QA Analyst III

Fujifilm; College Station (TX); On-site; USD 65,000 - 85,000; Full time

Job summary

Fujifilm is seeking a Quality Assurance (QA) Analyst III in College Station, TX to oversee documentation, quality audits, and compliance with standards. Candidates should possess relevant experience in pharmaceutical industries, with an emphasis on quality audits and regulatory support.

This position requires strong communication, organizational, and analytical skills, alongside a relevant degree. Join us to help ensure product quality and compliance.

Qualifications

• Master’s Degree and 1+ years’ experience in Pharmaceutical or other regulated industry.
• Bachelor’s degree and 3+ years’ experience in Pharmaceutical or other regulated industry.
• Associates Degree and 5+ years’ experience in Pharmaceutical or other regulated industry.
• High school or equivalent and 8+ years’ experience in Pharmaceutical or other regulated industry.
• Certified Quality Auditor preferred.

Responsibilities

• Review and/or approve technical documentation with minimal supervisory oversight.
• Draft and review internal Quality policies and procedures.
• Perform Quality audit functions and identify process improvement opportunities.
• Act as QA liaison to departments and external client Quality groups.
• Support regulatory audits and notify Senior Management of compliance issues.

Skills

Excellent written and oral communication skills

Excellent organizational skills

Analytical skills

Proficiency in Microsoft Excel

Proficiency in Microsoft Word

Proficiency in Microsoft PowerPoint

Education

Master's Degree in Pharmaceutical or regulated industry

Bachelor's Degree in Pharmaceutical or regulated industry

Associate's Degree in Pharmaceutical or regulated industry

High school or equivalent in Pharmaceutical or regulated industry

Job description

Position Overview

The Quality Assurance (QA) Analyst III, under minimal direction, will be responsible for review and/or approval of basic and technical documentation, drafting and reviewing of internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally.

Job Description

Reports to: Director, Quality Assurance/Senior Manager, Quality Assurance

Work Location: College Station, TX (On-site at NCTM building)

Primary Responsibilities

• Review and/or approve basic and technical documentation with minimal supervisory oversight to include, but not limited to:
  • Standard Operating Procedures
  • Batch Production Records (completed and approval)
  • Commissioning, qualification and validation protocols and reports
  • Deviation Reports
  • Corrective Action/Preventive Action Plans
  • Technical data review and approval
  • QC data review and approval
  • Drug Substance/Product Reports
  • Trending QA data
• Draft and review internal Quality policies, procedures, and reports.
• Perform inspection of final product containers and review and/or approval of executed process records and data.
• Perform Quality audit functions to include, but not limited to:
  • Audit of lab notebooks
  • Audit of equipment logbooks
  • Review of vendor, supplier, contract laboratory audit questionnaires
  • Lead vendor, supplier, contract laboratory and client audits
  • Identify process and Quality System improvement opportunities.
• Provide daily guidance for the compliance of the QA department to national and international standards and regulations.
• Support Regulatory, client, and internal audits.
• Act as QA liaison to internal Departments and external Client Quality Groups and Vendor/Contract Laboratory Quality Groups.
• Promptly notify Senior Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.
• Assist with technical oversight/training for the QA team.
• Assist with compliance related functions.
• All other duties as assigned.

Qualifications

• Master’s Degree and 1+ years’ experience in Pharmaceutical or other regulated industry.
• Bachelor’s degree and 3+ years’ experience in Pharmaceutical or other regulated industry.
• Associates Degree and 5+ years’ experience in Pharmaceutical or other regulated industry.
• High school or equivalent and 8+ years’ experience in Pharmaceutical or other regulated industry.
• Certified Quality Auditor preferred.
• Degree in Biology or Chemistry preferred.
• 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 your work.
• Ability to work independently with little supervision.
• Proficient in Microsoft Excel, Word and PowerPoint.
• All candidates must have a working knowledge of cGMP regulations for the production of drug, biologics or vaccine products.
• Role model for company core values of trust, delighting our customers, and Gemba.

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.
• 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.
• Attendance is mandatory.

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 ([e-mail] or [phone]).