Quality Assurance Supervisor (Weekend/Day Shift)

We need to output HTML fragment with sections: h3 for headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. We must not repeat job title as heading. No Job ID etc. Remove boilerplate: Company Overview, Mission, Location, Position Type, Schedule, Compensation Range, Position Summary, etc. We need to preserve substantive info. We need to parse the posting. Let's extract sections: Company Overview: description of Strive Pharmacy. Could be "About the role"? Actually "Company Overview" is about company, not role. Could be "About the role"? The instruction says use headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. So we can map content accordingly. We have: - Company Overview: description of company mission etc. Could go under "About the role"? Might be better as "About the role" includes overview of role and company? Usually "About the role" includes summary of role. We have Position Summary. So we can put Position Summary under "About the role". Also Company Overview could be part of that. - Responsibilities: Key Responsibilities bullet list. - Requirements: Required Qualifications (Education & Experience, Technical Expertise, Core Skills, Physical & Environmental). Could be under Requirements. - Qualifications: Preferred Qualifications (Advanced Education, Leadership Experience, Regulatory Knowledge, Audit Experience). Could be under Qualifications. - Skills: maybe Core Competencies list. - Benefits: Benefits/Perks list. - Pay: Compensation Range / Hourly Pay Rate. - Schedule: Schedule (Friday - Sunday; 6:00 AM - 6:00 PM). We must not include sections with placeholder text. All have real content. We need to output only HTML fragment, no /. Use

for each section heading. Use

• for any list of duties/requirements/benefits. Use

  for prose. We must preserve all substantive information; do not invent or summarize away detail. So we need to include all details from the posting, but we can format as lists. We must remove boilerplate: EEO, Disclaimer, navigation, etc. Also remove "Join Us in Making an Impact:" maybe that's promotional but still substantive? It's more like marketing; but we can keep as part of About the role? Might be considered boilerplate? It's not EEO/legal, it's a motivational paragraph. Probably keep as part of About the role. We need to ensure we don't repeat job title as heading. No Job ID. Let's craft sections:

  About the role

  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: Gilbert, Arizona Position Type: Full-time Schedule: Friday - Sunday; 6:00 AM - 6:00 PM Compensation Range: $62,000- $70,000 Position Summary The Quality Assurance Supervisor provides day-to-day tactical oversight and direct supervisory support for site-specific quality activities, ensuring full compliance with Strive Pharmacy’s Standard Operating Procedures (SOPs), product specifications, and applicable state and federal regulatory standards. Reporting to the Quality Assurance Manager, this position oversees the routine operations of the site QA team, including documentation review, batch record auditing, label reconciliation, and non-conformance tracking. The QA Supervisor acts as a hands-on leader to support continuous improvement, promote cleanroom compliance, and ensure seamless communication between floor operations, compounding personnel, and Quality leadership.

