Werfen
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
If you’re a QA expert when it comes to manufacturing, Immucor has an exciting opportunity for you! We are looking to hire a Sr. Quality Assurance Specialist with a background in blood banking, medical device, and/or the pharmaceutical industry. This critical role is responsible for providing quality oversight at the shop floor level to address immediate quality issues. If you’ve got the necessary skills and experience to excel in this role, we want to hear from you!
This position is not eligible for sponsorship for work authorization by Immucor, Inc. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.
Sr. Quality Assurance Specialist (Operations)
Job Summary
The Senior Quality Assurance Specialist-Operations will support the organization by providing quality oversight of manufacturing/oprations and ensuring all applicable GMP and regulatory requirements (ex. 21 CFR Part 820 and ISO 13485) are followed.
Key Accountabilities
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Minimum Knowledge & Experience required for the position:
Minimum bachelor’s degree in a science related field (ex. Biology, chemistry, biomedical engineering). Five (5) years or more experience in quality assurance in a medical device or pharmaceutical industry. Two (2) years or more experience in DHR/batch record review and product release. Knowledge and experience enforcing FDA and EU regulations for medical device and/or pharmaceuticals (21 CFR Part 211 or 820, ISO 13485).
Sr. Quality Assurance Specialist (Operations)
Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 5,000 employees around the world comprise our Werfen team.
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