician Assistants, Medical Billers/Collectors, Coders, and Office Managers/Administrators. We never charge a fee to candidates and all conversations are kept confidential. We would like to be your career consultant and look forward to working with you! Company DescriptionTTF is a recruiting firm that partners with companies nationwide to find the talent they need for success.TTF is a recruiting firm that partners with companies nationwide to find the talent they need for success.

Job DescriptionAbout MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide. MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit or follow MMS on LinkedIn. This role is a remote, project-based consulting opportunity. Responsibilities • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias, • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals, • Complete writing assignments in a timely manner, • Maintain timelines and workflow of writing assignments, • Practice good internal and external customer service, • Highly proficient with styles of writing for various regulatory documents, • Expert proficiency with client templates & style guides, • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects, • Contribute substantially to, or manages, production of interpretive guides, • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary, • Mentor medical writers and other members of the project team who are involved in the writing processRequirements, • At least 3 years of previous experience in the pharmaceutical industry, • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience, • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline, • Substantial clinical study protocol experience as lead author, • Experience leading and managing teams while authoring regulatory documents with aggressive timelines, • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus, • Understanding of clinical data, • Exceptional writing skills are a must, • Excellent organizational skills and the ability to multi-task are essential prerequisites, • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools, • Experience being a project lead, or managing a project team Z0AqWTnM2L

Job DescriptionAbout MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide. MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit or follow MMS on LinkedIn. Responsibilities • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias, • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals, • Complete writing assignments in a timely manner, • Maintain timelines and workflow of writing assignments, • Practice good internal and external customer service, • Highly proficient with styles of writing for various regulatory documents, • Expert proficiency with client templates & style guides, • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects, • Contribute substantially to, or manages, production of interpretive guides, • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary, • Mentor medical writers and other members of the project team who are involved in the writing processRequirements, • At least 3 years of previous experience in the pharmaceutical industry, • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience, • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline, • Substantial clinical study protocol experience, as lead author, required, • Experience leading and managing teams while authoring regulatory documents with aggressive timelines, • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus, • Understanding of clinical data, • Exceptional writing skills are a must, • Excellent organizational skills and the ability to multi-task are essential prerequisites, • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools, • Experience being a project lead, or managing a project team, • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus DItLGbfwtI

Job Description Responsibilities: • Load and secure product from the Medline Facility into a truck., • Safely operate a Class A vehicle between the Medline Facility and multiple customer destinations on a delivery route. Abide by Medline’s safety regulations, including wearing safety equipment where needed, performing safety checks, etc., • Unload and deliver product at our customer facilities, ensuring timely deliveries., • Provide in-person support to the customer – addressing their questions and needs and providing appropriate documentation upon delivery., • Communicate with dispatching team regarding necessary adjustments to delivery route or schedule in order to meet customer needs and maintain safe operations., • Maintain a travel and cargo log in accordance with Federal and State regulations and company policy., • Perform inspection of vehicle to ensure safe operation and sufficient fuel levels for continued vehicle use. Required Experience: • Minimum 2 years tractor trailer driving experience, • Class A CDL; Licensed to operate assigned vehicle., • Ability to meet Federal and State requirements for operation of commercial motor vehicles., • Clean driving record with no serious violations. Preferred Qualifications • High school diploma or equivalent What can you expect when you’re on board? • Our drivers are home daily with our local routes – we care about work-life balance, • New and updated trucks and equipment, • Affordable medical, dental, vision & Rx plan, • Generous paid time off, • 401k with company match, • Professional growth and development opportunities, • Safety is our #1 priorityCompany DescriptionMedline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings. Due to continued growth we are in need of a Warehouse Operator to join our team. The Warehouse Operator is an integral part of our team’s success. Our Warehouse Operators are responsible for operating machinery to move materials around a facility for shipping, processing and receiving. This might include unloading, scanning, moving, staging, loading, locating, picking, relocating, and stacking product.Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings. Due to continued growth we are in need of a Warehouse Operator to join our team. The Warehouse Operator is an integral part of our team’s success. Our Warehouse Operators are responsible for operating machinery to move materials around a facility for shipping, processing and receiving. This might include unloading, scanning, moving, staging, loading, locating, picking, relocating, and stacking product.

Job DescriptionTTF is recruiting for a Back Office Medical Assistant for a specialty healthcare company located in the North Scottsdale/North Phoenix area. This is a full-time, Monday-Friday opportunity offering a competitive salary range. Qualified candidates will have at least 2 years of previous experience in back office medical assistant duties; vitals, injections, patient demographics, etc. This position will be working closely with lead surgeon as well as require travel to Tucson and Prescott Biweekly. Please send your resume to Chelle at for consideration. TTF is a search and staffing company that partners with hospitals, physician groups, TPA's, medical management companies, pharmaceutical and pharmacy benefit plan organizations, surgery centers, DME/home health, consulting companies, and all other healthcare fields. The TTF Physician Office Staffing Division places MA’s (Medical Assistants), Medical Front Office, Medical Back Office, Physician Referrals and Authorizations, Schedulers, Nurse Practitioners, Physician Assistants, Medical Billers/Collectors, Coders, and Office Managers/Administrators. We never charge a fee to candidates and all conversations are kept confidential. We would like to be your career consultant and look forward to working with you. #IND1

Cardinal Health Sonexus™ Access and Patient Support helps specialty pharmaceutical manufacturers remove barriers to care so that patients can access, afford and remain on the therapy they need for a better quality of life. Assists patients in accessing services such as funding, transportation, lod

Associate Director of Quality Assurance Full Time | On-Site | Salary: $100,000–$125,000 About the Company A fast-growing pharmaceutical manufacturer is seeking an Associate Director of Quality Assurance to oversee quality systems and regulatory compliance across its sterile production operations. The company specializes in producing high-quality pharmaceutical products for healthcare organizations nationwide and maintains a strong focus on cGMP standards, process reliability, and continuous improvement. Position Summary The Associate Director of Quality Assurance will provide both strategic and hands-on leadership for the QA function, ensuring all products, processes, and documentation meet applicable regulatory requirements. This role supports day-to-day oversight of manufacturing and laboratory activities, leads QA personnel, and drives the maturity of the company’s quality systems. Candidates with experience in sterile or aseptic manufacturing environments are strongly preferred. Key Responsibilities • Lead QA operations across multiple production and laboratory areas, ensuring consistent alignment with internal quality standards and federal regulations., • Manage batch record review, product disposition, deviation investigations, and CAPA processes., • Ensure ongoing compliance with FDA 21 CFR regulations, cGMP requirements, and applicable industry standards such as ISO 9001., • Conduct internal audits and support external inspections from regulatory agencies and customer auditors., • Collaborate with cross-functional teams (Manufacturing, QC, Validation, Engineering) to resolve quality issues and maintain a compliant production environment., • Oversee training programs related to cGMP, aseptic practices, and quality procedures., • Review and approve SOPs, validation protocols, and other controlled documents., • Provide leadership for cleanroom oversight, environmental monitoring programs, and process validation activities., • Participate in risk assessments and support root-cause investigations for quality-related events. Required: • Bachelor’s degree in Chemistry, Microbiology, Pharmacy, or a related scientific field., • 7+ years of quality experience in pharmaceutical manufacturing or another FDA-regulated environment., • Strong knowledge of cGMP, quality systems, and regulatory expectations., • Demonstrated success leading QA teams or managing key quality functions., • Experience in sterile/aseptic operations or parenteral manufacturing., • Advanced degree (MS, PharmD, MBA, or similar)., • Familiarity with QMS software, electronic batch records, LIMS, or related systems. This is a fully on-site role requiring routine interaction with production, laboratory, and cleanroom areas. Occasional flexibility may be needed during audits, investigations, or time-sensitive production activities. Some travel between company locations may be required. Compensation & Benefits • Salary range: $100,000–$125,000, depending on experience., • Annual performance bonus eligibility., • Medical, dental, and vision coverage., • 401(k) with employer match., • Paid time off and company-observed holidays., • Ongoing training and professional development opportunities.