  But we have separate sections for Schedule, Pay, etc. So we might not repeat schedule and pay in About the role. Better to keep About the role as just the Position Summary and maybe company overview. But schedule and pay will be separate sections. Thus About the role could contain company overview, mission, position summary. We'll keep location? Location maybe not needed as separate heading; could be part of About the role. We'll avoid duplication. Now Responsibilities: list from Key Responsibilities. We need to capture each bullet as
• . The bullet list includes multiple sentences with semicolons. We'll keep as is. Responsibilities list: - Team Supervision & Coaching: Supervise the daily activities of the site QA team (e.g., QA Specialists/Technicians), including scheduling, workload distribution, timecard approval, and initial performance feedback. Assist with candidate interviews, facilitate onboarding, deliver hands-on competency training, and lead daily cross-departmental huddles. - Documentation & Compliance Auditing: Perform detailed, routine audits of compounding, production, cleaning, environmental monitoring, and validation records (including media fills and BMS/temperature alarms) for compliance with GDP and USP /// standards. Assist in reviewing routine equipment calibration and preventive maintenance logs. - Material & Label Accountability: Oversee routine physical and electronic labeling verification, line clearances, and reconciliation processes. Monitor supplier qualification documentation and verify incoming raw materials against approved vendor lists. - Quality Systems Support: Triage initial customer complaints and assist in gathering data for adverse drug event reporting. Perform initial investigations for deviations, non-conformances, and CAPA tasks in coordination with QA Specialists. Assist in managing sample staging and tracking for third-party analytical testing. - Internal Audits & Metrics Tracking: Support site preparation and documentation retrieval during external regulatory, partner, or client audits. Conduct routine internal compliance walkthroughs of compounding and storage areas. Collect, track, and log weekly site quality metrics and trend data for manager review. - Site Authority & Escalation: Serve as first-line authorization for routine product/component staging and release based on verified testing results. Hold the authority and responsibility to temporarily pause floor operations and immediately escalate to the QA Manager or Pharmacist-in-Charge (PIC) when immediate quality, safety, or compliance risks are identified. We need to preserve the "///" and "//" etc. Keep as is. Now Requirements: Required Qualifications. We have subparts: Education & Experience, Technical Expertise, Core Skills, Physical & Environmental. We can make a list. Education & Experience: High School Diploma or GED with a minimum of three (3) to five (5) years of experience in a quality assurance, quality control, or manufacturing role within a pharmaceutical compounding, medical device, or allied health science environment. Technical Expertise: Proven hands-on experience in aseptic operations and cleanroom environments, with strong foundational knowledge of core QA practices (documentation review, batch release, line clearances, and basic deviation handling). Core Skills: Proficiency with Microsoft Office Suite and digital Quality Management Systems (QMS). Strong organizational, analytical, communication, and problem-solving skills. Physical & Environmental: Ability to stand, sit, or walk for extended periods, and occasionally lift up to 45 pounds. Ability to work in controlled cleanroom environments, fully gown in required PPE, and tolerate controlled cleanroom temperatures and background noise. We'll put each as
• . Now Qualifications: Preferred Qualifications. - Advanced Education: Associate’s or Bachelor’s degree in Biology, Microbiology, Chemistry, Pharmacy, or a related scientific discipline. - Leadership Experience: Prior experience serving as a team lead, senior specialist, or shift supervisor in a pharmaceutical compounding (503A or 503B) or regulated manufacturing setting. - Regulatory Knowledge: Working knowledge of USP // standards, cGMP guidelines, and state pharmacy board regulations. - Audit Experience: Direct involvement in supporting internal or external quality audits. Now Skills: Core Competencies list. - Operational Leadership: Guides and supports daily QA staff to maintain high standards of accuracy and quality culture. - Attention to Detail: Demonstrates meticulous accuracy in reviewing batch records, labels, and quality logs. - Accountability: Takes personal ownership of daily site compliance tasks and timely problem resolution. - Problem-Solving & Escalation: Identifies process discrepancies early and knows when to apply immediate controls and escalate to site leadership. - Effective Communication: Clear, professional verbal and written communication across floor operators, compounding staff, and Quality management. Now Benefits: Benefits/Perks list. - 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 Now Pay: Compensation Range: $62,000- $70,000 (also Hourly Pay Rate: $62,000 USD - $70,000 USD). We'll include as

  maybe. Now Schedule: Schedule: Friday - Sunday; 6:00 AM - 6:00 PM. Now we need to ensure we don't include any boilerplate like EEO, Disclaimer, etc. Also remove "Join Us in Making an Impact:" and "Culture:" maybe we can incorporate into About the role? The "Culture:" paragraph is about culture building; could be part of About the role or maybe separate but we don't have a heading for Culture. Could include in About the role as extra paragraph. We'll include that paragraph in About the role after Position Summary. Thus About the role will contain company overview, mission, position summary, and culture paragraph. Now we need to ensure we don't repeat location etc. We'll include location in About the role maybe. Let's craft final HTML. We'll start with

  About the role

  then

  containing the combined prose. We need to be careful not to break into multiple

  unnecessarily; but we can have multiple

  if needed. We'll produce:

  About the role

  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: Gilbert, Arizona Position Type: Full-time Schedule: Friday - Sunday; 6:00 AM - 6:00 PM Compensation Range: $62,000- $70,000 Position Summary The Quality Assurance Supervisor