Project information
- IMP Quality Operations Switzerland is responsible for delivering Investigational Medicinal Products (IMPs) to the patients in compliance with cGMP. They are the Quality Partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and Compliance oversight of all. They are committed to transform itself from the inside out towards a purpose driven organization based on strength and role based working. They do this in order to create a great place to work, so each of they can thrive and to unleash our full potential.
Responsibilities
- Support all quality-relevant packaging processes and collaborate with packaging operations and all relevant interfaces with regard to GMP topics
- Partner with stakeholders and provide GMP support to ensure successful delivery of the company goals
- Review and release of manufacturing specifications and Batch Records (BR) of finished and semi-finished goods
- Manage actively Deviations and Changes
- Collaboration through to the management of local and global projectsActively engage in optimization activities and improvements within IMP Quality Clinical Packaging Switzerland.
- Coordinate improvement projects and engage in corrective and preventive measures (CAPA)
- Build, verify and implement standard documents (SOPs)
- Joy in a human-centered and self-managed way of working based on NewWork, with a key focus to support the ongoing cultural and organizational change towards collaboration, agility and innovation mindset
Profile
- Min. Master Degree preferably in Life Sciences or Engineering or similar degree
- Solid experience in the pharmaceutical industry in a quality manager role
- Knowledge of cGMP and quality requirements for clinical development phases
- Experience in the area of pharmaceutical development such as packaging lines or materials, master data management, quality control or quality assurance is an advantage
- Proven track record to work towards outcomes and an innovative manner of solving problems
- Strong team-player with a high level of self-motivation and being able to inspire others
- Ability to work in a purpose driven organization, taking full ownership for assigned roles and tasks, continuously willing to improve individual and team effectiveness
- Ability to communicate clearly and professionally verbally and in writing in BOTH German and in English is necessary
- Experience with SAP and Veeva is an advantage
Benefits
- A very renowned company
- You will work in an international environment
About Hays
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
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