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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Company Description. LGC Clinical Diagnostics Business Unit is comprised of our operating entities including LGC Clinical Diagnostics, Inc. (f/k/a Maine Standards Company & SeraCare Life Sciences), Technopath Clinical Diagnostics, and the Native Antigen Company. Our 400 employees operate FDA-registered and ISO 13485-accredited facilities in Maine (USA), Massachusetts (USA), Maryland (USA), Tipperary (Ireland), and an ISO 9001-accredited facility ...
About HireRight. HireRight is the premier global background screening and workforce solutions provider. We bring clarity and confidence to vetting and hiring decisions through integrated, tailored solutions, driving a higher standard of accuracy in everything we do. Combining in-house talent, personalized services, and proprietary technology, we ensure the best candidate experience possible. PBSA accredited and based in Nashville, TN, we offer ex...
This position is an excellent opportunity for a quality-minded individual wanting to have an impact in a technology-based pharmaceutical manufacturing company. You will be collaborating with other members of the QA team in coordination with other departments to help ensure that our products maintain the highest product quality. Essential job functions include. Obtain and maintain ISO gowning certification for access to the aseptic areas (ISO 5 an...
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...
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...
This position is an excellent opportunity for a quality-minded individual wanting to have an impact in a technology-based pharmaceutical manufacturing company. You will be collaborating with other members of the QA team in coordination with other departments to help ensure that our products maintain the highest product quality. Essential job functions include. . Obtain and maintain ISO gowning certification for access to the aseptic areas (ISO 5 ...
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...
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...
