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Quality Control Project Coordinator III

Position Overview

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 Analyst’s 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.  

Company Overview

The work we do at FUJIFILM Diosynth Biotechnologies 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 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 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.

 

Job Description

Essential Functions:

  • Follow Standard Operating Procedures (SOP’s), 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 multi-task 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 hand-eye 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
  • Bachelor’s degree and minimum of 4 years of relevant experience
  • Master’s 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 FDBTHR@fujifilm.com or call 979-431-3528.

 

EEO Information

Fujifilm is committed to 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.

ADA Information

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBTHR@fujifilm.com or (979) 431-3500).

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Average salary estimate

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$60000K
$90000K

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What You Should Know About Quality Control Project Coordinator III, FUJIFILM

Are you an organized and detail-oriented professional ready to take your career to new heights? At FUJIFILM Diosynth Biotechnologies, we're searching for a passionate Quality Control Project Coordinator III in College Station. In this key role, you'll construct and maintain our Quality Control Testing Schedule, ensuring everything runs smoothly from release testing to method qualifications. With general direction, you'll implement a comprehensive Quality Control Master Schedule to support batch releases and stability testing. Communication is vital, as you'll often liaise with our Analytical Development and Assay Method Transfer teams to coordinate scheduling effectively. Attention to detail is a must, as you'll be responsible for daily updates to the Master Schedule to help meet vital QC deadlines. You’ll also compile Batch Disposition data, attend planning meetings, and communicate any schedule changes with QC Area Managers. At FUJIFILM Diosynth, you'll join a mission-driven team that is dedicated to shaping the future of biopharma solutions, including groundbreaking vaccines and therapies. Nestled in the vibrant College Station, Texas, you’ll enjoy a small-town feel with access to a lively culture and amenities, making it an ideal place to work and live. If you have a strong foundation in GMP documents, exhibit excellent communication skills, and are eager to dive into new technologies, we want to hear from you. Come be a part of our mission to make a difference in lives worldwide!

Frequently Asked Questions (FAQs) for Quality Control Project Coordinator III Role at FUJIFILM
What responsibilities does the Quality Control Project Coordinator III at FUJIFILM Diosynth Biotechnologies have?

The Quality Control Project Coordinator III at FUJIFILM Diosynth Biotechnologies is responsible for maintaining and overseeing the Quality Control Testing Schedule, which includes tasks such as release testing, stability testing, and method qualification. This role requires frequent communication with various teams to coordinate and schedule activities effectively, ensuring that all QC deadlines and milestones are met while following GMP guidelines.

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What qualifications are needed for the Quality Control Project Coordinator III position at FUJIFILM Diosynth Biotechnologies?

To be considered for the Quality Control Project Coordinator III role at FUJIFILM Diosynth Biotechnologies, candidates must possess a minimum of a high school diploma or GED, along with relevant experience depending on educational qualifications. Preferred qualifications include a degree in a scientific discipline, experience with GMP/GLP, and project management training, ensuring candidates have a solid foundation for this role.

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How does the Quality Control Project Coordinator III contribute to team communication at FUJIFILM Diosynth Biotechnologies?

In the Quality Control Project Coordinator III role, effective communication is key. The coordinator interacts with QC Area Managers and other departments to relay schedule changes, compliance updates, and team meeting outcomes. This ensures that everyone involved in QC activities maintains alignment and is informed about timely execution of tasks, ultimately supporting efficient operations at FUJIFILM Diosynth Biotechnologies.

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What skills are essential for success as a Quality Control Project Coordinator III at FUJIFILM Diosynth Biotechnologies?

Successful candidates for the Quality Control Project Coordinator III position at FUJIFILM Diosynth Biotechnologies must exhibit strong organizational skills, attention to detail, and the ability to manage multiple tasks effectively. Proficiency in Microsoft Office and electronic planning tools is also important, as is the capacity to adapt to new technologies relevant to laboratory operations and project management in biopharma.

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What is the work environment like for a Quality Control Project Coordinator III at FUJIFILM Diosynth Biotechnologies?

The work environment for a Quality Control Project Coordinator III at FUJIFILM Diosynth Biotechnologies is collaborative and fast-paced. The role requires a mix of independent work and teamwork, often in compliance with GMP and other regulatory guidelines. Employees are expected to foster a culture of innovation and safety while contributing to the impact of biopharma solutions within their community and beyond.

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Common Interview Questions for Quality Control Project Coordinator III
What motivated you to apply for the Quality Control Project Coordinator III position at FUJIFILM Diosynth Biotechnologies?

When answering this question, highlight your passion for biopharma and your desire to contribute positively to developing important therapies. Mention how FUJIFILM Diosynth's mission aligns with your professional goals and values.

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Can you describe your experience with quality control processes and how it relates to this role?

Discuss specific quality control processes you've been involved with, emphasizing your familiarity with GMP and GLP standards. Provide examples of how your past experiences have prepared you for the responsibilities associated with the Quality Control Project Coordinator III position.

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How do you handle tight deadlines and ensure tasks are completed on time?

Emphasize your organizational skills and ability to prioritize tasks effectively. Share a time when you managed multiple priorities, ensuring you met all deadlines without compromising quality.

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What tools and software have you used for project management or scheduling, and how familiar are you with them?

Detail your experience with tools such as Microsoft Project or Laboratory Information Management Systems (LIMS). Explain how you've utilized these tools in your previous roles to enhance productivity and organization.

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Describe a situation where you had to communicate important updates to a team. How did you ensure clarity?

Provide an example where clear communication was essential. Discuss your approach to delivering information, using concise language and confirming understanding among team members.

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How do you ensure compliance with GMP guidelines in your work?

Discuss specific methods you use to stay informed about GMP regulations and your approach to ensuring compliance within quality control processes. Provide examples of how you’ve successfully implemented GMP practices in past positions.

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Can you give an example of how you have contributed to a team environment in a previous role?

Share a specific instance demonstrating your collaborative skills, emphasizing how your contributions helped the team meet its objectives. Highlight your ability to build rapport and foster teamwork.

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What challenges do you anticipate in this role, and how would you address them?

Recognize potential challenges such as changes in regulatory guidelines or unexpected testing results. Discuss strategies for addressing such issues proactively while maintaining flexibility and adaptability.

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How do you stay updated with industry best practices and advancements?

Mention your commitment to continuous learning through professional organizations, attending conferences, or engaging in relevant online courses. Highlight how this knowledge enhances your performance in quality control roles.

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Why do you believe you are a good fit for this position at FUJIFILM Diosynth Biotechnologies?

Summarize your key qualifications, relevant experience, and personal values aligned with FUJIFILM Diosynth's mission. Highlight your enthusiasm for contributing to innovative biopharmaceutical solutions.

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FUJIFILM Holdings no longer dwells only on the negatives. Its Imaging Solutions unit makes color photographic films and papers, digital cameras, photofinishing equipment, and chemicals. It leads the film market in Japan and has hammered away at ri...

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