Regulatory Recruitment Subject Matter Expert In Pharma & Biotech With Unprecedented Access To Excellent Candidates
As a Recruitment Specialists in Regulatory Affairs, we have a proven track record for securing the very best candidates for a role within an agreed time frame.
Specialising in Regulatory Affairs for the Pharmaceutical and Biotechnology sector, we have built an unprecedented following of excellent candidates each of whom we know well and trust only Turner Regulatory to introduce them to new opportunities that fit within their areas of specialisation, career trajectory and personal circumstances.
This is why, when we call, they trust that we are not wasting their time and have something of interest. In fact, we may well have placed them in their current role.
For clients, our USP means we access a large database of potential candidates who aren’t on the job market, and therefore a significant number of candidates cannot be sourced via regular job boards or without an introduction.
Typically, for each role we are entrusted with, we will have in excess of ten excellent candidates to put forward within a matter of days. For us, the right candidate is someone who, in addition to having the right qualifications and personality fit, has something interesting to bring to the role.
Our in-depth knowledge and close industry relationships allow us to fully understand the requirements of a role and make the correct candidate recommendations.
In addition to putting suitable candidates forward, my clients also trust me to feedback on the latest insights and trends within the industry so they stay competitive as an employer.
If you or your organisation are struggling to find the right candidate for a role, or you feel having someone like Turner Regulatory in your network would benefit you, we invite you to contact us. We believe our track record speaks for itself (see below).
Turner Regulatory specialises at placing permanent and contract roles within Pharmaceuticals, Biotechnology, CROs, Generics and OTC across the UK, Continental Europe, USA and beyond.
New Biotech. Director or Senior Director, Regulatory Affairs - Biologics/ATMP/Gene Therapies. Europe, UK, and USA. Point of contact with the Regulat
Associate Director, Regulatory Affairs, ATMP's/Cell Therapy/CAR-T, Clinical/Development & Strategy /
Associate Director, Regulatory Affairs, ATMP's/Cell Therapy/CAR-T, Clinical/Development & Strategy. Rare Diseases Regulatory Development, New Drug A
Associate Director, Regulatory Strategy / Clinical/Development / Complex Submissions - MAA's & New I
Associate Director, Regulatory Strategy Regulatory Strategy, Clinical/Development and Complex Submissions - MAA's & New Indications across European
Senior Associate Regulatory CMC - Biologics, top Biopharma Excellent opportunity for a Senior Associate Regulatory CMC, or an experienced Regulatory
Director Global Regulatory Affairs / Oncology / Strategy / Development / New MAA's & Indications / L
Director, Global Regulatory Affairs - Oncology. Biologic & Pharma Products. Leadership, Strategy, Clinical/Development, Complex/New MAA's/New Indicati
Associate Director Regulatory Affairs, Clinical Development. Regulatory Strategy, 'hands-on' and high-level Project Leading in European and US Markets
Director, Regulatory CMC - Fast-growing Biotech. Leadership, Strategy, Development, Registrations and Lifecycle management. Lead Scientific Advice m
Senior Regulatory Officer - Labelling Compliance Lead or Specialist This outstanding Labelling opportunity could represent the next stage in your ca
Senior Manager Regulatory CMC / ROW / Emerging Markets / Leading Biopharma Exciting Regulatory CMC role: this is a rare opportunity to join a fast-g
Manager, Core Global Labelling Strategy Remote/Hybrid Working This outstanding Labelling opportunity could represent the next stage in your career