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QC Sample Receipt Analyst III

Position Overview

Summary:  The Sample Management Analyst III, under general direction, will be responsible for performing routine and non-routine support of samples submitted to the Quality Control (QC) Laboratory for evaluation. This position works as part of the Sample Management team to manage the receipt, organization and inventory of samples from manufacturing, clients, other Fujifilm facilities and third parties. The Sample Management Analyst III arranges sample shipments for outsource testing and shipments to Clients or other facilities and controls dispensing of samples for QC testing.  

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

Primary Responsibilities:

  • Follow Standard Operating Procedures (SOPs) and other related Good Laboratory Practices. (GLP)/Good Manufacturing Practices (GMP).
  • Manage test samples, critical reagents and reference materials.
  • Perform shipments to external testing facilities and clients.
  • Responsible for cleaning Sample Management laboratories and stocking with necessary supplies. Able to order supplies when needed.
  • Maintaining inventory.
  • Fulfill QC Analyst sample requests.
  • Stability coordination.
  • Train new hires.
  • Practices (GLP)/Good Manufacturing Practices (GMP) documentation.
  • Technical Writing to include:
    • Writes and revises Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP) documentation as appropriate.
    • Lead the initiation and closure of deviations, CAPAs and Change Controls.
  • Discuss inventory requests with Project Managers
  • Ability to work independently, along with ability to work well within a team.
  • Ensure samples are put into SmartQC for testing.
  • Acknowledge DeltaV alarms for chambers.
  • Ensure laboratory equipment is functioning properly, and submit order works if needed.
  • Previous pipetting experience.
  • Perform other duties as assigned.

Required Skills & Abilities:

  • Ability to build and foster relationships, cooperation, and collaboration across the organization.
  • Aptitude to follow safety procedures outlined in the Chemical Hygiene Plan.
  • Utilize SDS sheets to properly assess chemical hazards, spill response procedures, and PPE requirements if indicated.
  • Excellent attention to detail.
  • Computer proficiency required.
  • Ability to accurately complete required documentation.
  • Excellent written and oral communication skills.
  • Excellent organization and analytical 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.
  • Lift up to 15 lbs regularly and up to 30 lbs on occasion.
  • Potential for exposure to hazardous chemicals, gases, fumes, odors, mists, and dusts, and other hazardous materials.
  • Ability to wear personal protective equipment including safety glasses, lab coat, gloves, specialized clothing including laboratory scrubs (pants and shirt) and appropriate shoes required in most areas associated with this position.
  • Attendance is mandatory

Minimum Qualifications:

  • High School Diploma or GED, AND at least four (4) years of relevant GMP Experience OR;
  • Associate’s degree preferably in Biochemistry, Chemistry, Biology or related field AND at least two (2) years of relevant GMP Experience OR;
  • Bachelor’s degree preferably in Biochemistry, Chemistry, Biology or related field AND at least one (1) years of relevant GMP Experience OR;
  • Master’s degree preferably in Biochemistry, Chemistry, Biology or related field AND at least one (1) year of relevant GMP Experience

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

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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CEO of FUJIFILM
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Average salary estimate

$70000 / YEARLY (est.)
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$60000K
$80000K

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What You Should Know About QC Sample Receipt Analyst III, FUJIFILM

Are you passionate about quality control in the biotechnology sector? Join FUJIFILM Diosynth Biotechnologies as a QC Sample Receipt Analyst III in College Station! In this exciting role, you'll be an essential part of our Sample Management team, overseeing the receipt, organization, and inventory of samples arriving at our Quality Control (QC) Laboratory for evaluation. You'll perform both routine and non-routine support functions while ensuring compliance with standard operating procedures and good manufacturing practices. Managing shipments for outsource testing and handling sample requests will be part of your daily activities, as will maintaining a clean and well-stocked laboratory. We value collaboration, and as a QC Sample Receipt Analyst III, you’ll have the opportunity to train new hires, write and revise documentation, and discuss inventory requests with project managers. With a strong focus on detail and excellent communication skills, you’ll thrive in our dynamic work environment where innovation and passion meet. College Station is not just a great place to work; it's a vibrant community with a rich cultural scene and access to Texas' major cities. Come be a part of something bigger with FUJIFILM, where you can contribute to groundbreaking work in vaccines and therapies that truly make a difference in people's lives.

Frequently Asked Questions (FAQs) for QC Sample Receipt Analyst III Role at FUJIFILM
What are the primary responsibilities of a QC Sample Receipt Analyst III at FUJIFILM Diosynth Biotechnologies?

