Quality Assurance Engineer - Process and Validation (930) at Civica in Petersburg, Virginia

Job Description:

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. (https://catalyst.nejm.org/doi/full/10.1056/CAT.21.0189)


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


(https://www.biospace.com/article/civica-is-rallying-leaders-to-make-insulin-affordable-by-2024-/)



Job Description



Responsibilities of the position include supporting quality systems and oversight to ensure the product process validation, cleaning validation, Quality Risk Management and quality laboratory 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 to ensure FDA requirements are met.



Essential Duties and Responsibilities:

• Work with validation and engineering teams to provide Quality oversight for validation and qualification activities and ensure work is performed in a compliant and controlled manner.


• Participate in Quality Risk Management and analysis.


• 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.


• Support product process transfers, including validation, from and/or to other manufacturing sites.


• Support activities related to product introduction to the site.


• Support aseptic process simulations.


• Support quality processes and systems across the product lifecycle including, but not limited to, change control, CAPA, deviations and investigations, laboratory control, Annual Product Quality Review (APQR), and management notification.


• Provide quality review and support for laboratory method validation/verification and laboratory information management system (LIMS).


• Provide support to equipment, facilities and utilities qualification as needed.


• Work collaboratively to resolve problems by 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. Travel (up to 5%) may be required

Basic Qualifications and Capabilities:

• Bachelor's degree in a scientific discipline with 4+ years Quality/cGMP experience in the pharmaceutical industry.


• Experience in process and cleaning validation, LIMS systems, Aseptic Process Simulations and Quality Risk Management.


• Knowledge in 21CFR Part 11, Electronic Records and Signatures and data integrity is required.


• Participation and leading activities to support regulatory agency inspections required.


• Project management, organization, and execution skills are required.


• Ability to apply technical expertise to solve problems and issues.


• Participating in and leading activities that support regulatory agency inspections is required.


• 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.


• Committed to delivering high-quality results, working with others to overcome challenges, and focusing on what matters.


• Continuously looking for opportunities to learn, build skills, and share knowledge with others.

Preferred Qualifications:



Technical expertise in sterile pharmaceutical isolator technology, combination product and medical devices. Apply Now