Principal Registration Officer EU regs

This vacancy has now expired

Principal Registration Officer EU regs- Life Science – Permanent- Hybrid- Hatfield

The facility is a responsible for tablet manufacturing (OSD) and secondary packaging (blister packing and bottle primarily for tablets and capsules), and our client is looking for an Principal Registration Officer EU regs to help maintain manufacturing operations.

Principal Registration Officer EU regs Responsibilities:

Must have 5-10yrs experience of full lifecycle of existing or new product registrations including strategy/planning, registrations, monitoring, post marketing approvals, through to launching in accordance with EU regulations.
Must have experience mentoring / managing teams
Must have MRP/DCP experience
Experienced in MA applications and CMC changes
Pharma experience is prioritized over medical devices but mix of it would work.

Are you a good fit for a Principal Registration Officer EU regs? Get in touch with us today.

The candidate must have the rights to work in the location stated in the job advert.

Please note, Quanta part of QCS Staffing does not sponsor Visa applications.

To view Quanta's privacy policy, please visit our website

We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.

Engineering Director
Global Pharmaceutical firm

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Principal Registration Officer EU regs

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