Job DescriptionTTF is recruiting for a Patient Access Representative to work at a well-respected hospital in Mesa, AZ. This is a full-time position that is offering a rotating schedule, including weekends. Qualified candidates will have at least 1 year of experience working in a healthcare setting, be comfortable in a fast paced environment, provide excellent customer service, and be computer literate. For consideration, please send resumes to Tannia at TTF is a search and staffing company that partners with hospitals, physician groups, TPA's, medical management companies, pharmaceutical and pharmacy benefit plan organizations, surgery centers, DME/home health, consulting companies, and all other healthcare fields. We place candidates in the PFS field with the following specialties and titles: Hospital Collector, Commercial, Government, Managed Care, Billing Representative, Medical Biller, AHCCCS, Medicare, Medicaid, Medical Claims, Follow-Up Rep, Medical Collections Representative, Medical Collector, Medical Reimbursement Specialist, Patient Account Rep, Patient Financial Representative, Medical Scheduler, Reimbursement Representative, Reimbursement Specialist, Coding, Patient Access, Patient Admitting, and Claims Processing. IND #1

A-V Services Inc., a leading AV company with multiple fortune 100 contracts within the financial, pharmaceutical and computing industry, seeks a freelance Audio/Visual/Multimedia Technician for on-site support. Must have great customer service with emphasis supporting the corporate work sector. Additionally, comprehensive audio video skills. Ideal candidate would have Associates level college degree in a technology related field and/or minimum 3 years of previous employment with AV support responsibilities in the AV industry. Our corporation is looking for an individual who possesses a full understanding of all areas of the A/V field including but not limited to: Ability to operate and troubleshoot most AV equipment and systems, like: • Projection systems / display devices, • Crestron control systems, • Switching / routing / interfacing technology, • Videoconferencing & Audio conferencing technologies Technical understanding of AV and IT systems • Up-to-date awareness of AV and IT technologies and their features, • Ability to operate digital audio consoles (A1) for Live Events, • Ability to read and follow AV system flow diagrams and support documentation Excellent interpersonal skills, accuracy and attention to detail • Technical AV certifications such as CTS a plus, • Proficiency in the use of personal computers including such programs as MS Word, Excel and Outlook., • Positive, professional image, • Ability to remain calm under pressure, • Ability to operate related AV technologies required for the job, i.e. Town Hall events, conference room meetings, video conference-based events (sometimes using Telepresence), • Ability to work with an onsite AV team on a daily basis Join Our Diverse and Inclusive Team! At AV Services Inc. we are committed to fostering an inclusive and diverse workplace where every team member is valued and empowered. We are proud to be an equal opportunity employer, welcoming all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability status, or any other characteristic that makes you unique. Our Commitment to Diversity and Inclusion: Our employees are our greatest asset, and we believe that the diverse perspectives and experiences they bring are key to our success. We celebrate and encourage differences in age, ethnicity, family or marital status, language, physical and mental abilities, socio-economic status, and more. These unique attributes contribute to our vibrant culture, enhance our reputation, and drive our achievements. Why Work With Us? • Inclusive Culture: We embrace diversity in all its forms and are dedicated to creating an environment where everyone feels respected and valued., • Empowerment: We support our employees' growth and self-expression, recognizing that their individual talents and innovations are vital to our success.

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Job DescriptionDescription:PCI Nuclear Pharmacy-Driver PCI Nuclear Pharmacy, a division of Arizona Home Care, is looking for a responsible friendly driver to join our team for deliveries. Why Work For Us: • Company vehicles, phones and gas payment are provided during deliveries 3:30 AM - 9:30 PM Monday through Friday 5:00 AM - 10:00 AM Monday through Friday Our business depends on referrals from doctors and patients alike. The best candidates will not only be excellent drivers, but excellent customer service representatives. Responsibilities: • Managing the outbound delivery process of recurring radiopharmaceuticals and supplies to hospitals, clinics, and imaging centers., • Making timely, efficient deliveries., • Cleaning equipment and the pharmacy in preparation for each day’s deliveries. Requirements:PCI Nuclear Pharmacy- Driver Qualified candidates: • Have an extensive knowledge of the Metro Phoenix Area and are able to delivery Valley wide, • Are interested in cross-training and learning about a successful nuclear pharmacy, • Possess a valid driver’s license and a clean driving record, • Are able to lift 50 pounds repetitively, • Applicants MUST be non-smokers and willing to wear steal toed shoes (steal toed shoes are provided)

This position is ideal for a highly analytical and client-focused professional with deep expertise in pharmaceutical data and a strong ability to translate business requirements into analytics plans and subsequently, analytics insights into strategies. We are seeking a Senior Manager, Data and Analy

AV company with multiple fortune 100 contracts within the financial, pharmaceutical and computing industry, seeks a freelance Audio/Visual/Multimedia Technician for on-site support.

Cardinal Health Sonexus Access and Patient Support helps specialty pharmaceutical manufacturers remove barriers to care so that patients can access, afford, and remain on the therapy they need for a better quality of life. Oversee daily operations for patient access support contact center team of up

A fast-growing pharmaceutical manufacturer is seeking an Associate Director of Quality Assurance to oversee quality systems and regulatory compliance across its sterile production operations. Associate Director of Quality Assurance. The Associate Director of Quality Assurance will provide both strat

Minimum of 3 years of experience as a warehouse or distribution manager. The Warehouse Manager position involves managing inventory, ensuring compliance with regulatory requirements, and optimizing efficiency in the storage and distribution of pharmaceutical products. Strong background in inventory

Job Description Description Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities. Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day. Company Culture Guidelines & Values: • We empower and support our colleagues, • We commit to client success at every turn, • We have the courage to do the right thing, • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged., • We constantly acquire new skills and learn from our experiences to enhance our collective expertiseProject Manager Key Responsibilities Capital Project Management: Lead and manage full lifecycle of capital projects, including planning, budgeting, execution, and closeout, ensuring alignment with site and corporate goals. * Technical Leadership: Oversee engineering activities for sterile fill-finish operations and lyophilization systems, ensuring compliance with cGMP, FDA, and international regulatory standards. * Process & Equipment Integration: Support design and implementation of process and facility modifications to accommodate new products and clients, ensuring smooth technology transfer and process validation. * Budget & Financial Oversight: Develop and maintain accurate project budgets and forecasts; monitor project spend, track variances, and ensure financial accountability for capital expenditures. * Documentation & Phase Deliverables: Ensure adherence to established project documentation, phase gates, and change management processes for technical and operational projects. * Cross-Functional Collaboration: Partner with Manufacturing, Quality, Validation, EHS, and Supply Chain to deliver integrated project outcomes and support site readiness for commercial and clinical operations. * Operational Transition Support: Contribute to the site's transformation toward a CDMO business model by aligning engineering practices, capacity planning, and infrastructure to client-driven production needs. * Vendor & Contractor Management: Manage external engineering firms, equipment vendors, and contractors to ensure adherence to project scope, quality, safety, and schedule requirements. Qualifications & Requirements * Education: Bachelor's degree in Engineering (Mechanical, Chemical, Industrial, or related discipline). Advanced degree preferred. * Experience: * Minimum 7–10 years of experience in pharmaceutical manufacturing with a focus on sterile fill-finish and lyophilization. * Proven track record in capital project management, ideally within a CDMO or CMO environment. * Experience handling cytotoxic or high-potent compound manufacturing operations preferred. * Technical Expertise: * Strong understanding of aseptic processing, lyophilization systems, and cleanroom operations. * Knowledge of pharmaceutical packaging (bulk naked pack for Japan, full inspection and labeling for U.S. distribution). * Familiarity with process utilities and equipment qualification protocols (IQ/OQ/PQ). * Project & Financial Skills: * Demonstrated success in managing multi-million-dollar capital projects. * Skilled in budgeting, forecasting, and cost control within complex, regulated environments. * Soft Skills: * Strong leadership and communication skills, with the ability to influence cross-functional teams. * Highly organized, detail-oriented, and capable of managing multiple priorities in a dynamic environment. * Other: * Local candidates preferred (Phoenix, AZ area). * Willingness to work onsite at a GMP manufacturing facility. For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future. *Verista is an equal opportunity employer. National (US) Range$87,780—$136,225 USD Benefits Why Choose Verista? • High growth potential and fast-paced organization with a people-focused culture, • Competitive pay plus performance-based incentive programs, • Company-paid Life, Short-Term, and Long-Term Disability Insurance., • Medical, Dental & Vision insurances, • FSA, DCARE, Commuter Benefits, • Supplemental Life, Hospital, Critical Illness and Legal Insurance, • Health Savings Account, • 401(k) Retirement Plan (Employer Matching benefit), • Paid Time Off (Rollover Option) and Holidays, • As Needed Sick Time, • Tuition Reimbursement, • Team Social Activities (We have fun!), • Employee Recognition, • Employee Referral Program For more information about our company, please visit us at Verista.com

