LHH is seeking a detail-oriented GMP Documentation Specialist to join its Manufacturing Operations team in Switzerland. This role is crucial for ensuring compliance in clinical biologics manufacturing through detailed review and documentation best practices. The ideal candidate will have
Overview Are you passionate about quality, precision, and working in a GMP-regulated environment? We are currently seeking a detail-oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment. The
The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ standards and GMP expectations. The role is part of the Operational Excellence team within Manufacturing Operations and
Aristo Group is seeking a GMP Documentation Specialist in Luzern, Switzerland, to support clinical biologics manufacturing. This role involves reviewing executed batch records, ensuring compliance with ALCOA+ standards, and aiding in documentation creation and lifecycle support. The ideal
LHH is seeking a GMP Documentation Specialist (m/w/d) in Luzern, Switzerland, to support clinical biologics manufacturing. This role involves reviewing executed batch records, ensuring compliance with ALCOA+ standards, and enhancing documentation practices. The candidate must have a Bachelor’s degree
Overview Luzern, CH Office manager Full time job Bachelor Allwyn Group is a multi-national lottery operator with a market-leading presence in Austria, the Czech Republic, UK, Greece, Cyprus, Italy and USA. Allwyn became the operator of
Aristo Group is seeking a Batch Record Reviewer in Luzern, Switzerland. This role supports clinical biologics manufacturing by ensuring compliance with ALCOA+, GDP, and GMP standards through operational reviews and documentation management. The ideal candidate has a
About Our Client For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking a Batch Record Review Specialist (m/f/d). In this role, you will support clinical biologics
Michael Page International (Switzerland) SA is seeking a Batch Record Review Specialist in Luzern, Switzerland. The successful candidate will be responsible for ensuring the accuracy and compliance of batch records in clinical biologics manufacturing. Applicants should
International pharma company 18 months contract with extensionoption About Our Client Our client is a well-established organization within the pharma industry, renowned for delivering innovative solutions and maintaining a strong commitment to quality and compliance. Operating
Manager Supply Chain Business Intelligence (Supply Planning) (m/f/d) Purpose & Overall Relevance for the Organization Are you enthusiastic about the prospect of driving excellence in reporting & analytics capabilities to increase transparency and visibility across the
The Batch Record Reviewer supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation meets ALCOA+ , GDP , and GMP expectations. As part of the Manufacturing Operational Excellence team, this role
GeoSolutions is looking for a Head of Engineering to help us coordinate, structure and grow our engineering organization while remaining deeply involved in technical decisions and delivery. This is a senior, hands-on leadership role. The ideal