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Contribute to the success of strategic QA projects in this challenging QA position
Het bedrijf / The company
The organisation is a global contract packaging organisation (CPO) specializing in primary and secondary pharmaceutical packaging and supply chain management services. They are dedicated to shape the future of the pharmaceutical supply chain to be safer and more reliable for customers and for patients. With more than 30 years of track record in contract packaging, they use their knowledge and experience to offer flexible solutions to customers challenges. Furthermore, they use the latest technologies to continuously improve operations. As QA Manager (GMP-compliance focus) you will be part of the Quality Unit. It is the Quality Unit’s responsibility to make sure that people, processes, materials, and machines work together to assure patient safety. You will be reporting to the Director Corporate Development.
De functie / The role
As a QA Manager, you will be part of a dynamic, fast-paced, and innovation-inclined Quality Assurance team, consisting of three other QA Managers. The QA team is responsible for defining evidence-based quality standards, contributing to the robustness, efficiency and effectiveness of production and back-office processes and methods. Members of the QA team combine project-based work with operational release and approval work. As a member of the team, you will be an expert on European and international pharmaceutical regulation, drawing on your knowledge and experience to develop, implement and deliver excellent quality services. As such, you will have a direct impact on the success of the organisation and on the safety of the patients. As part of your work, you will be working in multi-disciplinary teams with partners from across the internal supply chain, communicating with local and international customers, and playing an integral part in the market delivery of complex and innovative pharmaceutical products that make a real difference to patients’ lives. You will lead several foreign inspections, supplier qualifications and around 30 customer audits per year. Furthermore, in this role you will work closely with other teams within Quality to lead, execute and monitor strategic QA projects. In addition, you will work closely with Commercial to enable an efficient and effective onboarding of new customers. Lastly, you will work closely with Operations Management to ensure oversight over suppliers and their timely qualification.
Het profiel / Your profile
• M.Sc (or equivalent degree) in a technical or scientific subject
• +3 year of experience with inspections, audits and supplier qualifications in a pharmaceutical company
• profound familiarity and in-depth experience with EU cGMP/cGDP and FDA regulations
• demonstrable experience with and interest in working in a fast-paced environment
• demonstrable experience with planning, scheduling and monitoring work to meet time and quality targets
• ability to work collaboratively in teams
• good professional and interpersonal communication skills; both oral and written in English
Het aanbod / The offer
• a diverse job at a pharmaceutical packaging organisation
• working at a stable and growing organisation
• having a personal development plan to become successful
• freedom to work independently
• good working conditions
Reactie / Reaction
Interested? Please send your resume and motivational letter by e-mail, with reference to WL/21-044-FMF, to Pieter van Gelderen: firstname.lastname@example.org.
For further information, please call Pieter van Gelderen at number +31 (0)33 472 80 87.
Tenslotte ..... / Finally ....
An individual assessment may be part of the selection procedure.
Our client has chosen Derks & Derks B.V. as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.