Skip to main contentA logo with &quat;the muse&quat; in dark blue text.

Quality Specialist II - Records

AT Thermo Fisher Scientific
Thermo Fisher Scientific

Quality Specialist II - Records

Cincinnati, OH

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

The QA Specialist II will perform activities in support of disposition of product while ensuring compliance with Thermo Fisher directives and procedures, customer requirements, and regulatory standards. Performs Quality batch record and documentation review. Works with manufacturing and cross-functional team members to ensure deliverables are met to support release.

Essential Functions

  • Provide Quality expertise and oversight of the batch disposition process which includes assessment of documentation to ensure quality and compliance by site procedures and cGMPs.
  • Responsible for compilation and review of batch release documentation packages (BPR, LPR, COA/COC, etc.)
  • Daily interaction with cross-functional teams including but not limited to Planning, Operations, and Business Management to assist with troubleshooting, documentation corrections/notes, and guidance.
  • Aids in identification of continuous improvement opportunities; participates in practical process improvement initiatives.

Want more jobs like this?

Get jobs in Cincinnati, OH delivered to your inbox every week.

By signing up, you agree to our Terms of Service & Privacy Policy.

Education

  • Bachelor's degree, preferably in technology, engineering or microbiology, or related field preferred.
  • High school diploma or equivalent required.

Experience

  • 3+ Years Preferred with previous experience in cGMP or Pharmaceutical, Medical Device, or related manufacturing industry.

Equivalency:

  • Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skill, and Requirements

  • Proficiency in using technology and computers, including common software applications and tools, is required (Microsoft Office Applications, Microsoft Excel, SAP, TrackWise, etc.)
  • Knowledge of FDA/EMA regulatory requirements applicable to biologics or pharmaceuticals.
  • Knowledge of Quality oversight of batch disposition.
  • Excellent organizational skills and analytical and problem-solving abilities, strong verbal and writing skills and good interpersonal and leadership skills.
  • Possesses exceptional time management and multi-tasking abilities to meet commitments and deadlines.

#qualitycinci

Client-provided location(s): Cincinnati, OH, USA
Job ID: ThermoFisher-R-01299037
Employment Type: Full Time

Perks and Benefits

  • Health and Wellness

    • Health Insurance
    • Dental Insurance
    • Vision Insurance
    • Life Insurance
    • Short-Term Disability
    • Long-Term Disability
    • FSA
    • HSA
    • HSA With Employer Contribution
    • Mental Health Benefits
    • Fitness Subsidies
  • Parental Benefits

    • Adoption Leave
    • Birth Parent or Maternity Leave
    • Non-Birth Parent or Paternity Leave
    • Fertility Benefits
    • Adoption Assistance Program
    • Family Support Resources
  • Work Flexibility

    • Flexible Work Hours
    • Hybrid Work Opportunities
    • Remote Work Opportunities
  • Office Life and Perks

    • Commuter Benefits Program
    • On-Site Cafeteria
  • Vacation and Time Off

    • Paid Vacation
    • Paid Holidays
    • Volunteer Time Off
  • Financial and Retirement

    • 401(K) With Company Matching
    • Stock Purchase Program
    • Financial Counseling
    • Performance Bonus
  • Professional Development

    • Tuition Reimbursement
    • Access to Online Courses
    • Internship Program
    • Mentor Program
  • Diversity and Inclusion

    • Employee Resource Groups (ERG)
    • Diversity, Equity, and Inclusion Program