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Hiring Quality Assurance – Supervisor, Operations

FUJIFILM Diosynth Biotechnologies

This is a Full-time position in College Station, TX posted June 21, 2021.


Summary: The Quality Assurance (QA) Supervisor of Operations will be responsible for the overall performance of a team of Quality Assurance Analysts, ensuring appropriate scheduling and training as well as ensuring that all work generated by the team is accurate, complete and in conformance with Fujifilm policies and procedures.

External US

Essential Functions:
LeadershipThe Quality Assurance Supervisor shall have oversight or more of one of the following areas:Deviation ManagementBatch Record ReviewManufacturing Quality
Incoming Quality
Demonstrates ability to problem solve and effectively communicate quality issues across multiple functions.Develop, motivate and lead direct reports towards achieving organizational and individual goals.
Provide strong guidance in the personal development of direct reports.
Operational DeliveryEnsure appropriate tracking and timely resolution of quality issues (Deviations, Corrective/Preventive Actions and Change Controls).Ensure Appropriate Organization and Control of In Process DocumentationTimely review / approval of basic and technical documentation to include, but not limited to:Standard Operating ProceduresWork InstructionsBatch Production Records
QC data review and approval
ComplianceEnsure self, and team, have no overdue training, or site actions.

Support other QA teams and other functions in completion of site actions.Continuously improve the processes specified in Standard Operating Procedures and Work Instructions operated by self and direct reports whilst still ensuring the operations meet all current regulatory requirements.Provide GMP guidance to other site departments such as Manufacturing, Facilities, and QC
Prompt notification of Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.
All other duties as assigned.
Required Skills & Abilities:
Apply knowledge of and adhere to cGMPs, company Quality Policies and site SOPs on a daily basis, as applicable.Excellent written and oral communication skills.Excellent organization, detail oriented and accurate.Self-motivated with a drive for excellence.Positive attitude and strong interpersonal skills.Creative independent thinking and can work with minimal supervision following internal procedures .Resilient through operational and organizational change.Exceptional planning and organizational skills and the ability to multi-task and meet deadlines is requiredProven effective teamwork skills: able to adapt to diverse interpersonal styles.Develop staff to maximize contributions to the team and the company.Interacts with all departmental staff, including giving training and / or presentations to small and large groups.Proficient with Microsoft Office products (Excel, Word, and PowerPoint).
Preferred Experience, Behavioral Competencies, Skills & Abilities:
Excellent presentation skills.

Author and/or update standard operating procedures, work instructions, or policies.Experience with Google Sheets, SmartSheets, and Microsoft SharePointExperience with the following applications: Trackwise, MasterControl, ComplianceWire, SAP, Blue Mountain Regulatory Asset Manager (BMRAM), MODA, Delta-V.
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 stretchingAbility to sit for long periods to work on a computerPotential for exposure to chemical, 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 hoursAbility to work weekends and off-shift hours, as needed to support manufacturing activities.Attendance is mandatory
Bachelor’s degree in related science concentration with 6 years of experience in Quality Assurance supporting pharmaceutical, biopharmaceutical or biotechnology products; ORMaster’s degree in related science concentration with 4 years of experience in Quality Assurance supporting pharmaceutical, biopharmaceutical or biotechnology products.At least 4 years of cGMP experience.
Preferred Qualifications:
Certified Quality AuditorDegree in Biology or Chemistry
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 e-mail or call 979-431-3500.

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