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
- Payrange, defined by client: 66,09 – 89,12 chf/h, Example: for a month with 160 worked hours*89,12 chf = 14.259,2 chf gross salary
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
Did we catch your interest?
The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).
Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.