Minimum of 3 years of experience as a warehouse or distribution manager. The Warehouse Manager position involves managing inventory, ensuring compliance with regulatory requirements, and optimizing efficiency in the storage and distribution of pharmaceutical products. This role offers the unique opp

Job Description This is a nationwide traveling role. We are seeking an industrial maintenance field service technician to become an integral part of our team! You will perform maintenance duties in the Industrial Automation Field including but not limited to the following industries: Automotive, Pharmaceutical, Aerospace, Ecommerce, Military Agricultural and Entertainment. Specifically requirements for this position will be as follows Job Overview We are seeking a skilled Industrial Maintenance Technician to join our team. The ideal candidate will have a strong background in electromechanical systems, PLC troubleshooting, and hydraulics/pneumatics. This position is crucial for maintaining and optimizing our industrial equipment and processes. Responsibilities • Perform preventive maintenance on various industrial equipment and machinery, • Diagnose and troubleshoot mechanical, electrical, and electronic issues in industrial systems, • Repair and maintain PLC systems, including programming and troubleshooting, • Install, maintain, and repair hydraulic and pneumatic systems, • Read and interpret technical documents, including schematics, blueprints, and maintenance manuals, • Respond promptly to emergency maintenance requests, • Collaborate with production teams to minimize downtime and optimize equipment performance, • Maintain accurate maintenance records and documentation, • Adhere to all safety protocols and procedures, • Knowledge of electromechanical systems, including motors, drives, and control circuits, • Experience with hydraulic and pneumatic systems, • Familiarity with predictive and preventive maintenance techniques, • Ability to use various hand tools, power tools, and precision measuring instruments, • Excellent communication and teamwork abilities, • Ability to lift and move up to 50 pounds, • Capable of standing, walking, and climbing for extended periods, • Comfortable working in various environmental conditions (heat, cold, noise, etc.), • Competitive salary commensurate with experience, • Comprehensive benefits package including health, dental, and vision insurance, • 401(k) retirement plan with company match, • Ongoing training and professional development opportunities

Job DescriptionCompany Description At EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. How? Our global team of more than 7,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry. We are grounded in our cultural beliefs and serve more than 650 clients ranging from innovative biotech start-ups to established pharmaceutical companies. Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them. Our jobs, skills and talents are unique, but together we make an impact every day. Join us! Across our growing organization, we embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry. We believe our people make all the difference in cultivating an inclusive culture that embraces our cultural beliefs. We are deliberate and self-reflective about the kind of team and culture we are building. We look for team members that are not only strong in their own aptitudes but also who care deeply about EVERSANA, our people, clients and most importantly, the patients we serve. We are EVERSANA. Job Description The Cardiovascular Sales Representative will be a part of Milestone Pharmaceuticals new sales team provided by EVERSANA that will be launching a new therapy in the cardiovascular therapeutic space. The Cardiovascular Sales Representative will achieve territory sales goals by promoting Milestone Pharmaceuticals new therapy to physicians as well as other medical personnel within their assigned geography. The Representative will educate physicians and office staff on the use, characteristics, advantages, indications, and all other developments related to promoted product(s). The Representative will professionally represent Milestone Pharmaceuticals and EVERSANA in the field and ensure high levels of visibility and customer satisfaction in the territory. The Representative will maintain effective communication and relationships with key external and internal customers. This position is responsible for achieving both territory product sales goals and territory sales activity goals through company defined metrics. This position needs someone who is self-driven and has had a high record of personal and professional achievements. Often seen as a go-getter, inspirational, motivating — someone with initiative and drive, someone who's ambitious; someone who'd instead take the reins themselves than wait for things to get done. Someone highly motivated, proactive, and actively seeks opportunities to achieve goals, often going above and beyond their assigned tasks. EVERSANA Deployment Solutions offers our employees competitive compensation, fleet vehicle package, paid time off, company paid holidays, excellent training, employee development programs, 401K plan with an employer match, and an incredible list of comprehensive employer benefits that includes medical, dental, and vision insurance along with a whole host of other valuable programs. ESSENTIAL DUTIES AND RESPONSIBILITIES: Our employees are tasked with delivering excellent business results through the efforts of their teams. These results are achieved by: • Achieve territory product sales goals while adhering to ethical sales practices, compliance guidelines, and required promotional regulations, • Effectively promote and educate targeted physicians/HCPs on the use of product portfolio through one-on-one meetings and group presentations, company-approved promotional speaker programs, and other company-approved means., • Work 5 days in the field each week, supported by office time as needed for call planning, customer follow-up, preparing presentations, making appointments, report generation, etc., • Ensure high performance levels of call and field productivity., • Meet call plan expectations and achieve territory product sales goals while adhering to ethical sales practices, compliance guidelines, and required promotional regulations, • Execute company-approved product marketing plans and territory/regional business plan activities, • Support targeted customers using company-approved resources, sales materials, and promotional activities/programs/ initiatives as identified by sales management, • Ensure territory sales strategy execution using periodic territory business plan, regional business plan, and call activity reports, • Accurately report/submit sales call activities, territory expenses and written reports in a timely manner and within deadlines defined by leadership, • Attend all company-sponsored sales and medical meetings as directed by sales leadership, • Balance territory and regional work and projects while maintaining a solid level of sales performance, • Exhibit an acceptable level of skill in all competencies, • Demonstrate sales influence within territory, • Travel as needed throughout the territory (to include overnights) to see targeted HCPs as required by call plan Qualifications MINIMUM KNOWLEDGE, SKILLS AND ABILITIES: The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required. • Bachelor’s Degree or higher from an accredited College or University is required, • 2 + years of current related pharmaceutical/med device/diagnostics sales experience, • Cardiovascular experience preferred, • Ability to learn, comprehend and apply medical, scientific, and commercial information to drive increased product utilization among assigned customers, • Strong sales aptitude and selling related experience through education and/or work experience, • Documented record of sales success from previously held positions, • Solid communication, facilitation and presentation skills, • Proactive; can do approach, • Problem solving ability, • Solid motivational and persuasion skills, • Demonstrates team orientation, • Proficient in MS Office Suite, • Ability to travel (to include overnight) as required Additional Information OUR CULTURAL BELIEFS Patient Minded - I act with the patient’s best interest in mind. Client Delight - I own every client experience and its impact on results. Take Action - I am empowered and hold myself accountable. Grow Talent - I own my development and invest in the development of others. Win Together - I passionately connect with anyone, anywhere, anytime to achieve results. Communication Matters - I speak up to create transparent, thoughtful and timely dialogue. Embrace Diversity - I create an environment of awareness and respect. Our team is aware of recent fraudulent job offers in the market, misrepresenting EVERSANA. Recruitment fraud is a sophisticated scam commonly perpetrated through online services using fake websites, unsolicited e-mails, or even text messages claiming to be a legitimate company. Some of these scams request personal information and even payment for training or job application fees. Please know EVERSANA would never require personal information nor payment of any kind during the employment process. We respect the personal rights of all candidates looking to explore careers at EVERSANA. EVERSANA is committed to providing competitive salaries and benefits for all employees. If this job posting includes a base salary range, it represents the low and high end of the salary range for this position and is not applicable to locations outside of the U.S. Compensation will be determined based on relevant experience, other job-related qualifications/skills, and geographic location (to account for comparative cost of living). More information about EVERSANA’s benefits package can be found at eversana.com/careers. EVERSANA reserves the right to modify this base salary range and benefits at any time. From EVERSANA’s inception, Diversity, Equity & Inclusion have always been key to our success. We are an Equal Opportunity Employer, and our employees are people with different strengths, experiences, and backgrounds who share a passion for improving the lives of patients and leading innovation within the healthcare industry. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All of our employees’ points of view are key to our success, and inclusion is everyone's responsibility. Consistent with the Americans with Disabilities Act (ADA) and applicable state and local laws, it is the policy of EVERSANA to provide reasonable accommodation when requested by a qualified applicant or candidate with a disability, unless such accommodation would cause an undue hardship for EVERSANA. The policy regarding requests for reasonable accommodations applies to all aspects of the hiring process. If reasonable accommodation is needed to participate in the interview and hiring process, please contact us at . Follow us on LinkedIn | Twitter

