Implements company and regulatory quality standards for product manufacturing. Knowledgeable of industry and governmental quality regulations. Audits and reviews quality data according to existing procedures. Documents results in required format. Requires a bachelor's degree or equivalent. Typically reports to a manager or head of a unit/department. Occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Typically requires 2-4 years of related experience.
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Requisition. 7396. of openings. 1. Employment Type. Full time. Position Status. Permanent. Category. Non-Bargaining. Workplace Arrangement. Hybrid. Fund. 1199SEIU National Benefit Fund. Job Classification. Non-Exempt. Responsibilities. Review and authorize pension benefits for retired 1199SEIU members, surviving spouses, beneficiaries and their estates. ensure benefits are processed in compliance with Federal and Plan regulations. Verify pension ...
Matica Biotechnology is at the forefront of biopharmaceutical research and development. The Matica Bio team brings an average of 15 years of cell and viral vector manufacturing experience to the development and manufacture of advanced therapy products. At our purpose-built GMP facility in College Station, Texas, we provide rapid development and scale-up of cell and gene therapies, vaccines, and Oncolytics meeting worldwide regulatory compliance. ...
Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Eur...
RESPONSIBILITIES. . Reviews and approves Change Requests, Reactive Maintenance, Deviations/CAPA as assigned. Assist with validations as assigned. Review records and forms to ensure compliance with established LSL procedures and regulations. Maintain Quality files as applicable: Scan, Save to appropriate online storage, file. Perform warehouse walkthroughs to ensure the facility is maintained in a clean, safe, compliant manner. Be a part of the in...
RESPONSIBILITIES. . Reviews and approves Change Requests, Reactive Maintenance, Deviations/CAPA as assigned. Assist with validations as assigned. Review records and forms to ensure compliance with established LSL procedures and regulations. Maintain Quality files as applicable: Scan, Save to appropriate online storage, file. Perform warehouse walkthroughs to ensure the facility is maintained in a clean, safe, compliant manner. Be a part of the in...
Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to pati...
At PBI-Gordon Companies, and our subsidiaries PBI-Gordon Corporation, Pegasus Laboratories, and PetAg, Inc, our priority is people, pets, and the places they go. As employee owners, we support each other in building our careers as well as our companies. Our foundation is rooted in integrity, innovation, partnership, and pride. Come grow with us. Job Summary. Support the Quality Compliance function by ensuring the effectiveness, consistency, and c...
Performing critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what we get to do every day at KCAS Bio. If that gets you excited too, then maybe working at KCAS Bio is for you. As a Quality Assurance Specialist II at KCAS Bio, you will be accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure qu...
Would you like to join an innovative team driven by a bold vision –. unleashing tools to accelerate breakthroughs in human health. Would you like to join an innovative team creating technology to power ground-breaking insights in academic, clinical, pharma and biotech research. It is an extraordinary time for Standard BioTools. Our technology is empowering customers to improve life through comprehensive health insight. We invite you to join a lea...
Would you like to join an innovative team driven by a bold vision –. unleashing tools to accelerate breakthroughs in human health. Would you like to join an innovative team creating technology to power ground-breaking insights in academic, clinical, pharma and biotech research. It is an extraordinary time for Standard BioTools. Our technology is empowering customers to improve life through comprehensive health insight. We invite you to join a lea...
