Lee Hecht Harrison Nederland B.V.
Quality Assurance Analyst
Lee Hecht Harrison Nederland B.V., San Francisco, California, United States, 94199
Job Posting: Quality Assurance SpecialistLocation:
San Francisco, CAPay:
$37hr to $41hr depending on experience levelPosition:
Full-time, OnsiteShift:
Monday - Friday, 09:00 AM - 05:00 PMJob Description:
We are seeking an experienced and detail-oriented Quality Assurance Specialist to join our team. This role is crucial in ensuring the quality and compliance of our products in a regulated industry. The successful candidate will demonstrate independence, strong decision-making skills, and a thorough understanding of relevant regulations.Key Responsibilities:Ensure adherence to quality standards and regulatory requirements in an FDA-regulated environment.Conduct thorough inspections and evaluations to identify issues and implement solutions.Maintain up-to-date knowledge of Federal and State regulations and policies.Communicate effectively, both orally and in writing, with internal teams and stakeholders.Manage multiple tasks efficiently, prioritizing work and adapting to changing priorities.Operate and utilize computer software for data retrieval, storage, and merging.Qualifications:Experience:
At least 5 years in a quality role within an FDA-regulated industry such as cell therapy, biotechnology, pharmaceuticals, or medical devices.Education:
Bachelor’s degree in a related field or equivalent experience/training.Pay Details:
$37.00 to $41.00 per hourEqual Opportunity Employer/Veterans/Disabled
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San Francisco, CAPay:
$37hr to $41hr depending on experience levelPosition:
Full-time, OnsiteShift:
Monday - Friday, 09:00 AM - 05:00 PMJob Description:
We are seeking an experienced and detail-oriented Quality Assurance Specialist to join our team. This role is crucial in ensuring the quality and compliance of our products in a regulated industry. The successful candidate will demonstrate independence, strong decision-making skills, and a thorough understanding of relevant regulations.Key Responsibilities:Ensure adherence to quality standards and regulatory requirements in an FDA-regulated environment.Conduct thorough inspections and evaluations to identify issues and implement solutions.Maintain up-to-date knowledge of Federal and State regulations and policies.Communicate effectively, both orally and in writing, with internal teams and stakeholders.Manage multiple tasks efficiently, prioritizing work and adapting to changing priorities.Operate and utilize computer software for data retrieval, storage, and merging.Qualifications:Experience:
At least 5 years in a quality role within an FDA-regulated industry such as cell therapy, biotechnology, pharmaceuticals, or medical devices.Education:
Bachelor’s degree in a related field or equivalent experience/training.Pay Details:
$37.00 to $41.00 per hourEqual Opportunity Employer/Veterans/Disabled
#J-18808-Ljbffr