Supervisor, Quality Assurance 2nd Shift

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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.

• Supervises Quality Assurance staff on assigned shift
• Oversees failure and discrepancy investigations and documents 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 reviews records to verify that quality standards for each drug product is met
• Maintains 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

• Detail-oriented with strong verbal and written communications skills
• Expresses energy, shows accountability, and multitasks
• Fulfills expectations, establishes sustainable relationships with team members, maintains effective and meaningful communication channels
• Has good interpersonal skills and the ability to work effectively and efficiently in a team environment to accomplish goals

• 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

• Bachelor’s Degree in Life Science or other related field

• 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
• The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions
• Range: $74,766 - $102,812 / Hour or Year

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 Bright Stream partners with health systems to aggregate, normalize, and…