Pharma Quality Assurance Associate

**THE JOB**: We are currently searching for a **Product Complaint Associate** to join our QA team to be responsible for ensuring that product complaints are processed in compliance with Good Manufacturing Practice (GMP), effectively and efficiently supports this business processes, is continually improved and inspection ready. **WHAT YOU CAN EXPECT TO DO IN...

**Company Overview**: Meditrial is a dynamic and rapidly growing multinational company specializing in providing clinical and regulatory services to medical device companies in the USA and Europe. With a commitment to excellence and innovation, we empower our clients to navigate complex regulatory landscapes and bring life-changing medical devices to market...

JOIN OUR TEAM! For the verope Service Center GmbH (Contwig/DE) we are looking for a Quality assurance employee (M/F/d) Who we are verope combines customers‘ requirements for highest quality and competitive prices in production, sales and service of special wire ropes with a global reach. verope AG is a joint venture between KISWIRE Ltd. (South Korea) and...

Job Description **Site Name**: Switzerland - Rotkreuz **Posted Date**: Jun 1 2023 **Hello. We’re Haleon.** A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol,...

**Quality Partner (m/w/d) - Quality Assurance / ISO 13485 / FDA Regulation / Prozess-Risikoanalysen / Deutsch** **Projekt**: Für unseren Kunden Roche Diagnostics International AG mit Sitz in Rotkreuz suchen wir einen Quality Partner (m/w/d) **Hintergrund**: Für das Operations Quality Netzwerk RDI/RDA suchen wir für das Product Partnering im Bereich BG&E...

Job Description Writes, edits, and reviews Essential Documents, including informed consent forms, patient information, and other project-specific clinical documentation Writes, edits, reviews, finalizes, and tracks clinical study report (CSR) patient safety narratives Collects and tracks documents for CSR appendices, in support of the Quality Control...

**Job Title: Product Complaint Associate** **Company Description**: Join a reputable pharmaceutical company focused on improving patient outcomes. As a global specialty pharmaceutical company, we market therapeutic solutions in over 50 countries, serving patients with life-threatening conditions and chronic illnesses. Our organization is backed by private...

**The role can be based in Munich, Germany or Zug, Switzerland** **Position Summary**: The Associate Director Pharmacovigilance (PV) International is responsible for managing local PV processes and systems in ex-US territories (focusing on Europe), maintaining compliance with local/regional PV regulations and guidance, particularly EU Good Pharmacovigilance...

**Job Overview** The position of the Director global Quality of SHL Medical AG holds overall responsibility for compliance to all applicable regulations pertaining to all operations functioning on the assigned site as well as corporate compliance to all applicable regulations including cGMP pertaining to all the markets currently being served by the...

Job Overview The position of the Director global Quality of SHL Medical AG holds overall responsibility for compliance to all applicable regulations pertaining to all operations functioning on the assigned site as well as corporate compliance to all applicable regulations including cGMP pertaining to all the markets currently being served by the...

Position Summary: The Associate Manager, Clinical Business Operations is responsible to manage assigned, dedicated Seagen staff as applicable and guide clinical trial operations. Position will serve as key contributor to clinical systems, process development, and support or drive quality initiatives. Position guides day-to-day operational...

Job Overview The Process Quality Engineer (PQE) is responsible for supporting new process development, automation equipment development and product transfer by applying quality engineering skills in compliance with medical devices industry standards and regulations. Sr PQE will handle projects and tasks, from product/process inception through product...

Position Summary: The Regulatory Affairs Associate Manager will report to and support the Regulatory Affairs Director/Associate Director by leading the preparation and submissions of regulatory dossiers to European and Swiss competent authorities, in line with the global regulatory plan for one or more Oncology products. Principal Responsibilities: -...

Seagen is a global, multi-product biotechnology company dedicated to developing and commercializing transformative cancer medicines. As the industry leader in antibody-drug conjugate (ADC) technology, we pioneered a new generation in the science of harnessing antibodies to deliver cell-killing agents directly to cancer cells. Seagen’s dedication to...

**Position**: Associate Director, International Commercial Training **Reports to**:Head of Insights, Analytics and Distribution **Location**:Zug Switzerland **Position Summary**: Apellis is seeking an experienced and engaged commercial professional for the role of Associate Director, Commercial Training, International Region. It is an outstanding...

**Job highlights** - Full time - Baar, Zug, Switzerland - Group Internal Audit and Assurance **Job ID** - R200000648**Closing date** - Never**Last Updated** - 08/03/2024*** We are looking for a motivated **Audit and Assurance Manager** with specialisation in Technology (Information and Operational) and Data Analytics to join our Group Internal Audit and...

**Global Supplier Quality Strategy & Performance Sr. Manager **-2206090097W **Description** Kenvue, part of the Johnson & Johnson Family of Companies is recruiting for a **Global Supplier Quality Strategy & Performance Sr. Manager**, located in Zug, Switzerland. The Global Supplier Quality Strategy & Performance, within Global Supplier Quality Management...

Janssen Supply Group is recruiting a Pharmaceutical Regulatory Compliance Manager within the Johnson & Johnson Regulatory Compliance (JJRC) team! The position will be preferably located in Latina, Italy, Zug, Switzerland, Horsham, PA, Malvern, PA, Titusville, NJ, Raritan, NJ, Beerse, Belgium, Leiden, Netherlands or Cork, Ireland. The Pharmaceutical...

**Project**: For our customer a big pharmaceutical company in Kaiseraugst we are looking for a highly qualified **Recipe Author Pharmasuite** For the MES Business Management Team we are looking for a temporary employee to support our Manufacturing Execution Systems in the manufacturing area in Kaiseraugst. Your main responsibility will be the support of the...

**Reports to**:Head of MSAT **Position Summary**: As part of the MSAT team, the Associate Director of Drug Substance, Manufacturing Science and Technology (MSAT), will assume broad responsibility for tech transfer, process qualification and validation at contract drug substance manufacturing sites. The Associate Director of DS MSAT is responsible for...