Quality Assurance Specialist
Job in
New Castle, New Castle County, Delaware, 19721, USA
Listed on 2026-06-05
Listing for:
FUJIFILM Diosynth Biotechnologies
Full Time
position Listed on 2026-06-05
Job specializations:
-
Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager -
Manufacturing / Production
QA Specialist / Manager
Job Description & How to Apply Below
Position Overview
GENERAL PURPOSE
The Quality Assurance Specialist I is responsible for executing and supporting the routine QA systems at the Fujifilm New Castle site. This role ensures that all routine products consistently meet established business quality standards. The incumbent will manage documentation related to Controlled Documents, Management of Change (MOC), Training Records, Audits, and Sample Shipping. Additionally, the specialist will identify and escalate non-routine or non-compliance issues to the appropriate functional leads, maintaining strict adherence to quality protocols
NATURE OF POSITION
Reporting directly to the Quality Assurance Supervisor, this role supports all QA requirements across the New Castle production site. Key tasks include daily batch clearance of routine production products, conducting internal and external audits, responding to routine customer complaints, and identifying opportunities to enhance current QA systems. The Quality Assurance Specialist I will maintain comprehensive documentation for Quality Systems, identify system gaps or inefficiencies, and liaise cross-functionally with departments such as Supply Chain, Production Support, Quality Control, Operations, Engineering, customers, and suppliers.
Non-compliance matters or issues beyond routine scope will be escalated seamlessly to the QA Supervisor for resolution.
Company Overview
If you're ready to "think ink," FUJIFILM Imaging Colorants is the place for you! As part of Fujifilm's global Ink Solutions Group, we develop state-of-the-art aqueous dyes, pigment dispersions, and innovative inks for digital printing applications like packaging, commercial printing, and displays. We're driven by creativity and a dedication to quality, and we're looking for passionate problem-solvers to join the team.
We believe in investing in our people, offering a collaborative culture and a flexible environment to help you thrive. If you're ready to roll up your sleeves and help create solutions that make an impact, let's make a splash together!
Our manufacturing facility is in New Castle, Delaware, a lively town with rich history, open parks, museums, and a vibrant community that offers recreation and culture at every turn.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit:
Job Description
KEY RESPONSIBILITIES
* Execute routine batch clearance of base materials and finished products. This process includes but is not limited to the following day-to-day activities:
* Review internal QC and manufacturing process results for compliance against specification and following the approved batch clearance process. Ensure all QC and QA documentation is complete and auditable. Ensure all manufacturing paperwork is reviewed for legibility, completeness, and filed properly for final products.
* Perform routine physical inspection of finished goods prior to release.
* Review the control limits for final products and specifications of base material and final products and relay any issues to the QA Supervisor.
* Identify materials requiring formal batch review.
* Administer deviations of finished goods when necessary and progress with appropriate personnel (manufacturing, technical, QC, etc.) through to completion.
* Progress all non-conforming, questionable or non-routine issues to the QA Supervisor. Monitors non-RFT finished goods and documents appropriately.
* Manage the updating of QA status into SAP inventory records, generate and issue COA's, and arrange pre-shipment samples and shipping documentation as appropriate.
* Participate in internal and external audits.
* Support the MOC process by performing actions as assigned, maintaining records, and updating MOC documentation with batch status.
* Act as the administrator for document control and training systems. Review and update QA procedures and work instructions as they relate to routine production and business needs. Must be capable of evaluating existing systems and streamlining where…
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