Quality Assurance Engineer

About Civica

Civica is a 501(c)(4) social welfare organization established in 2018 by health systems and philanthropies to reduce chronic generic drug shortages and related high prices in the United States.

Civica is led by an experienced team of healthcare and pharmaceutical industry leaders.

Today, more than 55 health systems have joined Civica. They represent over 1,500 hospitals and one-third of all U.S. hospital beds. Civica has also begun to supply the U.S. Department of Veteran's Affairs, the U.S. Department of Defense and the U.S. Strategic National Stockpile of essential medicines.

Civica recently announced plans to expand its mission, via a unit called CivicaScript, to into the outpatient pharmacy space and to manufacture and distribute insulins that, once approved, will be available to people with diabetes at significantly lower prices than insulins currently on the market.

The availability of Civica's affordable insulins, beginning in 2024, will benefit people with diabetes who have been forced to choose between life sustaining medicines and living expenses, particularly those uninsured or underinsured who often pay the most out of pocket for their medications.

Civica's mission is to ensure that quality generic medications are accessible and affordable to everyone.

Since established, the #1 Policy for the Civica team has been "Do What Is in the Best Interest of Patients." Civica's manufacturing facility in Petersburg, Virginia, is the future home of affordable insulin and essential sterile injectable medicines.

The facility is currently in late-stage construction and hiring for the site is well-underway.

To find out more about how Civica's innovative model is directly impacting patient care, click here to read a summary from the New England Journal of Medicine.

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To learn more about Civica's plans to bring affordable insulin to Americans living with diabetes, click here to read an article in BioSpace.)

Job Description

The Quality Assurance Engineer will join the Civica, Inc.

("Civica") Quality organization at the Petersburg, Virginia site by bringing their knowledge and experience in service to patients and pursuit of excellence in quality and compliance.

The Petersburg site serves as Civica's new fill finish facility dedicated to the manufacture and supply of essential generic sterile injectable medications.

Responsibilities of the position include maintaining quality systems and oversight to ensure the validation/qualification and operation of computerized systems meet cGMP and Civica compliance requirements at the onset of building the facility leading to successful U.S.

Food and Drug Administration (FDA) approval of the facility and the ongoing introduction and approval of new medications.

Responsibilities also include, but are not limited to, the generation, review and/or approval of policies, procedures, reports, and other records necessary to provide quality oversight of Civica Engineering functions including computerized system validation and ongoing operation activities of facility, utilities, process, equipment, instrumentation and to ensure FDA data integrity requirements are met.

Essential Duties and Responsibilities:

Working across functions, to ensuring the site's quality system processes related to GMP compliance of the facility, equipment, computer systems and processes.

Work with validation and engineering teams to provide Quality oversight for computerized system validation activities to ensure work is performed in a compliant and controlled manner and leverage experience and share industry best practices to support continuous improvement of site CSV program.

Maintain current knowledge of local and international regulatory and legislative requirements and trends to ensure that expert advice and appropriate technical support on all quality related matters is provided to the site with a focus on data integrity.

Support implementation and quality oversight related to the overall compliance of the facility, equipment, and manufacturing processes.

Support quality processes and systems across the product lifecycle including, but not limited to, change control, CAPA, deviations and investigations.

Participate or lead in quality risk analysis.
Proactively identify and work collaboratively to resolve problems taking risk-based and compliant approaches to solutions.
Promote a quality mindset and quality excellence approach to all activities.
Promote a safety mindset and focus on safety for all operations activities.

Basic Qualifications and Capabilities:
A bachelor's degree in a scientific discipline or computerized systems with a minimum of 4+ years relevant experience.
Experience providing computer system validation oversight.
Knowledge in 21CFR Part 11, Electronic Records and Signatures and data integrity is required.

Experience in developing and managing scientific studies, identifying critical aspects of the topic being studied, and defining appropriate acceptance criteria to the study.

Strong project management, organization, and execution skills to manage multiple projects and priorities.
Participation and leading activities to support regulatory agency inspections required.
Leverage experience and share industry best practices to support continuous improvement of site procedures.
Excellent interpersonal and written communication skills and experience using various software/electronic applications required.
Self-motivated, flexible, and able to work in a small, fast-paced, dynamic, environment.
Ability to work autonomously and within established guidelines, procedures, and practices.
Committed to delivering high quality results, working with others to overcome challenges, and focusing on what matters. Continuously looking for opportunities to learn, build

Preferred Qualifications:
Experience in facility, utilities and equipment qualification.
Experience across the product development and commercialization lifecycle including change management and associated implementation strategies.
Technical expertise in sterile pharmaceutical isolator technology, combination product and medical devices.

Physical Demands and Work Environment:

This role will be expected to be on site for 80% of the work week, with exception of one day remote per week.

In addition, the role will be required to be on site to perform Essential Duties and Responsibilities when physical activities are being performed on site.

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