Quality Control Project Coordinator III

Summary: The Quality Control Project Coordinator III will construct maintain and oversee the Quality Control Testing Schedule to include release testing stability testing and method qualification activities.

The Quality Control Coordinator III under general direction will be responsible for implementing a Quality Control Master Schedule to guide QC activities supporting batch release and stability testing. The position will also require frequent communication with the Analytical Development and Assay Method Transfer groups to coordinate and schedule method qualification activities. The Coordinator will assist the QC Analysts and QC Management to navigate GMP documents through the EQMS system. Close attention to detail is required to update the Master Schedule on a daily basis to ensure QC deadlines and milestones are met. Other responsibilities may include but are not limited to: Compiling data for Batch Disposition. Attending planning meetings as needed. Communicating gaps and schedule changes to QC Area Managers.

The work we do at FUJIFILM Diosynth Biotechnologies has never been more importantand we are looking for talented candidates to join us. We are growing our locations our capabilities and our teams and looking for passionate missiondriven people like you who want to make a real difference in peoples 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 FUJIFILM Diosynth Biotechnologies call Genki.

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 smalltown life and the convenience of living close to the vibrant pulse of big cities. Eightyseven percent of Texas population lives within a 180mile 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.

Essential Functions:

• Follow Standard Operating Procedures (SOPs) other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) and other site procedure documents (such as Chemical Hygiene Plan SDS sheets)
• Construct and maintain a QC Master Schedule
• Assists in preparing QC metrics on a monthly basis
• Alignment of QC Master Schedule to projected manufacturing schedules
• Assist in generating POs for external testing
• Work directly with Contract laboratories to coordinate and monitor testing per timelines
• Work directly with customers to update and confirm schedules and deadlines
• Attend daily briefings and update as needed.
• Lead team and department meetings
• Assist QC Director and QC Managers to oversee and coordinate departmental training
• Ability to work cross functionally with Quality Assurance Manufacturing and Project Management to establish timelines
• Work with customer and other appropriate parties to establish GMP documents.
• Provide technical suggestions to customers based on industry guidelines.
• Follow all established laboratory regulatory safety and environmental procedures.
• Perform other duties as assigned.

Required Skills & Abilities:

• Must be highly organized driven and possess the skills and capability to plan ahead and stay on schedule.
• Ability to evolve and adapt to new technologies to include electronic planning tools and Laboratory Information Management Systems (LIMS)
• Computer skills in Microsoft Office and Microsoft Project
• Ability to multitask and prioritize work assignments with little supervision.
• Excellent attention to detail.
• Ability to work in a team or independent setting and collaborate with employees from various departments.
• Excellent analytical and planning skills.
• Must have excellent organizational written and oral communication skills.

Working Conditions & Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job the employee is regularly required to:

• Experience prolonged standing some bending stooping and stretching.
• Use handeye coordination and manual dexterity sufficient to operate a keyboard photocopier telephone calculator and other office equipment is required.
• Ability to sit for long periods to work on a computer.
• Attendance is mandatory.

Minimum Qualifications:

• High school or GED and minimum of 8 years of relevant experience
• Associates degree and minimum of 6 years of relevant experience
• Bachelors degree and minimum of 4 years of relevant experience
• Masters degree and minimum of 2 years of relevant experience

Preferred Qualifications:

• Degree in a scientific discipline
• GMP/GLP experience

• PMP Certificate
• Analytical background
• Client relations background and/or Customer interaction training

We are an equal opportunity and affirmative action employer. All qualified applicants will receive consideration without regard to race color national origin sex gender identity sexual orientation religion disability protected veteran status or any other characteristic protected by applicable federal state or local law.

If an accommodation to the application process is needed please email or call.

Fujifilm is committedto providing equal opportunities in hiring promotion and advancement compensation benefits and training regardless of nationality age gender sexual orientation or gender identity race ethnicity religion political creed ideology national or social origin disability veteran status etc.

If you require reasonable accommodation in completing this application interviewing completing any preemployment testing or otherwise participating in the employee selection process please direct your inquiries to our HR Department or.