Gmp Documents

For our _Techfirm Industrial Services _team, we would like to integrate an **Document Controller (M/W/D)** Ready to join us in Switzerland to take up new challenges together! **WHAT WILL BE YOUR TASKS** - Ensure uniform document procedures across all organization departments. - Verify and approve documents prior to filing. - Coordinate with internal and...

The Department of Biomedicine is a joint effort between the University of Basel and the University Hospitals Basel. It unites basic and clinical scientists to advance our understanding of health and disease and to develop pioneering therapies benefiting the lives of patients in areas of unmet need. With more than 70 research groups and 900 employees, the...

GMP Compliance Expert Contract Duration: 12 months **Responsibilities**: - Ensuring that the official and regulatory requirements are met in operational operations - Responsible for ensuring operational compliance for site media systems (process water and gases) in the GMP regulated environment Initiating and processing deviation, change, risk and change...

**About Idorsia Pharmaceuticals Ltd** Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients. In order to achieve this, we want to develop Idorsia into one of Europe’s leading biopharmaceutical companies, with a strong scientific core. Headquartered in Switzerland - a European biotech hub -...

For our client, a well-known pharmaceutical company in Basel, we are looking for a QA Associate (M/F/d). **Background** The Quality Assurance (QA) Associate ensures the integrity and compliance of GMP-relevant documents and batches. This role supports the timely release of GMP materials and adheres to cGMP standards within the Technical Research and...

JobdescriptionFor our client, we are seeking a highly skilled Qualification and Validation Manager to join their team in the Basel area on a temporary contract via Randstad. This position offers the opportunity to work in a GMP-relevant environment, focusing on CSV (Computerized System Validation) and qualification programs in pharmaceutical...

**Bioengineer Associate** Executes manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution. **Responsibilities** - Provides front line technical and procedural support, working with the...

**Technical QA Manager** **Technical QA Manager (M/F/d) - GMP / Pharma / Qualification / Validation / CSV** **Projekt**: For our client, a big pharmaceutical company in Basel we are looking for Technical QA Manager (M/F/d). **Background**: **Tasks & Responsibilities**: - Running, maintaining and continuously improving Qualification/Validation activities...

For our client, we are seeking a highly skilled Qualification and Validation Manager to join their team in the Basel area on a temporary contract via Randstad. This position offers the opportunity to work in a GMP-relevant environment, focusing on CSV (Computerized System Validation) and qualification programs in pharmaceutical manufacturing.Key...

Switzerland, Basel Switzerland, Stein Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their...

Switzerland, Basel Switzerland, Stein Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their...

**Beschreibung**: We are looking for a motivated and committed **Technical QA Manager** for our client, F. Hoffmann-La Roche Ltd. based in Basel, for a 12 month assignment with the option to extend. The IMP Quality Operations Unit Switzerland in Global Technical Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in...

................ For our client from the pharmaceutical industry in Basel, we are looking for a technical QA manager **General Information**: - start date: asap - extension: possible - workplace: Basel - remote: on-site required, home office upon discussion - travel: no **Tasks & Responsibilities**: - QA supervision of qualification - and...

**INTRODUCTION**: As a preferred supplier for F. Hoffmann - La Roche Ltd. in Basel, we are looking for a motivated **Technical QA Manager (M/F/d)** - This is a full-time position, with a 12-months duration with possible extension. The earliest start date is as soon as possible. Home Office is allowed on a case by case basis. **ASSIGNMENT DESCRIPTION**: -...

**Technical QA Manager** You will support the end to end cGMP activities, in maintaining the Right to Operate at the Swiss Technical R&D sites and in ensuring quality and compliance of IMP products according to Health Authority requirements and Company Standards for IMP products. You will be reponsible for running, maintaining and continuously improving...

Hobson Prior is seeking an experienced Scientist to join a dynamic Analytical Chemistry team. This role will focus on writing and reviewing various analytical documents and ensuring compliance with health and safety guidelines. The successful candidate will support regulatory submissions and the overall quality of our analytical processes. Please note that...

Please note that to be considered for this role you must have the right to work in this location. **Responsibilities**: - Manually label and package primary packed medications for clinical studies. - Execute assigned tasks according to production plans and GMP, safety, and environmental guidelines. - Create batch documentation accurately and on time. -...

Secure a rewarding career as Senior Quality Assurance Specialist for Pharmaceutical Supply Chain with gloor&lang AG in Basel, Switzerland. This challenging role offers a competitive salary of €80,000 - €110,000 per year.Job Description:We are seeking an experienced and highly skilled professional to join our team as Senior Quality Assurance Specialist...

Gi Group SA is seeking a Quality Assurance Manager to join their team in Basel. As a Senior Quality Expert, you will be responsible for reviewing and approving SOPs, protocols, reports, Certificate of Analysis, and other quality-related documents.About the RoleThis is a unique opportunity to work with a dynamic team in the pharmaceutical industry. The...

For our client, a well-known pharmaceutical company in Basel, we are looking for a Laboratory Scientist (M/F/d). **Background** Perform and document scientific experiments in the laboratory for drug substances (DS) and drug products (DP) in collaboration with multifunctional project teams. Contribute to maintenance of lab instruments/day-to-day operations....