GMP Compliance Specialist

Wir suchen einen Quality Assurance Associate, der die Einhaltung der Good Manufacturing Practices (GMP) sicherstellt.In dieser Rolle werden Sie Abweichungen analysieren, Produktreklamationen bearbeiten und komplexe Qualitätsfragen lösen.Aufgaben:Koordination und Untersuchung von Produktreklamationen und Meldungen zu NebenwirkungenSicherstellung...

Hauptaufgaben:GMP-Anforderungen überprüfenUnterstützung bei Entscheidungen zu Qualität und ComplianceRisikobeurteilung und -managementÄnderungsanträge bearbeitenFachliche Review von GMP-DokumentenBesondere Anforderungen:Gute analytische FähigkeitenHohe KommunikationsfähigkeitZielsetzung:Als Teil unseres Teams werden Sie dazu beitragen, dass wir als...

About UsGXP CONSULTING Switzerland is a Swiss company with a passion for delivering outstanding industry expertise and support to our clients. Our team of Life Sciences professionals is dedicated to helping our clients achieve their goals and succeed in the market.We are seeking a Technical Project Manager to join our team and contribute to our mission. In...

About the TeamOur Laboratory Operations Specialist will play a vital role in supporting our laboratory operations, ensuring the quality and compliance of our products. Your primary responsibilities will include:Performing routine release and stability tests for various products, adhering to cGMP guidelines and internal regulations.Contributing to building a...

German Language Content Compliance Specialist / Relocation to LisbonLocation: Lisbon, PortugalPosition Type: Full-time (Monday to Friday)About Us:Join our dynamic team in Lisbon as a German Language Content Compliance Specialist. We are committed to maintaining a safe and compliant online environment for our users.Role Overview:In this back-office position,...

Job Title: Content Compliance Specialist - German Language Expert\About Us:\Cross Border Talents is committed to creating a safe and compliant online environment. We're seeking a skilled Content Compliance Specialist to join our team in Lisbon.\Job Description:\We're looking for a highly analytical individual with strong attention to detail to review flagged...

About the RoleWe are seeking a highly skilled Senior QC Specialist to join our Quality Control team. As a key member of our laboratory operations, you will be responsible for performing routine release and stability tests for novel clinical phase materials as well as ENVM and CVAL samples.Your primary focus will be on ensuring the quality and compliance of...

Job Description:At Oxford Global Resources, we are seeking a skilled Biopharmaceutical Production Specialist to join our team. In this role, you will be responsible for carrying out biopharmaceutical production activities in either upstream (USP) or downstream (DSP) processing.The ideal candidate will have 1-5 years of experience in USP or DSP in the...

We are seeking a seasoned EHS professional to join our CapEx/CAR-T project team in Bern, Switzerland. As an EHS specialist, you will be responsible for overseeing EHS aspects of annual CAPEX projects and driving EHS initiatives.Main Responsibilities:Review and approve work permits, conduct site inspections, and coordinate with on-site suppliers to ensure EHS...

Job DescriptionWe are seeking a skilled Process Commissioning Specialist to support the startup of critical utilities and HVAC systems in a cutting-edge life sciences environment.This role involves commissioning, troubleshooting, and optimizing systems to ensure compliance with industry standards and operational efficiency.Commission and qualify black &...

Clinical trial supply management is a critical component of our pharmaceutical industry operations. We are seeking a skilled professional to manage and execute clinical trial supplies from setup through to closeout.This role involves coordinating the timely delivery, packaging, distribution, and destruction of clinical trial supplies, ensuring compliance...

About the RoleOxford Global Resources is currently seeking skilled bioprocess specialists to join our team. As a leading provider of innovative solutions for pharmaceutical, biotech, and clinical research industries, we specialize in biologics manufacturing, sterile drug production, and advanced analytical services. This role offers an exciting opportunity...

We are seeking a highly skilled GMP Compliance Specialist to join our team at Advanced Clinical.The ideal candidate will have experience in a pharmaceutical company and a strong understanding of GMP regulations.Key Responsibilities:Investigate and resolve product complaints and adverse eventsEnsure timely and quality-compliant investigationsPrepare...

At TieTalent, we are seeking a highly skilled Senior Equipment Procurement Specialist to join our team. As a key member of our quality excellence team, you will be responsible for coordinating the end-to-end acquisition process of laboratory equipment, ensuring compliance with GxP requirements.Job DescriptionThe successful candidate will assist in writing...

In dieser Rolle sind Sie für die Einhaltung der Good Manufacturing Practices (GMP) verantwortlich, indem Sie Abweichungen analysieren, Produktreklamationen bearbeiten und komplexe Qualitätsfragen lösen.Als GMP Compliance Specialist arbeiten Sie eng mit Behörden und internen Teams zusammen, um höchste Qualitätsstandards...

About the JobThis is a fantastic opportunity to join our team as a Pharmaceutical Industry Electrical Specialist at Gi Group. As a key member of our team, you will contribute significantly to ensuring the smooth operation of our manufacturing processes.Your Main Responsibilities:Identify opportunities for process improvement and implement changes to increase...

We are seeking a highly skilled Quality Assurance Specialist QC Microbiology to join our team. As a key member of our Quality Control department, you will be responsible for performing routine release and stability tests for new materials in the clinical and commercial phase.Key Responsibilities:Develop and implement microbiological laboratory operations and...

We are seeking a Quality Control Laboratory Instrument Specialist to join our team. As a key member of our quality excellence team, you will be responsible for coordinating the end-to-end acquisition process of laboratory equipment, ensuring compliance with GxP requirements.ResponsibilitiesThe successful candidate will assist in writing technical and...

Oxford Global Resources is proud to partner with a leading company in the life sciences industry. As an Upstream and Downstream Specialist, you will play a critical role in the development and production of innovative biopharmaceutical products.About the ClientOur client is a global leader in life sciences and biotechnology, providing cutting-edge solutions...

Job SummaryOxford Global Resources is seeking a skilled Biopharmaceutical Process Specialist to join our team. As a key member of our production team, you will be responsible for carrying out biopharmaceutical production activities in either upstream (USP) or downstream (DSP) processing.Perform daily manufacturing activities in USP or DSP, including...