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Manufacturing Process Engineer I

Position Overview

Summary:  The Manufacturing Process Engineer I is an integral part of the Manufacturing Technical Operations department located in College Station, Texas.  This position will report directly to the Manager of Technical Operations, Manufacturing.

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:

Works independently and with colleagues to provide expertise and assistance for the design, development, standardization, and maintenance of an operational biotechnology utilized to manufacture various proteins and other drug substances.  This person would become the subject matter expert on core manufacturing and operational technologies for the manufacturing unit.  Operational biotechnologies include 1. USP: Isolators and biosafety cabinets and their use in cell propagation, Cell Culture/Single Use Technology for adherent and suspension culture; 2. DSP: Dispensing and Mixing and Buffer Preparation, Chromatography, Tangential Flow Filtration, various filtration technologies, centrifugation, and Bulk Fill.  This position will also create training programs and perform training for manufacturing technicians in the unit operation categories.

 

Develop and maintain equipment and unit operation standards and procedures utilizing the 4M (Man, Materials, Machinery, and Methods) approach, including:

 

(Man) Develop and deliver practical skill-building and training plans for a given operational technology to manufacturing technicians.

  • Collaborate with individuals and teams of technicians & managers on self-development plans.
  • Responsible for interfacing with internal/external technical experts and peers to maintain a broad knowledge of the technology and regulatory issues that impact the biopharmaceutical business, enabling technology options to be identified, evaluated and compared.
  • Responsible for specifying, purchasing, designing, qualifying, and handing over effective manufacturing systems, ensuring plant modifications have credible delivery plans.
  • Implement e-learning, video, classroom, and in-suite design and delivery as appropriate.
  • Take the lead in investigating and resolving events that arise from compliance issues.
  • Assist in identifying improvement to and managing change in technology transfer practices to deliver continuous improvements.
  • Create and maintain the technical training manuals and personnel certification process.
  • Develop and ensure training and skill-building activities align to site business requirements.
  • Assure local operational practice reflect local procedure and instruction.
  • Provide guidance and direction on cross-functional training initiatives.

 

(Materials) Understand process control and material inputs to ensure capable and acceptable process output.

 

  • Ensure supplies are in place to execute water runs and Engineering Test Plans/Studies.

 

(Machinery) Understand technology operation capabilities, limits, and control strategies.

  • Review and/or Approve equipment qualification limits.
  • Review Calibration Tolerances and Approve Out of Tolerance Investigations
  • Coordinate validation, calibration, and PM completion of manufacturing lab equipment
  • Creation and or revision of recipes or methods for various platforms.
  • Represent the manufacturing unit for equipment purchase, new technology, and changes to equipment.

(Methods) Develop and maintain Technical Operational Manuals/Standard Operating Procedures/Work Instructions/Batch Records.

  • Lead operational technology standardization, standard batch templates, and instruction interfaces and lead continuous improvement for a given technology.
  • Assist in transferring and scaling new processes and technologies to the manufacturing plant, ensuring requirements for EHS and cGMP compliance.
  • Ensure procedures are in place to execute water runs and Engineering Test Plans/Studies
  • Interface with Process Development and Process Science to ensure a smooth transfer of processes into the manufacturing plant.
  • Develop and approve procedures and batch records.
  • Author URS (user requirement specification) documents
  • Ensure best practice operating methods are deployed and assist in resolving operational problems such as deviations, QIPs, CAPAs, change controls, etc.
  • Review and approve batch records, process validation protocols, process specifications, BOMs, campaign summary reports, and other documentation.

 

All other duties as may be assigned.

 

Required Skills & Abilities:

  • Excellent oral and written communication skills and interpersonal and organizational skills.
  • Strong leadership skills.
  • Ability to train others to perform to cGMP standards.
  • Proficient with Microsoft Office applications.
  • Good self-discipline and attention to detail; ability to work under minimal supervision.
  • Must have flexible work hours –willing to work outside of normally-scheduled hours, including opportunities for alternative shift hours and weekends as required.
  • Experience working in cleanroom environments under sterile or aseptic conditions; must have experience in engineering standards required for this type of operation.
  • Must have good planning skills and be willing to interface with and guide colleagues in many different roles and functions throughout the manufacturing facilities.

Working Conditions & Physical Requirements:

 

An employee must meet the physical demands described here to perform the essential functions of this job successfully.  Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.  While performing the duties of this job, the employee is regularly required to:

 

  • Experience prolonged standing, some bending, stooping, pushing, pulling, reaching above shoulders, and stretching.
  • Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment.
  • Lift up to 25 pounds frequently and up to 50 pounds occasionally.
  • Attendance is mandatory. This is a manufacturing support position. Work remotely is only allowed occasionally with previous coordination and management approval. (90% on the side; 10% from home). 
  • This position requires being on-call or on-site during critical manufacturing activities.

 

 

 

Minimum Qualifications:

  • Bachelor’s degree in Science, Engineering, or other related field and one (1) year of biotech manufacturing experience; OR
  • Associate degree in Science, Engineering, or other related field and two (2) years of biotech manufacturing experience; OR
  • High School/GED with four (4) years of biotech manufacturing experience
  • All above must have one (1) year of GMP experience

Preferred Qualifications:

  • Previous Process Engineering experience
  • Experience in developing training materials
  • Experience conducting and evaluating training
  • Experience with laboratory and or manufacturing instruments/equipment
  • Previous leadership roles
  • GMP experience

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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What You Should Know About Manufacturing Process Engineer I, FUJIFILM

