Quality & Compliance Manager – Compounding Pharmacy

Remedy; Houston (TX); On-site; USD 130,000 - 180,000; Full time

Benefits offered by this job

Health plan

Flexible time off policy

Job summary

Remedy, now part of Thirty Madison, seeks a Quality & Compliance Manager for our compounding pharmacy. You will own the quality system, author SOPs, and train staff; ensure inspection readiness and accreditation readiness. You’ll manage environmental monitoring, personnel qualifications, CAPA, change control, and audits, with deep USP/797/800 and DEA compliance in a high-stakes sterile setting. This role offers competitive pay and benefits.

Qualifications

• 5+ years in sterile compounding with quality system accountability.
• Experience building or rebuilding EM programs and sampling rationale.
• Knowledge of USP <795>/<797>/<800> and state board regulations.
• Experience with licensure, DEA, and multistate operations.
• Strong communication and training skills.

Responsibilities

• Write the quality system from scratch: SOPs, training, and document control.
• Design environmental monitoring programs with risk-based plans.
• Lead personnel qualification and data trend analysis.
• Approve facility SOPs and third-party reports; manage investigations.
• Own the 503A framework and licensure processes across states.
• Coordinate licensure and regulatory documentation for inspections.

Skills

Sterile compounding

Quality system

SOP development

Audit readiness

Regulatory compliance

Education

Pharmacy Technician certification

CHC

RAC

CPHQ

BCSCP

Tools

USP compliance

DEA registration

PCAB/ACHC

Job description

Quality & Compliance Manager – Compounding Pharmacy

Houston, TX

Thirty Madison is now part of Remedy ! You can read more about the acquisition here . We are excited to join forces and continue to revolutionize healthcare accessibility!

Quality & Compliance Manager – Compounding Pharmacy you will own the quality system for our 503A compounding pharmacy, ensuring the facility is always inspection-ready and accreditation-ready. You will be responsible for authoring, maintaining, and training staff on SOPs across every facet of operations. This includes environmental monitoring and personnel qualifications to deviation/CAPA and change control. You must have prior experience in hands‑on experience building or running a quality system in a sterile compounding environment and be comfortable serving as the subject matter expert when state, federal, or accreditation auditors walk through the door. You are detail‑driven, autonomous, and confident defending quality decisions and documentation under scrutiny. You also have a strong working knowledge of USP <795>/<797>/<800>, state board regulations and PCAB/ACHC accreditation standards.

Pharmacist license is not required. We welcome experienced pharmacy technicians (CPhT), sterile compounding professionals, and quality professionals with relevant sterile/aseptic experience.

• Robust and affordable Medical, Dental, and Vision plan options
• Flexible time off policy

**Base pay offered may vary depending on job-related knowledge, skills, and experience. An annual incentive plan and stock options may be provided as part of the compensation package, in addition to a full range of medical, financial, and/or other benefits, dependent on the position offered.

What you get to do every day

• Write the quality system from scratch: SOPs and document control, training and competency, cleaning and disinfection, BUD assignment, deviation/CAPA, change control, complaints, recall
• Design the environmental monitoring program — risk‑based sampling plans, alert and action levels, and the contract micro lab behind it
• Build and run personnel qualification (garbing, gloved fingertip, media fill, technique observation), then trend the data and investigate every excursion to real root cause
• Approve facility SOPs and third‑party certification reports, and partner with facilities on joint excursion investigations and change control on anything touching classified space
• Own the 503A framework: bulk substance eligibility, "essentially a copy" analysis, prescriber‑patient documentation, Texas office‑use limits
• Manage the licensure lifecycle: Class A‑S, DEA registration and controlled substance recordkeeping, [nonresident licensure and the renewal calendar that comes with it]
• Qualify suppliers and outsourcing facilities, run HIPAA privacy and security with [IT/Legal], and handle adverse event, complaint, and recall processes
• Track USP revisions, TSBP rule changes, and FDA guidance in our space, and translate them into action before they’re a finding — including clearing prescriber‑facing materials
• Prepare the quality and regulatory content of the licensure package for the PIC's signature, and be the SME in the room when the Board inspector arrives
• Build and run the internal audit and self‑inspection programHost TSBP, FDA, DEA, accreditation, and customer audits, and own deficiency responses and the commitments in them
• Keep the PIC and Head of Compounding current on compliance status, open investigations, and anything heading toward a reportable event

What you bring to the role

• §291.133 training requirements met, with current gloved fingertip and media‑fill qualification
• 5+ years in sterile compounding with real accountability for the quality system. You have been responsible for it, not adjacent to it
• Demonstrated experience designing or substantially rebuilding an EM program, including sampling rationale and action‑level setting
• Track record trending microbial data, calling an excursion, and defending that call to someone who didn’t want to hear it
• Direct experience with pharmacy regulatory compliance beyond USP <797> – licensure, DEA, multistate operations
• SOP authorship and hands‑on owners of a formal deviation/CAPA and change‑control system
• Experience being questioned by an inspector about your records
• Strong verbal and written communication skills, with the ability to train staff clearly and build relationships with regulators, leadership, and cross‑functional teams
• Well developed organizational and time management skills; comfortable managing multiple open investigations and audit preparations simultaneously
• Certified in Healthcare Compliance (CHC), RAPS RAC, ASQ CQA, or CPHQ
• CriticalPoint or ASHP sterile compounding training certificate
• PCAB (ACHC) accreditation experience, or cGMP quality‑system exposure from a 503B or manufacturer
• Multistate nonresident pharmacy licensure management at scale
• Microbiology coursework or lab background — enough to argue with your contract lab productively
• Experience opening a pharmacy or cleanroom from construction through first licensure
• Telehealth or mail‑order pharmacy compliance background
• Board Certified Sterile Compounding Pharmacist (BCSCP), in good standing

Physical Requirements

• Gown and enter ISO 7/8 classified areas regularly for sampling, observation, and audit
• Extended standing and periods at a workstation and ability to lift up to 25 lb

All Company policies and procedures are subject to change without notice based on business needs. This includes, but is not limited to, the locations where we hire remote, hybrid, or onsite employees.

U.S. Applicants Only

Don’t meet every single requirement?

Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Remedy we are dedicated to building a diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right candidate for this or other roles.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions. Contact us at [e-mail] to request accommodation.

*This employer participates in E-Verify and will provide the federal government with your I-9 Form information to confirm that you are authorized to work in the U.S.*