# Quality Control Supervisor at Revance

> United States · Unspecified · Other · open. Source: https://alderhq.app/jobs/greenhouse%3Arevance%3A8920430002 (read 2026-11-07).

## Facts (observed)

- Company: [Revance](https://alderhq.app/companies/revance)
- Location text: Johnson City, TN; Johnson City - Plant
- Where it can be done from (inferred): United States (evidence: "Location: Johnson City, TN; Johnson City - Plant")
- Posted: 2026-10-28 (10 days ago)
- First seen by alder: 2026-11-02 · last verified: 2026-11-04
- Reposted: 0 times · edited: 0 times
- Apply on the employer's site: http://www.revance.com/careers/job-listings/?gh_jid=8920430002

## Pay and sponsorship

- Posted pay: not posted
- Market band for similar posted roles (United States, n 21890): p25 $55k, median $90k, p75 $154k

## Description (the employer's text)

### Job Summary

The Quality Control Supervisor leads daily laboratory operations and personnel to ensure accurate, timely, and compliant testing of raw materials, in-process samples, bulk intermediates, stability samples, and finished products. This role provides technical and operational oversight for analytical testing, investigations, method lifecycle activities, instrument readiness, data integrity, safety, and continuous improvement while partnering cross-functionally to support product quality, commercial operations, and regulatory readiness.

Reporting to: Manager, Quality Control

Location: Johnson City, TN – onsite 5 days/week

Responsibilities/Essential Duties:

- Supervise, coach, develop, and schedule QC laboratory personnel; set priorities, review performance, and foster a culture of accountability, scientific excellence, safety, and continuous improvement.
- Direct routine and non-routine testing of raw materials, in-process samples, bulk intermediates, stability samples, components, and finished products in accordance with approved procedures, compendial requirements, and regulatory expectations.
- Ensure analytical data and records are accurate, complete, timely, and compliant with cGMP, GLP, ALCOA+ data integrity principles, and applicable electronic laboratory system requirements.
- Provide technical oversight for HPLC, GC, UV-Vis, FTIR, Karl Fischer, wet chemistry, ICP or equivalent elemental analysis, and other laboratory instrumentation; escalate or coordinate resolution of complex issues.
- Review and approve laboratory data, notebooks, electronic records, calculations, specifications, certificates of analysis, SOPs, test methods, protocols, and reports.
- Manage OOS, OOT, deviation, and nonconformance investigations; ensure scientifically sound root cause analysis, impact assessment, and timely CAPA completion.
- Plan and oversee method development, verification, transfer, qualification, validation, robustness assessment, and lifecycle management in alignment with USP, EP, JP, ICH Q2(R2), and FDA expectations.
- Maintain instrument lifecycle readiness through qualification, calibration, preventive maintenance, troubleshooting, and technology upgrades in partnership with Validation and Engineering.
- Manage internal and contract laboratory workloads, priorities, turnaround times, staffing plans, supplies, and departmental budget inputs to support operational commitments.
- Maintain laboratory safety, cleanliness, documentation, and inspection readiness; enforce EHS, PPE, hazardous-material, and near-miss reporting requirements.
- Represent QC during internal and external audits and serve as a technical escalation point for analytical methods, laboratory systems, and data integrity practices.
- Partner with Quality Assurance, Manufacturing, R&D, QA Validation and Supply Chain to resolve product-quality issues and support method readiness, technology transfers, and commercial operations.
- Lead continuous improvement initiatives, including 5S, Lean or kaizen activities, workflow optimization, error prevention, analytical throughput improvements, and harmonization of laboratory practices.
- Establish and monitor training and qualification programs for laboratory personnel, including chromatography, instrumentation, investigations, documentation, and data integrity.
- Perform additional duties, projects, and training assignments as directed by senior Quality leadership.
### Basic Qualifications

- Bachelor’s degree & 7+ years’ directly related experience.
### Preferred Qualifications

- Bachelor’s degree in Chemistry, or a related scientific discipline.
- Typically 7+ years’ experience in a cGMP/GLP laboratory environment, including at least 1 years’ direct supervisory or team-lead experience.
- Demonstrated knowledge of cGMP, GLP, FDA 21 CFR Part 211, USP/EP/JP compendial requirements, ICH Q2(R2), and ALCOA+ data integrity principles.
- Strong technical knowledge of chromatography and analytical instrumentation, including HPLC, GC, ICP-MS, UV-Vis, FTIR, Karl Fischer, wet chemistry, and related laboratory systems.

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Data: alder (https://alderhq.app). Cite https://alderhq.app/jobs/greenhouse%3Arevance%3A8920430002 and the date you read it. Observed facts come from the employer's own listing; location reach, level, family and skills are inferences.