Job DescriptionPharmaceutical Sales Representative (Specialty or Entry Level) Pharmaceutical Sales Rep - Job Description We are a healthcare industry specialty distributor serving the healthcare and medical supply markets. We are driven to meet the needs of healthcare professionals in several therapeutic areas. Our healthcare professional and physician customers benefit from a diverse group of products and services. Who are we looking for in our Pharmaceutical Sales Rep professionals? We are looking for healthcare and business-minded professionals, with successful sales track records who strive for organizational success, and seek career growth. What can you expect from a career with us as a Pharmaceutical Sales Representative? As a Pharmaceutical Sales Representative, you are responsible for driving profitable sales growth by developing, maintaining, and advancing accounts by regularly contacting medical offices, hospitals, and rehabilitation institutions within a defined territory. Pharmaceutical Sales Rep responsibilities include: • Providing healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers., • Consulting with physicians, nursing, phlebotomists as well as medical office staff to secure product orders for and increase product usage., • Sustaining or generating new or repeat orders for all products and programs., • Supplying necessary information to operate the overall business effectively by completing all required reports accurately, completely and in a timely fashion., • Other duties related to the positionOur Pharmaceutical Sales Rep - Job opening pre-requisites: What background and experience is needed to be one of our Pharmaceutical Sales Reps? The ideal candidate will possess some college and sales experience. A strong initiative with exceptional customer service, presentation, and communication skills is desired. Previous success attaining and exceeding sales goals is a plus. Proficiency in Microsoft Office Products (Word, Excel, Power Point, etc.) as well knowledge of contact management software is helpful.. List of other qualifications that our current Pharmaceutical Sales Reps have and what we are looking for. • Proven customer acumen and relationship building skills in a healthcare environment, • Experience interfacing with both internal team members and external customers as a part of a solution-based sales process, • Experience collaborating with, supporting and driving sales through sales channel partner organizations, • Attend all CME seminars and already have some pharmaceutical sales training or industry knowledge, • Strong written and verbal communication and clear thinking skills with the ability to synthesize complex issues into simple messages, • Solid process orientation, demonstrated resource management and allocation experience, and the ability to perform multiple tasks simultaneously ub9v5joUnL

Job Description Lead with Purpose. Deliver with Care. Join Potter’s House Apothecary and make every patient interaction count. Where exceptional service meets personalized medicine. Patient Care Team Manager – Pharmacy Operations Leadership Location: Peoria, AZ Company: Potter’s House Apothecary – PCAB Accredited Compounding Pharmacy Are you a proven retail pharmacy leader ready to take your career to the next level? Potter’s House Apothecary is seeking a Patient Care Team Manager to lead our front-end operations and deliver exceptional patient care – our number one priority. As a PCAB Accredited compounding pharmacy, we specialize in creating custom medications tailored to individual patient needs. We pride ourselves on compassion, humility, and respect, and we’re looking for a leader who shares these values while driving sales performance, customer satisfaction, and team retention. What You’ll Do • Lead and develop a high-performing Patient Care Team (Technicians, Coordinators, Associates)., • Ensure timely, accurate, and compassionate service for every patient and provider., • Drive productivity metrics, customer service outcomes, and retention goals., • Oversee scheduling, workflow, and process management., • Maintain compliance with USP standards and State Board regulations., • Resolve patient concerns quickly and professionally., • Collaborate with leadership to identify growth opportunities and optimize revenue. What We’re Looking For • Certified Pharmacy Technician License., • 5+ years of pharmacy management experience, preferably in retail or multi-site operations., • Proven ability to deliver on KPIs and lead teams to success., • Strong communication and leadership skills., • Commitment to ethical performance and patient-first care. Benefits & Perks • Competitive Salary + Performance-Based Incentives, • Health, Dental, and Vision Insurance, • Paid Time Off (PTO) & Holidays, • 401(k) Retirement Plan with Company Match, • Employee Discounts on Pharmacy Services, • Professional Development & Leadership Training, • Supportive, Mission-Driven Culture Focused on Patient Care Apply today and help us redefine pharmacy care – where patients come first, and results matter. Company DescriptionPotter’s House Apothecary is a PCAB Accredited compounding pharmacy specializing in Sterile and Non-Sterile Compounding. Compounding is the art of making custom made prescription medications specifically for an individual patient and their unique needs. Our desire is to provide optimal pharmaceutical care while demonstrating superior customer service through compassion, humility, and respect. By partnering with physicians in our community, we aim to enhance our patient’s treatment options and improve their results by customizing medications to meet their specific needs. Our Core Values: -\tCompassion – We care deeply about our patients and treat every interaction with empathy. -\tInnovation – We embrace creativity and new solutions to improve patient outcomes. -\tQuality Service – We deliver timely, accurate, and personalized care every time. -\tIntegrity – We uphold the highest ethical standards in all we do. -\tRespect – We value every patient, provider, and team member equally.Potter’s House Apothecary is a PCAB Accredited compounding pharmacy specializing in Sterile and Non-Sterile Compounding. Compounding is the art of making custom made prescription medications specifically for an individual patient and their unique needs. Our desire is to provide optimal pharmaceutical care while demonstrating superior customer service through compassion, humility, and respect. By partnering with physicians in our community, we aim to enhance our patient’s treatment options and improve their results by customizing medications to meet their specific needs.\n\nOur Core Values:\n•\tCompassion – We care deeply about our patients and treat every interaction with empathy.\n•\tInnovation – We embrace creativity and new solutions to improve patient outcomes.\n•\tQuality Service – We deliver timely, accurate, and personalized care every time.\n•\tIntegrity – We uphold the highest ethical standards in all we do.\n•\tRespect – We value every patient, provider, and team member equally.

