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. Work is closely managed. Works on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience.
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Job Description. As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some ...
Job Description. As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some ...
The Opportunity: Avantor is looking for a detail-centric Quality Assurance Specialist I to join our Quality Assurance Specialist team. Our Quality Assurance Specialist Team upholds and maintains Avantor’s operational continuity, including documentation ownership by maintaining quality and industry standards, meeting production deadlines, and closely working with associates interdepartmentally. This role will be a full-time, Monday through Friday ...
The. Opportunity. Avantor is looking for a detail-centric Quality Assurance Specialist I to join our Quality Assurance Specialist team. Our Quality Assurance Specialist Team upholds and maintains Avantor's operational continuity, including documentation ownership by maintaining quality and industry standards, meeting production deadlines, and closely working with associates interdepartmentally. This role will be a full-time, Monday through Friday...
Quality Assurance Specialist I. Full time 40 hrs/week. Company Overview. Rocky Mountain Biologicals (RMBIO) is an international biotechnology company located in Missoula, Montana. RMBIO manufactures cell culture media, sera, transport media, and protein fractions for the global research, biopharma, medical, and clinical diagnostic industries. We are currently seeking candidates to fill a permanent position as an administrative assistant. Position...
About Us Live Oak Bank is a digital bank that serves small business owners across the country. Our groundbreaking spin on service and technology has fueled our mission to be America’s Small Business Bank. Our products help customers buy, build, and expand their business, and our high-yield savings and CD products help them grow their hard-earned money. At Live Oak, we never lose sight of the well-being of our people. We believe our employees are ...
Objective. The Quality Assurance Specialist I will support the design, implementation and maintenance of QA and compliance programs including, but not limited to an SOP system and corrective action and preventative actions (CAPAs). In addition, the Quality Assurance Specialist I will provide consultation in the interpretation of good manufacturing practice (GMP), good laboratory practice (GLP), and good clinical practice (GCP) regulations, guidel...
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplie...
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...
Cambridge Isotope Laboratories (CIL) has an outstanding opportunity for a Quality Assurance Specialist I to join the team responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components based onsite in our Tewksbury, MA location. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology...
Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing Quality Assurance professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics. Reporting directly to the Senior Manager, Quality Operations at Vericel, this is a great opportunity to join a hig...
Quality Assurance (QA) Specialist I in Springfield, MO. . Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. . Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. . Summary. The Quality Assuran...
