Quality Project Manager / no-436

For our customer located in Basel/Switzerland we are currently looking for a: Quality Project Manager (m/f/d)

• Fully On-Site based position
• Start date ASAP
• 18 month contract
• possible extension +6 month, based on project needs

Tasks & Responsibilities

• Acts as TRD excipient portfolio manager

Performs following activities:

• Interacts and collaborates with internal and external stakeholders, customers and/or suppliers, according to specific area of responsibility.
• Maintains TRD excipient portfolio regarding supplier approval.
• Ensures change control management of excipient related matters notified by suppliers or triggered internally.
• Supports project teams in case of excipient-related request
• Handling of change actions and CAPAs, related to excipient involving multiple project users in TRD about supplier or product specifications.
• Guides project teams through new excipient implementation operations
• Performs following additional activities, as portfolio manager
• Acts as line unit representative to TRD Third Party QA organization with respect to TRD excipient portfolio and ensures that own deliverables are met.
• Acts as line unit representative and SME for interactions within TRD and with NTO excipient counterparts on local sites when needed.
• Supports PHAD Excipient Supply and Demand planning coordinators.
• Acts as key expert for new excipient/supplier implementation in TRD portfolio.
• Coordinates activities linked to transfer of excipient ownership from commercial site back to TRD in case of discontinuation.
• Maintains effective information channel with all involved parties. Communicates issues to involved partners.
• Ensures compliance to our client and other relevant regulations.
• Shows positive work ethics and influences others.
• Proposes and implements ideas for continuous process improvement also outside area of expertise/ organization.
• 1QEM: CAPA and Actions.

Must Haves

• Very good English (oral & written)
• Degree in science, logistics & supply chain, business administration or equivalent with SAP knowledge
• Min. 5 years of successful industry experience in the development of pharmaceutical industry (including GMP knowhow)
• Strong knowledge of relevant GMP regulations and policies.
• Expertise in supply chain (esp. material planning, logistics), business support and/or customer service roles, ideally in a pharmaceutical/chemical/biotechnical development or manufacturing environment
• Interdisciplinary thinking and interest in collaboration with other functions.
• Excellent communication skills, organizational, planning and negotiation skills.

Nice to Haves

• German skills