Company Overview:
Strive Pharmacy is a personalized compounding pharmacy built on a simple conviction: medicine should fit the patient, not the other way around. We started Strive because we believed the pharmaceutical industry was overdue for a more human approach—one that prioritizes individualized care, clinical nuance, and genuine partnership with patients and providers.
Compounding gives us the tools to do that. Every formulation we prepare is built to the specific needs of a specific person, and every interaction we have is guided by that same commitment to personalized care.
We're growing, and we're looking for people who share that conviction. If you're ready to be part of a pharmacy that takes the work seriously and the people even more seriously, we'd like to meet you.
Mission:
Strive exists to disrupt an industry long overdue for a more personal approach to care. We put the human element at the center of everything: every formulation, every patient interaction, every provider partnership. We're not just a compounding pharmacy. We're a team on a mission to change what personalized healthcare looks and feels like.
Location: Tampa, Florida
Position Type: Full Time
Schedule: 1st Shift; 8am - 4pm
Compensation Range: $80,000 - $90,000
Position Summary:
The Quality Assurance (QA) Manager provides site-specific quality oversight and ensures full compliance with Strive Pharmacy’s Standard Operating Procedures (SOPs), specifications, and applicable state and federal regulatory standards. Reporting to the National Quality Assurance Manager, this position leads and manages the QA function at the assigned pharmacy location. Responsibilities include documentation review, label control, investigations, change control, audits, and product release. Additionally, the QA Manager supports continuous improvement initiatives and serves as the primary on-site liaison between pharmacy operations, compounding, and corporate Quality leadership.
Key Responsibilities:- Team Leadership & Development: Supervise the site QA team by managing workloads, timecards, performance reviews, and discipline. Lead candidate interviews, oversee onboarding and competency training, and conduct routine team meetings and cross-department huddles.
- Documentation & Compliance Review: Conduct regular audits of compounding, production, cleaning, and validation records (including media fills and BMS/temperature alarms) to ensure absolute accuracy and compliance with GDP and USP <795>/<797>/<800>/<1163> standards. Approve equipment calibration and preventive maintenance records.
- Material & Label Control: Verify and reconcile all physical and electronic labeling to maintain strict accountability. Review supplier qualification records to ensure materials are sourced exclusively from approved, compliant vendors.
- Quality Systems & Event Management: Triage customer complaints and coordinate with corporate QA to report adverse drug events. Review and approve deviations, non-conformances, Corrective and Preventive Action (CAPA), and change controls, partnering with QA Specialists to investigate non-compliance events and manage third-party testing.
- Auditing & Metrics Reporting: Lead external regulatory, partner, or client audits in collaboration with the Pharmacist-in-Charge (PIC), and conduct regular internal compliance audits. Track and report weekly site quality metrics and trend data directly to the Director of Quality.
- Site Authority: Authorized to approve or reject compounded products, raw materials, and components based on testing results. Fully authorized to pause or halt pharmacy operations when immediate quality, safety, or compliance risks are identified.
- Education & Experience: High School Diploma or GED with a minimum of five (5) years of experience in a quality or manufacturing role within a pharmaceutical, medical device, or allied health science environment.
- Technical Expertise: Proven experience in aseptic operations and regulated environments , alongside strong knowledge of QA practices (deviation management, CAPA, change control, and documentation review)
- Core Skills: Proficiency with Microsoft Office Suite and quality management systems (QMS) , paired with strong data analysis, trend identification, organizational, and problem-solving skills.
- Physical & Environmental: Ability to stand, sit, or walk for extended periods, and occasionally lift up to 45 pounds. Must be able to work in controlled cleanroom environments, wear required protective attire, and tolerate controlled temperatures and background noise.
- Advanced Education: Associate’s or higher degree in Biology, Microbiology, Chemistry, or Pharmacy.
- Industry Leadership: Prior experience leading a QA team within a compounding or manufacturing environment.
- Regulatory Knowledge: Deep familiarity with 503A/503B compounding regulations, USP <795>/<797>/<800>, and FDA 21 CFR 210/211.
- Audit Experience: Direct experience participating in or leading regulatory or partner audits.
Work Environment: This position is primarily based in an onsite work environment. The role requires regular periods of sitting, standing, and computer use, with occasional lifting as needed. Reasonable accommodations may be made for individuals with disabilities.
Core Competencies
- Accountability: Takes ownership of site quality performance and compliance outcomes.
- Attention to Detail: Maintains exceptional accuracy in documentation and review activities.
- Leadership: Guides and develops QA personnel to uphold Strive’s culture of quality and excellence.
- Decision-Making: Exercises sound judgment in product release and quality escalation.
- Communication: Effectively collaborates across teams and with corporate leadership.
- Continuous Improvement: Proactively identifies opportunities to enhance quality systems and reduce risk.
Join Us in Making an Impact:
At Strive, the work is real and the impact is direct. Every role here contributes to a patient experience that's more personal, more attentive, and more human than what most people have come to expect from a pharmacy. Apply today and help us raise the bar.
Benefits/ Perks:
Strive Pharmacy offers a comprehensive benefits package, including:
- Employer-paid healthcare coverage, effective the 1st day of the following month of your hire date
- Free Strive compounded medications for employees based on a valid patient-specific prescription from a licensed healthcare provider
- Paid time off
- Sick time
- FSA and HSA options
- Parental leave
- 401(k) with employer matching
- Life insurance
- Vision and dental insurance
- Veterinary insurance
Culture:
Culture isn't an afterthought at Strive. It's something we actively build. At our Gilbert, Arizona location, that looks like Food Truck Fridays and Casual Fridays. Company-wide, we also celebrate throughout the year with holiday potlucks and seasonal gatherings. We're committed to supporting the personal and professional growth of every employee, inside and outside 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.
Skills Required
- High School Diploma or GED with a minimum of five (5) years in a quality or manufacturing role within pharmaceutical, medical device, or allied health.
- Proven experience in aseptic operations and regulated environments.
- Strong knowledge of QA practices: deviation management, CAPA, change control, and documentation review.
- Proficiency with Microsoft Office Suite and quality management systems (QMS).
- Ability to work in controlled cleanroom environments and occasionally lift up to 45 pounds.
- Associate's degree or higher in Biology, Microbiology, Chemistry, or Pharmacy.
- Prior experience leading a QA team within a compounding or manufacturing environment.
- Familiarity with 503A/503B compounding regulations, USP <795>/<797>/<800>, and FDA 21 CFR 210/211.
- Direct experience participating in or leading regulatory or partner audits.
What We Do
At Strive Compounding Pharmacy, we’re pioneering a movement in personalized medicine. Ditching the one-size-fits-all approach, we specialize in customizing medications to fit the unique health conditions and wellness goals of each individual. Our commitment to 'whole-person health' is evident in our comprehensive services ranging from hormone replacement and weight management to dermatology and veterinary care. As a rapidly growing company, we pride ourselves on our robust company culture, strong partnerships with healthcare providers, and the effectiveness, safety, and benefits of our compounded drugs. Our pursuit of uncompromised excellence in compounding, coupled with a proactive approach to healthcare, sets us apart in creating healthier and happier lives, while also educating the world on the crucial role that compound pharmacies play within a healthy society.