Are you ready to step into a pivotal role as a Manufacturing Process Engineer I with FUJIFILM Diosynth Biotechnologies in College Station? In this exciting position, you’ll be at the heart of our Manufacturing Technical Operations department, working closely with a passionate team dedicated to developing innovative biopharmaceutical solutions. Your expertise will shape the operational biotechnology processes, specifically focusing on key manufacturing technologies such as cell culture, chromatography, and filtration systems. Not only will you be responsible for the design and maintenance of these systems, but you will also become the go-to expert and mentor for manufacturing technicians, enhancing their skills with tailored training programs. At FUJIFILM Diosynth Biotechnologies, we believe in nurturing a culture that inspires creativity and dedication, allowing you to thrive while making a difference in the biopharmaceutical industry. College Station, a charming university town, offers a vibrant lifestyle and is perfectly positioned in the hub of Texas innovation, making it an ideal location for both personal and professional growth. If you’re looking for a meaningful career at a company driven by mission and collaboration, this Manufacturing Process Engineer I position at FUJIFILM Diosynth Biotechnologies could be the perfect fit for you!

Frequently Asked Questions (FAQs) for Manufacturing Process Engineer I Role at FUJIFILM
What are the key responsibilities of a Manufacturing Process Engineer I at FUJIFILM Diosynth Biotechnologies?

As a Manufacturing Process Engineer I at FUJIFILM Diosynth Biotechnologies, your primary responsibilities will include designing, developing, and maintaining operational biotechnologies. This involves becoming an expert in manufacturing technologies, creating training programs for technicians, and ensuring compliance with cGMP standards. You'll collaborate with diverse teams, manage equipment specifications, and oversee the execution of engineering test plans, making a significant impact on our manufacturing processes.

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What qualifications do I need to become a Manufacturing Process Engineer I at FUJIFILM Diosynth Biotechnologies?

To qualify for the Manufacturing Process Engineer I position at FUJIFILM Diosynth Biotechnologies, you should have a Bachelor’s degree in Science or Engineering along with at least one year of biotech manufacturing experience. Alternatively, you could have an Associate degree with two years of experience, or a High School diploma with four years of relevant experience. Previous experience in process engineering and GMP compliance is preferred but not mandatory.

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What opportunities for advancement exist for a Manufacturing Process Engineer I at FUJIFILM Diosynth Biotechnologies?

At FUJIFILM Diosynth Biotechnologies, a Manufacturing Process Engineer I has ample opportunities for career advancement. Your performance in this role can lead to higher-level engineering positions or specialized roles in process development or technical operations. The company also encourages continuous learning and development through training programs, paving the way for personal and professional growth within the organization.

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How does FUJIFILM Diosynth Biotechnologies promote a positive work culture for Manufacturing Process Engineers?

FUJIFILM Diosynth Biotechnologies fosters a vibrant and inclusive workplace culture that encourages collaboration, creativity, and passion. Manufacturing Process Engineers are supported in their roles through mentorship opportunities, team collaboration, and a commitment to personal and professional development. The unique culture, known as Genki, instills a sense of pride and camaraderie among employees, enhancing job satisfaction and overall engagement.

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What skills are essential for success as a Manufacturing Process Engineer I in College Station?

Success as a Manufacturing Process Engineer I at FUJIFILM Diosynth Biotechnologies entails having excellent communication and interpersonal skills, strong leadership capabilities, and the ability to work independently with a keen attention to detail. Proficiency in Microsoft Office applications, coupled with a solid understanding of cleanroom environments and engineering standards, will also set you apart in this dynamic role.

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Common Interview Questions for Manufacturing Process Engineer I
Can you describe your experience in biotech manufacturing?

In response, highlight your relevant positions, the responsibilities you undertook, and any specific technologies you worked with. Make sure to detail your experience with cGMP standards, training programs, and any improvements you implemented in past roles.

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How do you ensure compliance with regulatory standards in manufacturing?

Discuss your understanding of cGMP and related regulations. Provide examples of how you've maintained compliance in previous roles, such as conducting audits, documenting procedures, and maintaining equipment according to established protocols.

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Describe a time when you had to troubleshoot a production issue.

Offer a specific instance where you identified a problem, your method for troubleshooting it, and the successful resolution you achieved. This showcases your problem-solving skills, your ability to work under pressure, and your proactive approach.

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What training or mentorship experience do you have?

Detail your experience in creating and delivering training programs. Mention the types of materials you developed and how you assessed the effectiveness of the training to ensure colleagues were well-prepared to operate under cGMP standards.

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What methods do you use for maintaining operational efficiency?

Talk about your understanding of operational best practices, such as using the 4M approach (Man, Materials, Machinery, and Methods). Provide examples of how you've used these principles to identify inefficiencies and implement improvements.

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How do you manage change in technology transfer?

Explain your approach to facilitating technology transfers by highlighting your communication skills, coordination with cross-functional teams, and techniques for ensuring smooth transitions while adhering to compliance and operational standards.

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How do you assess the performance of manufacturing systems?

Discuss your experience with metrics and KPIs that you use to evaluate system performance. Give examples of how you have monitored these indicators and made recommendations for enhancements based on your assessments.

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Describe your experience with operational biotechnologies used in manufacturing.

Detail your specialization in areas like USP, DSP technologies, and other manufacturing processes. Discuss your familiarity with specific equipment and how you've applied this knowledge in practical settings.

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What steps do you take to ensure safety in the manufacturing environment?

Share your commitment to safety by discussing the protocols you follow, your role in training others on these standards, and any safety initiatives you introduced in past positions to promote a safer workplace.

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Why do you want to work at FUJIFILM Diosynth Biotechnologies?

Express your enthusiasm for the biopharmaceutical industry, the company's mission, and culture. Discuss how your professional goals align with their vision and the impact you hope to have as a Manufacturing Process Engineer I.

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Full-time, hybrid
DATE POSTED
April 16, 2025

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