Do you have the skills and motivation to take full responsibility for the product release at our clients in the pharmaceutical industry?
What are your responsibilities?
- You’re responsible for the regulatory compliance of the pharmaceutical products throughout their whole life cycle.
- You’re involved during inspections and audits from the government (e.g. FAGG or FDA) and clients (e.g. supplier audit).
- You follow up incoming complaints, maintain contacts and participate in third party deliberation.
- You set up an extensive network from internal and external contacts.
Who are we looking for?
- You are an industrial pharmacist and you hold a QP number.
- You have experience with sterile production processes (in line with GMP Annex 1), demonstrable affinity with aseptic production processes and/or medical devices and interest in the technical side of pharmacy.
- Good knowledge of and experience with the pharmaceutical laws and regulations (in the EU and US).
What's in it for you?
- QbD is a healthy company with a strong growth and international ambitions. In addition to a very attractive salary package, we can offer you the following advantages:
- A company with a clear strategy and ambition
- We've got your back! Our HR Business Partners follow you closely, giving you the opportunity to shape your career.
- Thanks to our flat organization, we have short communication lines and you can always come to us.
- Standing still means going backwards. With our extensive training package and our periodic knowledge-sharing moments, we offer you many opportunities to continuously learn, to expand or specialize your knowledge and skills and to gain new expertise.
- Get to know your colleagues outside the work environment! Teambuilding and fun activities are planned on a monthly basis.
Interested? Send your CV and motivation letter to jobs@qbd.eu. Want some more info? https://jobs.qbd.eu/en/vacancies/vacancy-qualified-person-qp-industrial-pharmacist/
