Benuvia Operations, LLC. · 9 hours ago
Quality Control Supervisor
Round Rock, TX
Full-time
Onsite
Senior Level
5+ years expBenuvia is a company focused on pharmaceutical manufacturing, and they are seeking a Quality Control Supervisor to lead laboratory operations. The role involves ensuring compliance with cGMP and FDA regulations, overseeing a team of chemists and technicians, and driving continuous improvement in laboratory processes.
HealthcareManufacturingPharmaceuticalMedical
No H1B
Hiring Manager
Gina Amaya, PHR, SHRM-CP
Responsibilities
Ensure a safe working environment by providing leadership on all safety-related issues in the quality and microbiology laboratories at the Round Rock site
Be an active champion for good housekeeping, cGMP and safety related issues
Maintain and develop strategy for the analytical equipment and instrumentation in both labs
Ensure the spare parts program is in place for instrumentation
Ensure analytical methods are maintained and validated
Coordinate internal and external laboratory tests, procedures and methods and the development of new product test methods and specifications in conjunction with manufacturing, marketing, product development and sales functions
Ensure that all finished product meets appropriate internal specifications to ensure customer satisfaction
Handle special projects assigned for method validations or equipment qualifications
Ensure necessary supplies are ordered and stocked for the laboratory operations
Supervise the quality department chemists, analysts, and technicians. Manage in accordance with the organization’s policies and applicable laws
Mentor and train employees; planning, assigning, and directing work
Support employee development through training and performance management
Managing complaints and resolving performance and collaboration issues
Ensure laboratory operations comply to relevant standards: GMP, GDP, ISO 9001:2015
Ensure instrumentation is compliant with current standards and follows recommended calibration frequencies and/or replacement schedules
Ensures proper compliance to OOS program and proper investigations are completed and documented
Participate in internal audits and conduct audits of the laboratory operations to ensure compliance is demonstrated
Identify opportunities for process improvements within the laboratory
Implement efficiency initiatives and best practices
Support method validation, method transfer, and analytical troubleshooting
Qualification
Required
Bachelor's degree or higher in a Life or Chemical Science; Chemistry, Analytical Chemistry or similar science-based degrees preferred
Minimum of 5 years in Quality Control within a pharmaceutical, chemical or manufacturing environment with a minimum of 2-5 years of experience in a supervisory or management role
Strong knowledge of cGMP, FDA, ICH, and USP requirements
Hands-on experience with HPLC, GC, spectroscopy, wet chemistry, and other analytical techniques
Demonstrated ability to lead and develop teams and resolve conflicts in support of organizational goals
Strong interpersonal skills: demonstrated ability to work effectively, professionally, and respectfully in a team-based environment to involve peers, customers, line management and technical competency experts
Company
Benuvia Operations, LLC.
Benuvia Manufacturing is a leading developer and manufacturer of high-purity, pharmaceutical cannabinoid ingredients and products.
51-200 employees
Funding
Current Stage
Growth StageCompany data provided by crunchbase