Bmsc Careers
Director of Quality
Fort Worth, TX · Director · Full-time
Sponsorship not specifiedDetected 26 days ago
Project ManagementSupply ChainGMPFDA RegulatoryLeadershipCommunicationProblem SolvingCritical ThinkingMicrosoft OfficeGxP
About the role
- The Director of Quality will be responsible for the development, implementation, and execution of processes that inspect and improve the quality of products.
- This position requires a full-time, five-day on-site presence at our Fort Worth, Texas office.
- Remote and hybrid work arrangements are not available.
Responsibilities
- These teams support the execution of testing, improvement, and disposition throughout the plant.
- The director is responsible for development of KPIs that drive performance and evaluation based on those metrics.
- Train and develop the Quality Team.
- Manage the Quality team to improve and enforce quality standards through QA, QC, and Microbiology.
- Design and develop new quality control processes to improve efficiency and consistency including testing, inspection, and production.
- Develop, review, and approve SOPs that meet and exceed Quality standards set forth in specifications for incoming raw materials, outgoing finished goods, and work-in-process materials.
- Support the Company's mission, values, and standards of ethics and integrity by incorporating these into the development and implementation of business plans.
- Set and maintain department goals and timelines (Key Performance Indicators).
- Drive Robust Notice of Event (NOE) investigations and CAPAs for Quality issues that arise.
Requirements
- Must be able to climb stairs, stand for periods of time and have the ability to bend, squat, kneel, turn, and stoop.
- Ability to work and function safely in a Laboratory environment.
Nice to have
- Position Summary The Director of Quality will be responsible for the development, implementation, and execution of processes that inspect and improve the quality of products.
- and Essential Duties Ensure the integration of Quality in all steps of the development, manufacturing, and supply chain process.
- Interact with Regulatory bodies, such as the FDA, to ensure compliance.
- Execute internal audits and guide third-party audits.
- Ensure a robust training framework based on cGMP, internal audits, and CAPAs.
- These responsibilities can and will change as we continue to grow.
- Technical Skills Required Must possess strong technical skills.
Skills
- Required Must possess strong technical skills.
- Certification by ASQ, as a CQM/OE is strongly preferred.
- Must be self-motivated and possess strong problem-solving and critical thinking skills.
- Must have excellent interpersonal and leadership skills to effectively meet objectives.
- Computer skills to include proficiency with Microsoft Office software.
- Understanding of cGMP and FDA CFR 21 Parts 210/211.
- Self-directed and motivated.
- Experience Required Bachelor's Degree.
- 10 or more years prior work experience in CPG or Pharmaceutical industry, contract manufacturing preferred.
- Experience in developing and managing budgets.
Company info
- The position ensures the alignment of department execution that supports the company goals and strategic initiatives while ensuring regulatory compliance.
- As head of the Quality department, the position sets the standard for quality throughout the company and drives the quality culture.
- The Director ensures that the products meet and exceed standards set by customers and any regulatory bodies for cosmetic and OTC products through the design, adherence, and enforcement of quality processes.
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