Regulatory CMC Consultant

Based in Switzerland.
15 Years Biologics experience.
10 BLA Submissions.
Worked in: Rare diseases, Oncology, Infectious disease therapy areas.
Speaks: French, German and English.
Available end of November.

Regulatory CMC Consultant

Experience in development of CMC strategy for clinical phase programs (small molecules); Interaction with regulatory bodies, Technical CMC management, project management, Technology transfer and pharmaceutical process development (small molecules).
Available immediately.

Regulatory Affairs Consultant

Based in the UK.
20 Years Regulatory experience.
Small molecule expert.
Previous projects include: Interim head of regulatory, NDA submissions and post approval projects.
Available beginning November.

Regulatory Affairs Consultant

Experience in directives such as MDD 93/42/EEC, new European Regulation MDR 2017/745 and ICH/ GCP.
Significant experience in design, manufacture and conformity assessments of medical devices.
Submissions in: USA, China, Europe, Australia, Russia and Japan.
Speaks: English, French and Spanish.
Available Immediately.

Quality Consultant

Based in the UK.
Highly adaptable and detail-oriented professional with a strong background in pharmaceuticals and biologics development and manufacturing. My expertise lies in Supplier Development, Lead Auditing, Project Leadership, and Root Cause Analysis. They have successfully managed global projects and implemented effective Quality Management Systems.
Available Immediately

Quality Consultant

Based in the UK.
A proven experienced scientist & UKAS Certified Auditor of Laboratory Management Systems in Technical & Quality. Previous Management roles in Operations, Manufacturing, Medical device, Pharmaceutical, Wet Chemistry, Pathology, Biomolecular and Microbiology. Experience in leading pharmaceutical company to identifying, developing and leading continuous improvement through drugs batch release.
Available beginning of December

Quality Consultant

Based in the UK.
An experienced Quality Assurance (QA) Consultant with over 20 years of experience, specializing in project management, cross-sector expertise in Pharmaceuticals, Medical Devices, and Consumer Healthcare. Achievements include managing External Manufacturing Organization suppliers, implementing Approved Supplier Programs, and negotiating Technical Quality Agreements.
Available end of December.

Quality Consultant

Based in Switzerland.
Quality Assurance (QA) professional with over 18 years of experience in the pharmaceutical industry, specializing in GMP, GDP, and GxP areas. Proven track record of successful negotiation, structured planning, and organization. Their expertise encompasses managing international teams, conducting audits, and implementing robust quality assurance systems.
Speaks: Ukrainian, Russian, English and German.
Available end of November

Supply Chain Consultant

Based in the UK.
Over 30 years of experience with a proven track record of strategic vision and successful delivery of operational performance and profitability improvements.
Proficient in implementing and developing various systems, including SAP, JDE, Oracle, Formula 8, Relex-forecasting/MRP, data warehouse, and reporting.
Available mid November

Supply Chain Specialist

Based in Switzerland.
An experienced Supply Chain specialist with over 20 years experience who has a background in pharmaceuticals, biotech, and FMCG within global matrix organizations. Recognized for skills in defining and implementing supply chain strategies, the professional is known for cross-functional teamwork, a proactive and collaborative mindset.
Speaks: French and English.
Available end of December

Supply Chain Specialist

Based in Switzerland.
Expertise in managing international teams, conducting audits, and implementing robust quality assurance systems. Their experience spans roles such as Supplier Auditor, Quality Assurance Head, and Global Quality Assurance Head/Quality Assurance Manager. They have successfully overseen the development and implementation of quality assurance systems, conducted audits of partners and authority inspections, and managed various aspects of quality assurance in the pharmaceutical industry.
Speaks: English, Portuguese, French, German and Italian.
Available end of November

Supply Chain Manager

Based in Switzerland.
A seasoned supply chain professional with extensive experience in the pharmaceutical industry and FMCG. Armed with a master's degree in economics and certifications in APICS CPIM, Six Sigma Green Belt, and EJLog, you have showcased expertise in supply, demand, and inventory management, manufacturing planning, process improvement, project management, and ERP implementation.
Speaks: Russian, English, German and French.
Available immediately

CMC Consultant

Based in Switzerland.
A critical thinker with over 15 years of knowledge in pharmaceuticals, showcasing a successful track record and leadership in biologics drug development and manufacturing. Noted for strategic thinking, problem-solving, and analytical reasoning, the individual possesses a diverse skill set.
Speaks: Polish, English, German and Portuguese.
Available end of November.

Based in the UK.
A comprehensive background in Pharmacovigilance (PV) and drug safety across various roles and companies with over 13 years experience. Demonstrating expertise in signal detection, risk management, compliance coordination, and safety monitoring. With extensive experience in handling adverse event reports, managing safety databases, and contributing to the preparation of aggregate reports.
Speaks: English and Tagalog
Available mid November