Watton Hall is a privately owned independent search and selection firm that specialises in recruiting life‑science professionals across the pharmaceutical, biotech, CRO, and medical‑device sectors. We provide executive, permanent and contract recruitment services at the mid‑to‑senior level, supported by relocation and conference solutions. Our core value proposition is a cost‑effective partnership with HR teams, on‑site recruiters, RPOs and line managers, delivering high‑quality talent that meets the rigorous standards of the life‑science industry. With a focus on quality, speed and industry expertise, Watton Hall consistently sources candidates of the highest calibre for its clients.
Open Positions
Country Manager (Italy)
Bachelors degree in Pharmacy or Business Management, 5+ years of experience in pharmaceutical industry, strong business strategy skills
Clinical Supply Manager (cell and gene therapy)
Relevant experience in clinical trial/supply management or project management, university education in pharmacy, chemistry, or supply chain management, and strong understanding of GCP/GMP regulations
CMC Specialist
Minimum 3 years of experience in Regulatory Affairs, Bachelor's degree in chemistry, biology, or biochemistry, strong understanding of international regulations
COO
10+ years of executive leadership experience in the medical device industry, Lean Six Sigma / Blackbelt certification, fluent in German and English
Director Business Development EMEA and Distributor Management
Successful degree in medical technology, business administration or a comparable field with at least 6 years of European commercial/sales experience in a related area
Director, Regulatory Affairs Strategy
Bachelors degree in life sciences, experience in regulatory affairs, leadership experience
Apheresis and Infusion Operations Manager
Bachelors degree in Nursing, Healthcare Administration, or related field; Strong background in healthcare operations management; Excellent communication skills
Director, DMPK
PhD in Pharmacology, experience with regulatory requirements, and track record in PK studies
AD_D Biostatistics
5-10 years of experience in the pharmaceutical industry, with a background in overseeing a team and experience with health authorities and regulatory submissions
DMPK Team Lead
Ph.D. in DMPK, 5+ years of leadership experience, and successful project management from preclinical to clinical stages
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