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Quality Assurance Compliance - Sr. Specialist - Audit and Inspection

FUJIFILM Diosynth Biotechnologies
College Station, TX
Start date
Sep 12, 2022

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Clinical, Clinical Medicine, Regulatory, Legal/Compliance
Required Education
Bachelors Degree
Position Type
Full time
Lone Star Bio
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Job Details

  The Quality Assurance – Sr. Compliance Specialist – Audit and Inspection, will support all associated audit responsibilities in compliance with FUJIFILM Diosynth Biotechnologies quality policies and site SOPs to ensure regulatory compliance.

External US

Essential Functions:


Compliance Delivery


  • QA support to the organization in conducting internal audits to determine suitability, effectiveness, and compliance with applicable standards and regulations.
  • Displays critical thinking expertise, with the ability to define and implement a strategic approach to audit- based on compliance and business knowledge.
  • Support client due diligence and Quality audits as well as regulatory inspections if needed.
  • Work with Quality management to ensure quality systems support cGMP manufacturing of pre-clinical to commercial products.
  • Ensure the company Internal Audit program complies with regulatory standard and internal audits are executed within the fiscal year.
  • Provide cGMP guidance to other functions such as Manufacturing, Facilities and QC, Warehouse and Validations.
  • Support Site Readiness Preparation for Regulatory Inspections.
  • Staying aware and up to date with agency regulations, guidance documents, and industry best practices, to ensure Fujifilm, Texas is held to current standards
  • Supporting Lessons Learned from audit/inspection findings to benefit other sites
  • Execute audit strategy and lead process audits
  • Act as a reviewer of audit reports from internal audits
  • Provides support during regulatory inspections or customer audits as requested by the company, before, during and/or after the event.
  • Promptly notify Senior Management of potential quality or regulatory issues encountered during internal audits.
  • Promptly notify Senior Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.
  • Works on complex problems in which analysis of situations or data requires in-depth evaluation of various factors from many sources. Is adept at interpreting GMP regulations in the resolution of problems and in the design of systems, processes or procedures.
  • Ability to effectively plan, organize, and execute work that ensures deliverables are consistently met.
  • Ensure self-have no overdue training, or site actions. Support other QA teams and other functions in completion of site actions.



  • Work collaboratively with site management to instill a ‘Quality Culture' by coaching in the application of GMP Principles including the underlying rational of those principles.
  • Mentor peers towards achieving organizational and individual goals.
  • All other duties as assigned.

Required Skills & Abilities:


  • Excellent written and oral communication skills.
  • Excellent organizational, analytical, data review and report writing skills.
  • Ability to set personal performance goals and provide input to departmental objectives.
  • Ability to multitask and easily prioritize work.

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.
  • Ability to sit for long periods to work on a computer.
  • Potential for exposure to chemicals, gases, fumes, odors, dusts, and other hazardous materials.
  • Ability to wear personal protective equipment including but not limited to safety glasses, lab coat, gloves, specialized clothing including laboratory scrubs (pants and shirt), cleanroom (ISO 8 to ISO 5) gowning material and appropriate shoes required in most areas associated with this position.
  • Lifting up to 25 pounds on occasion.
  • Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required.
  • Must be willing to work flexible hours.
  • Ability to work weekends and off-shift hours, as needed to support manufacturing activities.
  • Must be willing to travel occasionally, as needed.
  • Attendance is mandatory.



  • Bachelor's degree preferably in a science-related field with 6 -8 years of related experience
  • At least four (4) years of cGMP experience in a Quality/Compliance role.


Preferred Qualifications:

  • Certified Quality Auditor
  • Degree in Biology, Chemistry or Engineering
  • Supervisory/leadership experience

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 979-431-3528.




FUJIFILM Diosynth Biotechnologies is an industry leading cGMP Contract Development and Manufacturing Organization (CDMO) supporting our partners in the biopharmaceutical industry with the development and production of their biologic, vaccines and gene therapies.

With over 30 years of experience in process development and cGMP manufacturing, a dedicated staff of over 2,000 and a reputation for excellent customer service, flexibility and responsiveness, we’ve become a trusted partner to some of the most prominent biotech developers and pharmaceutical companies in the industry.

Our Process Development experience includes the development of processes for molecules expressed via fermentation (e.g., E. coli, P. pastoris), cell culture systems including CHO, HEK, Vero, MDCK, EB66 and insect cells, and from transgenic sources.

Our network expands within five development and manufacturing facilities located in Teesside, United Kingdom; Research Triangle Park, North Carolina, USA; College Station, Texas, Thousand Oaks CA USA and Hillerød, Denmark.


Find Us
Thousand Oaks, CA
Research Triangle Park, NC
College Station, TX
Holly Springs, NC
Watertown, MA
United States
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