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The role involves supporting quality assurance and operations by implementing and maintaining quality standards for products and services. The position requires specialized skills in quality control, adherence to regulatory guidelines, and operational processes.
Job Responsibility:
Develop and implement quality programs to maintain and improve product and service standards
Establish policies, procedures, and methods for checking and enhancing quality
Ensure compliance with GLP/GCP/cGMP and global Drug and Device Development processes
Support operations by executing tasks using specialized knowledge in an operational process area
Adhere to Standard Operating Procedures (SOPs) and quality guidelines
Maintain appropriate licenses, training, and certifications as required
Perform routine and some non-routine tasks within the department
Requirements:
1-2 years of experience reading drawings and using measuring tools like calipers, rulers, and vision systems (preferred)
Experience working within quality assurance and regulatory compliance frameworks (preferred)
Basic knowledge of operating procedures for a specific functional area
Understanding of quality systems and regulatory compliance
Strong attention to detail and adherence to SOPs
Excellent communication and interpersonal skills
Ability to work with a high degree of supervision and minimal discretion
Organized and self-motivated
High School diploma or GED required
Knowledge of GLP/GCP/cGMP standards is an advantage
Training or certifications in quality assurance and operational processes preferred
Nice to have:
1-2 years of experience reading drawings and using measuring tools like calipers, rulers, and vision systems (preferred)
Experience working within quality assurance and regulatory compliance frameworks (preferred)
Knowledge of GLP/GCP/cGMP standards is an advantage
Training or certifications in quality assurance and operational processes preferred