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Empower Pharmacy

Complaint and Clinical Pharmacist

Empower Pharmacy

. Receive, triage, investigate, and document assigned adverse drug event and product quality complaints under approved SOPs .

Posted 11/9/2026full-timeHouston • Texas • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in adverse drug event assessment, complaint investigations, and clinical risk evaluation, supported by a Doctor of Pharmacy degree and an active pharmacist license. Proven ability to analyze trends, recommend corrective actions, and coordinate cross-functional priorities while ensuring compliance with regulatory standards.

Highest-signal resume keywords
Doctor Of Pharmacy DegreeActive Pharmacist LicenseAdverse Drug Event AssessmentComplaint InvestigationsClinical Risk Evaluation

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Complaint Trend AnalysisCAPA RecommendationsPharmaceutical AssessmentsTechnical InvestigationsQuality Systems Knowledge
Soft Skills
Strong Technical WritingEffective CommunicationJudgment Application
Industry Keywords
Regulatory AffairsQuality AssuranceControlled SubstancesPatient SafetySOP Compliance

About the role

Key responsibilities & impact
  • Receive, triage, investigate, and document assigned adverse drug event and product quality complaints under approved SOPs
  • Gather patient, prescriber, product, lot, distribution, manufacturing, and laboratory information for investigations
  • Assess clinical impact and escalate serious adverse events, potential product defects, and patient safety concerns
  • Trend complaints by product, lot, event type, severity, recurrence, and potential root cause
  • Present complaint-trending findings and recommend CAPAs or further investigations
  • Provide clinical and pharmaceutical assessments for health hazard evaluations, nonconformances, protocols, stability reviews, and technical investigations
  • Coordinate potential reporting obligations with site pharmacists-in-charge, Regulatory Affairs, and Quality Assurance
  • Support state, DEA, FDA, and internal inspections and responses
  • Review escalated new controlled substance accounts, investigate red flags, and document recommendations
  • Provide formally designated pharmacist absence coverage when appropriately qualified and compliant with state requirements
  • Supervise assigned staff and coordinate work priorities
  • Assist Quality Assurance with overdue investigations, complaint-related CAPAs, and effectiveness checks

Requirements

What you’ll need
  • Doctor of Pharmacy degree from an accredited program required
  • An active pharmacist license in the applicable jurisdiction for assigned responsibilities required
  • 3-5 years of relevant pharmacist experience required
  • Ability to work onsite, particularly during training, meetings, and inspections
  • Ability to meet applicable state requirements for formally designated coverage
  • Experience in clinical pharmacy, compounding, complaint investigations, patient safety, or regulated quality systems preferred
  • Experience collaborating with quality or regulatory partners preferred
  • Experience supervising staff, coordinating investigation priorities, or supporting inspection preparation preferred
  • Knowledge of adverse drug event assessment, product quality complaints, clinical risk evaluation, and evidence requirements for scientifically defensible investigations
  • Ability to analyze complaint trends, identify recurring risks, and recommend CAPAs
  • Strong technical writing and communication skills
  • Ability to coordinate staff and cross-functional priorities, protect confidential information, and apply sound judgment within approved procedures

Benefits

Comp & perks
  • Medical coverage
  • Dental coverage
  • Vision coverage
  • Paid time off
  • 401(k) matching
  • Wellness perks
  • IV therapy
  • Compounded medications