Minimum of 5 years of relevant experience in quality assurance, compliance, training, or data evaluation
Strong analytical skills with attention to detail and the ability to assess risks and maintain quality standards
Working knowledge of industry regulations and audit procedures
Ability to interpret and apply guidelines and standards consistently across processes
Excellent written and verbal communication skills
Experience facilitating audits or regulatory inspections
Comfortable working within a structured environment with defined procedures and performance metrics
Job Duties :
Support the development and execution of evaluation standards and calibration activities
Implement and enforce quality control procedures across various stages of the process (e.g., lab studies, clinical research, operations, raw materials, production, and finished products or services)
Monitor compliance and assess potential risks; provide recommendations for corrective actions
Take full ownership of quality assurance processes to ensure adherence to internal and external standards
Facilitate audits and regulatory inspections by preparing documentation and ensuring operational readiness
Ensure consistent application of standards across teams and identify discrepancies or gaps
Use defined guidelines, procedures, and previous experience to make informed decisions and solve problems
Collaborate with cross-functional teams to align subject matter expertise and support continuous improvement efforts
Industry :
Medical Device Manufacturing
Estimated Start Date :
9 / 2 / 2025
Only those lawfully authorized to work in the designated country associated with the position will be considered.
Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.