As a QC Sample Receipt Analyst III at FUJIFILM Diosynth Biotechnologies, your primary responsibilities include managing the receipt and organization of samples, performing shipments to external testing facilities and clients, cleaning and maintaining the Sample Management laboratories, training new hires, and ensuring all procedures comply with Good Manufacturing Practices (GMP). You'll also need to handle inventory requests and ensure that samples are recorded accurately in SmartQC for testing.

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What are the required qualifications for the QC Sample Receipt Analyst III position at FUJIFILM Diosynth Biotechnologies?

To qualify for the QC Sample Receipt Analyst III position at FUJIFILM Diosynth Biotechnologies, candidates should have a relevant background in biochemistry, chemistry, or biology, with a minimum of one to four years of relevant GMP experience based on the level of education. A bachelor's degree or higher in a related field is preferred, along with strong attention to detail, organizational skills, and proficiency in computer systems.

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What skills are essential for success as a QC Sample Receipt Analyst III at FUJIFILM Diosynth Biotechnologies?

Essential skills for success as a QC Sample Receipt Analyst III at FUJIFILM Diosynth Biotechnologies include excellent organizational skills, attention to detail, strong written and verbal communication skills, and the ability to work both independently and as part of a team. Familiarity with GMP compliance and a good understanding of laboratory safety protocols are also critical.

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How does the QC Sample Receipt Analyst III position contribute to the overall mission of FUJIFILM Diosynth Biotechnologies?

The role of a QC Sample Receipt Analyst III is crucial in ensuring that the samples submitted for testing are managed effectively and comply with industry standards. By maintaining high-quality control practices, this position directly supports FUJIFILM Diosynth Biotechnologies' mission of delivering innovative biopharmaceutical solutions and contributes to the creation of life-saving therapies.

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What is the work environment like for a QC Sample Receipt Analyst III at FUJIFILM Diosynth Biotechnologies?

The work environment for a QC Sample Receipt Analyst III at FUJIFILM Diosynth Biotechnologies is collaborative and focused on innovation. Employees work within a clean, organized laboratory, where safety and efficiency are top priorities. The culture emphasizes teamwork, personal growth, and a shared mission to impact healthcare positively. College Station offers a blend of small-town convenience with access to larger cities, making it an appealing place to work.

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Common Interview Questions for QC Sample Receipt Analyst III
What motivates you to work in quality control within the biotechnology industry?

In answering this question, focus on your passion for ensuring product quality and safety in biotechnology. You can mention the importance of contributing to medical advancements and how being part of a team that impacts people's lives drives your motivation.

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How do you manage and prioritize your tasks when working with multiple samples?

To effectively manage multiple tasks, discuss your organizational skills and techniques such as using checklists, setting deadlines, or utilizing software systems to track inventory and sample requests. Emphasize your ability to adapt and remain flexible in a dynamic environment.

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Can you provide an example of a time you had to solve a problem related to sample management?

For this question, describe a specific scenario where you identified an issue, the steps you took to resolve it, and the outcome. Use this as an opportunity to showcase your analytical skills and ability to work under pressure.

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How do you ensure compliance with Good Manufacturing Practices (GMP)?

Discuss your knowledge of GMP guidelines and how you adhere to them in your daily tasks. Share examples of documentation you maintain, your attention to detail, and any experiences where you worked to improve compliance within a team setting.

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What experience do you have with technical writing for SOPs or GMP documentation?

Explain your background in technical writing, highlighting any relevant experiences in drafting, revising, or implementing SOPs. Mention any specific projects where your writing contributed to workplace efficiency or compliance.

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How do you handle deviations from standard operating procedures?

In your response, emphasize the importance of proper documentation and communication when handling deviations. Describe the processes you follow to ensure that deviations are recorded, reported, and resolved in a timely manner, and how you involve your team in this process.

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Describe your experience with sample inventory management.

Share specific instances where you've managed sample inventories, discussing the systems or tools used to track samples. Highlight your attention to detail, organizational skills, and any improvements you've implemented in your past roles.

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How do you prioritize sample shipments and ensure timely delivery?

Explain your process for managing shipment priorities based on urgency and the requirements of the client or testing facility. Discuss how you communicate with stakeholders to ensure everyone is aligned on timelines.

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What safety procedures have you followed in laboratory settings?

Highlight your familiarity with safety protocols, such as wearing personal protective equipment and following chemical hygiene plans. Mention any training you've received and how you incorporate safety into your daily routines.

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Why do you think teamwork is important in the role of a QC Sample Receipt Analyst III?

Emphasize that collaboration enhances problem-solving and fuels innovation. Share examples of how teamwork has positively impacted projects you've worked on and how you aim to foster a cooperative environment within the Sample Management team.

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