Job Description TTF is recruiting for a Patient Access Representative to work at a well-respected hospital in the Ahwatukee area. This is a full-time position that is offering a rotating schedule, including weekends. Evening and night shifts available. Qualified candidates will have at least 1 year of experience working in a healthcare setting, be comfortable in a fast paced environment, provide excellent customer service, and be computer literate. For consideration, please send resumes to Tannia at TTF is a search and staffing company that partners with hospitals, physician groups, TPA's, medical management companies, pharmaceutical and pharmacy benefit plan organizations, surgery centers, DME/home health, consulting companies, and all other healthcare fields. We place candidates in the PFS field with the following specialties and titles: Hospital Collector, Commercial, Government, Managed Care, Billing Representative, Medical Biller, AHCCCS, Medicare, Medicaid, Medical Claims, Follow-Up Rep, Medical Collections Representative, Medical Collector, Medical Reimbursement Specialist, Patient Account Rep, Patient Financial Representative, Medical Scheduler, Reimbursement Representative, Reimbursement Specialist, Coding, Patient Access, Patient Admitting, and Claims Processing. Company DescriptionTTF is a recruiting firm that partners with companies nationwide to find the talent they need for success.TTF is a recruiting firm that partners with companies nationwide to find the talent they need for success.

Job Description Doctor of Pharmacy (PharmD) degree, active Pharmacist license, and minimum 1+ years Pharmacist experience required. Applicants who do not meet these qualifications will not be considered. An experienced pharmacist opportunity is available in San Carlos, AZ, to provide expert pharmaceutical services in a hospital and clinic setting. This contract position requires dedicated professionals with inpatient/ER pharmacy experience, offering a dynamic and impactful role. Position Details: • Location: San Carlos, AZ (with assignment in Peridot, AZ), • Job Type: Contract (13+ weeks), • Schedule: 4 days per week, 10-hour shifts, • Shifts: Variable (nights, days, swing, weekends), • Oversee daily pharmacy operations ensuring compliance with professional and regulatory standards, • Develop and monitor operational and financial metrics aligned with quality improvement systems, • Create and evaluate policies and procedures to optimize departmental functions, • Lead continuous process improvements and program effectiveness assessments, • Provide leadership and professional development opportunities to pharmacy staff, • Manage pharmacy information systems and dispensing operations for accuracy and efficiency, • Oversee purchasing and inventory management to ensure cost-effectiveness and availability, • Prepare comprehensive reports identifying operational progress and areas for improvement, • Bachelors degree in Pharmacy required; PharmD preferred with at least one year of residency, • Minimum of five years of professional pharmacy experience, including two years in a managerial role, • Current, unrestricted pharmacy license; Arizona license preferred, • BLS certification required within 30 days of hire; ACLS and PALS preferred (PALS training available on-site)

Job DescriptionCompany Overview Before we opened Strive Pharmacy we were unsatisfied with the current state of the pharmaceutical industry. Most of the current pharmaceuticals only offer a one size fits all approach and often come with unwanted and potentially dangerous side effects. We found that through compounding we can offer a much more personalized solution to medicine. Through this we have been able to help patients get the results they are seeking for their personal needs. After years of working for corporate chains we took the risk and opened Strive Pharmacy. We are dedicated to providing a better experience for each customer and clinic that we work with. Come see the Strive difference. Our Mission We're flipping the script with personal medicine. We strive to interrupt an industry that has been closed to personalized care, accessibility, and nuance for too long. We strive to shift a reactive view of self-care and ignite a proactive baseline-shifting approach to health for all. 'The human element' is our crux and catalyst, driving all that we do, whether we're interacting with patients, providers, or practices. We're here to partner with those ready for a change. More than a compounding pharmacy, we're on a mission to positively disrupt healthcare as we know it. Strive is about more than medicine. Strive is about striving for the personal side of healthcare. Position: Full Time, Salaried Salary: $90000-$105000 Location: USA based Remote - Preference in Mesa, AZ area or Fenton, MO area. Our ideal candidate will be able to work in office periodically in either of these locations This position is not eligible for any type of employment or visa sponsorship. Job Summary: As a Talent Acquisition Manager, you will play a pivotal role in flipping the script of recruitment strategy and processes to attract top talent to Strive. You will collaborate closely with hiring managers and stakeholders to drive hires that reflect the excitement of Strive's mission, develop sourcing strategies, and execute recruitment plans to ensure the acquisition of the best-in-class talent to continue to Strive for more. Key Responsibilities: • Strategic Recruitment Planning: Work closely with hiring managers to understand current and future staffing needs, align recruitment strategies with business objectives, and develop comprehensive hiring plans., • Candidate Sourcing: Utilize a variety of sourcing methods, including online channels, networking, social media, referrals, and direct sourcing, to attract qualified candidates for open positions., • Candidate Assessment and Selection: Screen resumes, conduct initial interviews, and evaluate candidates to determine their fit for specific roles and organizational culture. Coordinate and facilitate interview processes, including scheduling, feedback collection, and offer negotiation., • Employer Branding: Represent the company professionally and effectively communicate its values, culture, and opportunities to prospective candidates. Develop and maintain strong employer branding initiatives to attract top talent., • Talent Pipeline Management: Proactively build and maintain a pipeline of qualified candidates for current and future hiring needs. Implement talent acquisition best practices to ensure a consistent and efficient recruitment process., • Data Analysis and Reporting: Track recruitment metrics and analyze data to measure the effectiveness of sourcing strategies, identify areas for improvement, and provide regular reporting to stakeholders., • Collaboration and Relationship Management: Foster strong partnerships with hiring managers, department heads, and cross-functional teams to ensure alignment on recruitment priorities, timelines, and objectives., • 5 years + proven experience in talent acquisition or recruitment, preferably in a fast-paced manufacturing environment., • Strong understanding of recruitment best practices, sourcing techniques, and candidate assessment methods., • Excellent communication and interpersonal skills, with the ability to build rapport and influence stakeholders at all levels., • Demonstrated ability to manage multiple priorities and deliver results in a deadline-driven environment., • Proficiency in applicant tracking systems, specifically Workday and Greenhouse., • Commitment to upholding ethical standards, confidentiality, and professionalism in all aspects of recruitment., • Experience with Pharmaceutical hiring, • Experience with high volume req loads; consistently between 20-25 active reqs, • Experience with high volume hiring in a regulated manufacturing environment Disclaimer*** Please do not call the pharmacy location with questions about your application or interview. A talent acquisition partner will reach out to you.

