QC Manager, Drug Product Operations

Overview

The work we do at FDB has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what FDB call Genki. 

External US

College Station, Texas may be a small, university town, but the lively cultural scene and local amenities make it a great place for families as well as those who want the ease of small-town life and the convenience of living close to the vibrant pulse of big cities. Eighty-seven percent of Texas' population lives within a 180-mile radius, so we are in the center of it all in Texas. And our site is nestled in the hub of innovation, representing a source of pride for the area.

 

The QC Manager of Drug Product Operations under general direction from the Associate Director, Contamination Control, will be required to oversee all activities involved with Drug Product Quality Operations.  The Manager is responsible for Aseptic Process Simulations (APS) and all aspects of the visual inspection program including 100% inspection, AQL inspections, automated inspections, particulate investigations, and identification of required particulates.  The position also requires oversight of all container closure integrity testing activities for component release and final product testing.  These methodologies will also encompass sub-visible particulate testing via USP <787>, USP <788> and USP <789>.  Candidates for this managerial position must have experience in Drug Product visual inspection as well as sub-visible particulates testing in a regulated pharmaceutical and /or biotechnologies setting.  Strong candidates will have a working knowledge of GMP functions and USP guidelines.

 

Other responsibilities may include but are not limited to staff hiring, supervision, training, discipline and performing annual review assessments. Preparing and reporting out monthly metrics for all worked performed within the department.  Ensuring all equipment is in a state of GMP readiness.  Writing and Reviewing SOPs, verification protocols and reports. 

 

Reports to                Associate Director, Contamination Control

Work Location         College Station, TX 

 

Primary Responsibilities:

• Provide clear and understandable direction and goals for the team.
• Interpret applicable quality and regulatory requirements and develop associated policies for the laboratories operations.
• Manage operating costs for the outsourced testing and laboratory supplies.
• Develop and enhance the Company Visual Inspection program. Establish, monitor and investigate Action and Alert limit excursions and implement corrective and preventive actions, as needed.
• Oversee and guide investigations regarding invalid and out-of-specification results.
• Assure the implementation and effectiveness of appropriate and timely corrective actions.
• Work closely with Quality Assurance and other departments to continuously improve the effectiveness of the Quality Management Team.
• Work collaboratively with manufacturing and product development teams to improve quality, increase efficiency, solve problems, generate cost savings, and provide new product support.
• Interface with current and potential clients.
• Interface with investigators during both internal and external inspections and audits.
• Evaluate external audit observations and develop responses and oversight for related action plans.
• Adapt, develop, or review and approve procedures, protocols and reports.
• Follow and enforce all established laboratory, regulatory, safety, and environmental procedures.
• Adhere and enforce the standards of quality ruled by current GMP and the company Quality Policies and site SOPs.
• Identify and assist in deviation investigations and report possible preventative and corrective actions.
• Knowledge base in USP 790 / 1790 / USP 787 / USP 788/ USP 789
• Familiar with qualification of personnel for visual inspection and perform training and routine in-line audit assessment of personnel performance
• Review and approve associated documentation (Sample Plans, Product Specification)
• Must follow good documentation practices in all aspects and phases of the work; provide reports for review in a timely manner; work with other lab personnel on projects and participate in (OOS) Out-of-Specification and fail