For our client specialized in biotechnology, localized in the French part of Switzerland, we are looking for a :
PM and QMS - 6-month mission
Your missions
- Drive execution of product care and sustaining engineering projects
- Lead projects ensuring proper execution to deliver results on-time, accurate reporting and resource allocation
- Work within a cross-functional multidisciplinary team spanning over multiple global sites
Your responsibilities
Project management
- Plan project, define specifications and drive projects up to completion
- Report and track project resources and budget allocation
- Lead cross-functional program activities for biotechnology projects responsibility for timely completion within budget
- Work closely with Product Management team to drive product direction and resolve issues
- Manage and optimize project plans, product/project risk, project budgets, and resources/task assignments
- Liaise with and work with Suppliers and our CMOs to ensure seamless production and maintenance of quality
- Effectively facilitate cross-functional decision making to deliver effective and timely improvements to existing products and processes
- Ensure compliance with Design History File (DHF) and other QMS requirements
- Manage customer critical-to-quality (CTQ) objectives, regulatory requirements, schedules, and program risks and making decisions based on business objectives
- Provide periodic stakeholder communications and escalating concerns and issues as necessary
Quality Specific Goals
- Aware of and comply with the Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
- Complete all planned Quality & Compliance training within the defined deadlines
- Identify and report any quality or compliance concerns and take immediate corrective action as required
Your profile
- Degree in Mechanical, Biology, Pharmacy or Sciences,
- Minimum a 5-year experience in product development, sustaining or manufacturing in Healthcare or Life Sciences industry
- Familiarity with ISO, FDA and/or other regulatory standards
- Demonstrated engineering knowledge, program management, and business planning processes, with the full product lifecycle management experience
- Fluent in French & English
- Experience in regulated industries highly desirable, preferably in Healthcare, Life Sciences
Your application
Please apply on-line. For more information, contact Ms Sophie Darthenay on