Job Description United Integrated Services (USA) Corp. was founded in Phoenix, Arizona in 2020. UIS is a U.S. subsidiary of United Integrated Services Co., Ltd. (UIS Taiwan) which was founded in Taiwan in 1982. UIS is a multidisciplinary engineering and construction company. We provide fully integrated design-build services to our clients in the high-technology industry for their manufacturing facility needs. Our scope of services includes engineering design, high-tech factory planning, and on-time equipment and material delivery in which clean-room systems, HVAC, electrical systems, and tool hook-up, are all vital parts in need of total coordination. Summary: The QA/QC Inspector is responsible for conducting field inspections of various systems in industrial construction project, ensuring compliance with local, state, and federal codes. This role involves reviewing building plans, identifying non-compliance issues, documenting inspection results, and collaborating with contractors and city officials to uphold safety and quality standards. This is a full time onsite position located in North Phoenix, AZ (85027). Essential Duties and Responsibilities include the following. Other duties may be assigned. * • Perform daily inspections for electrical installations, including conduit, cable tray, wire pulls, terminations, grounding/bonding, equipment installation, lighting, PDUs, panels, switchgear, and MCCs. • Verify compliance with NEC 2017, IBC/IFC, IMC/IPC (as applicable), ASHRAE, TSMC standards, and local amendments., • Confirm conductor types, sizes, tags, routing, and proper labeling are installed per drawings and project specifications., • Inspect grounding/bonding systems per NEC Article 250 and project requirements., • Inspect medium-voltage and low-voltage systems for correct installation practices., • Review torque logs, insulation resistance tests, megger results, and equipment functional tests. Fire Alarm Systems • Inspect installation of fire alarm devices, including pull stations, smoke detectors, heat detectors, beam detectors, duct detectors, horns/strobes, and tamper/flow switches., • Verify that wiring, junction boxes, device mounting, and labeling comply with NFPA 72, NFPA 70, and project specifications., • Witness and document fire alarm testing, including:, • Device testing and mapping, • Network communication tests, • Power transfer testing (primary/secondary), • Acceptance testing with Fire Department and AHJ, • Ensure fire alarm pathways are installed per code (Class A/Class B circuits). Low-Voltage Systems • Inspect and verify low-voltage installations such as:, • Data, telecom, fiber optics, • Access control, • Security systems, • Paging and mass notification, • Review cable routes, separation requirements, and labeling per project drawings and standards., • Inspect cable testing results (OTDR, continuity, performance testing). Documentation & Reporting • Prepare daily inspection reports with photos, comments, and status details., • Issue Non-Conformance Reports (NCRs) and track corrective actions., • Maintain up-to-date logs for inspections, deficiencies, re-inspections, and turnover packages., • Review contractor QAQC documentation, including checklists, test reports, as-built drawings, redlines, and equipment submittals., • Support creation and maintenance of Quality Turnover Packages (QTPs). Coordination & Communication • Work closely with field crews, superintendents, subcontractors, and engineers., • Coordinate inspections with City of Phoenix inspectors and third-party special inspectors., • Attend daily coordination meetings and integrate QAQC updates into trackers., • Support commissioning teams for electrical, fire alarm, and low-voltage systems. Safety & Compliance • Enforce electrical safety requirements (LOTO, arc flash, PPE, energized work rules)., • Identify and report unsafe practices or conditions., • Ensure all work complies with TSMC safety policies and industrial cleanroom standards. Job Requirements Education & Experience • Minimum 3–5 years of experience as an Electrical QAQC Inspector, Electrician, or Electrical Field Engineer., • Experience on large industrial, semiconductor, pharmaceutical, or mission-critical projects preferred., • Experience with fire alarm and low-voltage systems required., • Strong understanding of NEC, NFPA 72, NFPA 70, IPC/IMC, and related codes., • Prior experience working with City of Phoenix or similar AHJ is a plus. Certifications (Preferred but Not Required) • OSHA 30, • NICET Level I–III (Fire Alarm Systems), • Journeyman or Master Electrician license, • ASNT Level II (Visual) – optional, • NFPA Fire Alarm Certification, • BICSI Technician / Installer for low-voltage systems, • CPR/First Aid Technical Skills • Ability to read and interpret construction drawings, one-lines, riser diagrams, and specifications., • Familiar with Smartsheet, BIM 360 / ACC, Bluebeam, Procore, Smartsheet's, Viewpoint, or similar platforms., • Knowledge of commissioning processes (FAT/SAT, integrated systems testing)., • Strong documentation, photo capture, and reporting skills. Physical Requirements • Ability to walk large industrial sites daily., • Ability to climb ladders, access elevated work areas, and navigate construction zones., • Ability to lift up to 40 lbs. occasionally. Soft Skills • Strong attention to detail., • Clear and concise communication., • Problem-solving mindset with the ability to identify root causes., • Ability to work independently and in coordination with teams., • High level of professionalism representing the GC to owner and inspectors. Additional Project-Specific Requirements • Ability to work in cleanroom or sub-fab environments., • Willingness to work extended hours or weekends when required for testing or inspections., • Must pass background checks, safety orientations, and site-specific training. UIS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status. Or any other characteristic protected by federal, state, or local law. We believe in fostering a diverse and inclusive workplace where all individuals are treated with respect and dignity. Disclaimer: The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties as assigned by their supervisor. Physical Demands & Work Environment This position requires the ability to lift and carry up to 50 lbs for transporting documents, equipment, and other materials as needed. The role involves extended periods standing, walking and/or of sitting while working at a computer. Frequent movement between the construction trailer and various areas of the construction site is necessary. The position is based at the construction job site (trailer office). Even though the exposure of hazardous work conditions would be minimal, the employee may be required to visit the work area of the jobsite and thus be exposed to some typical work hazards that may be present on a construction site, such as dust, moving machineries, weather, caustic chemicals, noise etc. UIS would provide the required safety protection to ensure the safety of UIS employees and comply with all OSHA standards. Equal Employment Opportunity: UIS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status. Or any other characteristic protected by federal, state, or local law. We believe in fostering a diverse and inclusive workplace where all individuals are treated with respect and dignity. Disclaimer: The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties as assigned by their supervisor.

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. Job Purpose: Track, prepare, and account for all investigational products. Act as a resource for study teams by utilizingpharmacological expertise and knowledge of pharmacy practice.Essential Functions: • Responsible for staff management in accordance with the organization's policies and applicable laws., • Responsibilities include interviewing, hiring, and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems; development and coaching of employees, • Knowledge of relevant United States Pharmacopeia guidelines, including chapters 795, 797, 800, 1163, and 1168 as well as the FDA Guidance for Industry CGMP for Phase 1 Investigational Drugs required., • Responsible in conjunction with the Designated Person for ensuring compounding suites are maintained and certified on an ongoing basis., • Management of pharmacy schedule and assignment of studies., • Responsible for receipt, storage, preparation, disposition, and retention of all study drug products in compliance with standard operating procedures, EU, FDA, and DEA regulations (as applicable) concerning investigational product handling, accountability and security. Review and understand study protocol requirements in regard to investigational product handling. Preparation of study specific pharmacy manuals for any type of compounding studies., • Overall responsibility for pharmacy operations., • Active member of study team providing expertise and support such as evaluating study feasibility, study set up and conduct, participating in internal and/or external client meetings. Provide internal and/or external client communication and interaction regarding investigational product handling and protocol specific requirements., • Ensure EU, Controlled Drug, and DEA license (if applicable) is current and all federal and state laws pertaining to prescription medications are being followed. Interact with all applicable regulatory agencies, as necessary, regarding investigational product and investigational product supply handling., • Track and maintain appropriate pharmacy metrics as necessary, including retention follow up/invoicing., • Track and manage pharmacy expenses including supplies, fees, contractors, and payroll., • Provide training and monitoring for administration of investigational products as needed., • Develop and review standard operating procedures and procedure guides pertaining to pharmacy and including pharmacy training as necessary., • Maintain pharmacy department equipment and applicable records as necessary in conjunction with the lead pharmacy technician., • Document and report any and all pharmacy deviations and implement process improvement changes as applicable., • Institutional Review Board consultant and resource., • Assist with special projects as needed., • Active member in the clinic leadership team and attending management meetings as necessary.Knowledge/Skills/Education/Licenses, • Registered Pharmacist required, • Doctor of Pharmacy preferred but not required, • Proven pharmaceutical experience of minimum 1-2 years, • Proven record keeping skills with extreme attention to detail, • Knowledge of United States Pharmacopeia guidelines, including chapters 795, 797, 800, 1163, and 1168 as well as the FDA Guidance for Industry CGMP for Phase 1 Investigational Drugs required., • Completion of media bi-annual media fill and fingertip testing (as applicable per site), • Knowledge of FDA and EU regulations preferred (if appropriate)

Global Oncology Marketing Intern.Join a Legacy of Innovation 125 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our worl

Senior Pharmaceutical Sales Specialist For R&I Primary Care Team. As a Senior Pharmaceutical Sales Specialist for R&I Primary Care Team, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives!. Knowledge of the medical, healthcare o

Job Description A dynamic opportunity is available for a licensed pharmacist with experience in pharmacy operations, prescription management, and mail order pharmacy services. This role is based in Mesa, AZ and offers a contract-to-hire arrangement, providing a pathway to permanent employment with competitive benefits. Key Responsibilities: • Supervise pharmacy technicians in compounding preparations, filling and labeling prescriptions, and prepackaging bulk medications., • Communicate effectively to clarify prescriptions and refill authorizations, perform final prescription checks, and oversee sterile and non-sterile compounding., • Ensure compliance with USP guidelines, Board of Pharmacy regulations, and maintain high standards for accuracy, potency, and pharmaceutical quality., • Current Arizona State Pharmacist license in good standing is mandatory., • Solid knowledge of pharmacy principles, laws, regulations, and pharmacy practice standards., • Experience with non-sterile and sterile compounding including capsules, oral liquids, injectables, topical medications, and other preparations., • Detail-oriented mindset with strong analytical, communication, and interpersonal skills. If you are a licensed pharmacist in Arizona ready to take on a challenging role with a reputable organization, apply now to explore this rewarding career path.

