Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Job Description
Key Responsibilities:
- Perform incoming inspection of raw materials to ensure flawless quality.
- Conduct in-process control of CDR manufacturing lines to maintain outstanding standards.
- Handle non-conformances and investigate issues with the support of Quality Engineers.
- Review Device History Records (DHR) and release products for delivery.
- Collect statistical data to resolve trends and improve processes.
Requirements/Qualifications:- Familiarity with ISO13485:2016 Quality management system.
- QA/QC experience in the IVD (In Vitro Diagnostics) industry is preferred.
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Client-provided location(s): China
Job ID: ThermoFisher-R-01256602-1
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
