Quva
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Supervisor, Quality Assurance 2nd Shift
role at
Quva .
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 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
Our Most Successful Supervisor, Quality Assurance
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
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
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
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.”
Seniority level Mid-Senior level
Employment type Full-time
Job function Quality Assurance
Industries Pharmaceutical Manufacturing
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Supervisor, Quality Assurance 2nd Shift
role at
Quva .
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 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
Our Most Successful Supervisor, Quality Assurance
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
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
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
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.”
Seniority level Mid-Senior level
Employment type Full-time
Job function Quality Assurance
Industries Pharmaceutical Manufacturing
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