Job Description A full-time Lab Pharmacist opportunity is available with a contract-to-hire arrangement in Chandler, AZ. The position offers a Monday through Friday schedule from 1:30 pm to 10:00 pm. Upon conversion to permanent status, the company provides benefits including 401(k), paid time off, and more. Key Responsibilities: • Supervise pharmacy technicians in compounding, filling, labeling prescriptions, and prepackaging bulk medications., • Clarify prescriptions and refill authorizations, finalize prescription checks, and oversee compounding processes., • Ensure all preparations meet standards for accuracy, pharmaceutical quality, and potency., • Comply with USP guidelines, Board of Pharmacy rules, and relevant regulations., • Current Arizona Pharmacist license in good standing., • Knowledge of both sterile and non-sterile compounding techniques, including capsules, oral liquids, injectables, topical medications, nasal preparations, suppositories, and related forms., • Strong attention to detail and analytical abilities., • Excellent communication and interpersonal skills. This contract-to-hire position offers a competitive rate up to $65 per hour. If you are a skilled pharmacist ready to contribute your expertise in a dynamic environment, consider applying for this opportunity today.

Job Description A full-time Lab Pharmacist position is available in Chandler, AZ, offering a contract-to-hire opportunity. This role involves supervising pharmacy technicians in compounding, filling, and labeling prescriptions, ensuring accuracy and compliance with USP standards and Board of Pharmacy regulations. The position requires exceptional attention to detail and strong communication skills. Responsibilities: • Supervise pharmacy technicians during compounding, filling, and labeling processes, • Clarify prescriptions or refill authorizations and perform final prescription checks, • Ensure adherence to pharmaceutical standards for accuracy and potency, • Follow USP guidelines and relevant pharmacy laws and regulations, • Current Arizona pharmacist license in good standing is required, • Knowledge of non-sterile and sterile compounding, including capsules, injectables, topical medications, and other preparations, • Strong analytical, communication, and interpersonal skills, • Familiarity with pharmacy regulations, laws, policies, and procedures, • Monday through Friday Qualified Arizona-licensed pharmacists with a passion for pharmaceutical excellence are encouraged to apply for this opportunity to contribute to a dynamic pharmacy setting. Take the next step in your pharmacy career by applying today.

Strategic Sourcing & Procurement Role. This position will report to the Strategic Sourcing & Procurement leader and will maintain strong alignment to the pharmaceutical operations network strategy and initiatives.

Job Description Blending Operator - Food & Nutraceutical Manufacturing Position Summary We're seeking an experienced Blending Room Operator to join our solid dose manufacturing team. In this role, you'll operate ergonomic and modern blending and processing equipment in our climate-controlled, GMP-certified facility. This position offers competitive compensation, comprehensive benefits, and opportunities for career advancement in solid-dose manufacturing. What You'll Do • Operate ergonomic and modern blending/ processing equipment including IBC mixers, mills, and material handling systems in a GMP and cross-contamination environment and control systems, • Process pharmaceutical-grade powder ingredients following strict GMP protocols, • Execute granulation, milling, and sifting operations for premium quality supplements, • Maintain detailed batch records and ensure compliance with FDA regulations, • High school diploma or equivalent, • 2+ years experience in food, pharmaceutical, or supplement manufacturing, • Understanding of GMP requirements and FDA regulations, • Physical ability to lift 50 pounds and stand for extended periods, • Competitive salary and comprehensive benefits package, • Modern, climate-controlled work environment, • Professional development opportunities, • Stable company with 60+ year history, • Make a difference in consumer health and wellnessCompany DescriptionMarlyn Nutraceuticals is a trusted leader in the dietary supplement industry with over 60 years of dedication to quality, innovation, and sustainability. We leverage a science-based approach to enhance lives through natural wellness solutions. Join our passionate team and contribute to our mission of improving health and well-being. Marlyn offers you not only an opportunity to work for a company that is dedicated to the environment and its people, but also offers competitive salaries and comprehensive benefit packages. We offer paid holidays, vacation, and sick time, a 401(k) retirement plan with company match as well as gift cards and luncheons/parties before major holidays. A wide range of benefit choices includes options for medical, dental, vision, life, short and long-term disability insurance plans, legal plans and pet insurance. Marlyn Nutraceuticals is an equal opportunity employer. We are committed to equality for everyone, regardless of age, sex, sexual orientation, race, color, creed, religion, ethnicity, national origin, disability, military or veteran status, or any other legally recognized protected basis under federal, state, or local laws.Marlyn Nutraceuticals is a trusted leader in the dietary supplement industry with over 60 years of dedication to quality, innovation, and sustainability. We leverage a science-based approach to enhance lives through natural wellness solutions. Join our passionate team and contribute to our mission of improving health and well-being.\r\n\r\nMarlyn offers you not only an opportunity to work for a company that is dedicated to the environment and its people, but also offers competitive salaries and comprehensive benefit packages. We offer paid holidays, vacation, and sick time, a 401(k) retirement plan with company match as well as gift cards and luncheons/parties before major holidays. A wide range of benefit choices includes options for medical, dental, vision, life, short and long-term disability insurance plans, legal plans and pet insurance.\r\n\r\nMarlyn Nutraceuticals is an equal opportunity employer. We are committed to equality for everyone, regardless of age, sex, sexual orientation, race, color, creed, religion, ethnicity, national origin, disability, military or veteran status, or any other legally recognized protected basis under federal, state, or local laws.

