Quality Assurance Specialist

3 days ago


Concord, New Hampshire, United States Oxford Global Resources Full time
Job Summary:
As a Quality Assurance Consultant at Oxford Global Resources, you will play a critical role in ensuring the quality and compliance of our manufacturing processes. This includes reviewing and approving manufacturing records, change controls, investigations, and analytical data. You will also be responsible for reviewing and approving test methods and method validations, as well as manufacturing validation protocols and reports.

Key Responsibilities:
Review and approve manufacturing records, change controls, investigations, and analytical data
Review and approve test methods and method validations
Review manufacturing validation protocols and reports
Collaborate with cross-functional teams to ensure quality and compliance

Requirements:
Bachelor's degree in Engineering, Chemistry, Biology, or related discipline
Minimum 5+ years' experience in Quality Assurance in a Medical Device and/or Pharmaceutical company
Knowledge and experience in CAPA, Root Cause Investigation, Validation, Environmental Monitoring, and Manufacturing Operations
Excellent verbal and written communication skills
Ability to effectively collaborate and partner with all levels of management

Language Required:
English
Oxford Global Resources is an Equal Employment Opportunity Employer. We consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. We provide a comprehensive benefits package, including medical, dental, vision, life, and disability insurance, as well as a 401(k) Retirement Savings Plan. Paid holidays and sick leave are also provided.

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