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Full-time
high school, bachelor degree
Medical Insurance, Dental Insurance, Vision Insurance, 401k Retirement Program With Company Match, 22 Paid Days Off, 8 Paid Holidays Per Year
Posted 17d ago
~40 hrs/week
Responsibilities
Supervise Quality Assurance staff and oversee the compounding of pharmaceuticals to ensure compliance with FDA 503B and cGMP guidelines. Manage failure investigations, implement corrective actions, and ensure the timely disposition of finished products.
Requirements
Requires a high school diploma, one year of supervisory experience, and two years of experience in a QA/cGMP/FDA regulated industry. Candidates must be physically able to lift up to 50 lbs and be authorized to work in the US without sponsorship.
Full job description
Our Supervisor, Quality Assurance plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include supervising all Quality Assurance (QA) aspects of compounding pharmaceuticals for compliance within the facility. This position operates within the legal and regulatory compliance, producing a quality product. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.
What the Supervisor, Quality Assurance Does Each Day:
Supervises Quality Assurance staff on assigned shift
Oversees failure and discrepancy investigations and documenting investigations on process deviations or equipment malfunctions
Develops and provides oversight to identification and implementation of appropriate corrective actions and preventive actions
Oversight of the environmental monitoring program including appropriate escalation of environmental and personnel monitoring results that exceed alert or action limits and interpreting results.
Responsible for timely and accurate disposition of finished product to assure each batch meets specification prior to release
Periodically review records to verify that quality standards for each drug product is met
Maintain compliance with FDA 503B and cGMP guidelines / state and federal laws
Responsible for maintaining QA records associated with internal and external testing
Responsible to maintain all testing equipment in compliance, calibration, and certification
Assists in developing policies and procedures related to QA
Promptly communicates with Operations regarding complaints, product issues/variance
Assists in maintaining compliant controlled substance documentation specifically associated with sample handling and reconciliation
Enforces applicable personnel policies and procedures
Our Most Successful Supervisor, Quality Assurance:
Are detail-oriented with strong verbal and written communications skills
Express energy, show accountability, and multi-task
Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels
Have good interpersonal skills and the ability to work effectively and efficiently in a team environment to accomplish goals
Minimum Requirements for this Role:
A High School diploma or equivalent
Able to successfully complete a drug and background check
1 year of supervisory or management experience required
2 years’ experience in Quality Assurance / cGMP / FDA regulated industry
Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas
Any of the Following Will Give You an Edge:
Bachelor’s Degree in Life Science or other related field
Benefits of Working at Quva:
Set, full-time, consistent work schedule
Comprehensive health and wellness benefits including medical, dental and vision
401k retirement program with company match
22 paid days off plus 8 paid holidays per year
Occasional weekend and overtime opportunities with advance notice
National, industry-leading high growth company with future career advancement opportunities
About Quva:
Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma’s multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva’s overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.
Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.”
Quva is a national, industry-leading provider of health-system pharmacy services and solutions, including 503B sterile injectable outsourcing and data software solutions that generate insights to help power the business of pharmacy.
Quva Pharma’s FDA-registered 503B outsourcing facilities provide hospitals with essential medications in ready-to-administer formats that are demanded by health care providers and critical to effective patient care. Quva’s unmatched cGMP expertise and pharmaceutical manufacturing background, broad sterile-to-sterile product portfolio, expansive capacity across multiple production facilities that leverage automation and integrated technologies, industry-first dedicated forward distribution capabilities, transparent and accountable customer service, and a patient-first safety orientation combine to help hospitals better meet their patient care and operational needs while reducing compliance risk.
Quva BrightStream’s predictive analytics and data insights software solutions partners with health systems to aggregate, normalize, and analyze large amounts of complex data across all sites of care, and through our proprietary machine learning and AI platform, transforms complex data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more so health-system pharmacy can have total clarity to make better decisions.
Quva’s overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value by operating more efficiently and effectively in delivering high-quality patient care.
Offices: 3 Sugar Creek Center Blvd, Sugar Land, Texas 77478, US · 521 NJ-173, Bloomsbury, New Jersey 08804, US · 1075 W Park One Dr, Sugar Land, Texas 77478, US · 305 N. 5th Avenue, $560, Minneapolis, MN 55401, US · 4717 E Hilton Ave, Suite 400, Phoenix, Arizona 85034, US
503B Compounding503B Outsourcing ServicesAntibioticsAnticoagulationAntiemeticCardiovascularElectrolyte SolutionsEmergency DepartmentEpiduralGeneral Medicine
Based on 2357 listings with disclosed salaries, most security & safety jobs in Texas pay between $69k–$183k per year. Individual offers vary with seniority, company size, and specialization.
How many Security & Safety jobs are open in Texas right now?
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