Job Description Tablet Machine Operator, GMP Manufacturing Shape the Future of Wellness Manufacturing Our Mission: For over 60 years, Marlyn Nutraceuticals has been a respected independent Contract Development and Manufacturing Organization (CDMO) specializing in complex solid dose dietary supplements. We partner with leading supplement brand owners, major pharmacy chains, Fortune 500 pharmaceutical companies, and specialized healthcare organizations to transform sensitive natural ingredients into high-quality consumer products. What Sets Us Apart: We don't just manufacture solid dose tablets, 2-piece capsules, and functional powdered supplement products —we're innovation leaders in solvent-free dry granulation, advanced taste masking technologies, and temperature-controlled processing of nature-derived herbals and botanicals. Our state-of-the-art facility features specialized IBC (Intermediate Bulk Container) systems to minimize cross-contamination while preserving the potency of delicate natural compounds that degrade easily under standard manufacturing conditions. Our Impact: From early-stage formulation development through commercial-scale production, we ensure millions of consumers receive consistent, bioavailable dietary supplements that genuinely improve their daily wellness. Every tablet we release are made according to GMP-grade standards while maintaining the integrity of natural active compounds. Why This Matters: In an industry where up to 70% of natural ingredient potency is typically lost during conventional processing, our specialized expertise in solvent free granulation, dehumidified environments, and sensitive material handling allows us to deliver products that retain their natural wellness value—making us the trusted choice for companies whose reputations depend on product efficacy. The Impact You'll Make: As our Tablet Machine Operator, you'll be the quality guardian for our modern solid dose process equipment, operating advanced equipment including Korsch XL 400 and Kilian KTP 420/590 rotary tablet equipment according to GMP standards. Your precision and expertise directly ensure that every processed and finished product meets FDA's current cGMP regulation to ensure safety and quality. What Success Looks Like: • Quality Leadership: Maintain 99.5%+ specification compliance while setting-up, dialing-in, and operating tablet press and auxiliary equipment, • Process Optimization: Identify and implement efficiency improvements that reduce waste, increase throughput, and quality, • Technical Mastery: Troubleshoot complex mechanical issues independently, minimizing costly production delays, • 3+ years hands-on experience with high-speed rotary tablet presses (Korsch, Kilian, or equivalent), • Demonstrated mechanical troubleshooting abilities with tablet press turrets, punch guide damage, die pockets and keyways wear and tear issues, verify punch alignment, and turrets for punch guide damage, die pockets and keyways for wear, and verify punch alignment settings, • Knowledge of hydraulic and pneumatic systems, gear trains, cam mechanism, and servo-driven components that control compression forces and production yields, • You prefer routine, predictable work environments, • You're uncomfortable with strict quality documentation requirements, • You can't maintain focus during long production runs, • Competitive Pay: Based on experience, plus year-end performance bonus, • Advanced Solid Dose Equipment**: Work with industry-leading solid dose equipment and technology, • Career Growth: Clear advancement paths to Lead Operator and Supervisor roles, • Respectable Clients: Make supplements available nationwide and internationally, • Comprehensive Benefits: Medical, dental, 401k matching, and paid training, • Location: Close To Phoenix Sky Harbor Airport, • Schedule: M-F day shiftCompany DescriptionMarlyn Nutraceuticals is a trusted leader in the dietary supplement industry with over 60 years of dedication to quality, innovation, and sustainability. We leverage a science-based approach to enhance lives through natural wellness solutions. Join our passionate team and contribute to our mission of improving health and well-being. Marlyn offers you not only an opportunity to work for a company that is dedicated to the environment and its people, but also offers competitive salaries and comprehensive benefit packages. We offer paid holidays, vacation, and sick time, a 401(k) retirement plan with company match as well as gift cards and luncheons/parties before major holidays. A wide range of benefit choices includes options for medical, dental, vision, life, short and long-term disability insurance plans, legal plans and pet insurance. Marlyn Nutraceuticals is an equal opportunity employer. We are committed to equality for everyone, regardless of age, sex, sexual orientation, race, color, creed, religion, ethnicity, national origin, disability, military or veteran status, or any other legally recognized protected basis under federal, state, or local laws.Marlyn Nutraceuticals is a trusted leader in the dietary supplement industry with over 60 years of dedication to quality, innovation, and sustainability. We leverage a science-based approach to enhance lives through natural wellness solutions. Join our passionate team and contribute to our mission of improving health and well-being.\r\n\r\nMarlyn offers you not only an opportunity to work for a company that is dedicated to the environment and its people, but also offers competitive salaries and comprehensive benefit packages. We offer paid holidays, vacation, and sick time, a 401(k) retirement plan with company match as well as gift cards and luncheons/parties before major holidays. A wide range of benefit choices includes options for medical, dental, vision, life, short and long-term disability insurance plans, legal plans and pet insurance.\r\n\r\nMarlyn Nutraceuticals is an equal opportunity employer. We are committed to equality for everyone, regardless of age, sex, sexual orientation, race, color, creed, religion, ethnicity, national origin, disability, military or veteran status, or any other legally recognized protected basis under federal, state, or local laws.

Job DescriptionCompany Overview Before we opened Strive Pharmacy we were unsatisfied with the current state of the pharmaceutical industry. Most of the current pharmaceuticals only offer a one size fits all approach and often come with unwanted and potentially dangerous side effects. We found that through compounding we can offer a much more personalized solution to medicine. Through this we have been able to help patients get the results they are seeking for their personal needs. After years of working for corporate chains we took the risk and opened Strive Pharmacy. We are dedicated to providing a better experience for each customer and clinic that we work with. Come see the Strive difference. Our Mission We're flipping the script with personal medicine. We strive to interrupt an industry that has been closed to personalized care, accessibility, and nuance for too long. We strive to shift a reactive view of self-care and ignite a proactive baseline-shifting approach to health for all. 'The human element' is our crux and catalyst, driving all that we do, whether we're interacting with patients, providers, or practices. We're here to partner with those ready for a change. More than a compounding pharmacy, we're on a mission to positively disrupt healthcare as we know it. Strive is about more than medicine. Strive is about striving for the personal side of healthcare. Position Overview: The Vice President of Quality is a strategic and operational executive responsible for leading the design, implementation, and continuous improvement of the organization's Quality strategy and systems. This leader will ensure that products, processes, and facilities meet the highest standards of quality, safety, compliance, and customer trust. The VP of Quality oversees Quality Assurance, Quality Control, Quality Improvement, Validation, Document Control, and training functions, partnering closely with Operations, Supply Chain, and Enterprise teams to drive business excellence. Location: Remote Salary Range: $180,000 - $200,000 + Bonus Opportunity Key Responsibilities: Strategic Leadership * Develop and lead a comprehensive Quality strategy aligned with organizational priorities and growth objectives. * Build and scale world-class Quality Management Systems (QMS) that support operational reliability, regulatory excellence, and continuous improvement. * Act as a key advisor to the Executive team on quality related risk, compliance health, and improvement opportunities. * Champion a culture of quality, accountability, and proactive problem-solving across all levels of the organization. * Execution & Delivery Compliance & Regulatory * Ensure full compliance with applicable regulations such as FDA, cGMP, 21 CFR, USP, ISO standards, state board regulations, and other governing bodies relevant to the business. * Lead preparation for and responses to regulatory inspections, customer audits, and certification activities. * Oversee internal audit programs, CAPA management, risk assessments, product release processes, and validation activities. Operational Quality Management * Lead Quality Assurance, Quality Control, training, and documentation teams to achieve performance, throughput, and reliability expectations. * Establish and track Quality KPIs and dashboards (such as, complaint trends, deviation rates, batch failure rates, inspection outcomes). * Collaborate with Operations and Supply Chain to drive defect reduction, process optimization, and preventive quality initiatives. * Oversee product recall processes, quality incident investigations, root-cause analysis, and corrective actions. Organizational Leadership * Develop talent, build bench strength, and create scalable organizational structures that support rapid growth. * Manage budgets, staffing plans, and resource allocation across the Quality organization. * Inspire and mentor teams, driving an environment of trust, integrity, performance, and accountability. Qualifications: * Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, Chemistry, Biology, or related field. * 15+ years of progressively responsible Quality leadership experience. * Demonstrated success scaling Quality systems in a highly regulated environment. * Deep expertise in cGMP, FDA regulations, ISO or equivalent industry standards. * Proven track record leading audit readiness, compliance, and continuous improvement programs. * Executive presence with strong communication, influence, and stakeholder alignment capability. Preferred Qualifications: * Master's degree, MBA, or PharmD. * Experience in pharmaceutical manufacturing, medical devices, biologics, or sterile compounding. * Experience with digital QMS systems, Lean, Six Sigma, or operational excellence methodologies. * Background leading multi-site, multi-state, or high-growth operations. Annual Salary$180,000—$200,000 USDBenefits/ Perks Strive Pharmacy provides a comprehensive benefits package that encompasses various perks such as employer paid healthcare coverage available after 30 days of employment, the choice of an FSA/HSA, a voucher for new hire scrubs (if applicable), parental leave, a 401(k) plan with matching contributions, and the benefit of weekends and holidays off. FREE COMPOUNDED MEDS to employees and immediate family members. Culture At Strive, culture plays a fundamental role in shaping our workplace atmosphere. Beyond our exceptional benefits package, we foster a sense of community. Throughout the year, we arrange various holiday potlucks and festive celebrations. Strive is committed to promoting both personal and professional development, striving for our employees to excel and grow in every aspect of their lives, both within and outside of the workplace. EEO Strive Pharmacy is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristics as outlined by federal, state or local laws. Disclaimer*** Please do not call the pharmacy location with questions about your application or interview. A talent acquisition partner will reach out to you.