Alfasigma - IT - Administration

Manager, Regulatory Lead role in Morristown, US, driving regional regulatory strategy for low-complexity programs. Requires 3-5 years’ experience in regulatory affairs, IND/CTA submissions, and cross-functional drug development. Key responsibilities include regulatory document review, submission ...

Senior Specialist, HR Systems role in Milan, Italy. Act as the trusted SuccessFactors expert, driving HR technology strategy, governance, and user adoption. Requires 5–7 years HRIS experience, strong stakeholder advisory skills, and a customer-centric mindset. Enjoy a competitive salary, comprehe...

Senior Specialist, Global IT Network sought to design, secure, and manage enterprise and industrial networks across Italy (Pomezia, Milano, Alanno, Bologna). This role demands deep Cisco expertise (Catalyst, Nexus, Meraki), routing protocols, and firewalling in a regulated GxP/GMP environment. Yo...

Lead global labeling and regulatory policy strategy for a top pharma firm in Bologna, Italy. Drive FDA, EMA, and ICH compliance, oversee end-to-end labeling for the Innovative Rx portfolio, and influence global frameworks. Requires 10+ years in regulatory affairs, strong leadership, and an advanc...

Lead global CMC regulatory strategy for pharmaceutical and biologics across the product lifecycle. This senior role in Bologna, Milan, or Pomezia, Italy requires 15+ years of regulatory affairs expertise, deep knowledge of FDA/EMA/ICH guidelines, and a proven record of major filings. Drive submis...

Director, Clinical and Safety Quality sought to lead GCP/GVP compliance and QMS strategy for Phase II–IV trials in Mechelen, UK. Requires 10+ years pharma experience, 5+ in Clinical/PV Quality, and proven inspection readiness with regulators. Drive quality oversight, audits, and CRO management in...

Senior Manager, Commercial Training role in Morristown, NJ (hybrid). Drive innovative training programs for a leading US commercial team advancing non-viral chronic liver disease treatments. Requires 3+ years pharma/biotech experience, sales training background, and hepatology/gastroenterology kn...

Quality Validation Specialist sought in Pomezia, Italy, to ensure GMP compliance through data integrity governance and equipment qualification. Requires a Master’s in Chemistry or Engineering, 5+ years in pharma, and ALCOA+ expertise. Key duties include managing DIRAs, CAPAs, and audit support. O...

Seeking a skilled **Supply Planning Specialist** to join our ESO team in **Milan or Bologna, Italy**. You will manage external supplier products and inventory for a specific pharmaceutical line, utilizing **ERP systems (IBP preferred)**. The role demands strong analytical skills for 24-month purc...

Sr Associate, Manufacturing Regulatory Affairs role in Pomezia, Italy. Ensure regulatory compliance for CMC variations and manufacturing changes within a pharmaceutical environment. Requires a Chemistry or CTF degree, 1-2 years of regulatory experience, and fluency in English. Join a cross-functi...

Seeking a Clinical Data Management Manager in Milano. Lead data strategy and oversee outsourced DM activities across all clinical trial phases. Requires 7+ years' experience, EDC expertise, and strong knowledge of CDISC standards. Competitive salary and professional development opportunities.