- International Regulatory Strategy Product Specialist
Currently looking for a senior regulatory affairs professional with expert experience in Emerging and International markets to join a leading biotechnology company in Hampshire.
- PW 6335 Global Submission Specialist / Regulatory Submissions Project Manager
Opportunity for a Submissions Manager to join this Top 20 Pharma on a fixed term contract as our Client’s Global Regulatory Submissions Specialist. The role is office based in the South East, focuses on compliant submissions, Ectd standardisation and sits within a cross functional global team. Contract length is 6 months and strong likelihood to extend further.
- Regulatory and Quality Specialist
An opportunity has arisen for experienced Regulatory affairs professional to join a market leading Medical Device company based in Hampshire.
The company are global leader in Eye care products, having a strong worldwide presence, with aspirations of penetrating the US market. They are currently in a period of high and sustained growth, and are looking to expand their regulatory department to cope with the increased work load associated with getting new and existing products into new markets.
- Director - Regulatory Strategy Lead
European Regulatory Strategy, Product Lead - Biotech/Pharmaceutical - UK - Excellent salary, bonus and benefits packageIf you would like to apply for the position or wish to learn more about the role and company please call Mark on 0044 (0) 207 255 6665 or email your CV with a brief covering note to firstname.lastname@example.org
- Regulatory Affairs Specialist/Senior Regulatory Affairs Specialist - EMEA-122360
PPD is recruiting for Regulatory Affairs Specialists.
In this role you will provide regulatory advice and carry out projects in the provision of regulatory affairs services. You will also act as liaison with internal and external clients in the provision and marketing of regulatory affairs services. ...
- Regulatory Affairs Specialist - 12 Month Maternity Cover-120887
PPD has a new vacancy for a Regulatory Affairs Specialist. This opportunity is for 12 month maternity cover.
Position location will be in a PPD office where a regulatory team exists, and will depend upon candidate experience and business need.
In this role you will provide regulatory advice and carry out projects in the provision of regulatory affairs services. ...
- Associate Director, Regulatory Site Lead, Established Products & CMC (Chicago region USA)
Just Pharma are currently working on behalf of a leading company in the pharmaceutical industry looking for an experienced Associate Director, Regulatory Site Lead, Established Products & CMC to join their team.
- Regulatory Affairs Specialist Class I, II Medical Devices – Berlin – Permanent
If you are looking for a permanent role with progression opportunities in a multi-national company with impeccable reputation, apply for this position now with your most recent CV.
- Associate Director/Director /General Medicine Therapeutic Lead
A fantastic opportunity to working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level.
- QA/RA Specialist
Our client, a leading pharmaceutical company in South Dublin, have a vacancy for a QA/RA Specialist to join their team.