QA Compliance and System Specialist

We are currently looking for a QA Compliance and System Specialist to join our team at our site in St. Gallen. Your main responsibilities will include: providing support on GMP processes to ensure compliance with company standards and GMP regulatory guidelines; developing, maintaining and improving GMP-related standard operating procedures (SOPs); supporting quality processes related to Validation, Qualification, Document Management, Deviation Management, CAPA and Change Control in the Site GMP areas.In this position you will be directly reporting to the Head QA Compliance and Innovations....

January 21, 2025 · 3 min · 456 words · Joy Larson

QA Director, America

OverviewLead the Americas Quality Assurance organization, providing long-term strategic direction with the aim of supporting the Waters business in achieving the highest levels of corporate growth, product quality, business process quality/efficiency, operational excellence and customer satisfaction, while meeting regulatory needs, through ensuring that:The Quality Assurance organization within the Americas is aligned to the Waters business and collaborates effectively to support the achievement of Waters' long-term strategy and business goalsThe Global Quality Assurance Strategy is developed and implemented to support high levels of internal and external customer satisfaction through delivery of quality products and an effective and efficient service to the businessA strong, globally-consistent culture of Quality is developed and maintained throughout Americas to support increasing inclusion of all Waters staff in supporting customer satisfactionThere is ongoing development, implementation, and maintenance of the quality management system to 21 CFR 820, ISO 9001, ISO 13485, ISO17025 and ISO17034 and other relevant standards as requiredThe effectiveness of the Quality organization is supported through appropriately qualified, experienced and motivated staff, an optimized organization structure and a development-focused environment...

January 21, 2025 · 2 min · 242 words · Mary Gallagher

QA Engineer

Want more jobs like this?GetjobsinBangalore, Indiadelivered to your inbox every week. Want more jobs like this? GetjobsinBangalore, Indiadelivered to your inbox every week. Get Jobs Your deliverables as aQuality Assurance Professionalwill include, but are not limited to, the following:Deliver against performance engineering goalsExecute Performance Engineering and Testing activities leveraging Agile methodologyCreate, re-factor, extend, and maintain performance test scripts.Help determine appropriate metrics to be gathered during performance testing and be responsible for analyzing and tracking against these performance testing metrics on an ongoing basis....

January 21, 2025 · 2 min · 246 words · Kayla Murphy

QA Engineer - AI Application (EDAi)

Siemens Digital Industries Software is a global technology powerhouse. With some of the best-known brands in the world, Siemens has stood for engineering excellence, innovation, quality, and reliability for more than 175 years.We’re looking for QA Engineer for AI Application (EDAi) to join our team in Cairo, Egypt.Job Responsibilities:Design, develop, and execute comprehensive test plans and cases for the functionality of AI applications.Design innovative scenarios targeting different customer use models to identify issues and offer suggestions for improvement....

January 21, 2025 · 2 min · 410 words · Alison Rodriguez

QA Labelling Specialist - Tagalog Speaker - Monetization Integrity

ResponsibilitiesAbout TikTokTikTok is the leading destination for short-form mobile video. At TikTok, our mission is to inspire creativity and bring joy. TikTok’s global headquarters are in Los Angeles and Singapore, and its offices include New York, London, Dublin, Paris, Berlin, Dubai, Jakarta, Seoul, and Tokyo.Why Join UsCreation is the core of TikTok’s purpose. Our platform is built to help imaginations thrive. This is doubly true of the teams that make TikTok possible....

January 21, 2025 · 3 min · 449 words · William Carpenter

QA Process & Cleaning Validation Specialist

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, OfficeJob DescriptionThermo Fisher Monza site is a world class contract manufacturing and development facility, specialized in aseptic injectable drugs, with a growing focus on biologics and vaccines.Location/Division Specific InformationMonza (MB), ItalyAs Quality Assurance P&CV Specialist, you will become part of a proactive and dynamic team, which maintains an high quality standard on P&CV of new products manufacturing in Monza site....

January 21, 2025 · 3 min · 476 words · Trevor White

QA Software Student

Based: Airport City - Israel. Onsite. Part-Time.The Digital Industry (DI) Division offers a comprehensive portfolio of seamlessly coordinated hardware, software, and technology-based services to support manufacturing companies worldwide in improving the flexibility and efficiency of their manufacturing processes and reducing the time to market of their products.You will be part of Realtime Monitoring and Optimization division (RMO). RMO develops ACM Suite (Adaptive Control and Monitoring) and ACM Web Console products. ACM is a suite of efficiency products that strive to increase CNC machine efficiency, improve process stability, prevent and/or detect tool breakage etc....

January 21, 2025 · 2 min · 321 words · Joanna Barnes

QA Trainee CDAC 2

Testing AnalystThe Analyst, Testing job supports the evaluation of equipment and processes to ensure the safety, reliability and maintainability of products and systems. This job tests the performance of various systems, applications and databases, and works under close supervision.Key Responsibilities and DutiesReviews test cases, scenarios and scripts to ensure the quality of information systems, applications and databases delivered.Plans reliability tests and conducts analyses of field failures while developing reliability information systems for failure analysis and performance improvement....

January 21, 2025 · 2 min · 309 words · Cody Coleman

QA-Inspektor Etiketten (m/w/d)

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionDer QA-Inspektor in der Abteilung für Clinical Label Services ist verantwortlich für den Empfang von unbedruckten und bedruckten Etiketten sowie Booklets für klinische Studien. Darüber hinaus obliegt ihm/ihr die Gewährleistung des genauen Versands von Etiketten für klinische Studien.Er/Sie ist verantwortlich für die Freigabe von Wareneingängen sowie den Warenausgang an die interne Produktion und direkt an den Kunden.Die Rolle erfordert eine kompetente Nutzung der FCS-Computersysteme und SOPs sowie die Einhaltung der Qualitätsstandards und Zeitvorgaben von Fisher Clinical Services und Clinical Label Services....

January 21, 2025 · 2 min · 374 words · Christopher Lester

QA/QC Specialist

General information:It is needed to oversee QA and QC activities in the process of manufacture and testing of TR for Japanese utility market in the oversea factory and JP activities. He is also involved in the trouble shooting for overall Hitachi legacy products and newly products introduced from oversea factory. In addition, he is responsible health/safety/environment aspects of all activities done in the organization. It is needed to be linked with HSE structure in HE-J and HUB APMEA in order to achieve zero HSE issues....

January 21, 2025 · 2 min · 351 words · Julie Dickerson

QC Analyst II

OverviewPosition Summary:Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Microbiology controls and reagents using various automated and manual techniques in accordance with established Quality standards and GMP requirementsResponsibilitiesKey AccountabilitiesEssential Functions:Performs automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product.Interprets test results against specifications and decides if assays pass or fail. Overview Position Summary: Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Microbiology controls and reagents using various automated and manual techniques in accordance with established Quality standards and GMP requirements...

January 21, 2025 · 2 min · 341 words · Tiffany Duffy MD

QC Chemist

Why Patients Need YouEverything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.What You Will AchieveYou will be a member of Pfizer’s dedicated and highly effective quality assurance and control team....

January 21, 2025 · 4 min · 794 words · Michelle Williams

QC Cleaning analyst

Work ScheduleOtherEnvironmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety StandardsJob DescriptionThermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them....

January 21, 2025 · 2 min · 412 words · Andrew Scott